JP2001039906A - Compound bearing tetrahydronaphthalene skeleton and liquid crystal containing the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a novel compound bearing a tetrahydro-naphthalene skeleton that has a particularly wide range of liquid crystal temperature and is useful as a component of liquid crystal composition that needs a low-voltage driving and high-speed response. SOLUTION: This novel compound is represented by formula I [R is a (substituted) 1-20C alkyl; the linkage group V is a single bond, O or the like, the linkage groups W, X, Y are each a single bond, -CH2CH2-; Z is H, fluorine, chlorine or the like; Q1-Q3 are each H or fluorine; rings A and B are each trans-1,4-cyclohexylene or the like; ring C is 1,4-phenylene or the like; and (m) and (n) are each 0, 1], typically 6-propyl-2-(3,4,5-trifluoro-phenyl)-1,2,3,4- tetrahydronaphthalene. The compound of formula I is prepared, for example, by allowing a ketone of formula II [R2 is a (substituted) 1-20C alkyl] to react with a reactant of formula III (Z1 is H, fluorine, chlorine or the like; and Mtl1 is a metal ion such as Li) to form an alcohol of formula IV, then heating the alcohol of formula IV in the presence of an acid catalyst to form a dihydronaphthalene and hydrogenating the dihydronaphthalene.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

The present invention relates to a novel liquid crystalline compound which is a tetrahydronaphthalene derivative useful as an electro-optical liquid crystal display material, a liquid crystal composition containing the same, and a liquid crystal display device using the same.

[0002]

2. Description of the Related Art Liquid crystal display elements have been used in various measuring instruments such as watches and calculators, panels for automobiles, word processors, electronic organizers, printers, computers, televisions and the like. Typical liquid crystal display methods are TN (twisted nematic), STN (super twisted nematic), DS (dynamic light scattering), GH (guest / host), and FLC that can respond at high speed. (Ferroelectric liquid crystal) and AFLC (anti-ferroelectric liquid crystal). As a driving method, a multiplex driving has been generally used instead of the conventional static driving, and a simple matrix method, more recently, an active matrix method has been put to practical use.

As the liquid crystal material used for these, a great variety of liquid crystal compounds have been synthesized so far, and these are used according to the display system, the driving system, or the application. However, demands for improving the performance of liquid crystal display elements (improvement of display quality, enlargement of display screen, etc.) are increasing year by year, and new liquid crystal compounds are being developed to satisfy the demands.

A liquid crystal compound is usually composed of a central skeleton part called a core and terminal parts on both sides. Usually, as the ring structure constituting the core portion of the liquid crystal compound, a 1,4-phenylene group (may be substituted by one or two halogen atoms, a cyano group, a methyl group, etc.) and trans-1,4 -Cyclohexylene groups make up the majority. However
Liquid crystalline compounds composed only of 1,4-phenylene groups and trans-1,4-cyclohexylene groups are limited in their types and properties, and cannot satisfy the above requirements by themselves. It is.

The ring structure other than the 1,4-phenylene group and the trans-1,4-cyclohexylene group includes, for example, pyridine-
Heterocyclic systems such as 2,5-diyl group, pyrimidine-2,5-diyl group, 1,3-dioxane-trans-2,5-diyl group, and trans
-Decalin-2,6-diyl group, naphthalene-2,6-diyl group,
Tetrahydronaphthalene-2-6-diyl group, bicyclo [2.2.
2] octane-1,4-diyl group, spiro [3.3] heptane-2,6-
Condensed ring systems such as diyl groups are also being studied,
At present, only a few are practically used due to problems (technology, cost, etc.) and stability problems.

In these condensed ring systems, although the tetrahydronaphthalene-2-6-diyl group has a ring structure which has been reported for a long time, the synthesis examples thereof are extremely few, and the liquid crystal (phase transition) Properties other than temperature), in particular, properties as a nematic liquid crystal are hardly known. (Recently, it has been reported that optically active alcohol esters of tetrahydronaphthalene-2-carboxylic acid exhibit interesting properties as smectic liquid crystals, especially ferroelectric liquid crystals and antiferroelectric liquid crystals.) At least one of the portions is a chain (side chain) group, and in the case of a so-called p-type liquid crystal having a positive dielectric anisotropy, the other is often a polar group.

In order to reduce the driving voltage in the TN or STN display system, a compound (p-type) having a large positive dielectric anisotropy is required. For such a purpose, a compound having a cyano group at the molecular terminal and further containing one or more fluorine atoms in the same direction of the molecule is usually used. Most of the currently reported tetrahydronaphthalene derivatives are so-called n-type liquid crystals having a dielectric anisotropy of 0 to negative. Only compounds having a phenyl tetrahydronaphthalene-2-carboxylate skeleton have been reported, and there is no description of electro-optical properties or application examples (Helv. Chim. Acta, 65, 1
318-1330 (1982).

As the p-type compound to be used in the above-mentioned active matrix driving method, a compound having only a fluorine atom, a fluoroalkoxyl group or a fluoroalkyl group as a polar group is used. There are no reports. In addition, a liquid crystal compound that is a tetrahydronaphthalene derivative generally has poor compatibility with other liquid crystal compounds in many cases.However, in order to improve the compatibility, a lateral substituent (particularly, a fluorine atom (Preferably) is considered to be effective. In the use in the active matrix system, substitution with a fluorine atom is considered to be effective even when a polar group is directly introduced into a tetrahydronaphthalene ring. There is no example of such a fluorotetralin derivative actually synthesized, and it is not possible to estimate what characteristic values such a compound has.

Introducing an alkenyl group in a liquid crystal compound in place of an alkyl group usually used as a side chain portion has improved liquid crystallinity, reduced viscosity, and improved sharpness in display characteristics. It is known that an effect can be obtained. However, these alkenyl groups are usually introduced in a form directly linked to a cyclohexane ring, and no compound introduced into an aromatic ring, particularly a tetrahydronaphthalene ring, has been reported.

Similarly, no tetrahydronaphthalene derivative having an alkoxylalkyl group, fluoroalkyl group, fluoroalkenyl group, fluoroalkenyloxy group or the like as a side chain has been reported.

In the liquid crystal compound, the linking group having a ring structure in the core may be a 1,2-ethylene group (-CH ₂ CH _2- ) or an ethynylene group other than a single bond or an ester group (-COO-, -OCO-). (-C≡C
Many divalent organic groups such as-) and a difluoroethenylene group (-CF = CF-) are known, but not a tetrahydronaphthalene derivative.

[0012]

An object of the present invention is to provide a novel compound having a tetrahydronaphthalene skeleton, and to provide a practical liquid crystal composition using the compound. .

[0013]

Means for Solving the Problems The inventors of the present invention have conducted intensive studies to solve the above-mentioned problems, and as a result, compounds having a tetrahydronaphthalene skeleton can be easily produced, and many of them exhibit liquid crystallinity over a wide temperature range. In addition, regardless of the presence or absence of liquid crystallinity alone, when this is added to the composition, without slowing the response speed (in many cases speeding up the response speed), without significantly narrowing the target liquid crystal temperature range.
(In many cases, the temperature range was widened), they found that they could be mixed without layer separation, and completed the present invention.

That is, the present invention provides: General formula (I)

[0015]

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(Wherein R is 1-7 fluorine atoms or carbon atom
It may be substituted by an alkoxyl group having 1 to 7 children
And may have a saturated or unsaturated carbon number of 1
Represents an alkyl group of ~ 20, and the connecting group V is a single bond,
Atom, sulfur atom, -COO-, -OCO-, -OCOO-, -COS- or-
Represents SCO-, wherein the linking groups W, X and Y are each independently
Single bond, -CH_TwoCH_Two-, -CH = CH-, -CH (CH_Three) CH_Two-, -CH_TwoCH (CH
_Three)-, -CH (CH_Three) CH (CH_Three)-, -CF _TwoCF_Two-, -CF = CF-, -CH_TwoO-,
-OCH_Two-, -OCH (CH_Three)-, -CH (CH_Three) O-, -C≡C-, -CF_TwoO-, -O
CF_Two-, -COO-, -OCO-, -COS- or -SCO-, and Z is
Nitrogen atom, chlorine atom, cyano group, cyanato group, trifur
Oromethyl group, trifluoromethoxy group, difluoro
Represents a toxic group or a hydrogen atom, Q¹, Q^TwoAnd Q^ThreeIs it
Each independently represents a hydrogen atom or a fluorine atom, and represents a ring A or
And ring B are each independently trans-1,4-cyclohexyl
Len group, trans-decahydronaphthalene-2,6-diyl
Group, trans-1,3-dioxane-2,5-diyl group or one
Or 1,4-phenylene which may be substituted by two fluorine atoms
Len group, pyridine-2,5-diyl group, pyrimidine-2,5-diyl
Group, pyrazine-2,5-diyl group, pyridazine-3,6-diyl
Group and one or two fluorine atoms
Represents a naphthalene-2,6-diyl group, and ring C is one or two
1,4-phenylene groups which may be substituted with
Or a group which may be substituted by one or two fluorine atoms
Represents a phthalene-2,6-diyl group, m and n are each independently
Stands for 0 or 1. However, if Z is a hydrogen atom,
Ring C is 1,4 substituted by one or two fluorine atoms
-Substituted with a phenylene group or one or two fluorine atoms
Represents an optionally substituted naphthalene-2,6-diyl group, Q¹, Q
^TwoAnd Q^ThreeAre all hydrogen atoms, and m and n are
Are all 0, Y is -COO-, and Z is a fluorine atom
Is, ring C is substituted with one or two fluorine atoms
1,4-phenylene group or one or two fluorines
The naphthalene-2,6-diyl group which may be substituted
Then Q¹, Q^TwoAnd Q^ThreeAre all hydrogen atoms, and m and
And n are both 0, and Y is a single bond or -COO-
And when Z is a cyano group, one or two rings C
1,4-phenylene group or one substituted with a fluorine atom
Or naphthalene optionally substituted by two fluorine atoms
Represents a -2,6-diyl group. Tetrahydronaphtha represented by)
Len derivative. I will provide a.

Further, the present invention provides a liquid crystal composition containing at least one compound of the above general formula (I), and a liquid crystal element comprising the same, that is, 2. 2. The compound according to 1 above, wherein m is 0 in the general formula (I). 3. 2. The compound according to the above 1, wherein n is 0 in the general formula (I). 4. 4. The compound according to any one of the above items 1 to 3, wherein in formula (I), Q ¹ and Q ² are both hydrogen atoms. 5. General formula (I) in the linking group W, X and Y are each independently a single bond or -CH ₂ CH ₂ - the fourth compound according at which selected from. 6. In the general formula (I), ring A and ring B are each independently substituted with a trans-1,4-cyclohexylene group, trans-decahydronaphthalene-2,6-diyl group or one or two fluorine atoms The above 1 to 1 which is selected from 1,4-phenylene group and naphthalene-2,6-diyl group
5. The compound according to 5. 7. 1,4-phenylene group or naphthalene-2,6 wherein ring C is substituted by one or two fluorine atoms in the general formula (I)
-The compound of any one of the above 1 to 6, which is selected from a diyl group. 8. Wherein Z in the general formula (I) is selected from a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group or a hydrogen atom
The compound of any one of 1 to 7. 9. 9. The compound according to the above item 8, wherein in the general formula (I), Z is selected from a fluorine atom or a trifluoromethoxy group. 10. The above wherein V represents a single bond in the general formula (I)
The compound according to any one of 1 to 9 above. 11. 11. The compound according to any one of the above 1 to 10, wherein R is selected from a linear alkyl group having 1 to 10 carbon atoms in the general formula (I). 12. A liquid crystal composition comprising one or more compounds of the general formula (I) according to any one of the above 1 to 11. 13. The above used for active matrix drive
13. The liquid crystal composition according to 12. 14． 14. A liquid crystal device comprising the liquid crystal composition according to 13 above as a constituent element. 15. 15. An active matrix driven liquid crystal display device using the liquid crystal composition according to the above 14. I will provide a.

[0018]

BEST MODE FOR CARRYING OUT THE INVENTION As described above, in the compound of the above general formula (I), m, n, R, V, W, X, Y, Z, Q ¹ ,
Examples of Q ² , Q ³ , ring A, ring B and ring C include the following.

M and n are 0 or 1, and m = n = 0 and m = 0
Any combination of n = 0 and m = n = 1 at n = 1, m = 1 is possible, but if m = n = 1, the melting point and viscosity increase, so m = n = 0, m =
A combination of 0 at n = 1 and m = 1 at n = 0 is preferred.

R- represents a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, an undecyl group,
Dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, linear saturated alkyl group of eicosyl group, 1-methylethyl group, 1-methylpropyl group, 2-methylpropyl Group, 1,2-dimethylpropyl group, 1-methylbutyl group, 2-methylbutyl group, 3-methylbutyl group, 1,2-dimethylbutyl group, 1,3-dimethylbutyl group, 2,3-dimethylbutyl group, 1 -Methylpentyl group, 2-methylpentyl group, 3-
Methylpentyl group, 4-methylpentyl group, 1,2-dimethylpentyl group, 1,3-dimethylpentyl group, 1-methylhexyl group, 2-methylhexyl group, 3-methylhexyl group, 4-methylhexyl group, 5-methylhexyl, 1,2-dimethylhexyl, 1,3-dimethylhexyl, 1-methylheptyl, 2-methylheptyl, 3-methylheptyl, 4-methylheptyl, 5-methylheptyl Group, 6-methylheptyl group, 1,2-dimethylheptyl group, 1,3-dimethylheptyl group, 1-methyloctyl group, 2-methyloctyl group, 3-methyloctyl group, 4-methyloctyl group, 5- Methyloctyl, 6-methyloctyl, 7-methyloctyl, 1,2-dimethyloctyl, 1,3-dimethyloctyl, 1-methylnonyl, 2-methylnonyl, 3-methylnonyl, 4-methylnonyl Group, 5-methylnonyl group, 6-methylnonyl Group,
7-methylnonyl group, 8-methylnonyl group, 1,2-dimethylnonyl group, 1,3-dimethylnonyl group, 1-methyldecyl group, 2-
Methyldecyl group, 3-methyldecyl group, 1,2-dimethyldecyl group, 1,3-dimethyldecyl group, 1-methylundecyl group,
2-methylundecyl group, 3-methylundecyl group, 1,2-dimethylundecyl group, 1,3-dimethylundecyl group, 1-methyldodecyl group, 2-methyldodecyl group, 3-methyldodecyl group, 1,2-dimethyldodecyl group, 1,3-dimethyldodecyl group, 1-methyltridecyl group, 2-methyltridecyl group, 3-
Methyltridecyl group, 1,2-dimethyltridecyl group, 1,3-
Branched saturated alkyl groups such as dimethyltridecyl group, vinyl group, trans-1-propenyl group, 2-propenyl group, trans-1-butenyl group, trans-2-butenyl group, 3-butenyl group, trans-1- Pentenyl group, trans-2-pentenyl group, trans-3-pentenyl group, 4-pentenyl group,
Trans-1-hexenyl group, trans-2-hexenyl group,
Trans-3-hexenyl group, trans-4-hexenyl group,
5-hexenyl group, trans-1-heptenyl group, trans-
2-heptenyl group, trans-3-heptenyl group, trans-
4-heptenyl group, trans-5-heptenyl group, 6-heptenyl group, trans-1-octenyl group, trans-2-octenyl group, trans-3-octenyl group, trans-4-octenyl group, trans-5-octenyl Group, trans-6-octenyl group, 7-octenyl group, trans-1-nonenyl group, 8-
Nonenyl group, trans-1-decenyl group, 9-decenyl group,
Trans-1-undecenyl group, 10-undecenyl group, trans-1-dodecenyl group, 11-dodecenyl group, ethynyl group,
1-propynyl group, 2-propynyl group, 1-butynyl group, 2-butynyl group, 3-butynyl group, 1-pentenyl group, 2-pentenyl group, 3-pentenyl group, 4-pentenyl group, 1-hexynyl group, 2-hexynyl group, 3-hexynyl group, 4-hexynyl group, 5-hexynyl group, 1-heptynyl group, 2-heptynyl group, 3-heptynyl group, 4-heptynyl group, 5-heptynyl group, 6-heptynyl group, 1-octynyl group, 2-octynyl group, 3-octynyl group, 4-octynyl group, 5-octynyl group, 6-octynyl group, 7-octynyl group, 1-noninyl group,
Unsaturated alkyl groups such as 8-noninyl group, 1-decynyl group, 9-decynyl group, 1-undecynyl group, 10-undecynyl group, 1-dodecynyl group, 11-dodecynyl group, 1-tridecynyl group and 12-tridecynyl group , Fluoromethyl group, difluoromethyl group, trifluoromethyl group, 2-fluoromethyl group,
2,2-difluoroethyl group, 2,2,2-trifluoroethyl group, 1,1,2,2,2-pentafluoroethyl group, 3-fluoropropyl group, 2-fluoropropyl group, 1-fluoropropyl Group, 3,3-difluoropropyl group, 3,3,3-trifluoropropyl group, 2,2,3,3-tetrafluoropropyl group, 2,2,3,
3,3-pentafluoropropyl group, 1,1,2,2,3,3,3-heptafluoropropyl group, 4-fluorobutyl group, 3-fluorobutyl group, 2-fluorobutyl group, 1-fluorobutyl Group,
4,4-difluorobutyl group, 4,4,4-trifluorobutyl group, 3,3,4,4-tetrafluorobutyl group, 3,3,4,4,4-pentafluorobutyl group, 2,2 , 3,3,4,4,4-heptafluorobutyl, 5-fluoropentyl, 4-fluoropentyl, 3-fluoropentyl, 2-fluoropentyl, 1-
Fluoropentyl group, 5,5-difluoropentyl group, 5,5,
5-trifluoropentyl group, 4,4,5,5-tetrafluoropentyl group, 4,4,5,5,5-pentafluoropentyl group, 3,3,
4,4,5,5,5-heptafluoropentyl group, 6-fluorohexyl group, 5-fluorohexyl group, 4-fluorohexyl group, 3-fluorohexyl group, 2-fluorohexyl group, 1-
Fluorohexyl group, 6,6-difluorohexyl group, 6,6,
6-trifluorohexyl group, 5,5,6,6,6-pentafluorohexyl group, 4,4,5,5,6,6,6-heptafluorohexyl group, 7-fluoroheptyl group, 6-fluoro Heptyl group, 5-
Fluoroheptyl group, 4-fluoroheptyl group, 3-fluoroheptyl group, 2-fluoroheptyl group, 1-fluoroheptyl group, 7,7-difluoroheptyl group, 7,7,7-trifluoroheptyl group, 6,6 , 7,7-tetrafluoroheptyl group, 6,
6,7,7,7-pentafluoroheptyl group, 5,5,6,6,7,7,7-heptafluoroheptyl group, 8-fluorooctyl group, 7-fluorooctyl group, 6-fluorooctyl group, 5-fluorooctyl group, 4-fluorooctyl group, 3-fluorooctyl group, 2-fluorooctyl group, 1-fluorooctyl group,
8,8-difluorooctyl group, 8,8,8-trifluorooctyl group, 7,7,8,8-tetrafluorooctyl group, 7,7,8,8,8-
Pentafluorooctyl group, fluorine-substituted alkyl group such as 6,6,7,7,8,8,8-heptafluorooctyl group,

2,2-difluoroethenyl group, (E) -1,2-difluoroethenyl group, (Z) -1,2-difluoroethenyl group,
3-difluoro-2-propenyl group, (E) -2,3-difluoro-2-
Propenyl group, (Z) -2,3-difluoro-2-propenyl group,
4,4-difluoro-3-butenyl group, (E) -3,4-difluoro-3-
Butenyl group, (Z) -3,4-difluoro-3-butenyl group, 5,5-
Difluoro-4-pentenyl group, (E) -4,5-difluoro-4-pentenyl group, (Z) -4,5-difluoro-4-pentenyl group, 6,6
-Difluoro-5-hexenyl group, (E) -5,6-difluoro-5-
Hexenyl group, (Z) -5,6-difluoro-5-hexenyl group,
(E) -1,2-difluoro-1-propenyl group, (E) -1,2-difluoro-1-butenyl group, (E) -1,2-difluoro-1-pentenyl group, (E) -1 , 2-difluoro-1-hexenyl group, (Z) -1-fluoro-1-propenyl group, (Z) -1-fluoro-1-butenyl group,
(Z) -1-fluoro-1-pentenyl group, (Z) -1-fluoro-1-hexenyl group, (Z) -2-fluoro-1-propenyl group, (Z) -2-
Fluoro-1-butenyl group, (Z) -2-fluoro-1-pentenyl group, (Z) -2-fluoro-1-hexenyl group, (E) -2,3-difluoro-2-butenyl group, (E ) -2,3-difluoro-2-pentenyl group, (E) -2,3-difluoro-2-hexenyl group, (Z) -2-fluoro-2-butenyl group, (Z) -2-fluoro-2 -Pentenyl group,
(Z) -2-fluoro-2-hexenyl group, (Z) -3-fluoro-2-butenyl group, (Z) -3-fluoro-2-pentenyl group, (Z) -3-fluoro-2-hexenyl Groups such as fluorine-substituted unsaturated alkyl groups, methoxymethyl groups, ethoxymethyl groups, propoxymethyl groups, butoxymethyl groups, pentyloxymethyl groups, hexyloxymethyl groups, heptyloxymethyl groups, 1-methoxyethyl groups, 1-ethoxy Ethyl group, 1-propoxyethyl group, 1-butoxyethyl group, 1-pentyloxyethyl group, 1-hexyloxyethyl group, 1-heptyloxyethyl group, 2-methoxyethyl group, 2-ethoxyethyl group, 2- Propoxyethyl group, 2-butoxyethyl group, 2-pentyloxyethyl group, 2-hexyloxyethyl group, 2-
Heptyloxyethyl group, 1-methoxypropyl group, 1-ethoxypropyl group, 1-propoxypropyl group, 1-butoxypropyl group, 1-pentyloxypropyl group, 1-hexyloxypropyl group, 1-heptyloxypropyl group, 2-
Methoxypropyl group, 2-ethoxypropyl group, 2-propoxypropyl group, 2-butoxypropyl group, 2-pentyloxypropyl group, 2-hexyloxypropyl group, 2-heptyloxypropyl group, 3-methoxypropyl group, 3 -Ethoxypropyl group, 3-propoxypropyl group, 3-butoxypropyl group, 3-pentyloxypropyl group, 3-hexyloxypropyl group, 3-heptyloxypropyl group, 4-methoxybutyl group, 4-ethoxybutyl group, 4-propoxybutyl group, 4-butoxybutyl group, 4-pentyloxybutyl group, 4-hexyloxybutyl group, 4-heptyloxybutyl group, 5-methoxypentyl group, 5-ethoxypentyl group,
5-propoxypentyl group, 5-butoxypentyl group, 5-pentyloxypentyl group, 5-hexyloxypentyl group, 5-heptyloxypentyl group, 6-methoxyhexyl group, 6-ethoxyhexyl group, 6-propoxyhexyl group ,
6-butoxyhexyl group, 6-pentyloxyhexyl group,
6-hexyloxyhexyl group, alkoxyl group-substituted alkyl groups such as 6-heptyloxyhexyl group and the like, among which straight-chain saturated alkyl groups and unsaturated alkyl groups are preferred, methyl group, ethyl group, propyl group, butyl Group, pentyl group, hexyl group, heptyl group, octyl group, vinyl group, trans-1-propenyl group, 2-propenyl group, trans-1-butenyl group, trans-2-butenyl group, 3-butenyl group, trans- 1-pentenyl group, trans-2-pentenyl group, trans-3-pentenyl group, 4-pentenyl group, trans-1-hexenyl group, trans-2-hexenyl group, trans-3-hexenyl group, trans-4-hexenyl Group, 5-hexenyl group, trans-1-heptenyl group, trans-2-heptenyl group, trans-3-heptenyl group, trans-4-heptenyl group, trans-5-heptenyl Group, 6-heptenyl group is particularly preferred.

Examples of the linking group V include a single bond, an oxygen atom, a sulfur atom, -COO-, -OCO-, -OCOO-, -COS-, and -SCO-, with a single bond and an oxygen atom being preferred. Bonding is particularly preferred.

W, X and Y each represent a single bond, -CH ₂ CH
_{2 -, - CH = CH -} , - CH (CH 3) CH 2 -, - CH 2 CH (CH 3) -, - CH (CH 3) C
H (CH ₃ )-, -CF ₂ CF _2- , -CF = CF-, -CH ₂ O-, -OCH _2- , -OCH (C
H ₃ )-, -CH (CH ₃ ) O-, -C≡C-, -CF ₂ O-, -OCF _2- , -COO-,-
OCO -, - COS -, - SCO- . Of these, a single _{bond, -CH 2 CH 2 -, -} C≡C- , more preferably a single bond is particularly preferred.

Examples of Z include a fluorine atom, a chlorine atom, a cyano group, a cyanato group, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group, and a hydrogen atom. Groups are preferred, and fluorine and trifluoromethoxy groups are particularly preferred.

Q ¹ , Q ² and Q ³ represent a hydrogen atom or a fluorine atom. When Q ¹ , Q ² and Q ³ are a hydrogen atom, when Q ¹ and Q ² are a hydrogen atom and Q ³ is a fluorine atom Is preferred.

The ring A and the ring B include the structures shown in Formula Group 1.

[0027]

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Among them, the structures described in Formula 2 are preferable.

[0029]

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Among them, the structure described in Formula 3 is particularly preferable.

[0031]

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Examples of the ring C include structures as shown in Formula Group 4.

[0033]

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Among them, the structure described in Formula 5 is preferable.

[0035]

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Among them, the structure described in Formula 6 is particularly preferable.

[0037]

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However, when Z is a hydrogen atom, Q ¹ , Q ²
And Q ³ are all hydrogen atoms, m and n are both 0, Y is -COO-, and Z is a fluorine atom, or Q ¹ , Q ² and Q ³ are all When it is a hydrogen atom, m and n are both 0, Y is a single bond or —COO—, and Z is a cyano group, the 1,4-phenylene group is excluded.

As described above, the compound of the above general formula (I) has m, n, R, V, W, X, Y, Z, Q ¹ , Q ² , Q ³ , ring A, ring B and ring C Although it is possible to include a very wide variety of compounds depending on the selection of, the compound can be adapted to a wider range of applications by selecting each of its structural sites,
As a result, the compound of the general formula (I) is very useful because it has favorable characteristics for electro-optical devices such as a wide nematic temperature range, stability against light and heat, and high voltage holding ratio, particularly for STN-LCD and AM-LCD. It is. More specifically, among the compounds of the general formula (I), particularly preferred compounds include the following compounds.

The following abbreviations are used in the description of the compounds, and R ¹ is a methyl group, an ethyl group, a propyl group, a butyl group,
Pentyl group, hexyl group, peptyl group, octyl group, vinyl group, trans-1-propenyl group, 2-propenyl group,
Trans-1-butenyl group, trans-2-butenyl group, 3-butenyl group, trans-1-pentenyl group, trans-2-pentenyl group, trans-3-pentenyl group, 4-pentenyl group, trans-1-hexenyl Group, trans-2-hexenyl group, trans-3-hexenyl group, trans-4-hexenyl group, 5-hexenyl group, trans-1-heptenyl group, trans-2-heptenyl group, trans-3-heptenyl group, trans Represents any of a -4-heptenyl group, a trans-5-heptenyl group, and a 6-heptenyl group.

[0041]

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When m = n = 0, V is a single bond, and Z is a fluorine atom,

R ¹ -Te1-Ph1-F, R ¹ -Te1-Ph2-F, R ¹ -Te1-Ph3
-F, R ¹ -Te1-Np1-F, R ¹ -Te1-Np2-F, R ¹ -Te1-Np3-F, R ¹ -T
e1-Np4-F, R ¹ -Te2-Ph1-F, R ¹ -Te2-Ph2-F, R ¹ -Te2-Ph3-
F, R ¹ -Te2-Np1-F, R ¹ -Te2-Np2-F, R ¹ -Te2-Np3-F, R ¹ -Te
2-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-
F, R ¹ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Te
1-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂
-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-F,
R ¹ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-C
H ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-F,

When m = n = 0, V is a single bond and Z is a cyano group,

R ¹ -Te1-Ph2-CN, R ¹ -Te1-Ph3-CN, R ¹ -Te1-N
p1-CN, R ¹ -Te1-Np2-CN, R ¹ -Te1-Np3-CN, R ¹ -Te1-Np4-C
N, R ¹ -Te2-Ph1-CN, R ¹ -Te2-Ph2-CN, R ¹ -Te2-Ph3-CN, R ¹
-Te2-Np1-CN, R ¹ -Te2-Np2-CN, R ¹ -Te2-Np3-CN, R ¹ -Te2-
Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C
N, R ¹ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-CN, R ^1-
Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH
₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -P
h3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-C
N, R ¹ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CN,

When m = n = 0, V is a single bond, and Z is a trifluoromethoxy group,

R ¹ -Te1-Ph1-OCF ₃ , R ¹ -Te1-Ph2-OCF ₃ , R ¹ -T
e1-Ph3-OCF ₃ , R ¹ -Te1-Np1-OCF ₃ , R ¹ -Te1-Np2-OCF ₃ , R ^1-
Te1-Np3-OCF ₃ , R ¹ -Te1-Np4-OCF ₃ , R ¹ -Te2-Ph1-OCF ₃ , R ¹
-Te2-Ph2-OCF ₃ , R ¹ -Te2-Ph3-OCF ₃ , R ¹ -Te2-Np1-OCF ₃ , R
¹ -Te2-Np2-OCF ₃ , R ¹ -Te2-Np3-OCF ₃ , R ¹ -Te2-Np4-OCF ₃ ,
R ¹ -Te1-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹
-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Te1-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -T
e1-CH ₂ CH ₂ -Np3-OCF ₃ , R ¹ -Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ¹ -Te2
-CH ₂ CH ₂ -Ph1-OCF ₃ , R ¹ -Te2-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Te2-C
H ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Te2-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Te2-CH ₂
CH ₂ -Np2-OCF ₃ , R ¹ -Te2-CH ₂ CH ₂ -Np3-OCF ₃ , R ¹ -Te2-CH ₂ CH
₂ -Np4-OCF ₃ ,

When m = 1, n = 0, V is a single bond, and Z is a fluorine atom,

R ¹ -Cy-Te1-Ph1-F, R ¹ -Cy-Te1-Ph2-F, R ¹ -C
y-Te1-Ph3-F, R ¹ -Cy-Te1-Np1-F, R ¹ -Cy-Te1-Np2-F, R ^1-
Cy-Te1-Np3-F, R ¹ -Cy-Te1-Np4-F, R ¹ -Cy-Te2-Ph1-F, R ¹
-Cy-Te2-Ph2-F, R ¹ -Cy-Te2-Ph3-F, R ¹ -Cy-Te2-Np1-F, R
¹ -Cy-Te2-Np2-F, R ¹ -Cy-Te2-Np3-F, R ¹ -Cy-Te2-Np4-F,
R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph3-F, R ¹
-Cy-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -C
y-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Cy-
Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Cy-Te
2-CH ₂ CH ₂ -Ph3-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Cy-Te2-
CH ₂ CH ₂ -Np2-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Cy-Te2-CH
₂ CH ₂ -Np4-F,

