US20230354690A1 - Organic electroluminescent materials and devices - Google Patents

Abstract

A composition including a first compound capable of functioning as a phosphorescent emitter in an OLED is provided. The first compound has at least one aromatic ring and at least one substituent R directly bonded to one of the at least one aromatic rings. Each substituent R has the formula of

where (a) G¹ is selected from NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; and G² is a non-aromatic polycyclic group; (b) G¹ is a direct bond; and G² is a non-aromatic spiro polycyclic group; or (c) G¹ is selected from direct bond, NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; G² is a non-aromatic polycyclic group; and R is directly bonded to a phenyl, pyridine, or triazine. R¹, R², and R³ are are a variety of substituents. Formulations and devices, such as an OLEDs, that include the first compound are also described.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
• This application is a continuation of co-pending U.S. Pat. Application No. 16/438,819, filed on Jun. 12, 2019, which is a continuation of U.S. Pat. Application No. 15/240,044, filed on Aug. 18, 2016, which claims priority to U.S. Provisional applications No. 62/213,757, filed on Sep. 3, 2015; No. 62/232,194, filed on Sep. 24, 2015; No. 62/291,960, filed on Feb. 5, 2016; No. 62/322,510, filed on Apr. 14, 2016; and No. 62/330,412 filed on May 2, 2016, the entire contents of which are incorporated herein by reference.
PARTIES TO A JOINT RESEARCH AGREEMENT
• The claimed invention was made by, on behalf of, and/or in connection with one or more of the following parties to a joint university corporation research agreement: The Regents of the University of Michigan, Princeton University, University of Southern California, and the Universal Display Corporation. The agreement was in effect on and before the date the claimed invention was made, and the claimed invention was made as a result of activities undertaken within the scope of the agreement.
FIELD
• The present invention relates to compounds for use as emitters, and devices, such as organic light emitting diodes, including the same.
BACKGROUND
• Opto-electronic devices that make use of organic materials are becoming increasingly desirable for a number of reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting diodes/devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials. For example, the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.
• OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, illumination, and backlighting. Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.
• One application for phosphorescent emissive molecules is a full color display. Industry standards for such a display call for pixels adapted to emit particular colors, referred to as “saturated” colors. In particular, these standards call for saturated red, green, and blue pixels. Alternatively the OLED can be designed to emit white light. In conventional liquid crystal displays emission from a white backlight is filtered using absorption filters to produce red, green and blue emission. The same technique can also be used with OLEDs.The white OLED can be either a single EML device or a stack structure. Color may be measured using CIE coordinates, which are well known to the art.
• One example of a green emissive molecule is tris(2-phenylpyridine) iridium, denoted Ir(ppy)₃, which has the following structure:
• 
• In this, and later figures herein, we depict the dative bond from nitrogen to metal (here, Ir) as a straight line.
• As used herein, the term “organic” includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices. “Small molecule” refers to any organic material that is not a polymer, and “small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances. For example, using a long chain alkyl group as a substituent does not remove a molecule from the “small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter. A dendrimer may be a “small molecule,” and it is believed that all dendrimers currently used in the field of OLEDs are small molecules.
• As used herein, “top” means furthest away from the substrate, while “bottom” means closest to the substrate. Where a first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is “in contact with” the second layer. For example, a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.
• As used herein, “solution processible” means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.
• A ligand may be referred to as “photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material. A ligand may be referred to as “ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.
• As used herein, and as would be generally understood by one skilled in the art, a first “Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is “greater than” or “higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative). On a conventional energy level diagram, with the vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. A “higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a “lower” HOMO or LUMO energy level.
• As used herein, and as would be generally understood by one skilled in the art, a first work function is “greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a “higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.
• More details on OLEDs, and the definitions described above, can be found in U.S. Pat. No. 7,279,704, which is incorporated herein by reference in its entirety.
SUMMARY
• According to one embodiment, a composition comprising a first compound is provided. In the composition, the first compound is capable of functioning as a phosphorescent emitter in an organic light emitting device at room temperature, and the first compound has at least one aromatic ring and at least one substituent R, where each of the at least one substituent R is directly bonded to one of the at least one aromatic rings. Each of the at least one substituent R has the formula of
• 
• where :
• (a) G¹ is selected from the group consisting of NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; and G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³;
• (b) G¹ is a direct bond; and G² is a non-aromatic spiro polycyclic group, which can be further substituted by one or more R³; or
• (c) G¹ is selected from the group consisting of: direct bond, NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³; and R is directly bonded to an aromatic ring selected from the group consisting of phenyl, pyridine, and triazine, which can be further fused to other rings;
• R¹, R², and R³ are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and
• each G¹ and G² can be independently, partially or fully deuterated.
• According to another embodiment, an organic light emitting diode/device (OLED) is also provided. The OLED can include an anode, a cathode, and an organic layer, disposed between the anode and the cathode. The organic layer can include the first compound as described herein. According to yet another embodiment, the organic light emitting device is incorporated into one or more device selected from a consumer product, an electronic component module, and/or a lighting panel.
• According to yet another embodiment, a formulation containing the first compound as described herein is provided.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 shows an organic light emitting device.
• FIG. 2 shows an inverted organic light emitting device that does not have a separate electron transport layer.
DETAILED DESCRIPTION
• Generally, an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode. When a current is applied, the anode injects holes and the cathode injects electrons into the organic layer(s). The injected holes and electrons each migrate toward the oppositely charged electrode. When an electron and hole localize on the same molecule, an “exciton,” which is a localized electron-hole pair having an excited energy state, is formed. Light is emitted when the exciton relaxes via a photoemissive mechanism. In some cases, the exciton may be localized on an excimer or an exciplex. Non-radiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.
• The initial OLEDs used emissive molecules that emitted light from their singlet states (“fluorescence”) as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.
• More recently, OLEDs having emissive materials that emit light from triplet states (“phosphorescence”) have been demonstrated. Baldo et al., “Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices,” Nature, vol. 395, 151-154, 1998; (“Baldo-I”) and Baldo et al., “Very high-efficiency green organic light-emitting devices based on electrophosphorescence,” Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999) (“Baldo-II”), are incorporated by reference in their entireties. Phosphorescence is described in more detail in U.S. Pat. No. 7,279,704 at cols. 5-6, which are incorporated by reference.
• FIG. 1 shows an organic light emitting device 100. The figures are not necessarily drawn to scale. Device 100 may include a substrate 110, an anode 115, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, a cathode 160, and a barrier layer 170. Cathode 160 is a compound cathode having a first conductive layer 162 and a second conductive layer 164. Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in US 7,279,704 at cols. 6-10, which are incorporated by reference.
• More examples for each of these layers are available. For example, a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety. An example of a p-doped hole transport layer is m-MTDATA doped with F₄-TCNQ at a molar ratio of 50:1, as disclosed in U.S. Pat. Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which is incorporated by reference in its entirety. An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1:1, as disclosed in U.S. Pat. Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entireties, disclose examples of cathodes including compound cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electrically-conductive, sputter-deposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Pat. Application Publication No. 2003/0230980, which are incorporated by reference in their entireties. Examples of injection layers are provided in U.S. Pat. Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of protective layers may be found in U.S. Pat. Application Publication No. 2004/0174116, which is incorporated by reference in its entirety.
• FIG. 2 shows an inverted OLED 200. The device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230. Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an “inverted” OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200. FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.
• The simple layered structure illustrated in FIGS. 1 and 2 is provided by way of nonlimiting example, and it is understood that embodiments of the invention may be used in connection with a wide variety of other structures. The specific materials and structures described are exemplary in nature, and other materials and structures may be used. Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used. Also, the layers may have various sublayers. The names given to the various layers herein are not intended to be strictly limiting. For example, in device 200, hole transport layer 225 transports holes and injects holes into emissive layer 220, and may be described as a hole transport layer or a hole injection layer. In one embodiment, an OLED may be described as having an “organic layer” disposed between a cathode and an anode. This organic layer may comprise a single layer, or may further comprise multiple layers of different organic materials as described, for example, with respect to FIGS. 1 and 2 .
• Structures and materials not specifically described may also be used, such as OLEDs comprised of polymeric materials (PLEDs) such as disclosed in U.S. Pat. No. 5,247,190 to Friend et al., which is incorporated by reference in its entirety. By way of further example, OLEDs having a single organic layer may be used. OLEDs may be stacked, for example as described in U.S. Pat. No. 5,707,745 to Forrest et al, which is incorporated by reference in its entirety. The OLED structure may deviate from the simple layered structure illustrated in FIGS. 1 and 2 . For example, the substrate may include an angled reflective surface to improve out-coupling, such as a mesa structure as described in U.S. Pat. No. 6,091,195 to Forrest et al., and/or a pit structure as described in U.S. Pat. No. 5,834,893 to Bulovic et al., which are incorporated by reference in their entireties.
• Unless otherwise specified, any of the layers of the various embodiments may be deposited by any suitable method. For the organic layers, preferred methods include thermal evaporation, ink-jet, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102 to Forrest et al., which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. Pat. No. 7,431,968, which is incorporated by reference in its entirety. Other suitable deposition methods include spin coating and other solution based processes. Solution based processes are preferably carried out in nitrogen or an inert atmosphere. For the other layers, preferred methods include thermal evaporation. Preferred patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as ink-jet and OVJD. Other methods may also be used. The materials to be deposited may be modified to make them compatible with a particular deposition method. For example, substituents such as alkyl and aryl groups, branched or unbranched, and preferably containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having 20 carbons or more may be used, and 3-20 carbons is a preferred range. Materials with asymmetric structures may have better solution processibility than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize. Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.
• Devices fabricated in accordance with embodiments of the present invention may further optionally comprise a barrier layer. One purpose of the barrier layer is to protect the electrodes and organic layers from damaging exposure to harmful species in the environment including moisture, vapor and/or gases, etc. The barrier layer may be deposited over, under or next to a substrate, an electrode, or over any other parts of a device including an edge. The barrier layer may comprise a single layer, or multiple layers. The barrier layer may be formed by various known chemical vapor deposition techniques and may include compositions having a single phase as well as compositions having multiple phases. Any suitable material or combination of materials may be used for the barrier layer. The barrier layer may incorporate an inorganic or an organic compound or both. The preferred barrier layer comprises a mixture of a polymeric material and a non-polymeric material as described in U.S. Pat. No. 7,968,146, PCT Pat. Application Nos. PCT/US2007/023098 and PCT/US2009/042829, which are herein incorporated by reference in their entireties. To be considered a “mixture”, the aforesaid polymeric and non-polymeric materials comprising the barrier layer should be deposited under the same reaction conditions and/or at the same time. The weight ratio of polymeric to non-polymeric material may be in the range of 95:5 to 5:95. The polymeric material and the non-polymeric material may be created from the same precursor material. In one example, the mixture of a polymeric material and a non-polymeric material consists essentially of polymeric silicon and inorganic silicon.
• Devices fabricated in accordance with embodiments of the invention can be incorporated into a wide variety of electronic component modules (or units) that can be incorporated into a variety of electronic products or intermediate components. Examples of such electronic products or intermediate components include display screens, lighting devices such as discrete light source devices or lighting panels, etc. that can be utilized by the end-user product manufacturers. Such electronic component modules can optionally include the driving electronics and/or power source(s). Devices fabricated in accordance with embodiments of the invention can be incorporated into a wide variety of consumer products that have one or more of the electronic component modules (or units) incorporated therein. Such consumer products would include any kind of products that include one or more light source(s) and/or one or more of some type of visual displays. Some examples of such consumer products include flat panel displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, laser printers, telephones, cell phones, tablets, phablets, personal digital assistants (PDAs), wearable device, laptop computers, digital cameras, camcorders, viewfinders, micro-displays, 3-D displays, vehicles, a large area wall, theater or stadium screen, or a sign. Various control mechanisms may be used to control devices fabricated in accordance with the present invention, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18° C. to 30° C., and more preferably at room temperature (20-25° C.), but could be used outside this temperature range, for example, from -40° C. to + 80° C.
• The materials and structures described herein may have applications in devices other than OLEDs. For example, other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures. More generally, organic devices, such as organic transistors, may employ the materials and structures.
• In the field of organic chemistry, a polycyclic compound is an organic chemical featuring several closed rings of atoms, primarily carbon. These ring substructures comprises cycloalkanes, aromatics, and other ring types. They come in sizes of three atoms and upward, and in combinations of linkages that include tethering (such as in biaryls), fusing (edge-to-edge, such as in anthracene and steroids), links via a single atom (such as in spiro compounds), and bridged cyclics such as adamantane. Though “poly” literally means “many”, in this context polycyclic includes smaller rings such as bicyclic, tricyclic, and tetracyclic.
• The term “halo,” “halogen,” or “halide” as used herein includes fluorine, chlorine, bromine, and iodine.
• The term “alkyl” as used herein contemplates both straight and branched chain alkyl radicals. Preferred alkyl groups are those containing from one to fifteen carbon atoms and includes methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl,and the like. Additionally, the alkyl group may be optionally substituted.
• The term “cycloalkyl” as used herein contemplates cyclic alkyl radicals. Preferred cycloalkyl groups are those containing 3 to 10 ring carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, adamantyl, and the like. Additionally, the cycloalkyl group may be optionally substituted.
• The term “alkenyl” as used herein contemplates both straight and branched chain alkene radicals. Preferred alkenyl groups are those containing two to fifteen carbon atoms. Additionally, the alkenyl group may be optionally substituted.
• The term “alkynyl” as used herein contemplates both straight and branched chain alkyne radicals. Preferred alkynyl groups are those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted.
• The terms “aralkyl” or “arylalkyl” as used herein are used interchangeably and contemplate an alkyl group that has as a substituent an aromatic group. Additionally, the aralkyl group may be optionally substituted.
• The term “heterocyclic group” as used herein contemplates aromatic and non-aromatic cyclic radicals. Hetero-aromatic cyclic radicals also means heteroaryl. Preferred hetero-non-aromatic cyclic groups are those containing 3 to 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperdino, pyrrolidino, and the like, and cyclic ethers, such as tetrahydrofuran, tetrahydropyran, and the like. Additionally, the heterocyclic group may be optionally substituted.
• The term “aryl” or “aromatic group” as used herein contemplates single-ring groups and polycyclic ring systems. The polycyclic rings may have two or more rings in which two carbons are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is aromatic, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred aryl groups are those containing six to thirty carbon atoms, preferably six to twenty carbon atoms, more preferably six to twelve carbon atoms. Especially preferred is an aryl group having six carbons, ten carbons or twelve carbons. Suitable aryl groups include phenyl, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene, preferably phenyl, biphenyl, triphenyl, triphenylene, fluorene, and naphthalene. Additionally, the aryl group may be optionally substituted.
• The term “heteroaryl” as used herein contemplates single-ring hetero-aromatic groups that may include from one to five heteroatoms. The term heteroaryl also includes polycyclic hetero-aromatic systems having two or more rings in which two atoms are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred heteroaryl groups are those containing three to thirty carbon atoms, preferably three to twenty carbon atoms, more preferably three to twelve carbon atoms. Suitable heteroaryl groups include dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine, preferably dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, triazine, benzimidazole, 1,2-azaborine, 1,3-azaborine, 1,4-azaborine, borazine, and aza-analogs thereof. Additionally, the heteroaryl group may be optionally substituted.
• The alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, heterocyclic group, aryl, and heteroaryl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
• As used herein, “substituted” indicates that a substituent other than H is bonded to the relevant position, such as carbon. Thus, for example, where R¹ is mono-substituted, then one R¹ must be other than H. Similarly, where R¹ is di-substituted, then two of R¹ must be other than H. Similarly, where R¹ is unsubstituted, R¹ is hydrogen for all available positions.
• The “aza” designation in the fragments described herein, i.e. aza-dibenzofuran, aza-dibenzothiophene, etc. means that one or more of the C-H groups in the respective fragment can be replaced by a nitrogen atom, for example, and without any limitation, azatriphenylene encompasses both dibenzo[f,h]quinoxaline and dibenzo[f,h]quinoline. One of ordinary skill in the art can readily envision other nitrogen analogs of the aza-derivatives described above, and all such analogs are intended to be encompassed by the terms as set forth herein.
• It is to be understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. phenyl, phenylene, naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g. benzene, naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent.
• According to one embodiment, a composition comprising a first compound is described. In the composition, the first compound is capable of functioning as a phosphorescent emitter in an organic light emitting device at room temperature, and the first compound has at least one aromatic ring and at least one substituent R, where each of the at least one substituent R is directly bonded to one of the at least one aromatic rings. Each of the at least one substituent R has the formula of
• 
• where :
• (a) G¹ is selected from the group consisting of NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; and G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³;
• (b) G¹ is a direct bond; and G² is a non-aromatic spiro polycyclic group, which can be further substituted by one or more R³; or
• (c) G¹ is selected from the group consisting of: direct bond, NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³; and R is directly bonded to an aromatic ring selected from the group consisting of phenyl, pyridine, and triazine, which can be further fused to other rings;
• wherein R¹, R², and R³ are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and
• each G¹ and G² can be independently, partially or fully deuterated.
• In some embodiments, G¹ is SiR¹R². In some embodiments, G¹ is NR¹. In some embodiments, G¹ is alkyl. In some such embodiments, G¹ is selected from the gourp consisiting of divalent methyl, ethyl, propyl, and butyl. In some embodiments, G¹ is fully or partially deuterated.
• In some embodiments, G² is polycyclic alkyl. In some embodiments, G² is carborane. In some embodiments, G² contains at least one heteroatom. In some embodiments, G² includes at least one heterocyclic group.
• In some embodiments, the first compound is capable of emitting light from a triplet excited state to a ground singlet state at room temperature.
• In some embodiments, the first compound is a metal coordination complex having a metal-carbon bond. In some such embodiments, the metal is selected from the group consisting of Ir, Rh, Re, Ru, Os, Pt, Au, and Cu. In some such embodiments, the metal is Ir, while the metal is Pt is other embodiments.
• In some embodiments, the first compound has the formula of M(L¹)_x(L²)_y(L³)_z, where:
• L¹, L² and L³ can be the same or different;
• x is 1, 2, or 3;
• y is 0, 1, or 2;
• z is 0, 1, or 2;
• x+y+z is the oxidation state of the metal M;
• L¹, L² and L³ are each independently selected from the group consisting of:
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• , and
• 
• each X¹ to X¹⁷ are independently selected from the group consisting of carbon and nitrogen;
• X is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO₂, CR′R″, SiR′R″, and GeR′R″;
• each R′ and R″ is independently, optionally fused or joined to form a ring;
• each R_a, R_b, R_c, and R_d independently represents from mono substitution to the maximum possible number of substitutions, or no substitution;
• each R′, R″, R_a, R_b, R_c, and R_d is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;
• any two adjacent substitutents of R_a, R_b, R_c, and R_d are optionally fused or joined to form a ring or form a multidentate ligand; and
• at least one of the R_a, R_b, R_c, and R_d includes the at least one substituent R.
• In some embodiments where the first compound has the structure M(L¹)_x(L²)_y(L³)_z, the first compound has the formula of Ir(L¹)₂(L²). In some such embodiments, L¹ has the formula selected from the group consisting of:
• 
• 
• 
• and
• 
• and L² has the formula
• 
• In some such embodiments, L² has the formula:
• 
• where:
• R_e, R_f, R_h, and R_i are independently selected from group consisting of alkyl, cycloalkyl, aryl, and heteroaryl;
• at least one of R_e, R_f, R_h, and R_i has at least two carbon atoms; and
• R_g is selected from group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
• In some embodiments where the first compound has the formula of Ir(L¹)₂(L²), ligands L¹ and L² are different and each independently selected from the group consisting of:
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• , and
• 
• In some embodiments where the first compound has the formula of Ir(L¹)₂(L²), ligands L¹ and L² are each independently selected from the group consisting of:
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• , and
• 
• In some embodiments where the first compound has the structure M(L¹)_x(L²)_y(L³)_z, the first compound has the formula of Pt(L¹)₂ or Pt(L¹)(L²). In some embodiments where the first compound has the formula of Pt(L¹)₂ or Pt(L¹)(L²), one L¹ is connected to the other L¹ or L² to form a tetradentate ligand.
• In some embodiments where the first compound has the structure M(L¹)_x(L²)_y(L³)_z, at least one of R_a, R_b, R_c, and R_d includes an alkyl or cycloalkyl group that is partially or fully deuterated.
• In some embodiments, G² is selected from the group consisting of:
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• In some embodiments, each of the at least one substituent R is independently selected from the group consisting of:
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• , and
• 
• In some embodiments where the first compound has the structure M(L¹)_x(L²)_y(L³)_z,, at least one of L¹, L², and L³ is selected from the group consisting of:
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• 
• , and
• 
• In some embodiments where the first compound has the formula of Ir(L¹)₂(L²), ligands L¹ and L² are different and each independently selected from the group consisting of:
• 
• and
• 
• In some embodiments where the first compound has the formula of M(L¹)_x(L²)_y(L³)_z, ligand L¹ is L_A having the following structure:
• 
• selected from the group consisting of L_A1 to L_A2480 as listed below:

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1	RG1	H	H	H	H	H	LA1241	CD3	H	RG58	H	H	H
  LA2	RG2	H	H	H	H	H	LA1242	CD3	H	RG59	H	H	H
  LA3	RG3	H	H	H	H	H	LA1243	CD3	H	RG60	H	H	H
  LA4	RG4	H	H	H	H	H	LA1244	CD3	H	RG61	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA5	RG5	H	H	H	H	H	LA1245	CD3	H	RG62	H	H	H
  LA6	RG6	H	H	H	H	H	LA1246	CD3	H	RG63	H	H	H
  LA7	RG7	H	H	H	H	H	LA1247	CD3	H	RG64	H	H	H
  LA8	RG8	H	H	H	H	H	LA1248	CD3	H	RG65	H	H	H
  LA9	RG9	H	H	H	H	H	LA1249	CD3	H	RG66	H	H	H
  LA10	RG10	H	H	H	H	H	LA1250	CD3	H	RG67	H	H	H
  LA11	RG11	H	H	H	H	H	LA1251	CD3	H	RG68	H	H	H
  LA12	RG12	H	H	H	H	H	LA1252	CD3	H	RG69	H	H	H
  LA13	RG13	H	H	H	H	H	LA1253	CD3	H	RG70	H	H	H
  LA14	RG14	H	H	H	H	H	LA1254	CD3	H	RG71	H	H	H
  LA15	RG15	H	H	H	H	H	LA1255	CD3	H	RG72	H	H	H
  LA16	RG16	H	H	H	H	H	LA1256	CD3	H	RG73	H	H	H
  LA17	RG17	H	H	H	H	H	LA1257	CD3	H	RG74	H	H	H
  LA18	RG18	H	H	H	H	H	LA1258	CD3	H	RG75	H	H	H
  LA19	RG19	H	H	H	H	H	LA1259	CD3	H	RG76	H	H	H
  LA20	RG20	H	H	H	H	H	LA1260	CD3	H	RG77	H	H	H
  LA21	RG21	H	H	H	H	H	LA1261	CD3	H	RG78	H	H	H
  LA22	RG22	H	H	H	H	H	LA1262	CD3	H	RG79	H	H	H
  LA23	RG23	H	H	H	H	H	LA1263	CD3	H	RG80	H	H	H
  LA24	RG24	H	H	H	H	H	LA1264	CD3	H	RG81	H	H	H
  LA25	RG25	H	H	H	H	H	LA1265	CD3	H	RG82	H	H	H
  LA26	RG26	H	H	H	H	H	LA1266	CD3	H	RG83	H	H	H
  LA27	RG27	H	H	H	H	H	LA1267	CD3	H	RG84	H	H	H
  LA28	RG28	H	H	H	H	H	LA1268	CD3	H	RG85	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA29	RG29	H	H	H	H	H	LA1269	CD3	H	RG86	H	H	H
  LA30	RG30	H	H	H	H	H	LA1270	CD3	H	RG87	H	H	H
  LA31	RG31	H	H	H	H	H	LA1271	CD3	H	RG88	H	H	H
  LA32	RG32	H	H	H	H	H	LA1272	CD3	H	RG89	H	H	H
  LA33	RG33	H	H	H	H	H	LA1273	CD3	H	RG90	H	H	H
  LA34	RG34	H	H	H	H	H	LA1274	CD3	H	RG91	H	H	H
  LA35	RG35	H	H	H	H	H	LA1275	CD3	H	RG92	H	H	H
  LA36	RG36	H	H	H	H	H	LA1276	CD3	H	RG93	H	H	H
  LA37	RG37	H	H	H	H	H	LA1277	CD3	H	RG94	H	H	H
  LA38	RG38	H	H	H	H	H	LA1278	CD3	H	RG95	H	H	H
  LA39	RG39	H	H	H	H	H	LA1279	CD3	H	RG96	H	H	H
  LA40	RG40	H	H	H	H	H	LA1280	CD3	H	RG97	H	H	H
  LA41	RG41	H	H	H	H	H	LA1281	CD3	H	RG98	H	H	H
  LA42	RG42	H	H	H	H	H	LA1282	CD3	H	RG99	H	H	H
  LA43	RG43	H	H	H	H	H	LA1283	CD3	H	RG100	H	H	H
  LA44	RG44	H	H	H	H	H	LA1284	CD3	H	RG101	H	H	H
  LA45	RG45	H	H	H	H	H	LA1285	CD3	H	RG102	H	H	H
  LA46	RG46	H	H	H	H	H	LA1286	CD3	H	RG103	H	H	H
  LA47	RG47	H	H	H	H	H	LA1287	CD3	H	RG104	H	H	H
  LA48	RG48	H	H	H	H	H	LA1288	CD3	H	RG105	H	H	H
  LA49	RG49	H	H	H	H	H	LA1289	CD3	H	RG106	H	H	H
  LA50	RG50	H	H	H	H	H	LA1290	CD3	H	RG107	H	H	H
  LA51	RG51	H	H	H	H	H	LA1291	CD3	H	RG108	H	H	H
  LA52	RG52	H	H	H	H	H	LA1292	CD3	H	RG109	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA53	RG53	H	H	H	H	H	LA1293	CD3	H	RG110	H	H	H
  LA54	RG54	H	H	H	H	H	LA1294	CD3	H	RG111	H	H	H
  LA55	RG55	H	H	H	H	H	LA1295	CD3	H	RG112	H	H	H
  LA56	RG56	H	H	H	H	H	LA1296	CD3	H	RG113	H	H	H
  LA57	RG57	H	H	H	H	H	LA1297	CD3	H	RG114	H	H	H
  LA58	RG58	H	H	H	H	H	LA1298	CD3	H	RG115	H	H	H
  LA59	RG59	H	H	H	H	H	LA1299	CD3	H	RG116	H	H	H
  LA60	RG60	H	H	H	H	H	LA1300	CD3	H	RG117	H	H	H
  LA61	RG61	H	H	H	H	H	LA1301	CD3	H	RG118	H	H	H
  LA62	RG62	H	H	H	H	H	LA1302	CD3	H	RG119	H	H	H
  LA63	RG63	H	H	H	H	H	LA1303	CD3	H	RG120	H	H	H
  LA64	RG64	H	H	H	H	H	LA1304	CD3	H	RG121	H	H	H
  LA65	RG65	H	H	H	H	H	LA1305	CD3	H	RG122	H	H	H
  LA66	RG66	H	H	H	H	H	LA1306	CD3	H	RG123	H	H	H
  LA67	RG67	H	H	H	H	H	LA1307	CD3	H	RG124	H	H	H
  LA68	RG68	H	H	H	H	H	LA1308	CD3	H	RG125	H	H	H
  LA69	RG69	H	H	H	H	H	LA1309	CD3	H	RG126	H	H	H
  LA70	RG70	H	H	H	H	H	LA1310	CD3	H	RG127	H	H	H
  LA71	RG71	H	H	H	H	H	LA1311	CD3	H	RG128	H	H	H
  LA72	RG72	H	H	H	H	H	LA1312	CD3	H	RG129	H	H	H
  LA73	RG73	H	H	H	H	H	LA1313	CD3	H	RG130	H	H	H
  LA74	RG74	H	H	H	H	H	LA1314	CD3	H	RG131	H	H	H
  LA75	RG75	H	H	H	H	H	LA1315	CD3	H	RG132	H	H	H
  LA76	RG76	H	H	H	H	H	LA1316	CD3	H	RG133	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA77	RG77	H	H	H	H	H	LA1317	CD3	H	RG134	H	H	H
  LA78	RG78	H	H	H	H	H	LA1318	CD3	H	RG135	H	H	H
  LA79	RG79	H	H	H	H	H	LA1319	CD3	H	RG136	H	H	H
  LA80	RG80	H	H	H	H	H	LA1320	CD3	H	RG137	H	H	H
  LA81	RG81	H	H	H	H	H	LA1321	CD3	H	RG138	H	H	H
  LA82	RG82	H	H	H	H	H	LA1322	CD3	H	RG139	H	H	H
  LA83	RG83	H	H	H	H	H	LA1323	CD3	H	RG140	H	H	H
  LA84	RG84	H	H	H	H	H	LA1324	CD3	H	RG141	H	H	H
  LA85	RG85	H	H	H	H	H	LA13 25	CD3	H	RG142	H	H	H
  LA86	RG86	H	H	H	H	H	LA1326	CD3	H	RG143	H	H	H
  LA87	RG87	H	H	H	H	H	LA1327	CD3	H	RG144	H	H	H
  LA88	RG88	H	H	H	H	H	LA1328	CD3	H	RG145	H	H	H
  LA89	RG89	H	H	H	H	H	LA1329	CD3	H	RG146	H	H	H
  LA90	RG90	H	H	H	H	H	LA1330	CD3	H	RG147	H	H	H
  LA91	RG91	H	H	H	H	H	LA1331	CD3	H	RG148	H	H	H
  LA92	RG92	H	H	H	H	H	LA1332	CD3	H	RG149	H	H	H
  LA93	RG93	H	H	H	H	H	LA1333	CD3	H	RG150	H	H	H
  LA94	RG94	H	H	H	H	H	LA1334	CD3	H	RG151	H	H	H
  LA95	RG95	H	H	H	H	H	LA1335	CD3	H	RG152	H	H	H
  LA96	RG96	H	H	H	H	H	LA1336	CD3	H	RG153	H	H	H
  LA97	RG97	H	H	H	H	H	LA1337	CD3	H	RG154	H	H	H
  LA98	RG98	H	H	H	H	H	LA1338	CD3	H	RG155	H	H	H
  LA99	RG99	H	H	H	H	H	LA1339	CD3	H	RG156	H	H	H
  LA100	RG100	H	H	H	H	H	LA1340	CD3	H	RG157	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA101	RG101	H	H	H	H	H	LA1341	CD3	H	RG158	H	H	H
  LA102	RG102	H	H	H	H	H	LA1342	CD3	H	RG159	H	H	H
  LA103	RG103	H	H	H	H	H	LA1343	CD3	H	RG160	H	H	H
  LA104	RG104	H	H	H	H	H	LA1344	CD3	H	RG161	H	H	H
  LA105	RG105	H	H	H	H	H	LA1345	CD3	H	RG162	H	H	H
  LA106	RG106	H	H	H	H	H	LA1346	CD3	H	RG163	H	H	H
  LA107	RG107	H	H	H	H	H	LA1347	CD3	H	RG164	H	H	H
  LA108	RG108	H	H	H	H	H	LA1348	CD3	H	RG165	H	H	H
  LA109	RG109	H	H	H	H	H	LA1349	CD3	H	RG166	H	H	H
  LA110	RG110	H	H	H	H	H	LA1350	CD3	H	RG167	H	H	H
  LA111	RG111	H	H	H	H	H	LA1351	CD3	H	RG168	H	H	H
  LA112	RG112	H	H	H	H	H	LA1352	CD3	H	RG169	H	H	H
  LA113	RG113	H	H	H	H	H	LA1353	H	CD3	RG1	H	H	H
  LA114	RG114	H	H	H	H	H	LA1354	H	CD3	RG2	H	H	H
  LA115	RG115	H	H	H	H	H	LA1355	H	CD3	RG3	H	H	H
  LA116	RG116	H	H	H	H	H	LA1356	H	CD3	RG4	H	H	H
  LA117	RG117	H	H	H	H	H	LA1357	H	CD3	RG5	H	H	H
  LA118	RG118	H	H	H	H	H	LA1358	H	CD3	RG6	H	H	H
  LA119	RG119	H	H	H	H	H	LA1359	H	CD3	RG7	H	H	H
  LA120	RG120	H	H	H	H	H	LA1360	H	CD3	RG8	H	H	H
  LA121	RG121	H	H	H	H	H	LA1361	H	CD3	RG9	H	H	H
  LA122	RG122	H	H	H	H	H	LA1362	H	CD3	RG10	H	H	H
  LA123	RG123	H	H	H	H	H	LA1363	H	CD3	RG11	H	H	H
  LA124	RG124	H	H	H	H	H	LA1364	H	CD3	RG12	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA125	RG125	H	H	H	H	H	LA1365	H	CD3	RG13	H	H	H
  LA126	RG126	H	H	H	H	H	LA1366	H	CD3	RG14	H	H	H
  LA127	RG127	H	H	H	H	H	LA1367	H	CD3	RG15	H	H	H
  LA128	RG128	H	H	H	H	H	LA1368	H	CD3	RG16	H	H	H
  LA129	RG129	H	H	H	H	H	LA1369	H	CD3	RG17	H	H	H
  LA130	RG130	H	H	H	H	H	LA1370	H	CD3	RG18	H	H	H
  LA131	RG131	H	H	H	H	H	LA1371	H	CD3	RG19	H	H	H
  LA132	RG132	H	H	H	H	H	LA1372	H	CD3	RG20	H	H	H
  LA133	RG133	H	H	H	H	H	LA1373	H	CD3	RG21	H	H	H
  LA134	RG134	H	H	H	H	H	LA1374	H	CD3	RG22	H	H	H
  LA135	RG135	H	H	H	H	H	LA1375	H	CD3	RG23	H	H	H
  LA136	RG136	H	H	H	H	H	LA1376	H	CD3	RG24	H	H	H
  LA137	RG137	H	H	H	H	H	LA1377	H	CD3	RG25	H	H	H
  LA138	RG138	H	H	H	H	H	LA1378	H	CD3	RG26	H	H	H
  LA139	RG139	H	H	H	H	H	LA1379	H	CD3	RG27	H	H	H
  LA140	RG140	H	H	H	H	H	LA1380	H	CD3	RG28	H	H	H
  LA141	RG141	H	H	H	H	H	LA1381	H	CD3	RG29	H	H	H
  LA142	RG142	H	H	H	H	H	LA1382	H	CD3	RG30	H	H	H
  LA143	RG143	H	H	H	H	H	LA1383	H	CD3	RG31	H	H	H
  LA144	RG144	H	H	H	H	H	LA1384	H	CD3	RG32	H	H	H
  LA145	RG145	H	H	H	H	H	LA1385	H	CD3	RG33	H	H	H
  LA146	RG146	H	H	H	H	H	LA1386	H	CD3	RG34	H	H	H
  LA147	RG147	H	H	H	H	H	LA1387	H	CD3	RG35	H	H	H
  LA148	RG148	H	H	H	H	H	LA1388	H	CD3	RG36	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA149	RG149	H	H	H	H	H	LA1389	H	CD3	RG37	H	H	H
  LA150	RG150	H	H	H	H	H	LA1390	H	CD3	RG38	H	H	H
  LA151	RG151	H	H	H	H	H	LA1391	H	CD3	RG39	H	H	H
  LA152	RG152	H	H	H	H	H	LA1392	H	CD3	RG40	H	H	H
  LA153	RG153	H	H	H	H	H	LA1393	H	CD3	RG41	H	H	H
  LA154	RG154	H	H	H	H	H	LA1394	H	CD3	RG42	H	H	H
  LA155	RG155	H	H	H	H	H	LA1395	H	CD3	RG43	H	H	H
  LA156	RG156	H	H	H	H	H	LA1396	H	CD3	RG44	H	H	H
  LA157	RG157	H	H	H	H	H	LA1397	H	CD3	RG45	H	H	H
  LA158	RG158	H	H	H	H	H	LA1398	H	CD3	RG46	H	H	H
  LA159	RG159	H	H	H	H	H	LA1399	H	CD3	RG47	H	H	H
  LA160	RG160	H	H	H	H	H	LA1400	H	CD3	RG48	H	H	H
  LA161	RG161	H	H	H	H	H	LA1401	H	CD3	RG49	H	H	H
  LA162	RG162	H	H	H	H	H	LA1402	H	CD3	RG50	H	H	H
  LA163	RG163	H	H	H	H	H	LA1403	H	CD3	RG51	H	H	H
  LA164	RG164	H	H	H	H	H	LA1404	H	CD3	RG52	H	H	H
  LA165	RG165	H	H	H	H	H	LA1405	H	CD3	RG53	H	H	H
  LA166	RG166	H	H	H	H	H	LA1406	H	CD3	RG54	H	H	H
  LA167	RG167	H	H	H	H	H	LA1407	H	CD3	RG55	H	H	H
  LA168	RG168	H	H	H	H	H	LA1408	H	CD3	RG56	H	H	H
  LA169	RG169	H	H	H	H	H	LA1409	H	CD3	RG57	H	H	H
  LA170	RG1	H	CD3	H	H	H	LA1410	H	CD3	RG58	H	H	H
  LA171	RG2	H	CD3	H	H	H	LA1411	H	CD3	RG59	H	H	H
  LA172	RG3	H	CD3	H	H	H	LA1412	H	CD3	RG60	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA173	RG4	H	CD3	H	H	H	LA1413	H	CD3	RG61	H	H	H
  LA174	RG5	H	CD3	H	H	H	LA1414	H	CD3	RG62	H	H	H
  LA175	RG6	H	CD3	H	H	H	LA1415	H	CD3	RG63	H	H	H
  LA176	RG7	H	CD3	H	H	H	LA1416	H	CD3	RG64	H	H	H
  LA177	RG8	H	CD3	H	H	H	LA1417	H	CD3	RG65	H	H	H
  LA178	RG9	H	CD3	H	H	H	LA1418	H	CD3	RG66	H	H	H
  LA179	RG10	H	CD3	H	H	H	LA1419	H	CD3	RG67	H	H	H
  LA180	RG11	H	CD3	H	H	H	LA1420	H	CD3	RG68	H	H	H
  LA181	RG12	H	CD3	H	H	H	LA1421	H	CD3	RG69	H	H	H
  LA182	RG13	H	CD3	H	H	H	LA1422	H	CD3	RG70	H	H	H
  LA183	RG14	H	CD3	H	H	H	LA1423	H	CD3	RG71	H	H	H
  LA184	RG15	H	CD3	H	H	H	LA1424	H	CD3	RG72	H	H	H
  LA185	RG16	H	CD3	H	H	H	LA1425	H	CD3	RG73	H	H	H
  LA186	RG17	H	CD3	H	H	H	LA1426	H	CD3	RG74	H	H	H
  LA187	RG18	H	CD3	H	H	H	LA1427	H	CD3	RG75	H	H	H
  LA188	RG19	H	CD3	H	H	H	LA1428	H	CD3	RG76	H	H	H
  LA189	RG20	H	CD3	H	H	H	LA1429	H	CD3	RG77	H	H	H
  LA190	RG21	H	CD3	H	H	H	LA1430	H	CD3	RG78	H	H	H
  LA191	RG22	H	CD3	H	H	H	LA1431	H	CD3	RG79	H	H	H
  LA192	RG23	H	CD3	H	H	H	LA1432	H	CD3	RG80	H	H	H
  LA193	RG24	H	CD3	H	H	H	LA1433	H	CD3	RG81	H	H	H
  LA194	RG25	H	CD3	H	H	H	LA1434	H	CD3	RG82	H	H	H
  LA195	RG26	H	CD3	H	H	H	LA1435	H	CD3	RG83	H	H	H
  LA196	RG27	H	CD3	H	H	H	LA1436	H	CD3	RG84	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA197	RG28	H	CD3	H	H	H	LA1437	H	CD3	RG85	H	H	H
  LA198	RG29	H	CD3	H	H	H	LA1438	H	CD3	RG86	H	H	H
  LA199	RG30	H	CD3	H	H	H	LA1439	H	CD3	RG87	H	H	H
  LA200	RG31	H	CD3	H	H	H	LA1440	H	CD3	RG88	H	H	H
  LA201	RG32	H	CD3	H	H	H	LA1441	H	CD3	RG89	H	H	H
  LA202	RG33	H	CD3	H	H	H	LA1442	H	CD3	RG90	H	H	H
  LA203	RG34	H	CD3	H	H	H	LA1443	H	CD3	RG91	H	H	H
  LA204	RG35	H	CD3	H	H	H	LA1444	H	CD3	RG92	H	H	H
  LA205	RG36	H	CD3	H	H	H	LA1445	H	CD3	RG93	H	H	H
  LA206	RG37	H	CD3	H	H	H	LA1446	H	CD3	RG94	H	H	H
  LA207	RG38	H	CD3	H	H	H	LA1447	H	CD3	RG95	H	H	H
  LA208	RG39	H	CD3	H	H	H	LA1448	H	CD3	RG96	H	H	H
  LA209	RG40	H	CD3	H	H	H	LA1449	H	CD3	RG97	H	H	H
  LA210	RG41	H	CD3	H	H	H	LA1450	H	CD3	RG98	H	H	H
  LA211	RG42	H	CD3	H	H	H	LA1451	H	CD3	RG99	H	H	H
  LA212	RG43	H	CD3	H	H	H	LA1452	H	CD3	RG100	H	H	H
  LA213	RG44	H	CD3	H	H	H	LA1453	H	CD3	RG101	H	H	H
  LA214	RG45	H	CD3	H	H	H	LA1454	H	CD3	RG102	H	H	H
  LA215	RG46	H	CD3	H	H	H	LA1455	H	CD3	RG103	H	H	H
  LA216	RG47	H	CD3	H	H	H	LA1456	H	CD3	RG104	H	H	H
  LA217	RG48	H	CD3	H	H	H	LA1457	H	CD3	RG105	H	H	H
  LA218	RG49	H	CD3	H	H	H	LA1458	H	CD3	RG106	H	H	H
  LA219	RG50	H	CD3	H	H	H	LA1459	H	CD3	RG107	H	H	H
  LA220	RG51	H	CD3	H	H	H	LA1460	H	CD3	RG108	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA221	RG52	H	CD3	H	H	H	LA1461	H	CD3	RG109	H	H	H
  LA222	RG53	H	CD3	H	H	H	LA1462	H	CD3	RG110	H	H	H
  LA223	RG54	H	CD3	H	H	H	LA1463	H	CD3	RG111	H	H	H
  LA224	RG55	H	CD3	H	H	H	LA1464	H	CD3	RG112	H	H	H
  LA225	RG56	H	CD3	H	H	H	LA1465	H	CD3	RG113	H	H	H
  LA226	RG57	H	CD3	H	H	H	LA1466	H	CD3	RG114	H	H	H
  LA227	RG58	H	CD3	H	H	H	LA1467	H	CD3	RG115	H	H	H
  LA228	RG59	H	CD3	H	H	H	LA1468	H	CD3	RG116	H	H	H
  LA229	RG60	H	CD3	H	H	H	LA1469	H	CD3	RG117	H	H	H
  LA230	RG61	H	CD3	H	H	H	LA1470	H	CD3	RG118	H	H	H
  LA231	RG62	H	CD3	H	H	H	LA1471	H	CD3	RG119	H	H	H
  LA232	RG63	H	CD3	H	H	H	LA1472	H	CD3	RG120	H	H	H
  LA233	RG64	H	CD3	H	H	H	LA1473	H	CD3	RG121	H	H	H
  LA234	RG65	H	CD3	H	H	H	LA1474	H	CD3	RG122	H	H	H
  LA235	RG66	H	CD3	H	H	H	LA1475	H	CD3	RG123	H	H	H
  LA236	RG67	H	CD3	H	H	H	LA1476	H	CD3	RG124	H	H	H
  LA237	RG68	H	CD3	H	H	H	LA1477	H	CD3	RG125	H	H	H
  LA238	RG69	H	CD3	H	H	H	LA1478	H	CD3	RG126	H	H	H
  LA239	RG70	H	CD3	H	H	H	LA1479	H	CD3	RG127	H	H	H
  LA240	RG71	H	CD3	H	H	H	LA1480	H	CD3	RG128	H	H	H
  LA241	RG72	H	CD3	H	H	H	LA1481	H	CD3	RG129	H	H	H
  LA242	RG73	H	CD3	H	H	H	LA1482	H	CD3	RG130	H	H	H
  LA243	RG74	H	CD3	H	H	H	LA1483	H	CD3	RG131	H	H	H
  LA244	RG75	H	CD3	H	H	H	LA1484	H	CD3	RG132	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA245	RG76	H	CD3	H	H	H	LA1485	H	CD3	RG133	H	H	H
  LA246	RG77	H	CD3	H	H	H	LA1486	H	CD3	RG134	H	H	H
  LA247	RG78	H	CD3	H	H	H	LA1487	H	CD3	RG135	H	H	H
  LA248	RG79	H	CD3	H	H	H	LA1488	H	CD3	RG136	H	H	H
  LA249	RG80	H	CD3	H	H	H	LA1489	H	CD3	RG137	H	H	H
  LA250	RG81	H	CD3	H	H	H	LA1490	H	CD3	RG138	H	H	H
  LA251	RG82	H	CD3	H	H	H	LA1491	H	CD3	RG139	H	H	H
  LA252	RG83	H	CD3	H	H	H	LA1492	H	CD3	RG140	H	H	H
  LA253	RG84	H	CD3	H	H	H	LA1493	H	CD3	RG141	H	H	H
  LA254	RG85	H	CD3	H	H	H	LA1494	H	CD3	RG142	H	H	H
  LA255	RG86	H	CD3	H	H	H	LA1495	H	CD3	RG143	H	H	H
  LA256	RG87	H	CD3	H	H	H	LA1496	H	CD3	RG144	H	H	H
  LA257	RG88	H	CD3	H	H	H	LA1497	H	CD3	RG145	H	H	H
  LA258	RG89	H	CD3	H	H	H	LA1498	H	CD3	RG146	H	H	H
  LA259	RG90	H	CD3	H	H	H	LA1499	H	CD3	RG147	H	H	H
  LA260	RG91	H	CD3	H	H	H	LA1500	H	CD3	RG148	H	H	H
  LA261	RG92	H	CD3	H	H	H	LA1501	H	CD3	RG149	H	H	H
  LA262	RG93	H	CD3	H	H	H	LA1502	H	CD3	RG150	H	H	H
  LA263	RG94	H	CD3	H	H	H	LA1503	H	CD3	RG151	H	H	H
  LA264	RG95	H	CD3	H	H	H	LA1504	H	CD3	RG152	H	H	H
  LA265	RG96	H	CD3	H	H	H	LA1505	H	CD3	RG153	H	H	H
  LA266	RG97	H	CD3	H	H	H	LA1506	H	CD3	RG154	H	H	H
  LA267	RG98	H	CD3	H	H	H	LA1507	H	CD3	RG155	H	H	H
  LA268	RG99	H	CD3	H	H	H	LA1508	H	CD3	RG156	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA269	RG100	H	CD3	H	H	H	LA1509	H	CD3	RG157	H	H	H
  LA270	RG101	H	CD3	H	H	H	LA1510	H	CD3	RG158	H	H	H
  LA271	RG102	H	CD3	H	H	H	LA1511	H	CD3	RG159	H	H	H
  LA272	RG103	H	CD3	H	H	H	LA1512	H	CD3	RG160	H	H	H
  LA273	RG104	H	CD3	H	H	H	LA1513	H	CD3	RG161	H	H	H
  LA274	RG105	H	CD3	H	H	H	LA1514	H	CD3	RG162	H	H	H
  LA275	RG106	H	CD3	H	H	H	LA1515	H	CD3	RG163	H	H	H
  LA276	RG107	H	CD3	H	H	H	LA1516	H	CD3	RG164	H	H	H
  LA277	RG108	H	CD3	H	H	H	LA1517	H	CD3	RG165	H	H	H
  LA278	RG109	H	CD3	H	H	H	LA1518	H	CD3	RG166	H	H	H
  LA279	RG110	H	CD3	H	H	H	LA1519	H	CD3	RG167	H	H	H
  LA280	RG111	H	CD3	H	H	H	LA1520	H	CD3	RG168	H	H	H
  LA281	RG112	H	CD3	H	H	H	LA1521	H	CD3	RG169	H	H	H
  LA282	RG113	H	CD3	H	H	H	LA1522	RG1	CD3	CD3	H	H	H
  LA283	RG114	H	CD3	H	H	H	LA1523	RG2	CD3	CD3	H	H	H
  LA284	RG115	H	CD3	H	H	H	LA1524	RG3	CD3	CD3	H	H	H
  LA285	RG116	H	CD3	H	H	H	LA1525	RG4	CD3	CD3	H	H	H
  LA286	RG117	H	CD3	H	H	H	LA1526	RG5	CD3	CD3	H	H	H
  LA287	RG118	H	CD3	H	H	H	LA1527	RG6	CD3	CD3	H	H	H
  LA288	RG119	H	CD3	H	H	H	LA1528	RG7	CD3	CD3	H	H	H
  LA289	RG120	H	CD3	H	H	H	LA1529	RG8	CD3	CD3	H	H	H
  LA290	RG121	H	CD3	H	H	H	LA1530	RG9	CD3	CD3	H	H	H
  LA291	RG122	H	CD3	H	H	H	LA1531	RG10	CD3	CD3	H	H	H
  LA292	RG123	H	CD3	H	H	H	LA1532	RG11	CD3	CD3	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA293	RG124	H	CD3	H	H	H	LA1533	RG12	CD3	CD3	H	H	H
  LA294	RG125	H	CD3	H	H	H	LA1534	RG13	CD3	CD3	H	H	H
  LA295	RG126	H	CD3	H	H	H	LA1535	RG14	CD3	CD3	H	H	H
  LA296	RG127	H	CD3	H	H	H	LA1536	RG15	CD3	CD3	H	H	H
  LA297	RG128	H	CD3	H	H	H	LA1537	RG16	CD3	CD3	H	H	H
  LA298	RG129	H	CD3	H	H	H	LA1538	RG17	CD3	CD3	H	H	H
  LA299	RG130	H	CD3	H	H	H	LA1539	RG18	CD3	CD3	H	H	H
  LA300	RG131	H	CD3	H	H	H	LA1540	RG19	CD3	CD3	H	H	H
  LA301	RG132	H	CD3	H	H	H	LA1541	CD3	RG1	H	H	H	H
  LA302	RG133	H	CD3	H	H	H	LA1542	CD3	RG2	H	H	H	H
  LA303	RG134	H	CD3	H	H	H	LA1543	CD3	RG3	H	H	H	H
  LA304	RG135	H	CD3	H	H	H	LA1544	CD3	RG4	H	H	H	H
  LA305	RG136	H	CD3	H	H	H	LA1545	CD3	RG5	H	H	H	H
  LA306	RG137	H	CD3	H	H	H	LA1546	CD3	RG6	H	H	H	H
  LA307	RG138	H	CD3	H	H	H	LA1547	CD3	RG7	H	H	H	H
  LA308	RG139	H	CD3	H	H	H	LA1548	CD3	RG8	H	H	H	H
  LA309	RG140	H	CD3	H	H	H	LA1549	CD3	RG9	H	H	H	H
  LA310	RG141	H	CD3	H	H	H	LA1550	CD3	RG10	H	H	H	H
  LA311	RG142	H	CD3	H	H	H	LA1551	CD3	RG11	H	H	H	H
  LA312	RG143	H	CD3	H	H	H	LA1552	CD3	RG12	H	H	H	H
  LA313	RG144	H	CD3	H	H	H	LA1553	CD3	RG13	H	H	H	H
  LA314	RG145	H	CD3	H	H	H	LA1554	CD3	RG14	H	H	H	H
  LA315	RG146	H	CD3	H	H	H	LA1555	CD3	RG15	H	H	H	H
  LA316	RG147	H	CD3	H	H	H	LA1556	CD3	RG16	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA317	RG148	H	CD3	H	H	H	LA1557	CD3	RG17	H	H	H	H
  LA318	RG149	H	CD3	H	H	H	LA1558	CD3	RG18	H	H	H	H
  LA319	RG150	H	CD3	H	H	H	LA1559	CD3	RG19	H	H	H	H
  LA320	RG151	H	CD3	H	H	H	LA1560	CD3	CD3	RG1	H	H	CD3
  LA321	RG152	H	CD3	H	H	H	LA1561	CD3	CD3	RG2	H	H	CD3
  LA322	RG153	H	CD3	H	H	H	LA1562	CD3	CD3	RG3	H	H	CD3
  LA323	RG154	H	CD3	H	H	H	LA1563	CD3	CD3	RG4	H	H	CD3
  LA324	RG155	H	CD3	H	H	H	LA1564	CD3	CD3	RG5	H	H	CD3
  LA325	RG156	H	CD3	H	H	H	LA1565	CD3	CD3	RG6	H	H	CD3
  LA326	RG157	H	CD3	H	H	H	LA1566	CD3	CD3	RG7	H	H	CD3
  LA327	RG158	H	CD3	H	H	H	LA1567	CD3	CD3	RG8	H	H	CD3
  LA328	RG159	H	CD3	H	H	H	LA1568	CD3	CD3	RG9	H	H	CD3
  LA329	RG160	H	CD3	H	H	H	LA1569	CD3	CD3	RG10	H	H	CD3
  LA330	RG161	H	CD3	H	H	H	LA1570	CD3	CD3	RG11	H	H	CD3
  LA331	RG162	H	CD3	H	H	H	LA1571	CD3	CD3	RG12	H	H	CD3
  LA332	RG163	H	CD3	H	H	H	LA1572	CD3	CD3	RG13	H	H	CD3
  LA333	RG164	H	CD3	H	H	H	LA1573	CD3	CD3	RG14	H	H	CD3
  LA334	RG165	H	CD3	H	H	H	LA1574	CD3	CD3	RG15	H	H	CD3
  LA335	RG166	H	CD3	H	H	H	LA1575	CD3	CD3	RG16	H	H	CD3
  LA336	RG167	H	CD3	H	H	H	LA1576	CD3	CD3	RG17	H	H	CD3
  LA337	RG168	H	CD3	H	H	H	LA1577	CD3	CD3	RG18	H	H	CD3
  LA338	RG169	H	CD3	H	H	H	LA1578	CD3	CD3	RG19	H	H	CD3
  LA339	RG1	CD3	CD3	H	H	CD3	LA1579	CD3	H	RG1	H	H	CD3
  LA340	RG2	CD3	CD3	H	H	CD3	LA1580	CD3	H	RG2	H	H	CD3