R ¹ -Ph1-Te1-Ph1-F, R ¹ -Ph1-Te1-Ph2-F, R ¹
-Ph1-Te1-Ph3-F, R ¹ -Ph1-Te1-Np1-F, R ¹ -Ph1-Te1-Np2-
F, R ¹ -Ph1-Te1-Np3-F, R ¹ -Ph1-Te1-Np4-F, R ¹ -Ph1-Te2-
Ph1-F, R ¹ -Ph1-Te2-Ph2-F, R ¹ -Ph1-Te2-Ph3-F, R ¹ -Ph1-
Te2-Np1-F, R ¹ -Ph1-Te2-Np2-F, R ¹ -Ph1-Te2-Np3-F, R ^1-
Ph1-Te2-Np4-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-Te1
-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-Te1
-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-Te1
-CH ₂ CH ₂ -Np4-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph1-Te2
-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-Te2
-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-Te2
-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Ph2-Te1-Ph1-F, R ¹ -Ph2-Te1-Ph2-F, R ¹
-Ph2-Te1-Ph3-F, R ¹ -Ph2-Te1-Np1-F, R ¹ -Ph2-Te1-Np2-
F, R ¹ -Ph2-Te1-Np3-F, R ¹ -Ph2-Te1-Np4-F, R ¹ -Ph2-Te2-
Ph1-F, R ¹ -Ph2-Te2-Ph2-F, R ¹ -Ph2-Te2-Ph3-F, R ¹ -Ph2-
Te2-Np1-F, R ¹ -Ph2-Te2-Np2-F, R ¹ -Ph2-Te2-Np3-F, R ^1-
Ph2-Te2-Np4-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-Te1
-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-Te1
-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-Te1
-CH ₂ CH ₂ -Np4-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph2-Te2
-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-Te2
-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-Te2
-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Ph3-Te1-Ph1-F, R ¹ -Ph3-Te1-Ph2-F, R ¹
-Ph3-Te1-Ph3-F, R ¹ -Ph3-Te1-Np1-F, R ¹ -Ph3-Te1-Np2-
F, R ¹ -Ph3-Te1-Np3-F, R ¹ -Ph3-Te1-Np4-F, R ¹ -Ph3-Te2-
Ph1-F, R ¹ -Ph3-Te2-Ph2-F, R ¹ -Ph3-Te2-Ph3-F, R ¹ -Ph3-
Te2-Np1-F, R ¹ -Ph3-Te2-Np2-F, R ¹ -Ph3-Te2-Np3-F, R ^1-
Ph3-Te2-Np4-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-Te1
-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-Te1
-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-Te1
-CH ₂ CH ₂ -Np4-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph3-Te2
-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-Te2
-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-Te2
-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Np1-Te1-Ph1-F, R ¹ -Np1-Te1-Ph2-F, R ¹
-Np1-Te1-Ph3-F, R ¹ -Np1-Te1-Np1-F, R ¹ -Np1-Te1-Np2-
F, R ¹ -Np1-Te1-Np3-F, R ¹ -Np1-Te1-Np4-F, R ¹ -Np1-Te2-
Ph1-F, R ¹ -Np1-Te2-Ph2-F, R ¹ -Np1-Te2-Ph3-F, R ¹ -Np1-
Te2-Np1-F, R ¹ -Np1-Te2-Np2-F, R ¹ -Np1-Te2-Np3-F, R ^1-
Np1-Te2-Np4-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-Te1
-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-Te1
-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-Te1
-CH ₂ CH ₂ -Np4-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np1-Te2
-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-Te2
-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-Te2
-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Np2-Te1-Ph1-F, R ¹ -Np2-Te1-Ph2-F, R ¹
-Np2-Te1-Ph3-F, R ¹ -Np2-Te1-Np1-F, R ¹ -Np2-Te1-Np2-
F, R ¹ -Np2-Te1-Np3-F, R ¹ -Np2-Te1-Np4-F, R ¹ -Np2-Te2-
Ph1-F, R ¹ -Np2-Te2-Ph2-F, R ¹ -Np2-Te2-Ph3-F, R ¹ -Np2-
Te2-Np1-F, R ¹ -Np2-Te2-Np2-F, R ¹ -Np2-Te2-Np3-F, R ^1-
Np2-Te2-Np4-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-Te1
-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-Te1
-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-Te1
-CH ₂ CH ₂ -Np4-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np2-Te2
-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-Te2
-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-Te2
-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Np3-Te1-Ph1-F, R ¹ -Np3-Te1-Ph2-F, R ¹
-Np3-Te1-Ph3-F, R ¹ -Np3-Te1-Np1-F, R ¹ -Np3-Te1-Np2-
F, R ¹ -Np3-Te1-Np3-F, R ¹ -Np3-Te1-Np4-F, R ¹ -Np3-Te2-
Ph1-F, R ¹ -Np3-Te2-Ph2-F, R ¹ -Np3-Te2-Ph3-F, R ¹ -Np3-
Te2-Np1-F, R ¹ -Np3-Te2-Np2-F, R ¹ -Np3-Te2-Np3-F, R ^1-
Np3-Te2-Np4-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-Te1
-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-Te1
-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-Te1
-CH ₂ CH ₂ -Np4-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np3-Te2
-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-Te2
-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-Te2
-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Np4-Te1-Ph1-F, R ¹ -Np4-Te1-Ph2-F, R ¹
-Np4-Te1-Ph3-F, R ¹ -Np4-Te1-Np1-F, R ¹ -Np4-Te1-Np2-
F, R ¹ -Np4-Te1-Np3-F, R ¹ -Np4-Te1-Np4-F, R ¹ -Np4-Te2-
Ph1-F, R ¹ -Np4-Te2-Ph2-F, R ¹ -Np4-Te2-Ph3-F, R ¹ -Np4-
Te2-Np1-F, R ¹ -Np4-Te2-Np2-F, R ¹ -Np4-Te2-Np3-F, R ^1-
Np4-Te2-Np4-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-Te1
-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-Te1
-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-Te1
-CH ₂ CH ₂ -Np4-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np4-Te2
-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-Te2
-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-Te2
-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Cy-CH ₂ CH ₂ -T
e1-Ph2-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Cy-CH ₂ CH ₂ -Te1
-Np1-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-N
p3-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph1
-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph3-
F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np2-
F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np4-
F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Cy-CH ₂ CH ₂ -Te1
-CH ₂ CH ₂ -Ph3-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -C
y-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Np3-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Cy-CH ₂ CH
₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-
F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Cy-CH ₂ CH ₂ -Te2
-CH ₂ CH ₂ -Np1-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -C
y-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂
-Np4-F,

R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Ph1-CH ₂ CH ₂
-Te1-Ph2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Ph1-CH ₂ CH ₂
-Te1-Np1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Ph1-CH ₂ CH ₂
-Te1-Np3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Ph1-CH ₂ CH ₂
-Te2-Ph1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Ph1-CH ₂ CH ₂
-Te2-Ph3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Ph1-CH ₂ CH ₂
-Te2-Np2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Ph1-CH ₂ CH ₂
-Te2-Np4-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1
-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Np1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-CH ₂
CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4
-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph1-CH ₂ CH _2-
Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F,
R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-
CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -P
h1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Ph2-CH ₂ CH ₂
-Te1-Ph2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Ph2-CH ₂ CH ₂
-Te1-Np1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Ph2-CH ₂ CH ₂
-Te1-Np3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Ph2-CH ₂ CH ₂
-Te2-Ph1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Ph2-CH ₂ CH ₂
-Te2-Ph3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Ph2-CH ₂ CH ₂
-Te2-Np2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Ph2-CH ₂ CH ₂
-Te2-Np4-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2
-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Np1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-CH ₂
CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4
-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph2-CH ₂ CH _2-
Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F,
R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-
CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -P
h2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Ph3-CH ₂ CH ₂
-Te1-Ph2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Ph3-CH ₂ CH ₂
-Te1-Np1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Ph3-CH ₂ CH ₂
-Te1-Np3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Ph3-CH ₂ CH ₂
-Te2-Ph1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Ph3-CH ₂ CH ₂
-Te2-Ph3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Ph3-CH ₂ CH ₂
-Te2-Np2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Ph3-CH ₂ CH ₂
-Te2-Np4-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3
-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Np1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-CH ₂
CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4
-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph3-CH ₂ CH _2-
Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F,
R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-
CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -P
h3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Np1-CH ₂ CH ₂
-Te1-Ph2-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Np1-CH ₂ CH ₂
-Te1-Np1-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Np1-CH ₂ CH ₂
-Te1-Np3-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Np1-CH ₂ CH ₂
-Te2-Ph1-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Np1-CH ₂ CH ₂
-Te2-Ph3-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Np1-CH ₂ CH ₂
-Te2-Np2-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Np1-CH ₂ CH ₂
-Te2-Np4-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1
-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Np1-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-CH ₂
CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4
-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np1-CH ₂ CH _2-
Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F,
R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-
CH ₂ CH ₂ -Np2-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -N
p1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Np2-CH ₂ CH ₂
-Te1-Ph2-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Np2-CH ₂ CH ₂
-Te1-Np1-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Np2-CH ₂ CH ₂
-Te1-Np3-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Np2-CH ₂ CH ₂
-Te2-Ph1-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Np2-CH ₂ CH ₂
-Te2-Ph3-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Np2-CH ₂ CH ₂
-Te2-Np2-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Np2-CH ₂ CH ₂
-Te2-Np4-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2
-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Np1-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-CH ₂
CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4
-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np2-CH ₂ CH _2-
Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F,
R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-
CH ₂ CH ₂ -Np2-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -N
p2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Np3-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Np3-CH ₂ CH ₂
-Te1-Ph2-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Np3-CH ₂ CH ₂
-Te1-Np1-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Np3-CH ₂ CH ₂
-Te1-Np3-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Np3-CH ₂ CH ₂
-Te2-Ph1-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Np3-CH ₂ CH ₂
-Te2-Ph3-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Np3-CH ₂ CH ₂
-Te2-Np2-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Np3-CH ₂ CH ₂
-Te2-Np4-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3
-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Np1-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-CH ₂
CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4
-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np3-CH ₂ CH _2-
Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F,
R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-
CH ₂ CH ₂ -Np2-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -N
p3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,

R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Np4-CH ₂ CH ₂
-Te1-Ph2-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Np4-CH ₂ CH ₂
-Te1-Np1-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Np4-CH ₂ CH ₂
-Te1-Np3-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Np4-CH ₂ CH ₂
-Te2-Ph1-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Np4-CH ₂ CH ₂
-Te2-Ph3-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Np4-CH ₂ CH ₂
-Te2-Np2-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Np4-CH ₂ CH ₂
-Te2-Np4-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4
-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Np1-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-CH ₂
CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4
-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np4-CH ₂ CH _2-
Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F,
R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-
CH ₂ CH ₂ -Np2-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -N
p4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,

R¹-Ph1-C≡C-Te1-Ph1-F, R¹-Ph1-C≡C-Te1
-Ph2-F, R¹-Ph1-C≡C-Te1-Ph3-F, R¹-Ph1-C≡C-Te1-Np1
-F, R¹-Ph1-C≡C-Te1-Np2-F, R¹-Ph1-C≡C-Te1-Np3-F,
R¹-Ph1-C≡C-Te1-Np4-F, R¹-Ph1-C≡C-Te2-Ph1-F, R¹-P
h1-C≡C-Te2-Ph2-F, R¹-Ph1-C≡C-Te2-Ph3-F, R¹-Ph1-C
≡C-Te2-Np1-F, R¹-Ph1-C≡C-Te2-Np2-F, R¹-Ph1-C≡C-
Te2-Np3-F, R¹-Ph1-C≡C-Te2-Np4-F, R¹-Ph1-C≡C-Te1-
CH_TwoCH_Two-Ph2-F, R¹-Ph1-C≡C-Te1-CH_TwoCH_Two-Ph3-F, R¹-Ph1
-C≡C-Te1-CH_TwoCH_Two-Np1-F, R¹-Ph1-C≡C-Te1-CH_TwoCH_Two-Np2
-F, R¹-Ph1-C≡C-Te1-CH_TwoCH_Two-Np3-F, R¹-Ph1-C≡C-Te1-
CH_TwoCH_Two-Np4-F, R ¹-Ph1-C≡C-Te2-CH_TwoCH_Two-Ph1-F, R¹-Ph1
-C≡C-Te2-CH_TwoCH_Two-Ph2-F, R¹-Ph1-C≡C-Te2-CH_TwoCH_Two-Ph3
-F, R¹-Ph1-C≡C-Te2-CH_TwoCH_Two-Np1-F, R¹-Ph1-C≡C-Te2-
CH_TwoCH_Two-Np2-F, R¹-Ph1-C≡C-Te2-CH_TwoCH_Two-Np3-F, R¹-Ph1
-C≡C-Te2-CH_TwoCH_Two-Np4-F,

R¹-Ph2-C≡C-Te1-Ph1-F, R¹-Ph2-C≡C-Te1
-Ph2-F, R¹-Ph2-C≡C-Te1-Ph3-F, R¹-Ph2-C≡C-Te1-Np1
-F, R¹-Ph2-C≡C-Te1-Np2-F, R¹-Ph2-C≡C-Te1-Np3-F,
R¹-Ph2-C≡C-Te1-Np4-F, R¹-Ph2-C≡C-Te2-Ph1-F, R¹-P
h2-C≡C-Te2-Ph2-F, R¹-Ph2-C≡C-Te2-Ph3-F, R¹-Ph2-C
≡C-Te2-Np1-F, R¹-Ph2-C≡C-Te2-Np2-F, R¹-Ph2-C≡C-
Te2-Np3-F, R¹-Ph2-C≡C-Te2-Np4-F, R¹-Ph2-C≡C-Te1-
CH_TwoCH_Two-Ph2-F, R¹-Ph2-C≡C-Te1-CH_TwoCH_Two-Ph3-F, R¹-Ph2
-C≡C-Te1-CH_TwoCH_Two-Np1-F, R¹-Ph2-C≡C-Te1-CH_TwoCH_Two-Np2
-F, R¹-Ph2-C≡C-Te1-CH_TwoCH_Two-Np3-F, R¹-Ph2-C≡C-Te1-
CH_TwoCH_Two-Np4-F, R ¹-Ph2-C≡C-Te2-CH_TwoCH_Two-Ph1-F, R¹-Ph2
-C≡C-Te2-CH_TwoCH_Two-Ph2-F, R¹-Ph2-C≡C-Te2-CH_TwoCH_Two-Ph3
-F, R¹-Ph2-C≡C-Te2-CH_TwoCH_Two-Np1-F, R¹-Ph2-C≡C-Te2-
CH_TwoCH_Two-Np2-F, R¹-Ph2-C≡C-Te2-CH_TwoCH_Two-Np3-F, R¹-Ph2
-C≡C-Te2-CH_TwoCH_Two-Np4-F,

R¹-Ph3-C≡C-Te1-Ph1-F, R¹-Ph3-C≡C-Te1
-Ph2-F, R¹-Ph3-C≡C-Te1-Ph3-F, R¹-Ph3-C≡C-Te1-Np1
-F, R¹-Ph3-C≡C-Te1-Np2-F, R¹-Ph3-C≡C-Te1-Np3-F,
R¹-Ph3-C≡C-Te1-Np4-F, R¹-Ph3-C≡C-Te2-Ph1-F, R¹-P
h3-C≡C-Te2-Ph2-F, R¹-Ph3-C≡C-Te2-Ph3-F, R¹-Ph3-C
≡C-Te2-Np1-F, R¹-Ph3-C≡C-Te2-Np2-F, R¹-Ph3-C≡C-
Te2-Np3-F, R¹-Ph3-C≡C-Te2-Np4-F, R¹-Ph3-C≡C-Te1-
CH_TwoCH_Two-Ph2-F, R¹-Ph3-C≡C-Te1-CH_TwoCH_Two-Ph3-F, R¹-Ph3
-C≡C-Te1-CH_TwoCH_Two-Np1-F, R¹-Ph3-C≡C-Te1-CH_TwoCH_Two-Np2
-F, R¹-Ph3-C≡C-Te1-CH_TwoCH_Two-Np3-F, R¹-Ph3-C≡C-Te1-
CH_TwoCH_Two-Np4-F, R ¹-Ph3-C≡C-Te2-CH_TwoCH_Two-Ph1-F, R¹-Ph3
-C≡C-Te2-CH_TwoCH_Two-Ph2-F, R¹-Ph3-C≡C-Te2-CH_TwoCH_Two-Ph3
-F, R¹-Ph3-C≡C-Te2-CH_TwoCH_Two-Np1-F, R¹-Ph3-C≡C-Te2-
CH_TwoCH_Two-Np2-F, R¹-Ph3-C≡C-Te2-CH_TwoCH_Two-Np3-F, R¹-Ph3
-C≡C-Te2-CH_TwoCH_Two-Np4-F,

R¹-Np1-C≡C-Te1-Ph1-F, R¹-Np1-C≡C-Te1
-Ph2-F, R¹-Np1-C≡C-Te1-Ph3-F, R¹-Np1-C≡C-Te1-Np1
-F, R¹-Np1-C≡C-Te1-Np2-F, R¹-Np1-C≡C-Te1-Np3-F,
R¹-Np1-C≡C-Te1-Np4-F, R¹-Np1-C≡C-Te2-Ph1-F, R¹-N
p1-C≡C-Te2-Ph2-F, R¹-Np1-C≡C-Te2-Ph3-F, R¹-Np1-C
≡C-Te2-Np1-F, R¹-Np1-C≡C-Te2-Np2-F, R¹-Np1-C≡C-
Te2-Np3-F, R¹-Np1-C≡C-Te2-Np4-F, R¹-Np1-C≡C-Te1-
CH_TwoCH_Two-Ph2-F, R¹-Np1-C≡C-Te1-CH_TwoCH_Two-Ph3-F, R¹-Np1
-C≡C-Te1-CH_TwoCH_Two-Np1-F, R¹-Np1-C≡C-Te1-CH_TwoCH_Two-Np2
-F, R¹-Np1-C≡C-Te1-CH_TwoCH_Two-Np3-F, R¹-Np1-C≡C-Te1-
CH_TwoCH_Two-Np4-F, R ¹-Np1-C≡C-Te2-CH_TwoCH_Two-Ph1-F, R¹-Np1
-C≡C-Te2-CH_TwoCH_Two-Ph2-F, R¹-Np1-C≡C-Te2-CH_TwoCH_Two-Ph3
-F, R¹-Np1-C≡C-Te2-CH_TwoCH_Two-Np1-F, R¹-Np1-C≡C-Te2-
CH_TwoCH_Two-Np2-F, R¹-Np1-C≡C-Te2-CH_TwoCH_Two-Np3-F, R¹-Np1
-C≡C-Te2-CH_TwoCH_Two-Np4-F,

R¹-Np2-C≡C-Te1-Ph1-F, R¹-Np2-C≡C-Te1
-Ph2-F, R¹-Np2-C≡C-Te1-Ph3-F, R¹-Np2-C≡C-Te1-Np1
-F, R¹-Np2-C≡C-Te1-Np2-F, R¹-Np2-C≡C-Te1-Np3-F,
R¹-Np2-C≡C-Te1-Np4-F, R¹-Np2-C≡C-Te2-Ph1-F, R¹-N
p2-C≡C-Te2-Ph2-F, R¹-Np2-C≡C-Te2-Ph3-F, R¹-Np2-C
≡C-Te2-Np1-F, R¹-Np2-C≡C-Te2-Np2-F, R¹-Np2-C≡C-
Te2-Np3-F, R¹-Np2-C≡C-Te2-Np4-F, R¹-Np2-C≡C-Te1-
CH_TwoCH_Two-Ph2-F, R¹-Np2-C≡C-Te1-CH_TwoCH_Two-Ph3-F, R¹-Np2
-C≡C-Te1-CH_TwoCH_Two-Np1-F, R¹-Np2-C≡C-Te1-CH_TwoCH_Two-Np2
-F, R¹-Np2-C≡C-Te1-CH_TwoCH_Two-Np3-F, R¹-Np2-C≡C-Te1-
CH_TwoCH_Two-Np4-F, R ¹-Np2-C≡C-Te2-CH_TwoCH_Two-Ph1-F, R¹-Np2
-C≡C-Te2-CH_TwoCH_Two-Ph2-F, R¹-Np2-C≡C-Te2-CH_TwoCH_Two-Ph3
-F, R¹-Np2-C≡C-Te2-CH_TwoCH_Two-Np1-F, R¹-Np2-C≡C-Te2-
CH_TwoCH_Two-Np2-F, R¹-Np2-C≡C-Te2-CH_TwoCH_Two-Np3-F, R¹-Np2
-C≡C-Te2-CH_TwoCH_Two-Np4-F,

R¹-Np3-C≡C-Te1-Ph1-F, R¹-Np3-C≡C-Te1
-Ph2-F, R¹-Np3-C≡C-Te1-Ph3-F, R¹-Np3-C≡C-Te1-Np1
-F, R¹-Np3-C≡C-Te1-Np2-F, R¹-Np3-C≡C-Te1-Np3-F,
R¹-Np3-C≡C-Te1-Np4-F, R¹-Np3-C≡C-Te2-Ph1-F, R¹-N
p3-C≡C-Te2-Ph2-F, R¹-Np3-C≡C-Te2-Ph3-F, R¹-Np3-C
≡C-Te2-Np1-F, R¹-Np3-C≡C-Te2-Np2-F, R¹-Np3-C≡C-
Te2-Np3-F, R¹-Np3-C≡C-Te2-Np4-F, R¹-Np3-C≡C-Te1-
CH_TwoCH_Two-Ph2-F, R¹-Np3-C≡C-Te1-CH_TwoCH_Two-Ph3-F, R¹-Np3
-C≡C-Te1-CH_TwoCH_Two-Np1-F, R¹-Np3-C≡C-Te1-CH_TwoCH_Two-Np2
-F, R¹-Np3-C≡C-Te1-CH_TwoCH_Two-Np3-F, R¹-Np3-C≡C-Te1-
CH_TwoCH_Two-Np4-F, R ¹-Np3-C≡C-Te2-CH_TwoCH_Two-Ph1-F, R¹-Np3
-C≡C-Te2-CH_TwoCH_Two-Ph2-F, R¹-Np3-C≡C-Te2-CH_TwoCH_Two-Ph3
-F, R¹-Np3-C≡C-Te2-CH_TwoCH_Two-Np1-F, R¹-Np3-C≡C-Te2-
CH_TwoCH_Two-Np2-F, R¹-Np3-C≡C-Te2-CH_TwoCH_Two-Np3-F, R¹-Np3
-C≡C-Te2-CH_TwoCH_Two-Np4-F,

R¹-Np4-C≡C-Te1-Ph1-F, R¹-Np4-C≡C-Te1
-Ph2-F, R¹-Np4-C≡C-Te1-Ph3-F, R¹-Np4-C≡C-Te1-Np1
-F, R¹-Np4-C≡C-Te1-Np2-F, R¹-Np4-C≡C-Te1-Np3-F,
R¹-Np4-C≡C-Te1-Np4-F, R¹-Np4-C≡C-Te2-Ph1-F, R¹-N
p4-C≡C-Te2-Ph2-F, R¹-Np4-C≡C-Te2-Ph3-F, R¹-Np4-C
≡C-Te2-Np1-F, R¹-Np4-C≡C-Te2-Np2-F, R¹-Np4-C≡C-
Te2-Np3-F, R¹-Np4-C≡C-Te2-Np4-F, R¹-Np4-C≡C-Te1-
CH_TwoCH_Two-Ph2-F, R¹-Np4-C≡C-Te1-CH_TwoCH_Two-Ph3-F, R¹-Np4
-C≡C-Te1-CH_TwoCH_Two-Np1-F, R¹-Np4-C≡C-Te1-CH_TwoCH_Two-Np2
-F, R¹-Np4-C≡C-Te1-CH_TwoCH_Two-Np3-F, R¹-Np4-C≡C-Te1-
CH_TwoCH_Two-Np4-F, R ¹-Np4-C≡C-Te2-CH_TwoCH_Two-Ph1-F, R¹-Np4
-C≡C-Te2-CH_TwoCH_Two-Ph2-F, R¹-Np4-C≡C-Te2-CH_TwoCH_Two-Ph3
-F, R¹-Np4-C≡C-Te2-CH_TwoCH_Two-Np1-F, R¹-Np4-C≡C-Te2-
CH_TwoCH_Two-Np2-F, R¹-Np4-C≡C-Te2-CH_TwoCH_Two-Np3-F, R¹-Np4
-C≡C-Te2-CH_TwoCH_Two-Np4-F,

When m = 1, n = 0, V is a single bond and Z is a cyano group,

R ¹ -Cy-Te1-Ph1-CN, R ¹ -Cy-Te1-Ph2-CN, R ¹
-Cy-Te1-Ph3-CN, R ¹ -Cy-Te1-Np1-CN, R ¹ -Cy-Te1-Np2-C
N, R ¹ -Cy-Te1-Np3-CN, R ¹ -Cy-Te1-Np4-CN, R ¹ -Cy-Te2-P
h1-CN, R ¹ -Cy-Te2-Ph2-CN, R ¹ -Cy-Te2-Ph3-CN, R ¹ -Cy-T
e2-Np1-CN, R ¹ -Cy-Te2-Np2-CN, R ¹ -Cy-Te2-Np3-CN, R ^1-
Cy-Te2-Np4-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Cy-Te1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Cy-Te1-
CH ₂ CH ₂ -Np2-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Cy-Te1-
CH ₂ CH ₂ -Np4-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Cy-Te2-
CH ₂ CH ₂ -Ph2-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Cy-Te2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Cy-Te2-
CH ₂ CH ₂ -Np3-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np4-CN,

R¹-Ph1-Te1-Ph1-CN, R¹-Ph1-Te1-Ph2-CN,
R¹-Ph1-Te1-Ph3-CN, R¹-Ph1-Te1-Np1-CN, R¹-Ph1-Te1-N
p2-CN, R¹-Ph1-Te1-Np3-CN, R¹-Ph1-Te1-Np4-CN, R¹-Ph
1-Te2-Ph1-CN, R¹-Ph1-Te2-Ph2-CN, R¹-Ph1-Te2-Ph3-C
N, R¹-Ph1-Te2-Np1-CN, R¹-Ph1-Te2-Np2-CN, R¹-Ph1-Te
2-Np3-CN, R¹-Ph1-Te2-Np4-CN, R¹-Ph1-Te1-CH_TwoCH_Two-Ph2
-CN, R¹-Ph1-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Ph1-Te1-CH_TwoCH_Two-N
p1-CN, R¹-Ph1-Te1-CH_TwoCH _Two-Np2-CN, R¹-Ph1-Te1-CH_TwoCH_Two
-Np3-CN, R¹-Ph1-Te1-CH_TwoCH_Two-Np4-CN, R¹-Ph1-Te2-CH_TwoC
H_Two-Ph1-CN, R¹-Ph1-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Ph1-Te2-CH
_TwoCH_Two-Ph3-CN, R¹-Ph1-Te2-CH_TwoCH_Two-Np1-CN, R¹-Ph1-Te2-
CH_TwoCH_Two-Np2-CN, R¹-Ph1-Te2-CH_TwoCH_Two-Np3-CN, R¹-Ph1-Te
2-CH_TwoCH_Two-Np4-CN,

R¹-Ph2-Te1-Ph1-CN, R¹-Ph2-Te1-Ph2-CN,
R¹-Ph2-Te1-Ph3-CN, R¹-Ph2-Te1-Np1-CN, R¹-Ph2-Te1-N
p2-CN, R¹-Ph2-Te1-Np3-CN, R¹-Ph2-Te1-Np4-CN, R¹-Ph
2-Te2-Ph1-CN, R¹-Ph2-Te2-Ph2-CN, R¹-Ph2-Te2-Ph3-C
N, R¹-Ph2-Te2-Np1-CN, R¹-Ph2-Te2-Np2-CN, R¹-Ph2-Te
2-Np3-CN, R¹-Ph2-Te2-Np4-CN, R¹-Ph2-Te1-CH_TwoCH_Two-Ph2
-CN, R¹-Ph2-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Ph2-Te1-CH_TwoCH_Two-N
p1-CN, R¹-Ph2-Te1-CH_TwoCH _Two-Np2-CN, R¹-Ph2-Te1-CH_TwoCH_Two
-Np3-CN, R¹-Ph2-Te1-CH_TwoCH_Two-Np4-CN, R¹-Ph2-Te2-CH_TwoC
H_Two-Ph1-CN, R¹-Ph2-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Ph2-Te2-CH
_TwoCH_Two-Ph3-CN, R¹-Ph2-Te2-CH_TwoCH_Two-Np1-CN, R¹-Ph2-Te2-
CH_TwoCH_Two-Np2-CN, R¹-Ph2-Te2-CH_TwoCH_Two-Np3-CN, R¹-Ph2-Te
2-CH_TwoCH_Two-Np4-CN,

R¹-Ph3-Te1-Ph1-CN, R¹-Ph3-Te1-Ph2-CN,
R¹-Ph3-Te1-Ph3-CN, R¹-Ph3-Te1-Np1-CN, R¹-Ph3-Te1-N
p2-CN, R¹-Ph3-Te1-Np3-CN, R¹-Ph3-Te1-Np4-CN, R¹-Ph
3-Te2-Ph1-CN, R¹-Ph3-Te2-Ph2-CN, R¹-Ph3-Te2-Ph3-C
N, R¹-Ph3-Te2-Np1-CN, R¹-Ph3-Te2-Np2-CN, R¹-Ph3-Te
2-Np3-CN, R¹-Ph3-Te2-Np4-CN, R¹-Ph3-Te1-CH_TwoCH_Two-Ph2
-CN, R¹-Ph3-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Ph3-Te1-CH_TwoCH_Two-N
p1-CN, R¹-Ph3-Te1-CH_TwoCH _Two-Np2-CN, R¹-Ph3-Te1-CH_TwoCH_Two
-Np3-CN, R¹-Ph3-Te1-CH_TwoCH_Two-Np4-CN, R¹-Ph3-Te2-CH_TwoC
H_Two-Ph1-CN, R¹-Ph3-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Ph3-Te2-CH
_TwoCH_Two-Ph3-CN, R¹-Ph3-Te2-CH_TwoCH_Two-Np1-CN, R¹-Ph3-Te2-
CH_TwoCH_Two-Np2-CN, R¹-Ph3-Te2-CH_TwoCH_Two-Np3-CN, R¹-Ph3-Te
2-CH_TwoCH_Two-Np4-CN,

R¹-Np1-Te1-Ph1-CN, R¹-Np1-Te1-Ph2-CN,
R¹-Np1-Te1-Ph3-CN, R¹-Np1-Te1-Np1-CN, R¹-Np1-Te1-N
p2-CN, R¹-Np1-Te1-Np3-CN, R¹-Np1-Te1-Np4-CN, R¹-Np
1-Te2-Ph1-CN, R¹-Np1-Te2-Ph2-CN, R¹-Np1-Te2-Ph3-C
N, R¹-Np1-Te2-Np1-CN, R¹-Np1-Te2-Np2-CN, R¹-Np1-Te
2-Np3-CN, R¹-Np1-Te2-Np4-CN, R¹-Np1-Te1-CH_TwoCH_Two-Ph2
-CN, R¹-Np1-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Np1-Te1-CH_TwoCH_Two-N
p1-CN, R¹-Np1-Te1-CH_TwoCH _Two-Np2-CN, R¹-Np1-Te1-CH_TwoCH_Two
-Np3-CN, R¹-Np1-Te1-CH_TwoCH_Two-Np4-CN, R¹-Np1-Te2-CH_TwoC
H_Two-Ph1-CN, R¹-Np1-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Np1-Te2-CH
_TwoCH_Two-Ph3-CN, R¹-Np1-Te2-CH_TwoCH_Two-Np1-CN, R¹-Np1-Te2-
CH_TwoCH_Two-Np2-CN, R¹-Np1-Te2-CH_TwoCH_Two-Np3-CN, R¹-Np1-Te
2-CH_TwoCH_Two-Np4-CN,

R¹-Np2-Te1-Ph1-CN, R¹-Np2-Te1-Ph2-CN,
R¹-Np2-Te1-Ph3-CN, R¹-Np2-Te1-Np1-CN, R¹-Np2-Te1-N
p2-CN, R¹-Np2-Te1-Np3-CN, R¹-Np2-Te1-Np4-CN, R¹-Np
2-Te2-Ph1-CN, R¹-Np2-Te2-Ph2-CN, R¹-Np2-Te2-Ph3-C
N, R¹-Np2-Te2-Np1-CN, R¹-Np2-Te2-Np2-CN, R¹-Np2-Te
2-Np3-CN, R¹-Np2-Te2-Np4-CN, R¹-Np2-Te1-CH_TwoCH_Two-Ph2
-CN, R¹-Np2-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Np2-Te1-CH_TwoCH_Two-N
p1-CN, R¹-Np2-Te1-CH_TwoCH _Two-Np2-CN, R¹-Np2-Te1-CH_TwoCH_Two
-Np3-CN, R¹-Np2-Te1-CH_TwoCH_Two-Np4-CN, R¹-Np2-Te2-CH_TwoC
H_Two-Ph1-CN, R¹-Np2-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Np2-Te2-CH
_TwoCH_Two-Ph3-CN, R¹-Np2-Te2-CH_TwoCH_Two-Np1-CN, R¹-Np2-Te2-
CH_TwoCH_Two-Np2-CN, R¹-Np2-Te2-CH_TwoCH_Two-Np3-CN, R¹-Np2-Te
2-CH_TwoCH_Two-Np4-CN,

R¹-Np3-Te1-Ph1-CN, R¹-Np3-Te1-Ph2-CN,
R¹-Np3-Te1-Ph3-CN, R¹-Np3-Te1-Np1-CN, R¹-Np3-Te1-N
p2-CN, R¹-Np3-Te1-Np3-CN, R¹-Np3-Te1-Np4-CN, R¹-Np
3-Te2-Ph1-CN, R¹-Np3-Te2-Ph2-CN, R¹-Np3-Te2-Ph3-C
N, R¹-Np3-Te2-Np1-CN, R¹-Np3-Te2-Np2-CN, R¹-Np3-Te
2-Np3-CN, R¹-Np3-Te2-Np4-CN, R¹-Np3-Te1-CH_TwoCH_Two-Ph2
-CN, R¹-Np3-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Np3-Te1-CH_TwoCH_Two-N
p1-CN, R¹-Np3-Te1-CH_TwoCH _Two-Np2-CN, R¹-Np3-Te1-CH_TwoCH_Two
-Np3-CN, R¹-Np3-Te1-CH_TwoCH_Two-Np4-CN, R¹-Np3-Te2-CH_TwoC
H_Two-Ph1-CN, R¹-Np3-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Np3-Te2-CH
_TwoCH_Two-Ph3-CN, R¹-Np3-Te2-CH_TwoCH_Two-Np1-CN, R¹-Np3-Te2-
CH_TwoCH_Two-Np2-CN, R¹-Np3-Te2-CH_TwoCH_Two-Np3-CN, R¹-Np3-Te
2-CH_TwoCH_Two-Np4-CN,

R¹-Np4-Te1-Ph1-CN, R¹-Np4-Te1-Ph2-CN,
R¹-Np4-Te1-Ph3-CN, R¹-Np4-Te1-Np1-CN, R¹-Np4-Te1-N
p2-CN, R¹-Np4-Te1-Np3-CN, R¹-Np4-Te1-Np4-CN, R¹-Np
4-Te2-Ph1-CN, R¹-Np4-Te2-Ph2-CN, R¹-Np4-Te2-Ph3-C
N, R¹-Np4-Te2-Np1-CN, R¹-Np4-Te2-Np2-CN, R¹-Np4-Te
2-Np3-CN, R¹-Np4-Te2-Np4-CN, R¹-Np4-Te1-CH_TwoCH_Two-Ph2
-CN, R¹-Np4-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Np4-Te1-CH_TwoCH_Two-N
p1-CN, R¹-Np4-Te1-CH_TwoCH _Two-Np2-CN, R¹-Np4-Te1-CH_TwoCH_Two
-Np3-CN, R¹-Np4-Te1-CH_TwoCH_Two-Np4-CN, R¹-Np4-Te2-CH_TwoC
H_Two-Ph1-CN, R¹-Np4-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Np4-Te2-CH
_TwoCH_Two-Ph3-CN, R¹-Np4-Te2-CH_TwoCH_Two-Np1-CN, R¹-Np4-Te2-
CH_TwoCH_Two-Np2-CN, R¹-Np4-Te2-CH_TwoCH_Two-Np3-CN, R¹-Np4-Te
2-CH_TwoCH_Two-Np4-CN,

R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Cy-CH ₂ CH _2-
Te1-Ph2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Cy-CH ₂ CH _2-
Te1-Np1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Cy-CH ₂ CH _2-
Te1-Np3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Cy-CH ₂ CH _2-
Te2-Ph1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Cy-CH ₂ CH _2-
Te2-Ph3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Cy-CH ₂ CH _2-
Te2-Np2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Cy-CH ₂ CH _2-
Te2-Np4-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Cy-
CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH _2-
Np1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Cy-CH ₂ C
H ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-
CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Cy-CH ₂ CH ₂ -T
e2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN,
R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-C
H ₂ CH ₂ -Np2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -C
y-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,

R¹-Ph1-CH_TwoCH_Two-Te1-Ph1-CN, R¹-Ph1-CH_TwoCH
_Two-Te1-Ph2-CN, R¹-Ph1-CH_TwoCH_Two-Te1-Ph3-CN, R¹-Ph1-CH_Two
CH_Two-Te1-Np1-CN, R¹-Ph1-CH_TwoCH_Two-Te1-Np2-CN, R¹-Ph1-C
H_TwoCH_Two-Te1-Np3-CN, R¹-Ph1-CH_TwoCH_Two-Te1-Np4-CN, R¹-Ph1
-CH_TwoCH_Two-Te2-Ph1-CN, R¹-Ph1-CH_TwoCH_Two-Te2-Ph2-CN, R¹-P
h1-CH_TwoCH_Two-Te2-Ph3-CN, R¹-Ph1-CH_TwoCH_Two-Te2-Np1-CN, R¹
-Ph1-CH_TwoCH_Two-Te2-Np2-CN, R¹-Ph1-CH_TwoCH_Two-Te2-Np3-CN,
R¹-Ph1-CH_TwoCH_Two-Te2-Np4-CN, R¹-Ph1-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Ph2-CN, R¹-Ph1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Ph1-C
H_TwoCH_Two-Te1-CH_TwoCH_Two-Np1-CN, R¹-Ph1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-
Np2-CN, R¹-Ph1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np3-CN, R¹-Ph1-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Np4-CN, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-P
h1-CN, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Ph1-CH_Two
CH_Two-Te2-CH _TwoCH_Two-Ph3-CN, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np
1-CN, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-CN, R¹-Ph1-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Np3-CN, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np4
-CN,

R¹-Ph2-CH_TwoCH_Two-Te1-Ph1-CN, R¹-Ph2-CH_TwoCH
_Two-Te1-Ph2-CN, R¹-Ph2-CH_TwoCH_Two-Te1-Ph3-CN, R¹-Ph2-CH_Two
CH_Two-Te1-Np1-CN, R¹-Ph2-CH_TwoCH_Two-Te1-Np2-CN, R¹-Ph2-C
H_TwoCH_Two-Te1-Np3-CN, R¹-Ph2-CH_TwoCH_Two-Te1-Np4-CN, R¹-Ph2
-CH_TwoCH_Two-Te2-Ph1-CN, R¹-Ph2-CH_TwoCH_Two-Te2-Ph2-CN, R¹-P
h2-CH_TwoCH_Two-Te2-Ph3-CN, R¹-Ph2-CH_TwoCH_Two-Te2-Np1-CN, R¹
-Ph2-CH_TwoCH_Two-Te2-Np2-CN, R¹-Ph2-CH_TwoCH_Two-Te2-Np3-CN,
R¹-Ph2-CH_TwoCH_Two-Te2-Np4-CN, R¹-Ph2-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Ph2-CN, R¹-Ph2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Ph2-C
H_TwoCH_Two-Te1-CH_TwoCH_Two-Np1-CN, R¹-Ph2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-
Np2-CN, R¹-Ph2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np3-CN, R¹-Ph2-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Np4-CN, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-P
h1-CN, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Ph2-CH_Two
CH_Two-Te2-CH _TwoCH_Two-Ph3-CN, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np
1-CN, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-CN, R¹-Ph2-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Np3-CN, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np4
-CN,

R¹-Ph3-CH_TwoCH_Two-Te1-Ph1-CN, R¹-Ph3-CH_TwoCH
_Two-Te1-Ph2-CN, R¹-Ph3-CH_TwoCH_Two-Te1-Ph3-CN, R¹-Ph3-CH_Two
CH_Two-Te1-Np1-CN, R¹-Ph3-CH_TwoCH_Two-Te1-Np2-CN, R¹-Ph3-C
H_TwoCH_Two-Te1-Np3-CN, R¹-Ph3-CH_TwoCH_Two-Te1-Np4-CN, R¹-Ph3
-CH_TwoCH_Two-Te2-Ph1-CN, R¹-Ph3-CH_TwoCH_Two-Te2-Ph2-CN, R¹-P
h3-CH_TwoCH_Two-Te2-Ph3-CN, R¹-Ph3-CH_TwoCH_Two-Te2-Np1-CN, R¹
-Ph3-CH_TwoCH_Two-Te2-Np2-CN, R¹-Ph3-CH_TwoCH_Two-Te2-Np3-CN,
R¹-Ph3-CH_TwoCH_Two-Te2-Np4-CN, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Ph2-CN, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Ph3-C
H_TwoCH_Two-Te1-CH_TwoCH_Two-Np1-CN, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-
Np2-CN, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np3-CN, R¹-Ph3-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Np4-CN, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-P
h1-CN, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Ph3-CH_Two
CH_Two-Te2-CH _TwoCH_Two-Ph3-CN, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np
1-CN, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-CN, R¹-Ph3-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Np3-CN, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np4
-CN,

R¹-Np1-CH_TwoCH_Two-Te1-Ph1-CN, R¹-Np1-CH_TwoCH
_Two-Te1-Ph2-CN, R¹-Np1-CH_TwoCH_Two-Te1-Ph3-CN, R¹-Np1-CH_Two
CH_Two-Te1-Np1-CN, R¹-Np1-CH_TwoCH_Two-Te1-Np2-CN, R¹-Np1-C
H_TwoCH_Two-Te1-Np3-CN, R¹-Np1-CH_TwoCH_Two-Te1-Np4-CN, R¹-Np1
-CH_TwoCH_Two-Te2-Ph1-CN, R¹-Np1-CH_TwoCH_Two-Te2-Ph2-CN, R¹-N
p1-CH_TwoCH_Two-Te2-Ph3-CN, R¹-Np1-CH_TwoCH_Two-Te2-Np1-CN, R¹
-Np1-CH_TwoCH_Two-Te2-Np2-CN, R¹-Np1-CH_TwoCH_Two-Te2-Np3-CN,
R¹-Np1-CH_TwoCH_Two-Te2-Np4-CN, R¹-Np1-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Ph2-CN, R¹-Np1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Np1-C
H_TwoCH_Two-Te1-CH_TwoCH_Two-Np1-CN, R¹-Np1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-
Np2-CN, R¹-Np1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np3-CN, R¹-Np1-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Np4-CN, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-P
h1-CN, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Np1-CH_Two
CH_Two-Te2-CH _TwoCH_Two-Ph3-CN, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np
1-CN, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-CN, R¹-Np1-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Np3-CN, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np4
-CN,

R¹-Np2-CH_TwoCH_Two-Te1-Ph1-CN, R¹-Np2-CH_TwoCH
_Two-Te1-Ph2-CN, R¹-Np2-CH_TwoCH_Two-Te1-Ph3-CN, R¹-Np2-CH_Two
CH_Two-Te1-Np1-CN, R¹-Np2-CH_TwoCH_Two-Te1-Np2-CN, R¹-Np2-C
H_TwoCH_Two-Te1-Np3-CN, R¹-Np2-CH_TwoCH_Two-Te1-Np4-CN, R¹-Np2
-CH_TwoCH_Two-Te2-Ph1-CN, R¹-Np2-CH_TwoCH_Two-Te2-Ph2-CN, R¹-N
p2-CH_TwoCH_Two-Te2-Ph3-CN, R¹-Np2-CH_TwoCH_Two-Te2-Np1-CN, R¹
-Np2-CH_TwoCH_Two-Te2-Np2-CN, R¹-Np2-CH_TwoCH_Two-Te2-Np3-CN,
R¹-Np2-CH_TwoCH_Two-Te2-Np4-CN, R¹-Np2-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Ph2-CN, R¹-Np2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Np2-C
H_TwoCH_Two-Te1-CH_TwoCH_Two-Np1-CN, R¹-Np2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-
Np2-CN, R¹-Np2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np3-CN, R¹-Np2-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Np4-CN, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-P
h1-CN, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Np2-CH_Two
CH_Two-Te2-CH _TwoCH_Two-Ph3-CN, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np
1-CN, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-CN, R¹-Np2-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Np3-CN, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np4
-CN,

R¹-Np3-CH_TwoCH_Two-Te1-Ph1-CN, R¹-Np3-CH_TwoCH
_Two-Te1-Ph2-CN, R¹-Np3-CH_TwoCH_Two-Te1-Ph3-CN, R¹-Np3-CH_Two
CH_Two-Te1-Np1-CN, R¹-Np3-CH_TwoCH_Two-Te1-Np2-CN, R¹-Np3-C
H_TwoCH_Two-Te1-Np3-CN, R¹-Np3-CH_TwoCH_Two-Te1-Np4-CN, R¹-Np3
-CH_TwoCH_Two-Te2-Ph1-CN, R¹-Np3-CH_TwoCH_Two-Te2-Ph2-CN, R¹-N
p3-CH_TwoCH_Two-Te2-Ph3-CN, R¹-Np3-CH_TwoCH_Two-Te2-Np1-CN, R¹
-Np3-CH_TwoCH_Two-Te2-Np2-CN, R¹-Np3-CH_TwoCH_Two-Te2-Np3-CN,
R¹-Np3-CH_TwoCH_Two-Te2-Np4-CN, R¹-Np3-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Ph2-CN, R¹-Np3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Np3-C
H_TwoCH_Two-Te1-CH_TwoCH_Two-Np1-CN, R¹-Np3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-
Np2-CN, R¹-Np3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np3-CN, R¹-Np3-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Np4-CN, R¹-Np3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-P
h1-CN, R¹-Np3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Np3-CH_Two
CH_Two-Te2-CH _TwoCH_Two-Ph3-CN, R¹-Np3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np
1-CN, R¹-Np3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-CN, R¹-Np3-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Np3-CN, R¹-Np3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np4
-CN,

R¹-Np4-CH_TwoCH_Two-Te1-Ph1-CN, R¹-Np4-CH_TwoCH
_Two-Te1-Ph2-CN, R¹-Np4-CH_TwoCH_Two-Te1-Ph3-CN, R¹-Np4-CH_Two
CH_Two-Te1-Np1-CN, R¹-Np4-CH_TwoCH_Two-Te1-Np2-CN, R¹-Np4-C
H_TwoCH_Two-Te1-Np3-CN, R¹-Np4-CH_TwoCH_Two-Te1-Np4-CN, R¹-Np4
-CH_TwoCH_Two-Te2-Ph1-CN, R¹-Np4-CH_TwoCH_Two-Te2-Ph2-CN, R¹-N
p4-CH_TwoCH_Two-Te2-Ph3-CN, R¹-Np4-CH_TwoCH_Two-Te2-Np1-CN, R¹
-Np4-CH_TwoCH_Two-Te2-Np2-CN, R¹-Np4-CH_TwoCH_Two-Te2-Np3-CN,
R¹-Np4-CH_TwoCH_Two-Te2-Np4-CN, R¹-Np4-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Ph2-CN, R¹-Np4-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-CN, R¹-Np4-C
H_TwoCH_Two-Te1-CH_TwoCH_Two-Np1-CN, R¹-Np4-CH_TwoCH_Two-Te1-CH_TwoCH_Two-
Np2-CN, R¹-Np4-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np3-CN, R¹-Np4-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Np4-CN, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-P
h1-CN, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-CN, R¹-Np4-CH_Two
CH_Two-Te2-CH _TwoCH_Two-Ph3-CN, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np
1-CN, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-CN, R¹-Np4-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Np3-CN, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np4
-CN,

R ¹ -Ph1-C≡C-Te1-Ph1-CN, R ¹ -Ph1-C≡C-Te
1-Ph2-CN, R ¹ -Ph1-C≡C-Te1-Ph3-CN, R ¹ -Ph1-C≡C-Te1-
Np1-CN, R ¹ -Ph1-C≡C-Te1-Np2-CN, R ¹ -Ph1-C≡C-Te1-Np
3-CN, R ¹ -Ph1-C≡C-Te1-Np4-CN, R ¹ -Ph1-C≡C-Te2-Ph1-
CN, R ¹ -Ph1-C≡C-Te2-Ph2-CN, R ¹ -Ph1-C≡C-Te2-Ph3-C
N, R ¹ -Ph1-C≡C-Te2-Np1-CN, R ¹ -Ph1-C≡C-Te2-Np2-C
N, R ¹ -Ph1-C≡C-Te2-Np3-CN, R ¹ -Ph1-C≡C-Te2-Np4-C
N, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph1-C≡C-Te1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -P
h1-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH _2-
Np3-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph1-C≡C
-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph1-C≡C-Te2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -P
h1-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH _2-
Np4-CN,

R ¹ -Ph2-C≡C-Te1-Ph1-CN, R ¹ -Ph2-C≡C-Te
1-Ph2-CN, R ¹ -Ph2-C≡C-Te1-Ph3-CN, R ¹ -Ph2-C≡C-Te1-
Np1-CN, R ¹ -Ph2-C≡C-Te1-Np2-CN, R ¹ -Ph2-C≡C-Te1-Np
3-CN, R ¹ -Ph2-C≡C-Te1-Np4-CN, R ¹ -Ph2-C≡C-Te2-Ph1-
CN, R ¹ -Ph2-C≡C-Te2-Ph2-CN, R ¹ -Ph2-C≡C-Te2-Ph3-C
N, R ¹ -Ph2-C≡C-Te2-Np1-CN, R ¹ -Ph2-C≡C-Te2-Np2-C
N, R ¹ -Ph2-C≡C-Te2-Np3-CN, R ¹ -Ph2-C≡C-Te2-Np4-C
N, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph2-C≡C-Te1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -P
h2-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH _2-
Np3-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph2-C≡C
-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph2-C≡C-Te2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -P
h2-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH _2-
Np4-CN,

R ¹ -Ph3-C≡C-Te1-Ph1-CN, R ¹ -Ph3-C≡C-Te
1-Ph2-CN, R ¹ -Ph3-C≡C-Te1-Ph3-CN, R ¹ -Ph3-C≡C-Te1-
Np1-CN, R ¹ -Ph3-C≡C-Te1-Np2-CN, R ¹ -Ph3-C≡C-Te1-Np
3-CN, R ¹ -Ph3-C≡C-Te1-Np4-CN, R ¹ -Ph3-C≡C-Te2-Ph1-
CN, R ¹ -Ph3-C≡C-Te2-Ph2-CN, R ¹ -Ph3-C≡C-Te2-Ph3-C
N, R ¹ -Ph3-C≡C-Te2-Np1-CN, R ¹ -Ph3-C≡C-Te2-Np2-C
N, R ¹ -Ph3-C≡C-Te2-Np3-CN, R ¹ -Ph3-C≡C-Te2-Np4-C
N, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph3-C≡C-Te1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -P
h3-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH _2-
Np3-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph3-C≡C
-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph3-C≡C-Te2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -P
h3-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH _2-
Np4-CN,

R ¹ -Np1-C≡C-Te1-Ph1-CN, R ¹ -Np1-C≡C-Te
1-Ph2-CN, R ¹ -Np1-C≡C-Te1-Ph3-CN, R ¹ -Np1-C≡C-Te1-
Np1-CN, R ¹ -Np1-C≡C-Te1-Np2-CN, R ¹ -Np1-C≡C-Te1-Np
3-CN, R ¹ -Np1-C≡C-Te1-Np4-CN, R ¹ -Np1-C≡C-Te2-Ph1-
CN, R ¹ -Np1-C≡C-Te2-Ph2-CN, R ¹ -Np1-C≡C-Te2-Ph3-C
N, R ¹ -Np1-C≡C-Te2-Np1-CN, R ¹ -Np1-C≡C-Te2-Np2-C
N, R ¹ -Np1-C≡C-Te2-Np3-CN, R ¹ -Np1-C≡C-Te2-Np4-C
N, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np1-C≡C-Te1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -N
p1-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH _2-
Np3-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np1-C≡C
-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np1-C≡C-Te2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -N
p1-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH _2-
Np4-CN,

R ¹ -Np2-C≡C-Te1-Ph1-CN, R ¹ -Np2-C≡C-Te
1-Ph2-CN, R ¹ -Np2-C≡C-Te1-Ph3-CN, R ¹ -Np2-C≡C-Te1-
Np1-CN, R ¹ -Np2-C≡C-Te1-Np2-CN, R ¹ -Np2-C≡C-Te1-Np
3-CN, R ¹ -Np2-C≡C-Te1-Np4-CN, R ¹ -Np2-C≡C-Te2-Ph1-
CN, R ¹ -Np2-C≡C-Te2-Ph2-CN, R ¹ -Np2-C≡C-Te2-Ph3-C
N, R ¹ -Np2-C≡C-Te2-Np1-CN, R ¹ -Np2-C≡C-Te2-Np2-C
N, R ¹ -Np2-C≡C-Te2-Np3-CN, R ¹ -Np2-C≡C-Te2-Np4-C
N, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np2-C≡C-Te1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -N
p2-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH _2-
Np3-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np2-C≡C
-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np2-C≡C-Te2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -N
p2-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH _2-
Np4-CN,

R ¹ -Np3-C≡C-Te1-Ph1-CN, R ¹ -Np3-C≡C-Te
1-Ph2-CN, R ¹ -Np3-C≡C-Te1-Ph3-CN, R ¹ -Np3-C≡C-Te1-
Np1-CN, R ¹ -Np3-C≡C-Te1-Np2-CN, R ¹ -Np3-C≡C-Te1-Np
3-CN, R ¹ -Np3-C≡C-Te1-Np4-CN, R ¹ -Np3-C≡C-Te2-Ph1-
CN, R ¹ -Np3-C≡C-Te2-Ph2-CN, R ¹ -Np3-C≡C-Te2-Ph3-C
N, R ¹ -Np3-C≡C-Te2-Np1-CN, R ¹ -Np3-C≡C-Te2-Np2-C
N, R ¹ -Np3-C≡C-Te2-Np3-CN, R ¹ -Np3-C≡C-Te2-Np4-C
N, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np3-C≡C-Te1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -N
p3-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH _2-
Np3-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np3-C≡C
-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np3-C≡C-Te2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -N
p3-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH _2-
Np4-CN,

R ¹ -Np4-C≡C-Te1-Ph1-CN, R ¹ -Np4-C≡C-Te
1-Ph2-CN, R ¹ -Np4-C≡C-Te1-Ph3-CN, R ¹ -Np4-C≡C-Te1-
Np1-CN, R ¹ -Np4-C≡C-Te1-Np2-CN, R ¹ -Np4-C≡C-Te1-Np
3-CN, R ¹ -Np4-C≡C-Te1-Np4-CN, R ¹ -Np4-C≡C-Te2-Ph1-
CN, R ¹ -Np4-C≡C-Te2-Ph2-CN, R ¹ -Np4-C≡C-Te2-Ph3-C
N, R ¹ -Np4-C≡C-Te2-Np1-CN, R ¹ -Np4-C≡C-Te2-Np2-C
N, R ¹ -Np4-C≡C-Te2-Np3-CN, R ¹ -Np4-C≡C-Te2-Np4-C
N, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np4-C≡C-Te1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -N
p4-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH _2-
Np3-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np4-C≡C
-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np4-C≡C-Te2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -N
p4-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH _2-
Np4-CN,

When m = 1, n = 0, V is a single bond and Z is a trifluoromethoxy group,

R ¹ -Cy-Te1-Ph1-OCF ₃ , R ¹ -Cy-Te1-Ph2-OC
F ₃ , R ¹ -Cy-Te1-Ph3-OCF ₃ , R ¹ -Cy-Te1-Np1-OCF ₃ , R ¹ -Cy-
Te1-Np2-OCF ₃ , R ¹ -Cy-Te1-Ph3-OCF ₃ , R ¹ -Cy-Te1-Np4-OC
F ₃ , R ¹ -Cy-Te2-Ph1-OCF ₃ , R ¹ -Cy-Te2-Ph2-OCF ₃ , R ¹ -Cy-
Te2-Ph3-OCF ₃ , R ¹ -Cy-Te2-Np1-OCF ₃ , R ¹ -Cy-Te2-Np2-OC
F ₃ , R ¹ -Cy-Te2-Ph3-OCF ₃ , R ¹ -Cy-Te2-Np4-OCF ₃ , R ¹ -Cy-
Te1-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹
-Cy-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Cy-Te1-CH ₂ CH ₂ -Np2-OC
F ₃ , R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Cy-Te1-CH ₂ CH ₂ -Np
4-OCF ₃ , R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph1-OCF ₃ , R ¹ -Cy-Te2-CH ₂ CH
₂ -Ph2-OCF ₃ , R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Cy-Te2-C
H ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Cy-Te2-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Cy-T
e2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Cy-Te2-CH ₂ CH ₂ -Np4-OCF ₃ ,

R¹-Ph1-Te1-Ph1-OCF_Three, R¹-Ph1-Te1-Ph2-OC
F_Three, R¹-Ph1-Te1-Ph3-OCF_Three, R¹-Ph1-Te1-Np1-OCF_Three, R¹-P
h1-Te1-Np2-OCF_Three, R¹-Ph1-Te1-Ph3-OCF_Three, R¹-Ph1-Te1-N
p4-OCF _Three, R¹-Ph1-Te2-Ph1-OCF_Three, R¹-Ph1-Te2-Ph2-OC
F_Three, R¹-Ph1-Te2-Ph3-OCF_Three, R¹-Ph1-Te2-Np1-OCF_Three, R¹-P
h1-Te2-Np2-OCF_Three, R¹-Ph1-Te2-Ph3-OCF_Three, R¹-Ph1-Te2-N
p4-OCF_Three, R¹-Ph1-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph1-Te1-CH
_TwoCH_Two-Ph3-OCF_Three, R¹-Ph1-Te1-CH_TwoCH_Two-Np1-OCF_Three, R¹-Ph1-
Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph1-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R
¹-Ph1-Te1-CH_TwoCH_Two-Np4-OCF_Three, R¹-Ph1-Te2-CH_TwoCH_Two-Ph1-O
CF_Three, R¹-Ph1-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph1-Te2-CH_TwoCH_Two
-Ph3-OCF_Three, R¹-Ph1-Te2-CH_TwoCH_Two-Np1-OCF_Three, R¹-Ph1-Te2-
CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph1-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph
1-Te2-CH_TwoCH_Two-Np4-OCF_Three,

R¹-Ph2-Te1-Ph1-OCF_Three, R¹-Ph2-Te1-Ph2-OC
F_Three, R¹-Ph2-Te1-Ph3-OCF_Three, R¹-Ph2-Te1-Np1-OCF_Three, R¹-P
h2-Te1-Np2-OCF_Three, R¹-Ph2-Te1-Ph3-OCF_Three, R¹-Ph2-Te1-N
p4-OCF _Three, R¹-Ph2-Te2-Ph1-OCF_Three, R¹-Ph2-Te2-Ph2-OC
F_Three, R¹-Ph2-Te2-Ph3-OCF_Three, R¹-Ph2-Te2-Np1-OCF_Three, R¹-P
h2-Te2-Np2-OCF_Three, R¹-Ph2-Te2-Ph3-OCF_Three, R¹-Ph2-Te2-N
p4-OCF_Three, R¹-Ph2-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph2-Te1-CH
_TwoCH_Two-Ph3-OCF_Three, R¹-Ph2-Te1-CH_TwoCH_Two-Np1-OCF_Three, R¹-Ph2-
Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph2-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R
¹-Ph2-Te1-CH_TwoCH_Two-Np4-OCF_Three, R¹-Ph2-Te2-CH_TwoCH_Two-Ph1-O
CF_Three, R¹-Ph2-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph2-Te2-CH_TwoCH_Two
-Ph3-OCF_Three, R¹-Ph2-Te2-CH_TwoCH_Two-Np1-OCF_Three, R¹-Ph2-Te2-
CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph2-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph
2-Te2-CH_TwoCH_Two-Np4-OCF_Three,

R¹-Ph3-Te1-Ph1-OCF_Three, R¹-Ph3-Te1-Ph2-OC
F_Three, R¹-Ph3-Te1-Ph3-OCF_Three, R¹-Ph3-Te1-Np1-OCF_Three, R¹-P
h3-Te1-Np2-OCF_Three, R¹-Ph3-Te1-Ph3-OCF_Three, R¹-Ph3-Te1-N
p4-OCF _Three, R¹-Ph3-Te2-Ph1-OCF_Three, R¹-Ph3-Te2-Ph2-OC
F_Three, R¹-Ph3-Te2-Ph3-OCF_Three, R¹-Ph3-Te2-Np1-OCF_Three, R¹-P
h3-Te2-Np2-OCF_Three, R¹-Ph3-Te2-Ph3-OCF_Three, R¹-Ph3-Te2-N
p4-OCF_Three, R¹-Ph3-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph3-Te1-CH
_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-Te1-CH_TwoCH_Two-Np1-OCF_Three, R¹-Ph3-
Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph3-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R
¹-Ph3-Te1-CH_TwoCH_Two-Np4-OCF_Three, R¹-Ph3-Te2-CH_TwoCH_Two-Ph1-O
CF_Three, R¹-Ph3-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph3-Te2-CH_TwoCH_Two
-Ph3-OCF_Three, R¹-Ph3-Te2-CH_TwoCH_Two-Np1-OCF_Three, R¹-Ph3-Te2-
CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph3-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph
3-Te2-CH_TwoCH_Two-Np4-OCF_Three,

R¹-Np1-Te1-Ph1-OCF_Three, R¹-Np1-Te1-Ph2-OC
F_Three, R¹-Np1-Te1-Ph3-OCF_Three, R¹-Np1-Te1-Np1-OCF_Three, R¹-N
p1-Te1-Np2-OCF_Three, R¹-Np1-Te1-Ph3-OCF_Three, R¹-Np1-Te1-N
p4-OCF _Three, R¹-Np1-Te2-Ph1-OCF_Three, R¹-Np1-Te2-Ph2-OC
F_Three, R¹-Np1-Te2-Ph3-OCF_Three, R¹-Np1-Te2-Np1-OCF_Three, R¹-N
p1-Te2-Np2-OCF_Three, R¹-Np1-Te2-Ph3-OCF_Three, R¹-Np1-Te2-N
p4-OCF_Three, R¹-Np1-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np1-Te1-CH
_TwoCH_Two-Ph3-OCF_Three, R¹-Np1-Te1-CH_TwoCH_Two-Np1-OCF_Three, R¹-Np1-
Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-Np1-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R
¹-Np1-Te1-CH_TwoCH_Two-Np4-OCF_Three, R¹-Np1-Te2-CH_TwoCH_Two-Ph1-O
CF_Three, R¹-Np1-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np1-Te2-CH_TwoCH_Two
-Ph3-OCF_Three, R¹-Np1-Te2-CH_TwoCH_Two-Np1-OCF_Three, R¹-Np1-Te2-
CH_TwoCH_Two-Np2-OCF_Three, R¹-Np1-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np
1-Te2-CH_TwoCH_Two-Np4-OCF_Three,

R¹-Np2-Te1-Ph1-OCF_Three, R¹-Np2-Te1-Ph2-OC
F_Three, R¹-Np2-Te1-Ph3-OCF_Three, R¹-Np2-Te1-Np1-OCF_Three, R¹-N
p2-Te1-Np2-OCF_Three, R¹-Np2-Te1-Ph3-OCF_Three, R¹-Np2-Te1-N
p4-OCF _Three, R¹-Np2-Te2-Ph1-OCF_Three, R¹-Np2-Te2-Ph2-OC
F_Three, R¹-Np2-Te2-Ph3-OCF_Three, R¹-Np2-Te2-Np1-OCF_Three, R¹-N
p2-Te2-Np2-OCF_Three, R¹-Np2-Te2-Ph3-OCF_Three, R¹-Np2-Te2-N
p4-OCF_Three, R¹-Np2-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np2-Te1-CH
_TwoCH_Two-Ph3-OCF_Three, R¹-Np2-Te1-CH_TwoCH_Two-Np1-OCF_Three, R¹-Np2-
Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-Np2-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R
¹-Np2-Te1-CH_TwoCH_Two-Np4-OCF_Three, R¹-Np2-Te2-CH_TwoCH_Two-Ph1-O
CF_Three, R¹-Np2-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np2-Te2-CH_TwoCH_Two
-Ph3-OCF_Three, R¹-Np2-Te2-CH_TwoCH_Two-Np1-OCF_Three, R¹-Np2-Te2-
CH_TwoCH_Two-Np2-OCF_Three, R¹-Np2-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np
2-Te2-CH_TwoCH_Two-Np4-OCF_Three,

R¹-Ph3-Te1-Ph1-OCF_Three, R¹-Ph3-Te1-Ph2-OC
F_Three, R¹-Ph3-Te1-Ph3-OCF_Three, R¹-Ph3-Te1-Np1-OCF_Three, R¹-P
h3-Te1-Np2-OCF_Three, R¹-Ph3-Te1-Ph3-OCF_Three, R¹-Ph3-Te1-N
p4-OCF _Three, R¹-Ph3-Te2-Ph1-OCF_Three, R¹-Ph3-Te2-Ph2-OC
F_Three, R¹-Ph3-Te2-Ph3-OCF_Three, R¹-Ph3-Te2-Np1-OCF_Three, R¹-P
h3-Te2-Np2-OCF_Three, R¹-Ph3-Te2-Ph3-OCF_Three, R¹-Ph3-Te2-N
p4-OCF_Three, R¹-Ph3-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph3-Te1-CH
_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-Te1-CH_TwoCH_Two-Np1-OCF_Three, R¹-Ph3-
Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph3-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R
¹-Ph3-Te1-CH_TwoCH_Two-Np4-OCF_Three, R¹-Ph3-Te2-CH_TwoCH_Two-Ph1-O
CF_Three, R¹-Ph3-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph3-Te2-CH_TwoCH_Two
-Ph3-OCF_Three, R¹-Ph3-Te2-CH_TwoCH_Two-Np1-OCF_Three, R¹-Ph3-Te2-
CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph3-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph
3-Te2-CH_TwoCH_Two-Np4-OCF_Three,

R¹-Np4-Te1-Ph1-OCF_Three, R¹-Np4-Te1-Ph2-OC
F_Three, R¹-Np4-Te1-Ph3-OCF_Three, R¹-Np4-Te1-Np1-OCF_Three, R¹-N
p4-Te1-Np2-OCF_Three, R¹-Np4-Te1-Ph3-OCF_Three, R¹-Np4-Te1-N
p4-OCF _Three, R¹-Np4-Te2-Ph1-OCF_Three, R¹-Np4-Te2-Ph2-OC
F_Three, R¹-Np4-Te2-Ph3-OCF_Three, R¹-Np4-Te2-Np1-OCF_Three, R¹-N
p4-Te2-Np2-OCF_Three, R¹-Np4-Te2-Ph3-OCF_Three, R¹-Np4-Te2-N
p4-OCF_Three, R¹-Np4-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np4-Te1-CH
_TwoCH_Two-Ph3-OCF_Three, R¹-Np4-Te1-CH_TwoCH_Two-Np1-OCF_Three, R¹-Np4-
Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-Np4-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R
¹-Np4-Te1-CH_TwoCH_Two-Np4-OCF_Three, R¹-Np4-Te2-CH_TwoCH_Two-Ph1-O
CF_Three, R¹-Np4-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np4-Te2-CH_TwoCH_Two
-Ph3-OCF_Three, R¹-Np4-Te2-CH_TwoCH_Two-Np1-OCF_Three, R¹-Np4-Te2-
CH_TwoCH_Two-Np2-OCF_Three, R¹-Np4-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np
4-Te2-CH_TwoCH_Two-Np4-OCF_Three,

R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph1-OCF ₃ , R ¹ -Cy-CH ₂ CH
₂ -Te1-Ph2-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph3-OCF ₃ , R ¹ -Cy-C
H ₂ CH ₂ -Te1-Np1-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te1-Np2-OCF ₃ , R ^1-
Cy-CH ₂ CH ₂ -Te1-Ph3-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te1-Np4-OC
F ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph1-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph
2-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph3-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te
2-Np1-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-Np2-OCF ₃ , R ¹ -Cy-CH ₂ CH
₂ -Te2-Ph3-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-Np4-OCF ₃ , R ¹ -Cy-C
H ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂
-Ph3-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Cy
-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ C
H ₂ -Ph3-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ^1-
Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH
₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R
¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-
CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OC
F ₃ , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF ₃ ,