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA341	RG3	CD3	CD3	H	H	CD3	LA1581	CD3	H	RG3	H	H	CD3
  LA342	RG4	CD3	CD3	H	H	CD3	LA1582	CD3	H	RG4	H	H	CD3
  LA343	RG5	CD3	CD3	H	H	CD3	LA1583	CD3	H	RG5	H	H	CD3
  LA344	RG6	CD3	CD3	H	H	CD3	LA1584	CD3	H	RG6	H	H	CD3
  LA345	RG7	CD3	CD3	H	H	CD3	LA1585	CD3	H	RG7	H	H	CD3
  LA346	RG8	CD3	CD3	H	H	CD3	LA1586	CD3	H	RG8	H	H	CD3
  LA347	RG9	CD3	CD3	H	H	CD3	LA1587	CD3	H	RG9	H	H	CD3
  LA348	RG10	CD3	CD3	H	H	CD3	LA1588	CD3	H	RG10	H	H	CD3
  LA349	RG11	CD3	CD3	H	H	CD3	LA1589	CD3	H	RG11	H	H	CD3
  LA350	RG12	CD3	CD3	H	H	CD3	LA1590	CD3	H	RG12	H	H	CD3
  LA351	RG13	CD3	CD3	H	H	CD3	LA1591	CD3	H	RG13	H	H	CD3
  LA352	RG14	CD3	CD3	H	H	CD3	LA1592	CD3	H	RG14	H	H	CD3
  LA353	RG15	CD3	CD3	H	H	CD3	LA1593	CD3	H	RG15	H	H	CD3
  LA354	RG16	CD3	CD3	H	H	CD3	LA1594	CD3	H	RG16	H	H	CD3
  LA355	RG17	CD3	CD3	H	H	CD3	LA1595	CD3	H	RG17	H	H	CD3
  LA356	RG18	CD3	CD3	H	H	CD3	LA1596	CD3	H	RG18	H	H	CD3
  LA357	RG19	CD3	CD3	H	H	CD3	LA1597	CD3	H	RG19	H	H	CD3
  LA358	RG20	CD3	CD3	H	H	CD3	LA1598	RG1	CD3	H	H	H	H
  LA359	RG21	CD3	CD3	H	H	CD3	LA1599	RG2	CD3	H	H	H	H
  LA360	RG22	CD3	CD3	H	H	CD3	LA1600	RG3	CD3	H	H	H	H
  LA361	RG23	CD3	CD3	H	H	CD3	LA1601	RG4	CD3	H	H	H	H
  LA362	RG24	CD3	CD3	H	H	CD3	LA1602	RG5	CD3	H	H	H	H
  LA363	RG25	CD3	CD3	H	H	CD3	LA1603	RG6	CD3	H	H	H	H
  LA364	RG26	CD3	CD3	H	H	CD3	LA1604	RG7	CD3	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA365	RG27	CD3	CD3	H	H	CD3	LA1605	RG8	CD3	H	H	H	H
  LA366	RG28	CD3	CD3	H	H	CD3	LA1606	RG9	CD3	H	H	H	H
  LA367	RG29	CD3	CD3	H	H	CD3	LA1607	RG10	CD3	H	H	H	H
  LA368	RG30	CD3	CD3	H	H	CD3	LA1608	RG11	CD3	H	H	H	H
  LA369	RG31	CD3	CD3	H	H	CD3	LA1609	RG12	CD3	H	H	H	H
  LA370	RG32	CD3	CD3	H	H	CD3	LA1610	RG13	CD3	H	H	H	H
  LA371	RG33	CD3	CD3	H	H	CD3	LA1611	RG14	CD3	H	H	H	H
  LA372	RG34	CD3	CD3	H	H	CD3	LA1612	RG15	CD3	H	H	H	H
  LA373	RG35	CD3	CD3	H	H	CD3	LA1613	RG16	CD3	H	H	H	H
  LA374	RG36	CD3	CD3	H	H	CD3	LA1614	RG17	CD3	H	H	H	H
  LA375	RG37	CD3	CD3	H	H	CD3	LA1615	RG18	CD3	H	H	H	H
  LA376	RG38	CD3	CD3	H	H	CD3	LA1616	RG19	CD3	H	H	H	H
  LA377	RG39	CD3	CD3	H	H	CD3	LA1617	H	CD3	RG1	H	H	CD3
  LA378	RG40	CD3	CD3	H	H	CD3	LA1618	H	CD3	RG2	H	H	CD3
  LA379	RG41	CD3	CD3	H	H	CD3	LA1619	H	CD3	RG3	H	H	CD3
  LA380	RG42	CD3	CD3	H	H	CD3	LA1620	H	CD3	RG4	H	H	CD3
  LA381	RG43	CD3	CD3	H	H	CD3	LA1621	H	CD3	RG5	H	H	CD3
  LA382	RG44	CD3	CD3	H	H	CD3	LA1622	H	CD3	RG6	H	H	CD3
  LA383	RG45	CD3	CD3	H	H	CD3	LA1623	H	CD3	RG7	H	H	CD3
  LA384	RG46	CD3	CD3	H	H	CD3	LA1624	H	CD3	RG8	H	H	CD3
  LA385	RG47	CD3	CD3	H	H	CD3	LA1625	H	CD3	RG9	H	H	CD3
  LA386	RG48	CD3	CD3	H	H	CD3	LA1626	H	CD3	RG10	H	H	CD3
  LA387	RG49	CD3	CD3	H	H	CD3	LA1627	H	CD3	RG11	H	H	CD3
  LA388	RG50	CD3	CD3	H	H	CD3	LA1628	H	CD3	RG12	H	H	CD3