R¹-Ph1-CH_TwoCH_Two-Te1-Ph1-OCF_Three, R¹-Ph1-CH_Two
CH_Two-Te1-Ph2-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-P
h1-CH_TwoCH_Two-Te1-Np1-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te1-Np2-OC
F_Three, R¹-Ph1-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te1-
Np4-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te2-Ph1-OCF_Three, R¹-Ph1-CH_TwoCH
_Two-Te2-Ph2-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Ph1
-CH_TwoCH_Two-Te2-Np1-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te2-Np2-OCF_Three,
R¹-Ph1-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te2-Np4-
OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph1-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Np1-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-P
h1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph1-CH _TwoCH_Two-Te1-C
H_TwoCH_Two-Np4-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph1-OC
F_Three, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph1-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-N
p1-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph1
-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph1-CH_TwoCH_Two-Te2-CH_Two
CH_Two-Np4-OCF_Three,

R¹-Ph2-CH_TwoCH_Two-Te1-Ph1-OCF_Three, R¹-Ph2-CH_Two
CH_Two-Te1-Ph2-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-P
h2-CH_TwoCH_Two-Te1-Np1-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te1-Np2-OC
F_Three, R¹-Ph2-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te1-
Np4-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te2-Ph1-OCF_Three, R¹-Ph2-CH_TwoCH
_Two-Te2-Ph2-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Ph2
-CH_TwoCH_Two-Te2-Np1-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te2-Np2-OCF_Three,
R¹-Ph2-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te2-Np4-
OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph2-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Np1-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-P
h2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph2-CH _TwoCH_Two-Te1-C
H_TwoCH_Two-Np4-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph1-OC
F_Three, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph2-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-N
p1-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph2
-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph2-CH_TwoCH_Two-Te2-CH_Two
CH_Two-Np4-OCF_Three,

R¹-Ph3-CH_TwoCH_Two-Te1-Ph1-OCF_Three, R¹-Ph3-CH_Two
CH_Two-Te1-Ph2-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-P
h3-CH_TwoCH_Two-Te1-Np1-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-Np2-OC
F_Three, R¹-Ph3-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-
Np4-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-Ph1-OCF_Three, R¹-Ph3-CH_TwoCH
_Two-Te2-Ph2-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Ph3
-CH_TwoCH_Two-Te2-Np1-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-Np2-OCF_Three,
R¹-Ph3-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-Np4-
OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph3-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Np1-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-P
h3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-CH _TwoCH_Two-Te1-C
H_TwoCH_Two-Np4-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph1-OC
F_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph3-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-N
p1-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph3
-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_Two
CH_Two-Np4-OCF_Three,

R¹-Np1-CH_TwoCH_Two-Te1-Ph1-OCF_Three, R¹-Np1-CH_Two
CH_Two-Te1-Ph2-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-N
p1-CH_TwoCH_Two-Te1-Np1-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te1-Np2-OC
F_Three, R¹-Np1-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te1-
Np4-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te2-Ph1-OCF_Three, R¹-Np1-CH_TwoCH
_Two-Te2-Ph2-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Np1
-CH_TwoCH_Two-Te2-Np1-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te2-Np2-OCF_Three,
R¹-Np1-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te2-Np4-
OCF_Three, R¹-Np1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np1-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Np1-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-N
p1-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np1-CH _TwoCH_Two-Te1-C
H_TwoCH_Two-Np4-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph1-OC
F_Three, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np1-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-N
p1-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-OCF_Three, R¹-Np1
-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np1-CH_TwoCH_Two-Te2-CH_Two
CH_Two-Np4-OCF_Three,

R¹-Np2-CH_TwoCH_Two-Te1-Ph1-OCF_Three, R¹-Np2-CH_Two
CH_Two-Te1-Ph2-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-N
p2-CH_TwoCH_Two-Te1-Np1-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te1-Np2-OC
F_Three, R¹-Np2-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te1-
Np4-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te2-Ph1-OCF_Three, R¹-Np2-CH_TwoCH
_Two-Te2-Ph2-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Np2
-CH_TwoCH_Two-Te2-Np1-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te2-Np2-OCF_Three,
R¹-Np2-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te2-Np4-
OCF_Three, R¹-Np2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np2-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Np1-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-N
p2-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np2-CH _TwoCH_Two-Te1-C
H_TwoCH_Two-Np4-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph1-OC
F_Three, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np2-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-N
p1-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-OCF_Three, R¹-Np2
-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np2-CH_TwoCH_Two-Te2-CH_Two
CH_Two-Np4-OCF_Three,

R¹-Ph3-CH_TwoCH_Two-Te1-Ph1-OCF_Three, R¹-Ph3-CH_Two
CH_Two-Te1-Ph2-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-P
h3-CH_TwoCH_Two-Te1-Np1-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-Np2-OC
F_Three, R¹-Ph3-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-
Np4-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-Ph1-OCF_Three, R¹-Ph3-CH_TwoCH
_Two-Te2-Ph2-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Ph3
-CH_TwoCH_Two-Te2-Np1-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-Np2-OCF_Three,
R¹-Ph3-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-Np4-
OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph3-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Np1-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-P
h3-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-CH _TwoCH_Two-Te1-C
H_TwoCH_Two-Np4-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph1-OC
F_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Ph3-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-N
p1-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-OCF_Three, R¹-Ph3
-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Ph3-CH_TwoCH_Two-Te2-CH_Two
CH_Two-Np4-OCF_Three,

R¹-Np4-CH_TwoCH_Two-Te1-Ph1-OCF_Three, R¹-Np4-CH_Two
CH_Two-Te1-Ph2-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-N
p4-CH_TwoCH_Two-Te1-Np1-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te1-Np2-OC
F_Three, R¹-Np4-CH_TwoCH_Two-Te1-Ph3-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te1-
Np4-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te2-Ph1-OCF_Three, R¹-Np4-CH_TwoCH
_Two-Te2-Ph2-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Np4
-CH_TwoCH_Two-Te2-Np1-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te2-Np2-OCF_Three,
R¹-Np4-CH_TwoCH_Two-Te2-Ph3-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te2-Np4-
OCF_Three, R¹-Np4-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np4-CH
_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te1-CH_TwoCH_Two
-Np1-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Np2-OCF_Three, R¹-N
p4-CH_TwoCH_Two-Te1-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np4-CH _TwoCH_Two-Te1-C
H_TwoCH_Two-Np4-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph1-OC
F_Three, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph2-OCF_Three, R¹-Np4-CH_TwoC
H_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-N
p1-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Np2-OCF_Three, R¹-Np4
-CH_TwoCH_Two-Te2-CH_TwoCH_Two-Ph3-OCF_Three, R¹-Np4-CH_TwoCH_Two-Te2-CH_Two
CH_Two-Np4-OCF_Three,

R ¹ -Ph1-C≡C-Te1-Ph1-OCF ₃ , R ¹ -Ph1-C≡C-
Te1-Ph2-OCF ₃ , R ¹ -Ph1-C≡C-Te1-Ph3-OCF ₃ , R ¹ -Ph1-C≡
C-Te1-Np1-OCF ₃ , R ¹ -Ph1-C≡C-Te1-Np2-OCF ₃ , R ¹ -Ph1-C
≡C-Te1-Ph3-OCF ₃ , R ¹ -Ph1-C≡C-Te1-Np4-OCF ₃ , R ¹ -Ph1
-C≡C-Te2-Ph1-OCF ₃ , R ¹ -Ph1-C≡C-Te2-Ph2-OCF ₃ , R ¹ -P
h1-C≡C-Te2-Ph3-OCF ₃ , R ¹ -Ph1-C≡C-Te2-Np1-OCF ₃ , R ¹
-Ph1-C≡C-Te2-Np2-OCF ₃ , R ¹ -Ph1-C≡C-Te2-Ph3-OCF ₃ ,
R ¹ -Ph1-C≡C-Te2-Np4-OCF ₃ , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -P
h2-OCF ₃ , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph1-C
≡C-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np
2-OCF ₃ , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph1-C
≡C-Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph
1-OCF ₃ , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Ph1-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np
1-OCF ₃ , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Ph1-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np
4-OCF ₃ ,

R ¹ -Ph2-C≡C-Te1-Ph1-OCF ₃ , R ¹ -Ph2-C≡C-
Te1-Ph2-OCF ₃ , R ¹ -Ph2-C≡C-Te1-Ph3-OCF ₃ , R ¹ -Ph2-C≡
C-Te1-Np1-OCF ₃ , R ¹ -Ph2-C≡C-Te1-Np2-OCF ₃ , R ¹ -Ph2-C
≡C-Te1-Ph3-OCF ₃ , R ¹ -Ph2-C≡C-Te1-Np4-OCF ₃ , R ¹ -Ph2
-C≡C-Te2-Ph1-OCF ₃ , R ¹ -Ph2-C≡C-Te2-Ph2-OCF ₃ , R ¹ -P
h2-C≡C-Te2-Ph3-OCF ₃ , R ¹ -Ph2-C≡C-Te2-Np1-OCF ₃ , R ¹
-Ph2-C≡C-Te2-Np2-OCF ₃ , R ¹ -Ph2-C≡C-Te2-Ph3-OCF ₃ ,
R ¹ -Ph2-C≡C-Te2-Np4-OCF ₃ , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -P
h2-OCF ₃ , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph2-C
≡C-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np
2-OCF ₃ , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph2-C
≡C-Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph
1-OCF ₃ , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Ph2-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np
1-OCF ₃ , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Ph2-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np
4-OCF ₃ ,

R ¹ -Ph3-C≡C-Te1-Ph1-OCF ₃ , R ¹ -Ph3-C≡C-
Te1-Ph2-OCF ₃ , R ¹ -Ph3-C≡C-Te1-Ph3-OCF ₃ , R ¹ -Ph3-C≡
C-Te1-Np1-OCF ₃ , R ¹ -Ph3-C≡C-Te1-Np2-OCF ₃ , R ¹ -Ph3-C
≡C-Te1-Ph3-OCF ₃ , R ¹ -Ph3-C≡C-Te1-Np4-OCF ₃ , R ¹ -Ph3
-C≡C-Te2-Ph1-OCF ₃ , R ¹ -Ph3-C≡C-Te2-Ph2-OCF ₃ , R ¹ -P
h3-C≡C-Te2-Ph3-OCF ₃ , R ¹ -Ph3-C≡C-Te2-Np1-OCF ₃ , R ¹
-Ph3-C≡C-Te2-Np2-OCF ₃ , R ¹ -Ph3-C≡C-Te2-Ph3-OCF ₃ ,
R ¹ -Ph3-C≡C-Te2-Np4-OCF ₃ , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -P
h2-OCF ₃ , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph3-C
≡C-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np
2-OCF ₃ , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph3-C
≡C-Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph
1-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Ph3-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np
1-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Ph3-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np
4-OCF ₃ ,

R ¹ -Np1-C≡C-Te1-Ph1-OCF ₃ , R ¹ -Np1-C≡C-
Te1-Ph2-OCF ₃ , R ¹ -Np1-C≡C-Te1-Ph3-OCF ₃ , R ¹ -Np1-C≡
C-Te1-Np1-OCF ₃ , R ¹ -Np1-C≡C-Te1-Np2-OCF ₃ , R ¹ -Np1-C
≡C-Te1-Ph3-OCF ₃ , R ¹ -Np1-C≡C-Te1-Np4-OCF ₃ , R ¹ -Np1
-C≡C-Te2-Ph1-OCF ₃ , R ¹ -Np1-C≡C-Te2-Ph2-OCF ₃ , R ¹ -N
p1-C≡C-Te2-Ph3-OCF ₃ , R ¹ -Np1-C≡C-Te2-Np1-OCF ₃ , R ¹
-Np1-C≡C-Te2-Np2-OCF ₃ , R ¹ -Np1-C≡C-Te2-Ph3-OCF ₃ ,
R ¹ -Np1-C≡C-Te2-Np4-OCF ₃ , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -P
h2-OCF ₃ , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np1-C
≡C-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np
2-OCF ₃ , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np1-C
≡C-Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph
1-OCF ₃ , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Np1-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np
1-OCF ₃ , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Np1-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np
4-OCF ₃ ,

R ¹ -Np2-C≡C-Te1-Ph1-OCF ₃ , R ¹ -Np2-C≡C-
Te1-Ph2-OCF ₃ , R ¹ -Np2-C≡C-Te1-Ph3-OCF ₃ , R ¹ -Np2-C≡
C-Te1-Np1-OCF ₃ , R ¹ -Np2-C≡C-Te1-Np2-OCF ₃ , R ¹ -Np2-C
≡C-Te1-Ph3-OCF ₃ , R ¹ -Np2-C≡C-Te1-Np4-OCF ₃ , R ¹ -Np2
-C≡C-Te2-Ph1-OCF ₃ , R ¹ -Np2-C≡C-Te2-Ph2-OCF ₃ , R ¹ -N
p2-C≡C-Te2-Ph3-OCF ₃ , R ¹ -Np2-C≡C-Te2-Np1-OCF ₃ , R ¹
-Np2-C≡C-Te2-Np2-OCF ₃ , R ¹ -Np2-C≡C-Te2-Ph3-OCF ₃ ,
R ¹ -Np2-C≡C-Te2-Np4-OCF ₃ , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -P
h2-OCF ₃ , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np2-C
≡C-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np
2-OCF ₃ , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np2-C
≡C-Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph
1-OCF ₃ , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Np2-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np
1-OCF ₃ , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Np2-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np
4-OCF ₃ ,

R ¹ -Ph3-C≡C-Te1-Ph1-OCF ₃ , R ¹ -Ph3-C≡C-
Te1-Ph2-OCF ₃ , R ¹ -Ph3-C≡C-Te1-Ph3-OCF ₃ , R ¹ -Ph3-C≡
C-Te1-Np1-OCF ₃ , R ¹ -Ph3-C≡C-Te1-Np2-OCF ₃ , R ¹ -Ph3-C
≡C-Te1-Ph3-OCF ₃ , R ¹ -Ph3-C≡C-Te1-Np4-OCF ₃ , R ¹ -Ph3
-C≡C-Te2-Ph1-OCF ₃ , R ¹ -Ph3-C≡C-Te2-Ph2-OCF ₃ , R ¹ -P
h3-C≡C-Te2-Ph3-OCF ₃ , R ¹ -Ph3-C≡C-Te2-Np1-OCF ₃ , R ¹
-Ph3-C≡C-Te2-Np2-OCF ₃ , R ¹ -Ph3-C≡C-Te2-Ph3-OCF ₃ ,
R ¹ -Ph3-C≡C-Te2-Np4-OCF ₃ , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -P
h2-OCF ₃ , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph3-C
≡C-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np
2-OCF ₃ , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph3-C
≡C-Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph
1-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Ph3-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np
1-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Ph3-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np
4-OCF ₃ ,

R ¹ -Np4-C≡C-Te1-Ph1-OCF ₃ , R ¹ -Np4-C≡C-
Te1-Ph2-OCF ₃ , R ¹ -Np4-C≡C-Te1-Ph3-OCF ₃ , R ¹ -Np4-C≡
C-Te1-Np1-OCF ₃ , R ¹ -Np4-C≡C-Te1-Np2-OCF ₃ , R ¹ -Np4-C
≡C-Te1-Ph3-OCF ₃ , R ¹ -Np4-C≡C-Te1-Np4-OCF ₃ , R ¹ -Np4
-C≡C-Te2-Ph1-OCF ₃ , R ¹ -Np4-C≡C-Te2-Ph2-OCF ₃ , R ¹ -N
p4-C≡C-Te2-Ph3-OCF ₃ , R ¹ -Np4-C≡C-Te2-Np1-OCF ₃ , R ¹
-Np4-C≡C-Te2-Np2-OCF ₃ , R ¹ -Np4-C≡C-Te2-Ph3-OCF ₃ ,
R ¹ -Np4-C≡C-Te2-Np4-OCF ₃ , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -P
h2-OCF ₃ , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np4-C
≡C-Te1-CH ₂ CH ₂ -Np1-OCF ₃ , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np
2-OCF ₃ , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np4-C
≡C-Te1-CH ₂ CH ₂ -Np4-OCF ₃ , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph
1-OCF ₃ , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF ₃ , R ¹ -Np4-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np
1-OCF ₃ , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF ₃ , R ¹ -Np4-C
≡C-Te2-CH ₂ CH ₂ -Ph3-OCF ₃ , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np
4-OCF ₃ ,

When m = 0, n = 1, V is a single bond, and Z is a fluorine atom,

R¹-Te1-Cy-Ph1-F, R¹-Te1-Cy-Ph2-F, R¹-T
e1-Cy-Ph3-F, R¹-Te1-Cy-Np1-F, R¹-Te1-Cy-Np2-F, R¹-
Te1-Cy-Np3-F, R¹-Te1-Cy-Np4-F, R¹-Te2-Cy-Ph1-F, R¹
-Te2-Cy-Ph2-F, R¹-Te2-Cy-Ph3-F, R¹-Te2-Cy-Np1-F, R
¹-Te2-Cy-Np2-F, R¹-Te2-Cy-Np3-F, R¹-Te2-Cy-Np4-F,
R¹-Te1-Cy-CH_TwoCH_Two-Ph2-F, R¹-Te1-Cy-CH_TwoCH_Two-Ph3-F, R¹
-Te1-Cy-CH_TwoCH_Two-Np1-F, R¹-Te1-Cy-CH_TwoCH_Two-Np2-F, R¹-T
e1-Cy-CH_TwoCH_Two-Np3-F, R¹-Te1-Cy-CH_TwoCH_Two-Np4-F, R¹-Te2
-Cy-CH_TwoCH_Two-Ph1-F, R¹-Te2-Cy-CH_TwoCH_Two-Ph2-F, R¹-Te2-C
y-CH_TwoCH_Two-Ph3-F, R¹-Te2-Cy-CH_TwoCH_Two-Np1-F, R¹-Te2-Cy-
CH_TwoCH_Two-Np2-F, R¹-Te2-Cy-CH_TwoCH_Two-Np3-F, R¹-Te2-Cy-CH
_TwoCH_Two-Np4-F, R¹-Te1-CH_TwoCH_Two-Cy-Ph1-F, R¹-Te1-CH_TwoCH_Two-
Cy-Ph2-F, R¹-Te1-CH_TwoCH_Two-Cy-Ph3-F, R¹-Te1-CH_TwoCH_Two-Cy
-Np1-F, R¹-Te1-CH_TwoCH_Two-Cy-Np2-F, R¹-Te1-CH_TwoCH_Two-Cy-N
p3-F, R¹-Te1-CH_TwoCH_Two-Cy-Np4-F, R¹-Te2-CH_TwoCH_Two-Cy-Ph1
-F, R¹-Te2-CH_TwoCH_Two-Cy-Ph2-F, R¹-Te2-CH_TwoCH_Two-Cy-Ph3-
F, R¹-Te2-CH_TwoCH_Two-Cy-Np1-F, R¹-Te2-CH_TwoCH_Two-Cy-Np2-
F, R¹-Te2-CH_TwoCH_Two-Cy-Np3-F, R¹-Te2-CH_TwoCH_Two-Cy-Np4-
F, R¹-Te1-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Ph2-F, R¹-Te1-CH_TwoCH_Two-Cy
-CH _TwoCH_Two-Ph3-F, R¹-Te1-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np1-F, R¹-T
e1-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np2-F, R¹-Te1-CH_TwoCH_Two-Cy-CH_TwoCH_Two
-Np3-F, R¹-Te1-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np4-F, R¹-Te2-CH_TwoC
H_Two-Cy-CH_TwoCH_Two-Ph1-F, R¹-Te2-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Ph2-
F, R¹-Te2-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Ph3-F, R¹-Te2-CH_TwoCH_Two-Cy
-CH_TwoCH_Two-Np1-F, R¹-Te2-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np2-F, R¹-T
e2-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np3-F, R¹-Te2-CH_TwoCH_Two-Cy-CH_TwoCH_Two
-Np4-F,

R¹-Te1-Ph1-Ph1-F, R¹-Te1-Ph1-Ph2-F, R¹
-Te1-Ph1-Ph3-F, R¹-Te1-Ph1-Np1-F, R¹-Te1-Ph1-Np2-
F, R¹-Te1-Ph1-Np3-F, R¹-Te1-Ph1-Np4-F, R¹-Te2-Ph1-
Ph1-F, R¹-Te2-Ph1-Ph2-F, R¹-Te2-Ph1-Ph3-F, R¹-Te2-
Ph1-Np1-F, R¹-Te2-Ph1-Np2-F, R¹-Te2-Ph1-Np3-F, R¹-
Te2-Ph1-Np4-F, R¹-Te1-Ph1-CH_TwoCH_Two-Ph2-F, R¹-Te1-Ph1
-CH_TwoCH_Two-Ph3-F, R¹-Te1-Ph1-CH_TwoCH_Two-Np1-F, R¹-Te1-Ph1
-CH_TwoCH_Two-Np2-F, R¹-Te1-Ph1-CH_TwoCH_Two-Np3-F, R¹-Te1-Ph1
-CH_TwoCH_Two-Np4-F, R¹-Te2-Ph1-CH_TwoCH_Two-Ph1-F, R¹-Te2-Ph1
-CH_TwoCH_Two-Ph2-F, R¹-Te2-Ph1-CH_TwoCH_Two-Ph3-F, R¹-Te2-Ph1
-CH_TwoCH_Two-Np1-F, R¹-Te2-Ph1-CH_TwoCH_Two-Np2-F, R¹-Te2-Ph1
-CH_TwoCH_Two-Np3-F, R¹-Te2-Ph1-CH_TwoCH_Two-Np4-F, R¹-Te1-Ph1
-C≡C-Ph2-F, R¹-Te1-Ph1-C≡C-Ph3-F, R¹-Te1-Ph1-C≡
C-Np1-F, R ¹-Te1-Ph1-C≡C-Np2-F, R¹-Te1-Ph1-C≡C-Np
3-F, R¹-Te1-Ph1-C≡C-Np4-F, R¹-Te2-Ph1-C≡C-Ph1-
F, R¹-Te2-Ph1-C≡C-Ph2-F, R¹-Te2-Ph1-C≡C-Ph3-F, R
¹-Te2-Ph1-C≡C-Np1-F, R¹-Te2-Ph1-C≡C-Np2-F, R¹-Te
2-Ph1-C≡C-Np3-F, R¹-Te2-Ph1-C≡C-Np4-F,

R¹-Te1-Ph2-Ph1-F, R¹-Te1-Ph2-Ph2-F, R¹
-Te1-Ph2-Ph3-F, R¹-Te1-Ph2-Np1-F, R¹-Te1-Ph2-Np2-
F, R¹-Te1-Ph2-Np3-F, R¹-Te1-Ph2-Np4-F, R¹-Te2-Ph2-
Ph1-F, R¹-Te2-Ph2-Ph2-F, R¹-Te2-Ph2-Ph3-F, R¹-Te2-
Ph2-Np1-F, R¹-Te2-Ph2-Np2-F, R¹-Te2-Ph2-Np3-F, R¹-
Te2-Ph2-Np4-F, R¹-Te1-Ph2-CH_TwoCH_Two-Ph2-F, R¹-Te1-Ph2
-CH_TwoCH_Two-Ph3-F, R¹-Te1-Ph2-CH_TwoCH_Two-Np1-F, R¹-Te1-Ph2
-CH_TwoCH_Two-Np2-F, R¹-Te1-Ph2-CH_TwoCH_Two-Np3-F, R¹-Te1-Ph2
-CH_TwoCH_Two-Np4-F, R¹-Te2-Ph2-CH_TwoCH_Two-Ph1-F, R¹-Te2-Ph2
-CH_TwoCH_Two-Ph2-F, R¹-Te2-Ph2-CH_TwoCH_Two-Ph3-F, R¹-Te2-Ph2
-CH_TwoCH_Two-Np1-F, R¹-Te2-Ph2-CH_TwoCH_Two-Np2-F, R¹-Te2-Ph2
-CH_TwoCH_Two-Np3-F, R¹-Te2-Ph2-CH_TwoCH_Two-Np4-F, R¹-Te1-Ph2
-C≡C-Ph2-F, R¹-Te1-Ph2-C≡C-Ph3-F, R¹-Te1-Ph2-C≡
C-Np1-F, R ¹-Te1-Ph2-C≡C-Np2-F, R¹-Te1-Ph2-C≡C-Np
3-F, R¹-Te1-Ph2-C≡C-Np4-F, R¹-Te2-Ph2-C≡C-Ph1-
F, R¹-Te2-Ph2-C≡C-Ph2-F, R¹-Te2-Ph2-C≡C-Ph3-F, R
¹-Te2-Ph2-C≡C-Np1-F, R¹-Te2-Ph2-C≡C-Np2-F, R¹-Te
2-Ph2-C≡C-Np3-F, R¹-Te2-Ph2-C≡C-Np4-F,

R¹-Te1-Ph3-Ph1-F, R¹-Te1-Ph3-Ph2-F, R¹
-Te1-Ph3-Ph3-F, R¹-Te1-Ph3-Np1-F, R¹-Te1-Ph3-Np2-
F, R¹-Te1-Ph3-Np3-F, R¹-Te1-Ph3-Np4-F, R¹-Te2-Ph3-
Ph1-F, R¹-Te2-Ph3-Ph2-F, R¹-Te2-Ph3-Ph3-F, R¹-Te2-
Ph3-Np1-F, R¹-Te2-Ph3-Np2-F, R¹-Te2-Ph3-Np3-F, R¹-
Te2-Ph3-Np4-F, R¹-Te1-Ph3-CH_TwoCH_Two-Ph2-F, R¹-Te1-Ph3
-CH_TwoCH_Two-Ph3-F, R¹-Te1-Ph3-CH_TwoCH_Two-Np1-F, R¹-Te1-Ph3
-CH_TwoCH_Two-Np2-F, R¹-Te1-Ph3-CH_TwoCH_Two-Np3-F, R¹-Te1-Ph3
-CH_TwoCH_Two-Np4-F, R¹-Te2-Ph3-CH_TwoCH_Two-Ph1-F, R¹-Te2-Ph3
-CH_TwoCH_Two-Ph2-F, R¹-Te2-Ph3-CH_TwoCH_Two-Ph3-F, R¹-Te2-Ph3
-CH_TwoCH_Two-Np1-F, R¹-Te2-Ph3-CH_TwoCH_Two-Np2-F, R¹-Te2-Ph3
-CH_TwoCH_Two-Np3-F, R¹-Te2-Ph3-CH_TwoCH_Two-Np4-F, R¹-Te1-Ph3
-C≡C-Ph2-F, R¹-Te1-Ph3-C≡C-Ph3-F, R¹-Te1-Ph3-C≡
C-Np1-F, R ¹-Te1-Ph3-C≡C-Np2-F, R¹-Te1-Ph3-C≡C-Np
3-F, R¹-Te1-Ph3-C≡C-Np4-F, R¹-Te2-Ph3-C≡C-Ph1-
F, R¹-Te2-Ph3-C≡C-Ph2-F, R¹-Te2-Ph3-C≡C-Ph3-F, R
¹-Te2-Ph3-C≡C-Np1-F, R¹-Te2-Ph3-C≡C-Np2-F, R¹-Te
2-Ph3-C≡C-Np3-F, R¹-Te2-Ph3-C≡C-Np4-F,

R¹-Te1-Np1-Ph1-F, R¹-Te1-Np1-Ph2-F, R¹
-Te1-Np1-Ph3-F, R¹-Te1-Np1-Np1-F, R¹-Te1-Np1-Np2-
F, R¹-Te1-Np1-Np3-F, R¹-Te1-Np1-Np4-F, R¹-Te2-Np1-
Ph1-F, R¹-Te2-Np1-Ph2-F, R¹-Te2-Np1-Ph3-F, R¹-Te2-
Np1-Np1-F, R¹-Te2-Np1-Np2-F, R¹-Te2-Np1-Np3-F, R¹-
Te2-Np1-Np4-F, R¹-Te1-Np1-CH_TwoCH_Two-Ph2-F, R¹-Te1-Np1
-CH_TwoCH_Two-Ph3-F, R¹-Te1-Np1-CH_TwoCH_Two-Np1-F, R¹-Te1-Np1
-CH_TwoCH_Two-Np2-F, R¹-Te1-Np1-CH_TwoCH_Two-Np3-F, R¹-Te1-Np1
-CH_TwoCH_Two-Np4-F, R¹-Te2-Np1-CH_TwoCH_Two-Ph1-F, R¹-Te2-Np1
-CH_TwoCH_Two-Ph2-F, R¹-Te2-Np1-CH_TwoCH_Two-Ph3-F, R¹-Te2-Np1
-CH_TwoCH_Two-Np1-F, R¹-Te2-Np1-CH_TwoCH_Two-Np2-F, R¹-Te2-Np1
-CH_TwoCH_Two-Np3-F, R¹-Te2-Np1-CH_TwoCH_Two-Np4-F, R¹-Te1-Np1
-C≡C-Ph2-F, R¹-Te1-Np1-C≡C-Ph3-F, R¹-Te1-Np1-C≡
C-Np1-F, R ¹-Te1-Np1-C≡C-Np2-F, R¹-Te1-Np1-C≡C-Np
3-F, R¹-Te1-Np1-C≡C-Np4-F, R¹-Te2-Np1-C≡C-Ph1-
F, R¹-Te2-Np1-C≡C-Ph2-F, R¹-Te2-Np1-C≡C-Ph3-F, R
¹-Te2-Np1-C≡C-Np1-F, R¹-Te2-Np1-C≡C-Np2-F, R¹-Te
2-Np1-C≡C-Np3-F, R¹-Te2-Np1-C≡C-Np4-F,

R¹-Te1-Np2-Ph1-F, R¹-Te1-Np2-Ph2-F, R¹
-Te1-Np2-Ph3-F, R¹-Te1-Np2-Np1-F, R¹-Te1-Np2-Np2-
F, R¹-Te1-Np2-Np3-F, R¹-Te1-Np2-Np4-F, R¹-Te2-Np2-
Ph1-F, R¹-Te2-Np2-Ph2-F, R¹-Te2-Np2-Ph3-F, R¹-Te2-
Np2-Np1-F, R¹-Te2-Np2-Np2-F, R¹-Te2-Np2-Np3-F, R¹-
Te2-Np2-Np4-F, R¹-Te1-Np2-CH_TwoCH_Two-Ph2-F, R¹-Te1-Np2
-CH_TwoCH_Two-Ph3-F, R¹-Te1-Np2-CH_TwoCH_Two-Np1-F, R¹-Te1-Np2
-CH_TwoCH_Two-Np2-F, R¹-Te1-Np2-CH_TwoCH_Two-Np3-F, R¹-Te1-Np2
-CH_TwoCH_Two-Np4-F, R¹-Te2-Np2-CH_TwoCH_Two-Ph1-F, R¹-Te2-Np2
-CH_TwoCH_Two-Ph2-F, R¹-Te2-Np2-CH_TwoCH_Two-Ph3-F, R¹-Te2-Np2
-CH_TwoCH_Two-Np1-F, R¹-Te2-Np2-CH_TwoCH_Two-Np2-F, R¹-Te2-Np2
-CH_TwoCH_Two-Np3-F, R¹-Te2-Np2-CH_TwoCH_Two-Np4-F, R¹-Te1-Np2
-C≡C-Ph2-F, R¹-Te1-Np2-C≡C-Ph3-F, R¹-Te1-Np2-C≡
C-Np1-F, R ¹-Te1-Np2-C≡C-Np2-F, R¹-Te1-Np2-C≡C-Np
3-F, R¹-Te1-Np2-C≡C-Np4-F, R¹-Te2-Np2-C≡C-Ph1-
F, R¹-Te2-Np2-C≡C-Ph2-F, R¹-Te2-Np2-C≡C-Ph3-F, R
¹-Te2-Np2-C≡C-Np1-F, R¹-Te2-Np2-C≡C-Np2-F, R¹-Te
2-Np2-C≡C-Np3-F, R¹-Te2-Np2-C≡C-Np4-F,