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA389	RG51	CD3	CD3	H	H	CD3	LA1629	H	CD3	RG13	H	H	CD3
  LA390	RG52	CD3	CD3	H	H	CD3	LA1630	H	CD3	RG14	H	H	CD3
  LA391	RG53	CD3	CD3	H	H	CD3	LA1631	H	CD3	RG15	H	H	CD3
  LA392	RG54	CD3	CD3	H	H	CD3	LA1632	H	CD3	RG16	H	H	CD3
  LA393	RG55	CD3	CD3	H	H	CD3	LA1633	H	CD3	RG17	H	H	CD3
  LA394	RG56	CD3	CD3	H	H	CD3	LA1634	H	CD3	RG18	H	H	CD3
  LA395	RG57	CD3	CD3	H	H	CD3	LA1635	H	CD3	RG19	H	H	CD3
  LA396	RG58	CD3	CD3	H	H	CD3	LA1636	H	RG1	H	H	H	H
  LA397	RG59	CD3	CD3	H	H	CD3	LA1637	H	RG2	H	H	H	H
  LA398	RG60	CD3	CD3	H	H	CD3	LA1638	H	RG3	H	H	H	H
  LA399	RG61	CD3	CD3	H	H	CD3	LA1639	H	RG4	H	H	H	H
  LA400	RG62	CD3	CD3	H	H	CD3	LA1640	H	RG5	H	H	H	H
  LA401	RG63	CD3	CD3	H	H	CD3	LA1641	H	RG6	H	H	H	H
  LA402	RG64	CD3	CD3	H	H	CD3	LA1642	H	RG7	H	H	H	H
  LA403	RG65	CD3	CD3	H	H	CD3	LA1643	H	RG8	H	H	H	H
  LA404	RG66	CD3	CD3	H	H	CD3	LA1644	H	RG9	H	H	H	H
  LA405	RG67	CD3	CD3	H	H	CD3	LA1645	H	RG10	H	H	H	H
  LA406	RG68	CD3	CD3	H	H	CD3	LA1646	H	RG11	H	H	H	H
  LA407	RG69	CD3	CD3	H	H	CD3	LA1647	H	RG12	H	H	H	H
  LA408	RG70	CD3	CD3	H	H	CD3	LA1648	H	RG13	H	H	H	H
  LA409	RG71	CD3	CD3	H	H	CD3	LA1649	H	RG14	H	H	H	H
  LA410	RG72	CD3	CD3	H	H	CD3	LA1650	H	RG15	H	H	H	H
  LA411	RG73	CD3	CD3	H	H	CD3	LA1651	H	RG16	H	H	H	H
  LA412	RG74	CD3	CD3	H	H	CD3	LA1652	H	RG17	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA413	RG75	CD3	CD3	H	H	CD3	LA1653	H	RG18	H	H	H	H
  LA414	RG76	CD3	CD3	H	H	CD3	LA1654	H	RG19	H	H	H	H
  LA415	RG77	CD3	CD3	H	H	CD3	LA1655	H	RG20	H	H	H	H
  LA416	RG78	CD3	CD3	H	H	CD3	LA1656	H	RG21	H	H	H	H
  LA417	RG79	CD3	CD3	H	H	CD3	LA1657	H	RG22	H	H	H	H
  LA418	RG80	CD3	CD3	H	H	CD3	LA1658	H	RG23	H	H	H	H
  LA419	RG81	CD3	CD3	H	H	CD3	LA1659	H	RG24	H	H	H	H
  LA420	RG82	CD3	CD3	H	H	CD3	LA1660	H	RG25	H	H	H	H
  LA421	RG83	CD3	CD3	H	H	CD3	LA1661	H	RG26	H	H	H	H
  LA422	RG84	CD3	CD3	H	H	CD3	LA1662	H	RG27	H	H	H	H
  LA423	RG85	CD3	CD3	H	H	CD3	LA1663	H	RG28	H	H	H	H
  LA424	RG86	CD3	CD3	H	H	CD3	LA1664	H	RG29	H	H	H	H
  LA425	RG87	CD3	CD3	H	H	CD3	LA1665	H	RG30	H	H	H	H
  LA426	RG88	CD3	CD3	H	H	CD3	LA1666	H	RG31	H	H	H	H
  LA427	RG89	CD3	CD3	H	H	CD3	LA1667	H	RG32	H	H	H	H
  LA428	RG90	CD3	CD3	H	H	CD3	LA1668	H	RG33	H	H	H	H
  LA429	RG91	CD3	CD3	H	H	CD3	LA1669	H	RG34	H	H	H	H
  LA430	RG92	CD3	CD3	H	H	CD3	LA1670	H	RG35	H	H	H	H
  LA431	RG93	CD3	CD3	H	H	CD3	LA1671	H	RG36	H	H	H	H
  LA432	RG94	CD3	CD3	H	H	CD3	LA1672	H	RG37	H	H	H	H
  LA433	RG95	CD3	CD3	H	H	CD3	LA1673	H	RG38	H	H	H	H
  LA434	RG96	CD3	CD3	H	H	CD3	LA1674	H	RG39	H	H	H	H
  LA435	RG97	CD3	CD3	H	H	CD3	LA1675	H	RG40	H	H	H	H
  LA436	RG98	CD3	CD3	H	H	CD3	LA1676	H	RG41	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA437	RG99	CD3	CD3	H	H	CD3	LA1677	H	RG42	H	H	H	H
  LA438	RG100	CD3	CD3	H	H	CD3	LA1678	H	RG43	H	H	H	H
  LA439	RG101	CD3	CD3	H	H	CD3	LA1679	H	RG44	H	H	H	H
  LA440	RG102	CD3	CD3	H	H	CD3	LA1680	H	RG45	H	H	H	H
  LA441	RG103	CD3	CD3	H	H	CD3	LA1681	H	RG46	H	H	H	H
  LA442	RG104	CD3	CD3	H	H	CD3	LA1682	H	RG47	H	H	H	H
  LA443	RG105	CD3	CD3	H	H	CD3	LA1683	H	RG48	H	H	H	H
  LA444	RG106	CD3	CD3	H	H	CD3	LA1684	H	RG49	H	H	H	H
  LA445	RG107	CD3	CD3	H	H	CD3	LA1685	H	RG50	H	H	H	H
  LA446	RG108	CD3	CD3	H	H	CD3	LA1686	H	RG51	H	H	H	H
  LA447	RG109	CD3	CD3	H	H	CD3	LA1687	H	RG52	H	H	H	H
  LA448	RG110	CD3	CD3	H	H	CD3	LA1688	H	RG53	H	H	H	H
  LA449	RG111	CD3	CD3	H	H	CD3	LA1689	H	RG54	H	H	H	H
  LA450	RG112	CD3	CD3	H	H	CD3	LA1690	H	RG55	H	H	H	H
  LA451	RG113	CD3	CD3	H	H	CD3	LA1691	H	RG56	H	H	H	H
  LA452	RG114	CD3	CD3	H	H	CD3	LA1692	H	RG57	H	H	H	H
  LA453	RG115	CD3	CD3	H	H	CD3	LA1693	H	RG58	H	H	H	H
  LA454	RG116	CD3	CD3	H	H	CD3	LA1694	H	RG59	H	H	H	H
  LA455	RG117	CD3	CD3	H	H	CD3	LA1695	H	RG60	H	H	H	H
  LA456	RG118	CD3	CD3	H	H	CD3	LA1696	H	RG61	H	H	H	H
  LA457	RG119	CD3	CD3	H	H	CD3	LA1697	H	RG62	H	H	H	H
  LA458	RG120	CD3	CD3	H	H	CD3	LA1698	H	RG63	H	H	H	H
  LA459	RG121	CD3	CD3	H	H	CD3	LA1699	H	RG64	H	H	H	H
  LA460	RG122	CD3	CD3	H	H	CD3	LA1700	H	RG65	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA461	RG123	CD3	CD3	H	H	CD3	LA1701	H	RG66	H	H	H	H
  LA462	RG124	CD3	CD3	H	H	CD3	LA1702	H	RG67	H	H	H	H
  LA463	RG125	CD3	CD3	H	H	CD3	LA1703	H	RG68	H	H	H	H
  LA464	RG126	CD3	CD3	H	H	CD3	LA1704	H	RG69	H	H	H	H
  LA465	RG127	CD3	CD3	H	H	CD3	LA1705	H	RG70	H	H	H	H
  LA466	RG128	CD3	CD3	H	H	CD3	LA1706	H	RG71	H	H	H	H
  LA467	RG129	CD3	CD3	H	H	CD3	LA1707	H	RG72	H	H	H	H
  LA468	RG130	CD3	CD3	H	H	CD3	LA1708	H	RG73	H	H	H	H
  LA469	RG131	CD3	CD3	H	H	CD3	LA1709	H	RG74	H	H	H	H
  LA470	RG132	CD3	CD3	H	H	CD3	LA1710	H	RG75	H	H	H	H
  LA471	RG133	CD3	CD3	H	H	CD3	LA1711	H	RG76	H	H	H	H
  LA472	RG134	CD3	CD3	H	H	CD3	LA1712	H	RG77	H	H	H	H
  LA473	RG135	CD3	CD3	H	H	CD3	LA1713	H	RG78	H	H	H	H
  LA474	RG136	CD3	CD3	H	H	CD3	LA1714	H	RG79	H	H	H	H
  LA475	RG137	CD3	CD3	H	H	CD3	LA1715	H	RG80	H	H	H	H
  LA476	RG138	CD3	CD3	H	H	CD3	LA1716	H	RG81	H	H	H	H
  LA477	RG139	CD3	CD3	H	H	CD3	LA1717	H	RG82	H	H	H	H
  LA478	RG140	CD3	CD3	H	H	CD3	LA1718	H	RG83	H	H	H	H
  LA479	RG141	CD3	CD3	H	H	CD3	LA1719	H	RG84	H	H	H	H
  LA480	RG142	CD3	CD3	H	H	CD3	LA1720	H	RG85	H	H	H	H
  LA481	RG143	CD3	CD3	H	H	CD3	LA1721	H	RG86	H	H	H	H
  LA482	RG144	CD3	CD3	H	H	CD3	LA1722	H	RG87	H	H	H	H
  LA483	RG145	CD3	CD3	H	H	CD3	LA1723	H	RG88	H	H	H	H
  LA484	RG146	CD3	CD3	H	H	CD3	LA1724	H	RG89	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA485	RG147	CD3	CD3	H	H	CD3	LA1725	H	RG90	H	H	H	H
  LA486	RG148	CD3	CD3	H	H	CD3	LA1726	H	RG91	H	H	H	H
  LA487	RG149	CD3	CD3	H	H	CD3	LA1727	H	RG92	H	H	H	H
  LA488	RG150	CD3	CD3	H	H	CD3	LA1728	H	RG93	H	H	H	H
  LA489	RG151	CD3	CD3	H	H	CD3	LA1729	H	RG94	H	H	H	H
  LA490	RG152	CD3	CD3	H	H	CD3	LA1730	H	RG95	H	H	H	H
  LA491	RG153	CD3	CD3	H	H	CD3	LA1731	H	RG96	H	H	H	H
  LA492	RG154	CD3	CD3	H	H	CD3	LA1732	H	RG97	H	H	H	H
  LA493	RG155	CD3	CD3	H	H	CD3	LA1733	H	RG98	H	H	H	H
  LA494	RG156	CD3	CD3	H	H	CD3	LA1734	H	RG99	H	H	H	H
  LA495	RG157	CD3	CD3	H	H	CD3	LA1735	H	RG100	H	H	H	H
  LA496	RG158	CD3	CD3	H	H	CD3	LA1736	H	RG101	H	H	H	H
  LA497	RG159	CD3	CD3	H	H	CD3	LA1737	H	RG102	H	H	H	H
  LA498	RG160	CD3	CD3	H	H	CD3	LA1738	H	RG103	H	H	H	H
  LA499	RG161	CD3	CD3	H	H	CD3	LA1739	H	RG104	H	H	H	H
  LA500	RG162	CD3	CD3	H	H	CD3	LA1740	H	RG105	H	H	H	H
  LA501	RG163	CD3	CD3	H	H	CD3	LA1741	H	RG106	H	H	H	H
  LA502	RG164	CD3	CD3	H	H	CD3	LA1742	H	RG107	H	H	H	H
  LA503	RG165	CD3	CD3	H	H	CD3	LA1743	H	RG108	H	H	H	H
  LA504	RG166	CD3	CD3	H	H	CD3	LA1744	H	RG109	H	H	H	H
  LA505	RG167	CD3	CD3	H	H	CD3	LA1745	H	RG110	H	H	H	H
  LA506	RG168	CD3	CD3	H	H	CD3	LA1746	H	RG111	H	H	H	H
  LA507	RG169	CD3	CD3	H	H	CD3	LA1747	H	RG112	H	H	H	H
  LA508	H	RG1	CD3	H	H	H	LA1748	H	RG113	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA509	H	RG2	CD3	H	H	H	LA1749	H	RG114	H	H	H	H
  LA510	H	RG3	CD3	H	H	H	LA1750	H	RG115	H	H	H	H
  LA511	H	RG4	CD3	H	H	H	LA1751	H	RG116	H	H	H	H
  LA512	H	RG5	CD3	H	H	H	LA1752	H	RG117	H	H	H	H
  LA513	H	RG6	CD3	H	H	H	LA1753	H	RG118	H	H	H	H
  LA514	H	RG7	CD3	H	H	H	LA1754	H	RG119	H	H	H	H
  LA515	H	RG8	CD3	H	H	H	LA1755	H	RG120	H	H	H	H
  LA516	H	RG9	CD3	H	H	H	LA1756	H	RG121	H	H	H	H
  LA517	H	RG10	CD3	H	H	H	LA1757	H	RG122	H	H	H	H
  LA518	H	RG11	CD3	H	H	H	LA1758	H	RG123	H	H	H	H
  LA519	H	RG12	CD3	H	H	H	LA1759	H	RG124	H	H	H	H
  LA520	H	RG13	CD3	H	H	H	LA1760	H	RG125	H	H	H	H
  LA521	H	RG14	CD3	H	H	H	LA1761	H	RG126	H	H	H	H
  LA522	H	RG15	CD3	H	H	H	LA1762	H	RG127	H	H	H	H
  LA523	H	RG16	CD3	H	H	H	LA1763	H	RG128	H	H	H	H
  LA524	H	RG17	CD3	H	H	H	LA1764	H	RG129	H	H	H	H
  LA525	H	RG18	CD3	H	H	H	LA1765	H	RG130	H	H	H	H
  LA526	H	RG19	CD3	H	H	H	LA1766	H	RG131	H	H	H	H
  LA527	H	RG20	CD3	H	H	H	LA1767	H	RG132	H	H	H	H
  LA528	H	RG21	CD3	H	H	H	LA1768	H	RG133	H	H	H	H
  LA529	H	RG22	CD3	H	H	H	LA1769	H	RG134	H	H	H	H
  LA530	H	RG23	CD3	H	H	H	LA1770	H	RG135	H	H	H	H
  LA531	H	RG24	CD3	H	H	H	LA1771	H	RG136	H	H	H	H
  LA532	H	RG25	CD3	H	H	H	LA1772	H	RG137	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA533	H	RG26	CD3	H	H	H	LA1773	H	RG138	H	H	H	H
  LA534	H	RG27	CD3	H	H	H	LA1774	H	RG139	H	H	H	H
  LA535	H	RG28	CD3	H	H	H	LA1775	H	RG140	H	H	H	H
  LA536	H	RG29	CD3	H	H	H	LA1776	H	RG141	H	H	H	H
  LA537	H	RG30	CD3	H	H	H	LA1777	H	RG142	H	H	H	H
  LA538	H	RG31	CD3	H	H	H	LA1778	H	RG143	H	H	H	H
  LA539	H	RG32	CD3	H	H	H	LA1779	H	RG144	H	H	H	H
  LA540	H	RG33	CD3	H	H	H	LA1780	H	RG145	H	H	H	H
  LA541	H	RG34	CD3	H	H	H	LA1781	H	RG146	H	H	H	H
  LA542	H	RG35	CD3	H	H	H	LA1782	H	RG147	H	H	H	H
  LA543	H	RG36	CD3	H	H	H	LA1783	H	RG148	H	H	H	H
  LA544	H	RG37	CD3	H	H	H	LA1784	H	RG149	H	H	H	H
  LA545	H	RG38	CD3	H	H	H	LA1785	H	RG150	H	H	H	H
  LA546	H	RG39	CD3	H	H	H	LA1786	H	RG151	H	H	H	H
  LA547	H	RG40	CD3	H	H	H	LA1787	H	RG152	H	H	H	H
  LA548	H	RG41	CD3	H	H	H	LA1788	H	RG153	H	H	H	H
  LA549	H	RG42	CD3	H	H	H	LA1789	H	RG154	H	H	H	H
  LA550	H	RG43	CD3	H	H	H	LA1790	H	RG155	H	H	H	H
  LA551	H	RG44	CD3	H	H	H	LA1791	H	RG156	H	H	H	H
  LA552	H	RG45	CD3	H	H	H	LA1792	H	RG157	H	H	H	H
  LA553	H	RG46	CD3	H	H	H	LA1793	H	RG158	H	H	H	H
  LA554	H	RG47	CD3	H	H	H	LA1794	H	RG159	H	H	H	H
  LA555	H	RG48	CD3	H	H	H	LA1795	H	RG160	H	H	H	H
  LA556	H	RG49	CD3	H	H	H	LA1796	H	RG161	H	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA557	H	RG50	CD3	H	H	H	LA1797	H	RG162	H	H	H	H
  LA558	H	RG51	CD3	H	H	H	LA1798	H	RG163	H	H	H	H
  LA559	H	RG52	CD3	H	H	H	LA1799	H	RG164	H	H	H	H
  LA560	H	RG53	CD3	H	H	H	LA1800	H	RG165	H	H	H	H
  LA561	H	RG54	CD3	H	H	H	LA1801	H	RG166	H	H	H	H
  LA562	H	RG55	CD3	H	H	H	LA1802	H	RG167	H	H	H	H
  LA563	H	RG56	CD3	H	H	H	LA1803	H	RG168	H	H	H	H
  LA564	H	RG57	CD3	H	H	H	LA1804	H	RG169	H	H	H	H
  LA565	H	RG58	CD3	H	H	H	LA1805	H	H	RG1	H	H	H
  LA566	H	RG59	CD3	H	H	H	LA1806	H	H	RG2	H	H	H
  LA567	H	RG60	CD3	H	H	H	LA1807	H	H	RG3	H	H	H
  LA568	H	RG61	CD3	H	H	H	LA1808	H	H	RG4	H	H	H
  LA569	H	RG62	CD3	H	H	H	LA1809	H	H	RG5	H	H	H
  LA570	H	RG63	CD3	H	H	H	LA1810	H	H	RG6	H	H	H
  LA571	H	RG64	CD3	H	H	H	LA1811	H	H	RG7	H	H	H
  LA572	H	RG65	CD3	H	H	H	LA1812	H	H	RG8	H	H	H
  LA573	H	RG66	CD3	H	H	H	LA1813	H	H	RG9	H	H	H
  LA574	H	RG67	CD3	H	H	H	LA1814	H	H	RG10	H	H	H
  LA575	H	RG68	CD3	H	H	H	LA1815	H	H	RG11	H	H	H
  LA576	H	RG69	CD3	H	H	H	LA1816	H	H	RG12	H	H	H
  LA577	H	RG70	CD3	H	H	H	LA1817	H	H	RG13	H	H	H
  LA578	H	RG71	CD3	H	H	H	LA1818	H	H	RG14	H	H	H
  LA579	H	RG72	CD3	H	H	H	LA1819	H	H	RG15	H	H	H
  LA580	H	RG73	CD3	H	H	H	LA1820	H	H	RG16	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA581	H	RG74	CD3	H	H	H	LA1821	H	H	RG17	H	H	H
  LA582	H	RG75	CD3	H	H	H	LA1822	H	H	RG18	H	H	H
  LA583	H	RG76	CD3	H	H	H	LA1823	H	H	RG19	H	H	H
  LA584	H	RG77	CD3	H	H	H	LA1824	H	H	RG20	H	H	H
  LA585	H	RG78	CD3	H	H	H	LA1825	H	H	RG21	H	H	H
  LA586	H	RG79	CD3	H	H	H	LA1826	H	H	RG22	H	H	H
  LA587	H	RG80	CD3	H	H	H	LA1827	H	H	RG23	H	H	H
  LA588	H	RG81	CD3	H	H	H	LA1828	H	H	RG24	H	H	H
  LA589	H	RG82	CD3	H	H	H	LA1829	H	H	RG25	H	H	H
  LA590	H	RG83	CD3	H	H	H	LA1830	H	H	RG26	H	H	H
  LA591	H	RG84	CD3	H	H	H	LA1831	H	H	RG27	H	H	H
  LA592	H	RG85	CD3	H	H	H	LA1832	H	H	RG28	H	H	H
  LA593	H	RG86	CD3	H	H	H	LA1833	H	H	RG29	H	H	H
  LA594	H	RG87	CD3	H	H	H	LA1834	H	H	RG30	H	H	H
  LA595	H	RG88	CD3	H	H	H	LA1835	H	H	RG31	H	H	H
  LA596	H	RG89	CD3	H	H	H	LA1836	H	H	RG32	H	H	H
  LA597	H	RG90	CD3	H	H	H	LA1837	H	H	RG33	H	H	H
  LA598	H	RG91	CD3	H	H	H	LA1838	H	H	RG34	H	H	H
  LA599	H	RG92	CD3	H	H	H	LA1839	H	H	RG35	H	H	H
  LA600	H	RG93	CD3	H	H	H	LA1840	H	H	RG36	H	H	H
  LA601	H	RG94	CD3	H	H	H	LA1841	H	H	RG37	H	H	H
  LA602	H	RG95	CD3	H	H	H	LA1842	H	H	RG38	H	H	H
  LA603	H	RG96	CD3	H	H	H	LA1843	H	H	RG39	H	H	H
  LA604	H	RG97	CD3	H	H	H	LA1844	H	H	RG40	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA605	H	RG98	CD3	H	H	H	LA1845	H	H	RG41	H	H	H
  LA606	H	RG99	CD3	H	H	H	LA1846	H	H	RG42	H	H	H
  LA607	H	RG100	CD3	H	H	H	LA1847	H	H	RG43	H	H	H
  LA608	H	RG101	CD3	H	H	H	LA1848	H	H	RG44	H	H	H
  LA609	H	RG102	CD3	H	H	H	LA1849	H	H	RG45	H	H	H
  LA610	H	RG103	CD3	H	H	H	LA1850	H	H	RG46	H	H	H
  LA611	H	RG104	CD3	H	H	H	LA1851	H	H	RG47	H	H	H
  LA612	H	RG105	CD3	H	H	H	LA1852	H	H	RG48	H	H	H
  LA613	H	RG106	CD3	H	H	H	LA1853	H	H	RG49	H	H	H
  LA614	H	RG107	CD3	H	H	H	LA1854	H	H	RG50	H	H	H
  LA615	H	RG108	CD3	H	H	H	LA1855	H	H	RG51	H	H	H
  LA616	H	RG109	CD3	H	H	H	LA1856	H	H	RG52	H	H	H
  LA617	H	RG110	CD3	H	H	H	LA1857	H	H	RG53	H	H	H
  LA618	H	RG111	CD3	H	H	H	LA1858	H	H	RG54	H	H	H
  LA619	H	RG112	CD3	H	H	H	LA1859	H	H	RG55	H	H	H
  LA620	H	RG113	CD3	H	H	H	LA1860	H	H	RG56	H	H	H
  LA621	H	RG114	CD3	H	H	H	LA1861	H	H	RG57	H	H	H
  LA622	H	RG115	CD3	H	H	H	LA1862	H	H	RG58	H	H	H
  LA623	H	RG116	CD3	H	H	H	LA1863	H	H	RG59	H	H	H
  LA624	H	RG117	CD3	H	H	H	LA1864	H	H	RG60	H	H	H
  LA625	H	RG118	CD3	H	H	H	LA1865	H	H	RG61	H	H	H
  LA626	H	RG119	CD3	H	H	H	LA1866	H	H	RG62	H	H	H
  LA627	H	RG120	CD3	H	H	H	LA1867	H	H	RG63	H	H	H
  LA628	H	RG121	CD3	H	H	H	LA1868	H	H	RG64	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA629	H	RG122	CD3	H	H	H	LA1869	H	H	RG65	H	H	H
  LA630	H	RG123	CD3	H	H	H	LA1870	H	H	RG66	H	H	H
  LA631	H	RG124	CD3	H	H	H	LA1871	H	H	RG67	H	H	H
  LA632	H	RG125	CD3	H	H	H	LA1872	H	H	RG68	H	H	H
  LA633	H	RG126	CD3	H	H	H	LA1873	H	H	RG69	H	H	H
  LA634	H	RG127	CD3	H	H	H	LA1874	H	H	RG70	H	H	H
  LA635	H	RG128	CD3	H	H	H	LA1875	H	H	RG71	H	H	H
  LA636	H	RG129	CD3	H	H	H	LA1876	H	H	RG72	H	H	H
  LA637	H	RG130	CD3	H	H	H	LA1877	H	H	RG73	H	H	H
  LA638	H	RG131	CD3	H	H	H	LA1878	H	H	RG74	H	H	H
  LA639	H	RG132	CD3	H	H	H	LA1879	H	H	RG75	H	H	H
  LA640	H	RG133	CD3	H	H	H	LA1880	H	H	RG76	H	H	H
  LA641	H	RG134	CD3	H	H	H	LA1881	H	H	RG77	H	H	H
  LA642	H	RG135	CD3	H	H	H	LA1882	H	H	RG78	H	H	H
  LA643	H	RG136	CD3	H	H	H	LA1883	H	H	RG79	H	H	H
  LA644	H	RG137	CD3	H	H	H	LA1884	H	H	RG80	H	H	H
  LA645	H	RG133	CD3	H	H	H	LA1885	H	H	RG81	H	H	H
  LA646	H	RG139	CD3	H	H	H	LA1886	H	H	RG82	H	H	H
  LA647	H	RG140	CD3	H	H	H	LA1887	H	H	RG83	H	H	H
  LA648	H	RG141	CD3	H	H	H	LA1888	H	H	RG84	H	H	H
  LA649	H	RG142	CD3	H	H	H	LA1889	H	H	RG85	H	H	H
  LA650	H	RG143	CD3	H	H	H	LA1890	H	H	RG86	H	H	H
  LA651	H	RG144	CD3	H	H	H	LA1891	H	H	RG87	H	H	H
  LA652	H	RG145	CD3	H	H	H	LA1892	H	H	RG88	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA653	H	RG146	CD3	H	H	H	LA1893	H	H	RG89	H	H	H
  LA654	H	RG147	CD3	H	H	H	LA1894	H	H	RG90	H	H	H
  LA655	H	RG148	CD3	H	H	H	LA1895	H	H	RG91	H	H	H
  LA656	H	RG149	CD3	H	H	H	LA1896	H	H	RG92	H	H	H
  LA657	H	RG150	CD3	H	H	H	LA1897	H	H	RG93	H	H	H
  LA658	H	RG151	CD3	H	H	H	LA1898	H	H	RG94	H	H	H
  LA659	H	RG152	CD3	H	H	H	LA1899	H	H	RG95	H	H	H
  LA660	H	RG153	CD3	H	H	H	LA1900	H	H	RG96	H	H	H
  LA661	H	RG154	CD3	H	H	H	LA1901	H	H	RG97	H	H	H
  LA662	H	RG155	CD3	H	H	H	LA1902	H	H	RG98	H	H	H
  LA663	H	RG156	CD3	H	H	H	LA1903	H	H	RG99	H	H	H
  LA664	H	RG157	CD3	H	H	H	LA1904	H	H	RG100	H	H	H
  LA665	H	RG158	CD3	H	H	H	LA1905	H	H	RG101	H	H	H
  LA666	H	RG159	CD3	H	H	H	LA1906	H	H	RG102	H	H	H
  LA667	H	RG160	CD3	H	H	H	LA1907	H	H	RG103	H	H	H
  LA668	H	RG161	CD3	H	H	H	LA1908	H	H	RG104	H	H	H
  LA669	H	RG162	CD3	H	H	H	LA1909	H	H	RG105	H	H	H
  LA670	H	RG163	CD3	H	H	H	LA1910	H	H	RG106	H	H	H
  LA671	H	RG164	CD3	H	H	H	LA1911	H	H	RG107	H	H	H
  LA672	H	RG165	CD3	H	H	H	LA1912	H	H	RG108	H	H	H
  LA673	H	RG166	CD3	H	H	H	LA1913	H	H	RG109	H	H	H
  LA674	H	RG167	CD3	H	H	H	LA1914	H	H	RG110	H	H	H
  LA675	H	RG168	CD3	H	H	H	LA1915	H	H	RG111	H	H	H
  LA676	H	RG169	CD3	H	H	H	LA1916	H	H	RG112	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA677	CD3	RG1	CD3	H	H	CD3	LA1917	H	H	RG113	H	H	H
  LA678	CD3	RG2	CD3	H	H	CD3	LA1918	H	H	RG114	H	H	H
  LA679	CD3	RG3	CD3	H	H	CD3	LA1919	H	H	RG115	H	H	H
  LA680	CD3	RG4	CD3	H	H	CD3	LA1920	H	H	RG116	H	H	H
  LA681	CD3	RG5	CD3	H	H	CD3	LA1921	H	H	RG117	H	H	H
  LA682	CD3	RG6	CD3	H	H	CD3	LA1922	H	H	RG118	H	H	H
  LA683	CD3	RG7	CD3	H	H	CD3	LA1923	H	H	RG119	H	H	H
  LA684	CD3	RG8	CD3	H	H	CD3	LA1924	H	H	RG120	H	H	H
  LA685	CD3	RG9	CD3	H	H	CD3	LA1925	H	H	RG121	H	H	H
  LA686	CD3	RG10	CD3	H	H	CD3	LA1926	H	H	RG122	H	H	H
  LA687	CD3	RG11	CD3	H	H	CD3	LA1927	H	H	RG123	H	H	H
  LA688	CD3	RG12	CD3	H	H	CD3	LA1928	H	H	RG124	H	H	H
  LA689	CD3	RG13	CD3	H	H	CD3	LA1929	H	H	RG125	H	H	H
  LA690	CD3	RG14	CD3	H	H	CD3	LA1930	H	H	RG126	H	H	H
  LA691	CD3	RG15	CD3	H	H	CD3	LA1931	H	H	RG127	H	H	H
  LA692	CD3	RG16	CD3	H	H	CD3	LA1932	H	H	RG128	H	H	H
  LA693	CD3	RG17	CD3	H	H	CD3	LA1933	H	H	RG129	H	H	H
  LA694	CD3	RG18	CD3	H	H	CD3	LA1934	H	H	RG130	H	H	H
  LA695	CD3	RG19	CD3	H	H	CD3	LA1935	H	H	RG131	H	H	H
  LA696	CD3	RG20	CD3	H	H	CD3	LA1936	H	H	RG132	H	H	H
  LA697	CD3	RG21	CD3	H	H	CD3	LA1937	H	H	RG133	H	H	H
  LA698	CD3	RG22	CD3	H	H	CD3	LA1938	H	H	RG134	H	H	H
  LA699	CD3	RG23	CD3	H	H	CD3	LA1939	H	H	RG135	H	H	H
  LA700	CD3	RG24	CD3	H	H	CD3	LA1940	H	H	RG136	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA701	CD3	RG25	CD3	H	H	CD3	LA1941	H	H	RG137	H	H	H
  LA702	CD3	RG26	CD3	H	H	CD3	LA1942	H	H	RG138	H	H	H
  LA703	CD3	RG27	CD3	H	H	CD3	LA1943	H	H	RG139	H	H	H
  LA704	CD3	RG28	CD3	H	H	CD3	LA1944	H	H	RG140	H	H	H
  LA705	CD3	RG29	CD3	H	H	CD3	LA1945	H	H	RG141	H	H	H
  LA706	CD3	RG30	CD3	H	H	CD3	LA1946	H	H	RG142	H	H	H
  LA707	CD3	RG31	CD3	H	H	CD3	LA1947	H	H	RG143	H	H	H
  LA708	CD3	RG32	CD3	H	H	CD3	LA1948	H	H	RG144	H	H	H
  LA709	CD3	RG33	CD3	H	H	CD3	LA1949	H	H	RG145	H	H	H
  LA710	CD3	RG34	CD3	H	H	CD3	LA1950	H	H	RG146	H	H	H
  LA711	CD3	RG35	CD3	H	H	CD3	LA1951	H	H	RG147	H	H	H
  LA712	CD3	RG36	CD3	H	H	CD3	LA1952	H	H	RG148	H	H	H
  LA713	CD3	RG37	CD3	H	H	CD3	LA1953	H	H	RG149	H	H	H
  LA714	CD3	RG38	CD3	H	H	CD3	LA1954	H	H	RG150	H	H	H
  LA715	CD3	RG39	CD3	H	H	CD3	LA1955	H	H	RG151	H	H	H
  LA716	CD3	RG40	CD3	H	H	CD3	LA1956	H	H	RG152	H	H	H
  LA717	CD3	RG41	CD3	H	H	CD3	LA1957	H	H	RG153	H	H	H
  LA718	CD3	RG42	CD3	H	H	CD3	LA1958	H	H	RG154	H	H	H
  LA719	CD3	RG43	CD3	H	H	CD3	LA1959	H	H	RG155	H	H	H
  LA720	CD3	RG44	CD3	H	H	CD3	LA1960	H	H	RG156	H	H	H
  LA721	CD3	RG45	CD3	H	H	CD3	LA1961	H	H	RG157	H	H	H
  LA722	CD3	RG46	CD3	H	H	CD3	LA1962	H	H	RG158	H	H	H
  LA723	CD3	RG47	CD3	H	H	CD3	LA1963	H	H	RG159	H	H	H
  LA724	CD3	RG48	CD3	H	H	CD3	LA1964	H	H	RG160	H	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA725	CD3	RG49	CD3	H	H	CD3	LA1965	H	H	RG161	H	H	H
  LA726	CD3	RG50	CD3	H	H	CD3	LA1966	H	H	RG162	H	H	H
  LA727	CD3	RG51	CD3	H	H	CD3	LA1967	H	H	RG163	H	H	H
  LA728	CD3	RG52	CD3	H	H	CD3	LA1968	H	H	RG164	H	H	H
  LA729	CD3	RG53	CD3	H	H	CD3	LA1969	H	H	RG165	H	H	H
  LA730	CD3	RG54	CD3	H	H	CD3	LA1970	H	H	RG166	H	H	H
  LA731	CD3	RG55	CD3	H	H	CD3	LA1971	H	H	RG167	H	H	H
  LA732	CD3	RG56	CD3	H	H	CD3	LA1972	H	H	RG168	H	H	H
  LA733	CD3	RG57	CD3	H	H	CD3	LA1973	H	H	RG169	H	H	H
  LA734	CD3	RGS8	CD3	H	H	CD3	LA1974	H	H	H	RG1	H	H
  LA735	CD3	RG59	CD3	H	H	CD3	LA1975	H	H	H	RG2	H	H
  LA736	CD3	RG60	CD3	H	H	CD3	LA1976	H	H	H	RG3	H	H
  LA737	CD3	RG61	CD3	H	H	CD3	LA1977	H	H	H	RG4	H	H
  LA738	CD3	RG62	CD3	H	H	CD3	LA1978	H	H	H	RG5	H	H
  LA739	CD3	RG63	CD3	H	H	CD3	LA1979	H	H	H	RG6	H	H
  LA740	CD3	RG64	CD3	H	H	CD3	LA1980	H	H	H	RG7	H	H
  LA741	CD3	RG65	CD3	H	H	CD3	LA1981	H	H	H	RG8	H	H
  LA742	CD3	RG66	CD3	H	H	CD3	LA1982	H	H	H	RG9	H	H
  LA743	CD3	RG67	CD3	H	H	CD3	LA1983	H	H	H	RG10	H	H
  LA744	CD3	RG68	CD3	H	H	CD3	LA1984	H	H	H	RG11	H	H
  LA745	CD3	RG69	CD3	H	H	CD3	LA1985	H	H	H	RG12	H	H
  LA746	CD3	RG70	CD3	H	H	CD3	LA1986	H	H	H	RG13	H	H
  LA747	CD3	RG71	CD3	H	H	CD3	LA1987	H	H	H	RG14	H	H
  LA748	CD3	RG72	CD3	H	H	CD3	LA1988	H	H	H	RG15	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA749	CD3	RG73	CD3	H	H	CD3	LA1989	H	H	H	RG16	H	H
  LA750	CD3	RG74	CD3	H	H	CD3	LA1990	H	H	H	RG17	H	H
  LA751	CD3	RG75	CD3	H	H	CD3	LA1991	H	H	H	RG18	H	H
  LA752	CD3	RG76	CD3	H	H	CD3	LA1992	H	H	H	RG19	H	H
  LA753	CD3	RG77	CD3	H	H	CD3	LA1993	H	H	H	RG20	H	H
  LA754	CD3	RG78	CD3	H	H	CD3	LA1994	H	H	H	RG21	H	H
  LA755	CD3	RG79	CD3	H	H	CD3	LA1995	H	H	H	RG22	H	H
  LA756	CD3	RG80	CD3	H	H	CD3	LA1996	H	H	H	RG23	H	H
  LA757	CD3	RG81	CD3	H	H	CD3	LA1997	H	H	H	RG24	H	H
  LA758	CD3	RG82	CD3	H	H	CD3	LA1998	H	H	H	RG25	H	H
  LA759	CD3	RG83	CD3	H	H	CD3	LA1999	H	H	H	RG26	H	H
  LA760	CD3	RG84	CD3	H	H	CD3	LA2000	H	H	H	RG27	H	H
  LA761	CD3	RG85	CD3	H	H	CD3	LA2001	H	H	H	RG28	H	H
  LA762	CD3	RG86	CD3	H	H	CD3	LA2002	H	H	H	RG29	H	H
  LA763	CD3	RG87	CD3	H	H	CD3	LA2003	H	H	H	RG30	H	H
  LA764	CD3	RG88	CD3	H	H	CD3	LA2004	H	H	H	RG31	H	H
  LA765	CD3	RG89	CD3	H	H	CD3	LA2005	H	H	H	RG32	H	H
  LA766	CD3	RG90	CD3	H	H	CD3	LA2006	H	H	H	RG33	H	H
  LA767	CD3	RG91	CD3	H	H	CD3	LA2007	H	H	H	RG34	H	H
  LA768	CD3	RG92	CD3	H	H	CD3	LA2008	H	H	H	RG35	H	H
  LA769	CD3	RG93	CD3	H	H	CD3	LA2009	H	H	H	RG36	H	H
  LA770	CD3	RG94	CD3	H	H	CD3	LA2010	H	H	H	RG37	H	H
  LA771	CD3	RG95	CD3	H	H	CD3	LA2011	H	H	H	RG38	H	H
  LA772	CD3	RG96	CD3	H	H	CD3	LA2012	H	H	H	RG39	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA773	CD3	RG97	CD3	H	H	CD3	LA2013	H	H	H	RG40	H	H
  LA774	CD3	RG98	CD3	H	H	CD3	LA2014	H	H	H	RG41	H	H
  LA775	CD3	RG99	CD3	H	H	CD3	LA2015	H	H	H	RG42	H	H
  LA776	CD3	RG100	CD3	H	H	CD3	LA2016	H	H	H	RG43	H	H
  LA777	CD3	RG101	CD3	H	H	CD3	LA2017	H	H	H	RG44	H	H
  LA778	CD3	RG102	CD3	H	H	CD3	LA2018	H	H	H	RG45	H	H
  LA779	CD3	RG103	CD3	H	H	CD3	LA2019	H	H	H	RG46	H	H
  LA780	CD3	RG104	CD3	H	H	CD3	LA2020	H	H	H	RG47	H	H
  LA781	CD3	RG105	CD3	H	H	CD3	LA2021	H	H	H	RG48	H	H
  LA782	CD3	RG106	CD3	H	H	CD3	LA2022	H	H	H	RG49	H	H
  LA783	CD3	RG107	CD3	H	H	CD3	LA2023	H	H	H	RG50	H	H
  LA784	CD3	RG108	CD3	H	H	CD3	LA2024	H	H	H	RG51	H	H
  LA785	CD3	RG109	CD3	H	H	CD3	LA2025	H	H	H	RG52	H	H
  LA786	CD3	RG110	CD3	H	H	CD3	LA2026	H	H	H	RG53	H	H
  LA787	CD3	RG111	CD3	H	H	CD3	LA2027	H	H	H	RG54	H	H
  LA788	CD3	RG112	CD3	H	H	CD3	LA2028	H	H	H	RG55	H	H
  LA789	CD3	RG113	CD3	H	H	CD3	LA2029	H	H	H	RG56	H	H
  LA790	CD3	RG114	CD3	H	H	CD3	LA2030	H	H	H	RG57	H	H
  LA791	CD3	RG115	CD3	H	H	CD3	LA2031	H	H	H	RGS8	H	H
  LA792	CD3	RG116	CD3	H	H	CD3	LA2032	H	H	H	RG59	H	H
  LA793	CD3	RG117	CD3	H	H	CD3	LA2033	H	H	H	RG60	H	H
  LA794	CD3	RG118	CD3	H	H	CD3	LA2034	H	H	H	RG61	H	H
  LA795	CD3	RG119	CD3	H	H	CD3	LA2035	H	H	H	RG62	H	H
  LA796	CD3	RG120	CD3	H	H	CD3	LA2036	H	H	H	RG63	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA797	CD3	RG121	CD3	H	H	CD3	LA2037	H	H	H	RG64	H	H
  LA798	CD3	RG122	CD3	H	H	CD3	LA2038	H	H	H	RG65	H	H
  LA799	CD3	RG123	CD3	H	H	CD3	LA2039	H	H	H	RG66	H	H
  LA800	CD3	RG124	CD3	H	H	CD3	LA2040	H	H	H	RG67	H	H
  LA801	CD3	RG125	CD3	H	H	CD3	LA2041	H	H	H	RG68	H	H
  LA802	CD3	RG126	CD3	H	H	CD3	LA2042	H	H	H	RG69	H	H
  LA803	CD3	RG127	CD3	H	H	CD3	LA2043	H	H	H	RG70	H	H
  LA804	CD3	RG128	CD3	H	H	CD3	LA2044	H	H	H	RG71	H	H
  LA805	CD3	RG129	CD3	H	H	CD3	LA2045	H	H	H	RG72	H	H
  LA806	CD3	RG130	CD3	H	H	CD3	LA2046	H	H	H	RG73	H	H
  LA807	CD3	RG131	CD3	H	H	CD3	LA2047	H	H	H	RG74	H	H
  LA808	CD3	RG132	CD3	H	H	CD3	LA2048	H	H	H	RG75	H	H
  LA809	CD3	RG133	CD3	H	H	CD3	LA2049	H	H	H	RG76	H	H
  LA810	CD3	RG134	CD3	H	H	CD3	LA2050	H	H	H	RG77	H	H
  LA811	CD3	RG135	CD3	H	H	CD3	LA2051	H	H	H	RG78	H	H
  LA812	CD3	RG136	CD3	H	H	CD3	LA2052	H	H	H	RG79	H	H
  LA813	CD3	RG137	CD3	H	H	CD3	LA2053	H	H	H	RG80	H	H
  LA814	CD3	RG138	CD3	H	H	CD3	LA2054	H	H	H	RG81	H	H
  LA815	CD3	RG139	CD3	H	H	CD3	LA2055	H	H	H	RG82	H	H
  LA816	CD3	RG140	CD3	H	H	CD3	LA2056	H	H	H	RG83	H	H
  LA817	CD3	RG141	CD3	H	H	CD3	LA2057	H	H	H	RG84	H	H
  LA818	CD3	RG142	CD3	H	H	CD3	LA2058	H	H	H	RG85	H	H
  LA819	CD3	RG143	CD3	H	H	CD3	LA2059	H	H	H	RG86	H	H
  LA820	CD3	RG144	CD3	H	H	CD3	LA2060	H	H	H	RG87	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA821	CD3	RG145	CD3	H	H	CD3	LA2061	H	H	H	RG88	H	H
  LA822	CD3	RG146	CD3	H	H	CD3	LA2062	H	H	H	RG89	H	H
  LA823	CD3	RG147	CD3	H	H	CD3	LA2063	H	H	H	RG90	H	H
  LA824	CD3	RG148	CD3	H	H	CD3	LA2064	H	H	H	RG91	H	H
  LA825	CD3	RG149	CD3	H	H	CD3	LA2065	H	H	H	RG92	H	H
  LA826	CD3	RG150	CD3	H	H	CD3	LA2066	H	H	H	RG93	H	H
  LA827	CD3	RG151	CD3	H	H	CD3	LA2067	H	H	H	RG94	H	H
  LA828	CD3	RG152	CD3	H	H	CD3	LA2068	H	H	H	RG95	H	H
  LA829	CD3	RG153	CD3	H	H	CD3	LA2069	H	H	H	RG96	H	H
  LA830	CD3	RG154	CD3	H	H	CD3	LA2070	H	H	H	RG97	H	H
  LA831	CD3	RG155	CD3	H	H	CD3	LA2071	H	H	H	RG98	H	H
  LA832	CD3	RG156	CD3	H	H	CD3	LA2072	H	H	H	RG99	H	H
  LA833	CD3	RG157	CD3	H	H	CD3	LA2073	H	H	H	RG100	H	H
  LA834	CD3	RG158	CD3	H	H	CD3	LA2074	H	H	H	RG101	H	H
  LA835	CD3	RG159	CD3	H	H	CD3	LA2075	H	H	H	RG102	H	H
  LA836	CD3	RG160	CD3	H	H	CD3	LA2076	H	H	H	RG103	H	H
  LA837	CD3	RG161	CD3	H	H	CD3	LA2077	H	H	H	RG104	H	H
  LA838	CD3	RG162	CD3	H	H	CD3	LA2078	H	H	H	RG105	H	H
  LA839	CD3	RG163	CD3	H	H	CD3	LA2079	H	H	H	RG106	H	H
  LA840	CD3	RG164	CD3	H	H	CD3	LA2080	H	H	H	RG107	H	H
  LA841	CD3	RG165	CD3	H	H	CD3	LA2081	H	H	H	RG108	H	H
  LA842	CD3	RG166	CD3	H	H	CD3	LA2082	H	H	H	RG109	H	H
  LA843	CD3	RG167	CD3	H	H	CD3	LA2083	H	H	H	RG110	H	H
  LA844	CD3	RG168	CD3	H	H	CD3	LA2084	H	H	H	RG111	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA845	CD3	RG169	CD3	H	H	CD3	LA2085	H	H	H	RG112	H	H
  LA846	CD3	RG1	CD3	H	H	H	LA2086	H	H	H	RG113	H	H
  LA847	CD3	RG2	CD3	H	H	H	LA2087	H	H	H	RG114	H	H
  LA848	CD3	RG3	CD3	H	H	H	LA2088	H	H	H	RG115	H	H
  LA849	CD3	RG4	CD3	H	H	H	LA2089	H	H	H	RG116	H	H
  LA850	CD3	RG5	CD3	H	H	H	LA2090	H	H	H	RG117	H	H
  LA851	CD3	RG6	CD3	H	H	H	LA2091	H	H	H	RG118	H	H
  LA852	CD3	RG7	CD3	H	H	H	LA2092	H	H	H	RG119	H	H
  LA853	CD3	RG8	CD3	H	H	H	LA2093	H	H	H	RG120	H	H
  LA854	CD3	RG9	CD3	H	H	H	LA2094	H	H	H	RG121	H	H
  LA855	CD3	RG10	CD3	H	H	H	LA2095	H	H	H	RG122	H	H
  LA856	CD3	RG11	CD3	H	H	H	LA2096	H	H	H	RG123	H	H
  LA857	CD3	RG12	CD3	H	H	H	LA2097	H	H	H	RG124	H	H
  LA858	CD3	RG13	CD3	H	H	H	LA2098	H	H	H	RG125	H	H
  LA859	CD3	RG14	CD3	H	H	H	LA2099	H	H	H	RG126	H	H
  LA860	CD3	RG15	CD3	H	H	H	LA2100	H	H	H	RG127	H	H
  LA861	CD3	RG16	CD3	H	H	H	LA2101	H	H	H	RG128	H	H
  LA862	CD3	RG17	CD3	H	H	H	LA2102	H	H	H	RG129	H	H
  LA863	CD3	RG18	CD3	H	H	H	LA2103	H	H	H	RG130	H	H
  LA864	CD3	RG19	CD3	H	H	H	LA2104	H	H	H	RG131	H	H
  LA865	CD3	RG20	CD3	H	H	H	LA2105	H	H	H	RG132	H	H
  LA866	CD3	RG21	CD3	H	H	H	LA2106	H	H	H	RG133	H	H
  LA867	CD3	RG22	CD3	H	H	H	LA2107	H	H	H	RG134	H	H
  LA868	CD3	RG23	CD3	H	H	H	LA2108	H	H	H	RG135	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA869	CD3	RG24	CD3	H	H	H	LA2109	H	H	H	RG136	H	H
  LA870	CD3	RG25	CD3	H	H	H	LA2110	H	H	H	RG137	H	H
  LA871	CD3	RG26	CD3	H	H	H	LA2111	H	H	H	RG138	H	H
  LA872	CD3	RG27	CD3	H	H	H	LA2112	H	H	H	RG139	H	H
  LA873	CD3	RG28	CD3	H	H	H	LA2113	H	H	H	RG140	H	H
  LA874	CD3	RG29	CD3	H	H	H	LA2114	H	H	H	RG141	H	H
  LA875	CD3	RG30	CD3	H	H	H	LA2115	H	H	H	RG142	H	H
  LA876	CD3	RG31	CD3	H	H	H	LA2116	H	H	H	RG143	H	H
  LA877	CD3	RG32	CD3	H	H	H	LA2117	H	H	H	RG144	H	H
  LA878	CD3	RG33	CD3	H	H	H	LA2118	H	H	H	RG145	H	H
  LA879	CD3	RG34	CD3	H	H	H	LA2119	H	H	H	RG146	H	H
  LA880	CD3	RG35	CD3	H	H	H	LA2120	H	H	H	RG147	H	H
  LA881	CD3	RG36	CD3	H	H	H	LA2121	H	H	H	RG148	H	H
  LA882	CD3	RG37	CD3	H	H	H	LA2122	H	H	H	RG149	H	H
  LA883	CD3	RG38	CD3	H	H	H	LA2123	H	H	H	RG150	H	H
  LA884	CD3	RG39	CD3	H	H	H	LA2124	H	H	H	RG151	H	H
  LA885	CD3	RG40	CD3	H	H	H	LA2125	H	H	H	RG152	H	H
  LA886	CD3	RG41	CD3	H	H	H	LA2126	H	H	H	RG153	H	H
  LA887	CD3	RG42	CD3	H	H	H	LA2127	H	H	H	RG154	H	H
  LA888	CD3	RG43	CD3	H	H	H	LA2128	H	H	H	RG155	H	H
  LA889	CD3	RG44	CD3	H	H	H	LA2129	H	H	H	RG156	H	H
  LA890	CD3	RG45	CD3	H	H	H	LA2130	H	H	H	RG157	H	H
  LA891	CD3	RG46	CD3	H	H	H	LA2131	H	H	H	RG158	H	H
  LA892	CD3	RG47	CD3	H	H	H	LA2132	H	H	H	RG159	H	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA893	CD3	RG48	CD3	H	H	H	LA2133	H	H	H	RG160	H	H
  LA894	CD3	RG49	CD3	H	H	H	LA2134	H	H	H	RG161	H	H
  LA895	CD3	RG50	CD3	H	H	H	LA2135	H	H	H	RG162	H	H
  LA896	CD3	RG51	CD3	H	H	H	LA2136	H	H	H	RG163	H	H
  LA897	CD3	RG52	CD3	H	H	H	LA2137	H	H	H	RG164	H	H
  LA898	CD3	RG53	CD3	H	H	H	LA2138	H	H	H	RG165	H	H
  LA899	CD3	RG54	CD3	H	H	H	LA2139	H	H	H	RG166	H	H
  LA900	CD3	RG55	CD3	H	H	H	LA2140	H	H	H	RG167	H	H
  LA901	CD3	RG56	CD3	H	H	H	LA2141	H	H	H	RG168	H	H
  LA902	CD3	RG57	CD3	H	H	H	LA2142	H	H	H	RG169	H	H
  LA903	CD3	RG58	CD3	H	H	H	LA2143	H	H	H	H	RG1	H
  LA904	CD3	RG59	CD3	H	H	H	LA2144	H	H	H	H	RG2	H
  LA905	CD3	RG60	CD3	H	H	H	LA2145	H	H	H	H	RG3	H
  LA906	CD3	RG61	CD3	H	H	H	LA2146	H	H	H	H	RG4	H
  LA907	CD3	RG62	CD3	H	H	H	LA2147	H	H	H	H	RG5	H
  LA908	CD3	RG63	CD3	H	H	H	LA2148	H	H	H	H	RG6	H
  LA909	CD3	RG64	CD3	H	H	H	LA2149	H	H	H	H	RG7	H
  LA910	CD3	RG65	CD3	H	H	H	LA2150	H	H	H	H	RG8	H
  LA911	CD3	RG66	CD3	H	H	H	LA2151	H	H	H	H	RG9	H
  LA912	CD3	RG67	CD3	H	H	H	LA2152	H	H	H	H	RG10	H
  LA913	CD3	RG68	CD3	H	H	H	LA2153	H	H	H	H	RG11	H
  LA914	CD3	RG69	CD3	H	H	H	LA2154	H	H	H	H	RG12	H
  LA915	CD3	RG70	CD3	H	H	H	LA2155	H	H	H	H	RG13	H
  LA916	CD3	RG71	CD3	H	H	H	LA2156	H	H	H	H	RG14	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA917	CD3	RG72	CD3	H	H	H	LA2157	H	H	H	H	RG15	H
  LA918	CD3	RG73	CD3	H	H	H	LA2158	H	H	H	H	RG16	H
  LA919	CD3	RG74	CD3	H	H	H	LA2159	H	H	H	H	RG17	H
  LA920	CD3	RG75	CD3	H	H	H	LA2160	H	H	H	H	RG18	H
  LA921	CD3	RG76	CD3	H	H	H	LA2161	H	H	H	H	RG19	H
  LA922	CD3	RG77	CD3	H	H	H	LA2162	H	H	H	H	RG20	H
  LA923	CD3	RG78	CD3	H	H	H	LA2163	H	H	H	H	RG21	H
  LA924	CD3	RG79	CD3	H	H	H	LA2164	H	H	H	H	RG22	H
  LA925	CD3	RG80	CD3	H	H	H	LA2165	H	H	H	H	RG23	H
  LA926	CD3	RG81	CD3	H	H	H	LA2166	H	H	H	H	RG24	H
  LA927	CD3	RG82	CD3	H	H	H	LA2167	H	H	H	H	RG25	H
  LA928	CD3	RG83	CD3	H	H	H	LA2168	H	H	H	H	RG26	H
  LA929	CD3	RG84	CD3	H	H	H	LA2169	H	H	H	H	RG27	H
  LA930	CD3	RG85	CD3	H	H	H	LA2170	H	H	H	H	RG28	H
  LA931	CD3	RG86	CD3	H	H	H	LA2171	H	H	H	H	RG29	H
  LA932	CD3	RG87	CD3	H	H	H	LA2172	H	H	H	H	RG30	H
  LA933	CD3	RG88	CD3	H	H	H	LA2173	H	H	H	H	RG31	H
  LA934	CD3	RG89	CD3	H	H	H	LA2174	H	H	H	H	RG32	H
  LA935	CD3	RG90	CD3	H	H	H	LA2175	H	H	H	H	RG33	H
  LA936	CD3	RG91	CD3	H	H	H	LA2176	H	H	H	H	RG34	H
  LA937	CD3	RG92	CD3	H	H	H	LA2177	H	H	H	H	RG35	H
  LA938	CD3	RG93	CD3	H	H	H	LA2178	H	H	H	H	RG36	H
  LA939	CD3	RG94	CD3	H	H	H	LA2179	H	H	H	H	RG37	H
  LA940	CD3	RG95	CD3	H	H	H	LA2180	H	H	H	H	RG38	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA941	CD3	RG96	CD3	H	H	H	LA2181	H	H	H	H	RG39	H
  LA942	CD3	RG97	CD3	H	H	H	LA2182	H	H	H	H	RG40	H
  LA943	CD3	RG98	CD3	H	H	H	LA2183	H	H	H	H	RG41	H
  LA944	CD3	RG99	CD3	H	H	H	LA2184	H	H	H	H	RG42	H
  LA945	CD3	RG100	CD3	H	H	H	LA2185	H	H	H	H	RG43	H
  LA946	CD3	RG101	CD3	H	H	H	LA2186	H	H	H	H	RG44	H
  LA947	CD3	RG102	CD3	H	H	H	LA2187	H	H	H	H	RG45	H
  LA948	CD3	RG103	CD3	H	H	H	LA2188	H	H	H	H	RG46	H
  LA949	CD3	RG104	CD3	H	H	H	LA2189	H	H	H	H	RG47	H
  LA950	CD3	RG105	CD3	H	H	H	LA2190	H	H	H	H	RG48	H
  LA951	CD3	RG106	CD3	H	H	H	LA2191	H	H	H	H	RG49	H
  LA952	CD3	RG107	CD3	H	H	H	LA2192	H	H	H	H	RG50	H
  LA953	CD3	RG108	CD3	H	H	H	LA2193	H	H	H	H	RG51	H
  LA954	CD3	RG109	CD3	H	H	H	LA2194	H	H	H	H	RG52	H
  LA955	CD3	RG110	CD3	H	H	H	LA2195	H	H	H	H	RG53	H
  LA956	CD3	RG111	CD3	H	H	H	LA2196	H	H	H	H	RG54	H
  LA957	CD3	RG112	CD3	H	H	H	LA2197	H	H	H	H	RG55	H
  LA958	CD3	RG113	CD3	H	H	H	LA2198	H	H	H	H	RG56	H
  LA959	CD3	RG114	CD3	H	H	H	LA2199	H	H	H	H	RG57	H
  LA960	CD3	RG115	CD3	H	H	H	LA2200	H	H	H	H	RG58	H
  LA961	CD3	RG116	CD3	H	H	H	LA2201	H	H	H	H	RG59	H
  LA962	CD3	RG117	CD3	H	H	H	LA2202	H	H	H	H	RG60	H
  LA963	CD3	RG118	CD3	H	H	H	LA2203	H	H	H	H	RG61	H
  LA964	CD3	RG119	CD3	H	H	H	LA2204	H	H	H	H	RG62	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA965	CD3	RG120	CD3	H	H	H	LA2205	H	H	H	H	RG63	H
  LA966	CD3	RG121	CD3	H	H	H	LA2206	H	H	H	H	RG64	H
  LA967	CD3	RG122	CD3	H	H	H	LA2207	H	H	H	H	RG65	H
  LA968	CD3	RG123	CD3	H	H	H	LA2208	H	H	H	H	RG66	H
  LA969	CD3	RG124	CD3	H	H	H	LA2209	H	H	H	H	RG67	H
  LA970	CD3	RG125	CD3	H	H	H	LA2210	H	H	H	H	RG68	H
  LA971	CD3	RG126	CD3	H	H	H	LA2211	H	H	H	H	RG69	H
  LA972	CD3	RG127	CD3	H	H	H	LA2212	H	H	H	H	RG70	H
  LA973	CD3	RG128	CD3	H	H	H	LA2213	H	H	H	H	RG71	H
  LA974	CD3	RG129	CD3	H	H	H	LA2214	H	H	H	H	RG72	H
  LA975	CD3	RG130	CD3	H	H	H	LA2215	H	H	H	H	RG73	H
  LA976	CD3	RG131	CD3	H	H	H	LA2216	H	H	H	H	RG74	H
  LA977	CD3	RG132	CD3	H	H	H	LA2217	H	H	H	H	RG75	H
  LA978	CD3	RG133	CD3	H	H	H	LA2218	H	H	H	H	RG76	H
  LA979	CD3	RG134	CD3	H	H	H	LA2219	H	H	H	H	RG77	H
  LA980	CD3	RG135	CD3	H	H	H	LA2220	H	H	H	H	RG78	H
  LA981	CD3	RG136	CD3	H	H	H	LA2221	H	H	H	H	RG79	H
  LA982	CD3	RG137	CD3	H	H	H	LA2222	H	H	H	H	RG80	H
  LA983	CD3	RG138	CD3	H	H	H	LA2223	H	H	H	H	RG81	H
  LA984	CD3	RG139	CD3	H	H	H	LA2224	H	H	H	H	RG82	H
  LA985	CD3	RG140	CD3	H	H	H	LA2225	H	H	H	H	RG83	H
  LA986	CD3	RG141	CD3	H	H	H	LA2226	H	H	H	H	RG84	H
  LA987	CD3	RG142	CD3	H	H	H	LA2227	H	H	H	H	RG85	H
  LA988	CD3	RG143	CD3	H	H	H	LA2228	H	H	H	H	RG86	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA989	CD3	RG144	CD3	H	H	H	LA2229	H	H	H	H	RG87	H
  LA990	CD3	RG145	CD3	H	H	H	LA2230	H	H	H	H	RG88	H
  LA991	CD3	RG146	CD3	H	H	H	LA2231	H	H	H	H	RG89	H
  LA992	CD3	RG147	CD3	H	H	H	LA2232	H	H	H	H	RG90	H
  LA993	CD3	RG148	CD3	H	H	H	LA2233	H	H	H	H	RG91	H
  LA994	CD3	RG149	CD3	H	H	H	LA2234	H	H	H	H	RG92	H
  LA995	CD3	RG150	CD3	H	H	H	LA2235	H	H	H	H	RG93	H
  LA996	CD3	RG151	CD3	H	H	H	LA2236	H	H	H	H	RG94	H
  LA997	CD3	RG152	CD3	H	H	H	LA2237	H	H	H	H	RG95	H
  LA998	CD3	RG153	CD3	H	H	H	LA2238	H	H	H	H	RG96	H
  LA999	CD3	RG154	CD3	H	H	H	LA2239	H	H	H	H	RG97	H
  LA1000	CD3	RG155	CD3	H	H	H	LA2240	H	H	H	H	RG98	H
  LA1001	CD3	RG156	CD3	H	H	H	LA2241	H	H	H	H	RG99	H
  LA1002	CD3	RG157	CD3	H	H	H	LA2242	H	H	H	H	RG100	H
  LA1003	CD3	RG158	CD3	H	H	H	LA2243	H	H	H	H	RG101	H
  LA1004	CD3	RG159	CD3	H	H	H	LA2244	H	H	H	H	RG102	H
  LA1005	CD3	RG160	CD3	H	H	H	LA2245	H	H	H	H	RG103	H
  LA1006	CD3	RG161	CD3	H	H	H	LA2246	H	H	H	H	RG104	H
  LA1007	CD3	RG162	CD3	H	H	H	LA2247	H	H	H	H	RG105	H
  LA1008	CD3	RG163	CD3	H	H	H	LA2248	H	H	H	H	RG106	H
  LA1009	CD3	RG164	CD3	H	H	H	LA2249	H	H	H	H	RG107	H
  LA1010	CD3	RG165	CD3	H	H	H	LA2250	H	H	H	H	RG108	H
  LA1011	CD3	RG166	CD3	H	H	H	LA2251	H	H	H	H	RG109	H
  LA1012	CD3	RG167	CD3	H	H	H	LA2252	H	H	H	H	RG110	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1013	CD3	RG168	CD3	H	H	H	LA2253	H	H	H	H	RG111	H
  LA1014	CD3	RG169	CD3	H	H	H	LA2254	H	H	H	H	RG112	H
  LA1015	CD3	CD3	RG1	H	H	H	LA2255	H	H	H	H	RG113	H
  LA1016	CD3	CD3	RG2	H	H	H	LA2256	H	H	H	H	RG114	H
  LA1017	CD3	CD3	RG3	H	H	H	LA2257	H	H	H	H	RG115	H
  LA1018	CD3	CD3	RG4	H	H	H	LA2258	H	H	H	H	RG116	H
  LA1019	CD3	CD3	RG5	H	H	H	LA2259	H	H	H	H	RG117	H
  LA1020	CD3	CD3	RG6	H	H	H	LA2260	H	H	H	H	RG118	H
  LA1021	CD3	CD3	RG7	H	H	H	LA2261	H	H	H	H	RG119	H
  LA1022	CD3	CD3	RG8	H	H	H	LA2262	H	H	H	H	RG120	H
  LA1023	CD3	CD3	RG9	H	H	H	LA2263	H	H	H	H	RG121	H
  LA1024	CD3	CD3	RG10	H	H	H	LA2264	H	H	H	H	RG122	H
  LA1025	CD3	CD3	RG11	H	H	H	LA2265	H	H	H	H	RG123	H
  LA1026	CD3	CD3	RG12	H	H	H	LA2266	H	H	H	H	RG124	H
  LA1027	CD3	CD3	RG13	H	H	H	LA2267	H	H	H	H	RG125	H
  LA1028	CD3	CD3	RG14	H	H	H	LA2268	H	H	H	H	RG126	H
  LA1029	CD3	CD3	RG15	H	H	H	LA2269	H	H	H	H	RG127	H
  LA1030	CD3	CD3	RG16	H	H	H	LA2270	H	H	H	H	RG128	H
  LA1031	CD3	CD3	RG17	H	H	H	LA2271	H	H	H	H	RG129	H
  LA1032	CD3	CD3	RG18	H	H	H	LA2272	H	H	H	H	RG130	H
  LA1033	CD3	CD3	RG19	H	H	H	LA2273	H	H	H	H	RG131	H
  LA1034	CD3	CD3	RG20	H	H	H	LA2274	H	H	H	H	RG132	H
  LA1035	CD3	CD3	RG21	H	H	H	LA2275	H	H	H	H	RG133	H
  LA1036	CD3	CD3	RG22	H	H	H	LA2276	H	H	H	H	RG134	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1037	CD3	CD3	RG23	H	H	H	LA2277	H	H	H	H	RG135	H
  LA1038	CD3	CD3	RG24	H	H	H	LA2278	H	H	H	H	RG136	H
  LA1039	CD3	CD3	RG25	H	H	H	LA2279	H	H	H	H	RG137	H
  LA1040	CD3	CD3	RG26	H	H	H	LA2280	H	H	H	H	RG138	H
  LA1041	CD3	CD3	RG27	H	H	H	LA2281	H	H	H	H	RG139	H
  LA1042	CD3	CD3	RG28	H	H	H	LA2282	H	H	H	H	RG140	H
  LA1043	CD3	CD3	RG29	H	H	H	LA2283	H	H	H	H	RG141	H
  LA1044	CD3	CD3	RG30	H	H	H	LA2284	H	H	H	H	RG142	H
  LA1045	CD3	CD3	RG31	H	H	H	LA2285	H	H	H	H	RG143	H
  LA1046	CD3	CD3	RG32	H	H	H	LA2286	H	H	H	H	RG144	H
  LA1047	CD3	CD3	RG33	H	H	H	LA2287	H	H	H	H	RG145	H
  LA1048	CD3	CD3	RG34	H	H	H	LA2288	H	H	H	H	RG146	H
  LA1049	CD3	CD3	RG35	H	H	H	LA2289	H	H	H	H	RG147	H
  LA1050	CD3	CD3	RG36	H	H	H	LA2290	H	H	H	H	RG148	H
  LA1051	CD3	CD3	RG37	H	H	H	LA2291	H	H	H	H	RG149	H
  LA1052	CD3	CD3	RG38	H	H	H	LA2292	H	H	H	H	RG150	H
  LA1053	CD3	CD3	RG39	H	H	H	LA2293	H	H	H	H	RG151	H
  LA1054	CD3	CD3	RG40	H	H	H	LA2294	H	H	H	H	RG152	H
  LA1055	CD3	CD3	RG41	H	H	H	LA2295	H	H	H	H	RG153	H
  LA1056	CD3	CD3	RG42	H	H	H	LA2296	H	H	H	H	RG154	H
  LA1057	CD3	CD3	RG43	H	H	H	LA2297	H	H	H	H	RG155	H
  LA1058	CD3	CD3	RG44	H	H	H	LA2298	H	H	H	H	RG156	H
  LA1059	CD3	CD3	RG45	H	H	H	LA2299	H	H	H	H	RG157	H
  LA1060	CD3	CD3	RG46	H	H	H	LA2300	H	H	H	H	RG158	H

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1061	CD3	CD3	RG47	H	H	H	LA2301	H	H	H	H	RG159	H
  LA1062	CD3	CD3	RG48	H	H	H	LA2302	H	H	H	H	RG160	H
  LA1063	CD3	CD3	RG49	H	H	H	LA2303	H	H	H	H	RG161	H
  LA1064	CD3	CD3	RG50	H	H	H	LA2304	H	H	H	H	RG162	H
  LA1065	CD3	CD3	RG51	H	H	H	LA2305	H	H	H	H	RG163	H
  LA1066	CD3	CD3	RG52	H	H	H	LA2306	H	H	H	H	RG164	H
  LA1067	CD3	CD3	RG53	H	H	H	LA2307	H	H	H	H	RG165	H
  LA1068	CD3	CD3	RG54	H	H	H	LA2308	H	H	H	H	RG166	H
  LA1069	CD3	CD3	RG55	H	H	H	LA2309	H	H	H	H	RG167	H
  LA1070	CD3	CD3	RG56	H	H	H	LA2310	H	H	H	H	RG168	H
  LA1071	CD3	CD3	RG57	H	H	H	LA2311	H	H	H	H	RG169	H
  LA1072	CD3	CD3	RG58	H	H	H	LA2312	H	H	H	H	H	RG1
  LA1073	CD3	CD3	RG59	H	H	H	LA2313	H	H	H	H	H	RG2
  LA1074	CD3	CD3	RG60	H	H	H	LA2314	H	H	H	H	H	RG3
  LA1075	CD3	CD3	RG61	H	H	H	LA2315	H	H	H	H	H	RG4
  LA1076	CD3	CD3	RG62	H	H	H	LA2316	H	H	H	H	H	RG5
  LA1077	CD3	CD3	RG63	H	H	H	LA2317	H	H	H	H	H	RG6
  LA1078	CD3	CD3	RG64	H	H	H	LA2318	H	H	H	H	H	RG7
  LA1079	CD3	CD3	RG65	H	H	H	LA2319	H	H	H	H	H	RG8
  LA1080	CD3	CD3	RG66	H	H	H	LA2320	H	H	H	H	H	RG9
  LA1081	CD3	CD3	RG67	H	H	H	LA2321	H	H	H	H	H	RG10
  LA1082	CD3	CD3	RG68	H	H	H	LA2322	H	H	H	H	H	RG11
  LA1083	CD3	CD3	RG69	H	H	H	LA2323	H	H	H	H	H	RG12
  LA1084	CD3	CD3	RG70	H	H	H	LA2324	H	H	H	H	H	RG13

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1085	CD3	CD3	RG71	H	H	H	LA2325	H	H	H	H	H	RG14
  LA1086	CD3	CD3	RG72	H	H	H	LA2326	H	H	H	H	H	RG15
  LA1087	CD3	CD3	RG73	H	H	H	LA2327	H	H	H	H	H	RG16
  LA1088	CD3	CD3	RG74	H	H	H	LA2328	H	H	H	H	H	RG17
  LA1089	CD3	CD3	RG75	H	H	H	LA2329	H	H	H	H	H	RG18
  LA1090	CD3	CD3	RG76	H	H	H	LA2330	H	H	H	H	H	RG19
  LA1091	CD3	CD3	RG77	H	H	H	LA2331	H	H	H	H	H	RG20
  LA1092	CD3	CD3	RG78	H	H	H	LA2332	H	H	H	H	H	RG21
  LA1093	CD3	CD3	RG79	H	H	H	LA2333	H	H	H	H	H	RG22
  LA1094	CD3	CD3	RG80	H	H	H	LA2334	H	H	H	H	H	RG23
  LA1095	CD3	CD3	RG81	H	H	H	LA2335	H	H	H	H	H	RG24
  LA1096	CD3	CD3	RG82	H	H	H	LA2336	H	H	H	H	H	RG25
  LA1097	CD3	CD3	RG83	H	H	H	LA2337	H	H	H	H	H	RG26
  LA1098	CD3	CD3	RG84	H	H	H	LA2338	H	H	H	H	H	RG27
  LA1099	CD3	CD3	RG85	H	H	H	LA2339	H	H	H	H	H	RG28
  LA1100	CD3	CD3	RG86	H	H	H	LA2340	H	H	H	H	H	RG29
  LA1101	CD3	CD3	RG87	H	H	H	LA2341	H	H	H	H	H	RG30
  LA1102	CD3	CD3	RG88	H	H	H	LA2342	H	H	H	H	H	RG31
  LA1103	CD3	CD3	RG89	H	H	H	LA2343	H	H	H	H	H	RG32
  LA1104	CD3	CD3	RG90	H	H	H	LA2344	H	H	H	H	H	RG33
  LA1105	CD3	CD3	RG91	H	H	H	LA2345	H	H	H	H	H	RG34
  LA1106	CD3	CD3	RG92	H	H	H	LA2346	H	H	H	H	H	RG35
  LA1107	CD3	CD3	RG93	H	H	H	LA2347	H	H	H	H	H	RG36
  LA1108	CD3	CD3	RG94	H	H	H	LA2348	H	H	H	H	H	RG37

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1109	CD3	CD3	RG95	H	H	H	LA2349	H	H	H	H	H	RG38
  LA1110	CD3	CD3	RG96	H	H	H	LA2350	H	H	H	H	H	RG39
  LA1111	CD3	CD3	RG97	H	H	H	LA2351	H	H	H	H	H	RG40
  LA1112	CD3	CD3	RG98	H	H	H	LA2352	H	H	H	H	H	RG41
  LA1113	CD3	CD3	RG99	H	H	H	LA2353	H	H	H	H	H	RG42
  LA1114	CD3	CD3	RG100	H	H	H	LA2354	H	H	H	H	H	RG43
  LA1115	CD3	CD3	RG101	H	H	H	LA2355	H	H	H	H	H	RG44
  LA1116	CD3	CD3	RG102	H	H	H	LA2356	H	H	H	H	H	RG45
  LA1117	CD3	CD3	RG103	H	H	H	LA2357	H	H	H	H	H	RG46
  LA1118	CD3	CD3	RG104	H	H	H	LA2358	H	H	H	H	H	RG47
  LA1119	CD3	CD3	RG105	H	H	H	LA2359	H	H	H	H	H	RG48
  LA1120	CD3	CD3	RG106	H	H	H	LA2360	H	H	H	H	H	RG49
  LA1121	CD3	CD3	RG107	H	H	H	LA2361	H	H	H	H	H	RG50
  LA1122	CD3	CD3	RG108	H	H	H	LA2362	H	H	H	H	H	RG51
  LA1123	CD3	CD3	RG109	H	H	H	LA2363	H	H	H	H	H	RG52
  LA1124	CD3	CD3	RG110	H	H	H	LA2364	H	H	H	H	H	RG53
  LA1125	CD3	CD3	RG111	H	H	H	LA2365	H	H	H	H	H	RG54
  LA1126	CD3	CD3	RG112	H	H	H	LA2366	H	H	H	H	H	RG55
  LA1127	CD3	CD3	RG113	H	H	H	LA2367	H	H	H	H	H	RG56
  LA1128	CD3	CD3	RG114	H	H	H	LA2368	H	H	H	H	H	RG57
  LA1129	CD3	CD3	RG115	H	H	H	LA2369	H	H	H	H	H	RG58
  LA1130	CD3	CD3	RG116	H	H	H	LA2370	H	H	H	H	H	RG59
  LA1131	CD3	CD3	RG117	H	H	H	LA2371	H	H	H	H	H	RG60
  LA1132	CD3	CD3	RG118	H	H	H	LA2372	H	H	H	H	H	RG61

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1133	CD3	CD3	RG119	H	H	H	LA2373	H	H	H	H	H	RG62
  LA1134	CD3	CD3	RG120	H	H	H	LA2374	H	H	H	H	H	RG63
  LA1135	CD3	CD3	RG121	H	H	H	LA2375	H	H	H	H	H	RG64
  LA1136	CD3	CD3	RG122	H	H	H	LA2376	H	H	H	H	H	RG65
  LA1137	CD3	CD3	RG123	H	H	H	LA2377	H	H	H	H	H	RG66
  LA1138	CD3	CD3	RG124	H	H	H	LA2378	H	H	H	H	H	RG67
  LA1139	CD3	CD3	RG125	H	H	H	LA2379	H	H	H	H	H	RG68
  LA1140	CD3	CD3	RG126	H	H	H	LA2380	H	H	H	H	H	RG69
  LA1141	CD3	CD3	RG127	H	H	H	LA2381	H	H	H	H	H	RG70
  LA1142	CD3	CD3	RG128	H	H	H	LA2382	H	H	H	H	H	RG71
  LA1143	CD3	CD3	RG129	H	H	H	LA2383	H	H	H	H	H	RG72
  LA1144	CD3	CD3	RG130	H	H	H	LA2384	H	H	H	H	H	RG73
  LA1145	CD3	CD3	RG131	H	H	H	LA2385	H	H	H	H	H	RG74
  LA1146	CD3	CD3	RG132	H	H	H	LA2386	H	H	H	H	H	RG75
  LA1147	CD3	CD3	RG133	H	H	H	LA2387	H	H	H	H	H	RG76
  LA1148	CD3	CD3	RG134	H	H	H	LA2388	H	H	H	H	H	RG77
  LA1149	CD3	CD3	RG135	H	H	H	LA2389	H	H	H	H	H	RG78
  LA1150	CD3	CD3	RG136	H	H	H	LA2390	H	H	H	H	H	RG79
  LA1151	CD3	CD3	RG137	H	H	H	LA2391	H	H	H	H	H	RG80
  LA1152	CD3	CD3	RG138	H	H	H	LA2392	H	H	H	H	H	RG81
  LA1153	CD3	CD3	RG139	H	H	H	LA2393	H	H	H	H	H	RG82
  LA1154	CD3	CD3	RG140	H	H	H	LA2394	H	H	H	H	H	RG83
  LA1155	CD3	CD3	RG141	H	H	H	LA2395	H	H	H	H	H	RG84
  LA1156	CD3	CD3	RG142	H	H	H	LA2396	H	H	H	H	H	RG85

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1157	CD3	CD3	RG143	H	H	H	LA2397	H	H	H	H	H	RG86
  LA1158	CD3	CD3	RG144	H	H	H	LA2398	H	H	H	H	H	RG87
  LA1159	CD3	CD3	RG145	H	H	H	LA2399	H	H	H	H	H	RG88
  LA1160	CD3	CD3	RG146	H	H	H	LA2400	H	H	H	H	H	RG89
  LA1161	CD3	CD3	RG147	H	H	H	LA2401	H	H	H	H	H	RG90
  LA1162	CD3	CD3	RG148	H	H	H	LA2402	H	H	H	H	H	RG91
  LA1163	CD3	CD3	RG149	H	H	H	LA2403	H	H	H	H	H	RG92
  LA1164	CD3	CD3	RG150	H	H	H	LA2404	H	H	H	H	H	RG93
  LA1165	CD3	CD3	RG151	H	H	H	LA2405	H	H	H	H	H	RG94
  LA1166	CD3	CD3	RG152	H	H	H	LA2406	H	H	H	H	H	RG95
  LA1167	CD3	CD3	RG153	H	H	H	LA2407	H	H	H	H	H	RG96
  LA1168	CD3	CD3	RG154	H	H	H	LA2408	H	H	H	H	H	RG97
  LA1169	CD3	CD3	RG155	H	H	H	LA2409	H	H	H	H	H	RG98
  LA1170	CD3	CD3	RG156	H	H	H	LA2410	H	H	H	H	H	RG99
  LA1171	CD3	CD3	RG157	H	H	H	LA2411	H	H	H	H	H	RG100
  LA1172	CD3	CD3	RG158	H	H	H	LA2412	H	H	H	H	H	RG101
  LA1173	CD3	CD3	RG159	H	H	H	LA2413	H	H	H	H	H	RG102
  LA1174	CD3	CD3	RG160	H	H	H	LA2414	H	H	H	H	H	RG103
  LA1175	CD3	CD3	RG161	H	H	H	LA2415	H	H	H	H	H	RG104
  LA1176	CD3	CD3	RG162	H	H	H	LA2416	H	H	H	H	H	RG105
  LA1177	CD3	CD3	RG163	H	H	H	LA2417	H	H	H	H	H	RG106
  LA1178	CD3	CD3	RG164	H	H	H	LA2418	H	H	H	H	H	RG107
  LA1179	CD3	CD3	RG165	H	H	H	LA2419	H	H	H	H	H	RG108
  LA1180	CD3	CD3	RG166	H	H	H	LA2420	H	H	H	H	H	RG109