R¹-Te1-Np3-Ph1-F, R¹-Te1-Np3-Ph2-F, R¹
-Te1-Np3-Ph3-F, R¹-Te1-Np3-Np1-F, R¹-Te1-Np3-Np2-
F, R¹-Te1-Np3-Np3-F, R¹-Te1-Np3-Np4-F, R¹-Te2-Np3-
Ph1-F, R¹-Te2-Np3-Ph2-F, R¹-Te2-Np3-Ph3-F, R¹-Te2-
Np3-Np1-F, R¹-Te2-Np3-Np2-F, R¹-Te2-Np3-Np3-F, R¹-
Te2-Np3-Np4-F, R¹-Te1-Np3-CH_TwoCH_Two-Ph2-F, R¹-Te1-Np3
-CH_TwoCH_Two-Ph3-F, R¹-Te1-Np3-CH_TwoCH_Two-Np1-F, R¹-Te1-Np3
-CH_TwoCH_Two-Np2-F, R¹-Te1-Np3-CH_TwoCH_Two-Np3-F, R¹-Te1-Np3
-CH_TwoCH_Two-Np4-F, R¹-Te2-Np3-CH_TwoCH_Two-Ph1-F, R¹-Te2-Np3
-CH_TwoCH_Two-Ph2-F, R¹-Te2-Np3-CH_TwoCH_Two-Ph3-F, R¹-Te2-Np3
-CH_TwoCH_Two-Np1-F, R¹-Te2-Np3-CH_TwoCH_Two-Np2-F, R¹-Te2-Np3
-CH_TwoCH_Two-Np3-F, R¹-Te2-Np3-CH_TwoCH_Two-Np4-F, R¹-Te1-Np3
-C≡C-Ph2-F, R¹-Te1-Np3-C≡C-Ph3-F, R¹-Te1-Np3-C≡
C-Np1-F, R ¹-Te1-Np3-C≡C-Np2-F, R¹-Te1-Np3-C≡C-Np
3-F, R¹-Te1-Np3-C≡C-Np4-F, R¹-Te2-Np3-C≡C-Ph1-
F, R¹-Te2-Np3-C≡C-Ph2-F, R¹-Te2-Np3-C≡C-Ph3-F, R
¹-Te2-Np3-C≡C-Np1-F, R¹-Te2-Np3-C≡C-Np2-F, R¹-Te
2-Np3-C≡C-Np3-F, R¹-Te2-Np3-C≡C-Np4-F,

R¹-Te1-Np4-Ph1-F, R¹-Te1-Np4-Ph2-F, R¹
-Te1-Np4-Ph3-F, R¹-Te1-Np4-Np1-F, R¹-Te1-Np4-Np2-
F, R¹-Te1-Np4-Np3-F, R¹-Te1-Np4-Np4-F, R¹-Te2-Np4-
Ph1-F, R¹-Te2-Np4-Ph2-F, R¹-Te2-Np4-Ph3-F, R¹-Te2-
Np4-Np1-F, R¹-Te2-Np4-Np2-F, R¹-Te2-Np4-Np3-F, R¹-
Te2-Np4-Np4-F, R¹-Te1-Np4-CH_TwoCH_Two-Ph2-F, R¹-Te1-Np4
-CH_TwoCH_Two-Ph3-F, R¹-Te1-Np4-CH_TwoCH_Two-Np1-F, R¹-Te1-Np4
-CH_TwoCH_Two-Np2-F, R¹-Te1-Np4-CH_TwoCH_Two-Np3-F, R¹-Te1-Np4
-CH_TwoCH_Two-Np4-F, R¹-Te2-Np4-CH_TwoCH_Two-Ph1-F, R¹-Te2-Np4
-CH_TwoCH_Two-Ph2-F, R¹-Te2-Np4-CH_TwoCH_Two-Ph3-F, R¹-Te2-Np4
-CH_TwoCH_Two-Np1-F, R¹-Te2-Np4-CH_TwoCH_Two-Np2-F, R¹-Te2-Np4
-CH_TwoCH_Two-Np3-F, R¹-Te2-Np4-CH_TwoCH_Two-Np4-F, R¹-Te1-Np4
-C≡C-Ph2-F, R¹-Te1-Np4-C≡C-Ph3-F, R¹-Te1-Np4-C≡
C-Np1-F, R ¹-Te1-Np4-C≡C-Np2-F, R¹-Te1-Np4-C≡C-Np
3-F, R¹-Te1-Np4-C≡C-Np4-F, R¹-Te2-Np4-C≡C-Ph1-
F, R¹-Te2-Np4-C≡C-Ph2-F, R¹-Te2-Np4-C≡C-Ph3-F, R
¹-Te2-Np4-C≡C-Np1-F, R¹-Te2-Np4-C≡C-Np2-F, R¹-Te
2-Np4-C≡C-Np3-F, R¹-Te2-Np4-C≡C-Np4-F,

R¹-Te1-CH_TwoCH_Two-Ph1-Ph1-F, R¹-Te1-CH_TwoCH_Two
-Ph1-Ph2-F, R¹-Te1-CH_TwoCH_Two-Ph1-Ph3-F, R¹-Te1-CH_TwoCH_Two
-Ph1-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph1-Np2-F, R¹-Te1-CH_TwoCH_Two
-Ph1-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph1-Np4-F, R¹-Te2-CH_TwoCH_Two
-Ph1-Ph1-F, R¹-Te2-CH_TwoCH_Two-Ph1-Ph2-F, R¹-Te2-CH_TwoCH_Two
-Ph1-Ph3-F, R¹-Te2-CH_TwoCH_Two-Ph1-Np1-F, R¹-Te2-CH_TwoCH_Two
-Ph1-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph1-Np3-F, R¹-Te2-CH_TwoCH_Two
-Ph1-Np4-F, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph2-F, R¹-Te1
-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph3-F, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two
-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np2-F, R¹-Te1-CH_Two
CH_Two-Ph1-CH_TwoCH_Two-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np4
-F, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph1-F, R¹-Te2-CH_TwoCH_Two-
Ph1-CH_TwoCH_Two-Ph2-F, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph3-F,
R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np1-F, R¹-Te2-CH_TwoCH_Two-Ph1-
CH_TwoCH_Two-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np3-F, R¹-T
e2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np4-F, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C
-Ph2-F, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C-Ph3-F, R¹-Te1-CH_TwoCH
_Two-Ph1-C≡C-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C-Np2-F, R¹
-Te1-CH_TwoCH_Two-Ph1-C≡C-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C
-Np4-F, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Ph1-F, R¹-Te2-CH_TwoCH
_Two-Ph1-C≡C-Ph2-F, R ¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Ph3-F, R¹
-Te2-CH_TwoCH_Two-Ph1-C≡C-Np1-F, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C
-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Np3-F, R¹-Te2-CH_TwoCH
_Two-Ph1-C≡C-Np4-F,

R¹-Te1-CH_TwoCH_Two-Ph2-Ph1-F, R¹-Te1-CH_TwoCH_Two
-Ph2-Ph2-F, R¹-Te1-CH_TwoCH_Two-Ph2-Ph3-F, R¹-Te1-CH_TwoCH_Two
-Ph2-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph2-Np2-F, R¹-Te1-CH_TwoCH_Two
-Ph2-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph2-Np4-F, R¹-Te2-CH_TwoCH_Two
-Ph2-Ph1-F, R¹-Te2-CH_TwoCH_Two-Ph2-Ph2-F, R¹-Te2-CH_TwoCH_Two
-Ph2-Ph3-F, R¹-Te2-CH_TwoCH_Two-Ph2-Np1-F, R¹-Te2-CH_TwoCH_Two
-Ph2-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph2-Np3-F, R¹-Te2-CH_TwoCH_Two
-Ph2-Np4-F, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph2-F, R¹-Te1
-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph3-F, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two
-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np2-F, R¹-Te1-CH_Two
CH_Two-Ph2-CH_TwoCH_Two-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np4
-F, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph1-F, R¹-Te2-CH_TwoCH_Two-
Ph2-CH_TwoCH_Two-Ph2-F, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph3-F,
R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np1-F, R¹-Te2-CH_TwoCH_Two-Ph2-
CH_TwoCH_Two-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np3-F, R¹-T
e2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np4-F, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C
-Ph2-F, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C-Ph3-F, R¹-Te1-CH_TwoCH
_Two-Ph2-C≡C-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C-Np2-F, R¹
-Te1-CH_TwoCH_Two-Ph2-C≡C-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C
-Np4-F, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Ph1-F, R¹-Te2-CH_TwoCH
_Two-Ph2-C≡C-Ph2-F, R ¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Ph3-F, R¹
-Te2-CH_TwoCH_Two-Ph2-C≡C-Np1-F, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C
-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Np3-F, R¹-Te2-CH_TwoCH
_Two-Ph2-C≡C-Np4-F,

R¹-Te1-CH_TwoCH_Two-Ph3-Ph1-F, R¹-Te1-CH_TwoCH_Two
-Ph3-Ph2-F, R¹-Te1-CH_TwoCH_Two-Ph3-Ph3-F, R¹-Te1-CH_TwoCH_Two
-Ph3-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph3-Np2-F, R¹-Te1-CH_TwoCH_Two
-Ph3-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph3-Np4-F, R¹-Te2-CH_TwoCH_Two
-Ph3-Ph1-F, R¹-Te2-CH_TwoCH_Two-Ph3-Ph2-F, R¹-Te2-CH_TwoCH_Two
-Ph3-Ph3-F, R¹-Te2-CH_TwoCH_Two-Ph3-Np1-F, R¹-Te2-CH_TwoCH_Two
-Ph3-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph3-Np3-F, R¹-Te2-CH_TwoCH_Two
-Ph3-Np4-F, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph2-F, R¹-Te1
-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph3-F, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two
-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np2-F, R¹-Te1-CH_Two
CH_Two-Ph3-CH_TwoCH_Two-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np4
-F, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph1-F, R¹-Te2-CH_TwoCH_Two-
Ph3-CH_TwoCH_Two-Ph2-F, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph3-F,
R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np1-F, R¹-Te2-CH_TwoCH_Two-Ph3-
CH_TwoCH_Two-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np3-F, R¹-T
e2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np4-F, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C
-Ph2-F, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C-Ph3-F, R¹-Te1-CH_TwoCH
_Two-Ph3-C≡C-Np1-F, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C-Np2-F, R¹
-Te1-CH_TwoCH_Two-Ph3-C≡C-Np3-F, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C
-Np4-F, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Ph1-F, R¹-Te2-CH_TwoCH
_Two-Ph3-C≡C-Ph2-F, R ¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Ph3-F, R¹
-Te2-CH_TwoCH_Two-Ph3-C≡C-Np1-F, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C
-Np2-F, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Np3-F, R¹-Te2-CH_TwoCH
_Two-Ph3-C≡C-Np4-F,

R¹-Te1-CH_TwoCH_Two-Np1-Ph1-F, R¹-Te1-CH_TwoCH_Two
-Np1-Ph2-F, R¹-Te1-CH_TwoCH_Two-Np1-Ph3-F, R¹-Te1-CH_TwoCH_Two
-Np1-Np1-F, R¹-Te1-CH_TwoCH_Two-Np1-Np2-F, R¹-Te1-CH_TwoCH_Two
-Np1-Np3-F, R¹-Te1-CH_TwoCH_Two-Np1-Np4-F, R¹-Te2-CH_TwoCH_Two
-Np1-Ph1-F, R¹-Te2-CH_TwoCH_Two-Np1-Ph2-F, R¹-Te2-CH_TwoCH_Two
-Np1-Ph3-F, R¹-Te2-CH_TwoCH_Two-Np1-Np1-F, R¹-Te2-CH_TwoCH_Two
-Np1-Np2-F, R¹-Te2-CH_TwoCH_Two-Np1-Np3-F, R¹-Te2-CH_TwoCH_Two
-Np1-Np4-F, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph2-F, R¹-Te1
-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph3-F, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two
-Np1-F, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np2-F, R¹-Te1-CH_Two
CH_Two-Np1-CH_TwoCH_Two-Np3-F, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np4
-F, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph1-F, R¹-Te2-CH_TwoCH_Two-
Np1-CH_TwoCH_Two-Ph2-F, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph3-F,
R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np1-F, R¹-Te2-CH_TwoCH_Two-Np1-
CH_TwoCH_Two-Np2-F, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np3-F, R¹-T
e2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np4-F, R¹-Te1-CH_TwoCH_Two-Np1-C≡C
-Ph2-F, R¹-Te1-CH_TwoCH_Two-Np1-C≡C-Ph3-F, R¹-Te1-CH_TwoCH
_Two-Np1-C≡C-Np1-F, R¹-Te1-CH_TwoCH_Two-Np1-C≡C-Np2-F, R¹
-Te1-CH_TwoCH_Two-Np1-C≡C-Np3-F, R¹-Te1-CH_TwoCH_Two-Np1-C≡C
-Np4-F, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-Ph1-F, R¹-Te2-CH_TwoCH
_Two-Np1-C≡C-Ph2-F, R ¹-Te2-CH_TwoCH_Two-Np1-C≡C-Ph3-F, R¹
-Te2-CH_TwoCH_Two-Np1-C≡C-Np1-F, R¹-Te2-CH_TwoCH_Two-Np1-C≡C
-Np2-F, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-Np3-F, R¹-Te2-CH_TwoCH
_Two-Np1-C≡C-Np4-F,

R¹-Te1-CH_TwoCH_Two-Np2-Ph1-F, R¹-Te1-CH_TwoCH_Two
-Np2-Ph2-F, R¹-Te1-CH_TwoCH_Two-Np2-Ph3-F, R¹-Te1-CH_TwoCH_Two
-Np2-Np1-F, R¹-Te1-CH_TwoCH_Two-Np2-Np2-F, R¹-Te1-CH_TwoCH_Two
-Np2-Np3-F, R¹-Te1-CH_TwoCH_Two-Np2-Np4-F, R¹-Te2-CH_TwoCH_Two
-Np2-Ph1-F, R¹-Te2-CH_TwoCH_Two-Np2-Ph2-F, R¹-Te2-CH_TwoCH_Two
-Np2-Ph3-F, R¹-Te2-CH_TwoCH_Two-Np2-Np1-F, R¹-Te2-CH_TwoCH_Two
-Np2-Np2-F, R¹-Te2-CH_TwoCH_Two-Np2-Np3-F, R¹-Te2-CH_TwoCH_Two
-Np2-Np4-F, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph2-F, R¹-Te1
-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph3-F, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two
-Np1-F, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np2-F, R¹-Te1-CH_Two
CH_Two-Np2-CH_TwoCH_Two-Np3-F, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np4
-F, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph1-F, R¹-Te2-CH_TwoCH_Two-
Np2-CH_TwoCH_Two-Ph2-F, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph3-F,
R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np1-F, R¹-Te2-CH_TwoCH_Two-Np2-
CH_TwoCH_Two-Np2-F, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np3-F, R¹-T
e2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np4-F, R¹-Te1-CH_TwoCH_Two-Np2-C≡C
-Ph2-F, R¹-Te1-CH_TwoCH_Two-Np2-C≡C-Ph3-F, R¹-Te1-CH_TwoCH
_Two-Np2-C≡C-Np1-F, R¹-Te1-CH_TwoCH_Two-Np2-C≡C-Np2-F, R¹
-Te1-CH_TwoCH_Two-Np2-C≡C-Np3-F, R¹-Te1-CH_TwoCH_Two-Np2-C≡C
-Np4-F, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-Ph1-F, R¹-Te2-CH_TwoCH
_Two-Np2-C≡C-Ph2-F, R ¹-Te2-CH_TwoCH_Two-Np2-C≡C-Ph3-F, R¹
-Te2-CH_TwoCH_Two-Np2-C≡C-Np1-F, R¹-Te2-CH_TwoCH_Two-Np2-C≡C
-Np2-F, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-Np3-F, R¹-Te2-CH_TwoCH
_Two-Np2-C≡C-Np4-F,

R¹-Te1-CH_TwoCH_Two-Np3-Ph1-F, R¹-Te1-CH_TwoCH_Two
-Np3-Ph2-F, R¹-Te1-CH_TwoCH_Two-Np3-Ph3-F, R¹-Te1-CH_TwoCH_Two
-Np3-Np1-F, R¹-Te1-CH_TwoCH_Two-Np3-Np2-F, R¹-Te1-CH_TwoCH_Two
-Np3-Np3-F, R¹-Te1-CH_TwoCH_Two-Np3-Np4-F, R¹-Te2-CH_TwoCH_Two
-Np3-Ph1-F, R¹-Te2-CH_TwoCH_Two-Np3-Ph2-F, R¹-Te2-CH_TwoCH_Two
-Np3-Ph3-F, R¹-Te2-CH_TwoCH_Two-Np3-Np1-F, R¹-Te2-CH_TwoCH_Two
-Np3-Np2-F, R¹-Te2-CH_TwoCH_Two-Np3-Np3-F, R¹-Te2-CH_TwoCH_Two
-Np3-Np4-F, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph2-F, R¹-Te1
-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph3-F, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two
-Np1-F, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np2-F, R¹-Te1-CH_Two
CH_Two-Np3-CH_TwoCH_Two-Np3-F, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np4
-F, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph1-F, R¹-Te2-CH_TwoCH_Two-
Np3-CH_TwoCH_Two-Ph2-F, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph3-F,
R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np1-F, R¹-Te2-CH_TwoCH_Two-Np3-
CH_TwoCH_Two-Np2-F, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np3-F, R¹-T
e2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np4-F, R¹-Te1-CH_TwoCH_Two-Np3-C≡C
-Ph2-F, R¹-Te1-CH_TwoCH_Two-Np3-C≡C-Ph3-F, R¹-Te1-CH_TwoCH
_Two-Np3-C≡C-Np1-F, R¹-Te1-CH_TwoCH_Two-Np3-C≡C-Np2-F, R¹
-Te1-CH_TwoCH_Two-Np3-C≡C-Np3-F, R¹-Te1-CH_TwoCH_Two-Np3-C≡C
-Np4-F, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-Ph1-F, R¹-Te2-CH_TwoCH
_Two-Np3-C≡C-Ph2-F, R ¹-Te2-CH_TwoCH_Two-Np3-C≡C-Ph3-F, R¹
-Te2-CH_TwoCH_Two-Np3-C≡C-Np1-F, R¹-Te2-CH_TwoCH_Two-Np3-C≡C
-Np2-F, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-Np3-F, R¹-Te2-CH_TwoCH
_Two-Np3-C≡C-Np4-F,

R¹-Te1-CH_TwoCH_Two-Np4-Ph1-F, R¹-Te1-CH_TwoCH_Two
-Np4-Ph2-F, R¹-Te1-CH_TwoCH_Two-Np4-Ph3-F, R¹-Te1-CH_TwoCH_Two
-Np4-Np1-F, R¹-Te1-CH_TwoCH_Two-Np4-Np2-F, R¹-Te1-CH_TwoCH_Two
-Np4-Np3-F, R¹-Te1-CH_TwoCH_Two-Np4-Np4-F, R¹-Te2-CH_TwoCH_Two
-Np4-Ph1-F, R¹-Te2-CH_TwoCH_Two-Np4-Ph2-F, R¹-Te2-CH_TwoCH_Two
-Np4-Ph3-F, R¹-Te2-CH_TwoCH_Two-Np4-Np1-F, R¹-Te2-CH_TwoCH_Two
-Np4-Np2-F, R¹-Te2-CH_TwoCH_Two-Np4-Np3-F, R¹-Te2-CH_TwoCH_Two
-Np4-Np4-F, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph2-F, R¹-Te1
-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph3-F, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two
-Np1-F, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np2-F, R¹-Te1-CH_Two
CH_Two-Np4-CH_TwoCH_Two-Np3-F, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np4
-F, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph1-F, R¹-Te2-CH_TwoCH_Two-
Np4-CH_TwoCH_Two-Ph2-F, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph3-F,
R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np1-F, R¹-Te2-CH_TwoCH_Two-Np4-
CH_TwoCH_Two-Np2-F, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np3-F, R¹-T
e2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np4-F, R¹-Te1-CH_TwoCH_Two-Np4-C≡C
-Ph2-F, R¹-Te1-CH_TwoCH_Two-Np4-C≡C-Ph3-F, R¹-Te1-CH_TwoCH
_Two-Np4-C≡C-Np1-F, R¹-Te1-CH_TwoCH_Two-Np4-C≡C-Np2-F, R¹
-Te1-CH_TwoCH_Two-Np4-C≡C-Np3-F, R¹-Te1-CH_TwoCH_Two-Np4-C≡C
-Np4-F, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-Ph1-F, R¹-Te2-CH_TwoCH
_Two-Np4-C≡C-Ph2-F, R ¹-Te2-CH_TwoCH_Two-Np4-C≡C-Ph3-F, R¹
-Te2-CH_TwoCH_Two-Np4-C≡C-Np1-F, R¹-Te2-CH_TwoCH_Two-Np4-C≡C
-Np2-F, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-Np3-F, R¹-Te2-CH_TwoCH
_Two-Np4-C≡C-Np4-F,

R¹-Te1-C≡C-Ph1-Ph1-F, R¹-Te1-C≡C-Ph1
-Ph2-F, R¹-Te1-C≡C-Ph1-Ph3-F, R¹-Te1-C≡C-Ph1-Np1
-F, R¹-Te1-C≡C-Ph1-Np2-F, R¹-Te1-C≡C-Ph1-Np3-F,
R¹-Te1-C≡C-Ph1-Np4-F, R¹-Te2-C≡C-Ph1-Ph1-F, R¹-T
e2-C≡C-Ph1-Ph2-F, R¹-Te2-C≡C-Ph1-Ph3-F, R¹-Te2-C
≡C-Ph1-Np1-F, R¹-Te2-C≡C-Ph1-Np2-F, R¹-Te2-C≡C-
Ph1-Np3-F, R¹-Te2-C≡C-Ph1-Np4-F, R¹-Te1-C≡C-Ph1-
CH_TwoCH_Two-Ph2-F, R¹-Te1-C≡C-Ph1-CH_TwoCH_Two-Ph3-F, R¹-Te1
-C≡C-Ph1-CH_TwoCH_Two-Np1-F, R¹-Te1-C≡C-Ph1-CH_TwoCH_Two-Np2
-F, R¹-Te1-C≡C-Ph1-CH_TwoCH_Two-Np3-F, R¹-Te1-C≡C-Ph1-
CH_TwoCH_Two-Np4-F, R ¹-Te2-C≡C-Ph1-CH_TwoCH_Two-Ph1-F, R¹-Te2
-C≡C-Ph1-CH_TwoCH_Two-Ph2-F, R¹-Te2-C≡C-Ph1-CH_TwoCH_Two-Ph3
-F, R¹-Te2-C≡C-Ph1-CH_TwoCH_Two-Np1-F, R¹-Te2-C≡C-Ph1-
CH_TwoCH_Two-Np2-F, R¹-Te2-C≡C-Ph1-CH_TwoCH_Two-Np3-F, R¹-Te2
-C≡C-Ph1-CH_TwoCH_Two-Np4-F, R¹-Te1-C≡C-Ph1-C≡C-Ph2-
F, R¹-Te1-C≡C-Ph1-C≡C-Ph3-F, R¹-Te1-C≡C-Ph1-C≡
C-Np1-F, R¹-Te1-C≡C-Ph1-C≡C-Np2-F, R¹-Te1-C≡C-P
h1-C≡C-Np3-F, R¹-Te1-C≡C-Ph1-C≡C-Np4-F, R¹-Te2-
C≡C-Ph1-C≡C-Ph1-F, R¹-Te2-C≡C-Ph1-C≡C-Ph2-F, R
¹-Te2-C≡C-Ph1-C≡C-Ph3-F, R¹-Te2-C≡C-Ph1-C≡C-Np
1-F, R¹-Te2-C≡C-Ph1-C≡C-Np2-F, R¹-Te2-C≡C-Ph1-C
≡C-Np3-F, R¹-Te2-C≡C-Ph1-C≡C-Np4-F,

R¹-Te1-C≡C-Ph2-Ph1-F, R¹-Te1-C≡C-Ph2
-Ph2-F, R¹-Te1-C≡C-Ph2-Ph3-F, R¹-Te1-C≡C-Ph2-Np1
-F, R¹-Te1-C≡C-Ph2-Np2-F, R¹-Te1-C≡C-Ph2-Np3-F,
R¹-Te1-C≡C-Ph2-Np4-F, R¹-Te2-C≡C-Ph2-Ph1-F, R¹-T
e2-C≡C-Ph2-Ph2-F, R¹-Te2-C≡C-Ph2-Ph3-F, R¹-Te2-C
≡C-Ph2-Np1-F, R¹-Te2-C≡C-Ph2-Np2-F, R¹-Te2-C≡C-
Ph2-Np3-F, R¹-Te2-C≡C-Ph2-Np4-F, R¹-Te1-C≡C-Ph2-
CH_TwoCH_Two-Ph2-F, R¹-Te1-C≡C-Ph2-CH_TwoCH_Two-Ph3-F, R¹-Te1
-C≡C-Ph2-CH_TwoCH_Two-Np1-F, R¹-Te1-C≡C-Ph2-CH_TwoCH_Two-Np2
-F, R¹-Te1-C≡C-Ph2-CH_TwoCH_Two-Np3-F, R¹-Te1-C≡C-Ph2-
CH_TwoCH_Two-Np4-F, R ¹-Te2-C≡C-Ph2-CH_TwoCH_Two-Ph1-F, R¹-Te2
-C≡C-Ph2-CH_TwoCH_Two-Ph2-F, R¹-Te2-C≡C-Ph2-CH_TwoCH_Two-Ph3
-F, R¹-Te2-C≡C-Ph2-CH_TwoCH_Two-Np1-F, R¹-Te2-C≡C-Ph2-
CH_TwoCH_Two-Np2-F, R¹-Te2-C≡C-Ph2-CH_TwoCH_Two-Np3-F, R¹-Te2
-C≡C-Ph2-CH_TwoCH_Two-Np4-F, R¹-Te1-C≡C-Ph2-C≡C-Ph2-
F, R¹-Te1-C≡C-Ph2-C≡C-Ph3-F, R¹-Te1-C≡C-Ph2-C≡
C-Np1-F, R¹-Te1-C≡C-Ph2-C≡C-Np2-F, R¹-Te1-C≡C-P
h2-C≡C-Np3-F, R¹-Te1-C≡C-Ph2-C≡C-Np4-F, R¹-Te2-
C≡C-Ph2-C≡C-Ph1-F, R¹-Te2-C≡C-Ph2-C≡C-Ph2-F, R
¹-Te2-C≡C-Ph2-C≡C-Ph3-F, R¹-Te2-C≡C-Ph2-C≡C-Np
1-F, R¹-Te2-C≡C-Ph2-C≡C-Np2-F, R¹-Te2-C≡C-Ph2-C
≡C-Np3-F, R¹-Te2-C≡C-Ph2-C≡C-Np4-F,

R¹-Te1-C≡C-Ph3-Ph1-F, R¹-Te1-C≡C-Ph3
-Ph2-F, R¹-Te1-C≡C-Ph3-Ph3-F, R¹-Te1-C≡C-Ph3-Np1
-F, R¹-Te1-C≡C-Ph3-Np2-F, R¹-Te1-C≡C-Ph3-Np3-F,
R¹-Te1-C≡C-Ph3-Np4-F, R¹-Te2-C≡C-Ph3-Ph1-F, R¹-T
e2-C≡C-Ph3-Ph2-F, R¹-Te2-C≡C-Ph3-Ph3-F, R¹-Te2-C
≡C-Ph3-Np1-F, R¹-Te2-C≡C-Ph3-Np2-F, R¹-Te2-C≡C-
Ph3-Np3-F, R¹-Te2-C≡C-Ph3-Np4-F, R¹-Te1-C≡C-Ph3-
CH_TwoCH_Two-Ph2-F, R¹-Te1-C≡C-Ph3-CH_TwoCH_Two-Ph3-F, R¹-Te1
-C≡C-Ph3-CH_TwoCH_Two-Np1-F, R¹-Te1-C≡C-Ph3-CH_TwoCH_Two-Np2
-F, R¹-Te1-C≡C-Ph3-CH_TwoCH_Two-Np3-F, R¹-Te1-C≡C-Ph3-
CH_TwoCH_Two-Np4-F, R ¹-Te2-C≡C-Ph3-CH_TwoCH_Two-Ph1-F, R¹-Te2
-C≡C-Ph3-CH_TwoCH_Two-Ph2-F, R¹-Te2-C≡C-Ph3-CH_TwoCH_Two-Ph3
-F, R¹-Te2-C≡C-Ph3-CH_TwoCH_Two-Np1-F, R¹-Te2-C≡C-Ph3-
CH_TwoCH_Two-Np2-F, R¹-Te2-C≡C-Ph3-CH_TwoCH_Two-Np3-F, R¹-Te2
-C≡C-Ph3-CH_TwoCH_Two-Np4-F, R¹-Te1-C≡C-Ph3-C≡C-Ph2-
F, R¹-Te1-C≡C-Ph3-C≡C-Ph3-F, R¹-Te1-C≡C-Ph3-C≡
C-Np1-F, R¹-Te1-C≡C-Ph3-C≡C-Np2-F, R¹-Te1-C≡C-P
h3-C≡C-Np3-F, R¹-Te1-C≡C-Ph3-C≡C-Np4-F, R¹-Te2-
C≡C-Ph3-C≡C-Ph1-F, R¹-Te2-C≡C-Ph3-C≡C-Ph2-F, R
¹-Te2-C≡C-Ph3-C≡C-Ph3-F, R¹-Te2-C≡C-Ph3-C≡C-Np
1-F, R¹-Te2-C≡C-Ph3-C≡C-Np2-F, R¹-Te2-C≡C-Ph3-C
≡C-Np3-F, R¹-Te2-C≡C-Ph3-C≡C-Np4-F,

R¹-Te1-C≡C-Np1-Ph1-F, R¹-Te1-C≡C-Np1
-Ph2-F, R¹-Te1-C≡C-Np1-Ph3-F, R¹-Te1-C≡C-Np1-Np1
-F, R¹-Te1-C≡C-Np1-Np2-F, R¹-Te1-C≡C-Np1-Np3-F,
R¹-Te1-C≡C-Np1-Np4-F, R¹-Te2-C≡C-Np1-Ph1-F, R¹-T
e2-C≡C-Np1-Ph2-F, R¹-Te2-C≡C-Np1-Ph3-F, R¹-Te2-C
≡C-Np1-Np1-F, R¹-Te2-C≡C-Np1-Np2-F, R¹-Te2-C≡C-
Np1-Np3-F, R¹-Te2-C≡C-Np1-Np4-F, R¹-Te1-C≡C-Np1-
CH_TwoCH_Two-Ph2-F, R¹-Te1-C≡C-Np1-CH_TwoCH_Two-Ph3-F, R¹-Te1
-C≡C-Np1-CH_TwoCH_Two-Np1-F, R¹-Te1-C≡C-Np1-CH_TwoCH_Two-Np2
-F, R¹-Te1-C≡C-Np1-CH_TwoCH_Two-Np3-F, R¹-Te1-C≡C-Np1-
CH_TwoCH_Two-Np4-F, R ¹-Te2-C≡C-Np1-CH_TwoCH_Two-Ph1-F, R¹-Te2
-C≡C-Np1-CH_TwoCH_Two-Ph2-F, R¹-Te2-C≡C-Np1-CH_TwoCH_Two-Ph3
-F, R¹-Te2-C≡C-Np1-CH_TwoCH_Two-Np1-F, R¹-Te2-C≡C-Np1-
CH_TwoCH_Two-Np2-F, R¹-Te2-C≡C-Np1-CH_TwoCH_Two-Np3-F, R¹-Te2
-C≡C-Np1-CH_TwoCH_Two-Np4-F, R¹-Te1-C≡C-Np1-C≡C-Ph2-
F, R¹-Te1-C≡C-Np1-C≡C-Ph3-F, R¹-Te1-C≡C-Np1-C≡
C-Np1-F, R¹-Te1-C≡C-Np1-C≡C-Np2-F, R¹-Te1-C≡C-N
p1-C≡C-Np3-F, R¹-Te1-C≡C-Np1-C≡C-Np4-F, R¹-Te2-
C≡C-Np1-C≡C-Ph1-F, R¹-Te2-C≡C-Np1-C≡C-Ph2-F, R
¹-Te2-C≡C-Np1-C≡C-Ph3-F, R¹-Te2-C≡C-Np1-C≡C-Np
1-F, R¹-Te2-C≡C-Np1-C≡C-Np2-F, R¹-Te2-C≡C-Np1-C
≡C-Np3-F, R¹-Te2-C≡C-Np1-C≡C-Np4-F,

R¹-Te1-C≡C-Np2-Ph1-F, R¹-Te1-C≡C-Np2
-Ph2-F, R¹-Te1-C≡C-Np2-Ph3-F, R¹-Te1-C≡C-Np2-Np1
-F, R¹-Te1-C≡C-Np2-Np2-F, R¹-Te1-C≡C-Np2-Np3-F,
R¹-Te1-C≡C-Np2-Np4-F, R¹-Te2-C≡C-Np2-Ph1-F, R¹-T
e2-C≡C-Np2-Ph2-F, R¹-Te2-C≡C-Np2-Ph3-F, R¹-Te2-C
≡C-Np2-Np1-F, R¹-Te2-C≡C-Np2-Np2-F, R¹-Te2-C≡C-
Np2-Np3-F, R¹-Te2-C≡C-Np2-Np4-F, R¹-Te1-C≡C-Np2-
CH_TwoCH_Two-Ph2-F, R¹-Te1-C≡C-Np2-CH_TwoCH_Two-Ph3-F, R¹-Te1
-C≡C-Np2-CH_TwoCH_Two-Np1-F, R¹-Te1-C≡C-Np2-CH_TwoCH_Two-Np2
-F, R¹-Te1-C≡C-Np2-CH_TwoCH_Two-Np3-F, R¹-Te1-C≡C-Np2-
CH_TwoCH_Two-Np4-F, R ¹-Te2-C≡C-Np2-CH_TwoCH_Two-Ph1-F, R¹-Te2
-C≡C-Np2-CH_TwoCH_Two-Ph2-F, R¹-Te2-C≡C-Np2-CH_TwoCH_Two-Ph3
-F, R¹-Te2-C≡C-Np2-CH_TwoCH_Two-Np1-F, R¹-Te2-C≡C-Np2-
CH_TwoCH_Two-Np2-F, R¹-Te2-C≡C-Np2-CH_TwoCH_Two-Np3-F, R¹-Te2
-C≡C-Np2-CH_TwoCH_Two-Np4-F, R¹-Te1-C≡C-Np2-C≡C-Ph2-
F, R¹-Te1-C≡C-Np2-C≡C-Ph3-F, R¹-Te1-C≡C-Np2-C≡
C-Np1-F, R¹-Te1-C≡C-Np2-C≡C-Np2-F, R¹-Te1-C≡C-N
p2-C≡C-Np3-F, R¹-Te1-C≡C-Np2-C≡C-Np4-F, R¹-Te2-
C≡C-Np2-C≡C-Ph1-F, R¹-Te2-C≡C-Np2-C≡C-Ph2-F, R
¹-Te2-C≡C-Np2-C≡C-Ph3-F, R¹-Te2-C≡C-Np2-C≡C-Np
1-F, R¹-Te2-C≡C-Np2-C≡C-Np2-F, R¹-Te2-C≡C-Np2-C
≡C-Np3-F, R¹-Te2-C≡C-Np2-C≡C-Np4-F,

R¹-Te1-C≡C-Np3-Ph1-F, R¹-Te1-C≡C-Np3
-Ph2-F, R¹-Te1-C≡C-Np3-Ph3-F, R¹-Te1-C≡C-Np3-Np1
-F, R¹-Te1-C≡C-Np3-Np2-F, R¹-Te1-C≡C-Np3-Np3-F,
R¹-Te1-C≡C-Np3-Np4-F, R¹-Te2-C≡C-Np3-Ph1-F, R¹-T
e2-C≡C-Np3-Ph2-F, R¹-Te2-C≡C-Np3-Ph3-F, R¹-Te2-C
≡C-Np3-Np1-F, R¹-Te2-C≡C-Np3-Np2-F, R¹-Te2-C≡C-
Np3-Np3-F, R¹-Te2-C≡C-Np3-Np4-F, R¹-Te1-C≡C-Np3-
CH_TwoCH_Two-Ph2-F, R¹-Te1-C≡C-Np3-CH_TwoCH_Two-Ph3-F, R¹-Te1
-C≡C-Np3-CH_TwoCH_Two-Np1-F, R¹-Te1-C≡C-Np3-CH_TwoCH_Two-Np2
-F, R¹-Te1-C≡C-Np3-CH_TwoCH_Two-Np3-F, R¹-Te1-C≡C-Np3-
CH_TwoCH_Two-Np4-F, R ¹-Te2-C≡C-Np3-CH_TwoCH_Two-Ph1-F, R¹-Te2
-C≡C-Np3-CH_TwoCH_Two-Ph2-F, R¹-Te2-C≡C-Np3-CH_TwoCH_Two-Ph3
-F, R¹-Te2-C≡C-Np3-CH_TwoCH_Two-Np1-F, R¹-Te2-C≡C-Np3-
CH_TwoCH_Two-Np2-F, R¹-Te2-C≡C-Np3-CH_TwoCH_Two-Np3-F, R¹-Te2
-C≡C-Np3-CH_TwoCH_Two-Np4-F, R¹-Te1-C≡C-Np3-C≡C-Ph2-
F, R¹-Te1-C≡C-Np3-C≡C-Ph3-F, R¹-Te1-C≡C-Np3-C≡
C-Np1-F, R¹-Te1-C≡C-Np3-C≡C-Np2-F, R¹-Te1-C≡C-N
p3-C≡C-Np3-F, R¹-Te1-C≡C-Np3-C≡C-Np4-F, R¹-Te2-
C≡C-Np3-C≡C-Ph1-F, R¹-Te2-C≡C-Np3-C≡C-Ph2-F, R
¹-Te2-C≡C-Np3-C≡C-Ph3-F, R¹-Te2-C≡C-Np3-C≡C-Np
1-F, R¹-Te2-C≡C-Np3-C≡C-Np2-F, R¹-Te2-C≡C-Np3-C
≡C-Np3-F, R¹-Te2-C≡C-Np3-C≡C-Np4-F,

R¹-Te1-C≡C-Np4-Ph1-F, R¹-Te1-C≡C-Np4
-Ph2-F, R¹-Te1-C≡C-Np4-Ph3-F, R¹-Te1-C≡C-Np4-Np1
-F, R¹-Te1-C≡C-Np4-Np2-F, R¹-Te1-C≡C-Np4-Np3-F,
R¹-Te1-C≡C-Np4-Np4-F, R¹-Te2-C≡C-Np4-Ph1-F, R¹-T
e2-C≡C-Np4-Ph2-F, R¹-Te2-C≡C-Np4-Ph3-F, R¹-Te2-C
≡C-Np4-Np1-F, R¹-Te2-C≡C-Np4-Np2-F, R¹-Te2-C≡C-
Np4-Np3-F, R¹-Te2-C≡C-Np4-Np4-F, R¹-Te1-C≡C-Np4-
CH_TwoCH_Two-Ph2-F, R¹-Te1-C≡C-Np4-CH_TwoCH_Two-Ph3-F, R¹-Te1
-C≡C-Np4-CH_TwoCH_Two-Np1-F, R¹-Te1-C≡C-Np4-CH_TwoCH_Two-Np2
-F, R¹-Te1-C≡C-Np4-CH_TwoCH_Two-Np3-F, R¹-Te1-C≡C-Np4-
CH_TwoCH_Two-Np4-F, R ¹-Te2-C≡C-Np4-CH_TwoCH_Two-Ph1-F, R¹-Te2
-C≡C-Np4-CH_TwoCH_Two-Ph2-F, R¹-Te2-C≡C-Np4-CH_TwoCH_Two-Ph3
-F, R¹-Te2-C≡C-Np4-CH_TwoCH_Two-Np1-F, R¹-Te2-C≡C-Np4-
CH_TwoCH_Two-Np2-F, R¹-Te2-C≡C-Np4-CH_TwoCH_Two-Np3-F, R¹-Te2
-C≡C-Np4-CH_TwoCH_Two-Np4-F, R¹-Te1-C≡C-Np4-C≡C-Ph2-
F, R¹-Te1-C≡C-Np4-C≡C-Ph3-F, R¹-Te1-C≡C-Np4-C≡
C-Np1-F, R¹-Te1-C≡C-Np4-C≡C-Np2-F, R¹-Te1-C≡C-N
p4-C≡C-Np3-F, R¹-Te1-C≡C-Np4-C≡C-Np4-F, R¹-Te2-
C≡C-Np4-C≡C-Ph1-F, R¹-Te2-C≡C-Np4-C≡C-Ph2-F, R
¹-Te2-C≡C-Np4-C≡C-Ph3-F, R¹-Te2-C≡C-Np4-C≡C-Np
1-F, R¹-Te2-C≡C-Np4-C≡C-Np2-F, R¹-Te2-C≡C-Np4-C
≡C-Np3-F, R¹-Te2-C≡C-Np4-C≡C-Np4-F,

When m = 0, n = 1, V is a single bond and Z is a cyano group,

R ¹ -Te1-Cy-Ph1-CN, R ¹ -Te1-Cy-Ph2-CN, R ¹
-Te1-Cy-Ph3-CN, R ¹ -Te1-Cy-Np1-CN, R ¹ -Te1-Cy-Np2-C
N, R ¹ -Te1-Cy-Np3-CN, R ¹ -Te1-Cy-Np4-CN, R ¹ -Te2-Cy-P
h1-CN, R ¹ -Te2-Cy-Ph2-CN, R ¹ -Te2-Cy-Ph3-CN, R ¹ -Te2-
Cy-Np1-CN, R ¹ -Te2-Cy-Np2-CN, R ¹ -Te2-Cy-Np3-CN, R ^1-
Te2-Cy-Np4-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Cy-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Cy-
CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Cy-
CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Cy-
CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Cy-
CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Cy-
CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂
CH ₂ -Cy-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph2-CN, R ¹ -Te1-CH ₂
CH ₂ -Cy-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np1-CN, R ¹ -Te1-CH ₂
CH ₂ -Cy-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np3-CN, R ¹ -Te1-CH ₂
CH ₂ -Cy-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph1-CN, R ¹ -Te2-CH ₂
CH ₂ -Cy-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph3-CN, R ¹ -Te2-CH ₂
CH ₂ -Cy-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np2-CN, R ¹ -Te2-CH ₂
CH ₂ -Cy-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np4-CN, R ¹ -Te1-CH ₂
CH ₂ -Cy-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph3-
CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH _2-
Cy-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np3-CN,
R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-C
H ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph2-CN, R ¹ -T
e2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH
₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-C
H ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np
4-CN,

R¹-Te1-Ph1-Ph1-CN, R¹-Te1-Ph1-Ph2-CN,
R¹-Te1-Ph1-Ph3-CN, R¹-Te1-Ph1-Np1-CN, R¹-Te1-Ph1-N
p2-CN, R¹-Te1-Ph1-Np3-CN, R¹-Te1-Ph1-Np4-CN, R¹-Te
2-Ph1-Ph1-CN, R¹-Te2-Ph1-Ph2-CN, R¹-Te2-Ph1-Ph3-C
N, R¹-Te2-Ph1-Np1-CN, R¹-Te2-Ph1-Np2-CN, R¹-Te2-Ph
1-Np3-CN, R¹-Te2-Ph1-Np4-CN, R¹-Te1-Ph1-CH_TwoCH_Two-Ph2
-CN, R¹-Te1-Ph1-CH_TwoCH_Two-Ph3-CN, R¹-Te1-Ph1-CH_TwoCH_Two-N
p1-CN, R¹-Te1-Ph1-CH_TwoCH _Two-Np2-CN, R¹-Te1-Ph1-CH_TwoCH_Two
-Np3-CN, R¹-Te1-Ph1-CH_TwoCH_Two-Np4-CN, R¹-Te2-Ph1-CH_TwoC
H_Two-Ph1-CN, R¹-Te2-Ph1-CH_TwoCH_Two-Ph2-CN, R¹-Te2-Ph1-CH
_TwoCH_Two-Ph3-CN, R¹-Te2-Ph1-CH_TwoCH_Two-Np1-CN, R¹-Te2-Ph1-
CH_TwoCH_Two-Np2-CN, R¹-Te2-Ph1-CH_TwoCH_Two-Np3-CN, R¹-Te2-Ph
1-CH_TwoCH_Two-Np4-CN, R¹-Te1-Ph1-C≡C-Ph2-CN, R¹-Te1-Ph
1-C≡C-Ph3-CN, R¹-Te1-Ph1-C≡C-Np1-CN, R¹-Te1-Ph1-
C≡C-Np2-CN, R¹-Te1-Ph1-C≡C-Np3-CN, R¹-Te1-Ph1-C
≡C-Np4-CN, R¹-Te2-Ph1-C≡C-Ph1-CN, R¹-Te2-Ph1-C≡
C-Ph2-CN, R¹-Te2-Ph1-C≡C-Ph3-CN, R¹-Te2-Ph1-C≡C-
Np1-CN, R¹-Te2-Ph1-C≡C-Np2-CN, R¹-Te2-Ph1-C≡C-Np
3-CN, R¹-Te2-Ph1-C≡C-Np4-CN,

R¹-Te1-Ph2-Ph1-CN, R¹-Te1-Ph2-Ph2-CN,
R¹-Te1-Ph2-Ph3-CN, R¹-Te1-Ph2-Np1-CN, R¹-Te1-Ph2-N
p2-CN, R¹-Te1-Ph2-Np3-CN, R¹-Te1-Ph2-Np4-CN, R¹-Te
2-Ph2-Ph1-CN, R¹-Te2-Ph2-Ph2-CN, R¹-Te2-Ph2-Ph3-C
N, R¹-Te2-Ph2-Np1-CN, R¹-Te2-Ph2-Np2-CN, R¹-Te2-Ph
2-Np3-CN, R¹-Te2-Ph2-Np4-CN, R¹-Te1-Ph2-CH_TwoCH_Two-Ph2
-CN, R¹-Te1-Ph2-CH_TwoCH_Two-Ph3-CN, R¹-Te1-Ph2-CH_TwoCH_Two-N
p1-CN, R¹-Te1-Ph2-CH_TwoCH _Two-Np2-CN, R¹-Te1-Ph2-CH_TwoCH_Two
-Np3-CN, R¹-Te1-Ph2-CH_TwoCH_Two-Np4-CN, R¹-Te2-Ph2-CH_TwoC
H_Two-Ph1-CN, R¹-Te2-Ph2-CH_TwoCH_Two-Ph2-CN, R¹-Te2-Ph2-CH
_TwoCH_Two-Ph3-CN, R¹-Te2-Ph2-CH_TwoCH_Two-Np1-CN, R¹-Te2-Ph2-
CH_TwoCH_Two-Np2-CN, R¹-Te2-Ph2-CH_TwoCH_Two-Np3-CN, R¹-Te2-Ph
2-CH_TwoCH_Two-Np4-CN, R¹-Te1-Ph2-C≡C-Ph2-CN, R¹-Te1-Ph
2-C≡C-Ph3-CN, R¹-Te1-Ph2-C≡C-Np1-CN, R¹-Te1-Ph2-
C≡C-Np2-CN, R¹-Te1-Ph2-C≡C-Np3-CN, R¹-Te1-Ph2-C
≡C-Np4-CN, R¹-Te2-Ph2-C≡C-Ph1-CN, R¹-Te2-Ph2-C≡
C-Ph2-CN, R¹-Te2-Ph2-C≡C-Ph3-CN, R¹-Te2-Ph2-C≡C-
Np1-CN, R¹-Te2-Ph2-C≡C-Np2-CN, R¹-Te2-Ph2-C≡C-Np
3-CN, R¹-Te2-Ph2-C≡C-Np4-CN,

R¹-Te1-Ph3-Ph1-CN, R¹-Te1-Ph3-Ph2-CN,
R¹-Te1-Ph3-Ph3-CN, R¹-Te1-Ph3-Np1-CN, R¹-Te1-Ph3-N
p2-CN, R¹-Te1-Ph3-Np3-CN, R¹-Te1-Ph3-Np4-CN, R¹-Te
2-Ph3-Ph1-CN, R¹-Te2-Ph3-Ph2-CN, R¹-Te2-Ph3-Ph3-C
N, R¹-Te2-Ph3-Np1-CN, R¹-Te2-Ph3-Np2-CN, R¹-Te2-Ph
3-Np3-CN, R¹-Te2-Ph3-Np4-CN, R¹-Te1-Ph3-CH_TwoCH_Two-Ph2
-CN, R¹-Te1-Ph3-CH_TwoCH_Two-Ph3-CN, R¹-Te1-Ph3-CH_TwoCH_Two-N
p1-CN, R¹-Te1-Ph3-CH_TwoCH _Two-Np2-CN, R¹-Te1-Ph3-CH_TwoCH_Two
-Np3-CN, R¹-Te1-Ph3-CH_TwoCH_Two-Np4-CN, R¹-Te2-Ph3-CH_TwoC
H_Two-Ph1-CN, R¹-Te2-Ph3-CH_TwoCH_Two-Ph2-CN, R¹-Te2-Ph3-CH
_TwoCH_Two-Ph3-CN, R¹-Te2-Ph3-CH_TwoCH_Two-Np1-CN, R¹-Te2-Ph3-
CH_TwoCH_Two-Np2-CN, R¹-Te2-Ph3-CH_TwoCH_Two-Np3-CN, R¹-Te2-Ph
3-CH_TwoCH_Two-Np4-CN, R¹-Te1-Ph3-C≡C-Ph2-CN, R¹-Te1-Ph
3-C≡C-Ph3-CN, R¹-Te1-Ph3-C≡C-Np1-CN, R¹-Te1-Ph3-
C≡C-Np2-CN, R¹-Te1-Ph3-C≡C-Np3-CN, R¹-Te1-Ph3-C
≡C-Np4-CN, R¹-Te2-Ph3-C≡C-Ph1-CN, R¹-Te2-Ph3-C≡
C-Ph2-CN, R¹-Te2-Ph3-C≡C-Ph3-CN, R¹-Te2-Ph3-C≡C-
Np1-CN, R¹-Te2-Ph3-C≡C-Np2-CN, R¹-Te2-Ph3-C≡C-Np
3-CN, R¹-Te2-Ph3-C≡C-Np4-CN,

R¹-Te1-Np1-Ph1-CN, R¹-Te1-Np1-Ph2-CN,
R¹-Te1-Np1-Ph3-CN, R¹-Te1-Np1-Np1-CN, R¹-Te1-Np1-N
p2-CN, R¹-Te1-Np1-Np3-CN, R¹-Te1-Np1-Np4-CN, R¹-Te
2-Np1-Ph1-CN, R¹-Te2-Np1-Ph2-CN, R¹-Te2-Np1-Ph3-C
N, R¹-Te2-Np1-Np1-CN, R¹-Te2-Np1-Np2-CN, R¹-Te2-Np
1-Np3-CN, R¹-Te2-Np1-Np4-CN, R¹-Te1-Np1-CH_TwoCH_Two-Ph2
-CN, R¹-Te1-Np1-CH_TwoCH_Two-Ph3-CN, R¹-Te1-Np1-CH_TwoCH_Two-N
p1-CN, R¹-Te1-Np1-CH_TwoCH _Two-Np2-CN, R¹-Te1-Np1-CH_TwoCH_Two
-Np3-CN, R¹-Te1-Np1-CH_TwoCH_Two-Np4-CN, R¹-Te2-Np1-CH_TwoC
H_Two-Ph1-CN, R¹-Te2-Np1-CH_TwoCH_Two-Ph2-CN, R¹-Te2-Np1-CH
_TwoCH_Two-Ph3-CN, R¹-Te2-Np1-CH_TwoCH_Two-Np1-CN, R¹-Te2-Np1-
CH_TwoCH_Two-Np2-CN, R¹-Te2-Np1-CH_TwoCH_Two-Np3-CN, R¹-Te2-Np
1-CH_TwoCH_Two-Np4-CN, R¹-Te1-Np1-C≡C-Ph2-CN, R¹-Te1-Np
1-C≡C-Ph3-CN, R¹-Te1-Np1-C≡C-Np1-CN, R¹-Te1-Np1-
C≡C-Np2-CN, R¹-Te1-Np1-C≡C-Np3-CN, R¹-Te1-Np1-C
≡C-Np4-CN, R¹-Te2-Np1-C≡C-Ph1-CN, R¹-Te2-Np1-C≡
C-Ph2-CN, R¹-Te2-Np1-C≡C-Ph3-CN, R¹-Te2-Np1-C≡C-
Np1-CN, R¹-Te2-Np1-C≡C-Np2-CN, R¹-Te2-Np1-C≡C-Np
3-CN, R¹-Te2-Np1-C≡C-Np4-CN,

R¹-Te1-Np2-Ph1-CN, R¹-Te1-Np2-Ph2-CN,
R¹-Te1-Np2-Ph3-CN, R¹-Te1-Np2-Np1-CN, R¹-Te1-Np2-N
p2-CN, R¹-Te1-Np2-Np3-CN, R¹-Te1-Np2-Np4-CN, R¹-Te
2-Np2-Ph1-CN, R¹-Te2-Np2-Ph2-CN, R¹-Te2-Np2-Ph3-C
N, R¹-Te2-Np2-Np1-CN, R¹-Te2-Np2-Np2-CN, R¹-Te2-Np
2-Np3-CN, R¹-Te2-Np2-Np4-CN, R¹-Te1-Np2-CH_TwoCH_Two-Ph2
-CN, R¹-Te1-Np2-CH_TwoCH_Two-Ph3-CN, R¹-Te1-Np2-CH_TwoCH_Two-N
p1-CN, R¹-Te1-Np2-CH_TwoCH _Two-Np2-CN, R¹-Te1-Np2-CH_TwoCH_Two
-Np3-CN, R¹-Te1-Np2-CH_TwoCH_Two-Np4-CN, R¹-Te2-Np2-CH_TwoC
H_Two-Ph1-CN, R¹-Te2-Np2-CH_TwoCH_Two-Ph2-CN, R¹-Te2-Np2-CH
_TwoCH_Two-Ph3-CN, R¹-Te2-Np2-CH_TwoCH_Two-Np1-CN, R¹-Te2-Np2-
CH_TwoCH_Two-Np2-CN, R¹-Te2-Np2-CH_TwoCH_Two-Np3-CN, R¹-Te2-Np
2-CH_TwoCH_Two-Np4-CN, R¹-Te1-Np2-C≡C-Ph2-CN, R¹-Te1-Np
2-C≡C-Ph3-CN, R¹-Te1-Np2-C≡C-Np1-CN, R¹-Te1-Np2-
C≡C-Np2-CN, R¹-Te1-Np2-C≡C-Np3-CN, R¹-Te1-Np2-C
≡C-Np4-CN, R¹-Te2-Np2-C≡C-Ph1-CN, R¹-Te2-Np2-C≡
C-Ph2-CN, R¹-Te2-Np2-C≡C-Ph3-CN, R¹-Te2-Np2-C≡C-
Np1-CN, R¹-Te2-Np2-C≡C-Np2-CN, R¹-Te2-Np2-C≡C-Np
3-CN, R¹-Te2-Np2-C≡C-Np4-CN,

R¹-Te1-Np3-Ph1-CN, R¹-Te1-Np3-Ph2-CN,
R¹-Te1-Np3-Ph3-CN, R¹-Te1-Np3-Np1-CN, R¹-Te1-Np3-N
p2-CN, R¹-Te1-Np3-Np3-CN, R¹-Te1-Np3-Np4-CN, R¹-Te
2-Np3-Ph1-CN, R¹-Te2-Np3-Ph2-CN, R¹-Te2-Np3-Ph3-C
N, R¹-Te2-Np3-Np1-CN, R¹-Te2-Np3-Np2-CN, R¹-Te2-Np
3-Np3-CN, R¹-Te2-Np3-Np4-CN, R¹-Te1-Np3-CH_TwoCH_Two-Ph2
-CN, R¹-Te1-Np3-CH_TwoCH_Two-Ph3-CN, R¹-Te1-Np3-CH_TwoCH_Two-N
p1-CN, R¹-Te1-Np3-CH_TwoCH _Two-Np2-CN, R¹-Te1-Np3-CH_TwoCH_Two
-Np3-CN, R¹-Te1-Np3-CH_TwoCH_Two-Np4-CN, R¹-Te2-Np3-CH_TwoC
H_Two-Ph1-CN, R¹-Te2-Np3-CH_TwoCH_Two-Ph2-CN, R¹-Te2-Np3-CH
_TwoCH_Two-Ph3-CN, R¹-Te2-Np3-CH_TwoCH_Two-Np1-CN, R¹-Te2-Np3-
CH_TwoCH_Two-Np2-CN, R¹-Te2-Np3-CH_TwoCH_Two-Np3-CN, R¹-Te2-Np
3-CH_TwoCH_Two-Np4-CN, R¹-Te1-Np3-C≡C-Ph2-CN, R¹-Te1-Np
3-C≡C-Ph3-CN, R¹-Te1-Np3-C≡C-Np1-CN, R¹-Te1-Np3-
C≡C-Np2-CN, R¹-Te1-Np3-C≡C-Np3-CN, R¹-Te1-Np3-C
≡C-Np4-CN, R¹-Te2-Np3-C≡C-Ph1-CN, R¹-Te2-Np3-C≡
C-Ph2-CN, R¹-Te2-Np3-C≡C-Ph3-CN, R¹-Te2-Np3-C≡C-
Np1-CN, R¹-Te2-Np3-C≡C-Np2-CN, R¹-Te2-Np3-C≡C-Np
3-CN, R¹-Te2-Np3-C≡C-Np4-CN,

R¹-Te1-Np4-Ph1-CN, R¹-Te1-Np4-Ph2-CN,
R¹-Te1-Np4-Ph3-CN, R¹-Te1-Np4-Np1-CN, R¹-Te1-Np4-N
p2-CN, R¹-Te1-Np4-Np3-CN, R¹-Te1-Np4-Np4-CN, R¹-Te
2-Np4-Ph1-CN, R¹-Te2-Np4-Ph2-CN, R¹-Te2-Np4-Ph3-C
N, R¹-Te2-Np4-Np1-CN, R¹-Te2-Np4-Np2-CN, R¹-Te2-Np
4-Np3-CN, R¹-Te2-Np4-Np4-CN, R¹-Te1-Np4-CH_TwoCH_Two-Ph2
-CN, R¹-Te1-Np4-CH_TwoCH_Two-Ph3-CN, R¹-Te1-Np4-CH_TwoCH_Two-N
p1-CN, R¹-Te1-Np4-CH_TwoCH _Two-Np2-CN, R¹-Te1-Np4-CH_TwoCH_Two
-Np3-CN, R¹-Te1-Np4-CH_TwoCH_Two-Np4-CN, R¹-Te2-Np4-CH_TwoC
H_Two-Ph1-CN, R¹-Te2-Np4-CH_TwoCH_Two-Ph2-CN, R¹-Te2-Np4-CH
_TwoCH_Two-Ph3-CN, R¹-Te2-Np4-CH_TwoCH_Two-Np1-CN, R¹-Te2-Np4-
CH_TwoCH_Two-Np2-CN, R¹-Te2-Np4-CH_TwoCH_Two-Np3-CN, R¹-Te2-Np
4-CH_TwoCH_Two-Np4-CN, R¹-Te1-Np4-C≡C-Ph2-CN, R¹-Te1-Np
4-C≡C-Ph3-CN, R¹-Te1-Np4-C≡C-Np1-CN, R¹-Te1-Np4-
C≡C-Np2-CN, R¹-Te1-Np4-C≡C-Np3-CN, R¹-Te1-Np4-C
≡C-Np4-CN, R¹-Te2-Np4-C≡C-Ph1-CN, R¹-Te2-Np4-C≡
C-Ph2-CN, R¹-Te2-Np4-C≡C-Ph3-CN, R¹-Te2-Np4-C≡C-
Np1-CN, R¹-Te2-Np4-C≡C-Np2-CN, R¹-Te2-Np4-C≡C-Np
3-CN, R¹-Te2-Np4-C≡C-Np4-CN,

R¹-Te1-CH_TwoCH_Two-Ph1-Ph1-CN, R¹-Te1-CH_TwoCH
_Two-Ph1-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Ph1-Ph3-CN, R¹-Te1-CH_Two
CH_Two-Ph1-Np1-CN, R¹-Te1-CH_TwoCH_Two-Ph1-Np2-CN, R¹-Te1-C
H_TwoCH_Two-Ph1-Np3-CN, R¹-Te1-CH_TwoCH_Two-Ph1-Np4-CN, R¹-Te2
-CH_TwoCH_Two-Ph1-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Ph1-Ph2-CN, R¹-T
e2-CH_TwoCH_Two-Ph1-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph1-Np1-CN, R¹
-Te2-CH_TwoCH_Two-Ph1-Np2-CN, R¹-Te2-CH_TwoCH_Two-Ph1-Np3-CN,
R¹-Te2-CH_TwoCH_Two-Ph1-Np4-CN, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two
-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph3-CN, R¹-Te1-C
H_TwoCH_Two-Ph1-CH_TwoCH_Two-Np1-CN, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-
Np2-CN, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np3-CN, R¹-Te1-CH
_TwoCH_Two-Ph1-CH_TwoCH_Two-Np4-CN, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-P
h1-CN, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph2-CN, R¹-Te2-CH_Two
CH_Two-Ph1-CH _TwoCH_Two-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np
1-CN, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np2-CN, R¹-Te2-CH_TwoC
H_Two-Ph1-CH_TwoCH_Two-Np3-CN, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np4
-CN, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C-Ph2-CN, R¹-Te1-CH_TwoCH_Two-
Ph1-C≡C-Ph3-CN, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C-Np1-CN, R¹
-Te1-CH_TwoCH_Two-Ph1-C≡C-Np2-CN, R¹-Te1-CH_TwoCH_Two-Ph1-C≡
C-Np3-CN, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C-Np4-CN, R¹-Te2-CH
_TwoCH_Two-Ph1-C≡C-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Ph2-C
N, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph
1-C≡C-Np1-CN, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Np2-CN, R¹-T
e2-CH_TwoCH_Two-Ph1-C≡C-Np3-CN, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-
Np4-CN,

R¹-Te1-CH_TwoCH_Two-Ph2-Ph1-CN, R¹-Te1-CH_TwoCH
_Two-Ph2-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Ph2-Ph3-CN, R¹-Te1-CH_Two
CH_Two-Ph2-Np1-CN, R¹-Te1-CH_TwoCH_Two-Ph2-Np2-CN, R¹-Te1-C
H_TwoCH_Two-Ph2-Np3-CN, R¹-Te1-CH_TwoCH_Two-Ph2-Np4-CN, R¹-Te2
-CH_TwoCH_Two-Ph2-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Ph2-Ph2-CN, R¹-T
e2-CH_TwoCH_Two-Ph2-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph2-Np1-CN, R¹
-Te2-CH_TwoCH_Two-Ph2-Np2-CN, R¹-Te2-CH_TwoCH_Two-Ph2-Np3-CN,
R¹-Te2-CH_TwoCH_Two-Ph2-Np4-CN, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two
-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph3-CN, R¹-Te1-C
H_TwoCH_Two-Ph2-CH_TwoCH_Two-Np1-CN, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-
Np2-CN, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np3-CN, R¹-Te1-CH
_TwoCH_Two-Ph2-CH_TwoCH_Two-Np4-CN, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-P
h1-CN, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph2-CN, R¹-Te2-CH_Two
CH_Two-Ph2-CH _TwoCH_Two-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np
1-CN, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np2-CN, R¹-Te2-CH_TwoC
H_Two-Ph2-CH_TwoCH_Two-Np3-CN, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np4
-CN, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C-Ph2-CN, R¹-Te1-CH_TwoCH_Two-
Ph2-C≡C-Ph3-CN, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C-Np1-CN, R¹
-Te1-CH_TwoCH_Two-Ph2-C≡C-Np2-CN, R¹-Te1-CH_TwoCH_Two-Ph2-C≡
C-Np3-CN, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C-Np4-CN, R¹-Te2-CH
_TwoCH_Two-Ph2-C≡C-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Ph2-C
N, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph
2-C≡C-Np1-CN, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Np2-CN, R¹-T
e2-CH_TwoCH_Two-Ph2-C≡C-Np3-CN, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-
Np4-CN,

R¹-Te1-CH_TwoCH_Two-Ph3-Ph1-CN, R¹-Te1-CH_TwoCH
_Two-Ph3-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Ph3-Ph3-CN, R¹-Te1-CH_Two
CH_Two-Ph3-Np1-CN, R¹-Te1-CH_TwoCH_Two-Ph3-Np2-CN, R¹-Te1-C
H_TwoCH_Two-Ph3-Np3-CN, R¹-Te1-CH_TwoCH_Two-Ph3-Np4-CN, R¹-Te2
-CH_TwoCH_Two-Ph3-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Ph3-Ph2-CN, R¹-T
e2-CH_TwoCH_Two-Ph3-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph3-Np1-CN, R¹
-Te2-CH_TwoCH_Two-Ph3-Np2-CN, R¹-Te2-CH_TwoCH_Two-Ph3-Np3-CN,
R¹-Te2-CH_TwoCH_Two-Ph3-Np4-CN, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two
-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph3-CN, R¹-Te1-C
H_TwoCH_Two-Ph3-CH_TwoCH_Two-Np1-CN, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-
Np2-CN, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np3-CN, R¹-Te1-CH
_TwoCH_Two-Ph3-CH_TwoCH_Two-Np4-CN, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-P
h1-CN, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph2-CN, R¹-Te2-CH_Two
CH_Two-Ph3-CH _TwoCH_Two-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np
1-CN, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np2-CN, R¹-Te2-CH_TwoC
H_Two-Ph3-CH_TwoCH_Two-Np3-CN, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np4
-CN, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C-Ph2-CN, R¹-Te1-CH_TwoCH_Two-
Ph3-C≡C-Ph3-CN, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C-Np1-CN, R¹
-Te1-CH_TwoCH_Two-Ph3-C≡C-Np2-CN, R¹-Te1-CH_TwoCH_Two-Ph3-C≡
C-Np3-CN, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C-Np4-CN, R¹-Te2-CH
_TwoCH_Two-Ph3-C≡C-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Ph2-C
N, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Ph
3-C≡C-Np1-CN, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Np2-CN, R¹-T
e2-CH_TwoCH_Two-Ph3-C≡C-Np3-CN, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-
Np4-CN,