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1181	CD3	CD3	RG167	H	H	H	LA2421	H	H	H	H	H	RG110
  LA1182	CD3	CD3	RG168	H	H	H	LA2422	H	H	H	H	H	RG111
  LA1183	CD3	CD3	RG169	H	H	H	LA2423	H	H	H	H	H	RG112
  LA1184	CD3	H	RG1	H	H	H	LA2424	H	H	H	H	H	RG113
  LA1185	CD3	H	RG2	H	H	H	LA2425	H	H	H	H	H	RG114
  LA1186	CD3	H	RG3	H	H	H	LA2426	H	H	H	H	H	RG115
  LA1187	CD3	H	RG4	H	H	H	LA2427	H	H	H	H	H	RG116
  LA1188	CD3	H	RG5	H	H	H	LA2428	H	H	H	H	H	RG117
  LA1189	CD3	H	RG6	H	H	H	LA2429	H	H	H	H	H	RG118
  LA1190	CD3	H	RG7	H	H	H	LA2430	H	H	H	H	H	RG119
  LA1191	CD3	H	RG8	H	H	H	LA2431	H	H	H	H	H	RG120
  LA1192	CD3	H	RG9	H	H	H	LA2432	H	H	H	H	H	RG121
  LA1193	CD3	H	RG10	H	H	H	LA2433	H	H	H	H	H	RG122
  LA1194	CD3	H	RG11	H	H	H	LA2434	H	H	H	H	H	RG123
  LA1195	CD3	H	RG12	H	H	H	LA2435	H	H	H	H	H	RG124
  LA1196	CD3	H	RG13	H	H	H	LA2436	H	H	H	H	H	RG125
  LA1197	CD3	H	RG14	H	H	H	LA2437	H	H	H	H	H	RG126
  LA1198	CD3	H	RG15	H	H	H	LA2438	H	H	H	H	H	RG127
  LA1199	CD3	H	RG16	H	H	H	LA2439	H	H	H	H	H	RG128
  LA1200	CD3	H	RG17	H	H	H	LA2440	H	H	H	H	H	RG129
  LA1201	CD3	H	RG18	H	H	H	LA2441	H	H	H	H	H	RG130
  LA1202	CD3	H	RG19	H	H	H	LA2442	H	H	H	H	H	RG131
  LA1203	CD3	H	RG20	H	H	H	LA2443	H	H	H	H	H	RG132
  LA1204	CD3	H	RG21	H	H	H	LA2444	H	H	H	H	H	RG133

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1205	CD3	H	RG22	H	H	H	LA2445	H	H	H	H	H	RG134
  LA1206	CD3	H	RG23	H	H	H	LA2446	H	H	H	H	H	RG135
  LA1207	CD3	H	RG24	H	H	H	LA2447	H	H	H	H	H	RG136
  LA1208	CD3	H	RG25	H	H	H	LA2448	H	H	H	H	H	RG137
  LA1209	CD3	H	RG26	H	H	H	LA2449	H	H	H	H	H	RG138
  LA1210	CD3	H	RG27	H	H	H	LA2450	H	H	H	H	H	RG139
  LA1211	CD3	H	RG28	H	H	H	LA2451	H	H	H	H	H	RG140
  LA1212	CD3	H	RG29	H	H	H	LA2452	H	H	H	H	H	RG141
  LA1213	CD3	H	RG30	H	H	H	LA2453	H	H	H	H	H	RG142
  LA1214	CD3	H	RG31	H	H	H	LA2454	H	H	H	H	H	RG143
  LA1215	CD3	H	RG32	H	H	H	LA2455	H	H	H	H	H	RG144
  LA1216	CD3	H	RG33	H	H	H	LA2456	H	H	H	H	H	RG145
  LA1217	CD3	H	RG34	H	H	H	LA2457	H	H	H	H	H	RG146
  LA1218	CD3	H	RG35	H	H	H	LA2458	H	H	H	H	H	RG147
  LA1219	CD3	H	RG36	H	H	H	LA2459	H	H	H	H	H	RG148
  LA1220	CD3	H	RG37	H	H	H	LA2460	H	H	H	H	H	RG149
  LA1221	CD3	H	RG38	H	H	H	LA2461	H	H	H	H	H	RG150
  LA1222	CD3	H	RG39	H	H	H	LA2462	H	H	H	H	H	RG151
  LA1223	CD3	H	RG40	H	H	H	LA2463	H	H	H	H	H	RG152
  LA1224	CD3	H	RG41	H	H	H	LA2464	H	H	H	H	H	RG153
  LA1225	CD3	H	RG42	H	H	H	LA2465	H	H	H	H	H	RG154
  LA1226	CD3	H	RG43	H	H	H	LA2456	H	H	H	H	H	RG155
  LA1227	CD3	H	RG44	H	H	H	LA2467	H	H	H	H	H	RG156
  LA1228	CD3	H	RG45	H	H	H	LA2456	H	H	H	H	H	RG157

• Ligand	RA1	RA2	RA3	RA4	RA5	RA6	Ligand	RA1	RA2	RA3	RA4	RA5	RA6
  LA1229	CD3	H	RG46	H	H	H	LA2469	H	H	H	H	H	RG158
  LA1230	CD3	H	RG47	H	H	H	LA2470	H	H	H	H	H	RG159
  LA1231	CD3	H	RG48	H	H	H	LA2471	H	H	H	H	H	RG160
  LA1232	CD3	H	RG49	H	H	H	LA2472	H	H	H	H	H	RG161
  LA1233	CD3	H	RG50	H	H	H	LA2473	H	H	H	H	H	RG162
  LA1234	CD3	H	RG51	H	H	H	LA2474	H	H	H	H	H	RG163
  LA1235	CD3	H	RG52	H	H	H	LA2475	H	H	H	H	H	RG164
  LA1236	CD3	H	RG53	H	H	H	LA2476	H	H	H	H	H	RG165
  LA1237	CD3	H	RG54	H	H	H	LA2477	H	H	H	H	H	RG166
  LA1238	CD3	H	RG55	H	H	H	LA2478	H	H	H	H	H	RG167
  LA1239	CD3	H	RG56	H	H	H	LA2479	H	H	H	H	H	RG168
  LA1240	CD3	H	RG57	H	H	H	LA2480	H	H	H	H	H	RG169

• wherein R^G1 to R^G169 have the following structures:
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• In some embodiments where L₁ is L_A, the compound is Compound x selected from the group consisting of Compound 1 through Compound 2120400, where:
• Compound x has the formula Ir(L_Ai)(L_Bj)₂, where
• x = 2480j + i – 2480,
• i is an integer from 1 to 2480,
• j is an integer from 1 to 855; and
• L_Bj is listed in the following table based on the following structure:
• 

• LBj, where j is	RB1	RB2	RB3	RB4
  1.	H	H	H	H
  2.	CH3	H	H	H
  3.	H	CH3	H	H
  4.	H	H	CH3	H
  5.	H	H	H	CH3
  6.	CH3	H	CH3	H
  7.	CH3	H	H	CH3
  8.	H	CH3	CH3	H
  9.	H	CH3	H	CH3
  10.	H	H	CH3	CH3
  11.	CH3	CH3	CH3	H
  12.	CH3	CH3	H	CH3
  13.	CH3	H	CH3	CH3
  14.	H	CH3	CH3	CH3
  15.	CH3	CH3	CH3	CH3
  16.	CH2CH3	H	H	H
  17.	CH2CH3	CH3	H	H
  18.	CH2CH3	H	CH3	H
  19.	CH2CH3	H	H	CH3
  20.	CH2CH3	CH3	CH3	H
  21.	CH2CH3	CH3	H	CH3
  22.	CH2CH3	H	CH3	CH3
  23.	CH2CH3	CH3	CH3	CH3
  24.	H	CH2CH3	H	H
  25.	CH3	CH2CH3	H	H
  26.	H	CH2CH3	CH3	H
  27.	H	CH2CH3	H	CH3
  28.	CH3	CH2CH3	CH3	H
  29.	CH3	CH2CH3	H	CH3
  30.	H	CH2CH3	CH3	CH3
  31.	CH3	CH2CH3	CH3	CH3
  32.	H	H	CH2CH3	H
  33.	CH3	H	CH2CH3	H
  34.	H	CH3	CH2CH3	H
  35.	H	H	CH2CH3	CH3
  36.	CH3	CH3	CH2CH3	H
  37.	CH3	H	CH2CH3	CH3
  38.	H	CH3	CH2CH3	CH3
  39.	CH3	CH3	CH2CH3	CH3
  40.	CH(CH3)2	H	H	H
  41.	CH(CH3)2	CH3	H	H
  42.	CH(CH3)2	H	CH3	H
  43.	CH(CH3)2	H	H	CH3
  44.	CH(CH3)2	CH3	CH3	H
  45.	CH(CH3)2	CH3	H	CH3
  46.	CH(CH3)2	H	CH3	CH3
  47.	CH(CH3)2	CH3	CH3	CH3
  48.	H	CH(CH3)2	H	H
  49.	CH3	CH(CH3)2	H	H
  50.	H	CH(CH3)2	CH3	H
  51.	H	CH(CH3)2	H	CH3
  52.	CH3	CH(CH3)2	CH3	H
  53.	CH3	CH(CH3)2	H	CH3
  54.	H	CH(CH3)2	CH3	CH3
  55.	CH3	CH(CH3)2	CH3	CH3
  56.	H	H	CH(CH3)2	H
  57.	CH3	H	CH(CH3)2	H
  58.	H	CH3	CH(CH3)2	H
  59.	H	H	CH(CH3)2	CH3
  60.	CH3	CH3	CH(CH3)2	H
  61.	CH3	H	CH(CH3)2	CH3
  62.	H	CH3	CH(CH3)2	CH3
  63.	CH3	CH3	CH(CH3)2	CH3
  64.	CH2CH(CH3)2	H	H	H
  65.	CH2CH(CH3)2	CH3	H	H
  66.	CH2CH(CH3)2	H	CH3	H
  67.	CH2CH(CH3)2	H	H	CH3
  68.	CH2CH(CH3)2	CH3	CH3	H
  69.	CH2CH(CH3)2	CH3	H	CH3
  70.	CH2CH(CH3)2	H	CH3	CH3
  71.	CH2CH(CH3)2	CH3	CH3	CH3
  72.	H	CH2CH(CH3)2	H	H
  73.	CH3	CH2CH(CH3)2	H	H
  74.	H	CH2CH(CH3)2	CH3	H
  75.	H	CH2CH(CH3)2	H	CH3
  76.	CH3	CH2CH(CH3)2	CH3	H
  77.	CH3	CH2CH(CH3)2	H	CH3
  78.	H	CH2CH(CH3)2	CH3	CH3
  79.	CH3	CH2CH(CH3)2	CH3	CH3
  80.	H	H	CH2CH(CH3)2	H
  81.	CH3	H	CH2CH(CH3)2	H
  82.	H	CH3	CH2CH(CH3)2	H
  83.	H	H	CH2CH(CH3)2	CH3
  84.	CH3	CH3	CH2CH(CH3)2	H
  85.	CH3	H	CH2CH(CH3)2	CH3
  86.	H	CH3	CH2CH(CH3)2	CH3
  87.	CH3	CH3	CH2CH(CH3)2	CH3
  88.	C(CH3)3	H	H	H
  89.	C(CH3)3	CH3	H	H
  90.	C(CH3)3	H	CH3	H
  91.	C(CH3)3	H	H	CH3
  92.	C(CH3)3	CH3	CH3	H
  93.	C(CH3)3	CH3	H	CH3
  94.	C(CH3)3	H	CH3	CH3
  95.	C(CH3)3	CH3	CH3	CH3
  96.	H	C(CH3)3	H	H
  97.	CH3	C(CH3)3	H	H
  98.	H	C(CH3)3	CH3	H
  99.	H	C(CH3)3	H	CH3
  100.	CH3	C(CH3)3	CH3	H
  101.	CH3	C(CH3)3	H	CH3
  102.	H	C(CH3)3	CH3	CH3
  103.	CH3	C(CH3)3	CH3	CH3
  104.	H	H	C(CH3)3	H
  105.	CH3	H	C(CH3)3	H
  106.	H	CH3	C(CH3)3	H
  107.	H	H	C(CH3)3	CH3
  108.	CH3	CH3	C(CH3)3	H
  109.	CH3	H	C(CH3)3	CH3
  110.	H	CH3	C(CH3)3	CH3
  111.	CH3	CH3	C(CH3)3	CH3
  112.	CH2C(CH3)3	H	H	H
  113.	CH2C(CH3)3	CH3	H	H
  114.	CH2C(CH3)3	H	CH3	H
  115.	CH2C(CH3)3	H	H	CH3
  116.	CH2C(CH3)3	CH3	CH3	H
  117.	CH2C(CH3)3	CH3	H	CH3
  118.	CH2C(CH3)3	H	CH3	CH3
  119.	CH2C(CH3)3	CH3	CH3	CH3
  120.	H	CH2C(CH3)3	H	H
  121.	CH3	CH2C(CH3)3	H	H
  122.	H	CH2C(CH3)3	CH3	H
  123.	H	CH2C(CH3)3	H	CH3
  124.	CH3	CH2C(CH3)3	CH3	H
  125.	CH3	CH2C(CH3)3	H	CH3
  126.	H	CH2C(CH3)3	CH3	CH3
  127.	CH3	CH2C(CH3)3	CH3	CH3
  128.	H	H	CH2C(CH3)3	H
  129.	CH3	H	CH2C(CH3)3	H
  130.	H	CH3	CH2C(CH3)3	H
  131.	H	H	CH2C(CH3)3	CH3
  132.	CH3	CH3	CH2C(CH3)3	H
  133.	CH3	H	CH2C(CH3)3	CH3
  134.	H	CH3	CH2C(CH3)3	CH3
  135.	CH3	CH3	CH2C(CH3)3	CH3
  136.	CH2C(CH3)2CF3	H	H	H
  137.	CH2C(CH3)2CF3	CH3	H	H
  138.	CH2C(CH3)2CF3	H	CH3	H
  139.	CH2C(CH3)2CF3	H	H	CH3
  140.	CH2C(CH3)2CF3	CH3	CH3	H
  141.	CH2C(CH3)2CF3	CH3	H	CH3
  142.	CH2C(CH3)2CF3	H	CH3	CH3
  143.	CH2C(CH3)2CF3	CH3	CH3	CH3
  144.	H	CH2C(CH3)2CF3	H	H
  145.	CH3	CH2C(CH3)2CF3	H	H
  146.	H	CH2C(CH3)2CF3	CH3	H
  147.	H	CH2C(CH3)2CF3	H	CH3
  148.	CH3	CH2C(CH3)2CF3	CH3	H
  149.	CH3	CH2C(CH3)2CF3	H	CH3
  150.	H	CH2C(CH3)2CF3	CH3	CH3
  151.	CH3	CH2C(CH3)2CF3	CH3	CH3
  152.	H	H	CH2C(CH3)2CF3	H
  153.	CH3	H	CH2C(CH3)2CF3	H
  154.	H	CH3	CH2C(CH3)2CF3	H
  155.	H	H	CH2C(CH3)2CF3	CH3
  156.	CH3	CH3	CH2C(CH3)2CF3	H
  157.	CH3	H	CH2C(CH3)2CF3	CH3
  158.	H	CH3	CH2C(CH3)2CF3	CH3
  159.	CH3	CH3	CH2C(CH3)2CF3	CH3
  160.	CH2CH2CF3	H	H	H
  161.	CH2CH2CF3	CH3	H	H
  162.	CH2CH2CF3	H	CH3	H
  163.	CH2CH2CF3	H	H	CH3
  164.	CH2CH2CF3	CH3	CH3	H
  165.	CH2CH2CF3	CH3	H	CH3
  166.	CH2CH2CF3	H	CH3	CH3
  167.	CH2CH2CF3	CH3	CH3	CH3
  168.	H	CH2CH2CF3	H	H
  169.	CH3	CH2CH2CF3	H	H
  170.	H	CH2CH2CF3	CH3	H
  171.	H	CH2CH2CF3	H	CH3
  172.	CH3	CH2CH2CF3	CH3	H
  173.	CH3	CH2CH2CF3	H	CH3
  174.	H	CH2CH2CF3	CH3	CH3
  175.	CH3	CH2CH2CF3	CH3	CH3
  176.	H	H	CH2CH2CF3	H
  177.	CH3	H	CH2CH2CF3	H
  178.	H	CH3	CH2CH2CF3	H
  179.	H	H	CH2CH2CF3	CH3
  180.	CH3	CH3	CH2CH2CF3	H
  181.	CH3	H	CH2CH2CF3	CH3
  182.	H	CH3	CH2CH2CF3	CH3
  183.	CH3	CH3	CH2CH2CF3	CH3
  184.		H	H	H
  185.		CH3	H	H
  186.		H	CH3	H
  187.		H	H	CH3
  188.		CH3	CH3	H
  189.		CH3	H	CH3
  190.		H	CH3	CH3
  191.		CH3	CH3	CH3
  192.	H		H	H
  193.	CH3		H	H
  194.	H		CH3	H
  195.	H		H	CH3
  196.	CH3		CH3	H
  197.	CH3		H	CH3
  198.	H		CH3	CH3
  199.	CH3		CH3	CH3
  200.	H	H		H
  201.	CH3	H		H
  202.	H	CH3		H
  203.	H	H		CH3
  204.	CH3	CH3		H
  205.	CH3	H		CH3
  206.	H	CH3		CH3
  207.	CH3	CH3		CH3
  208.		H	H	H
  209.		CH3	H	H
  210.		H	CH3	H
  211.		H	H	CH3
  212.		CH3	CH3	H
  213.		CH3	H	CH3
  214.		H	CH3	CH3
  215.		CH3	CH3	CH3
  216.	H		H	H
  217.	CH3		H	H
  218.	H		CH3	H
  219.	H		H	CH	3
  220.	CH3		CH3	H
  221.	CH3		H	CH3
  222.	H		CH3	CH3
  223.	CH3		CH3	CH3
  224.	H	H		H
  225.	CH3	H		H
  226.	H	CH3		H
  227.	H	H		CH3
  228.	CH3	CH3		H
  229.	CH3	H		CH 3
  230.	H	CH3		CH3
  231.	CH3	CH3		CH3
  232.		H	H	H
  233.		CH3	H	H
  234.		H	CH3	H
  235.		H	H	CH3
  236.		CH3	CH3	H
  237.		CH3	H	CH3
  238.		H	CH3	CH3
  239.		CH3	CH3	CH3
  240.	H		H	H
  241.	CH3		H	H
  242.	H		CH3	H
  243.	H		H	CH3
  244.	CH3		CH3	H
  245.	CH3		H	CH3
  246.	H		CH3	CH3
  247.	CH3		CH3	CH3
  248.	H	H		H
  249.	CH3	H		H
  250.	H	CH3		H
  251.	H	H		CH3
  252.	CH3	CH3		H
  253.	CH3	H		CH3
  254.	H	CH3		CH3
  255.	CH3	CH3		CH3
  256.		H	H	H
  257.		CH3	H	H
  258.		H	CH3	H
  259.		H	H	CH3
  260.		CH3	CH3	H
  261.		CH3	H	CH3
  262.		H	CH3	CH3
  263.		CH3	CH3	CH3
  264.	H		H	H
  265.	CH3		H	H
  266.	H		CH3	H
  267.	H		H	CH3
  268.	CH3		CH3	H
  269.	CH3		H	CH3
  270.	H		CH3	CH3
  271.	CH3		CH3	CH3
  272.	H	H		H
  273.	CH3	H		H
  274.	H	CH3		H
  275.	H	H		CH3
  276.	CH3	CH3		H
  277.	CH3	H		CH3
  278.	H	CH3		CH3
  279.	CH3	CH3		CH3
  280.		H	H	H
  281.		CH3	H	H
  282.		H	CH3	H
  283.		H	H	CH3
  284.		CH3	CH3	H
  285.		CH3	H	CH3
  286.		H	CH3	CH3
  287.		CH3	CH3	CH3
  288.	H		H	H
  289.	CH3		H	H
  290.	H		CH3	H
  291.	H		H	CH3
  292.	CH3		CH3	H
  293.	CH3		H	CH3
  294.	H		CH3	CH3
  295.	CH3		CH3	CH3
  296.	H	H		H
  297.	CH3	H		H
  298.	H	CH3		H
  299.	H	H		CH3
  300.	CH3	CH3		H
  301.	CH3	H		CH3
  302.	H	CH3		CH3
  303.	CH3	CH3		CH3
  304.		H	H	H
  305.		CH3	H	H
  306.		H	CH3	H
  307.		H	H	CH3
  308.		CH3	CH3	H
  309.		CH3	H	CH3
  310.		H	CH3	CH3
  311.		CH3	CH3	CH3
  312.	H		H	H
  313.	CH3		H	H
  314.	H		CH3	H
  315.	H		H	CH3
  316.	CH3		CH3	H
  317.	CH3		H	CH3
  318.	H		CH3	CH3
  319.	CH3		CH3	CH3
  320.	H	H		H
  321.	CH3	H		H
  322.	H	CH3		H
  323.	H	H		CH3
  324.	CH3	CH3		H
  325.	CH3	H		CH3
  326.	H	CH3		CH3
  327.	CH3	CH3		CH3
  328.	CH(CH3)2	H	CH2CH3	H
  329.	CH(CH3)2	H	CH(CH3)2	H
  330.	CH(CH3)2	H	CH2CH(CH3)2	H
  331.	CH(CH3)2	H	C(CH3)3	H
  332.	CH(CH3)2	H	CH2C(CH3)3	H
  333.	CH(CH3)2	H	CH2CH2CF3	H
  334.	CH(CH3)2	H	CH2C(CH3)2CF3	H
  335.	CH(CH3)2	H		H
  336.	CH(CH3)2	H		H
  337.	CH(CH3)2	H		H
  338.	CH(CH3)2	H		H
  339.	CH(CH3)2	H		H
  340.	CH(CH3)2	H		H
  341.	C(CH3)3	H	CH2CH3	H
  342.	C(CH3)3	H	CH(CH3)2	H
  343.	C(CH3)3	H	CH2CH(CH3)2	H
  344.	C(CH3)3	H	C(CH3)3	H
  345.	C(CH3)3	H	CH2C(CH3)3	H
  346.	C(CH3)3	H	CH2CH2CF3	H
  347.	C(CH3)3	H	CH2C(CH3)2CF3	H
  348.	C(CH3)3	H		H
  349.	C(CH3)3	H		H
  350.	C(CH3)3	H		H
  351.	C(CH3)3	H		H
  352.	C(CH3)3	H		H
  353.	C(CH3)3	H		H
  354.	CH2C(CH3)3	H	CH2CH3	H
  355.	CH2C(CH3)3	H	CH(CH3)2	H
  356.	CH2C(CH3)3	H	CH2CH(CH3)2	H
  357.	CH2C(CH3)3	H	C(CH3)3	H
  358.	CH2C(CH3)3	H	CH2C(CH3)3	H
  359.	CH2C(CH3)3	H	CH2CH2CF3	H
  360.	CH2C(CH3)3	H	CH2C(CH3)2CF3	H
  361.	CH2C(CH3)3	H		H
  362.	CH2C(CH3)3	H		H
  363.	CH2C(CH3)3	H		H
  364.	CH2C(CH3)3	H		H
  365.	CH2C(CH3)3	H		H
  366.	CH2C(CH3)3	H		H
  367.		H	CH2CH3	H
  368.		H	CH(CH3)2	H
  369.		H	CH2CH(CH3)2	H
  370.		H	C(CH3)3	H
  371.		H	CH2C(CH3)3	H
  372.		H	CH2CH2CF3	H
  373.		H	CH2C(CH3)2CF3	H
  374.		H		H
  375.		H		H
  376.		H		H
  377.		H		H
  378.		H		H
  379.		H		H
  380.		H	CH2CH3	H
  381.		H	CH(CH3)2	H
  382.		H	CH2CH(CH3)2	H
  383.		H	C(CH3)3	H
  384.		H	CH2C(CH3)3	H
  385.		H	CH2CH2CF3	H
  386.		H	CH2C(CH3)2CF3	H
  387.		H		H
  388.		H		H
  389.		H		H
  390.		H		H
  391.		H		H
  392.		H		H
  393.		H	CH2CH(CH3)2	H
  394.		H	C(CH3)3	H
  395.		H	CH2C(CH3)3	H
  396.		H	CH2CH2CF3	H
  397.		H	CH2C(CH3)2CF3	H
  398.		H		H
  399.		H		H
  400.		H		H
  401.		H		H
  402.		H		H
  403.		H		H
  404.		H	CH2CH(CH3)2	H
  405.		H	C(CH3)3	H
  406.		H	CH2C(CH3)3	H
  407.		H	CH2CH2CF3	H
  408.		H	CH2C(CH3)2CF3	H
  409.		H		H
  410.		H		H
  411.		H		H
  412.		H		H
  413.		H		H
  414.		H		H
  415.		H	CH2CH(CH3)2	H
  416.		H	C(CH3)3	H
  417.		H	CH2C(CH3)3	H
  418.		H	CH2CH2CF3	H
  419.		H	CH2C(CH3)2CF3	H
  420.		H		H
  421.		H		H
  422.		H		H
  423.		H		H
  424.		H		H
  425.		H		H
  426.	CD3	H	H	H
  427.	H	CD3	H	H
  428.	H	H	CD3	H
  429.	H	H	H	CD3
  430.	CD3	H	CD3	H
  431.	CD3	H	H	CD3
  432.	H	CD3	CD3	H
  433.	H	CD3	H	CD3
  434.	H	H	CD3	CD3
  435.	CD3	CD3	CD3	H
  436.	CD3	CD3	H	CD3
  437.	CD3	H	CD3	CD3
  438.	H	CD3	CD3	CD3
  439.	CD3	CD3	CD3	CD3
  440.	CD2CH3	H	H	H
  441.	CD2CH3	CD3	H	H
  442.	CD2CH3	H	CD3	H
  443.	CD2CH3	H	H	CD3
  444.	CD2CH3	CD3	CD3	H
  445.	CD2CH3	CD3	H	CD3
  446.	CD2CH3	H	CD3	CD3
  447.	CD2CH3	CD3	CD3	CD3
  448.	H	CD2CH3	H	H
  449.	CD3	CD2CH3	H	H
  450.	H	CD2CH3	CD3	H
  451.	H	CD2CH3	H	CD3
  452.	CD3	CD2CH3	CD3	H
  453.	CD3	CD2CH3	H	CD3
  454.	H	CD2CH3	CD3	CD3
  455.	CD3	CD2CH3	CD3	CD3
  456.	H	H	CD2CH3	H
  457.	CD3	H	CD2CH3	H
  458.	H	CD3	CD2CH3	H
  459.	H	H	CD2CH3	CD3
  460.	CD3	CD3	CD2CH3	H
  461.	CD3	H	CD2CH3	CD3
  462.	H	CD3	CD2CH3	CD3
  463.	CD3	CD3	CD2CH3	CD3
  464.	CD(CH3)2	H	H	H
  465.	CD(CH3)2	CD3	H	H
  466.	CD(CH3)2	H	CD3	H
  467.	CD(CH3)2	H	H	CD3
  468.	CD(CH3)2	CD3	CD3	H
  469.	CD(CH3)2	CD3	H	CD3
  470.	CD(CH3)2	H	CD3	CD3
  471.	CD(CH3)2	CD3	CD3	CD3
  472.	H	CD(CH3)2	H	H
  473.	CD3	CD(CH3)2	H	H
  474.	H	CD(CH3)2	CD3	H
  475.	H	CD(CH3)2	H	CD3
  476.	CD3	CD(CH3)2	CD3	H
  477.	CD3	CD(CH3)2	H	CD3
  478.	H	CD(CH3)2	CD3	CD3
  479.	CD3	CD(CH3)2	CD3	CD3
  480.	H	H	CD(CH3)2	H
  481.	CD3	H	CD(CH3)2	H
  482.	H	CD3	CD(CH3)2	H
  483.	H	H	CD(CH3)2	CD3
  484.	CD3	CD3	CD(CH3)2	H
  485.	CD3	H	CD(CH3)2	CD3
  486.	H	CD3	CD(CH3)2	CD3
  487.	CD3	CD3	CD(CH3)2	CD3
  488.	CD(CD3)2	H	H	H
  489.	CD(CD3)2	CD3	H	H
  490.	CD(CD3)2	H	CD3	H
  491.	CD(CD3)2	H	H	CD3
  492.	CD(CD3)2	CD3	CD3	H
  493.	CD(CD3)2	CD3	H	CD3
  494.	CD(CD3)2	H	CD3	CD3
  495.	CD(CD3)2	CD3	CD3	CD3
  496.	H	CD(CD3)2	H	H
  497.	CD3	CD(CD3)2	H	H
  498.	H	CD(CD3)2	CD3	H
  499.	H	CD(CD3)2	H	CD3
  500.	CD3	CD(CD3)2	CD3	H
  501.	CD3	CD(CD3)2	H	CD3
  502.	H	CD(CD3)2	CD3	CD3
  503.	CD3	CD(CD3)2	CD3	CD3
  504.	H	H	CD(CD3)2	H
  505.	CD3	H	CD(CD3)2	H
  506.	H	CD3	CD(CD3)2	H
  507.	H	H	CD(CD3)2	CD3
  508.	CD3	CD3	CD(CD3)2	H
  509.	CD3	H	CD(CD3)2	CD3
  510.	H	CD3	CD(CD3)2	CD3
  511.	CD3	CD3	CD(CD3)2	CD3
  512.	CD2CH(CH3)2	H	H	H
  513.	CD2CH(CH3)2	CD3	H	H
  514.	CD2CH(CH3)2	H	CD3	H
  515.	CD2CH(CH3)2	H	H	CD3
  516.	CD2CH(CH3)2	CD3	CD3	H
  517.	CD2CH(CH3)2	CD3	H	CD3
  518.	CD2CH(CH3)2	H	CD3	CD3
  519.	CD2CH(CH3)2	CD3	CD3	CD3
  520.	H	CD2CH(CH3)2	H	H
  521.	CD3	CD2CH(CH3)2	H	H
  522.	H	CD2CH(CH3)2	CD3	H
  523.	H	CD2CH(CH3)2	H	CD3
  524.	CD3	CD2CH(CH3)2	CD3	H
  525.	CD3	CD2CH(CH3)2	H	CD3
  526.	H	CD2CH(CH3)2	CD3	CD3
  527.	CD3	CD2CH(CH3)2	CD3	CD3
  528.	H	H	CD2CH(CH3)2	H
  529.	CD3	H	CD2CH(CH3)2	H
  530.	H	CD3	CD2CH(CH3)2	H
  531.	H	H	CD2CH(CH3)2	CD3
  532.	CD3	CD3	CD2CH(CH3)2	H
  533.	CD3	H	CD2CH(CH3)2	CD3
  534.	H	CD3	CD2CH(CH3)2	CD3
  535.	CD3	CD3	CD2CH(CH3)2	CD3
  536.	CD2C(CH3)3	H	H	H
  537.	CD2C(CH3)3	CD3	H	H
  538.	CD2C(CH3)3	H	CD3	H
  539.	CD2C(CH3)3	H	H	CD3
  540.	CD2C(CH3)3	CD3	CD3	H
  541.	CD2C(CH3)3	CD3	H	CD3
  542.	CD2C(CH3)3	H	CD3	CD3
  543.	CD2C(CH3)3	CH3	CD3	CD3
  544.	H	CD2C(CH3)3	H	H
  545.	CD3	CD2C(CH3)3	H	H
  546.	H	CD2C(CH3)3	CD3	H
  547.	H	CD2C(CH3)3	H	CD3
  548.	CD3	CD2C(CH3)3	CD3	H
  549.	CD3	CD2C(CH3)3	H	CD3
  550.	H	CD2C(CH3)3	CD3	CD3
  551.	CD3	CD2C(CH3)3	CD3	CD3
  552.	H	H	CD2C(CH3)3	H
  553.	CD3	H	CD2C(CH3)3	H
  554.	H	CD3	CD2C(CH3)3	H
  555.	H	H	CD2C(CH3)3	CD3
  556.	CD3	CD3	CD2C(CH3)3	H
  557.	CD3	H	CD2C(CH3)3	CD3
  558.	H	CD3	CD2C(CH3)3	CD3
  559.	CD3	CD3	CD2C(CH3)3	CD3
  560.	CD2C(CH3)2CF3	H	H	H
  561.	CD2C(CH3)2CF3	CD3	H	H
  562.	CD2C(CH3)2CF3	H	CD3	H
  563.	CD2C(CH3)2CF3	H	H	CD3
  564.	CD2C(CH3)2CF3	CD3	CD3	H
  565.	CD2C(CH3)2CF3	CD3	H	CD3
  566.	CD2C(CH3)2CF3	H	CD3	CD3
  567.	CD2C(CH3)2CF3	CD3	CD3	CD3
  568.	H	CD2C(CH3)2CF3	H	H
  569.	CD3	CD2C(CH3)2CF3	H	H
  570.	H	CD2C(CH3)2CF3	CD3	H
  571.	H	CD2C(CH3)2CF3	H	CD3
  572.	CD3	CD2C(CH3)2CF3	CD3	H
  573.	CD3	CD2C(CH3)2CF3	H	CD3
  574.	H	CD2C(CH3)2CF3	CD3	CD3
  575.	CD3	CD2C(CH3)2CF3	CD3	CD3
  576.	H	H	CD2C(CH3)2CF3	H
  577.	CD3	H	CD2C(CH3)2CF3	H
  578.	H	CD3	CD2C(CH3)2CF3	H
  579.	H	H	CD2C(CH3)2CF3	CD3
  580.	CD3	CD3	CD2C(CH3)2CF3	H
  581.	CD3	H	CD2C(CH3)2CF3	CD3
  582.	H	CD3	CD2C(CH3)2CF3	CD3
  583.	CD3	CD3	CD2C(CH3)2CF3	CD3
  584.	CD2CH2CF3	H	H	H
  585.	CD2CH2CF3	CD3	H	H
  586.	CD2CH2CF3	H	CD3	H
  587.	CD2CH2CF3	H	H	CD3
  588.	CD2CH2CF3	CD3	CD3	H
  589.	CD2CH2CF3	CD3	H	CD3
  590.	CD2CH2CF3	H	CD3	CD3
  591.	CD2CH2CF3	CD3	CD3	CD3
  592.	H	CD2CH2CF3	H	H
  593.	CD3	CD2CH2CF3	H	H
  594.	H	CD2CH2CF3	CD3	H
  595.	H	CD2CH2CF3	H	CD3
  596.	CD3	CD2CH2CF3	CD3	H
  597.	CD3	CD2CH2CF3	H	CD3
  598.	H	CD2CH2CF3	CD3	CD3
  599.	CD3	CD2CH2CF3	CD3	CD3
  600.	H	H	CD2CH2CF3	H
  601.	CD3	H	CD2CH2CF3	H
  602.	H	CD3	CD2CH2CF3	H
  603.	H	H	CD2CH2CF3	CD3
  604.	CD3	CD3	CD2CH2CF3	H
  605.	CD3	H	CD2CH2CF3	CD3
  606.	H	CD3	CD2CH2CF3	CD3
  607.	CD3	CD3	CD2CH2CF3	CD3
  608.		H	H	H
  609.		CD3	H	H
  610.		H	CD3	H
  611.		H	H	CD3
  612.		CD3	CD3	H
  613.		CD3	H	CD3
  614.		H	CD3	CD3
  615.		CD3	CD3	CD3
  616.	H		H	H
  617.	CD3		H	H
  618.	H		CD3	H
  619.	H		H	CD3
  620.	CD3		CD3	H
  621.	CD3		H	CD3
  622.	H		CD3	CD3
  623.	CD3		CD3	CD3
  624.	H	H		H
  625.	CD3	H		H
  626.	H	CD3		H
  627.	H	H		CD3
  628.	CD3	CD3		H
  629.	CD3	H		CD3
  630.	H	CD3		CD3
  631.	CD3	CD3		CD3
  632.		H	H	H
  633.		CD3	H	H
  634.		H	CD3	H
  635.		H	H	CD3
  636.		CD3	CD3	H
  637.		CD3	H	CD3
  638.		H	CD3	CD3
  639.		CD3	CD3	CD3
  640.	H		H	H
  641.	CD3		H	H
  642.	H		CD3	H
  643.	H		H	CD3
  644.	CD3		CD3	H
  645.	CD3		H	CD3
  646.	H		CD3	CD3
  647.	CH3		CD3	CD3
  648.	H	H		H
  649.	CD3	H		H
  650.	H	CD3		H
  651.	H	H		CD3
  652.	CD3	CD3		H
  653.	CD3	H		CD3
  654.	H	CD3		CD3
  655.	CD3	CD3		CD3
  656.		H	H	H
  657.		CD3	H	H
  658.		H	CD3	H
  659.		H	H	CD3
  660.		CD3	CD3	H
  661.		CD3	H	CD3
  662.		H	CD3	CD3
  663.		CD3	CD3	CD3
  664.	H		H	H
  665.	CD3		H	H
  666.	H		CD3	H
  667.	H		H	CD3
  668.	CD3		CD3	H
  669.	CD3		H	CD3
  670.	H		CD3	CD3
  671.	CD3		CD3	CD3
  672.	H	H		H
  673.	CD3	H		H
  674.	H	CD3		H
  675.	H	H		CD3
  676.	CD3	CD3		H
  677.	CD3	H		CD3
  678.	H	CD3		CD3
  679.	CD3	CD3		CD3
  680.		H	H	H
  681.		CD3	H	H
  682.		H	CD3	H
  683.		H	H	CD3
  684.		CD3	CD3	H
  685.		CD3	H	CD3
  686.		H	CD3	CD3
  687.		CD3	CD3	CD3
  688.	H		H	H
  689.	CD3		H	H
  690.	H		CD3	H
  691.	H		H	CD3
  692.	CD3		CD3	H
  693.	CD3		H	CD3
  694.	H		CD3	CD3
  695.	CD3		CD3	CD3
  696.	H	H		H
  697.	CD3	H		H
  698.	H	CD3		H
  699.	H	H		CD3
  700.	CD3	CD3		H
  701.	CD3	H		CD3
  702.	H	CD3		CD3
  703.	CD3	CD3		CD3
  704.		H	H	H
  705.		CD3	H	H
  706.		H	CD3	H
  707.		H	H	CD3
  708.		CD3	CD3	H
  709.		CD3	H	CD3
  710.		H	CD3	CD3
  711.		CD3	CD3	CD3
  712.	H		H	H
  713.	CD3		H	H
  714.	H		CD3	H
  715.	H		H	CD3
  716.	CD3		CD3	H
  717.	CD3		H	CD3
  718.	H		CD3	CD3
  719.	CD3		CD3	CD3
  720.	H	H		H
  721.	CD3	H		H
  722.	H	CD3		H
  723.	H	H		CD3
  724.	CD3	CD3		H
  725.	CD3	H		CD3
  726.	H	CD3		CD3
  727.	CD3	CD3		CD3
  728.		H	H	H
  729.		CD3	H	H
  730.		H	CD3	H
  731.		H	H	CD3
  732.		CH3	CH3	H
  733.		CD3	H	CD3
  734.		H	CD3	CD3
  735.		CD3	CD3	CD3
  736.	H		H	H
  737.	CD3		H	H
  738.	H		CD3	H
  739.	H		H	CD3
  740.	CD3		CD3	H
  741.	CD3		H	CD3
  742.	H		CD3	CD3
  743.	CD3		CD3	CD3
  744.	H	H		H
  745.	CD3	H		H
  746.	H	CD3		H
  747.	H	H		CD3
  748.	CD3	CD3		H
  749.	CD3	H		CD3
  750.	H	CD3		CD3
  751.	CD3	CD3		CD3
  752.	CD(CH3)2	H	CD2CH3	H
  753.	CD(CH3)2	H	CD(CH3)2	H
  754.	CD(CH3)2	H	CD2CH(CH3)2	H
  755.	CD(CH3)2	H	C(CH3)3	H
  756.	CD(CH3)2	H	CD2C(CH3)3	H
  757.	CD(CH3)2	H	CD2CH2CF3	H
  758.	CD(CH3)2	H	CD2C(CH3)2CF3	H
  759.	CD(CH3)2	H		H
  760.	CD(CH3)2	H		H
  761.	CD(CH3)2	H		H
  762.	CD(CH3)2	H		H
  763.	CD(CH3)2	H		H
  764.	CD(CH3)2	H		H
  765.	C(CH3)3	H	CD2CH3	H
  766.	C(CH3)3	H	CD(CH3)2	H
  767.	C(CH3)3	H	CD2CH(CH3)2	H
  768.	C(CH3)3	H	C(CH3)3	H
  769.	C(CH3)3	H	CD2C(CH3)3	H
  770.	C(CH3)3	H	CD2CH2CF3	H
  771.	C(CH3)3	H	CD2C(CH3)2CF3	H
  772.	C(CH3)3	H		H
  773.	C(CH3)3	H		H
  774.	C(CH3)3	H		H
  775.	C(CH3)3	H		H
  776.	C(CH3)3	H		H
  777.	C(CH3)3	H		H
  778.	CD2C(CH3)3	H	CD2CH3	H
  779.	CD2C(CH3)3	H	CD(CH3)2	H
  780.	CD2C(CH3)3	H	CD2CH(CH3)2	H
  781.	CD2C(CH3)3	H	C(CH3)3	H
  782.	CD2C(CH3)3	H	CD2C(CH3)3	H
  783.	CD2C(CH3)3	H	CD2CH2CF3	H
  784.	CD2C(CH3)3	H	CD2C(CH3)2CF3	H
  785.	CD2C(CH3)3	H		H
  786.	CD2C(CH3)3	H		H
  787.	CD2C(CH3)3	H		H
  788.	CD2C(CH3)3	H		H
  789.	CD2C(CH3)3	H		H
  790.	CD2C(CH3)3	H		H
  791.		H	CD2CH3	H
  792.		H	CD(CH3)2	H
  793.		H	CD2CH(CH3)2	H
  794.		H	C(CH3)3	H
  795.		H	CD2C(CH3)3	H
  796.		H	CD2CH2CF3	H
  797.		H	CD2C(CH3)2CF3	H
  798.		H		H
  799.		H		H
  800.		H		H
  801.		H		H
  802.		H		H
  803.		H		H
  804.		H	CD2CH3	H
  805.		H	CD(CH3)2	H
  806.		H	CD2CH(CH3)2	H
  807.		H	C(CH3)3	H
  808.		H	CD2C(CH3)3	H
  809.		H	CD2CH2CF3	H
  810.		H	CD2C(CH3)2CF3	H
  811.		H		H
  812.		H		H
  813.		H		H
  814.		H		H
  815.		H		H
  816.		H		H
  817.		H	CD2CH3	H
  818.		H	CD(CH3)2	H
  819.		H	CD2CH(CH3)2	H
  820.		H	C(CH3)3	H
  821.		H	CD2C(CH3)3	H
  822.		H	CD2CH2CF3	H
  823.		H	CD2C(CH3)2CF3	H
  824.		H		H
  825.		H		H
  826.		H		H
  827.		H		H
  828.		H		H
  829.		H		H
  830.		H	CD2CH3	H
  831.		H	CD(CH3)2	H
  832.		H	CD2CH(CH3)2	H
  833.		H	C(CH3)3	H
  834.		H	CD2C(CH3)3	H
  835.		H	CD2CH2CF3	H
  836.		H	CD2C(CH3)2CF3	H
  837.		H		H
  838.		H		H
  839.		H		H
  840.		H		H
  841.		H		H
  842.		H		H
  843.		H	CD2CH3	H
  844.		H	CD(CH3)2	H
  845.		H	CD2CH(CH3)2	H
  846.		H	C(CH3)3	H
  847.		H	CD2C(CH3)3	H
  848.		H	CD2CH2CF3	H
  849.		H	CD2C(CH3)2CF3	H
  850.		H		H
  851.		H		H
  852.		H		H
  853.		H		H
  854.		H		H
  855.		H		H

• In some embodiments, the first compound can be an emissive dopant. In some embodiments, the compound can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence), triplet-triplet annihilation, or combinations of these processes.
• In another aspect of the present disclosure, an organic light-emitting device (OLED) comprising an anode; a cathode; and an organic layer, disposed between the anode and the cathode, comprising a first compound is disclosed. The first compound is capable of functioning as a phosphorescent emitter in an organic light emitting device at room temperature, and the first compound has at least one aromatic ring and at least one substituent R, where each of the at least one substituent R is directly bonded to one of the at least one aromatic rings. Each of the at least one substituent R has the formula of
• 
• where :
• G¹ is
  • (a) selected from the group consisting of NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; and G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³;
  • (b) a direct bond; and G² is a non-aromatic spiro polycyclic group, which can be further substituted by one or more R³; or
  • (c) selected from the group consisting of: direct bond, NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; G2 is a non-aromatic polycyclic group, which can be further substituted by one or more R3; and R is directly bonded to an aromatic ring selected from the group consisting of phenyl, pyridine, and triazine, which can be further fused to other rings;
• R¹, R², and R³ are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and
• each G¹ and G² is independently, optionally, partially or fully deuterated.
• The OLED disclosed herein can be incorporated into one or more of a consumer product, an electronic component module, and a lighting panel. The organic layer can be an emissive layer and the compound can be an emissive dopant in some embodiments, while the compound can be a non-emissive dopant in other embodiments.
• The organic layer can also include a host. In some embodiments, two or more hosts are preferred. In some embodiments, the hosts used maybe a) bipolar, b) electron transporting, c) hole transporting or d) wide band gap materials that play little role in charge transport. In some embodiments, the host can include a metal complex. The host can be a triphenylene containing benzo-fused thiophene or benzo-fused furan. Any substituent in the host can be an unfused substituent independently selected from the group consisting of C_nH_2n+1, OC_nH_2n+1, OAr₁, N(C_nH_2n+1)₂, N(Ar₁)(Ar₂), CH═CH—C_nH_2n+1, C≡C—C_nH_2n+1, Ar₁, Ar₁—Ar₂, and C_nH_2n—Ar₁, or the host has no substitution. In the preceding substituents n can range from 1 to 10; and Ar₁ and Ar₂ can be independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof. The host can be an inorganic compound. For example a Zn containing inorganic material e.g. ZnS.
• The host can be a compound comprising at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene. The host can include a metal complex. The host can be, but is not limited to, a specific compound selected from the group consisting of:
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• and combinations thereof. Additional information on possible hosts is provided below.
• In yet another aspect of the present disclosure, a formulation that comprises the first compound is described. The formulation can include one or more components selected from the group consisting of a solvent, a host, a hole injection material, hole transport material, and an electron transport layer material, disclosed herein.
Combination With Other Materials
• The materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device. For example, emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present. The materials described or referred to below are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.
Conductivity Dopants
• A charge transport layer can be doped with conductivity dopants to substantially alter its density of charge carriers, which will in turn alter its conductivity. The conductivity is increased by generating charge carriers in the matrix material, and depending on the type of dopant, a change in the Fermi level of the semiconductor may also be achieved. Hole-transporting layer can be doped by p-type conductivity dopants and n-type conductivity dopants are used in the electron-transporting layer.
• Non-limiting examples of the conductivity dopants that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP01617493, EP01968131, EP2020694, EP2684932, US20050139810, US20070160905, US20090167167, US2010288362, WO06081780, WO2009003455, WO2009008277, WO2009011327, WO2014009310, US2007252140, US2015060804 and US2012146012.
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HIL/HTL
• A hole injecting/transporting material to be used in the present invention is not particularly limited, and any compound may be used as long as the compound is typically used as a hole injecting/transporting material. Examples of the material include, but are not limited to: a phthalocyanine or porphyrin derivative; an aromatic amine derivative; an indolocarbazole derivative; a polymer containing fluorohydrocarbon; a polymer with conductivity dopants; a conducting polymer, such as PEDOT/PSS; a self-assembly monomer derived from compounds such as phosphonic acid and silane derivatives; a metal oxide derivative, such as MoO_x; a p-type semiconducting organic compound, such as 1,4,5,8,9,12-Hexaazatriphenylenchexacarbonitrile; a metal complex, and a crosslinkable compounds.
• Examples of aromatic amine derivatives used in HIL or HTL include, but not limit to the following general structures:
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• Each of Ar¹ to Ar⁹ is selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each Ar may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
• In one aspect, Ar¹ to Ar⁹ is independently selected from the group consisting of:
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• wherein k is an integer from 1 to 20; X¹⁰¹ to X¹⁰⁸ is C (including CH) or N; Z¹⁰¹ is NAr¹, O, or S; Ar¹ has the same group defined above.
• Examples of metal complexes used in HIL or HTL include, but are not limited to the following general formula:
• 
• wherein Met is a metal, which can have an atomic weight greater than 40; (Y¹⁰¹-Y¹⁰²) is a bidentate ligand, Y¹⁰¹ and Y¹⁰¹ are independently selected from C, N, O, P, and S; L¹⁰¹ is an ancillary ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.
• In one aspect, (Y¹⁰¹-Y¹⁰²) is a 2-phenylpyridine derivative. In another aspect, (Y¹⁰¹-Y¹⁰²) is a carbene ligand. In another aspect, Met is selected from Ir, Pt, Os, and Zn. In a further aspect, the metal complex has a smallest oxidation potential in solution vs. Fc⁺/Fc couple less than about 0.6 V.
• Non-limiting examples of the HIL and HTL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN102702075, DE102012005215, EP01624500, EP01698613, EP01806334, EP01930964, EP01972613, EP01997799, EP02011790, EP02055700, EP02055701, EP1725079, EP2085382, EP2660300, EP650955, JP07-073529, JP2005112765, JP2007091719, JP2008021687, JP2014-009196, KR20110088898, KR20130077473, TW201139402, US06517957, US20020158242, US20030162053, US20050123751, US20060182993, US20060240279, US20070145888, US20070181874, US20070278938, US20080014464, US20080091025, US20080106190, US20080124572, US20080145707, US20080220265, US20080233434, US20080303417, US2008107919, US20090115320, US20090167161, US2009066235, US2011007385, US20110163302, US2011240968, US2011278551, US2012205642, US2013241401, US20140117329, US2014183517, US5061569, US5639914, WO05075451, WO07125714, WO08023550, WO08023759, WO2009145016, WO2010061824, WO2011075644, WO2012177006, WO2013018530, WO2013039073, WO2013087142, WO2013118812, WO2013120577, WO2013157367, WO2013175747, WO2014002873, WO2014015935, WO2014015937, WO2014030872, WO2014030921, WO2014034791, WO2014104514, WO2014157018.
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EBL
• An electron blocking layer (EBL) may be used to reduce the number of electrons and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies, and/or longer lifetime, as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than the emitter closest to the EBL interface. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than one or more of the hosts closest to the EBL interface. In one aspect, the compound used in EBL contains the same molecule or the same functional groups used as one of the hosts described below.
Host
• The light emitting layer of the organic EL device of the present invention preferably contains at least a metal complex as light emitting material, and may contain a host material using the metal complex as a dopant material. Examples of the host material are not particularly limited, and any metal complexes or organic compounds may be used as long as the triplet energy of the host is larger than that of the dopant. Any host material may be used with any dopant so long as the triplet criteria is satisfied.
• Examples of metal complexes used as host are preferred to have the following general formula:
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• wherein Met is a metal; (Y¹⁰³-Y¹⁰⁴) is a bidentate ligand, Y¹⁰³ and Y¹⁰⁴ are independently selected from C, N, O, P, and S; L¹⁰¹ is an another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.
• In one aspect, the metal complexes are:
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• wherein (O—N) is a bidentate ligand, having metal coordinated to atoms O and N.
• In another aspect, Met is selected from Ir and Pt. In a further aspect, (Y¹⁰³-Y¹⁰⁴) is a carbene ligand.
• Examples of other organic compounds used as host are selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each option within each group may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
• In one aspect, the host compound contains at least one of the following groups in the molecule:
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• wherein each of R¹⁰¹ to R¹⁰⁷ is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and when it is aryl or heteroaryl, it has the similar definition as Ar’s mentioned above. k is an integer from 0 to 20 or 1 to 20; k‴ is an integer from 0 to 20. X¹⁰¹ to X¹⁰⁸ is selected from C (including CH) or N. Z¹⁰¹ and Z¹⁰² is selected from NR¹⁰¹, O, or S.
• Non-limiting examples of the host materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP2034538, EP2034538A, EP2757608, JP2007254297, KR20100079458, KR20120088644, KR20120129733, KR20130115564, TW201329200, US20030175553, US20050238919, US20060280965, US20090017330, US20090030202, US20090167162, US20090302743, US20090309488, US20100012931, US20100084966, US20100187984, US2010187984, US2012075273, US2012126221, US2013009543, US2013105787, US2013175519, US2014001446, US20140183503, US20140225088, US2014034914, US7154114, WO2001039234, WO2004093207, WO2005014551, WO2005089025, WO2006072002, WO2006114966, WO2007063754, WO2008056746, WO2009003898, WO2009021126, WO2009063833, WO2009066778, WO2009066779, WO2009086028, WO2010056066, WO2010107244, WO2011081423, WO2011081431, WO2011086863, WO2012128298, WO2012133644, WO2012133649, WO2013024872, WO2013035275, WO2013081315, WO2013191404, WO2014142472,
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Additional Emitters
• One or more additional emitter dopants may be used in conjunction with the compound of the present disclosure. Examples of the additional emitter dopants are not particularly limited, and any compounds may be used as long as the compounds are typically used as emitter materials. Examples of suitable emitter materials include, but are not limited to, compounds which can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence), triplet-triplet annihilation, or combinations of these processes.
• Non-limiting examples of the emitter materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103694277, CN1696137, EB01238981, EP01239526, EP01961743, EP1239526, EP1244155, EP1642951, EP1647554, EP1841834, EP1841834B, EP2062907, EP2730583, JP2012074444, JP2013110263, JP4478555, KR1020090133652, KR20120032054, KR20130043460, TW201332980, US06699599, US06916554, US20010019782, US20020034656, US20030068526, US20030072964, US20030138657, US20050123788, US20050244673, US2005123791, US2005260449, US20060008670, US20060065890, US20060127696, US20060134459, US20060134462, US20060202194, US20060251923, US20070034863, US20070087321, US20070103060, US20070111026, US20070190359, US20070231600, US2007034863, US2007104979, US2007104980, US2007138437, US2007224450, US2007278936, US20080020237, US20080233410, US20080261076, US20080297033, US200805851, US2008161567, US2008210930, US20090039776, US20090108737, US20090115322, US20090179555, US2009085476, US2009104472, US20100090591, US20100148663, US20100244004, US20100295032, US2010102716, US2010105902, US2010244004, US2010270916, US20110057559, US20110108822, US20110204333, US2011215710, US2011227049, US2011285275, US2012292601, US20130146848, US2013033172, US2013165653, US2013181190, US2013334521, US20140246656, US2014103305, US6303238, US6413656, US6653654, US6670645, US6687266, US6835469, US6921915, US7279704, US7332232, US7378162, US7534505, US7675228, US7728137, US7740957, US7759489, US7951947, US8067099, US8592586, US8871361, WO06081973, WO06121811, WO07018067, WO07108362, WO07115970, WO07115981, WO08035571, WO2002015645, WO2003040257, WO2005019373, WO2006056418, WO2008054584, WO2008078800, WO2008096609, WO2008101842, WO2009000673, WO2009050281, WO2009100991, WO2010028151, WO2010054731, WO2010086089, WO2010118029, WO2011044988, WO2011051404, WO2011107491, WO2012020327, WO2012163471, WO2013094620, WO2013107487, WO2013174471, WO2014007565, WO2014008982, WO2014023377, WO2014024131, WO2014031977, WO2014038456, WO2014112450.
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HBL
• A hole blocking layer (HBL) may be used to reduce the number of holes and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies and/or longer lifetime as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and or higher triplet energy than the emitter closest to the HBL interface. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and or higher triplet energy than one or more of the hosts closest to the HBL interface.
• In one aspect, compound used in HBL contains the same molecule or the same functional groups used as host described above.
• In another aspect, compound used in HBL contains at least one of the following groups in the molecule:
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• wherein k is an integer from 1 to 20; L¹⁰¹ is an another ligand, k′ is an integer from 1 to 3.
ETL
• Electron transport layer (ETL) may include a material capable of transporting electrons. Electron transport layer may be intrinsic (undoped), or doped. Doping may be used to enhance conductivity. Examples of the ETL material are not particularly limited, and any metal complexes or organic compounds may be used as long as they are typically used to transport electrons.
• In one aspect, compound used in ETL contains at least one of the following groups in the molecule:
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• wherein R¹⁰¹ is selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, when it is aryl or heteroaryl, it has the similar definition as Ar’s mentioned above. Ar¹ to Ar³ has the similar definition as Ar’s mentioned above. k is an integer from 1 to 20. X¹⁰¹ to X¹⁰⁸ is selected from C (including CH) or N.
• In another aspect, the metal complexes used in ETL contains, but not limit to the following general formula:
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• wherein (O—N) or (N—N) is a bidentate ligand, having metal coordinated to atoms O, N or N, N; L¹⁰¹ is another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal.
• Non-limiting examples of the ETL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103508940, EP01602648, EP01734038, EP01956007, JP2004-022334, JP2005149918, JP2005-268199, KR0117693, KR20130108183, US20040036077, US20070104977, US2007018155, US20090101870, US20090115316, US20090140637, US20090179554, US2009218940, US2010108990, US2011156017, US2011210320, US2012193612, US2012214993, US2014014925, US2014014927, US20140284580, US6656612, US8415031, WO2003060956, WO2007111263, WO2009148269, WO2010067894, WO2010072300, WO2011074770, WO2011105373, WO2013079217, WO2013145667, WO2013180376, WO2014104499, WO2014104535,
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Charge Generation Layer (CGL)
• In tandem or stacked OLEDs, the CGL plays an essential role in the performance, which is composed of an n-doped layer and a p-doped layer for injection of electrons and holes, respectively. Electrons and holes are supplied from the CGL and electrodes. The consumed electrons and holes in the CGL are refilled by the electrons and holes injected from the cathode and anode, respectively; then, the bipolar currents reach a steady state gradually. Typical CGL materials include n and p conductivity dopants used in the transport layers.
• In any above-mentioned compounds used in each layer of the OLED device, the hydrogen atoms can be partially or fully deuterated. Thus, any specifically listed substituent, such as, without limitation, methyl, phenyl, pyridyl, etc. may be undeuterated, partially deuterated, and fully deuterated versions thereof. Similarly, classes of substituents such as, without limitation, alkyl, aryl, cycloalkyl, heteroaryl, etc. also may be undeuterated, partially deuterated, and fully deuterated versions thereof.
EXPERIMENTAL Synthesis Examples Synthesis Example 1 Synthesis of 8-(4-(bicyclo[2.2.1]heptan-2-yl)pyridin-2-yl)-2-methylbenzofuro[2,3-b] pyridine
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• 8-(4-chloropyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine (4.75 g, 16.12 mmol) and [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) dichloride (PEPPSI-IPr) (1.094 g, 1.612 mmol) were charged into a reaction flask with 50 mL of tetrahydrofuran (THF). This mixture was degassed with nitrogen then was stirred at room temperature (~22° C.). Then, bicyclo[2.2.1]heptan-2-ylzinc(II) bromide (97 ml, 48.3 mmol) was added to the reaction mixture via syringe. Stirring was continued at room temperature for 18 hours. The reaction mixture was quenched with aqueous ammonium chloride solution, then extracted with ethyl acetate. The extracts were dried over magnesium sulfate then filtered and concentrated to a reduced volume under vacuum. A solid was filtered from the resulting concentrate. The filtrate was passed through a silica gel column eluting with 2.5-5% THF/dichloromethane (DCM). The cleanest fractions were combined and concentrated under vacuum yielding 8-(4-(bicyclo[2.2.1]heptan-2-yl)pyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine (4 g, 11.28 mmol, 70.0% yield) as a viscous light yellow oil.
Synthesis of 8-(4-(bicyclo[2.2.1]heptan-2-yl-2-d)pyridin-2-yl)-2-(methyl-d3)benzofuro[2,3-b]pyridine
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• 8-(4-(bicyclo[2.2.1]heptan-2-yl)pyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine (4 g, 11.28 mmol) was dissolved in 40 mL of THF. Dimethyl sulfoxide-d₆ (37.9 g, 451 mmol) was syringed into the reaction mixture, followed by the addition of sodium tert-butoxide (0.542 g, 5.64 mmol). The resulting mixture was stirred and heated for 20 hours in a bath set at 65° C. The reaction mixture was quenched with 80 mL of D₂O. The mixture was extracted two times with 400 mL ethyl acetate. The extracts were combined, washed with an aqueous LiCl solution, then dried over magnesium sulfate. The extracts were then filtered and concentrated under vacuum. The residue was passed through 3 × 120 g silica gel columns using 2.5-3.5% THF/ DCM. The clean product fractions yielded 8-(4-(bicyclo[2.2.1]heptan-2-yl-2-d)pyridin-2-yl)-2-(methyl- d3)benzofuro[2,3-b]pyridine (2.7 g, 7.53 mmol, 66.7% yield).
Synthesis of Compound 1064460 [Ir(L_A540)(L_B430)₂]
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• 8-(4-(bicyclo[2.2.1]heptan-2-yl-2-d)pyridin-2-yl)-2-(methyl-d3)benzofuro[2,3-b]pyridine (2.6 g, 7.25 mmol) and the iridium salt shown in the synthetic scheme above (3.28 g, 4.19 mmol) were charged into a reaction flask with ethanol (32 mL) and methanol (32 mL). The reaction mixture was degassed with nitrogen then was heated for 3 days in an oil bath set at 70° C. The oil bath temperature was then raised to 80° C. and the raction mixture was stirred for two additional days. After this time, the reaction flask was cooled to room temperatrue (~ 20° C.). A yellow solid was isolated via filtration and was dried under vacuum with no heat. This solid was dissolved in toluene and was pre-absorbed on silica gel. This material was purified using silica gel chromatography through 6 × 125 g silica gel cartridges eluting with 0.7-0.8% ethyl acetate/toluene to yield a yellow solid that was triturated twicewith hot toluene. Compound 1064460 was then isolated as a yellow solid via filtration (0.60 g, 0.646 mmol, 15.4% yield) LC/MS confirmed the mass of the desired product.
Synthesis Example 2 Synthesis of 8-(5-(bicyclo[2.2.1]heptan-2-yl)pyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine:
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• 8-(5-bromopyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine (7 g, 20.64 mmol) and PEPPSI-IPr (1.051 g, 1.548 mmol) were charged into the reaction flask with 150 mL of THF. Bicyclo[2.2.1]heptan-2-ylzinc(II) bromide (70.2 ml, 35.1 mmol) was then syringed into the reaction flask and the mixture was degassed with nitrogen. This mixture was stirred at room temperature (~ 22° C.) for 16 hours. Gas chromatography/mass spetroscopy analysis showed the reaction to be complete. The reaction mixture was quenched with aqueous ammonium chloride, then the majority of the THF was removed under reduced pressure. Ethyl acetate was added to the aqueous mixture and this mixture was heated for several hours in a 70° C. bath. The organic layer was then separated and the aqueous layer was again extracted with ethyl acetate. The extracts were combined, washed with aqueous LiCl, then dried over magnesium sulfate. The extracts were then filtered and concentrated under vacuum. The crude residue was passed through 2 × 330 g silica gel columns using 3-6% THF/ toluene. Clean product fractions were combined and concentrated under vacuum yielding 8-(5-(bicyclo[2.2.1]heptan-2-yl)pyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine (6 g, 16.93 mmol, 82% yield) as a foamy solid.
Synthesis of 8-(5-(bicyclo[2.2.1]heptan-2-yl-2-d)pyridin-2-yl)-2-(methyl-d3)benzofuro [2,3-b] pyridine
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• 8-(5-(bicyclo[2.2.1]heptan-2-yl)pyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine (7.34 g, 20.71 mmol) was charged into a reaction flask with 60 mL of THF and dimethyl sulfoxide-d6 (35 ml, 500 mmol). Sodium tert-butoxide (0.596 g, 6.21 mmol) was then added all at once to the reaction mixture. This mixture was stirred and heated for 16 hours in an oil bath set at 65° C. The reaction mixture was cooled to room temperature (~ 22° C.) then was quenched with 80 mL of D₂O. The mixture was extracted two times with 400 mL ethyl acetate. The extracts were combined, washed with aqueous LiCl, then dried over magnesium sulfate. The extracts were then filtered and concentrated under vacuum. The residue was passed through 3 × 330 g silica gel columns using 2.5-3.5% THF/ toluene. Clean product fractions yielded 8-(5-(bicyclo[2.2.1]heptan-2-yl-2-d)pyridin-2-yl)-2-(methyl-d3)benzofuro[2,3-b]pyridine (3.3 g, 9.21 mmol, 44.5% yield).
Synthesis of Compound 1064122 [Ir(L_A202)(L_B430)₂]
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  8-(5-(bicyclo[2.2.1]heptan-2-yl-2-d)pyridin-2-yl)-2-(methyl-d3)benzofuro[2,3-b]pyridine (3.3 g, 9.21 mmol) and the iridium salt shown in the scheme above (4.2 g, 5.37 mmol) were charged into the reaction flask with 40 mL ethanol and 40 mL methanol. This mixture was degassed with nitrogen then heated for five days in an oil bath set at 75° C. The reaction mixture was cooled to room temperature (~ 22° C.). A yellow solid was filtered from solution, which was then dried under vacuum. The yellow solid was dissolved in 400 mL of DCM and then passed through an activated plug of basic alumina. The DCM filtrate was evaporated under reduced vacuum. The crude residue was passed through 7 × 120 g silica gel columns eluting the columns with 5% ethyl acetate/ toluene. The major product eluted 1^st from the columns was isolated as a yellow solid. This material was triturated twice with toluene/ heptane then isolated via filtration. The desired iridium complex was isolated as a yellow solid (0.8 g, 0.86 mmoL, 16.06% yield). Liquid chromatography/mass spectroscopy (LC/MS) analysis confirmed the mass of the desired product.
Device Examples
• All example devices were fabricated by high vacuum (<10-7 Torr) thermal evaporation. The anode electrode was 750 Å of indium tin oxide (ITO). The cathode consisted of 10 Å of Liq (8-hydroxyquinoline lithium) followed by 1,000 Å of Al. All devices were encapsulated with a glass lid sealed with an epoxy resin in a nitrogen glove box (<1 ppm of H₂O and O₂) immediately after fabrication, and a moisture getter was incorporated inside the package. The stack of the device examples consisted of sequentially, from the ITO surface, 100 Å of HATCN as the hole injection layer (HIL); 450 Å of HTM as a hole transporting layer (HTL); 50 Å of EBM as electron blocking layer, 400 Å of EML containing two component host (H1:H2 3:2 ratio) and emitter 12% (GD1 as Inventive Example 1 vs GD2 as comparison example CE 1), and 350 Å of Liq (8-hydroxyquinoline lithium) doped with 40% of ETM as the ETL. The chemical structures of the device materials are shown below.
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• Table 1 shows the device layer thicknesses and materials.
• TABLE 1

  Device structure for evaluation of green emitters
  Layer	Material	Thickness [Å]
  Anode	ITO	750
  HIL	HATCN		100
  HTL	HTM	450
  EBL	EBM	50
  G EML	H1:H2 (3:2):Emitter 12%	350
  ETL	Liq: ETM 40%	350
  EIL	Liq	10
  Cathode	Al	1000

• Emitter Example 1 (GD1) and Comparative Example CE1 (GD2) were used to demonstrate the superiority efficiency of the device with inventive vs. comparative compounds. The device External quantum efficiency (EQE) and luminance efficacy (LE) measured 10mA/cm² are shown in the Table 2.
• TABLE 2

  External quantum efficiency of devices with inventive and comparative examples
  Example	Emitter	LE at 10mA/cm2 [cd/A]	EQE at 10mA/cm2 [%]
  CE1	GD2	93.3	24.4
  Example 1	GD1	98.1	25.7

• The observed device LE and EQE of inventive emitter is significantly higher vs.comparative emitter.
• It is understood that the various embodiments described herein are by way of example only, and are not intended to limit the scope of the invention. For example, many of the materials and structures described herein may be substituted with other materials and structures without deviating from the spirit of the invention. The present invention as claimed may therefore include variations from the particular examples and preferred embodiments described herein, as will be apparent to one of skill in the art. It is understood that various theories as to why the invention works are not intended to be limiting.

Claims (20)

What is claimed is:

1. A composition comprising a first compound;

wherein the first compound is capable of functioning as a phosphorescent emitter in an organic light emitting device at room temperature;

wherein the first compound has at least one aromatic ring and at least one substituent R;

wherein each of the at least one substituent R is directly bonded to one of the at least one aromatic ring;

wherein each of the at least one substituent R has the formula of

wherein

(a) G¹ is selected from the group consisting of NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; and G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³;

(b) G¹ is a direct bond; and G² is a non-aromatic spiro polycyclic group, which can be further substituted by one or more R³; or

(c) G¹ is selected from the group consisting of: direct bond, NR¹, SiR¹R², GeR¹R², alkyl, cycloalkyl, and combinations thereof; G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³; and R is directly bonded to an aromatic ring selected from the group consisting of phenyl, pyridine, and triazine, which can be further fused to other rings;

wherein R¹, R², and R³ are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

wherein each G¹ and G² can be independently, partially or fully deuterated.

2. The composition of claim 1, wherein G² is polycyclic alkyl.

3. The composition of claim 1, wherein G² is carborane.

4. The composition of claim 1, wherein G² contains at least one heteroatom.

5. The composition of claim 1, wherein the first compound is capable of emitting light from a triplet excited state to a ground singlet state at room temperature.

6. The composition of claim 1, wherein the first compound has the formula of

$\text{M}{\left({\text{L}}^1\right)}_{\text{x}}{\left({\text{L}}^2\right)}_{\text{y}}{\left({\text{L}}^3\right)}_{\text{z}};$

wherein L¹, L², and L³ can be the same or different;

wherein x is 1, 2, or 3;

wherein y is 0, 1, or 2;

wherein z is 0, 1, or 2;

wherein x+y+z is the oxidation state of the metal M;

wherein L¹, L², and L³ are each independently selected from the group consisting of:

wherein each X¹ to X¹⁷ are independently selected from the group consisting of carbon and nitrogen;

wherein X is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO₂, CR′R″, SiR′R″, and GeR′R″;

wherein each R′ and R″ can be independently, fused or joined to form a ring;

wherein each R_a, R_b, R_c, and R_d independently represents from mono substitution to the maximum possible number of substitutions, or no substitution;

wherein each R′, R″, R_a, R_b, R_c, and R_d is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein any two adjacent substitutents of R_a, R_b, R_c, and R_d can be fused or joined to form a ring or form a multidentate ligand; and

wherein at least one of the R_a, R_b, R_c, and R_d includes the at least one substituent R.

7. The composition of claim 6, wherein the first compound has the formula of

$\text{Ir}{\left({\text{L}}^1\right)}_2\left({\text{L}}^2\right).$

.

8. The composition of claim 7, wherein L¹ has the formula selected from the group consisting of:

and

and wherein L

² has the formula:

.

9. The composition of claim 7, wherein L¹ and L² are different and each independently selected from the group consisting of:

and

.

10. The composition of claim 7, wherein L¹ and L² are each independently selected from the group consisting of:

and

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11. The composition of claim 1, wherein G² is selected from the group consisting of:

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12. The composition of claim 1, wherein each of the at least one substituent R is independently selected from the group consisting of:

and

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13. The composition of claim 6, wherein L¹ is L_A having the following structure:

selected from the group consisting of L

_A1 to L_A2480 as listed below:

Ligand R_A1 R_A2 R_A3 R_A4 R_A5 RA6 Ligand R_A1 R_A2 R_A3 R_A4 R_A5 R_A6 L_A1 R^G1 H H H H H L_A1241 CD₃ H R^G58 H H H L_A2 R^G2 H H H H H L_A1242 CD₃ H R^G59 H H H L_A3 R^G3 H H H H H L_A1243 CD₃ H R^G60 H H H L_A4 R^G4 H H H H H L_A1244 CD₃ H R^G61 H H H L_A5 R^G5 H H H H H L_A1245 CD₃ H R^G62 H H H L_A6 R^G6 H H H H H L_A1246 CD₃ H R^G63 H H H L_A7 R^G7 H H H H H L_A1247 CD₃ H R^G64 H H H LAB R^G8 H H H H H L_A1248 CD₃ H R^G65 H H H L_A9 R^G9 H H H H H L_A1249 CD₃ H R^G66 H H H LA₁₀ R^G10 H H H H H L_A1250 CD₃ H R^G67 H H H L_A11 R^G11 H H H H H L_A1251 CD₃ H R^G68 H H H L_A12 RG12 H H H H H L_A1252 CD₃ H R^G69 H H H LA13 R^G13 H H H H H L_A1253 CD₃ H R^G70 H H H L_A14 R^G14 H H H H H L_A1254 CD₃ H R^G71 H H H LA15 R^G15 H H H H H L_A1255 CD₃ H R^G72 H H H L_A16 R^G16 H H H H H L_A1256 CD₃ H R^G73 H H H L_A17 R^G17 H H H H H L_A1257 CD₃ H R^G74 H H H L_A18 R^G18 H H H H H L_A1258 CD₃ H RG75 H H H L_A19 R^G19 H H H H H L_A1259 CD₃ H R^G76 H H H L_A20 R^G20 H H H H H L_A1260 CD₃ H R^G77 H H H L_A21 R^G21 H H H H H L_A1261 CD₃ H R^G78 H H H L_A22 R^G22 H H H H H L_A1262 CD₃ H R^G79 H H H L_A23 R^G23 H H H H H L_A1263 CD₃ H R^G80 H H H L_A24 R^G24 H H H H H L_A1264 CD₃ H R^G81 H H H L_A25 R^G25 H H H H H L_A1265 CD₃ H R^G82 H H H L_A26 R^G26 H H H H H L_A1266 CD₃ H R^G84 H H H L_A27 R^G27 H H H H H L_A1267 CD₃ H R^G84 H H H L_A28 R^G28 H H H H H L_A1268 CD₃ H R^G85 H H H L_A29 R^G29 H H H H H L_A1269 CD₃ H R^G86 H H H L_A30 R^G30 H H H H H L_A1270 CD₃ H R^GB7 H H H L_A31 R^G31 H H H H H L_A1271 CD₃ H R^G88 H H H L_A32 R^G32 H H H H H L_A1272 CD₃ H R^G89 H H H L_A33 R^G33 H H H H H L_A1273 CD₃ H R^G90 H H H L_A34 R^G34 H H H H H L_A1274 CD₃ H R^G91 H H H L_A35 R^G35 H H H H H L_A1275 CD₃ H R^G92 H H H L_A36 R^G36 H H H H H L_A1276 CD₃ H R^G93 H H H L_A37 R^G37 H H H H H L_A1277 CD₃ H R^G94 H H H L_A38 R^G38 H H H H H L_A1278 CD₃ H R^G95 H H H L_A39 R^G39 H H H H H L_A1279 CD₃ H R^G96 H H H L_A40 R^G40 H H H H H L_A1280 CD₃ H R^G97 H H H L_A41 R^G41 H H H H H L_A1281 CD₃ H R^G98 H H H L_A42 R^G42 H H H H H L_A1282 CD₃ H R^G99 H H H L_A43 R^G43 H H H H H L_A1283 CD₃ H R^G100 H H H L_A44 R^G44 H H H H H L_A1284 CD₃ H R^G101 H H H L_A45 R^G45 H H H H H L_A1285 CD₃ H R^G102 H H H L_A46 R^G46 H H H H H L_A1286 CD₃ H R^G103 H H H L_A47 R^G47 H H H H H L_A1287 CD₃ H R^G104 H H H L_A48 R^G48 H H H H H L_A1288 CD₃ H R^G105 H H H L_A49 R^G49 H H H H H L_A1289 CD₃ H R^G106 H H H L_A50 R^G50 H H H H H L_A1290 CD₃ H R^G107 H H H L_A51 R^G51 H H H H H L_A1291 CD₃ H R^G108 H H H L_A52 R^G52 H H H H H L_A1292 CD₃ H R^G109 H H H L_A53 R^G53 H H H H H L_A1293 CD₃ H R^G110 H H H L_A54 R^G54 H H H H H L_A1294 CD₃ H R^{G11 1} H H H L_A55 R^G55 H H H H H L_A1295 CD₃ H R^{G11 2} H H H L_A56 R^G56 H H H H H L_A1296 CD₃ H R^{G11 3} H H H L_A57 R^G57 H H H H H L_A1297 CD₃ H R^{G11 4} H H H L_A58 R^G58 H H H H H L_A1298 CD₃ H R^{G11 5} H H H L_A59 R^G59 H H H H H L_A1299 CD₃ H R^{G11 6} H H H L_A60 R^G60 H H H H H L_A1300 CD₃ H R^{G11 7} H H H L_A61 R^G61 H H H H H L_A1301 CD₃ H R^{G1 1 8} H H H L_A62 R^G62 H H H H H L_A1302 CD₃ H R^{G11 9} H H H L_A63 R^G63 H H H H H L_A1303 CD₃ H R^{G1 2 0} H H H L_A64 R^G64 H H H H H L_A1304 CD₃ H R^{G1 2 1} H H H L_A65 R^G65 H H H H H L_A1305 CD₃ H R^{G1 2 2} H H H L_A66 R^G66 H H H H H L_A1306 CD₃ H R^{G1 2 3} H H H L_A67 R^G67 H H H H H L_A1307 CD₃ H R^{G 1 2 4} H H H L_A68 R^G68 H H H H H L_A1308 CD₃ H R^{G 1 2 5} H H H L_A69 R^G69 H H H H H L_A1309 CD₃ H R^{G 1 2 6} H H H L_A70 R^G70 H H H H H L_{A13 1 0} CD₃ H R^{G 1 2 7} H H H L_A71 R^G71 H H H H H L_{A13 1 1} CD₃ H R^{G 1 2 8} H H H L_A72 R^G72 H H H H H L_A1312 CD₃ H R^{G 1 2 9} H H H L_A73 R^G73 H H H H H L_A1313 CD₃ H R^{G 1 30} H H H L_A74 R^G74 H H H H H L_A1314 CD₃ H R^{G 1 3 1} H H H L_A75 R^G75 H H H H H L_A1315 CD₃ H R^{G 132} H H H L_A76 R^G76 H H H H H L_A1316 CD₃ H R^{G 13 3} H H H L_A77 R^G77 H H H H H L_A1317 CD₃ H R^{G 13 4} H H H L_A78 R^G78 H H H H H L_A1318 CD₃ H R^{G 135} H H H L_A79 R^G79 H H H H H L_A1319 CD₃ H R^{G 13 6} H H H L_A80 R^G80 H H H H H L_{A13 2 0} CD₃ H R^{G 137} H H H L_{A8 1} R^G81 H H H H H L_A1321 CD₃ H R^{G 138} H H H L_A82 R^G82 H H H H H L_A1322 CD₃ H R^{G 139} H H H L_A83 R^G83 H H H H H L_{A13 2 3} CD₃ H R^{G 140} H H H L_A84 R^G84 H H H H H L_A1324 CD₃ H R^{G 141} H H H L_A58 R^G85 H H H H H L_{A13 2 5} CD₃ H R^{G 142} H H H L_A86 R^G86 H H H H H L_{A13 2 6} CD₃ H R^{G 1 4 3} H H H L_A87 R^G87 H H H H H L_{A13 2 7} CD₃ H R^{G 144} H H H L_A58 R^G88 H H H H H L_{A13 2 8} CD₃ H R^{G 145} H H H L_A89 R^G89 H H H H H L_{A13 2 9} CD₃ H R^{G 146} H H H L_A90 R^G90 H H H H H L_A1330 CD₃ H R^{G 147} H H H L_A91 R^G91 H H H H H L_A1331 CD₃ H R^G148 H H H L_A92 R^G92 H H H H H L_A1332 CD₃ H R^G149 H H H L_A93 R^G93 H H H H H L_A1333 CD₃ H R^G150 H H H L_A94 R^G94 H H H H H L_A1334 CD₃ H R^G151 H H H L_A95 R^G95 H H H H H L_A1335 CD₃ H R^G152 H H H L_A96 R^G96 H H H H H L_A1336 CD₃ H R^G153 H H H L_A97 R^G97 H H H H H L_A1337 CD₃ H R^G154 H H H L_A98 R^G98 H H H H H L_A1338 CD₃ H R^G155 H H H L_A99 R^G99 H H H H H L_A1339 CD₃ H R^G156 H H H L_A100 R^G100 H H H H H L_A1340 CD₃ H R^G157 H H H L_A101 R^G101 H H H H H L_A1341 CD₃ H R^G158 H H H L_A102 R^G102 H H H H H L_A1342 CD₃ H R^G159 H H H L_A103 R^G103 H H H H H L_A1343 CD₃ H R^G160 H H H L_A104 R^G104 H H H H H L_A1344 CD₃ H R^G161 H H H L_A105 R^G105 H H H H H L_A1345 CD₃ H R^G162 H H H L_A106 R^G106 H H H H H L_A1346 CD₃ H R^G163 H H H L_A107 R^G107 H H H H H L_A1347 CD₃ H R^G164 H H H L_A108 R^G108 H H H H H L_A1348 CD₃ H R^G165 H H H L_A109 R^G109 H H H H H L_A1349 CD₃ H R^G166 H H H L_A110 R^G110 H H H H H L_A1350 CD₃ H R^G167 H H H L_A111 R^G111 H H H H H L_A1351 CD₃ H R^G168 H H H L_A112 R^G112 H H H H H L_A1352 CD₃ H R^G169 H H H L_A113 R^G113 H H H H H L_A1353 H CD₃ R^G1 H H H L_A114 R^G114 H H H H H L_A1354 H CD₃ R^G2 H H H L_A115 R^G115 H H H H H L_A1355 H CD₃ R^G3 H H H L_A116 R^G116 H H H H H L_A1356 H CD₃ R^G4 H H H L_A117 R^G117 H H H H H L_A1357 H CD₃ R^G5 H H H L_A118 R^G118 H H H H H L_A1358 H CD₃ R^G6 H H H L_A119 R^G119 H H H H H L_A1359 H CD₃ R^G7 H H H L_A120 R^G120 H H H H H L_A1360 H CD₃ R^G8 H H H L_A121 R^G121 H H H H H L_A1361 H CD₃ R^G9 H H H L_A122 R^G122 H H H H H L_A1362 H CD₃ R^G10 H H H L_A123 R^G123 H H H H H L_A1363 H CD₃ R^G11 H H H L_A124 R^G124 H H H H H L_A1364 H CD₃ R^G12 H H H L_A125 R^G125 H H H H H L_A1365 H CD₃ R^G13 H H H L_A126 R^G126 H H H H H L_A1366 H CD₃ R^G14 H H H L_A127 R^G127 H H H H H L_A1367 H CD₃ R^G15 H H H L_A128 R^G128 H H H H H L_A1368 H CD₃ R^G16 H H H L_A129 R^G129 H H H H H L_A1369 H CD₃ R^G17 H H H L_A130 R^G130 H H H H H L_A1370 H CD₃ R^G18 H H H L_A1311 R^G131 H H H H H L_A1371 H CD₃ R^G19 H H H L_A132 R^G132 H H H H H L_A1372 H CD₃ R^G20 H H H L_A133 R^G133 H H H H H L_A1373 H CD₃ R^G21 H H H L_A134 R^G134 H H H H H L_A1374 H CD₃ R^G22 H H H L_A135 R^G135 H H H H H L_A1375 H CD₃ R^G23 H H H L_A136 R^G136 H H H H H L_A1376 H CD₃ R^G24 H H H L_A137 R^G137 H H H H H L_A1377 H CD₃ R^G25 H H H L_A138 R^G138 H H H H H L_A1378 H CD₃ R^G26 H H H L_A139 R^G139 H H H H H L_A1379 H CD₃ R^G27 H H H L_A140 R^G140 H H H H H L_A1380 H CD₃ R^G28 H H H L_A141 R^G141 H H H H H L_A1381 H CD₃ R^G29 H H H L_A142 R^G142 H H H H H L_A1382 H CD₃ R^G30 H H H L_A143 R^G143 H H H H H L_A1383 H CD₃ R^G31 H H H L_A144 R^G144 H H H H H L_A1384 H CD₃ R^G32 H H H L_A145 R^G145 H H H H H L_A1385 H CD₃ R^G33 H H H L_A146 R^G146 H H H H H L_A1386 H CD₃ R^G34 H H H L_A147 R^G147 H H H H H L_A1387 H CD₃ R^G35 H H H L_A148 R^G148 H H H H H L_A1388 H CD₃ R^G36 H H H L_A149 R^G149 H H H H H L_A1389 H CD₃ R^G37 H H H L_A150 R^G150 H H H H H L_A1390 H CD₃ R^G38 H H H L_A151 R^G151 H H H H H L_A1391 H CD₃ R^G39 H H H L_A152 R^G152 H H H H H L_A1392 H CD₃ R^G40 H H H L_A153 R^G153 H H H H H L_A1393 H CD₃ R^G41 H H H L_A154 R^G154 H H H H H L_A1394 H CD₃ R^G42 H H H L_A155 R^G155 H H H H H L_A1395 H CD₃ R^G43 H H H L_A156 R^G156 H H H H H L_A1396 H CD₃ R^G44 H H H L_A157 R^G157 H H H H H L_A1397 H CD₃ R^G45 H H H L_A158 R^G158 H H H H H L_A1398 H CD₃ R^G46 H H H L_A159 R^G159 H H H H H L_A1399 H CD₃ R^G47 H H H L_A160 R^G160 H H H H H L_A1400 H CD₃ R^G48 H H H L_A161 R^G161 H H H H H L_A1401 H CD₃ R^G49 H H H L_A162 R^G162 H H H H H L_A1402 H CD₃ R^G50 H H H L_A163 R^G163 H H H H H L_A1403 H CD₃ R^G51 H H H L_A164 R^G164 H H H H H L_A1404 H CD₃ R^G52 H H H L_A165 R^G165 H H H H H L_A1405 H CD₃ R^G53 H H H L_A166 R^G166 H H H H H L_A1406 H CD₃ R^G54 H H H L_A167 R^G167 H H H H H L_A1407 H CD₃ R^G55 H H H L_A168 R^G168 H H H H H L_A1408 H CD₃ R^G56 H H H L_A169 R^G169 H H H H H L_A1409 H CD₃ R^G57 H H H L_A170 R^G1 H CD₃ H H H L_A1410 H CD₃ R^G58 H H H L_A171 R^G2 H CD₃ H H H L_A1411 H CD₃ R^G59 H H H L_A172 R^G3 H CD₃ H H H L_A1412 H CD₃ R^G60 H H H L_A173 R^G4 H CD₃ H H H L_A1413 H CD₃ R^G61 H H H L_A174 R^G5 H CD₃ H H H L_A1414 H CD₃ R^G62 H H H L_A175 R^G6 H CD₃ H H H L_A1415 H CD₃ R^G63 H H H L_A176 R^G7 H CD₃ H H H L_A1416 H CD₃ R^G64 H H H L_A177 R^G8 H CD₃ H H H L_A1417 H CD₃ R^G65 H H H L_A178 R^G9 H CD₃ H H H L_A1418 H CD₃ R^G66 H H H L_A179 R^G10 H CD₃ H H H L_A1419 H CD₃ R^G67 H H H L_A180 R^G11 H CD₃ H H H L_A1420 H CD₃ R^G68 H H H L_A181 R^G12 H CD₃ H H H L_A1421 H CD₃ R^G69 H H H L_A182 R^G13 H CD₃ H H H L_A1422 H CD₃ R^G70 H H H L_A183 R^G14 H CD₃ H H H L_A1423 H CD₃ R^G71 H H H L_A184 R^G15 H CD₃ H H H L_A1424 H CD₃ R^G72 H H H L_A185 R^G16 H CD₃ H H H L_A1425 H CD₃ R^G73 H H H L_A186 R^G17 H CD₃ H H H L_A1426 H CD₃ R^G74 H H H L_A187 R^G18 H CD₃ H H H L_A1427 H CD₃ R^G75 H H H L_A188 R^G19 H CD₃ H H H L_A1428 H CD₃ R^G76 H H H L_A189 R^G20 H CD₃ H H H L_A1429 H CD₃ R^G77 H H H L_A190 R^G21 H CD₃ H H H L_A1430 H CD₃ R^G78 H H H L_A191 R^G22 H CD₃ H H H L_A1431 H CD₃ R^G79 H H H L_A192 R^G23 H CD₃ H H H L_A1432 H CD₃ R^G80 H H H L_A193 R^G24 H CD₃ H H H L_A1433 H CD₃ R^G81 H H H L_A194 R^G25 H CD₃ H H H L_A1434 H CD₃ R^G82 H H H L_A195 R^G26 H CD₃ H H H L_A1435 H CD₃ R^G83 H H H L_A196 R^G27 H CD₃ H H H L_A1436 H CD₃ R^G84 H H H L_A197 R^G28 H CD₃ H H H L_A1437 H CD₃ R^G85 H H H L_A198 R^G29 H CD₃ H H H L_A1438 H CD₃ R^G86 H H H L_A199 R^G30 H CD₃ H H H L_A1439 H CD₃ R^G87 H H H L_A200 R^G31 H CD₃ H H H L_A1440 H CD₃ R^G88 H H H L_A201 R^G32 H CD₃ H H H L_A1441 H CD₃ R^G89 H H H L_A202 R^G33 H CD₃ H H H L_A1442 H CD₃ R^G90 H H H L_A203 R^G34 H CD₃ H H H L_A1443 H CD₃ R^G91 H H H L_A204 R^G35 H CD₃ H H H L_A1444 H CD₃ R^G92 H H H L_A205 R^G36 H CD₃ H H H L_A1445 H CD₃ R^G93 H H H L_A206 R^G37 H CD₃ H H H L_A1446 H CD₃ R^G94 H H H L_A207 R^G38 H CD₃ H H H L_A1447 H CD₃ R^G95 H H H L_A208 R^G39 H CD₃ H H H L_A1448 H CD₃ R^G96 H H H L_A209 R^G40 H CD₃ H H H L_A1449 H CD₃ R^G97 H H H L_A210 R^G41 H CD₃ H H H L_A1450 H CD₃ R^G98 H H H L_A211 R^G42 H CD₃ H H H L_A1451 H CD₃ R^G99 H H H L_A212 R^G43 H CD₃ H H H L_A1452 H CD₃ R^G100 H H H L_A213 R^G44 H CD₃ H H H L_A1453 H CD₃ R^G101 H H H L_A214 R^G46 H CD₃ H H H L_A1454 H CD₃ R^G102 H H H L_A215 R^G46 H CD₃ H H H L_A1455 H CD₃ R^G103 H H H L_A216 R^G47 H CD₃ H H H L_A1456 H CD₃ R^G104 H H H L_A217 R^G48 H CD₃ H H H L_A1457 H CD₃ R^G105 H H H L_A218 R^G49 H CD₃ H H H L_A1458 H CD₃ R^G106 H H H L_A219 R^G50 H CD₃ H H H L_A1459 H CD₃ R^G107 H H H L_A220 R^G51 H CD₃ H H H L_A1460 H CD₃ R^G108 H H H L_A221 R^G52 H CD₃ H H H L_A1461 H CD₃ R^G109 H H H L_A222 R^G53 H CD₃ H H H L_A1462 H CD₃ R^G110 H H H L_A223 R^G54 H CD₃ H H H L_A1463 H CD₃ R^G111 H H H L_A224 R^G55 H CD₃ H H H L_A1464 H CD₃ R^G112 H H H L_A225 R^G56 H CD₃ H H H L_A1465 H CD₃ R^G113 H H H L_A226 R^G57 H CD₃ H H H L_A1466 H CD₃ R^G114 H H H L_A227 R^G58 H CD₃ H H H L_A1467 H CD₃ R^G115 H H H L_A228 R^G59 H CD₃ H H H L_A1468 H CD₃ R^G116 H H H L_A229 R^G60 H CD₃ H H H L_A1469 H CD₃ R^G117 H H H L_A230 R^G61 H CD₃ H H H L_A1470 H CD₃ R^G118 H H H L_A231 R^G62 H CD₃ H H H L_A1471 H CD₃ R^G119 H H H L_A232 R^G63 H CD₃ H H H L_A1472 H CD₃ R^G120 H H H L_A233 R^G64 H CD₃ H H H L_A1473 H CD₃ R^G121 H H H L_A234 R^G65 H CD₃ H H H L_A1474 H CD₃ R^G122 H H H L_A235 R^G66 H CD₃ H H H L_A1475 H CD₃ R^G123 H H H L_A236 R^G67 H CD₃ H H H L_A1476 H CD₃ R^G124 H H H L_A237 R^G68 H CD₃ H H H L_A1477 H CD₃ R^G125 H H H L_A238 R^G69 H CD₃ H H H L_A1478 H CD₃ R^G126 H H H L_A239 R^G70 H CD₃ H H H L_A1479 H CD₃ R^G127 H H H L_A240 R^G71 H CD₃ H H H L_A1480 H CD₃ R^G128 H H H L_A241 R^G72 H CD₃ H H H L_A1481 H CD₃ R^G129 H H H L_A242 R^G73 H CD₃ H H H L_A1482 H CD₃ R^G130 H H H L_A243 R^G74 H CD₃ H H H L_A1483 H CD₃ R^G131 H H H L_A244 R^G75 H CD₃ H H H L_A1484 H CD₃ R^G132 H H H L_A245 R^G76 H CD₃ H H H L_A1485 H CD₃ R^G133 H H H L_A246 R^G77 H CD₃ H H H L_A1486 H CD₃ R^G134 H H H L_A247 R^G78 H CD₃ H H H L_A1487 H CD₃ R^G135 H H H L_A248 R^G79 H CD₃ H H H L_A1488 H CD₃ R^G136 H H H L_A249 R^G80 H CD₃ H H H L_A1489 H CD₃ R^G137 H H H L_A250 R^G81 H CD₃ H H H L_A1490 H CD₃ R^G138 H H H L_A251 R^G82 H CD₃ H H H L_A1491 H CD₃ R^G139 H H H L_A252 R^G83 H CD₃ H H H L_A1492 H CD₃ R^G140 H H H L_A253 R^G84 H CD₃ H H H L_A1493 H CD₃ R^G141 H H H L_A254 R^G85 H CD₃ H H H L_A1494 H CD₃ R^G142 H H H L_A255 R^G86 H CD₃ H H H L_A1495 H CD₃ R^G143 H H H L_A256 R^G87 H CD₃ H H H L_A1496 H CD₃ R^G144 H H H L_A257 R^G88 H CD₃ H H H L_A1497 H CD₃ R^G145 H H H L_A258 R^G89 H CD₃ H H H L_A1498 H CD₃ R^G146 H H H L_A259 R^G90 H CD₃ H H H L_A1499 H CD₃ R^G147 H H H L_A260 R^G91 H CD₃ H H H L_A1500 H CD₃ R^G148 H H H L_A261 R^G92 H CD₃ H H H L_A1501 H CD₃ R^G149 H H H L_A262 R^G93 H CD₃ H H H L_A1502 H CD₃ R^G150 H H H L_A263 R^G94 H CD₃ H H H L_A1503 H CD₃ R^G151 H H H L_A264 R^G95 H CD₃ H H H L_A1504 H CD₃ R^G152 H H H L_A265 R^G96 H CD₃ H H H L_A1505 H CD₃ R^G153 H H H L_A266 R^G97 H CD₃ H H H L_A1506 H CD₃ R^G154 H H H L_A267 R^G98 H CD₃ H H H L_A1507 H CD₃ R^G155 H H H L_A268 R^G99 H CD₃ H H H L_A1508 H CD₃ R^G156 H H H L_A269 R^G100 H CD₃ H H H L_A1509 H CD₃ R^G157 H H H L_A270 R^G101 H CD₃ H H H L_A1510 H CD₃ R^G158 H H H L_A271 R^G102 H CD₃ H H H L_A1511 H CD₃ R^G159 H H H L_A272 R^G103 H CD₃ H H H L_A1512 H CD₃ R^G160 H H H L_A273 R^G104 H CD₃ H H H L_A1513 H CD₃ R^G161 H H H L_A274 R^G105 H CD₃ H H H L_A1514 H CD₃ R^G162 H H H L_A275 R^G106 H CD₃ H H H L_A1515 H CD₃ R^G163 H H H L_A276 R^G107 H CD₃ H H H L_A1516 H CD₃ R^G164 H H H L_A277 R^G108 H CD₃ H H H L_A1517 H CD₃ R^G165 H H H L_A278 R^G109 H CD₃ H H H L_A1518 H CD₃ R^G166 H H H L_A279 R^G110 H CD₃ H H H L_A1519 H CD₃ R^G167 H H H L_A280 R^G111 H CD₃ H H H L_A1520 H CD₃ R^G168 H H H L_A281 R^G112 H CD₃ H H H L_A1521 H CD₃ R^G169 H H H L_A282 R^{G11 3} H CD₃ H H H L_A1522 R^G1 CD₃ CD₃ H H H L_A283 R^G114 H CD₃ H H H L_A1523 R^G2 CD₃ CD₃ H H H L_A284 R^G115 H CD₃ H H H L_A1524 R^G3 CD₃ CD₃ H H H L_A285 R^G116 H CD₃ H H H L_A1525 R^G4 CD₃ CD₃ H H H L_A286 R^G117 H CD₃ H H H L_A1526 R^G5 CD₃ CD₃ H H H L_A287 R^G118 H CD₃ H H H L_A1527 R^G6 CD₃ CD₃ H H H L_A288 R^G119 H CD₃ H H H L_A1528 R^G7 CD₃ CD₃ H H H L_A289 R^G120 H CD₃ H H H L_A1529 R^G8 CD₃ CD₃ H H H L_A290 R^G121 H CD₃ H H H L_A1530 R^G9 CD₃ CD₃ H H H L_A291 R^G122 H CD₃ H H H L_A1531 R^G10 CD₃ CD₃ H H H L_A292 R^G123 H CD₃ H H H L_A1532 R^G11 CD₃ CD₃ H H H L_A293 R^G124 H CD₃ H H H L_A1533 R^G12 CD₃ CD₃ H H H L_A294 R^G125 H CD₃ H H H L_A1534 R^G13 CD₃ CD₃ H H H L_A295 R^G126 H CD₃ H H H L_A1535 R^G14 CD₃ CD₃ H H H L_A296 R^G127 H CD₃ H H H L_A1536 R^G15 CD₃ CD₃ H H H L_A297 R^G128 H CD₃ H H H L_A1537 R^G16 CD₃ CD₃ H H H L_A298 R^G129 H CD₃ H H H L_A1538 R^G17 CD₃ CD₃ H H H L_A299 R^G130 H CD₃ H H H L_A1539 R^G18 CD₃ CD₃ H H H L_A300 R^G131 H CD₃ H H H L_A1540 R^G19 CD₃ CD₃ H H H L_A301 R^G132 H CD₃ H H H L_A1541 CD₃ R^G1 H H H H L_A302 R^G133 H CD₃ H H H L_A1542 CD₃ R^G2 H H H H L_A303 R^G134 H CD₃ H H H L_A1543 CD₃ R^G3 H H H H L_A304 R^G135 H CD₃ H H H L_A1544 CD₃ R^G4 H H H H L_A305 R^G136 H CD₃ H H H L_A1545 CD₃ R^G5 H H H H L_A306 R^G137 H CD₃ H H H L_A1546 CD₃ R^G6 H H H H L_A307 R^G138 H CD₃ H H H L_A1547 CD₃ R^G7 H H H H L_A308 R^G139 H CD₃ H H H L_A1548 CD₃ R^G8 H H H H L_A309 R^G140 H CD₃ H H H L_A1549 CD₃ R^G9 H H H H L_A310 R^G141 H CD₃ H H H L_A1550 CD₃ R^G10 H H H H L_A311 R^G142 H CD₃ H H H L_A1551 CD₃ R^G11 H H H H L_A312 R^G143 H CD₃ H H H L_A1552 CD₃ R^G12 H H H H L_A313 R^G144 H CD₃ H H H L_A1553 CD₃ R^G13 H H H H L_A314 R^G145 H CD₃ H H H L_A1554 CD₃ R^G14 H H H H L_A315 R^G146 H CD₃ H H H L_A1555 CD₃ R^G15 H H H H L_A316 R^G147 H CD₃ H H H L_A1556 CD₃ R^G16 H H H H L_A317 R^G148 H CD₃ H H H L_A1557 CD₃ R^G17 H H H H L_A318 R^G149 H CD₃ H H H L_A1558 CD₃ R^G18 H H H H L_A319 R^G150 H CD₃ H H H L_A1559 CD₃ R^G19 H H H H L_A320 R^G151 H CD₃ H H H L_A1560 CD₃ CD₃ R^G1 H H CD₃ L_A321 R^G152 H CD₃ H H H L_A1561 CD₃ CD₃ R^G2 H H CD₃ L_A322 R^G153 H CD₃ H H H L_A1562 CD₃ CD₃ R^G3 H H CD₃ L_A323 R^G154 H CD₃ H H H L_A1563 CD₃ CD₃ R^G4 H H CD₃ L_A324 R^G155 H CD₃ H H H L_A1564 CD₃ CD₃ R^G5 H H CD₃ L_A325 R^G156 H CD₃ H H H L_A1565 CD₃ CD₃ R^G6 H H CD₃ L_A326 R^{G15 7} H CD₃ H H H L_A1566 CD₃ CD₃ R^G7 H H CD₃ L_A327 R^G158 H CD₃ H H H L_A1567 CD₃ CD₃ R^G8 H H CD₃ L_A328 R^G159 H CD₃ H H H L_A1568 CD₃ CD₃ R^G9 H H CD₃ L_A329 R^G160 H CD₃ H H H L_A1569 CD₃ CD₃ R^G10 H H CD₃ L_A330 R^G161 H CD₃ H H H L_A1570 CD₃ CD₃ R^G11 H H CD₃ L_A331 R^G162 H CD₃ H H H L_A1571 CD₃ CD₃ R^G12 H H CD₃ L_A332 R^G163 H CD₃ H H H L_A1572 CD₃ CD₃ R^G13 H H CD₃ L_A333 R^G164 H CD₃ H H H L_A1573 CD₃ CD₃ R^G14 H H CD₃ L_A334 R^G165 H CD₃ H H H L_A1574 CD₃ CD₃ R^G15 H H CD₃ L_A335 R^G166 H CD₃ H H H L_A1575 CD₃ CD₃ R^G16 H H CD₃ L_A336 R^G167 H CD₃ H H H L_A1576 CD₃ CD₃ R^G17 H H CD₃ L_A337 R^G168 H CD₃ H H H L_A1577 CD₃ CD₃ R^G18 H H CD₃ L_A338 R^G69 H CD₃ H H H L_A1578 CD₃ CD₃ R^G19 H H CD₃ L_A339 R^G1 CD₃ CD₃ H H CD₃ L_A1579 CD₃ H R^G1 H H CD₃ L_A340 R^G2 CD₃ CD₃ H H CD₃ L_A1580 CD₃ H R^G2 H H CD₃ L_A341 R^G3 CD₃ CD₃ H H CD₃ L_A1581 CD₃ H R^G3 H H CD₃ L_A342 R^G4 CD₃ CD₃ H H CD₃ L_A1582 CD₃ H R^G4 H H CD₃ L_A343 R^G5 CD₃ CD₃ H H CD₃ L_A1583 CD₃ H R^G5 H H CD₃ L_A344 R^G6 CD₃ CD₃ H H CD₃ L_A1584 CD₃ H R^G6 H H CD₃ L_A345 R^G7 CD₃ CD₃ H H CD₃ L_A1585 CD₃ H R^G7 H H CD₃ L_A346 R^G8 CD₃ CD₃ H H CD₃ L_A1586 CD₃ H R^G8 H H CD₃ L_A347 R^G9 CD₃ CD₃ H H CD₃ L_A1587 CD₃ H R^G9 H H CD₃ L_A348 R^G10 CD₃ CD₃ H H CD₃ L_A1588 CD₃ H R^G10 H H CD₃ L_A349 R^G11 CD₃ CD₃ H H CD₃ L_A1589 CD₃ H R^G11 H H CD₃ L_A350 R^G12 CD₃ CD₃ H H CD₃ L_A1590 CD₃ H R^G12 H H CD₃ L_A351 R^G13 CD₃ CD₃ H H CD₃ L_A1591 CD₃ H R^G13 H H CD₃ L_A352 R^G14 CD₃ CD₃ H H CD₃ L_A1592 CD₃ H R^G14 H H CD₃ L_A353 R^G15 CD₃ CD₃ H H CD₃ L_A1593 CD₃ H R^G15 H H CD₃ L_A354 R^G16 CD₃ CD₃ H H CD₃ L_A1594 CD₃ H R^G16 H H CD₃ L_A355 R^G17 CD₃ CD₃ H H CD₃ L_A1595 CD₃ H R^G17 H H CD₃ L_A356 R^G18 CD₃ CD₃ H H CD₃ L_A1596 CD₃ H R^G18 H H CD₃ L_A357 R^G19 CD₃ CD₃ H H CD₃ L_A1597 CD₃ H R^G19 H H CD₃ L_A358 R^G20 CD₃ CD₃ H H CD₃ L_A1598 R^G1 CD₃ H H H H L_A359 R^G21 CD₃ CD₃ H H CD₃ L_A1599 R^G2 CD₃ H H H H L_A360 R^G22 CD₃ CD₃ H H CD₃ L_A1600 R^G3 CD₃ H H H H L_A361 R^G23 CD₃ CD₃ H H CD₃ L_A1601 R^G4 CD₃ H H H H L_A362 R^G24 CD₃ CD₃ H H CD₃ L_A1602 R^G5 CD₃ H H H H L_A363 R^G25 CD₃ CD₃ H H CD₃ L_A1603 R^G6 CD₃ H H H H L_A364 R^G26 CD₃ CD₃ H H CD₃ L_A1604 R^G7 CD₃ H H H H L_A365 R^G27 CD₃ CD₃ H H CD₃ L_A1605 R^G8 CD₃ H H H H L_A366 R^G28 CD₃ CD₃ H H CD₃ L_A1606 R^G9 CD₃ H H H H L_A367 R^G29 CD₃ CD₃ H H CD₃ L_A1607 R^G10 CD₃ H H H H L_A368 R^G30 CD₃ CD₃ H H CD₃ L_A1608 R^G11 CD₃ H H H H L_A369 R^G31 CD₃ CD₃ H H CD₃ L_A1609 R^G12 CD₃ H H H H L_A370 R^G32 CD₃ CD₃ H H CD₃ L_A1610 R^G13 CD₃ H H H H L_A371 R^G33 CD₃ CD₃ H H CD₃ L_A1611 R^G14 CD₃ H H H H L_A372 R^G34 CD₃ CD₃ H H CD₃ L_A1612 R^G15 CD₃ H H H H L_A373 R^G35 CD₃ CD₃ H H CD₃ L_A1613 R^G16 CD₃ H H H H L_A374 R^G36 CD₃ CD₃ H H CD₃ L_A1614 R^G17 CD₃ H H H H L_A375 R^G37 CD₃ CD₃ H H CD₃ L_A1615 R^G18 CD₃ H H H H L_A376 R^G38 CD₃ CD₃ H H CD₃ L_A1616 R^G19 CD₃ H H H H L_A377 R^G39 CD₃ CD₃ H H CD₃ L_A1617 H CD₃ R^G1 H H CD₃ L_A378 R^G40 CD₃ CD₃ H H CD₃ L_A1618 H CD₃ R^G2 H H CD₃ L_A379 R^G41 CD₃ CD₃ H H CD₃ L_A1619 H CD₃ R^G3 H H CD₃ L_A380 R^G42 CD₃ CD₃ H H CD₃ L_A1620 H CD₃ R^G4 H H CD₃ L_A381 R^G43 CD₃ CD₃ H H CD₃ L_A1621 H CD₃ R^G5 H H CD₃ L_A382 R^G44 CD₃ CD₃ H H CD₃ L_A1622 H CD₃ R^G6 H H CD₃ L_A383 R^G45 CD₃ CD₃ H H CD₃ L_A1623 H CD₃ R^G7 H H CD₃ L_A384 R^G46 CD₃ CD₃ H H CD₃ L_A1624 H CD₃ R^G8 H H CD₃ L_A385 R^G47 CD₃ CD₃ H H CD₃ L_A1625 H CD₃ R^G9 H H CD₃ L_A386 R^G48 CD₃ CD₃ H H CD₃ L_A1626 H CD₃ R^G10 H H CD₃ L_A387 R^G49 CD₃ CD₃ H H CD₃ L_A1627 H CD₃ R^G11 H H CD₃ L_A388 R^G50 CD₃ CD₃ H H CD₃ L_A1628 H CD₃ R^G12 H H CD₃ L_A389 R^G51 CD₃ CD₃ H H CD₃ L_A1629 H CD₃ R^G13 H H CD₃ L_A390 R^G52 CD₃ CD₃ H H CD₃ L_A1630 H CD₃ R^G14 H H CD₃ L_A391 R^G53 CD₃ CD₃ H H CD₃ L_A1631 H CD₃ R^G15 H H CD₃ L_A392 R^G54 CD₃ CD₃ H H CD₃ L_A1632 H CD₃ R^G16 H H CD₃ L_A393 R^G55 CD₃ CD₃ H H CD₃ L_A1633 H CD₃ R^G17 H H CD₃ L_A394 R^G56 CD₃ CD₃ H H CD₃ L_A1634 H CD₃ R^G18 H H CD₃ L_A395 R^G57 CD₃ CD₃ H H CD₃ L_A1635 H CD₃ R^G19 H H CD₃ L_A396 R^G58 CD₃ CD₃ H H CD₃ L_A1636 H R^G1 H H H H L_A397 R^G59 CD₃ CD₃ H H CD₃ L_A1637 H R^G2 H H H H L_A398 R^G60 CD₃ CD₃ H H CD₃ L_A1638 H R^G3 H H H H L_A399 R^G61 CD₃ CD₃ H H CD₃ L_A1639 H R^G4 H H H H L_A400 R^G62 CD₃ CD₃ H H CD₃ L_A1640 H R^G5 H H H H L_A401 R^G63 CD₃ CD₃ H H CD₃ L_A1641 H R^G6 H H H H L_A402 R^G64 CD₃ CD₃ H H CD₃ L_A1642 H R^G7 H H H H L_A403 R^G65 CD₃ CD₃ H H CD₃ L_A1643 H R^G8 H H H H L_A404 R^G66 CD₃ CD₃ H H CD₃ L_A1644 H R^G9 H H H H L_A405 R^G67 CD₃ CD₃ H H CD₃ L_A1645 H R^G10 H H H H L_A406 R^G68 CD₃ CD₃ H H CD₃ L_A1646 H R^G11 H H H H L_A407 R^G69 CD₃ CD₃ H H CD₃ L_A1647 H R^G12 H H H H L_A408 R^G70 CD₃ CD₃ H H CD₃ L_A1648 H R^G13 H H H H L_A409 R^G71 CD₃ CD₃ H H CD₃ L_A1649 H R^G14 H H H H L_A410 R^G72 CD₃ CD₃ H H CD₃ L_A1650 H R^G15 H H H H L_A41 R^G73 CD₃ CD₃ H H CD₃ L_A1651 H R^G16 H H H H L_A412 R^G74 CD₃ CD₃ H H CD₃ L_A1652 H R^G17 H H H H L_A413 R^G75 CD₃ CD₃ H H CD₃ L_A1653 H R^G18 H H H H L_A414 R^G76 CD₃ CD₃ H H CD₃ L_A1654 H R^G19 H H H H L_A415 R^G77 CD₃ CD₃ H H CD₃ L_A1655 H R^G20 H H H H L_A416 R^G78 CD₃ CD₃ H H CD₃ L_A1656 H R^G21 H H H H L_A417 R^G79 CD₃ CD₃ H H CD₃ L_A1657 H R^G22 H H H H L_A418 R^G80 CD₃ CD₃ H H CD₃ L_A1658 H R^G23 H H H H L_A419 R^G81 CD₃ CD₃ H H CD₃ L_A1659 H R^G24 H H H H L_A420 R^G82 CD₃ CD₃ H H CD₃ L_A1660 H R^G25 H H H H L_A421 R^G83 CD₃ CD₃ H H CD₃ L_A1661 H R^G26 H H H H L_A422 R^G84 CD₃ CD₃ H H CD₃ L_A1662 H R^G27 H H H H L_A423 R^G85 CD₃ CD₃ H H CD₃ L_A1663 H R^G28 H H H H L_A424 R^G86 CD₃ CD₃ H H CD₃ L_A1664 H R^G29 H H H H L_A425 R^GB7 CD₃ CD₃ H H CD₃ L_A1665 H R^G30 H H H H L_A426 R^G88 CD₃ CD₃ H H CD₃ L_A1666 H R^G31 H H H H L_A427 R^G89 CD₃ CD₃ H H CD₃ L_A1667 H R^G32 H H H H L_A428 R^G90 CD₃ CD₃ H H CD₃ L_A1668 H R^G33 H H H H L_A429 R^G91 CD₃ CD₃ H H CD₃ L_A1669 H R^G34 H H H H L_A430 R^G92 CD₃ CD₃ H H CD₃ L_A1670 H R^G35 H H H H L_A431 R^G93 CD₃ CD₃ H H CD₃ L_A1671 H R^G36 H H H H L_A432 R^G94 CD₃ CD₃ H H CD₃ L_A1672 H R^G37 H H H H L_A433 R^G95 CD₃ CD₃ H H CD₃ L_A1673 H R^G38 H H H H L_A434 R^G96 CD₃ CD₃ H H CD₃ L_A1674 H R^G39 H H H H L_A435 R^G97 CD₃ CD₃ H H CD₃ L_A1675 H R^G40 H H H H L_A436 R^G98 CD₃ CD₃ H H CD₃ L_A1676 H R^G41 H H H H L_A437 R^G99 CD₃ CD₃ H H CD₃ L_A1677 H R^G42 H H H H L_A438 R^G100 CD₃ CD₃ H H CD₃ L_A1678 H R^G43 H H H H L_A439 R^G101 CD₃ CD₃ H H CD₃ L_A1679 H R^G44 H H H H L_A440 R^G102 CD₃ CD₃ H H CD₃ L_A1680 H R^G45 H H H H L_A441 R^G103 CD₃ CD₃ H H CD₃ L_A1681 H R^G46 H H H H L_A442 R^G104 CD₃ CD₃ H H CD₃ L_A1682 H R^G47 H H H H L_A443 R^G105 CD₃ CD₃ H H CD₃ L_A1683 H R^G48 H H H H L_A444 R^G106 CD₃ CD₃ H H CD₃ L_A1684 H R^G49 H H H H L_A445 R^G107 CD₃ CD₃ H H CD₃ L_A1685 H R^G50 H H H H L_A446 R^G108 CD₃ CD₃ H H CD₃ L_A1686 H R^G51 H H H H L_A447 R^G109 CD₃ CD₃ H H CD₃ L_A1687 H R^G52 H H H H L_A448 R^G110 CD₃ CD₃ H H CD₃ L_A1688 H R^G53 H H H H L_A449 R^G111 CD₃ CD₃ H H CD₃ L_A1689 H R^G54 H H H H L_A450 R^G112 CD₃ CD₃ H H CD₃ L_A1690 H R^G55 H H H H L_A451 R^G113 CD₃ CD₃ H H CD₃ L_A1691 H R^G56 H H H H L_A452 R^G114 CD₃ CD₃ H H CD₃ L_A1692 H R^G57 H H H H L_A453 R^G115 CD₃ CD₃ H H CD₃ L_A1693 H R^G58 H H H H L_A454 R^G116 CD₃ CD₃ H H CD₃ L_A1694 H R^G59 H H H H L_A455 R^G117 CD₃ CD₃ H H CD₃ L_A1695 H R^G60 H H H H L_A456 R^G118 CD₃ CD₃ H H CD₃ L_A1696 H R^G61 H H H H L_A457 R^G119 CD₃ CD₃ H H CD₃ L_A1697 H R^G62 H H H H L_A458 R^G120 CD₃ CD₃ H H CD₃ L_A1698 H R^G63 H H H H L_A459 R^G121 CD₃ CD₃ H H CD₃ L_A1699 H R^G64 H H H H L_A460 R^G122 CD₃ CD₃ H H CD₃ L_A1700 H R^G65 H H H H L_A461 R^G123 CD₃ CD₃ H H CD₃ L_A1701 H R^G66 H H H H L_A462 R^G124 CD₃ CD₃ H H CD₃ L_A1702 H R^G67 H H H H L_A463 R^G125 CD₃ CD₃ H H CD₃ L_A1703 H R^G68 H H H H L_A464 R^G126 CD₃ CD₃ H H CD₃ L_A1704 H R^G69 H H H H L_A465 R^G127 CD₃ CD₃ H H CD₃ L_A1705 H R^G70 H H H H L_A466 R^G128 CD₃ CD₃ H H CD₃ L_A1706 H R^G71 H H H H L_A467 R^G129 CD₃ CD₃ H H CD₃ L_A1707 H R^G72 H H H H L_A468 R^G130 CD₃ CD₃ H H CD₃ L_A1708 H R^G73 H H H H L_A469 R^G131 CD₃ CD₃ H H CD₃ L_A1709 H R^G74 H H H H L_A470 R^G132 CD₃ CD₃ H H CD₃ L_A1710 H R^G75 H H H H L_A471 R^G133 CD₃ CD₃ H H CD₃ L_A1711 H R^G76 H H H H L_A472 R^G134 CD₃ CD₃ H H CD₃ L_A1712 H R^G77 H H H H L_A473 R^G135 CD₃ CD₃ H H CD₃ L_A1713 H R^G78 H H H H L_A474 R^G136 CD₃ CD₃ H H CD₃ L_A1714 H R^G79 H H H H L_A475 R^G137 CD₃ CD₃ H H CD₃ L_A1715 H R^G80 H H H H L_A476 R^G138 CD₃ CD₃ H H CD₃ L_A1716 H R^G81 H H H H L_A477 R^G139 CD₃ CD₃ H H CD₃ L_A1717 H R^G82 H H H H L_A478 R^G140 CD₃ CD₃ H H CD₃ L_A1718 H R^G83 H H H H L_A479 R^G141 CD₃ CD₃ H H CD₃ L_A1719 H R^G84 H H H H L_A480 R^G142 CD₃ CD₃ H H CD₃ L_A1720 H R^G85 H H H H L_A481 R^G143 CD₃ CD₃ H H CD₃ L_A1721 H R^css H H H H L_A482 R^G144 CD₃ CD₃ H H CD₃ L_A1722 H R^GB7 H H H H L_A483 R^G145 CD₃ CD₃ H H CD₃ L_A1723 H R^G88 H H H H L_A484 R^G146 CD₃ CD₃ H H CD₃ L_A1724 H R^G89 H H H H L_A485 R^G147 CD₃ CD₃ H H CD₃ L_A1725 H R^G90 H H H H L_A486 R^G148 CD₃ CD₃ H H CD₃ L_A1726 H R^G91 H H H H L_A487 R^G149 CD₃ CD₃ H H CD₃ L_A1727 H R^G92 H H H H L_A488 R^G150 CD₃ CD₃ H H CD₃ L_A1728 H R^G93 H H H H L_A489 R^G151 CD₃ CD₃ H H CD₃ L_A1729 H R^G94 H H H H L_A490 R^G152 CD₃ CD₃ H H CD₃ L_A1730 H R^G95 H H H H L_A491 R^G153 CD₃ CD₃ H H CD₃ L_A1731 H R^G96 H H H H L_A492 R^G154 CD₃ CD₃ H H CD₃ L_A1732 H R^G97 H H H H L_A493 R^G155 CD₃ CD₃ H H CD₃ L_A1733 H R^G98 H H H H L_A494 R^G156 CD₃ CD₃ H H CD₃ L_A1734 H R^G99 H H H H L_A495 R^G157 CD₃ CD₃ H H CD₃ L_A1735 H R^G100 H H H H L_A496 R^G158 CD₃ CD₃ H H CD₃ L_A1736 H R^G101 H H H H L_A497 R^G159 CD₃ CD₃ H H CD₃ L_A1737 H R^G102 H H H H L_A498 R^G160 CD₃ CD₃ H H CD₃ L_A1738 H R^G103 H H H H Ligand R_A1 R_A2 R_A3 R_A4 R_A5 R_A6 Ligand R_A1 R_A2 R_A3 R_A4 R_A5 R_A6 L_A499 R^G161 CD₃ CD₃ H H CD₃ L_A1739 H R^G104 H H H H L_A500 R^G162 CD₃ CD₃ H H CD₃ L_A1740 H R^G105 H H H H L_A501 R^G163 CD₃ CD₃ H H CD₃ L_A1741 H R^G106 H H H H L_A502 R^G164 CD₃ CD₃ H H CD₃ L_A1742 H R^G107 H H H H L_A503 R^G165 CD₃ CD₃ H H CD₃ L_A1743 H R^G108 H H H H L_A504 R^G166 CD₃ CD₃ H H CD₃ L_A1744 H R^G109 H H H H L_A505 R^G167 CD₃ CD₃ H H CD₃ L_A1745 H R^G110 H H H H L_A506 R^G168 CD₃ CD₃ H H CD₃ L_A1746 H R^G111 H H H H L_A507 R^G169 CD₃ CD₃ H H CD₃ L_A1747 H R^G112 H H H H L_A508 H R^G1 CD₃ H H H L_A1748 H R^G113 H H H H L_A509 H R^G2 CD₃ H H H L_A1749 H R^G114 H H H H L_A510 H R^G3 CD₃ H H H L_A1750 H R^G115 H H H H L_A511 H R^G4 CD₃ H H H L_A1751 H R^G116 H H H H L_A512 H R^G5 CD₃ H H H L_A1752 H R^G117 H H H H L_A513 H R^G6 CD₃ H H H L_A1753 H R^G118 H H H H L_A514 H R^G7 CD₃ H H H L_A1754 H R^G119 H H H H L_A515 H R^G8 CD₃ H H H L_A1755 H R^G120 H H H H L_A516 H R^G9 CD₃ H H H L_A1756 H R^G121 H H H H L_A517 H R^G10 CD₃ H H H L_A1757 H R^G122 H H H H L_A518 H R^G11 CD₃ H H H L_A1758 H R^G123 H H H H L_A519 H R^G12 CD₃ H H H L_A1759 H R^G124 H H H H L_A520 H R^G13 CD₃ H H H L_A1760 H R^G125 H H H H L_A521 H R^G14 CD₃ H H H L_A1761 H R^G126 H H H H L_A522 H R^G15 CD₃ H H H L_A1762 H R^G127 H H H H L_A523 H R^G16 CD₃ H H H L_A1763 H R^G128 H H H H L_A524 H R^G17 CD₃ H H H L_A1764 H R^G129 H H H H L_A525 H R^G18 CD₃ H H H L_A1765 H R^G130 H H H H L_A526 H R^G19 CD₃ H H H L_A1766 H R^G131 H H H H L_A527 H R^G20 CD₃ H H H L_A1767 H R^G132 H H H H L_A528 H R^G21 CD₃ H H H L_A1768 H R^G133 H H H H L_A529 H R^G22 CD₃ H H H L_A1769 H R^G134 H H H H L_A530 H R^G23 CD₃ H H H L_A1770 H R^G135 H H H H L_A531 H R^G24 CD₃ H H H L_A1771 H R^G136 H H H H L_A532 H R^G25 CD₃ H H H L_A1772 H R^G137 H H H H L_A533 H R^G26 CD₃ H H H L_A1773 H R^G138 H H H H L_A534 H R^G27 CD₃ H H H L_A1774 H R^G139 H H H H L_A535 H R^G28 CD₃ H H H L_A1775 H R^G140 H H H H L_A536 H R^G29 CD₃ H H H L_A1776 H R^G141 H H H H L_A537 H R^G30 CD₃ H H H L_A1777 H R^G142 H H H H L_A538 H R^G31 CD₃ H H H L_A1778 H R^G143 H H H H L_A539 H R^G32 CD₃ H H H L_A1779 H R^G144 H H H H L_A540 H R^G33 CD₃ H H H L_A1780 H R^G145 H H H H L_A541 H R^G34 CD₃ H H H L_A1781 H R^G146 H H H H L_A542 H R^G35 CD₃ H H H L_A1782 H R^G147 H H H H L_A543 H R^G36 CD₃ H H H L_A1783 H R^G148 H H H H L_A544 H R^G37 CD₃ H H H L_A1784 H R^G149 H H H H L_A545 H R^G38 CD₃ H H H L_A1785 H R^G150 H H H H L_A546 H R^G39 CD₃ H H H L_A1786 H R^G151 H H H H L_A547 H R^G40 CD₃ H H H L_A1787 H R^G152 H H H H L_A548 H R^G41 CD₃ H H H L_A1788 H R^G153 H H H H L_A549 H R^G42 CD₃ H H H L_A1789 H R^G154 H H H H L_ASS0 H R^G43 CD₃ H H H L_A1790 H R^G155 H H H H L_A551 H R^G44 CD₃ H H H L_A1791 H R^G156 H H H H L_A552 H R^G45 CD₃ H H H L_A1792 H R^G157 H H H H L_A553 H R^G46 CD₃ H H H L_A1793 H R^G158 H H H H L_A554 H R^G47 CD₃ H H H L_A1794 H R^G159 H H H H L_A555 H R^G48 CD₃ H H H L_A1795 H R^G160 H H H H L_A556 H R^G49 CD₃ H H H L_A1796 H R^G161 H H H H L_A557 H R^G50 CD₃ H H H L_A1797 H R^G162 H H H H L_A558 H R^G51 CD₃ H H H L_A1798 H R^G163 H H H H L_A559 H R^G52 CD₃ H H H L_A1799 H R^G164 H H H H L_A560 H R^G53 CD₃ H H H L_A1800 H R^G165 H H H H L_A561 H R^G54 CD₃ H H H L_A1801 H R^G166 H H H H L_A562 H R^G55 CD₃ H H H L_A1802 H R^G167 H H H H L_A563 H R^G56 CD₃ H H H L_A1803 H R^G168 H H H H L_A564 H R^G57 CD₃ H H H L_A1804 H R^G169 H H H H L_A565 H R^G58 CD₃ H H H L_A1805 H H R^G1 H H H L_A566 H R^G59 CD₃ H H H L_A1806 H H R^G2 H H H L_A567 H R^G60 CD₃ H H H L_A1807 H H R^G3 H H H L_A568 H R^G61 CD₃ H H H L_A1808 H H R^G4 H H H L_A569 H R^G62 CD₃ H H H L_A1809 H H R^G5 H H H L_A570 H R^G63 CD₃ H H H L_A1810 H H R^G6 H H H L_A571 H R^G64 CD₃ H H H L_A1811 H H R^G7 H H H L_A572 H R^G65 CD₃ H H H L_A1812 H H R^G8 H H H L_A573 H R^G66 CD₃ H H H L_A1813 H H R^G9 H H H L_A574 H R^G67 CD₃ H H H L_A1814 H H R^G10 H H H L_A575 H R^G68 CD₃ H H H L_A1815 H H R^G11 H H H L_A576 H R^G69 CD₃ H H H L_A1816 H H R^G12 H H H L_A577 H R^G70 CD₃ H H H L_A1817 H H R^G13 H H H L_A578 H R^G71 CD₃ H H H L_A1818 H H R^G14 H H H L_A579 H R^G72 CD₃ H H H L_A1819 H H R^G15 H H H L_A580 H R^G73 CD₃ H H H L_A1820 H H R^G16 H H H L_A581 H R^G74 CD₃ H H H L_A1821 H H R^G17 H H H L_A582 H R^G75 CD₃ H H H L_A1822 H H R^G18 H H H L_A583 H R^G76 CD₃ H H H L_A1823 H H R^G19 H H H L_A584 H R^G77 CD₃ H H H L_A1824 H H R^G20 H H H L_A585 H R^G78 CD₃ H H H L_A1825 H H R^G21 H H H L_A586 H R^G79 CD₃ H H H L_A1826 H H R^G22 H H H L_A587 H R^G80 CD₃ H H H L_A1827 H H R^G23 H H H L_A588 H R^G81 CD₃ H H H L_A1828 H H R^G24 H H H L_A589 H R^G82 CD₃ H H H L_A1829 H H R^G25 H H H L_A590 H R^G83 CD₃ H H H L_A1830 H H R^G26 H H H L_A591 H R^G84 CD₃ H H H L_A1831 H H R^G27 H H H L_A592 H R^G85 CD₃ H H H L_A1832 H H R^G28 H H H L_A593 H R^G86 CD₃ H H H L_A1833 H H R^G29 H H H L_A594 H R^G87 CD₃ H H H L_A1834 H H R^G30 H H H L_A595 H R^G88 CD₃ H H H L_A1835 H H R^G31 H H H L_A596 H R^G89 CD₃ H H H L_A1836 H H R^G32 H H H L_A597 H R^G90 CD₃ H H H L_A1837 H H R^G33 H H H L_A598 H R^G91 CD₃ H H H L_A1838 H H R^G34 H H H L_A599 H R^G92 CD₃ H H H L_A1839 H H R^G35 H H H L_A600 H R^G93 CD₃ H H H L_A1840 H H R^G36 H H H L_A601 H R^G94 CD₃ H H H L_A1841 H H R^G37 H H H L_A602 H R^G95 CD₃ H H H L_A1842 H H R^G38 H H H L_A603 H R^G96 CD₃ H H H L_A1843 H H R^G39 H H H L_A604 H R^G97 CD₃ H H H L_A1844 H H R^G40 H H H L_A605 H R^G98 CD₃ H H H L_A1845 H H R^G41 H H H L_A606 H R^G99 CD₃ H H H L_A1846 H H R^G42 H H H L_A607 H R^G100 CD₃ H H H L_A1847 H H R^G43 H H H L_A608 H R^G101 CD₃ H H H L_A1848 H H R^G44 H H H L_A609 H R^G102 CD₃ H H H L_A1849 H H R^G45 H H H L_A610 H R^G103 CD₃ H H H L_A1850 H H R^G46 H H H L_A611 H R^G104 CD₃ H H H L_A1851 H H R^G47 H H H L_A612 H R^G105 CD₃ H H H L_A1852 H H R^G48 H H H L_A613 H R^G106 CD₃ H H H L_A1853 H H R^G49 H H H L_A614 H R^G107 CD₃ H H H L_A1854 H H R^G50 H H H L_A615 H R^G108 CD₃ H H H L_A1855 H H R^G51 H H H L_A616 H R^G109 CD₃ H H H L_A1856 H H R^G52 H H H L_A617 H R^G110 CD₃ H H H L_A1857 H H R^G53 H H H L_A618 H R^G111 CD₃ H H H L_A1858 H H R^G54 H H H L_A619 H R^G112 CD₃ H H H L_A1859 H H R^G55 H H H L_A620 H R^G113 CD₃ H H H L_A1860 H H R^G56 H H H L_A621 H R^G114 CD₃ H H H L_A1861 H H R^G57 H H H L_A622 H R^G115 CD₃ H H H L_A1862 H H R^G58 H H H L_A623 H R^G116 CD₃ H H H L_A1863 H H R^G59 H H H L_A624 H R^G117 CD₃ H H H L_A1864 H H R^G60 H H H L_A625 H R^G118 CD₃ H H H L_A1865 H H R^G61 H H H L_A626 H