R¹-Te1-CH_TwoCH_Two-Np1-Ph1-CN, R¹-Te1-CH_TwoCH
_Two-Np1-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Np1-Ph3-CN, R¹-Te1-CH_Two
CH_Two-Np1-Np1-CN, R¹-Te1-CH_TwoCH_Two-Np1-Np2-CN, R¹-Te1-C
H_TwoCH_Two-Np1-Np3-CN, R¹-Te1-CH_TwoCH_Two-Np1-Np4-CN, R¹-Te2
-CH_TwoCH_Two-Np1-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Np1-Ph2-CN, R¹-T
e2-CH_TwoCH_Two-Np1-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np1-Np1-CN, R¹
-Te2-CH_TwoCH_Two-Np1-Np2-CN, R¹-Te2-CH_TwoCH_Two-Np1-Np3-CN,
R¹-Te2-CH_TwoCH_Two-Np1-Np4-CN, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two
-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph3-CN, R¹-Te1-C
H_TwoCH_Two-Np1-CH_TwoCH_Two-Np1-CN, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-
Np2-CN, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np3-CN, R¹-Te1-CH
_TwoCH_Two-Np1-CH_TwoCH_Two-Np4-CN, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-P
h1-CN, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph2-CN, R¹-Te2-CH_Two
CH_Two-Np1-CH _TwoCH_Two-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np
1-CN, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np2-CN, R¹-Te2-CH_TwoC
H_Two-Np1-CH_TwoCH_Two-Np3-CN, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np4
-CN, R¹-Te1-CH_TwoCH_Two-Np1-C≡C-Ph2-CN, R¹-Te1-CH_TwoCH_Two-
Np1-C≡C-Ph3-CN, R¹-Te1-CH_TwoCH_Two-Np1-C≡C-Np1-CN, R¹
-Te1-CH_TwoCH_Two-Np1-C≡C-Np2-CN, R¹-Te1-CH_TwoCH_Two-Np1-C≡
C-Np3-CN, R¹-Te1-CH_TwoCH_Two-Np1-C≡C-Np4-CN, R¹-Te2-CH
_TwoCH_Two-Np1-C≡C-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-Ph2-C
N, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np
1-C≡C-Np1-CN, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-Np2-CN, R¹-T
e2-CH_TwoCH_Two-Np1-C≡C-Np3-CN, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-
Np4-CN,

R¹-Te1-CH_TwoCH_Two-Np2-Ph1-CN, R¹-Te1-CH_TwoCH
_Two-Np2-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Np2-Ph3-CN, R¹-Te1-CH_Two
CH_Two-Np2-Np1-CN, R¹-Te1-CH_TwoCH_Two-Np2-Np2-CN, R¹-Te1-C
H_TwoCH_Two-Np2-Np3-CN, R¹-Te1-CH_TwoCH_Two-Np2-Np4-CN, R¹-Te2
-CH_TwoCH_Two-Np2-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Np2-Ph2-CN, R¹-T
e2-CH_TwoCH_Two-Np2-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np2-Np1-CN, R¹
-Te2-CH_TwoCH_Two-Np2-Np2-CN, R¹-Te2-CH_TwoCH_Two-Np2-Np3-CN,
R¹-Te2-CH_TwoCH_Two-Np2-Np4-CN, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two
-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph3-CN, R¹-Te1-C
H_TwoCH_Two-Np2-CH_TwoCH_Two-Np1-CN, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-
Np2-CN, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np3-CN, R¹-Te1-CH
_TwoCH_Two-Np2-CH_TwoCH_Two-Np4-CN, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-P
h1-CN, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph2-CN, R¹-Te2-CH_Two
CH_Two-Np2-CH _TwoCH_Two-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np
1-CN, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np2-CN, R¹-Te2-CH_TwoC
H_Two-Np2-CH_TwoCH_Two-Np3-CN, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np4
-CN, R¹-Te1-CH_TwoCH_Two-Np2-C≡C-Ph2-CN, R¹-Te1-CH_TwoCH_Two-
Np2-C≡C-Ph3-CN, R¹-Te1-CH_TwoCH_Two-Np2-C≡C-Np1-CN, R¹
-Te1-CH_TwoCH_Two-Np2-C≡C-Np2-CN, R¹-Te1-CH_TwoCH_Two-Np2-C≡
C-Np3-CN, R¹-Te1-CH_TwoCH_Two-Np2-C≡C-Np4-CN, R¹-Te2-CH
_TwoCH_Two-Np2-C≡C-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-Ph2-C
N, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np
2-C≡C-Np1-CN, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-Np2-CN, R¹-T
e2-CH_TwoCH_Two-Np2-C≡C-Np3-CN, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-
Np4-CN,

R¹-Te1-CH_TwoCH_Two-Np3-Ph1-CN, R¹-Te1-CH_TwoCH
_Two-Np3-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Np3-Ph3-CN, R¹-Te1-CH_Two
CH_Two-Np3-Np1-CN, R¹-Te1-CH_TwoCH_Two-Np3-Np2-CN, R¹-Te1-C
H_TwoCH_Two-Np3-Np3-CN, R¹-Te1-CH_TwoCH_Two-Np3-Np4-CN, R¹-Te2
-CH_TwoCH_Two-Np3-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Np3-Ph2-CN, R¹-T
e2-CH_TwoCH_Two-Np3-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np3-Np1-CN, R¹
-Te2-CH_TwoCH_Two-Np3-Np2-CN, R¹-Te2-CH_TwoCH_Two-Np3-Np3-CN,
R¹-Te2-CH_TwoCH_Two-Np3-Np4-CN, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two
-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph3-CN, R¹-Te1-C
H_TwoCH_Two-Np3-CH_TwoCH_Two-Np1-CN, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-
Np2-CN, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np3-CN, R¹-Te1-CH
_TwoCH_Two-Np3-CH_TwoCH_Two-Np4-CN, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-P
h1-CN, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph2-CN, R¹-Te2-CH_Two
CH_Two-Np3-CH _TwoCH_Two-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np
1-CN, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np2-CN, R¹-Te2-CH_TwoC
H_Two-Np3-CH_TwoCH_Two-Np3-CN, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np4
-CN, R¹-Te1-CH_TwoCH_Two-Np3-C≡C-Ph2-CN, R¹-Te1-CH_TwoCH_Two-
Np3-C≡C-Ph3-CN, R¹-Te1-CH_TwoCH_Two-Np3-C≡C-Np1-CN, R¹
-Te1-CH_TwoCH_Two-Np3-C≡C-Np2-CN, R¹-Te1-CH_TwoCH_Two-Np3-C≡
C-Np3-CN, R¹-Te1-CH_TwoCH_Two-Np3-C≡C-Np4-CN, R¹-Te2-CH
_TwoCH_Two-Np3-C≡C-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-Ph2-C
N, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np
3-C≡C-Np1-CN, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-Np2-CN, R¹-T
e2-CH_TwoCH_Two-Np3-C≡C-Np3-CN, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-
Np4-CN,

R¹-Te1-CH_TwoCH_Two-Np4-Ph1-CN, R¹-Te1-CH_TwoCH
_Two-Np4-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Np4-Ph3-CN, R¹-Te1-CH_Two
CH_Two-Np4-Np1-CN, R¹-Te1-CH_TwoCH_Two-Np4-Np2-CN, R¹-Te1-C
H_TwoCH_Two-Np4-Np3-CN, R¹-Te1-CH_TwoCH_Two-Np4-Np4-CN, R¹-Te2
-CH_TwoCH_Two-Np4-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Np4-Ph2-CN, R¹-T
e2-CH_TwoCH_Two-Np4-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np4-Np1-CN, R¹
-Te2-CH_TwoCH_Two-Np4-Np2-CN, R¹-Te2-CH_TwoCH_Two-Np4-Np3-CN,
R¹-Te2-CH_TwoCH_Two-Np4-Np4-CN, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two
-Ph2-CN, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph3-CN, R¹-Te1-C
H_TwoCH_Two-Np4-CH_TwoCH_Two-Np1-CN, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-
Np2-CN, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np3-CN, R¹-Te1-CH
_TwoCH_Two-Np4-CH_TwoCH_Two-Np4-CN, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-P
h1-CN, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph2-CN, R¹-Te2-CH_Two
CH_Two-Np4-CH _TwoCH_Two-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np
1-CN, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np2-CN, R¹-Te2-CH_TwoC
H_Two-Np4-CH_TwoCH_Two-Np3-CN, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np4
-CN, R¹-Te1-CH_TwoCH_Two-Np4-C≡C-Ph2-CN, R¹-Te1-CH_TwoCH_Two-
Np4-C≡C-Ph3-CN, R¹-Te1-CH_TwoCH_Two-Np4-C≡C-Np1-CN, R¹
-Te1-CH_TwoCH_Two-Np4-C≡C-Np2-CN, R¹-Te1-CH_TwoCH_Two-Np4-C≡
C-Np3-CN, R¹-Te1-CH_TwoCH_Two-Np4-C≡C-Np4-CN, R¹-Te2-CH
_TwoCH_Two-Np4-C≡C-Ph1-CN, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-Ph2-C
N, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-Ph3-CN, R¹-Te2-CH_TwoCH_Two-Np
4-C≡C-Np1-CN, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-Np2-CN, R¹-T
e2-CH_TwoCH_Two-Np4-C≡C-Np3-CN, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-
Np4-CN,

R ¹ -Te1-C≡C-Ph1-Ph1-CN, R ¹ -Te1-C≡C-Ph
1-Ph2-CN, R ¹ -Te1-C≡C-Ph1-Ph3-CN, R ¹ -Te1-C≡C-Ph1-
Np1-CN, R ¹ -Te1-C≡C-Ph1-Np2-CN, R ¹ -Te1-C≡C-Ph1-Np
3-CN, R ¹ -Te1-C≡C-Ph1-Np4-CN, R ¹ -Te2-C≡C-Ph1-Ph1-
CN, R ¹ -Te2-C≡C-Ph1-Ph2-CN, R ¹ -Te2-C≡C-Ph1-Ph3-C
N, R ¹ -Te2-C≡C-Ph1-Np1-CN, R ¹ -Te2-C≡C-Ph1-Np2-C
N, R ¹ -Te2-C≡C-Ph1-Np3-CN, R ¹ -Te2-C≡C-Ph1-Np4-C
N, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Ph1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np1-CN, R ¹ -T
e1-C≡C-Ph1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH _2-
Np3-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C
-Ph1-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Ph1-
CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np2-CN, R ¹ -T
e2-C≡C-Ph1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH _2-
Np4-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Ph2-CN, R ¹ -Te1-C≡CP
h1-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Np1-CN, R ¹ -Te
1-C≡C-Ph1-C≡C-Np2-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Np3-C
N, R ¹ -Te1-C≡C-Ph1-C≡C-Np4-CN, R ¹ -Te2-C≡C-Ph1-C
≡C-Ph1-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Ph2-CN, R ¹ -Te2-C
≡C-Ph1-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Np1-CN,
R ¹ -Te2-C≡C-Ph1-C≡C-Np2-CN, R ¹ -Te2-C≡C-Ph1-C≡C-
Np3-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Np4-CN,

R ¹ -Te1-C≡C-Ph2-Ph1-CN, R ¹ -Te1-C≡C-Ph
2-Ph2-CN, R ¹ -Te1-C≡C-Ph2-Ph3-CN, R ¹ -Te1-C≡C-Ph2-
Np1-CN, R ¹ -Te1-C≡C-Ph2-Np2-CN, R ¹ -Te1-C≡C-Ph2-Np
3-CN, R ¹ -Te1-C≡C-Ph2-Np4-CN, R ¹ -Te2-C≡C-Ph2-Ph1-
CN, R ¹ -Te2-C≡C-Ph2-Ph2-CN, R ¹ -Te2-C≡C-Ph2-Ph3-C
N, R ¹ -Te2-C≡C-Ph2-Np1-CN, R ¹ -Te2-C≡C-Ph2-Np2-C
N, R ¹ -Te2-C≡C-Ph2-Np3-CN, R ¹ -Te2-C≡C-Ph2-Np4-C
N, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Ph2-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np1-CN, R ¹ -T
e1-C≡C-Ph2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH _2-
Np3-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C
-Ph2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Ph2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np2-CN, R ¹ -T
e2-C≡C-Ph2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH _2-
Np4-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Ph2-CN, R ¹ -Te1-C≡CP
h2-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Np1-CN, R ¹ -Te
1-C≡C-Ph2-C≡C-Np2-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Np3-C
N, R ¹ -Te1-C≡C-Ph2-C≡C-Np4-CN, R ¹ -Te2-C≡C-Ph2-C
≡C-Ph1-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Ph2-CN, R ¹ -Te2-C
≡C-Ph2-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Np1-CN,
R ¹ -Te2-C≡C-Ph2-C≡C-Np2-CN, R ¹ -Te2-C≡C-Ph2-C≡C-
Np3-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Np4-CN,

R ¹ -Te1-C≡C-Ph3-Ph1-CN, R ¹ -Te1-C≡C-Ph
3-Ph2-CN, R ¹ -Te1-C≡C-Ph3-Ph3-CN, R ¹ -Te1-C≡C-Ph3-
Np1-CN, R ¹ -Te1-C≡C-Ph3-Np2-CN, R ¹ -Te1-C≡C-Ph3-Np
3-CN, R ¹ -Te1-C≡C-Ph3-Np4-CN, R ¹ -Te2-C≡C-Ph3-Ph1-
CN, R ¹ -Te2-C≡C-Ph3-Ph2-CN, R ¹ -Te2-C≡C-Ph3-Ph3-C
N, R ¹ -Te2-C≡C-Ph3-Np1-CN, R ¹ -Te2-C≡C-Ph3-Np2-C
N, R ¹ -Te2-C≡C-Ph3-Np3-CN, R ¹ -Te2-C≡C-Ph3-Np4-C
N, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Ph3-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np1-CN, R ¹ -T
e1-C≡C-Ph3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH _2-
Np3-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C
-Ph3-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Ph3-
CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np2-CN, R ¹ -T
e2-C≡C-Ph3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH _2-
Np4-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Ph2-CN, R ¹ -Te1-C≡CP
h3-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Np1-CN, R ¹ -Te
1-C≡C-Ph3-C≡C-Np2-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Np3-C
N, R ¹ -Te1-C≡C-Ph3-C≡C-Np4-CN, R ¹ -Te2-C≡C-Ph3-C
≡C-Ph1-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Ph2-CN, R ¹ -Te2-C
≡C-Ph3-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Np1-CN,
R ¹ -Te2-C≡C-Ph3-C≡C-Np2-CN, R ¹ -Te2-C≡C-Ph3-C≡C-
Np3-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Np4-CN,

R ¹ -Te1-C≡C-Np1-Ph1-CN, R ¹ -Te1-C≡C-Np
1-Ph2-CN, R ¹ -Te1-C≡C-Np1-Ph3-CN, R ¹ -Te1-C≡C-Np1-
Np1-CN, R ¹ -Te1-C≡C-Np1-Np2-CN, R ¹ -Te1-C≡C-Np1-Np
3-CN, R ¹ -Te1-C≡C-Np1-Np4-CN, R ¹ -Te2-C≡C-Np1-Ph1-
CN, R ¹ -Te2-C≡C-Np1-Ph2-CN, R ¹ -Te2-C≡C-Np1-Ph3-C
N, R ¹ -Te2-C≡C-Np1-Np1-CN, R ¹ -Te2-C≡C-Np1-Np2-C
N, R ¹ -Te2-C≡C-Np1-Np3-CN, R ¹ -Te2-C≡C-Np1-Np4-C
N, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Np1-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np1-CN, R ¹ -T
e1-C≡C-Np1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH _2-
Np3-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C
-Np1-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Np1-
CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np2-CN, R ¹ -T
e2-C≡C-Np1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH _2-
Np4-CN, R ¹ -Te1-C≡C-Np1-C≡C-Ph2-CN, R ¹ -Te1-C≡CN
p1-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Np1-C≡C-Np1-CN, R ¹ -Te
1-C≡C-Np1-C≡C-Np2-CN, R ¹ -Te1-C≡C-Np1-C≡C-Np3-C
N, R ¹ -Te1-C≡C-Np1-C≡C-Np4-CN, R ¹ -Te2-C≡C-Np1-C
≡C-Ph1-CN, R ¹ -Te2-C≡C-Np1-C≡C-Ph2-CN, R ¹ -Te2-C
≡C-Np1-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Np1-C≡C-Np1-CN,
R ¹ -Te2-C≡C-Np1-C≡C-Np2-CN, R ¹ -Te2-C≡C-Np1-C≡C-
Np3-CN, R ¹ -Te2-C≡C-Np1-C≡C-Np4-CN,

R ¹ -Te1-C≡C-Np2-Ph1-CN, R ¹ -Te1-C≡C-Np
2-Ph2-CN, R ¹ -Te1-C≡C-Np2-Ph3-CN, R ¹ -Te1-C≡C-Np2-
Np1-CN, R ¹ -Te1-C≡C-Np2-Np2-CN, R ¹ -Te1-C≡C-Np2-Np
3-CN, R ¹ -Te1-C≡C-Np2-Np4-CN, R ¹ -Te2-C≡C-Np2-Ph1-
CN, R ¹ -Te2-C≡C-Np2-Ph2-CN, R ¹ -Te2-C≡C-Np2-Ph3-C
N, R ¹ -Te2-C≡C-Np2-Np1-CN, R ¹ -Te2-C≡C-Np2-Np2-C
N, R ¹ -Te2-C≡C-Np2-Np3-CN, R ¹ -Te2-C≡C-Np2-Np4-C
N, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Np2-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np1-CN, R ¹ -T
e1-C≡C-Np2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH _2-
Np3-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C
-Np2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Np2-
CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np2-CN, R ¹ -T
e2-C≡C-Np2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH _2-
Np4-CN, R ¹ -Te1-C≡C-Np2-C≡C-Ph2-CN, R ¹ -Te1-C≡CN
p2-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Np2-C≡C-Np1-CN, R ¹ -Te
1-C≡C-Np2-C≡C-Np2-CN, R ¹ -Te1-C≡C-Np2-C≡C-Np3-C
N, R ¹ -Te1-C≡C-Np2-C≡C-Np4-CN, R ¹ -Te2-C≡C-Np2-C
≡C-Ph1-CN, R ¹ -Te2-C≡C-Np2-C≡C-Ph2-CN, R ¹ -Te2-C
≡C-Np2-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Np2-C≡C-Np1-CN,
R ¹ -Te2-C≡C-Np2-C≡C-Np2-CN, R ¹ -Te2-C≡C-Np2-C≡C-
Np3-CN, R ¹ -Te2-C≡C-Np2-C≡C-Np4-CN,

R ¹ -Te1-C≡C-Np3-Ph1-CN, R ¹ -Te1-C≡C-Np
3-Ph2-CN, R ¹ -Te1-C≡C-Np3-Ph3-CN, R ¹ -Te1-C≡C-Np3-
Np1-CN, R ¹ -Te1-C≡C-Np3-Np2-CN, R ¹ -Te1-C≡C-Np3-Np
3-CN, R ¹ -Te1-C≡C-Np3-Np4-CN, R ¹ -Te2-C≡C-Np3-Ph1-
CN, R ¹ -Te2-C≡C-Np3-Ph2-CN, R ¹ -Te2-C≡C-Np3-Ph3-C
N, R ¹ -Te2-C≡C-Np3-Np1-CN, R ¹ -Te2-C≡C-Np3-Np2-C
N, R ¹ -Te2-C≡C-Np3-Np3-CN, R ¹ -Te2-C≡C-Np3-Np4-C
N, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Np3-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np1-CN, R ¹ -T
e1-C≡C-Np3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH _2-
Np3-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C
-Np3-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Np3-
CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np2-CN, R ¹ -T
e2-C≡C-Np3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH _2-
Np4-CN, R ¹ -Te1-C≡C-Np3-C≡C-Ph2-CN, R ¹ -Te1-C≡CN
p3-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Np3-C≡C-Np1-CN, R ¹ -Te
1-C≡C-Np3-C≡C-Np2-CN, R ¹ -Te1-C≡C-Np3-C≡C-Np3-C
N, R ¹ -Te1-C≡C-Np3-C≡C-Np4-CN, R ¹ -Te2-C≡C-Np3-C
≡C-Ph1-CN, R ¹ -Te2-C≡C-Np3-C≡C-Ph2-CN, R ¹ -Te2-C
≡C-Np3-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Np3-C≡C-Np1-CN,
R ¹ -Te2-C≡C-Np3-C≡C-Np2-CN, R ¹ -Te2-C≡C-Np3-C≡C-
Np3-CN, R ¹ -Te2-C≡C-Np3-C≡C-Np4-CN,

R ¹ -Te1-C≡C-Np4-Ph1-CN, R ¹ -Te1-C≡C-Np
4-Ph2-CN, R ¹ -Te1-C≡C-Np4-Ph3-CN, R ¹ -Te1-C≡C-Np4-
Np1-CN, R ¹ -Te1-C≡C-Np4-Np2-CN, R ¹ -Te1-C≡C-Np4-Np
3-CN, R ¹ -Te1-C≡C-Np4-Np4-CN, R ¹ -Te2-C≡C-Np4-Ph1-
CN, R ¹ -Te2-C≡C-Np4-Ph2-CN, R ¹ -Te2-C≡C-Np4-Ph3-C
N, R ¹ -Te2-C≡C-Np4-Np1-CN, R ¹ -Te2-C≡C-Np4-Np2-C
N, R ¹ -Te2-C≡C-Np4-Np3-CN, R ¹ -Te2-C≡C-Np4-Np4-C
N, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Np4-
CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np1-CN, R ¹ -T
e1-C≡C-Np4-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH _2-
Np3-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C
-Np4-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph2-C
N, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Np4-
CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np2-CN, R ¹ -T
e2-C≡C-Np4-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH _2-
Np4-CN, R ¹ -Te1-C≡C-Np4-C≡C-Ph2-CN, R ¹ -Te1-C≡CN
p4-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Np4-C≡C-Np1-CN, R ¹ -Te
1-C≡C-Np4-C≡C-Np2-CN, R ¹ -Te1-C≡C-Np4-C≡C-Np3-C
N, R ¹ -Te1-C≡C-Np4-C≡C-Np4-CN, R ¹ -Te2-C≡C-Np4-C
≡C-Ph1-CN, R ¹ -Te2-C≡C-Np4-C≡C-Ph2-CN, R ¹ -Te2-C
≡C-Np4-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Np4-C≡C-Np1-CN,
R ¹ -Te2-C≡C-Np4-C≡C-Np2-CN, R ¹ -Te2-C≡C-Np4-C≡C-
Np3-CN, R ¹ -Te2-C≡C-Np4-C≡C-Np4-CN,

When m = 0, n = 1, V is a single bond and Z is a trifluoromethyl group,

R¹-Te1-Cy-Ph1-CF_Three, R¹-Te1-Cy-Ph2-CF_Three,
R¹-Te1-Cy-Ph3-CF_Three, R¹-Te1-Cy-Np1-CF_Three, R¹-Te1-Cy-Np
2-CF_Three, R¹-Te1-Cy-Np3-CF_Three, R¹-Te1-Cy-Np4-CF_Three, R¹-Te
2-Cy-Ph1-CF_Three, R¹-Te2-Cy-Ph2-CF_Three, R¹-Te2-Cy-Ph3-C
F_Three, R¹-Te2-Cy-Np1-CF_Three, R¹-Te2-Cy-Np2-CF_Three, R¹-Te2-C
y-Np3-CF_Three, R¹-Te2-Cy-Np4-CF_Three, R¹-Te1-Cy-CH_TwoCH_Two-Ph2
-CF_Three, R¹-Te1-Cy-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te1-Cy-CH_TwoCH_Two-N
p1-CF_Three, R¹-Te1-Cy-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-Cy-CH_TwoCH_Two
-Np3-CF_Three, R¹-Te1-Cy-CH_TwoCH_Two-Np4-CF_Three, R¹-Te2-Cy-CH_TwoC
H_Two-Ph1-CF_Three, R¹-Te2-Cy-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te2-Cy-CH
_TwoCH_Two-Ph3-CF_Three, R¹-Te2-Cy-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-Cy-
CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-Cy-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-C
y-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-CH_TwoCH_Two-Cy-Ph1-CF_Three, R¹-Te1
-CH_TwoCH_Two-Cy-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Cy-Ph3-CF_Three, R¹-T
e1-CH_TwoCH_Two-Cy-Np1-CF_Three, R¹-Te1-CH_TwoCH _Two-Cy-Np2-CF_Three, R¹
-Te1-CH_TwoCH_Two-Cy-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Cy-Np4-CF_Three,
R¹-Te2-CH_TwoCH_Two-Cy-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-Ph2-C
F_Three, R¹-Te2-CH_TwoCH_Two-Cy-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-Np1
-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-Np2-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-N
p3-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-Np4-CF_Three, R¹-Te1-CH_TwoCH_Two-Cy
-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Ph3-CF_Three,
R¹-Te1-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-Cy-
CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np3-CF_Three, R
¹-Te1-CH_TwoCH_Two-Cy-CH _TwoCH_Two-Np4-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-C
H_TwoCH_Two-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Ph2-CF_Three, R¹
-Te2-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-CH
_TwoCH_Two-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np2-CF_Three, R¹-
Te2-CH_TwoCH_Two-Cy-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-CH_TwoCH_Two-Cy-CH_Two
CH_Two-Np4-CF_Three,

R¹-Te1-Ph1-Ph1-CF_Three, R¹-Te1-Ph1-Ph2-C
F_Three, R¹-Te1-Ph1-Ph3-CF_Three, R¹-Te1-Ph1-Np1-CF_Three, R¹-Te1
-Ph1-Np2-CF_Three, R¹-Te1-Ph1-Np3-CF_Three, R¹-Te1-Ph1-Np4-C
F_Three, R¹-Te2-Ph1-Ph1-CF_Three, R¹-Te2-Ph1-Ph2-CF_Three, R¹-Te2
-Ph1-Ph3-CF_Three, R¹-Te2-Ph1-Np1-CF_Three, R¹-Te2-Ph1-Np2-C
F_Three, R¹-Te2-Ph1-Np3-CF_Three, R¹-Te2-Ph1-Np4-CF_Three, R¹-Te1
-Ph1-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-Ph1-CH_TwoCH_Two-Ph3-CF_Three, R¹
-Te1-Ph1-CH_TwoCH_Two-Np1-CF_Three, R¹-Te1-Ph1-CH_TwoCH_Two-Np2-C
F_Three, R¹-Te1-Ph1-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-Ph1-CH_TwoCH _Two-N
p4-CF_Three, R¹-Te2-Ph1-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-Ph1-CH_TwoC
H_Two-Ph2-CF_Three, R¹-Te2-Ph1-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te2-Ph1-
CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-Ph1-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-
Ph1-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-Ph1-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te1-Ph1-C≡C-Ph2-CF_Three, R¹-Te1-Ph1-C≡C-Ph3-CF_Three, R¹-
Te1-Ph1-C≡C-Np1-CF_Three, R¹-Te1-Ph1-C≡C-Np2-CF_Three, R¹-
Te1-Ph1-C≡C-Np3-CF_Three, R¹-Te1-Ph1-C≡C-Np4-CF_Three, R¹-
Te2-Ph1-C≡C-Ph1-CF_Three, R¹-Te2-Ph1-C≡C-Ph2-CF_Three, R¹-
Te2-Ph1-C≡C-Ph3-CF_Three, R¹-Te2-Ph1-C≡C-Np1-CF_Three, R¹-
Te2-Ph1-C≡C-Np2-CF_Three, R¹-Te2-Ph1-C≡C-Np3-CF_Three, R¹-
Te2-Ph1-C≡C-Np4-CF_Three,

R¹-Te1-Ph2-Ph1-CF_Three, R¹-Te1-Ph2-Ph2-C
F_Three, R¹-Te1-Ph2-Ph3-CF_Three, R¹-Te1-Ph2-Np1-CF_Three, R¹-Te1
-Ph2-Np2-CF_Three, R¹-Te1-Ph2-Np3-CF_Three, R¹-Te1-Ph2-Np4-C
F_Three, R¹-Te2-Ph2-Ph1-CF_Three, R¹-Te2-Ph2-Ph2-CF_Three, R¹-Te2
-Ph2-Ph3-CF_Three, R¹-Te2-Ph2-Np1-CF_Three, R¹-Te2-Ph2-Np2-C
F_Three, R¹-Te2-Ph2-Np3-CF_Three, R¹-Te2-Ph2-Np4-CF_Three, R¹-Te1
-Ph2-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-Ph2-CH_TwoCH_Two-Ph3-CF_Three, R¹
-Te1-Ph2-CH_TwoCH_Two-Np1-CF_Three, R¹-Te1-Ph2-CH_TwoCH_Two-Np2-C
F_Three, R¹-Te1-Ph2-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-Ph2-CH_TwoCH _Two-N
p4-CF_Three, R¹-Te2-Ph2-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-Ph2-CH_TwoC
H_Two-Ph2-CF_Three, R¹-Te2-Ph2-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te2-Ph2-
CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-Ph2-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-
Ph2-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-Ph2-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te1-Ph2-C≡C-Ph2-CF_Three, R¹-Te1-Ph2-C≡C-Ph3-CF_Three, R¹-
Te1-Ph2-C≡C-Np1-CF_Three, R¹-Te1-Ph2-C≡C-Np2-CF_Three, R¹-
Te1-Ph2-C≡C-Np3-CF_Three, R¹-Te1-Ph2-C≡C-Np4-CF_Three, R¹-
Te2-Ph2-C≡C-Ph1-CF_Three, R¹-Te2-Ph2-C≡C-Ph2-CF_Three, R¹-
Te2-Ph2-C≡C-Ph3-CF_Three, R¹-Te2-Ph2-C≡C-Np1-CF_Three, R¹-
Te2-Ph2-C≡C-Np2-CF_Three, R¹-Te2-Ph2-C≡C-Np3-CF_Three, R¹-
Te2-Ph2-C≡C-Np4-CF_Three,

R¹-Te1-Ph3-Ph1-CF_Three, R¹-Te1-Ph3-Ph2-C
F_Three, R¹-Te1-Ph3-Ph3-CF_Three, R¹-Te1-Ph3-Np1-CF_Three, R¹-Te1
-Ph3-Np2-CF_Three, R¹-Te1-Ph3-Np3-CF_Three, R¹-Te1-Ph3-Np4-C
F_Three, R¹-Te2-Ph3-Ph1-CF_Three, R¹-Te2-Ph3-Ph2-CF_Three, R¹-Te2
-Ph3-Ph3-CF_Three, R¹-Te2-Ph3-Np1-CF_Three, R¹-Te2-Ph3-Np2-C
F_Three, R¹-Te2-Ph3-Np3-CF_Three, R¹-Te2-Ph3-Np4-CF_Three, R¹-Te1
-Ph3-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-Ph3-CH_TwoCH_Two-Ph3-CF_Three, R¹
-Te1-Ph3-CH_TwoCH_Two-Np1-CF_Three, R¹-Te1-Ph3-CH_TwoCH_Two-Np2-C
F_Three, R¹-Te1-Ph3-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-Ph3-CH_TwoCH _Two-N
p4-CF_Three, R¹-Te2-Ph3-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-Ph3-CH_TwoC
H_Two-Ph2-CF_Three, R¹-Te2-Ph3-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te2-Ph3-
CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-Ph3-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-
Ph3-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-Ph3-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te1-Ph3-C≡C-Ph2-CF_Three, R¹-Te1-Ph3-C≡C-Ph3-CF_Three, R¹-
Te1-Ph3-C≡C-Np1-CF_Three, R¹-Te1-Ph3-C≡C-Np2-CF_Three, R¹-
Te1-Ph3-C≡C-Np3-CF_Three, R¹-Te1-Ph3-C≡C-Np4-CF_Three, R¹-
Te2-Ph3-C≡C-Ph1-CF_Three, R¹-Te2-Ph3-C≡C-Ph2-CF_Three, R¹-
Te2-Ph3-C≡C-Ph3-CF_Three, R¹-Te2-Ph3-C≡C-Np1-CF_Three, R¹-
Te2-Ph3-C≡C-Np2-CF_Three, R¹-Te2-Ph3-C≡C-Np3-CF_Three, R¹-
Te2-Ph3-C≡C-Np4-CF_Three,

R¹-Te1-Np1-Ph1-CF_Three, R¹-Te1-Np1-Ph2-C
F_Three, R¹-Te1-Np1-Ph3-CF_Three, R¹-Te1-Np1-Np1-CF_Three, R¹-Te1
-Np1-Np2-CF_Three, R¹-Te1-Np1-Np3-CF_Three, R¹-Te1-Np1-Np4-C
F_Three, R¹-Te2-Np1-Ph1-CF_Three, R¹-Te2-Np1-Ph2-CF_Three, R¹-Te2
-Np1-Ph3-CF_Three, R¹-Te2-Np1-Np1-CF_Three, R¹-Te2-Np1-Np2-C
F_Three, R¹-Te2-Np1-Np3-CF_Three, R¹-Te2-Np1-Np4-CF_Three, R¹-Te1
-Np1-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-Np1-CH_TwoCH_Two-Ph3-CF_Three, R¹
-Te1-Np1-CH_TwoCH_Two-Np1-CF_Three, R¹-Te1-Np1-CH_TwoCH_Two-Np2-C
F_Three, R¹-Te1-Np1-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-Np1-CH_TwoCH _Two-N
p4-CF_Three, R¹-Te2-Np1-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-Np1-CH_TwoC
H_Two-Ph2-CF_Three, R¹-Te2-Np1-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te2-Np1-
CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-Np1-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-
Np1-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-Np1-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te1-Np1-C≡C-Ph2-CF_Three, R¹-Te1-Np1-C≡C-Ph3-CF_Three, R¹-
Te1-Np1-C≡C-Np1-CF_Three, R¹-Te1-Np1-C≡C-Np2-CF_Three, R¹-
Te1-Np1-C≡C-Np3-CF_Three, R¹-Te1-Np1-C≡C-Np4-CF_Three, R¹-
Te2-Np1-C≡C-Ph1-CF_Three, R¹-Te2-Np1-C≡C-Ph2-CF_Three, R¹-
Te2-Np1-C≡C-Ph3-CF_Three, R¹-Te2-Np1-C≡C-Np1-CF_Three, R¹-
Te2-Np1-C≡C-Np2-CF_Three, R¹-Te2-Np1-C≡C-Np3-CF_Three, R¹-
Te2-Np1-C≡C-Np4-CF_Three,