R^G119 CD₃ H H H L_A1866 H H R^G62 H H H L_A627 H R^G120 CD₃ H H H L_A1867 H H R^G63 H H H L_A628 H R^G121 CD₃ H H H L_A1868 H H R^G64 H H H L_A629 H R^G122 CD₃ H H H L_A1869 H H R^G65 H H H L_A630 H R^G123 CD₃ H H H L_A1870 H H R^G66 H H H L_A631 H R^G124 CD₃ H H H L_A1871 H H R^G67 H H H L_A632 H R^G125 CD₃ H H H L_A1872 H H R^G68 H H H L_A633 H R^G126 CD₃ H H H L_A1873 H H R^G69 H H H L_A634 H R^G127 CD₃ H H H L_A1874 H H R^G70 H H H L_A635 H R^G128 CD₃ H H H L_A1875 H H R^G71 H H H L_A636 H R^G129 CD₃ H H H L_A1876 H H R^G72 H H H L_A637 H R^G130 CD₃ H H H L_A1877 H H R^G73 H H H L_A638 H R^G131 CD₃ H H H L_A1878 H H R^G74 H H H L_A639 H R^G132 CD₃ H H H L_A1879 H H R^G75 H H H L_A640 H R^G133 CD₃ H H H L_A1880 H H R^G76 H H H L_A641 H R^G134 CD₃ H H H L_A1881 H H R^G77 H H H L_A642 H R^G135 CD₃ H H H L_A1882 H H R^G78 H H H L_A643 H R^G136 CD₃ H H H L_A1883 H H R^G79 H H H L_A644 H R^G137 CD₃ H H H L_A1884 H H R^G80 H H H L_A645 H R^G138 CD₃ H H H L_A1885 H H R^G81 H H H L_A646 H R^G139 CD₃ H H H L_A1886 H H R^G82 H H H L_A647 H R^G140 CD₃ H H H L_A1887 H H R^G83 H H H L_A648 H R^G141 CD₃ H H H L_A1888 H H R^G84 H H H L_A649 H R^G142 CD₃ H H H L_A1889 H H R^G85 H H H L_A650 H R^{G1 4 3} CD₃ H H H L_A1890 H H R^G86 H H H L_A651 H R^{G1 4 4} CD₃ H H H L_A1891 H H R^G87 H H H L_A652 H R^{G1 4 5} CD₃ H H H L_A1892 H H R^G88 H H H L_A653 H R^{G1 4 6} CD₃ H H H L_A1893 H H R^G89 H H H L_A654 H R^{G1 4 7} CD₃ H H H L_A1894 H H R^G90 H H H L_A655 H R^{G1 4 8} CD₃ H H H L_A1895 H H R^G91 H H H L_A656 H R^{G1 4 9} CD₃ H H H L_A1896 H H R^G92 H H H L_A657 H R^{G1 5 0} CD₃ H H H L_A1897 H H R^G93 H H H L_A658 H R^{G1 5 1} CD₃ H H H L_A1898 H H R^G94 H H H L_A659 H R^{G1 5 2} CD₃ H H H L_A1899 H H R^G95 H H H L_A660 H R^{G1 5 3} CD₃ H H H L_A1900 H H R^G96 H H H L_A661 H R^{G1 5 4} CD₃ H H H L_A1901 H H R^G97 H H H L_A662 H R^{G1 5 5} CD₃ H H H L_A1902 H H R^G98 H H H L_A663 H R^{G1 5 6} CD₃ H H H L_A1903 H H R^G99 H H H L_A664 H R^{G1 5 7} CD₃ H H H L_A1904 H H R^G100 H H H L_A665 H R^G158 CD₃ H H H L_A1905 H H R^G101 H H H L_A666 H R^G159 CD₃ H H H L_A1906 H H RG102 H H H L_A667 H R^G160 CD₃ H H H L_A1907 H H R^G103 H H H L_A668 H R^G161 CD₃ H H H L_A1908 H H R^G104 H H H L_A669 H R^G162 CD₃ H H H L_A1909 H H R^G105 H H H L_A670 H R^G163 CD₃ H H H L_A1910 H H R^G106 H H H L_A671 H R^G164 CD₃ H H H L_A1911 H H R^G107 H H H L_A672 H R^G165 CD₃ H H H L_A1912 H H R^G108 H H H L_A673 H R^G166 CD₃ H H H L_A1913 H H R^G109 H H H L_A674 H R^G167 CD₃ H H H L_A1914 H H R^G110 H H H L_A675 H R^G168 CD₃ H H H L_A1915 H H R^G111 H H H L_A676 H R^G169 CD₃ H H H L_A1916 H H R^G112 H H H L_A677 CD3 R^G1 CD₃ H H CD₃ L_A1917 H H R^G113 H H H L_A678 CD3 R^G2 CD₃ H H CD₃ L_A1918 H H R^G114 H H H L_A679 CD3 R^G3 CD₃ H H CD₃ L_A1919 H H R^{G1 1 5} H H H L_A680 CD3 R^G4 CD₃ H H CD₃ L_A1920 H H R^G116 H H H L_A681 CD3 R^G5 CD₃ H H CD₃ L_A1921 H H R^G117 H H H L_A682 CD3 R^G6 CD₃ H H CD₃ L_A1922 H H R^G118 H H H L_A683 CD3 R^G7 CD₃ H H CD₃ L_A1923 H H R^G119 H H H L_A684 CD3 R^G8 CD₃ H H CD₃ L_A1924 H H R^G120 H H H L_A685 CD3 R^G9 CD₃ H H CD₃ L_A1925 H H R^G121 H H H L_A686 CD3 R^G10 CD₃ H H CD₃ L_A1926 H H R^G122 H H H L_A687 CD3 R^G11 CD₃ H H CD₃ L_A1927 H H R^G123 H H H L_A688 CD3 R^G12 CD₃ H H CD₃ L_A1928 H H R^G124 H H H L_A689 CD3 R^G13 CD₃ H H CD₃ L_A1929 H H R^G125 H H H L_A690 CD3 R^G14 CD₃ H H CD₃ L_A1930 H H R^G126 H H H L_A691 CD3 R^G15 CD₃ H H CD₃ L_A1931 H H R^G127 H H H L_A692 CD3 R^G16 CD₃ H H CD₃ L_A1932 H H R^G128 H H H L_A693 CD3 R^G17 CD₃ H H CD₃ L_A1933 H H R^{G12 9} H H H L_A694 CD3 R^G18 CD₃ H H CD₃ L_A1934 H H R^{G1 3 0} H H H L_A695 CD3 R^G19 CD₃ H H CD₃ L_A1935 H H R^{G1 3 1} H H H L_A696 CD3 R^G20 CD₃ H H CD₃ L_A1936 H H R^{G1 3 2} H H H L_A697 CD3 R^G21 CD₃ H H CD₃ L_A1937 H H R^{G1 3 3} H H H L_A698 CD3 R^G22 CD₃ H H CD₃ L_A1938 H H R^{G1 3 4} H H H L_A699 CD3 R^G23 CD₃ H H CD₃ L_A1939 H H R^{G1 3 5} H H H L_A700 CD3 R^G24 CD₃ H H CD₃ L_A1940 H H R^{G1 3 6} H H H L_A701 CD3 R^G25 CD₃ H H CD₃ L_A1941 H H R^{G1 3 7} H H H L_A702 CD₃ R^G26 CD₃ H H CD₃ L_A1942 H H R^{G1 3 8} H H H L_A703 CD₃ R^G27 CD₃ H H CD₃ L_A1943 H H R^{G1 3 9} H H H L_A704 CD₃ R^G28 CD₃ H H CD₃ L_A1944 H H R^{G1 4 0} H H H L_A705 CD₃ R^G29 CD₃ H H CD₃ L_A1945 H H R^{G1 4 1} H H H L_A706 CD₃ R^G30 CD₃ H H CD₃ L_A1946 H H R^{G1 4 2} H H H L_A707 CD₃ R^G31 CD₃ H H CD₃ L_A1947 H H R^{G1 4 3} H H H L_A708 CD₃ R^G32 CD₃ H H CD₃ L_A1948 H H R^{G1 4 4} H H H L_A709 CD₃ R^G33 CD₃ H H CD₃ L_A1949 H H R^{G1 4 5} H H H L_A710 CD₃ R^G34 CD₃ H H CD₃ L_A1950 H H R^{G1 4 6} H H H L_A711 CD₃ R^G35 CD₃ H H CD₃ L_A1951 H H R^{G1 4 7} H H H L_A712 CD₃ R^G36 CD₃ H H CD₃ L_A1952 H H R^{G1 4 8} H H H L_A713 CD₃ R^G37 CD₃ H H CD₃ L_A1953 H H R^{G1 4 9} H H H L_A714 CD₃ R^G38 CD₃ H H CD₃ L_A1954 H H R^{G1 5 0} H H H L_A715 CD₃ R^G39 CD₃ H H CD₃ L_A1955 H H R^G151 H H H L_A716 CD₃ R^G40 CD₃ H H CD₃ L_A1956 H H R^G152 H H H L_A717 CD₃ R^G41 CD₃ H H CD₃ L_A1957 H H R^{G151 3} H H H L_A718 CD₃ R^G42 CD₃ H H CD₃ L_A1958 H H R^G154 H H H L_A719 CD₃ R^G43 CD₃ H H CD₃ L_A1959 H H R^G155 H H H L_A720 CD₃ R^G44 CD₃ H H CD₃ L_A1960 H H R^G156 H H H L_A721 CD₃ R^G45 CD₃ H H CD₃ L_A1961 H H R^G157 H H H L_A722 CD₃ R^G46 CD₃ H H CD₃ L_A1962 H H R^G158 H H H L_A723 CD₃ R^G47 CD₃ H H CD₃ L_A1963 H H R^G159 H H H L_A724 CD₃ R^G48 CD₃ H H CD₃ L_A1964 H H R^G160 H H H L_A725 CD₃ R^G49 CD₃ H H CD₃ L_A1965 H H R^G161 H H H L_A726 CD₃ R^G50 CD₃ H H CD₃ L_A1966 H H R^G162 H H H L_A727 CD₃ R^G51 CD₃ H H CD₃ L_A1967 H H R^G163 H H H L_A728 CD₃ R^G52 CD₃ H H CD₃ L_A1968 H H R^G164 H H H L_A729 CD₃ R^G53 CD₃ H H CD₃ L_A1969 H H R^G165 H H H L_A730 CD₃ R^G54 CD₃ H H CD₃ L_A1970 H H R^G166 H H H L_A731 CD₃ R^G55 CD₃ H H CD₃ L_A1971 H H R^G167 H H H L_A732 CD₃ R^G56 CD₃ H H CD₃ L_A1972 H H R^G168 H H H L_A733 CD₃ R^G57 CD₃ H H CD₃ L_A1973 H H R^G169 H H H L_A734 CD₃ R^G58 CD₃ H H CD₃ L_A1974 H H H R^G1 H H L_A735 CD₃ R^G59 CD₃ H H CD₃ L_A1975 H H H R^G2 H H L_A736 CD₃ R^G60 CD₃ H H CD₃ L_A1976 H H H R^G3 H H L_A737 CD₃ R^G61 CD₃ H H CD₃ L_A1977 H H H R^G4 H H L_A738 CD₃ R^G62 CD₃ H H CD₃ L_A1978 H H H R^G5 H H L_A739 CD₃ R^G63 CD₃ H H CD₃ L_A1979 H H H R^G6 H H L_A740 CD₃ R^G64 CD₃ H H CD₃ L_A1980 H H H R^G7 H H L_A741 CD₃ R^G65 CD₃ H H CD₃ L_A1981 H H H R^G8 H H L_A742 CD₃ R^G66 CD₃ H H CD₃ L_A1982 H H H R^G9 H H L_A743 CD₃ R^G67 CD₃ H H CD₃ L_A1983 H H H R^G10 H H L_A744 CD₃ R^G68 CD₃ H H CD₃ L_A1984 H H H R^G11 H H L_A745 CD₃ R^G69 CD₃ H H CD₃ L_A1985 H H H R^G12 H H L_A746 CD₃ R^G70 CD₃ H H CD₃ L_A1986 H H H R^G13 H H L_A747 CD₃ R^G71 CD₃ H H CD₃ L_A1987 H H H R^G14 H H L_A748 CD₃ R^G72 CD₃ H H CD₃ L_A1988 H H H R^G15 H H L_A749 CD₃ R^G73 CD₃ H H CD₃ L_A1989 H H H R^G16 H H L_A750 CD₃ R^G74 CD₃ H H CD₃ L_A1990 H H H R^G17 H H L_A751 CD₃ R^G75 CD₃ H H CD₃ L_A1991 H H H R^G18 H H L_A752 CD₃ R^G76 CD₃ H H CD₃ L_A1992 H H H R^G19 H H L_A753 CD₃ R^G77 CD₃ H H CD₃ L_A1993 H H H R^G20 H H L_A754 CD₃ R^G78 CD₃ H H CD₃ L_A1994 H H H R^G21 H H L_A755 CD₃ R^G79 CD₃ H H CD₃ L_A1995 H H H R^G22 H H L_A756 CD₃ R^G80 CD₃ H H CD₃ L_A1996 H H H R^G23 H H L_A757 CD₃ R^G81 CD₃ H H CD₃ L_A1997 H H H R^G24 H H L_A758 CD₃ R^G82 CD₃ H H CD₃ L_A1998 H H H R^G25 H H L_A759 CD₃ R^G83 CD₃ H H CD₃ L_A1999 H H H R^G26 H H L_A760 CD₃ R^G84 CD₃ H H CD₃ L_A2000 H H H R^G27 H H L_A761 CD₃ R^G85 CD₃ H H CD₃ L_A2001 H H H R^G28 H H L_A762 CD₃ R^G86 CD₃ H H CD₃ L_A2002 H H H R^G29 H H L_A763 CD₃ R^G87 CD₃ H H CD₃ L_A2003 H H H R^G30 H H L_A764 CD₃ R^G88 CD₃ H H CD₃ L_A2004 H H H R^G31 H H L_A765 CD₃ R^G89 CD₃ H H CD₃ L_A2005 H H H R^G32 H H L_A766 CD₃ R^G90 CD₃ H H CD₃ L_A2006 H H H R^G33 H H L_A767 CD₃ R^G91 CD₃ H H CD₃ L_A2007 H H H R^G34 H H L_A768 CD₃ R^G92 CD₃ H H CD₃ L_A2008 H H H R^G35 H H L_A769 CD₃ R^G93 CD₃ H H CD₃ L_A2009 H H H R^G36 H H L_A770 CD₃ R^G94 CD₃ H H CD₃ L_A2010 H H H R^G37 H H L_A771 CD₃ R^G95 CD₃ H H CD₃ L_A2011 H H H R^G38 H H L_A772 CD₃ R^G96 CD₃ H H CD₃ L_A2012 H H H R^G39 H H L_A773 CD₃ R^G97 CD₃ H H CD₃ L_A2013 H H H R^G40 H H L_A774 CD₃ R^G98 CD₃ H H CD₃ L_A2014 H H H R^G41 H H L_A775 CD₃ R^G99 CD₃ H H CD₃ L_A2015 H H H R^G42 H H L_A776 CD₃ R^G100 CD₃ H H CD₃ L_A2016 H H H R^G43 H H L_A777 CD₃ R^G101 CD₃ H H CD₃ L_A2017 H H H R^G44 H H L_A778 CD₃ R^G102 CD₃ H H CD₃ L_A2018 H H H R^G45 H H L_A779 CD₃ R^G103 CD₃ H H CD₃ L_A2019 H H H R^G46 H H L_A780 CD₃ R^G104 CD₃ H H CD₃ L_A2020 H H H R^G47 H H L_A781 CD₃ R^G105 CD₃ H H CD₃ L_A2021 H H H R^G48 H H L_A782 CD₃ R^G106 CD₃ H H CD₃ L_A2022 H H H R^G49 H H L_A783 CD₃ R^G107 CD₃ H H CD₃ L_A2023 H H H R^G50 H H L_A784 CD₃ R^G108 CD₃ H H CD₃ L_A2024 H H H R^G51 H H L_A785 CD₃ R^G109 CD₃ H H CD₃ L_A2025 H H H R^G52 H H L_A786 CD₃ R^G110 CD₃ H H CD₃ L_A2026 H H H R^G53 H H L_A787 CD₃ R^G111 CD₃ H H CD₃ L_A2027 H H H R^G54 H H L_A788 CD₃ R^G112 CD₃ H H CD₃ L_A2028 H H H R^G55 H H L_A789 CD₃ R^G113 CD₃ H H CD₃ L_A2029 H H H R^G56 H H L_A790 CD₃ R^G114 CD₃ H H CD₃ L_A2030 H H H R^G57 H H L_A791 CD₃ R^G115 CD₃ H H CD₃ L_A2031 H H H R^G58 H H L_A792 CD₃ R^G116 CD₃ H H CD₃ L_A2032 H H H R^G59 H H L_A793 CD₃ R^G117 CD₃ H H CD₃ L_A2033 H H H R^G60 H H L_A794 CD₃ R^G118 CD₃ H H CD₃ L_A2034 H H H R^G61 H H L_A795 CD₃ R^G119 CD₃ H H CD₃ L_A2035 H H H R^G62 H H L_A796 CD₃ R^G120 CD₃ H H CD₃ L_A2036 H H H R^G63 H H L_A797 CD₃ R^G121 CD₃ H H CD₃ L_A2037 H H H R^G64 H H L_A798 CD₃ R^G122 CD₃ H H CD₃ L_A2038 H H H R^G65 H H L_A799 CD₃ R^G123 CD₃ H H CD₃ L_A2039 H H H R^G66 H H L_A800 CD₃ R^G124 CD₃ H H CD₃ L_A2040 H H H R^G67 H H L_A801 CD₃ R^G125 CD₃ H H CD₃ L_A2041 H H H R^G68 H H L_A802 CD₃ R^G126 CD₃ H H CD₃ L_A2042 H H H R^G69 H H L_A803 CD₃ R^G127 CD₃ H H CD₃ L_A2043 H H H R^G70 H H L_A804 CD₃ R^G128 CD₃ H H CD₃ L_A2044 H H H R^G71 H H L_A805 CD₃ R^G129 CD₃ H H CD₃ L_A2045 H H H R^G72 H H L_A806 CD₃ R^G130 CD₃ H H CD₃ L_A2046 H H H R^G73 H H L_A807 CD₃ R^G131 CD₃ H H CD₃ L_A2047 H H H R^G74 H H L_A808 CD₃ R^G132 CD₃ H H CD₃ L_A2048 H H H R^G75 H H L_A809 CD₃ R^G133 CD₃ H H CD₃ L_A2049 H H H R^G76 H H L_A810 CD₃ R^G134 CD₃ H H CD₃ L_A2050 H H H R^G77 H H L_A811 CD₃ R^G135 CD₃ H H CD₃ L_A2051 H H H R^G78 H H L_A812 CD₃ R^G136 CD₃ H H CD₃ L_A2052 H H H R^G79 H H L_A813 CD₃ R^G137 CD₃ H H CD₃ L_A2053 H H H R^G80 H H L_A814 CD₃ R^G138 CD₃ H H CD₃ L_A2054 H H H R^G81 H H L_A815 CD₃ R^G139 CD₃ H H CD₃ L_A2055 H H H R^G82 H H L_A816 CD₃ R^G140 CD₃ H H CD₃ L_A2056 H H H R^G83 H H L_A817 CD₃ R^G141 CD₃ H H CD₃ L_A2057 H H H R^G84 H H L_A818 CD₃ R^G142 CD₃ H H CD₃ L_A2058 H H H R^G85 H H L_A819 CD₃ R^G143 CD₃ H H CD₃ L_A2059 H H H R^G86 H H L_A820 CD₃ R^G144 CD₃ H H CD₃ L_A2060 H H H R^G87 H H L_A821 CD₃ R^G145 CD₃ H H CD₃ L_A2061 H H H R^G88 H H L_A822 CD₃ R^G146 CD₃ H H CD₃ L_A2062 H H H R^G89 H H L_A823 CD₃ R^G147 CD₃ H H CD₃ L_A2063 H H H R^G90 H H L_A824 CD₃ R^G148 CD₃ H H CD₃ L_A2064 H H H R^G91 H H L_A825 CD₃ R^G149 CD₃ H H CD₃ L_A2065 H H H R^G92 H H L_A826 CD₃ R^G150 CD₃ H H CD₃ L_A2066 H H H R^G93 H H L_A827 CD₃ R^G151 CD₃ H H CD₃ L_A2067 H H H R^G94 H H L_A828 CD₃ R^G152 CD₃ H H CD₃ L_A2068 H H H R^G95 H H L_A829 CD₃ R^G153 CD₃ H H CD₃ L_A2069 H H H R^G96 H H L_A830 CD₃ R^G154 CD₃ H H CD₃ L_A2070 H H H R^G97 H H L_A831 CD₃ R^G155 CD₃ H H CD₃ L_A2071 H H H R^G98 H H L_A832 CD₃ R^G156 CD₃ H H CD₃ L_A2072 H H H R^G99 H H L_A833 CD₃ R^G157 CD₃ H H CD₃ L_A2073 H H H R^G100 H H L_A834 CD₃ R^G158 CD₃ H H CD₃ L_A2074 H H H R^G101 H H L_A835 CD₃ R^G159 CD₃ H H CD₃ L_A2075 H H H R^G102 H H L_A836 CD₃ R^G160 CD₃ H H CD₃ L_A2076 H H H R^G103 H H L_A837 CD₃ R^G161 CD₃ H H CD₃ L_A2077 H H H R^G104 H H L_A838 CD₃ R^G162 CD₃ H H CD₃ L_A2078 H H H R^G105 H H L_A839 CD₃ R^G163 CD₃ H H CD₃ L_A2079 H H H R^G106 H H L_A840 CD₃ R^G164 CD₃ H H CD₃ L_A2080 H H H R^G107 H H L_A841 CD₃ R^G165 CD₃ H H CD₃ L_A2081 H H H R^G108 H H L_A842 CD₃ R^G166 CD₃ H H CD₃ L_A2082 H H H R^{G10 9} H H L_A843 CD₃ R^G167 CD₃ H H CD₃ L_A2083 H H H R^G110 H H L_A844 CD₃ R^G168 CD₃ H H CD₃ L_A2084 H H H R^G111 H H L_A845 CD₃ R^G169 CD₃ H H CD₃ L_A2085 H H H R^G112 H H L_A846 CD₃ R^G1 CD₃ H H H L_A2086 H H H R^G113 H H L_A847 CD₃ R^G2 CD₃ H H H L_A2087 H H H R^G114 H H L_A848 CD₃ R^G3 CD₃ H H H L_A2088 H H H R^{G11 5} H H L_A849 CD₃ R^G4 CD₃ H H H L_A2089 H H H R^G116 H H L_A850 CD₃ R^G5 CD₃ H H H L_A2090 H H H R^G117 H H L_A851 CD₃ R^G6 CD₃ H H H L_A2091 H H H R^G118 H H L_A852 CD₃ R^G7 CD₃ H H H L_A2092 H H H R^G119 H H L_A853 CD₃ R^G8 CD₃ H H H L_A2093 H H H R^G120 H H L_A854 CD₃ R^G9 CD₃ H H H L_A2094 H H H R^{G12 1} H H L_A855 CD₃ R^G10 CD₃ H H H L_A2095 H H H R^G122 H H L_A856 CD₃ R^G11 CD₃ H H H L_A2096 H H H R^G123 H H L_A857 CD₃ R^G12 CD₃ H H H L_A2097 H H H R^G124 H H L_A858 CD₃ R^G13 CD₃ H H H L_A2098 H H H R^G125 H H L_A859 CD₃ R^G14 CD₃ H H H L_A2099 H H H R^G126 H H L_A860 CD₃ R^G15 CD₃ H H H L_A2100 H H H R^G127 H H L_A861 CD₃ R^G16 CD₃ H H H L_A2101 H H H R^{G12 8} H H L_A862 CD₃ R^G17 CD₃ H H H L_A2102 H H H R^G129 H H L_A863 CD₃ R^G18 CD₃ H H H L_A2103 H H H R^G130 H H L_A864 CD₃ R^G19 CD₃ H H H L_A2104 H H H R^G131 H H L_A865 CD₃ R^G20 CD₃ H H H L_A2105 H H H R^G132 H H L_A866 CD₃ R^G21 CD₃ H H H L_A2106 H H H R^G133 H H L_A867 CD₃ R^G22 CD₃ H H H L_A2107 H H H R^G134 H H L_A868 CD₃ R^G23 CD₃ H H H L_A2108 H H H R^G135 H H L_A869 CD₃ R^G24 CD₃ H H H L_A2109 H H H R^G136 H H L_A870 CD₃ R^G25 CD₃ H H H L_A2110 H H H R^G137 H H L_A871 CD₃ R^G26 CD₃ H H H L_A2111 H H H R^G138 H H L_A872 CD₃ R^G27 CD₃ H H H L_A2112 H H H R^G139 H H L_A873 CD₃ R^G28 CD₃ H H H L_A2113 H H H R^{G1 4 0} H H L_A874 CD₃ R^G29 CD₃ H H H L_A2114 H H H R^{G1 4 1} H H L_A875 CD₃ R^G30 CD₃ H H H L_A2115 H H H R^{G1 4 2} H H L_A876 CD₃ R^G31 CD₃ H H H L_A2116 H H H R^{G1 4 3} H H L_A877 CD₃ R^G32 CD₃ H H H L_A2117 H H H R^{G1 4 4} H H L_A878 CD₃ R^G33 CD₃ H H H L_A2118 H H H R^{G1 4 5} H H L_A879 CD₃ R^G34 CD₃ H H H L_A2119 H H H R^{G1 4 6} H H L_A880 CD₃ R^G35 CD₃ H H H L_A2120 H H H R^{G1 4 7} H H L_A881 CD₃ R^G36 CD₃ H H H L_A2121 H H H R^{G1 4 8} H H L_A882 CD₃ R^G37 CD₃ H H H L_A2122 H H H R^{G1 4 9} H H L_A883 CD₃ R^{G 38} CD₃ H H H L_A2123 H H H R^{G1 5 0} H H L_A884 CD₃ R^G39 CD₃ H H H L_A2124 H H H R^{G1 5 1} H H L_A885 CD₃ R^G40 CD₃ H H H L_A2125 H H H R^{G1 5 2} H H L_A886 CD₃ R^G41 CD₃ H H H L_A2126 H H H R^{G1 5 3} H H L_A887 CD₃ R^G42 CD₃ H H H L_A2127 H H H R^{G1 5 4} H H L_A888 CD₃ R^G43 CD₃ H H H L_A2128 H H H R^{G1 5 5} H H L_A889 CD₃ R^G44 CD₃ H H H L_A2129 H H H R^{G1 5 6} H H L_A890 CD₃ R^G45 CD₃ H H H L_A2130 H H H R^{G1 5 7} H H L_A891 CD₃ R^G46 CD₃ H H H L_A2131 H H H R^{G1 5 8} H H L_A892 CD₃ R^G47 CD₃ H H H L_A2132 H H H R^{G1 5 9} H H L_A893 CD₃ R^G48 CD₃ H H H L_A2133 H H H R^{G1 6 0} H H L_A894 CD₃ R^G49 CD₃ H H H L_A2134 H H H R^{G1 6 1} H H L_A895 CD₃ R^G50 CD₃ H H H L_A2135 H H H R^{G1 6 2} H H L_A896 CD₃ R^G51 CD₃ H H H L_A2136 H H H R^{G1 6 3} H H L_A897 CD₃ R^G52 CD₃ H H H L_A2137 H H H R^{G1 6 4} H H L_A898 CD₃ R^G53 CD₃ H H H L_A2138 H H H R^{G1 6 5} H H L_A899 CD₃ R^G54 CD₃ H H H L_A2139 H H H R^{G1 6 6} H H L_A900 CD₃ R^G55 CD₃ H H H L_A2140 H H H R^{G1 6 7} H H L_A901 CD₃ R^G56 CD₃ H H H L_A2141 H H H R^{G1 6 8} H H L_A902 CD₃ R^G57 CD₃ H H H L_A2142 H H H R^{G1 6 9} H H L_A903 CD₃ R^G58 CD₃ H H H L_A2143 H H H H R^G1 H L_A904 CD₃ R^{G 5 9} CD₃ H H H L_A2144 H H H H R^G2 H L_A905 CD₃ R^G60 CD₃ H H H L_A2145 H H H H R^G3 H L_A906 CD₃ R^G61 CD₃ H H H L_A2146 H H H H R^G4 H L_A907 CD₃ R^G62 CD₃ H H H L_A2147 H H H H R^G5 H L_A908 CD₃ R^G63 CD₃ H H H L_A2148 H H H H R^G6 H L_A909 CD₃ R^G64 CD₃ H H H L_A2149 H H H H R^G7 H L_A910 CD₃ R^G65 CD₃ H H H L_A2150 H H H H R^G8 H L_A911 CD₃ R^G66 CD₃ H H H L_A2151 H H H H R^G9 H L_A912 CD₃ R^G67 CD₃ H H H L_A2152 H H H H R^G10 H L_A913 CD₃ R^G68 CD₃ H H H L_A2153 H H H H R^G11 H L_A914 CD₃ R^G69 CD₃ H H H L_A2154 H H H H R^G12 H L_A915 CD₃ R^G70 CD₃ H H H L_A2155 H H H H R^G13 H L_A916 CD₃ R^G71 CD₃ H H H L_A2156 H H H H R^G14 H L_A917 CD₃ R^G72 CD₃ H H H L_A2157 H H H H R^G15 H L_A918 CD₃ R^G73 CD₃ H H H L_A2158 H H H H R^G16 H L_A919 CD₃ R^G74 CD₃ H H H L_A2159 H H H H R^G17 H L_A920 CD₃ R^G75 CD₃ H H H L_A2160 H H H H R^G18 H L_A921 CD₃ R^G76 CD₃ H H H L_A2161 H H H H R^G19 H L_A922 CD₃ R^G77 CD₃ H H H L_A2162 H H H H R^G20 H L_A923 CD₃ R^G78 CD₃ H H H L_A2163 H H H H R^G21 H L_A924 CD₃ R^G79 CD₃ H H H L_A2164 H H H H R^G22 H L_A925 CD₃ R^G80 CD₃ H H H L_A2165 H H H H R^G23 H L_A926 CD₃ R^G81 CD₃ H H H L_A2166 H H H H R^G24 H L_A927 CD₃ R^G82 CD₃ H H H L_A2167 H H H H R^G25 H L_A928 CD₃ R^G83 CD₃ H H H L_A2168 H H H H R^G26 H L_A929 CD₃ R^G84 CD₃ H H H L_A2169 H H H H R^G27 H L_A930 CD₃ R^G85 CD₃ H H H L_A2170 H H H H R^G28 H L_A931 CD₃ R^G86 CD₃ H H H L_A2171 H H H H R^G29 H L_A932 CD₃ R^G87 CD₃ H H H L_A2172 H H H H R^G30 H L_A933 CD₃ R^G88 CD₃ H H H L_A2173 H H H H R^G31 H L_A934 CD₃ R^G89 CD₃ H H H L_A2174 H H H H R^G32 H L_A935 CD₃ R^G90 CD₃ H H H L_A2175 H H H H R^G33 H L_A936 CD₃ R^G91 CD₃ H H H L_A2176 H H H H R^G34 H L_A937 CD₃ R^G92 CD₃ H H H L_A2177 H H H H R^G35 H L_A938 CD₃ R^G93 CD₃ H H H L_A2178 H H H H R^G36 H L_A939 CD₃ R^G94 CD₃ H H H L_A2179 H H H H R^G37 H L_A940 CD₃ R^G95 CD₃ H H H L_A2180 H H H H R^G38 H L_A941 CD₃ R^G96 CD₃ H H H L_A2181 H H H H R^G39 H L_A942 CD₃ R^G97 CD₃ H H H L_A2182 H H H H R^G40 H L_A943 CD₃ R^G98 CD₃ H H H L_A2183 H H H H R^G41 H L_A944 CD₃ R^G99 CD₃ H H H L_A2184 H H H H R^G42 H L_A945 CD₃ R^G100 CD₃ H H H L_A2185 H H H H R^G43 H L_A946 CD₃ R^G101 CD₃ H H H L_A2186 H H H H R^G44 H L_A947 CD₃ R^G102 CD₃ H H H L_A2187 H H H H R^G45 H L_A948 CD₃ R^G103 CD₃ H H H L_A2188 H H H H R^G46 H L_A949 CD₃ R^G104 CD₃ H H H L_A2189 H H H H R^G47 H L_A950 CD₃ R^G105 CD₃ H H H L_A2190 H H H H R^G48 H L_A951 CD₃ R^G106 CD₃ H H H L_A2191 H H H H R^G49 H L_A952 CD₃ R^G107 CD₃ H H H L_A2192 H H H H R^G50 H L_A953 CD₃ R^G108 CD₃ H H H L_A2193 H H H H R^G51 H L_A954 CD₃ R^G109 CD₃ H H H L_A2194 H H H H R^G52 H L_A955 CD₃ R^G110 CD₃ H H H L_A2195 H H H H R^G53 H L_A956 CD₃ R^G111 CD₃ H H H L_A2196 H H H H R^G54 H L_A957 CD₃ R^G112 CD₃ H H H L_A2197 H H H H R^G55 H L_A958 CD₃ R^G113 CD₃ H H H L_A2198 H H H H R^G56 H L_A959 CD₃ R^G114 CD₃ H H H L_A2199 H H H H R^G57 H L_A960 CD₃ R^G115 CD₃ H H H L_A2200 H H H H R^G58 H L_A961 CD₃ R^G116 CD₃ H H H L_A2201 H H H H R^G59 H L_A962 CD₃ R^G117 CD₃ H H H L_A2202 H H H H R^G60 H L_A963 CD₃ R^G118 CD₃ H H H L_A2203 H H H H R^G61 H L_A964 CD₃ R^G119 CD₃ H H H L_A2204 H H H H R^G62 H L_A965 CD₃ R^G120 CD₃ H H H L_A2205 H H H H R^G63 H L_A966 CD₃ R^G121 CD₃ H H H L_A2206 H H H H R^G64 H L_A967 CD₃ R^G122 CD₃ H H H L_A2207 H H H H R^G65 H L_A968 CD₃ R^G123 CD₃ H H H L_A2208 H H H H R^G66 H L_A969 CD₃ R^G124 CD₃ H H H L_A2209 H H H H R^G67 H L_A970 CD₃ R^G125 CD₃ H H H L_A2210 H H H H R^G68 H L_A971 CD₃ R^G126 CD₃ H H H L_A2211 H H H H R^G69 H L_A972 CD₃ R^G127 CD₃ H H H L_A2212 H H H H R^G70 H L_A973 CD₃ R^G128 CD₃ H H H L_A2213 H H H H R^G71 H L_A974 CD₃ R^G129 CD₃ H H H L_A2214 H H H H R^G72 H L_A975 CD₃ R^G130 CD₃ H H H L_A2215 H H H H R^G73 H L_A976 CD₃ R^G131 CD₃ H H H L_A2216 H H H H R^G74 H L_A977 CD₃ R^G132 CD₃ H H H L_A2217 H H H H R^G75 H L_A978 CD₃ R^G133 CD₃ H H H L_A2218 H H H H R^G76 H L_A979 CD₃ R^G134 CD₃ H H H L_A2219 H H H H R^G77 H L_A980 CD₃ R^G135 CD₃ H H H L_A2220 H H H H R^G78 H L_A981 CD₃ R^G136 CD₃ H H H L_A2221 H H H H R^G79 H L_A982 CD₃ R^G137 CD₃ H H H L_A2222 H H H H R^G80 H L_A983 CD₃ R^G138 CD₃ H H H L_A2223 H H H H R^G81 H L_A984 CD₃ R^G139 CD₃ H H H L_A2224 H H H H R^G82 H L_A985 CD₃ R^G140 CD₃ H H H L_A2225 H H H H R^G83 H L_A986 CD₃ R^G141 CD₃ H H H L_A2226 H H H H R^G84 H L_A987 CD₃ R^G142 CD₃ H H H L_A2227 H H H H R^G85 H L_A988 CD₃ R^G143 CD₃ H H H L_A2228 H H H H R^G86 H L_A989 CD₃ R^G144 CD₃ H H H L_A2229 H H H H R^G87 H L_A990 CD₃ R^G145 CD₃ H H H L_A2230 H H H H R^G88 H L_A991 CD₃ R^G146 CD₃ H H H L_A2231 H H H H R^G89 H L_A992 CD₃ R^G147 CD₃ H H H L_A2232 H H H H R^G90 H L_A993 CD₃ R^G148 CD₃ H H H L_A2233 H H H H R^G91 H L_A994 CD₃ R^G149 CD₃ H H H L_A2234 H H H H R^G92 H L_A995 CD₃ R^G150 CD₃ H H H L_A2235 H H H H R^G93 H L_A996 CD₃ R^G151 CD₃ H H H L_A2236 H H H H R^G94 H L_A997 CD₃ R^G152 CD₃ H H H L_A2237 H H H H R^G95 H L_A998 CD₃ R^G153 CD₃ H H H L_A2238 H H H H R^G96 H L_A999 CD₃ R^G154 CD₃ H H H L_A2239 H H H H R^G97 H L_A1000 CD₃ R^G155 CD₃ H H H L_A2240 H H H H R^G98 H L_A1001 CD₃ R^G156 CD₃ H H H L_A2241 H H H H R^G99 H L_A1002 CD₃ R^G157 CD₃ H H H L_A2242 H H H H R^G100 H L_A1003 CD₃ R^G158 CD₃ H H H L_A2243 H H H H R^G101 H L_A1004 CD₃ R^G159 CD₃ H H H L_A2244 H H H H R^G102 H L_A1005 CD₃ R^G160 CD₃ H H H L_A2245 H H H H R^G103 H L_A1006 CD₃ R^G161 CD₃ H H H L_A2246 H H H H R^G104 H L_A1007 CD₃ R^G162 CD₃ H H H L_A2247 H H H H R^G105 H L_A1008 CD₃ R^G163 CD₃ H H H L_A2248 H H H H R^G106 H L_A1009 CD₃ R^G164 CD₃ H H H L_A2249 H H H H R^G107 H L_A1010 CD₃ R^G165 CD₃ H H H L_A2250 H H H H R^G108 H L_A1011 CD₃ R^G166 CD₃ H H H L_A2251 H H H H R^G109 H L_A1012 CD₃ R^G167 CD₃ H H H L_A2252 H H H H R^G110 H L_A1013 CD₃ R^G168 CD₃ H H H L_A2253 H H H H R^G111 H L_A1014 CD₃ R^G169 CD₃ H H H L_A2254 H H H H R^G112 H L_A1015 CD₃ CD₃ R^G1 H H H L_A2255 H H H H R^G113 H L_A1016 CD₃ CD₃ R^G2 H H H L_A2256 H H H H R^G114 H L_A1017 CD₃ CD₃ R^G3 H H H L_A2257 H H H H R^G115 H L_A1018 CD₃ CD₃ R^G4 H H H L_A2258 H H H H R^G116 H L_A1019 CD₃ CD₃ R^G5 H H H L_A2259 H H H H R^G117 H L_A1020 CD₃ CD₃ R^G6 H H H L_A2260 H H H H R^G118 H L_A1021 CD₃ CD₃ R^G7 H H H L_A2261 H H H H R^G119 H L_A1022 CD₃ CD₃ R^G8 H H H L_A2262 H H H H R^G120 H L_A1023 CD₃ CD₃ R^G9 H H H L_A2263 H H H H R^G121 H L_A1024 CD₃ CD₃ R^G10 H H H L_A2264 H H H H R^G122 H L_A1025 CD₃ CD₃ R^G11 H H H L_A2265 H H H H R^G123 H L_A1026 CD₃ CD₃ R^G12 H H H L_A2266 H H H H R^G124 H L_A1027 CD₃ CD₃ R^G13 H H H L_A2267 H H H H R^G125 H L_A1028 CD₃ CD₃ R^G14 H H H L_A2268 H H H H R^G126 H L_A1029 CD₃ CD₃ R^G15 H H H L_A2269 H H H H R^G127 H L_A1030 CD₃ CD₃ R^G16 H H H L_A2270 H H H H R^G128 H L_A1031 CD₃ CD₃ R^G17 H H H L_A2271 H H H H R^G129 H L_A1032 CD₃ CD₃ R^G18 H H H L_A2272 H H H H R^G130 H L_A1033 CD₃ CD₃ R^G19 H H H L_A2273 H H H H R^G131 H L_A1034 CD₃ CD₃ R^G20 H H H L_A2274 H H H H R^G132 H L_A1035 CD₃ CD₃ R^G21 H H H L_A2275 H H H H R^G133 H L_A1036 CD₃ CD₃ R^G22 H H H L_A2276 H H H H R^G134 H L_A1037 CD₃ CD₃ R^G23 H H H L_A2277 H H H H R^G135 H L_A1038 CD₃ CD₃ R^G24 H H H L_A2278 H H H H R^G136 H L_A1039 CD₃ CD₃ R^G25 H H H L_A2279 H H H H R^G137 H L_A1040 CD₃ CD₃ R^G26 H H H L_A2280 H H H H R^G138 H L_A1041 CD₃ CD₃ R^G27 H H H L_A2281 H H H H R^G139 H L_A1042 CD₃ CD₃ R^G28 H H H L_A2282 H H H H R^G140 H L_A1043 CD₃ CD₃ R^G29 H H H L_A2283 H H H H R^G141 H L_A1044 CD₃ CD₃ R^G30 H H H L_A2284 H H H H R^G142 H L_A1045 CD₃ CD₃ R^G31 H H H L_A2285 H H H H R^G143 H L_A1046 CD₃ CD₃ R^G32 H H H L_A2286 H H H H R^G144 H L_A1047 CD₃ CD₃ R^G33 H H H L_A2287 H H H H R^G145 H L_A1048 CD₃ CD₃ R^G34 H H H L_A2288 H H H H R^G146 H L_A1049 CD₃ CD₃ R^G35 H H H L_A2289 H H H H R^G147 H L_A1050 CD₃ CD₃ R^G36 H H H L_A2290 H H H H R^G148 H L_A1051 CD₃ CD₃ R^G37 H H H L_A2291 H H H H R^G149 H L_A1052 CD₃ CD₃ R^G38 H H H L_A2292 H H H H R^G150 H L_A1053 CD₃ CD₃ R^G39 H H H L_A2293 H H H H R^G151 H L_A1054 CD₃ CD₃ R^G40 H H H L_A2294 H H H H R^G152 H L_A1055 CD₃ CD₃ R^G41 H H H L_A2295 H H H H R^G153 H L_A1056 CD₃ CD₃ R^G42 H H H L_A2296 H H H H R^G154 H L_A1057 CD₃ CD₃ R^G43 H H H L_A2297 H H H H R^G155 H L_A1058 CD₃ CD₃ R^G44 H H H L_A2298 H H H H R^G156 H L_A1059 CD₃ CD₃ R^G45 H H H L_A2299 H H H H R^G157 H L_A1060 CD₃ CD₃ R^G46 H H H L_A2300 H H H H R^G158 H L_A1061 CD₃ CD₃ R^G47 H H H L_A2301 H H H H R^G159 H L_A1062 CD₃ CD₃ R^G48 H H H L_A2302 H H H H R^G160 H L_A1063 CD₃ CD₃ R^G49 H H H L_A2303 H H H H R^G161 H L_A1064 CD₃ CD₃ R^G50 H H H L_A2304 H H H H R^G162 H L_A1065 CD₃ CD₃ R^G51 H H H L_A2305 H H H H R^G163 H L_A1066 CD₃ CD₃ R^G52 H H H L_A2306 H H H H R^G164 H L_A1067 CD₃ CD₃ R^G53 H H H L_A2307 H H H H R^G165 H L_A1068 CD₃ CD₃ R^G54 H H H L_A2308 H H H H R^G166 H L_A1069 CD₃ CD₃ R^G55 H H H L_A2309 H H H H R^G167 H L_A1070 CD₃ CD₃ R^G56 H H H L_A2310 H H H H R^G168 H L_A1071 CD₃ CD₃ R^G57 H H H L_A2311 H H H H R^G169 H L_A1072 CD₃ CD₃ R^G58 H H H L_A2312 H H H H H R^G1 L_A1073 CD₃ CD₃ R^G59 H H H L_A2313 H H H H H R^G2 L_A1074 CD₃ CD₃ R^G60 H H H L_A2314 H H H H H R^G3 L_A1075 CD₃ CD₃ R^G61 H H H L_A2315 H H H H H R^G4 L_A1076 CD₃ CD₃ R^G62 H H H L_A2316 H H H H H R^G5 L_A1077 CD₃ CD₃ R^G63 H H H L_A2317 H H H H H R^G6 L_A1078 CD₃ CD₃ R^G64 H H H L_A2318 H H H H H R^G7 L_A1079 CD₃ CD₃ R^G65 H H H L_A2319 H H H H H R^G8 L_A1080 CD₃ CD₃ R^G66 H H H L_A2320 H H H H H R^G9 L_A1081 CD₃ CD₃ R^G67 H H H L_A2321 H H H H H R^G10 L_A1082 CD₃ CD₃ R^G68 H H H L_A2322 H H H H H R^G11 L_A1083 CD₃ CD₃ R^G69 H H H L_A2323 H H H H H R^G12 L_A1084 CD₃ CD₃ R^G70 H H H L_A2324 H H H H H R^G13 L_A1085 CD₃ CD₃ R^G71 H H H L_A2325 H H H H H R^G14 L_A1086 CD₃ CD₃ R^G72 H H H L_A2326 H H H H H R^G15 L_A1087 CD₃ CD₃ R^G73 H H H L_A2327 H H H H H R^G16 L_A1088 CD₃ CD₃ R^G74 H H H L_A2328 H H H H H R^G17 L_A1089 CD₃ CD₃ R^G75 H H H L_A2329 H H H H H R^G18 L_A1090 CD₃ CD₃ R^G76 H H H L_A2330 H H H H H R^G19 L_A1091 CD₃ CD₃ R^G77 H H H L_A2331 H H H H H R^G20 L_A1092 CD₃ CD₃ R^G78 H H H L_A2332 H H H H H R^G21 L_A1093 CD₃ CD₃ R^G79 H H H L_A2333 H H H H H R^G22 L_A1094 CD₃ CD₃ R^G80 H H H L_A2334 H H H H H R^G23 L_A1095 CD₃ CD₃ R^G81 H H H L_A2335 H H H H H R^G24 L_A1096 CD₃ CD₃ R^G82 H H H L_A2336 H H H H H R^G25 L_A1097 CD₃ CD₃ R^G83 H H H L_A2337 H H H H H R^G26 L_A1098 CD₃ CD₃ R^G84 H H H L_A2338 H H H H H R^G27 L_A1099 CD₃ CD₃ R^G85 H H H L_A2339 H H H H H R^G28 L_A1100 CD₃ CD₃ R^G86 H H H L_A2340 H H H H H R^G29 L_A1101 CD₃ CD₃ R^G87 H H H L_A2341 H H H H H R^G30 L_A1102 CD₃ CD₃ R^G88 H H H L_A2342 H H H H H R^G31 L_A1103 CD₃ CD₃ R^G89 H H H L_A2343 H H H H H R^G32 L_A1104 CD₃ CD₃ R^G90 H H H L_A2344 H H H H H R^G33 L_A1105 CD₃ CD₃ R^G91 H H H L_A2345 H H H H H R^G34 L_A1106 CD₃ CD₃ R^G92 H H H L_A2346 H H H H H R^G35 L_A1107 CD₃ CD₃ R^G93 H H H L_A2347 H H H H H R^G36 L_A1108 CD₃ CD₃ R^G94 H H H L_A2348 H H H H H R^G37 L_A1109 CD₃ CD₃ R^G95 H H H L_A2349 H H H H H R^G38 L_A1110 CD₃ CD₃ R^G96 H H H L_A2350 H H H H H R^G39 L_A1111 CD₃ CD₃ R^G97 H H H L_A2351 H H H H H R^G40 L_A1112 CD₃ CD₃ R^G98 H H H L_A2352 H H H H H R^G41 L_A1113 CD₃ CD₃ R^G99 H H H L_A2353 H H H H H R^G42 L_A1114 CD₃ CD₃ R^G100 H H H L_A2354 H H H H H R^G43 L_A1115 CD₃ CD₃ R^G101 H H H L_A2355 H H H H H R^G44 L_A1116 CD₃ CD₃ R^G102 H H H L_A2356 H H H H H R^G45 L_A1117 CD₃ CD₃ R^G103 H H H L_A2357 H H H H H R^G46 L_A1118 CD₃ CD₃ R^G104 H H H L_A2358 H H H H H R^G47 L_A1119 CD₃ CD₃ R^G105 H H H L_A2359 H H H H H R^G48 L_A1120 CD₃ CD₃ R^G106 H H H L_A2360 H H H H H R^G49 L_A1121 CD₃ CD₃ R^G107 H H H L_A2361 H H H H H R^G50 L_A1122 CD₃ CD₃ R^G108 H H H L_A2362 H H H H H R^G51 L_A1123 CD₃ CD₃ R^G109 H H H L_A2363 H H H H H R^G52 L_A1124 CD₃ CD₃ R^G110 H H H L_A2364 H H H H H R^G53 L_A1125 CD₃ CD₃ R^G111 H H H L_A2365 H H H H H R^G54 L_A1126 CD₃ CD₃ R^G112 H H H L_A2366 H H H H H R^G55 L_A1127 CD₃ CD₃ R^G113 H H H L_A2367 H H H H H R^G56 L_A1128 CD₃ CD₃ R^G114 H H H L_A2368 H H H H H R^G57 L_A1129 CD₃ CD₃ R^G115 H H H L_A2369 H H H H H R^G58 L_A1130 CD₃ CD₃ R^G116 H H H L_A2370 H H H H H R^G59 L_A1131 CD₃ CD₃ R^G117 H H H L_A2371 H H H H H R^G60 L_A1132 CD₃ CD₃ R^G118 H H H L_A2372 H H H H H R^G61 L_A1133 CD₃ CD₃ R^G119 H H H L_A2373 H H H H H R^G62 L_A1134 CD₃ CD₃ R^G120 H H H L_A2374 H H H H H R^G63 L_A1135 CD₃ CD₃ R^G121 H H H L_A2375 H H H H H R^G64 L_A1136 CD₃ CD₃ R^G122 H H H L_A2376 H H H H H R^G65 L_A1137 CD₃ CD₃ R^G123 H H H L_A2377 H H H H H R^G66 L_A1138 CD₃ CD₃ R^G124 H H H L_A2378 H H H H H R^G67 L_A1139 CD₃ CD₃ R^G125 H H H L_A2379 H H H H H R^G68 L_A1140 CD₃ CD₃ R^G126 H H H L_A2380 H H H H H R^G69 L_A1141 CD₃ CD₃ R^G127 H H H L_A2381 H H H H H R^G70 L_A1142 CD₃ CD₃ R^G128 H H H L_A2382 H H H H H R^G71 L_A1143 CD₃ CD₃ R^G129 H H H L_A2383 H H H H H R^G72 L_A1144 CD₃ CD₃ R^G130 H H H L_A2384 H H H H H R^G73 L_A1145 CD₃ CD₃ R^G131 H H H L_A2385 H H H H H R^G74 L_A1146 CD₃ CD₃ R^G132 H H H L_A2386 H H H H H R^G75 L_A1147 CD₃ CD₃ R^G133 H H H L_A2387 H H H H H R^G76 L_A1148 CD₃ CD₃ R^G134 H H H L_A2388 H H H H H R^G77 L_A1149 CD₃ CD₃ R^G135 H H H L_A2389 H H H H H R^G78 L_A1150 CD₃ CD₃ R^G136 H H H L_A2390 H H H H H R^G79 L_A1151 CD₃ CD₃ R^G137 H H H L_A2391 H H H H H R^G80 L_A1152 CD₃ CD₃ R^G138 H H H L_A2392 H H H H H R^G81 L_A1153 CD₃ CD₃ R^G139 H H H L_A2393 H H H H H R^G82 L_A1154 CD₃ CD₃ R^G140 H H H L_A2394 H H H H H R^G83 L_A1155 CD₃ CD₃ R^G141 H H H L_A2395 H H H H H R^G84 L_A1156 CD₃ CD₃ R^G142 H H H L_A2396 H H H H H R^G85 L_A1157 CD₃ CD₃ R^G143 H H H L_A2397 H H H H H R^G86 L_A1158 CD₃ CD₃ R^G144 H H H L_A2398 H H H H H R^G87 L_A1159 CD₃ CD₃ R^G145 H H H L_A2399 H H H H H R^G88 L_A1160 CD₃ CD₃ R^G146 H H H L_A2400 H H H H H R^G89 L_A1161 CD₃ CD₃ R^G147 H H H L_A2401 H H H H H R^G90 L_A1162 CD₃ CD₃ R^G148 H H H L_A2402 H H H H H R^G91 L_A1163 CD₃ CD₃ R^G149 H H H L_A2403 H H H H H R^G92 L_A1164 CD₃ CD₃ R^G150 H H H L_A2404 H H H H H R^G93 L_A1165 CD₃ CD₃ R^G151 H H H L_A2405 H H H H H R^G94 L_A1166 CD₃ CD₃ R^G152 H H H L_A2406 H H H H H R^G95 L_A1167 CD₃ CD₃ R^G153 H H H L_A2407 H H H H H R^G96 L_A1168 CD₃ CD₃ R^G154 H H H L_A2408 H H H H H R^G97 L_A1169 CD₃ CD₃ R^G155 H H H L_A2409 H H H H H R^G98 L_A1170 CD₃ CD₃ R^G156 H H H L_A2410 H H H H H R^G99 L_A1171 CD₃ CD₃ R^G157 H H H L_A2411 H H H H H R^G100 L_A1172 CD₃ CD₃ R^G158 H H H L_A2412 H H H H H R^G101 L_A1173 CD₃ CD₃ R^G159 H H H L_A2413 H H H H H R^G102 L_A1174 CD₃ CD₃ R^G160 H H H L_A2414 H H H H H R^G103 L_A1175 CD₃ CD₃ R^G161 H H H L_A2415 H H H H H R^G104 L_A1176 CD₃ CD₃ R^G162 H H H L_A2416 H H H H H R^G105 L_A1177 CD₃ CD₃ R^G163 H H H L_A2417 H H H H H R^G106 L_A1178 CD₃ CD₃ R^G164 H H H L_A2418 H H H H H R^G107 L_A1179 CD₃ CD₃ R^G165 H H H L_A2419 H H H H H R^G108 L_A1180 CD₃ CD₃ R^G166 H H H L_A2420 H H H H H R^G109 L_A1181 CD₃ CD₃ R^G167 H H H L_A2421 H H H H H R^G110 L_A1182 CD₃ CD₃ R^G168 H H H L_A2422 H H H H H R^G111 L_A1183 CD₃ CD₃ R^G169 H H H L_A2423 H H H H H R^G112 L_A1184 CD₃ H R^G1 H H H L_A2424 H H H H H R^G113 L_A1185 CD₃ H R^G2 H H H L_A2425 H H H H H R^G114 L_A1186 CD₃ H R^G3 H H H L_A2426 H H H H H R^G115 L_A1187 CD₃ H R^G4 H H H L_A2427 H H H H H R^G116 L_A1188 CD₃ H R^G5 H H H L_A2428 H H H H H R^G117 L_A1189 CD₃ H R^G6 H H H L_A2429 H H H H H R^G118 L_A1190 CD₃ H R^G7 H H H L_A2430 H H H H H R^G119 L_A1191 CD₃ H R^G8 H H H L_A2431 H H H H H R^G120 L_A1192 CD₃ H R^G9 H H H L_A2432 H H H H H R^G121 L_A1193 CD₃ H R^G10 H H H L_A2433 H H H H H R^G122 L_A1194 CD₃ H R^G11 H H H L_A2434 H H H H H R^G123 L_A1195 CD₃ H R^G12 H H H L_A2435 H H H H H R^G124 L_A1196 CD₃ H R^G13 H H H L_A2436 H H H H H R^G125 L_A1197 CD₃ H R^G14 H H H L_A2437 H H H H H R^G126 L_A1198 CD₃ H R^G15 H H H L_A2438 H H H H H R^G127 L_A1199 CD₃ H R^G16 H H H L_A2439 H H H H H R^G128 L_A1200 CD₃ H R^G17 H H H L_A2440 H H H H H R^G129 L_A1201 CD₃ H R^G18 H H H L_A2441 H H H H H R^G130 L_A1202 CD₃ H R^G19 H H H L_A2442 H H H H H R^G131 L_A1203 CD₃ H R^G20 H H H L_A2443 H H H H H R^G132 L_A1204 CD₃ H R^G21 H H H L_A2444 H H H H H R^G133 L_A1205 CD₃ H R^G22 H H H L_A2445 H H H H H R^G134 L_A1206 CD₃ H R^G23 H H H L_A2446 H H H H H R^G135 L_A1207 CD₃ H R^G24 H H H L_A2447 H H H H H R^G136 L_A1208 CD₃ H R^G25 H H H L_A2448 H H H H H R^G137 L_A1209 CD₃ H R^G26 H H H L_A2449 H H H H H R^G138 L_A1210 CD₃ H R^G27 H H H L_A2450 H H H H H R^G139 L_A1211 CD₃ H R^G28 H H H L_A2451 H H H H H R^G140 L_A1212 CD₃ H R^G29 H H H L_A2452 H H H H H R^G141 L_A1213 CD₃ H R^G30 H H H L_A2453 H H H H H R^G142 L_A1214 CD₃ H R^G31 H H H L_A2454 H H H H H R^G143 L_A1215 CD₃ H R^G32 H H H L_A2455 H H H H H R^G144 L_A1216 CD₃ H R^G33 H H H L_A2456 H H H H H R^G145 L_A1217 CD₃ H R^G34 H H H L_A2457 H H H H H R^G146 L_A1218 CD₃ H R^G35 H H H L_A2458 H H H H H R^G147 L_A1219 CD₃ H R^G36 H H H L_A2459 H H H H H R^G148 L_A1220 CD₃ H R^G37 H H H L_A2460 H H H H H R^G149 L_A1221 CD₃ H R^G38 H H H L_A2461 H H H H H R^G150 L_A1222 CD₃ H R^G39 H H H L_A2462 H H H H H R^G151 L_A1223 CD₃ H R^G40 H H H L_A2463 H H H H H R^G152 L_A1224 CD₃ H R^G41 H H H L_A2464 H H H H H R^G153 L_A1225 CD₃ H R^G42 H H H L_A2465 H H H H H R^G154 L_A1226 CD₃ H R^G43 H H H L_A2466 H H H H H R^G155 L_A1227 CD₃ H R^G44 H H H L_A2467 H H H H H R^G156 L_A1228 CD₃ H R^G45 H H H L_A2468 H H H H H R^G157 L_A1229 CD₃ H R^G46 H H H L_A2469 H H H H H R^G158 L_A1230 CD₃ H R^G47 H H H L_A2470 H H H H H R^G159 L_A1231 CD₃ H R^G48 H H H L_A2471 H H H H H R^G160 L_A1232 CD₃ H R^G49 H H H L_A2472 H H H H H R^G161 L_A1233 CD₃ H R^G50 H H H L_A2473 H H H H H R^G162 L_A1234 CD₃ H R^G51 H H H L_A2474 H H H H H R^G163 L_A1235 CD₃ H R^G52 H H H L_A2475 H H H H H R^G164 L_A1236 CD₃ H R^G53 H H H L_A2476 H H H H H R^G165 L_A1237 CD₃ H R^G54 H H H L_A2477 H H H H H R^G166 L_A1238 CD₃ H R^G55 H H H L_A2478 H H H H H R^G167 L_A1239 CD₃ H R^G56 H H H L_A2479 H H H H H R^G168 L_A1240 CD₃ H R^G57 H H H L_A2480 H H H H H R^G169

wherein R

^G1 to R^G169 have the following structures:

and

.

14. The composition of claim 13, wherein the compound is Compound x selected from the group consisting of Compound x, wherein x is an integer from 1 to 2120400;

wherein Compound x has the formula Ir(L_Ai)(L_Bj)₂;

wherein x = 2480j + i - 2480, i is an integer from 1 to 2480, and j is an integer from 1 to 855;

wherein each L_Bj has a structure based on the following structure:

and R

^B1, R^B2, R^B3, R^B4 for each j is defined as follows:

j R^B1 R^B2 R^B3 R^B4 1. H H H H 2. CH₃ H H H 3. H CH₃ H H 4. H H CH₃ H 5. H H H CH₃ 6. CH₃ H CH₃ H 7. CH₃ H H CH₃ 8. H CH₃ CH₃ H 9. H CH₃ H CH₃ 10. H H CH₃ CH₃ 11. CH₃ CH₃ CH₃ H 12. CH₃ CH₃ H CH₃ 13. CH₃ H CH₃ CH₃ 14. H CH₃ CH₃ CH₃ 15. CH₃ CH₃ CH₃ CH₃ 16. CH₂CH₃ H H H 17. CH₂CH₃ CH₃ H H 18. CH₂CH₃ H CH₃ H 19. CH₂CH₃ H H CH₃ 20. CH₂CH₃ CH₃ CH₃ H 21. CH₂CH₃ CH₃ H CH₃ 22. CH₂CH₃ H CH₃ CH₃ 23. CH₂CH₃ CH₃ CH₃ CH₃ 24. H CH₂CH₃ H H 25. CH₃ CH₂CH₃ H H 26. H CH₂CH₃ CH₃ H 27. H CH₂CH₃ H CH₃ 28. CH₃ CH₂CH₃ CH₃ H 29. CH₃ CH₂CH₃ H CH₃ 30. H CH₂CH₃ CH₃ CH₃ 31. CH₃ CH₂CH₃ CH₃ CH₃ 32. H H CH₂CH₃ H 33. CH₃ H CH₂CH₃ H 34. H CH₃ CH₂CH₃ H 35. H H CH₂CH₃ CH₃ 36. CH₃ CH₃ CH₂CH₃ H 37. CH₃ H CH₂CH₃ CH₃ 38. H CH₃ CH₂CH₃ CH₃ 39. CH₃ CH₃ CH₂CH₃ CH₃ 40. CH(CH₃)₂ H H H 41. CH(CH₃)₂ CH₃ H H 42. CH(CH₃)₂ H CH₃ H 43. CH(CH₃)₂ H H CH₃ 44. CH(CH₃)₂ CH₃ CH₃ H 45. CH(CH₃)₂ CH₃ H CH₃ 46. CH(CH₃)₂ H CH₃ CH₃ 47. CH(CH₃)₂ CH₃ CH₃ CH₃ 48. H CH(CH₃)₂ H H 49. CH₃ CH(CH₃)₂ H H 50. H CH(CH₃)₂ CH₃ H 51. H CH(CH₃)₂ H CH₃ 52. CH₃ CH(CH₃)₂ CH₃ H 53. CH₃ CH(CH₃)₂ H CH₃ 54. H CH(CH₃)₂ CH₃ CH₃ 55. CH₃ CH(CH₃)₂ CH₃ CH₃ 56. H H CH(CH₃)₂ H 57. CH₃ H CH(CH₃)₂ H 58. H CH₃ CH(CH₃)₂ H 59. H H CH(CH₃)₂ CH₃ 60. CH₃ CH₃ CH(CH₃)₂ H 61. CH₃ H CH(CH₃)₂ CH₃ 62. H CH₃ CH(CH₃)₂ CH₃ 63. CH₃ CH₃ CH(CH₃)₂ CH₃ 64. CH₂CH(CH₃)₂ H H H 65. CH₂CH(CH₃)₂ CH₃ H H 66. CH₂CH(CH₃)₂ H CH₃ H 67. CH₂CH(CH₃)₂ H H CH₃ 68. CH₂CH(CH₃)₂ CH₃ CH₃ H 69. CH₂CH(CH₃)₂ CH₃ H CH₃ 70. CH₂CH(CH₃)₂ H CH₃ CH₃ 71. CH₂CH(CH₃)₂ CH₃ CH₃ CH₃ 72. H CH₂CH(CH₃)₂ H H 73. CH₃ CH₂CH(CH₃)₂ H H 74. H CH₂CH(CH₃)₂ CH₃ H 75. H CH₂CH(CH₃)₂ H CH₃ 76. CH₃ CH₂CH(CH₃)₂ CH₃ H 77. CH₃ CH₂CH(CH₃)₂ H CH₃ 78. H CH₂CH(CH₃)₂ CH₃ CH₃ 79. CH₃ CH₂CH(CH₃)₂ CH₃ CH₃ 80. H H CH₂CH(CH₃)₂ H 81. CH₃ H CH₂CH(CH₃)₂ H 82. H CH₃ CH₂CH(CH₃)₂ H 83. H H CH₂CH(CH₃)₂ CH₃ 84. CH₃ CH₃ CH₂CH(CH₃)₂ H 85. CH₃ H CH₂CH(CH₃)₂ CH₃ 86. H CH₃ CH₂CH(CH₃)₂ CH₃ 87. CH₃ CH₃ CH₂CH(CH₃)₂ CH₃ 88. C(CH₃)₃ H H H 89. C(CH₃)₃ CH₃ H H 90. C(CH₃)₃ H CH₃ H 91. C(CH₃)₃ H H CH₃ 92. C(CH₃)₃ CH₃ CH₃ H 93. C(CH₃)₃ CH₃ H CH₃ 94. C(CH₃)₃ H CH₃ CH₃ 95. C(CH₃)₃ CH₃ CH₃ CH₃ 96. H C(CH₃)₃ H H 97. CH₃ C(CH₃)₃ H H 98. H C(CH₃)₃ CH₃ H 99. H C(CH₃)₃ H CH₃ 100. CH₃ C(CH₃)₃ CH₃ H 101. CH₃ C(CH₃)₃ H CH₃ 102. H C(CH₃)₃ CH₃ CH₃ 103. CH₃ C(CH₃)₃ CH₃ CH₃ 104. H H C(CH₃)₃ H 105. CH₃ H C(CH₃)₃ H 106. H CH₃ C(CH₃)₃ H 107. H H C(CH₃)₃ CH₃ 108. CH₃ CH₃ C(CH₃)₃ H 109. CH₃ H C(CH₃)₃ CH₃ 110. H CH₃ C(CH₃)₃ CH₃ 111. CH₃ CH₃ C(CH₃)₃ CH₃ 112. CH₂C(CH₃)₃ H H H 113. CH₂C(CH₃)₃ CH₃ H H 114. CH₂C(CH₃)₃ H CH₃ H 115. CH₂C(CH₃)₃ H H CH₃ 116. CH₂C(CH₃)₃ CH₃ CH₃ H 117. CH₂C(CH₃)₃ CH₃ H CH₃ 118. CH₂C(CH₃)₃ H CH₃ CH₃ 119. CH₂C(CH₃)₃ CH₃ CH₃ CH₃ 120. H CH₂C(CH₃)₃ H H 121. CH₃ CH₂C(CH₃)₃ H H 122. H CH₂C(CH₃)₃ CH₃ H 123. H CH₂C(CH₃)₃ H CH₃ 124. CH₃ CH₂C(CH₃)₃ CH₃ H 125. CH₃ CH₂C(CH₃)₃ H CH₃ 126. H CH₂C(CH₃)₃ CH₃ CH₃ 127. CH₃ CH₂C(CH₃)₃ CH₃ CH₃ 128. H H CH₂C(CH₃)₃ H 129. CH₃ H CH₂C(CH₃)₃ H 130. H CH₃ CH₂C(CH₃)₃ H 131. H H CH₂C(CH₃)₃ CH₃ 132. CH₃ CH₃ CH₂C(CH₃)₃ H 133. CH₃ H CH₂C(CH₃)₃ CH₃ 134. H CH₃ CH₂C(CH₃)₃ CH₃ 135. CH₃ CH₃ CH₂C(CH₃)₃ CH₃ 136. CH₂C(CH₃)₂CF₃ H H H 137. CH₂C(CH₃)₂CF₃ CH₃ H H 138. CH₂C(CH₃)₂CF₃ H CH₃ H 139. CH₂C(CH₃)₂CF₃ H H CH₃ 140. CH₂C(CH₃)₂CF₃ CH₃ CH₃ H 141. CH₂C(CH₃)₂CF₃ CH₃ H CH₃ 142. CH₂C(CH₃)₂CF₃ H CH₃ CH₃ 143. CH₂C(CH₃)₂CF₃ CH₃ CH₃ CH₃ 144. H CH₂C(CH₃)₂CF₃ H H 145. CH₃ CH₂C(CH₃)₂CF₃ H H 146. H CH₂C(CH₃)₂CF₃ CH₃ H 147. H CH₂C(CH₃)₂CF₃ H CH₃ 148. CH₃ CH₂C(CH₃)₂CF₃ CH₃ H 149. CH₃ CH₂C(CH₃)₂CF₃ H CH₃ 150. H CH₂C(CH₃)₂CF₃ CH₃ CH₃ 151. CH₃ CH₂C(CH₃)₂CF₃ CH₃ CH₃ 152. H H CH₂C(CH₃)₂CF₃ H 153. CH₃ H CH₂C(CH₃)₂CF₃ H 154. H CH₃ CH₂C(CH₃)₂CF₃ H 155. H H CH₂C(CH₃)₂CF₃ CH₃ 156. CH₃ CH₃ CH₂C(CH₃)₂CF₃ H 157. CH₃ H CH₂C(CH₃)₂CF₃ CH₃ 158. H CH₃ CH₂C(CH₃)₂CF₃ CH₃ 159. CH₃ CH₃ CH₂C(CH₃)₂CF₃ CH₃ 160. CH₂CH₂CF₃ H H H 161. CH₂CH₂CF₃ CH₃ H H 162. CH₂CH₂CF₃ H CH₃ H 163. CH₂CH₂CF₃ H H CH₃ 164. CH₂CH₂CF₃ CH₃ CH₃ H 165. CH₂CH₂CF₃ CH₃ H CH₃ 166. CH₂CH₂CF₃ H CH₃ CH₃ 167. CH₂CH₂CF₃ CH₃ CH₃ CH₃ 168. H CH₂CH₂CF₃ H H 169. CH₃ CH₂CH₂CF₃ H H 170. H CH₂CH₂CF₃ CH₃ H 171. H CH₂CH₂CF₃ H CH₃ 172. CH₃ CH₂CH₂CF₃ CH₃ H 173. CH₃ CH₂CH₂CF₃ H CH₃ 174. H CH₂CH₂CF₃ CH₃ CH₃ 175. CH₃ CH₂CH₂CF₃ CH₃ CH₃ 176. H H CH₂CH₂CF₃ H 177. CH₃ H CH₂CH₂CF₃ H 178. H CH₃ CH₂CH₂CF₃ H 179. H H CH₂CH₂CF₃ CH₃ 180. CH₃ CH₃ CH₂CH₂CF₃ H 181. CH₃ H CH₂CH₂CF₃ CH₃ 182. H CH₃ CH₂CH₂CF₃ CH₃ 183. CH₃ CH₃ CH₂CH₂CF₃ CH₃ 184.

H H H 185.

CH₃ H H 186.

H CH₃ H 187.

H H CH₃ 188.

CH₃ CH₃ H 189.

CH₃ H CH₃ 190.

H CH₃ CH₃ 191.

CH₃ CH₃ CH₃ 192. H

H H 193. CH₃

H H 194. H

CH₃ H 195. H

H CH₃ 196. CH₃

CH₃ H 197. CH₃

H CH₃ 198. H

CH₃ CH₃ 199. CH₃

CH₃ CH₃ 200. H H

H 201. CH₃ H

H 202. H CH₃

H 203. H H

CH₃ 204. CH₃ CH₃

H 205. CH₃ H

CH₃ 206. H CH₃

CH₃ 207. CH₃ CH₃

CH₃ 208.

H H H 209.

CH₃ H H 210.

H CH₃ H 211.

H H CH₃ 212.

CH₃ CH₃ H 213.

CH₃ H CH₃ 214.

H CH₃ CH₃ 215.

CH₃ CH₃ CH₃ 216. H

H H 217. CH₃

H H 218. H

CH₃ H 219. H

H CH₃ 220. CH₃

CH₃ H 221. CH₃

H CH₃ 222. H

CH₃ CH₃ 223. CH₃

CH₃ CH₃ 224. H H

H 225. CH₃ H

H 226. H CH₃

H 227. H H

CH₃ 228. CH₃ CH₃

H 229. CH₃ H

CH₃ 230. H CH₃

CH₃ 231. CH₃ CH₃

CH₃ 232.

H H H 233.

CH₃ H H 234.

H CH₃ H 235.

H H CH₃ 236.

CH₃ CH₃ H 237.

CH₃ H CH₃ 238.

H CH₃ CH₃ 239.

CH₃ CH₃ CH₃ 240. H

H H 241. CH₃

H H 242. H

CH₃ H 243. H

H CH₃ 244. CH₃

CH₃ H 245. CH₃

H CH₃ 246. H

CH₃ CH₃ 247. CH₃

CH₃ CH₃ 248. H H

H 249. CH₃ H

H 250. H CH₃

H 251. H H

CH₃ 252. CH₃ CH₃

H 253. CH₃ H

CH₃ 254. H CH₃

CH₃ 255. CH₃ CH₃

CH₃ 256.

H H H 257.

CH₃ H H 258.

H CH₃ H 259.

H H CH₃ 260.

CH₃ CH₃ H 261.

CH₃ H CH₃ 262.

H CH₃ CH₃ 263.

CH₃ CH₃ CH₃ 264. H

H H 265. CH₃

H H 266. H

CH₃ H 267. H

H CH₃ 268. CH₃

CH₃ H 269. CH₃

H CH₃ 270. H

CH₃ CH₃ 271. CH₃

CH₃ CH₃ 272. H H

H 273. CH₃ H

H 274. H CH₃

H 275. H H

CH₃ 276. CH₃ CH₃

H 277. CH₃ H

CH₃ 278. H CH₃

CH₃ 279. CH₃ CH₃

CH₃ 280.

H H H 281.

H H 282.

H CH₃ H 283.

H H CH₃ 284.

CH₃ CH₃ H 285.

CH₃ H CH₃ 286.

H CH₃ CH₃ 287.

CH₃ CH₃ CH₃ 288. H

H H 289. CH₃

H H 290. H

CH₃ H 291. H

H CH₃ 292. CH₃

CH₃ H 293. CH₃

H CH₃ 294. H

CH₃ CH₃ 295. CH₃

CH₃ CH₃ 296. H H

H 297. CH₃ H

H 298. H CH₃

H 299. H H

CH₃ 300. CH₃ CH₃

H 301. CH₃ H

CH₃ 302. H CH₃

CH₃ 303. CH₃ CH₃

CH₃ 304.

H H H 305.

CH₃ H H 306.

H CH₃ H 307.

H H CH₃ 308.

CH₃ CH₃ H 309.

CH₃ H CH₃ 310.

H CH₃ CH₃ 311.

CH₃ CH₃ CH₃ 312. H

H H 313. CH₃

H H 314. H

CH₃ H 315. H

H CH₃ 316. CH₃

CH₃ H 317. CH₃

H CH₃ 318. H

CH₃ CH₃ 319. CH₃

CH₃ CH₃ 320. H H

H 321. CH₃ H

H 322. H CH₃

H 323. H H

CH₃ 324. CH₃ CH₃

H 325. CH₃ H

CH₃ 326. H CH₃

CH₃ 327. CH₃ CH₃

CH₃ 328. CH(CH₃)₂ H CH₂CH₃ H 329. CH(CH₃)₂ H CH(CH₃)₂ H 330. CH(CH₃)₂ H CH₂CH(CH₃)₂ H 331. CH(CH₃)₂ H C(CH₃)₃ H 332. CH(CH₃)₂ H CH₂C(CH₃)₃ H 333. CH(CH₃)₂ H CH₂CH₂CF₃ H 334. CH(CH₃)₂ H CH₂C(CH₃)₂CF₃ H 335. CH(CH₃)₂ H

H 336. CH(CH₃)₂ H

H 337. CH(CH₃)₂ H

H 338. CH(CH₃)₂ H

H 339. CH(CH₃)₂ H

H 340. CH(CH₃)₂ H

H 341. C(CH₃)₃ H CH₂CH₃ H 342. C(CH₃)₃ H CH(CH₃)₂ H 343. C(CH₃)₃ H CH₂CH(CH₃)₂ H 344. C(CH₃)₃ H C(CH₃)₃ H 345. C(CH₃)₃ H CH₂C(CH₃)₃ H 346. C(CH₃)₃ H CH₂CH₂CF₃ H 347. C(CH₃)₃ H CH₂C(CH₃)₂CF₃ H 348. C(CH₃)₃ H

H 349. C(CH₃)₃ H

H 350. C(CH₃)₃ H

H 351. C(CH₃)₃ H

H 352. C(CH₃)₃ H

H 353. C(CH₃)₃ H

H 354. CH₂C(CH₃)₃ H CH₂CH₃ H 355. CH₂C(CH₃)₃ H CH(CH₃)₂ H 356. CH₂C(CH₃)₃ H CH₂CH(CH₃)₂ H 357. CH₂C(CH₃)₃ H C(CH₃)₃ H 358. CH₂C(CH₃)₃ H CH₂C(CH₃)₃ H 359. CH₂C(CH₃)₃ H CH₂CH₂CF₃ H 360. CH₂C(CH₃)₃ H CH₂C(CH₃)₂CF₃ H 361. CH₂C(CH₃)₃ H

H 362. CH₂C(CH₃)₃ H

H 363. CH₂C(CH₃)₃ H

H 364. CH₂C(CH₃)₃ H

H 365. CH₂C(CH₃)₃ H

H 366. CH₂C(CH₃)₃ H

H 367.

H CH₂CH₃ H 368.

H CH(CH₃)₂ H 369.

H CH₂CH(CH₃)₂ H 370.

H C(CH₃)₃ H 371.

H CH₂C(CH₃)₃ H 372.

H CH₂CH₂CF₃ H 373.

H CH₂C(CH₃)₂CF₃ H 374.

H

H 375.

H

H 376.

H

H 377.

H

H 378.

H

H 379.

H

H 380.

H CH₂CH₃ H 381.

H CH(CH₃)₂ H 382.

H CH₂CH(CH₃)₂ H 383.

H C(CH₃)₃ H 384.

H CH₂C(CH₃)₃ H 385.

H CH₂CH₂CF₃ H 386.

H CH₂C(CH₃)₂CF₃ H 387.

H

H 388.

H

H 389.

H

H 390.

H

H 391.

H

H 392.

H

H 393.

H CH₂CH(CH₃)₂ H 394.

H C(CH₃)₃ H 395.

H CH₂C(CH₃)₃ H 396.

H CH₂CH₂CF₃ H 397.

H CH₂C(CH₃)₂CF₃ H 398.

H

H 399.

H

H 400.

H

H 401.

H

H 402.

H

H 403.

H

H 404.

H CH₂CH(CH₃)₂ H 405.

H C(CH₃)₃ H 406.

H CH₂C(CH₃)₃ H 407.

H CH₂CH₂CF₃ H 408.

H CH₂C(CH₃)₂CF₃ H 409.

H

H 410.

H

H 411.

H

H 412.

H

H 413.

H

H 414.

H

H 415.

H CH₂CH(CH₃)₂ H 416.

H C(CH₃)₃ H 417.

H CH₂C(CH₃)₃ H 418.

H CH₂CH₂CF₃ H 419.

H CH₂C(CH₃)₂CF₃ H 420.

H

H 421.

H

H 422.

H

H 423.

H

H 424.

H

H 425.

H

H 426. CD₃ H H H 427. H CD₃ H H 428. H H CD₃ H 429. H H H CD₃ 430. CD₃ H CD₃ H 431. CD₃ H H CD₃ 432. H CD₃ CD₃ H 433. H CD₃ H CD₃ 434. H H CD₃ CD₃ 435. CD₃ CD₃ CD₃ H 436. CD₃ CD₃ H CD₃ 437. CD₃ H CD₃ CD₃ 438. H CD₃ CD₃ CD₃ 439. CD₃ CD₃ CD₃ CD₃ 440. CD₂CH₃ H H H 441. CD₂CH₃ CD₃ H H 442. CD₂CH₃ H CD₃ H 443. CD₂CH₃ H H CD₃ 444. CD₂CH₃ CD₃ CD₃ H 445. CD₂CH₃ CD₃ H CD₃ 446. CD₂CH₃ H CD₃ CD₃ 447. CD₂CH₃ CD₃ CD₃ CD₃ 448. H CD₂CH₃ H H 449. CD₃ CD₂CH₃ H H 450. H CD₂CH₃ CD₃ H 451. H CD₂CH₃ H CD₃ 452. CD₃ CD₂CH₃ CD₃ H 453. CD₃ CD₂CH₃ H CD₃ 454. H CD₂CH₃ CD₃ CD₃ 455. CD₃ CD₂CH₃ CD₃ CD₃ 456. H H CD₂CH₃ H 457. CD₃ H CD₂CH₃ H 458. H CD₃ CD₂CH₃ H 459. H H CD₂CH₃ CD₃ 460. CD₃ CD₃ CD₂CH₃ H 461. CD₃ H CD₂CH₃ CD₃ 462. H CD₃ CD₂CH₃ CD₃ 463. CD₃ CD₃ CD₂CH₃ CD₃ 464. CD(CH₃)₂ H H H 465. CD(CH₃)₂ CD₃ H H 466. CD(CH₃)₂ H CD₃ H 467. CD(CH₃)₂ H H CD₃ 468. CD(CH₃)₂ CD₃ CD₃ H 469. CD(CH₃)₂ CD₃ H CD₃ 470. CD(CH₃)₂ H CD₃ CD₃ 471. CD(CH₃)₂ CD₃ CD₃ CD₃ 472. H CD(CH₃)₂ H H 473. CD₃ CD(CH₃)₂ H H 474. H CD(CH₃)₂ CD₃ H 475. H CD(CH₃)₂ H CD₃ 476. CD₃ CD(CH₃)₂ CD₃ H 477. CD₃ CD(CH₃)₂ H CD₃ 478. H CD(CH₃)₂ CD₃ CD₃ 479. CD₃ CD(CH₃)₂ CD₃ CD₃ 480. H H CD(CH₃)₂ H 481. CD₃ H CD(CH₃)₂ H 482. H CD₃ CD(CH₃)₂ H 483. H H CD(CH₃)₂ CD₃ 484. CD₃ CD₃ CD(CH₃)₂ H 485. CD₃ H CD(CH₃)₂ CD₃ 486. H CD₃ CD(CH₃)₂ CD₃ 487. CD₃ CD₃ CD(CH₃)₂ CD₃ 488. CD(CD₃)₂ H H H 489. CD(CD₃)₂ CD₃ H H 490. CD(CD₃)₂ H CD₃ H 491. CD(CD₃)₂ H H CD₃ 492. CD(CD₃)₂ CD₃ CD₃ H 493. CD(CD₃)₂ CD₃ H CD₃ 494. CD(CD₃)₂ H CD₃ CD₃ 495. CD(CD₃)₂ CD₃ CD₃ CD₃ 496. H CD(CD₃)₂ H H 497. CD₃ CD(CD₃)₂ H H 498. H CD(CD₃)₂ CD₃ H 499. H CD(CD₃)₂ H CD₃ 500. CD₃ CD(CD₃)₂ CD₃ H 501. CD₃ CD(CD₃)₂ H CD₃ 502. H CD(CD₃)₂ CD₃ CD₃ 503. CD₃ CD(CD₃)₂ CD₃ CD₃ 504. H H CD(CD₃)₂ H 505. CD₃ H CD(CD₃)₂ H 506. H CD₃ CD(CD₃)₂ H 507. H H CD(CD₃)₂ CD₃ 508. CD₃ CD₃ CD(CD₃)₂ H 509. CD₃ H CD(CD₃)₂ CD₃ 510. H CD₃ CD(CD₃)₂ CD₃ 511. CD₃ CD₃ CD(CD₃)₂ CD₃ 512. CD₂CH(CH₃)₂ H H H 513. CD₂CH(CH₃)₂ CD₃ H H 514. CD₂CH(CH₃)₂ H CD₃ H 515. CD₂CH(CH₃)₂ H H CD₃ 516. CD₂CH(CH₃)₂ CD₃ CD₃ H 517. CD₂CH(CH₃)₂ CD₃ H CD₃ 518. CD₂CH(CH₃)₂ H CD₃ CD₃ 519. CD₂CH(CH₃)₂ CD₃ CD₃ CD₃ 520. H CD₂CH(CH₃)₂ H H 521. CD₃ CD₂CH(CH₃)₂ H H 522. H CD₂CH(CH₃)₂ CD₃ H 523. H CD₂CH(CH₃)₂ H CD₃ 524. CD₃ CD₂CH(CH₃)₂ CD₃ H 525. CD₃ CD₂CH(CH₃)₂ H CD₃ 526. H CD₂CH(CH₃)₂ CD₃ CD₃ 527. CD₃ CD₂CH(CH₃)₂ CD₃ CD₃ 528. H H CD₂CH(CH₃)₂ H 529. CD₃ H CD₂CH(CH₃)₂ H 530. H CD₃ CD₂CH(CH₃)₂ H 531. H H CD₂CH(CH₃)₂ CD₃ 532. CD₃ CD₃ CD₂CH(CH₃)₂ H 533. CD₃ H CD₂CH(CH₃)₂ CD₃ 534. H CD₃ CD₂CH(CH₃)₂ CD₃ 535. CD₃ CD₃ CD₂CH(CH₃)₂ CD₃ 536. CD₂C(CH₃)₃ H H H 537. CD₂C(CH₃)₃ CD₃ H H 538. CD₂C(CH₃)₃ H CD₃ H 539. CD₂C(CH₃)₃ H H CD₃ 540. CD₂C(CH₃)₃ CD₃ CD₃ H 541. CD₂C(CH₃)₃ CD₃ H CD₃ 542. CD₂C(CH₃)₃ H CD₃ CD₃ 543. CD₂C(CH₃)₃ CH₃ CD₃ CD₃ 544. H CD₂C(CH₃)₃ H H 545. CD₃ CD₂C(CH₃)₃ H H 546. H CD₂C(CH₃)₃ CD₃ H 547. H CD₂C(CH₃)₃ H CD₃ 548. CD₃ CD₂C(CH₃)₃ CD₃ H 549. CD₃ CD₂C(CH₃)₃ H CD₃ 550. H CD₂C(CH₃)₃ CD₃ CD₃ 551. CD₃ CD₂C(CH₃)₃ CD₃ CD₃ 552. H H CD₂C(CH₃)₃ H 553. CD₃ H CD₂C(CH₃)₃ H 554. H CD₃ CD₂C(CH₃)₃ H 555. H H CD₂C(CH₃)₃ CD₃ 556. CD₃ CD₃ CD₂C(CH₃)₃ H 557. CD₃ H CD₂C(CH₃)₃ CD₃ 558. H CD₃ CD₂C(CH₃)₃ CD₃ 559. CD₃ CD₃ CD₂C(CH₃)₃ CD₃ 560. CD₂C(CH₃)₂CF₃ H H H 561. CD₂C(CH₃)₂CF₃ CD₃ H H 562. CD₂C(CH₃)₂CF₃ H CD₃ H 563. CD₂C(CH₃)₂CF₃ H H CD₃ 564. CD₂C(CH₃)₂CF₃ CD₃ CD₃ H 565. CD₂C(CH₃)₂CF₃ CD₃ H CD₃ 566. CD₂C(CH₃)₂CF₃ H CD₃ CD₃ 567. CD₂C(CH₃)₂CF₃ CD₃ CD₃ CD₃ 568. H CD₂C(CH₃)₂CF₃ H H 569. CD₃ CD₂C(CH₃)₂CF₃ H H 570. H CD₂C(CH₃)₂CF₃ CD₃ H 571. H CD₂C(CH₃)₂CF₃ H CD₃ 572. CD₃ CD₂C(CH₃)₂CF₃ CD₃ H 573. CD₃ CD₂C(CH₃)₂CF₃ H CD₃ 574. H CD₂C(CH₃)₂CF₃ CD₃ CD₃ 575. CD₃ CD₂C(CH₃)₂CF₃ CD₃ CD₃ 576. H H CD₂C(CH₃)₂CF₃ H 577. CD₃ H CD₂C(CH₃)₂CF₃ H 578. H CD₃ CD₂C(CH₃)₂CF₃ H 579. H H CD₂C(CH₃)₂CF₃ CD₃ 580. CD₃ CD₃ CD₂C(CH₃)₂CF₃ H 581. CD₃ H CD₂C(CH₃)₂CF₃ CD₃ 582. H CD₃ CD₂C(CH₃)₂CF₃ CD₃ 583. CD₃ CD₃ CD₂C(CH₃)₂CF₃ CD₃ 584. CD₂CH₂CF₃ H H H 585. CD₂CH₂CF₃ CD₃ H H 586. CD₂CH₂CF₃ H CD₃ H 587. CD₂CH₂CF₃ H H CD₃ 588. CD₂CH₂CF₃ CD₃ CD₃ H 589. CD₂CH₂CF₃ CD₃ H CD₃ 590. CD₂CH₂CF₃ H CD₃ CD₃ 591. CD₂CH₂CF₃ CD₃ CD₃ CD₃ 592. H CD₂CH₂CF₃ H H 593. CD₃ CD₂CH₂CF₃ H H 594. H CD₂CH₂CF₃ CD₃ H 595. H CD₂CH₂CF₃ H CD₃ 596. CD₃ CD₂CH₂CF₃ CD₃ H 597. CD₃ CD₂CH₂CF₃ H CD₃ 598. H CD₂CH₂CF₃ CD₃ CD₃ 599. CD₃ CD₂CH₂CF₃ CD₃ CD₃ 600. H H CD₂CH₂CF₃ H 601. CD₃ H CD₂CH₂CF₃ H 602. H CD₃ CD₂CH₂CF₃ H 603. H H CD₂CH₂CF₃ CD₃ 604. CD₃ CD₃ CD₂CH₂CF₃ H 605. CD₃ H CD₂CH₂CF₃ CD₃ 606. H CD₃ CD₂CH₂CF₃ CD₃ 607. CD₃ CD₃ CD₂CH₂CF₃ CD₃ 608.

H H H 609.

CD₃ H H 610.

H CD₃ H 611.

H H CD₃ 612.

CD₃ CD₃ H 613.

CD₃ H CD₃ 614.

H CD₃ CD₃ 615.

CD₃ CD₃ CD₃ 616. H

H H 617. CD₃

H H 618. H

CD₃ H 619. H

H CD₃ 620. CD₃

CD₃ H 621. CD₃

H CD₃ 622. H

CD₃ CD₃ 623. CD₃

CD₃ CD₃ 624. H H

H 625. CD₃ H

H 626. H CD₃

H 627. H H

CD₃ 628. CD₃ CD₃

H 629. CD₃ H

CD₃ 630. H CD₃

CD₃ 631. CD₃ CD₃

CD₃ 632.

H H H 633.

CD₃ H H 634.

H CD₃ H 635.

H H CD₃ 636.

CD₃ CD₃ H 637.

CD₃ H CD₃ 638.

H CD₃ CD₃ 639.

CD₃ CD₃ CD₃ 640. H

H H 641. CD₃

H H 642. H

CD₃ H 643. H

H CD₃ 644. CD₃

CD₃ H 645. CD₃

H CD₃ 646. H

CD₃ CD₃ 647. CH₃

CD₃ CD₃ 648. H H

H 649. CD₃ H

H 650. H CD₃

H 651. H H

CD₃ 652. CD₃ CD₃

H 653. CD₃ H

CD₃ 654. H CD₃

CD₃ 655. CD₃ CD₃

CD₃ 656.

H H H 657.

CD₃ H H 658.

H CD₃ H 659.

H H CD₃ 660.

CD₃ CD₃ H 661.

CD₃ H CD₃ 662.

H CD₃ CD₃ 663.

CD₃ CD₃ CD₃ 664. H

H H 665. CD₃

H H 666. H

CD₃ H 667. H

H CD₃ 668. CD₃

CD₃ H 669. CD₃

H CD₃ 670. H

CD₃ CD₃ 671. CD₃

CD₃ CD₃ 672. H H

H 673. CD₃ H

H 674. H CD₃

H 675. H H

CD₃ 676. CD₃ CD₃

H 677. CD₃ H

CD₃ 678. H CD₃

CD₃ 679. CD₃ CD₃

CD₃ 680.

H H H 681.

CD₃ H H 682.

H CD₃ H 683.

H H CD₃ 684.

CD₃ CD₃ H 685.

CD₃ H CD₃ 686.

H CD₃ CD₃ 687.

CD₃ CD₃ CD₃ 688. H

H H 689. CD₃

H H 690. H

CD₃ H 691. H

H CD₃ 692. CD₃

CD₃ H 693. CD₃

H CD₃ 694. H

CD₃ CD₃ 695. CD₃

CD₃ CD₃ 696. H H

H 697. CD₃ H

H 698. H CD₃

H 699. H H

CD₃ 700. CD₃ CD₃

H 701. CD₃ H

CD₃ 702. H CD₃

CD₃ 703. CD₃ CD₃

CD₃ 704.

H H H 705.

CD₃ H H 706.

H CD₃ H 707.

H H CD₃ 708.

CD₃ CD₃ H 709.

CD₃ H CD₃ 710.

H CD₃ CD₃ 711.

CD₃ CD₃ CD₃ 712. H

H H 713. CD₃

H H 714. H

CD₃ H 715. H

H CD₃ 716. CD₃

CD₃ H 717. CD₃

H CD₃ 718. H

CD₃ CD₃ 719. CD₃

CD₃ CD₃ 720. H H

H 721. CD₃ H

H 722. H CD₃

H 723. H H

CD₃ 724. CD₃ CD₃

H 725. CD₃ H

CD₃ 726. H CD₃

CD₃ 727. CD₃ CD₃

CD₃ 728.

H H H 729.

CD₃ H H 730.

H CD₃ H 731.

H H CD₃ 732.

CH₃ CH₃ H 733.

CD₃ H CD₃ 734.

H CD₃ CD₃ 735.

CD₃ CD₃ CD₃ 736. H

H H 737. CD₃

H H 738. H

CD₃ H 739. H

H CD₃ 740. CD₃

CD₃ H 741. CD₃

H CD₃ 742. H

CD₃ CD₃ 743. CD₃

CD₃ CD₃ 744. H H

H 745. CD₃ H

H 746. H CD₃

H 747. H H

CD₃ 748. CD₃ CD₃

H 749. CD₃ H

CD₃ 750. H CD₃

CD₃ 751. CD₃ CD₃

CD₃ 752. CD(CH₃)₂ H CD₂CH₃ H 753. CD(CH₃)₂ H CD(CH₃)₂ H 754. CD(CH₃)₂ H CD₂CH(CH₃)₂ H 755. CD(CH₃)₂ H C(CH₃)₃ H 756. CD(CH₃)₂ H CD₂C(CH₃)₃ H 757. CD(CH₃)₂ H CD₂CH₂CF₃ H 758. CD(CH₃)₂ H CD₂C(CH₃)₂CF₃ H 759. CD(CH₃)₂ H

H 760. CD(CH₃)₂ H

H 761. CD(CH₃)₂ H

H 762. CD(CH₃)₂ H

H 763. CD(CH₃)₂ H

H 764. CD(CH₃)₂ H

H 765. C(CH₃)₃ H CD₂CH₃ H 766. C(CH₃)₃ H CD(CH₃)₂ H 767. C(CH₃)₃ H CD₂CH(CH₃)₂ H 768. C(CH₃)₃ H C(CH₃)₃ H 769. C(CH₃)₃ H CD₂C(CH₃)₃ H 770. C(CH₃)₃ H CD₂CH₂CF₃ H 771. C(CH₃)₃ H CD₂C(CH₃)₂CF₃ H 772. C(CH₃)₃ H

H 773. C(CH₃)₃ H

H 774. C(CH₃)₃ H

H 775. C(CH₃)₃ H

H 776. C(CH₃)₃ H

H 777. C(CH₃)₃ H

H 778. CD₂C(CH₃)₃ H CD₂CH₃ H 779. CD₂C(CH₃)₃ H CD(CH₃)₂ H 780. CD₂C(CH₃)₃ H CD₂CH(CH₃)₂ H 781. CD₂C(CH₃)₃ H C(CH₃)₃ H 782. CD₂C(CH₃)₃ H CD₂C(CH₃)₃ H 783. CD₂C(CH₃)₃ H CD₂CH₂CF₃ H 784. CD₂C(CH₃)₃ H CD₂C(CH₃)₂CF₃ H 785. CD₂C(CH₃)₃ H

H 786. CD₂C(CH₃)₃ H

H 787. CD₂C(CH₃)₃ H

H 788. CD₂C(CH₃)₃ H

H 789. CD₂C(CH₃)₃ H

H 790. CD₂C(CH₃)₃ H

H 791.

H CD₂CH₃ H 792.

H CD(CH₃)₂ H 793.

H CD₂CH(CH₃)₂ H 794.

H C(CH₃)₃ H 795.

H CD₂C(CH₃)₃ H 796.

H CD₂CH₂CF₃ H 797.

H CD₂C(CH₃)₂CF₃ H 798.

H

H 799.

H

H 800.

H

H 801.

H

H 802.

H

H 803.

H

H 804.

H CD₂CH₃ H 805.

H CD(CH₃)₂ H 806.

H CD₂CH(CH₃)₂ H 807.

H C(CH₃)₃ H 808.

H CD₂C(CH₃)₃ H 809.

H CD₂CH₂CF₃ H 810.

H CD₂C(CH₃)₂CF₃ H 811.

H

H 812.

H

H 813.

H

H 814.

H

H 815.

H

H 816.

H

H 817.

H CD₂CH₃ H 818.

H CD(CH₃)₂ H 819.

H CD₂CH(CH₃)₂ H 820.

H C(CH₃)₃ H 821.

H CD₂C(CH₃)₃ H 822.

H CD₂CH₂CF₃ H 823.

H CD₂C(CH₃)₂CF₃ H 824.

H

H 825.

H

H 826.

H

H 827.

H

H 828.

H

H 829.

H

H 830.

H CD₂CH₃ H 831.

H CD(CH₃)₂ H 832.

H CD₂CH(CH₃)₂ H 833.

H C(CH₃)₃ H 834.

H CD₂C(CH₃)₃ H 835.

H CD₂CH₂CF₃ H 836.

H CD₂C(CH₃)₂CF₃ H 837.

H

H 838.

H

H 839.

H

H 840.

H

H 841.

H

H 842.

H

H 843.

H CD₂CH₃ H 844.

H CD(CH₃)₂ H 845.

H CD₂CH(CH₃)₂ H 846.

H C(CH₃)₃ H 847.

H CD₂C(CH₃)₃ H 848.

H CD₂CH₂CF₃ H 849.

H CD₂C(CH₃)₂CF₃ H 850.

H

H 851.

H

H 852.

H

H 853.

H

H 854.

H

H 855.

H

H

.

15. An organic light-emitting device (OLED) comprising:

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, comprising a first compound;

wherein the first compound is capable of functioning as a phosphorescent emitter in an organic light emitting device at room temperature;

wherein the first compound has at least one aromatic ring and at least one substituent R;

wherein each of the at least one substituent R is directly bonded to one of the at least one aromatic ring;

wherein each of the at least one substituent R has the formula of

wherein

(a) G¹ is selected from the group consisting of NR¹, SiR¹R², Ge R¹R², alkyl, cycloalkyl, and combinations thereof; and G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³;

(b) G¹ is a direct bond; and G² is a non-aromatic spiro polycyclic group, which can be further substituted by one or more R³; or

(c) G¹ is selected from the group consisting of: direct bond, NR¹, SiR¹R², Ge R¹R², alkyl, cycloalkyl, and combinations thereof; G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³; and R is directly bonded to an aromatic ring selected from the group consisting of phenyl, pyridine, and triazine, which can be further fused to other rings;

wherein R¹, R², and R³ are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

wherein each G¹ and G² can be independently, partially or fully deuterated.

16. The OLED of claim 15, wherein the OLED is incorporated into a device selected from the group consisting of a consumer product, an electronic component module, and a lighting panel.

17. The OLED of claim 15, wherein the organic layer is an emissive layer and the compound is an emissive dopant or a non-emissive dopant.

18. The OLED of claim 15, wherein the organic layer further comprises a host, wherein host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, aza-triphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.

19. The OLED of claim 15, wherein the organic layer further comprises a host, wherein the host is selected from the group consisting of:

and combinations thereof.

20. A formulation comprising a composition including a first compound;

wherein the first compound is capable of functioning as a phosphorescent emitter in an organic light emitting device at room temperature;

wherein the first compound has at least one aromatic ring and at least one substituent R;

wherein each of the at least one substituent R is directly bonded to one of the at least one aromatic ring;

wherein each of the at least one substituent R has the formula of

wherein

(a) G¹ is selected from the group consisting of NR¹, SiR¹R², Ge R¹R², alkyl, cycloalkyl, and combinations thereof; and G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³;

(b) G¹ is a direct bond; and G² is a non-aromatic spiro polycyclic group, which can be further substituted by one or more R³; or

(c) G¹ is selected from the group consisting of: direct bond, NR¹, SiR¹R², Ge R¹R², alkyl, cycloalkyl, and combinations thereof; G² is a non-aromatic polycyclic group, which can be further substituted by one or more R³; and R is directly bonded to an aromatic ring selected from the group consisting of phenyl, pyridine, and triazine, which can be further fused to other rings;

wherein R¹, R², and R³ are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

wherein each G¹ and G² can be independently, partially or fully deuterated.

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