R¹-Te1-Np2-Ph1-CF_Three, R¹-Te1-Np2-Ph2-C
F_Three, R¹-Te1-Np2-Ph3-CF_Three, R¹-Te1-Np2-Np1-CF_Three, R¹-Te1
-Np2-Np2-CF_Three, R¹-Te1-Np2-Np3-CF_Three, R¹-Te1-Np2-Np4-C
F_Three, R¹-Te2-Np2-Ph1-CF_Three, R¹-Te2-Np2-Ph2-CF_Three, R¹-Te2
-Np2-Ph3-CF_Three, R¹-Te2-Np2-Np1-CF_Three, R¹-Te2-Np2-Np2-C
F_Three, R¹-Te2-Np2-Np3-CF_Three, R¹-Te2-Np2-Np4-CF_Three, R¹-Te1
-Np2-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-Np2-CH_TwoCH_Two-Ph3-CF_Three, R¹
-Te1-Np2-CH_TwoCH_Two-Np1-CF_Three, R¹-Te1-Np2-CH_TwoCH_Two-Np2-C
F_Three, R¹-Te1-Np2-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-Np2-CH_TwoCH _Two-N
p4-CF_Three, R¹-Te2-Np2-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-Np2-CH_TwoC
H_Two-Ph2-CF_Three, R¹-Te2-Np2-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te2-Np2-
CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-Np2-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-
Np2-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-Np2-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te1-Np2-C≡C-Ph2-CF_Three, R¹-Te1-Np2-C≡C-Ph3-CF_Three, R¹-
Te1-Np2-C≡C-Np1-CF_Three, R¹-Te1-Np2-C≡C-Np2-CF_Three, R¹-
Te1-Np2-C≡C-Np3-CF_Three, R¹-Te1-Np2-C≡C-Np4-CF_Three, R¹-
Te2-Np2-C≡C-Ph1-CF_Three, R¹-Te2-Np2-C≡C-Ph2-CF_Three, R¹-
Te2-Np2-C≡C-Ph3-CF_Three, R¹-Te2-Np2-C≡C-Np1-CF_Three, R¹-
Te2-Np2-C≡C-Np2-CF_Three, R¹-Te2-Np2-C≡C-Np3-CF_Three, R¹-
Te2-Np2-C≡C-Np4-CF_Three,

R¹-Te1-Np3-Ph1-CF_Three, R¹-Te1-Np3-Ph2-C
F_Three, R¹-Te1-Np3-Ph3-CF_Three, R¹-Te1-Np3-Np1-CF_Three, R¹-Te1
-Np3-Np2-CF_Three, R¹-Te1-Np3-Np3-CF_Three, R¹-Te1-Np3-Np4-C
F_Three, R¹-Te2-Np3-Ph1-CF_Three, R¹-Te2-Np3-Ph2-CF_Three, R¹-Te2
-Np3-Ph3-CF_Three, R¹-Te2-Np3-Np1-CF_Three, R¹-Te2-Np3-Np2-C
F_Three, R¹-Te2-Np3-Np3-CF_Three, R¹-Te2-Np3-Np4-CF_Three, R¹-Te1
-Np3-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-Np3-CH_TwoCH_Two-Ph3-CF_Three, R¹
-Te1-Np3-CH_TwoCH_Two-Np1-CF_Three, R¹-Te1-Np3-CH_TwoCH_Two-Np2-C
F_Three, R¹-Te1-Np3-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-Np3-CH_TwoCH _Two-N
p4-CF_Three, R¹-Te2-Np3-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-Np3-CH_TwoC
H_Two-Ph2-CF_Three, R¹-Te2-Np3-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te2-Np3-
CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-Np3-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-
Np3-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-Np3-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te1-Np3-C≡C-Ph2-CF_Three, R¹-Te1-Np3-C≡C-Ph3-CF_Three, R¹-
Te1-Np3-C≡C-Np1-CF_Three, R¹-Te1-Np3-C≡C-Np2-CF_Three, R¹-
Te1-Np3-C≡C-Np3-CF_Three, R¹-Te1-Np3-C≡C-Np4-CF_Three, R¹-
Te2-Np3-C≡C-Ph1-CF_Three, R¹-Te2-Np3-C≡C-Ph2-CF_Three, R¹-
Te2-Np3-C≡C-Ph3-CF_Three, R¹-Te2-Np3-C≡C-Np1-CF_Three, R¹-
Te2-Np3-C≡C-Np2-CF_Three, R¹-Te2-Np3-C≡C-Np3-CF_Three, R¹-
Te2-Np3-C≡C-Np4-CF_Three,

R¹-Te1-Np4-Ph1-CF_Three, R¹-Te1-Np4-Ph2-C
F_Three, R¹-Te1-Np4-Ph3-CF_Three, R¹-Te1-Np4-Np1-CF_Three, R¹-Te1
-Np4-Np2-CF_Three, R¹-Te1-Np4-Np3-CF_Three, R¹-Te1-Np4-Np4-C
F_Three, R¹-Te2-Np4-Ph1-CF_Three, R¹-Te2-Np4-Ph2-CF_Three, R¹-Te2
-Np4-Ph3-CF_Three, R¹-Te2-Np4-Np1-CF_Three, R¹-Te2-Np4-Np2-C
F_Three, R¹-Te2-Np4-Np3-CF_Three, R¹-Te2-Np4-Np4-CF_Three, R¹-Te1
-Np4-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-Np4-CH_TwoCH_Two-Ph3-CF_Three, R¹
-Te1-Np4-CH_TwoCH_Two-Np1-CF_Three, R¹-Te1-Np4-CH_TwoCH_Two-Np2-C
F_Three, R¹-Te1-Np4-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-Np4-CH_TwoCH _Two-N
p4-CF_Three, R¹-Te2-Np4-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-Np4-CH_TwoC
H_Two-Ph2-CF_Three, R¹-Te2-Np4-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te2-Np4-
CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-Np4-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-
Np4-CH_TwoCH_Two-Np3-CF_Three, R¹-Te2-Np4-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te1-Np4-C≡C-Ph2-CF_Three, R¹-Te1-Np4-C≡C-Ph3-CF_Three, R¹-
Te1-Np4-C≡C-Np1-CF_Three, R¹-Te1-Np4-C≡C-Np2-CF_Three, R¹-
Te1-Np4-C≡C-Np3-CF_Three, R¹-Te1-Np4-C≡C-Np4-CF_Three, R¹-
Te2-Np4-C≡C-Ph1-CF_Three, R¹-Te2-Np4-C≡C-Ph2-CF_Three, R¹-
Te2-Np4-C≡C-Ph3-CF_Three, R¹-Te2-Np4-C≡C-Np1-CF_Three, R¹-
Te2-Np4-C≡C-Np2-CF_Three, R¹-Te2-Np4-C≡C-Np3-CF_Three, R¹-
Te2-Np4-C≡C-Np4-CF_Three,

R¹-Te1-CH_TwoCH_Two-Ph1-Ph1-CF_Three, R¹-Te1-CH_TwoC
H_Two-Ph1-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph1-Ph3-CF_Three, R¹-Te1-
CH_TwoCH_Two-Ph1-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph1-Np2-CF_Three, R¹-
Te1-CH _TwoCH_Two-Ph1-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph1-Np4-C
F_Three, R¹-Te2-CH_TwoCH_Two-Ph1-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-P
h2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-P
h1-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-Np2-CF_Three, R¹-Te2-CH_TwoC
H_Two-Ph1-Np3-CF_Three, R¹-Te2-CH _TwoCH_Two-Ph1-Np4-CF_Three, R¹-Te1-
CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph1-CH _TwoCH
_Two-Ph3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np1-CF_Three, R¹-Te
1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph1-CH_Two
CH_Two-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-C
H_TwoCH_Two-Ph2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Ph3-CF_Three, R
¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1
-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np3-C
F_Three, R¹-Te2-CH_TwoCH_Two-Ph1-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-CH_TwoCH
_Two-Ph1-C≡C-Ph2-CF_Three, R¹-Te1-CH_TwoCH _Two-Ph1-C≡C-Ph3-C
F_Three, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-
Ph1-C≡C-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph1-C≡C-Np3-CF_Three,
R¹-Te1-CH_TwoCH_Two-Ph1-C≡C-Np4-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-
C≡C-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Ph2-CF_Three, R¹-T
e2-CH_TwoCH_Two-Ph1-C≡C-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C
-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Np2-CF_Three, R¹-Te2-C
H_TwoCH_Two-Ph1-C≡C-Np3-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph1-C≡C-Np4
-CF_Three,

R¹-Te1-CH_TwoCH_Two-Ph2-Ph1-CF_Three, R¹-Te1-CH_TwoC
H_Two-Ph2-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph2-Ph3-CF_Three, R¹-Te1-
CH_TwoCH_Two-Ph2-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph2-Np2-CF_Three, R¹-
Te1-CH _TwoCH_Two-Ph2-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph2-Np4-C
F_Three, R¹-Te2-CH_TwoCH_Two-Ph2-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-P
h2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-P
h2-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-Np2-CF_Three, R¹-Te2-CH_TwoC
H_Two-Ph2-Np3-CF_Three, R¹-Te2-CH _TwoCH_Two-Ph2-Np4-CF_Three, R¹-Te1-
CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph2-CH _TwoCH
_Two-Ph3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np1-CF_Three, R¹-Te
1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph2-CH_Two
CH_Two-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-C
H_TwoCH_Two-Ph2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Ph3-CF_Three, R
¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2
-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np3-C
F_Three, R¹-Te2-CH_TwoCH_Two-Ph2-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-CH_TwoCH
_Two-Ph2-C≡C-Ph2-CF_Three, R¹-Te1-CH_TwoCH _Two-Ph2-C≡C-Ph3-C
F_Three, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-
Ph2-C≡C-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph2-C≡C-Np3-CF_Three,
R¹-Te1-CH_TwoCH_Two-Ph2-C≡C-Np4-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-
C≡C-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Ph2-CF_Three, R¹-T
e2-CH_TwoCH_Two-Ph2-C≡C-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C
-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Np2-CF_Three, R¹-Te2-C
H_TwoCH_Two-Ph2-C≡C-Np3-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph2-C≡C-Np4
-CF_Three,

R¹-Te1-CH_TwoCH_Two-Ph3-Ph1-CF_Three, R¹-Te1-CH_TwoC
H_Two-Ph3-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph3-Ph3-CF_Three, R¹-Te1-
CH_TwoCH_Two-Ph3-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph3-Np2-CF_Three, R¹-
Te1-CH _TwoCH_Two-Ph3-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph3-Np4-C
F_Three, R¹-Te2-CH_TwoCH_Two-Ph3-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-P
h2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-P
h3-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-Np2-CF_Three, R¹-Te2-CH_TwoC
H_Two-Ph3-Np3-CF_Three, R¹-Te2-CH _TwoCH_Two-Ph3-Np4-CF_Three, R¹-Te1-
CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph3-CH _TwoCH
_Two-Ph3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np1-CF_Three, R¹-Te
1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph3-CH_Two
CH_Two-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-C
H_TwoCH_Two-Ph2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Ph3-CF_Three, R
¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3
-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np3-C
F_Three, R¹-Te2-CH_TwoCH_Two-Ph3-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-CH_TwoCH
_Two-Ph3-C≡C-Ph2-CF_Three, R¹-Te1-CH_TwoCH _Two-Ph3-C≡C-Ph3-C
F_Three, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-
Ph3-C≡C-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Ph3-C≡C-Np3-CF_Three,
R¹-Te1-CH_TwoCH_Two-Ph3-C≡C-Np4-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-
C≡C-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Ph2-CF_Three, R¹-T
e2-CH_TwoCH_Two-Ph3-C≡C-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C
-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Np2-CF_Three, R¹-Te2-C
H_TwoCH_Two-Ph3-C≡C-Np3-CF_Three, R¹-Te2-CH_TwoCH_Two-Ph3-C≡C-Np4
-CF_Three,

R¹-Te1-CH_TwoCH_Two-Np1-Ph1-CF_Three, R¹-Te1-CH_TwoC
H_Two-Np1-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np1-Ph3-CF_Three, R¹-Te1-
CH_TwoCH_Two-Np1-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-Np1-Np2-CF_Three, R¹-
Te1-CH _TwoCH_Two-Np1-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np1-Np4-C
F_Three, R¹-Te2-CH_TwoCH_Two-Np1-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-P
h2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-N
p1-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-Np2-CF_Three, R¹-Te2-CH_TwoC
H_Two-Np1-Np3-CF_Three, R¹-Te2-CH _TwoCH_Two-Np1-Np4-CF_Three, R¹-Te1-
CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np1-CH _TwoCH
_Two-Ph3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np1-CF_Three, R¹-Te
1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np1-CH_Two
CH_Two-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-C
H_TwoCH_Two-Ph2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Ph3-CF_Three, R
¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1
-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np3-C
F_Three, R¹-Te2-CH_TwoCH_Two-Np1-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-CH_TwoCH
_Two-Np1-C≡C-Ph2-CF_Three, R¹-Te1-CH_TwoCH _Two-Np1-C≡C-Ph3-C
F_Three, R¹-Te1-CH_TwoCH_Two-Np1-C≡C-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-
Np1-C≡C-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np1-C≡C-Np3-CF_Three,
R¹-Te1-CH_TwoCH_Two-Np1-C≡C-Np4-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-
C≡C-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-Ph2-CF_Three, R¹-T
e2-CH_TwoCH_Two-Np1-C≡C-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-C≡C
-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-Np2-CF_Three, R¹-Te2-C
H_TwoCH_Two-Np1-C≡C-Np3-CF_Three, R¹-Te2-CH_TwoCH_Two-Np1-C≡C-Np4
-CF_Three,

R¹-Te1-CH_TwoCH_Two-Np2-Ph1-CF_Three, R¹-Te1-CH_TwoC
H_Two-Np2-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np2-Ph3-CF_Three, R¹-Te1-
CH_TwoCH_Two-Np2-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-Np2-Np2-CF_Three, R¹-
Te1-CH _TwoCH_Two-Np2-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np2-Np4-C
F_Three, R¹-Te2-CH_TwoCH_Two-Np2-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-P
h2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-N
p2-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-Np2-CF_Three, R¹-Te2-CH_TwoC
H_Two-Np2-Np3-CF_Three, R¹-Te2-CH _TwoCH_Two-Np2-Np4-CF_Three, R¹-Te1-
CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np2-CH _TwoCH
_Two-Ph3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np1-CF_Three, R¹-Te
1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np2-CH_Two
CH_Two-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-C
H_TwoCH_Two-Ph2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Ph3-CF_Three, R
¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2
-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np3-C
F_Three, R¹-Te2-CH_TwoCH_Two-Np2-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-CH_TwoCH
_Two-Np2-C≡C-Ph2-CF_Three, R¹-Te1-CH_TwoCH _Two-Np2-C≡C-Ph3-C
F_Three, R¹-Te1-CH_TwoCH_Two-Np2-C≡C-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-
Np2-C≡C-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np2-C≡C-Np3-CF_Three,
R¹-Te1-CH_TwoCH_Two-Np2-C≡C-Np4-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-
C≡C-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-Ph2-CF_Three, R¹-T
e2-CH_TwoCH_Two-Np2-C≡C-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-C≡C
-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-Np2-CF_Three, R¹-Te2-C
H_TwoCH_Two-Np2-C≡C-Np3-CF_Three, R¹-Te2-CH_TwoCH_Two-Np2-C≡C-Np4
-CF_Three,

R¹-Te1-CH_TwoCH_Two-Np3-Ph1-CF_Three, R¹-Te1-CH_TwoC
H_Two-Np3-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np3-Ph3-CF_Three, R¹-Te1-
CH_TwoCH_Two-Np3-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-Np3-Np2-CF_Three, R¹-
Te1-CH _TwoCH_Two-Np3-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np3-Np4-C
F_Three, R¹-Te2-CH_TwoCH_Two-Np3-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-P
h2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-N
p3-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-Np2-CF_Three, R¹-Te2-CH_TwoC
H_Two-Np3-Np3-CF_Three, R¹-Te2-CH _TwoCH_Two-Np3-Np4-CF_Three, R¹-Te1-
CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np3-CH _TwoCH
_Two-Ph3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np1-CF_Three, R¹-Te
1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np3-CH_Two
CH_Two-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-C
H_TwoCH_Two-Ph2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Ph3-CF_Three, R
¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3
-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np3-C
F_Three, R¹-Te2-CH_TwoCH_Two-Np3-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-CH_TwoCH
_Two-Np3-C≡C-Ph2-CF_Three, R¹-Te1-CH_TwoCH _Two-Np3-C≡C-Ph3-C
F_Three, R¹-Te1-CH_TwoCH_Two-Np3-C≡C-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-
Np3-C≡C-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np3-C≡C-Np3-CF_Three,
R¹-Te1-CH_TwoCH_Two-Np3-C≡C-Np4-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-
C≡C-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-Ph2-CF_Three, R¹-T
e2-CH_TwoCH_Two-Np3-C≡C-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-C≡C
-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-Np2-CF_Three, R¹-Te2-C
H_TwoCH_Two-Np3-C≡C-Np3-CF_Three, R¹-Te2-CH_TwoCH_Two-Np3-C≡C-Np4
-CF_Three,

R¹-Te1-CH_TwoCH_Two-Np4-Ph1-CF_Three, R¹-Te1-CH_TwoC
H_Two-Np4-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np4-Ph3-CF_Three, R¹-Te1-
CH_TwoCH_Two-Np4-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-Np4-Np2-CF_Three, R¹-
Te1-CH _TwoCH_Two-Np4-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np4-Np4-C
F_Three, R¹-Te2-CH_TwoCH_Two-Np4-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-P
h2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-N
p4-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-Np2-CF_Three, R¹-Te2-CH_TwoC
H_Two-Np4-Np3-CF_Three, R¹-Te2-CH _TwoCH_Two-Np4-Np4-CF_Three, R¹-Te1-
CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np4-CH _TwoCH
_Two-Ph3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np1-CF_Three, R¹-Te
1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np4-CH_Two
CH_Two-Np3-CF_Three, R¹-Te1-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np4-CF_Three, R¹-
Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-C
H_TwoCH_Two-Ph2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Ph3-CF_Three, R
¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4
-CH_TwoCH_Two-Np2-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np3-C
F_Three, R¹-Te2-CH_TwoCH_Two-Np4-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-CH_TwoCH
_Two-Np4-C≡C-Ph2-CF_Three, R¹-Te1-CH_TwoCH _Two-Np4-C≡C-Ph3-C
F_Three, R¹-Te1-CH_TwoCH_Two-Np4-C≡C-Np1-CF_Three, R¹-Te1-CH_TwoCH_Two-
Np4-C≡C-Np2-CF_Three, R¹-Te1-CH_TwoCH_Two-Np4-C≡C-Np3-CF_Three,
R¹-Te1-CH_TwoCH_Two-Np4-C≡C-Np4-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-
C≡C-Ph1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-Ph2-CF_Three, R¹-T
e2-CH_TwoCH_Two-Np4-C≡C-Ph3-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-C≡C
-Np1-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-Np2-CF_Three, R¹-Te2-C
H_TwoCH_Two-Np4-C≡C-Np3-CF_Three, R¹-Te2-CH_TwoCH_Two-Np4-C≡C-Np4
-CF_Three,

R¹-Te1-C≡C-Ph1-Ph1-CF_Three, R¹-Te1-C≡C-P
h1-Ph2-CF_Three, R¹-Te1-C≡C-Ph1-Ph3-CF _Three, R¹-Te1-C≡C-P
h1-Np1-CF_Three, R¹-Te1-C≡C-Ph1-Np2-CF_Three, R¹-Te1-C≡C-P
h1-Np3-CF_Three, R¹-Te1-C≡C-Ph1-Np4-CF_Three, R¹-Te2-C≡C-P
h1-Ph1-CF_Three, R¹-Te2-C≡C-Ph1-Ph2-CF_Three, R¹-Te2-C≡C-P
h1-Ph3-CF_Three, R¹-Te2-C≡C-Ph1-Np1-CF_Three, R¹-Te2-C≡C-P
h1-Np2-CF_Three, R¹-Te2-C≡C-Ph1-Np3-CF_Three, R¹-Te2-C≡C-P
h1-Np4-CF_Three, R¹-Te1-C≡C-Ph1-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1
-C≡C-Ph1-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te1-C≡C-Ph1-CH _TwoCH_Two-N
p1-CF_Three, R¹-Te1-C≡C-Ph1-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-C≡
C-Ph1-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-C≡C-Ph1-CH_TwoCH_Two-Np4-C
F_Three, R¹-Te2-C≡C-Ph1-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-C≡C-Ph
1-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te2-C≡C-Ph1-CH_TwoCH_Two-Ph3-CF_Three,
R¹-Te2-C≡C-Ph1-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-C≡C-Ph1-CH
_TwoCH_Two-Np2-CF_Three, R¹-Te2-C≡C-Ph1-CH _TwoCH_Two-Np3-CF_Three, R¹-T
e2-C≡C-Ph1-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-C≡C-Ph1-C≡C-P
h2-CF_Three, R¹-Te1-C≡C-Ph1-C≡C-Ph3-CF_Three, R¹-Te1-C≡C-
Ph1-C≡C-Np1-CF_Three, R¹-Te1-C≡C-Ph1-C≡C-Np2-CF_Three, R¹
-Te1-C≡C-Ph1-C≡C-Np3-CF_Three, R¹-Te1-C≡C-Ph1-C≡C-N
p4-CF_Three, R¹-Te2-C≡C-Ph1-C≡C-Ph1-CF_Three, R¹-Te2-C≡C-
Ph1-C≡C-Ph2-CF_Three, R¹-Te2-C≡C-Ph1-C≡C-Ph3-CF_Three, R¹
-Te2-C≡C-Ph1-C≡C-Np1-CF_Three, R¹-Te2-C≡C-Ph1-C≡C-N
p2-CF_Three, R¹-Te2-C≡C-Ph1-C≡C-Np3-CF_Three, R¹-Te2-C≡C-
Ph1-C≡C-Np4-CF_Three,

R¹-Te1-C≡C-Ph2-Ph1-CF_Three, R¹-Te1-C≡C-P
h2-Ph2-CF_Three, R¹-Te1-C≡C-Ph2-Ph3-CF _Three, R¹-Te1-C≡C-P
h2-Np1-CF_Three, R¹-Te1-C≡C-Ph2-Np2-CF_Three, R¹-Te1-C≡C-P
h2-Np3-CF_Three, R¹-Te1-C≡C-Ph2-Np4-CF_Three, R¹-Te2-C≡C-P
h2-Ph1-CF_Three, R¹-Te2-C≡C-Ph2-Ph2-CF_Three, R¹-Te2-C≡C-P
h2-Ph3-CF_Three, R¹-Te2-C≡C-Ph2-Np1-CF_Three, R¹-Te2-C≡C-P
h2-Np2-CF_Three, R¹-Te2-C≡C-Ph2-Np3-CF_Three, R¹-Te2-C≡C-P
h2-Np4-CF_Three, R¹-Te1-C≡C-Ph2-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1
-C≡C-Ph2-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te1-C≡C-Ph2-CH _TwoCH_Two-N
p1-CF_Three, R¹-Te1-C≡C-Ph2-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-C≡
C-Ph2-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-C≡C-Ph2-CH_TwoCH_Two-Np4-C
F_Three, R¹-Te2-C≡C-Ph2-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-C≡C-Ph
2-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te2-C≡C-Ph2-CH_TwoCH_Two-Ph3-CF_Three,
R¹-Te2-C≡C-Ph2-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-C≡C-Ph2-CH
_TwoCH_Two-Np2-CF_Three, R¹-Te2-C≡C-Ph2-CH _TwoCH_Two-Np3-CF_Three, R¹-T
e2-C≡C-Ph2-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-C≡C-Ph2-C≡C-P
h2-CF_Three, R¹-Te1-C≡C-Ph2-C≡C-Ph3-CF_Three, R¹-Te1-C≡C-
Ph2-C≡C-Np1-CF_Three, R¹-Te1-C≡C-Ph2-C≡C-Np2-CF_Three, R¹
-Te1-C≡C-Ph2-C≡C-Np3-CF_Three, R¹-Te1-C≡C-Ph2-C≡C-N
p4-CF_Three, R¹-Te2-C≡C-Ph2-C≡C-Ph1-CF_Three, R¹-Te2-C≡C-
Ph2-C≡C-Ph2-CF_Three, R¹-Te2-C≡C-Ph2-C≡C-Ph3-CF_Three, R¹
-Te2-C≡C-Ph2-C≡C-Np1-CF_Three, R¹-Te2-C≡C-Ph2-C≡C-N
p2-CF_Three, R¹-Te2-C≡C-Ph2-C≡C-Np3-CF_Three, R¹-Te2-C≡C-
Ph2-C≡C-Np4-CF_Three,

R¹-Te1-C≡C-Ph3-Ph1-CF_Three, R¹-Te1-C≡C-P
h3-Ph2-CF_Three, R¹-Te1-C≡C-Ph3-Ph3-CF _Three, R¹-Te1-C≡C-P
h3-Np1-CF_Three, R¹-Te1-C≡C-Ph3-Np2-CF_Three, R¹-Te1-C≡C-P
h3-Np3-CF_Three, R¹-Te1-C≡C-Ph3-Np4-CF_Three, R¹-Te2-C≡C-P
h3-Ph1-CF_Three, R¹-Te2-C≡C-Ph3-Ph2-CF_Three, R¹-Te2-C≡C-P
h3-Ph3-CF_Three, R¹-Te2-C≡C-Ph3-Np1-CF_Three, R¹-Te2-C≡C-P
h3-Np2-CF_Three, R¹-Te2-C≡C-Ph3-Np3-CF_Three, R¹-Te2-C≡C-P
h3-Np4-CF_Three, R¹-Te1-C≡C-Ph3-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1
-C≡C-Ph3-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te1-C≡C-Ph3-CH _TwoCH_Two-N
p1-CF_Three, R¹-Te1-C≡C-Ph3-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-C≡
C-Ph3-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-C≡C-Ph3-CH_TwoCH_Two-Np4-C
F_Three, R¹-Te2-C≡C-Ph3-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-C≡C-Ph
3-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te2-C≡C-Ph3-CH_TwoCH_Two-Ph3-CF_Three,
R¹-Te2-C≡C-Ph3-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-C≡C-Ph3-CH
_TwoCH_Two-Np2-CF_Three, R¹-Te2-C≡C-Ph3-CH _TwoCH_Two-Np3-CF_Three, R¹-T
e2-C≡C-Ph3-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-C≡C-Ph3-C≡C-P
h2-CF_Three, R¹-Te1-C≡C-Ph3-C≡C-Ph3-CF_Three, R¹-Te1-C≡C-
Ph3-C≡C-Np1-CF_Three, R¹-Te1-C≡C-Ph3-C≡C-Np2-CF_Three, R¹
-Te1-C≡C-Ph3-C≡C-Np3-CF_Three, R¹-Te1-C≡C-Ph3-C≡C-N
p4-CF_Three, R¹-Te2-C≡C-Ph3-C≡C-Ph1-CF_Three, R¹-Te2-C≡C-
Ph3-C≡C-Ph2-CF_Three, R¹-Te2-C≡C-Ph3-C≡C-Ph3-CF_Three, R¹
-Te2-C≡C-Ph3-C≡C-Np1-CF_Three, R¹-Te2-C≡C-Ph3-C≡C-N
p2-CF_Three, R¹-Te2-C≡C-Ph3-C≡C-Np3-CF_Three, R¹-Te2-C≡C-
Ph3-C≡C-Np4-CF_Three,

R¹-Te1-C≡C-Np1-Ph1-CF_Three, R¹-Te1-C≡C-N
p1-Ph2-CF_Three, R¹-Te1-C≡C-Np1-Ph3-CF _Three, R¹-Te1-C≡C-N
p1-Np1-CF_Three, R¹-Te1-C≡C-Np1-Np2-CF_Three, R¹-Te1-C≡C-N
p1-Np3-CF_Three, R¹-Te1-C≡C-Np1-Np4-CF_Three, R¹-Te2-C≡C-N
p1-Ph1-CF_Three, R¹-Te2-C≡C-Np1-Ph2-CF_Three, R¹-Te2-C≡C-N
p1-Ph3-CF_Three, R¹-Te2-C≡C-Np1-Np1-CF_Three, R¹-Te2-C≡C-N
p1-Np2-CF_Three, R¹-Te2-C≡C-Np1-Np3-CF_Three, R¹-Te2-C≡C-N
p1-Np4-CF_Three, R¹-Te1-C≡C-Np1-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1
-C≡C-Np1-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te1-C≡C-Np1-CH _TwoCH_Two-N
p1-CF_Three, R¹-Te1-C≡C-Np1-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-C≡
C-Np1-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-C≡C-Np1-CH_TwoCH_Two-Np4-C
F_Three, R¹-Te2-C≡C-Np1-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-C≡C-Np
1-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te2-C≡C-Np1-CH_TwoCH_Two-Ph3-CF_Three,
R¹-Te2-C≡C-Np1-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-C≡C-Np1-CH
_TwoCH_Two-Np2-CF_Three, R¹-Te2-C≡C-Np1-CH _TwoCH_Two-Np3-CF_Three, R¹-T
e2-C≡C-Np1-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-C≡C-Np1-C≡C-P
h2-CF_Three, R¹-Te1-C≡C-Np1-C≡C-Ph3-CF_Three, R¹-Te1-C≡C-
Np1-C≡C-Np1-CF_Three, R¹-Te1-C≡C-Np1-C≡C-Np2-CF_Three, R¹
-Te1-C≡C-Np1-C≡C-Np3-CF_Three, R¹-Te1-C≡C-Np1-C≡C-N
p4-CF_Three, R¹-Te2-C≡C-Np1-C≡C-Ph1-CF_Three, R¹-Te2-C≡C-
Np1-C≡C-Ph2-CF_Three, R¹-Te2-C≡C-Np1-C≡C-Ph3-CF_Three, R¹
-Te2-C≡C-Np1-C≡C-Np1-CF_Three, R¹-Te2-C≡C-Np1-C≡C-N
p2-CF_Three, R¹-Te2-C≡C-Np1-C≡C-Np3-CF_Three, R¹-Te2-C≡C-
Np1-C≡C-Np4-CF_Three,

R¹-Te1-C≡C-Np2-Ph1-CF_Three, R¹-Te1-C≡C-N
p2-Ph2-CF_Three, R¹-Te1-C≡C-Np2-Ph3-CF _Three, R¹-Te1-C≡C-N
p2-Np1-CF_Three, R¹-Te1-C≡C-Np2-Np2-CF_Three, R¹-Te1-C≡C-N
p2-Np3-CF_Three, R¹-Te1-C≡C-Np2-Np4-CF_Three, R¹-Te2-C≡C-N
p2-Ph1-CF_Three, R¹-Te2-C≡C-Np2-Ph2-CF_Three, R¹-Te2-C≡C-N
p2-Ph3-CF_Three, R¹-Te2-C≡C-Np2-Np1-CF_Three, R¹-Te2-C≡C-N
p2-Np2-CF_Three, R¹-Te2-C≡C-Np2-Np3-CF_Three, R¹-Te2-C≡C-N
p2-Np4-CF_Three, R¹-Te1-C≡C-Np2-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1
-C≡C-Np2-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te1-C≡C-Np2-CH _TwoCH_Two-N
p1-CF_Three, R¹-Te1-C≡C-Np2-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-C≡
C-Np2-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-C≡C-Np2-CH_TwoCH_Two-Np4-C
F_Three, R¹-Te2-C≡C-Np2-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-C≡C-Np
2-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te2-C≡C-Np2-CH_TwoCH_Two-Ph3-CF_Three,
R¹-Te2-C≡C-Np2-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-C≡C-Np2-CH
_TwoCH_Two-Np2-CF_Three, R¹-Te2-C≡C-Np2-CH _TwoCH_Two-Np3-CF_Three, R¹-T
e2-C≡C-Np2-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-C≡C-Np2-C≡C-P
h2-CF_Three, R¹-Te1-C≡C-Np2-C≡C-Ph3-CF_Three, R¹-Te1-C≡C-
Np2-C≡C-Np1-CF_Three, R¹-Te1-C≡C-Np2-C≡C-Np2-CF_Three, R¹
-Te1-C≡C-Np2-C≡C-Np3-CF_Three, R¹-Te1-C≡C-Np2-C≡C-N
p4-CF_Three, R¹-Te2-C≡C-Np2-C≡C-Ph1-CF_Three, R¹-Te2-C≡C-
Np2-C≡C-Ph2-CF_Three, R¹-Te2-C≡C-Np2-C≡C-Ph3-CF_Three, R¹
-Te2-C≡C-Np2-C≡C-Np1-CF_Three, R¹-Te2-C≡C-Np2-C≡C-N
p2-CF_Three, R¹-Te2-C≡C-Np2-C≡C-Np3-CF_Three, R¹-Te2-C≡C-
Np2-C≡C-Np4-CF_Three,

R¹-Te1-C≡C-Np3-Ph1-CF_Three, R¹-Te1-C≡C-N
p3-Ph2-CF_Three, R¹-Te1-C≡C-Np3-Ph3-CF _Three, R¹-Te1-C≡C-N
p3-Np1-CF_Three, R¹-Te1-C≡C-Np3-Np2-CF_Three, R¹-Te1-C≡C-N
p3-Np3-CF_Three, R¹-Te1-C≡C-Np3-Np4-CF_Three, R¹-Te2-C≡C-N
p3-Ph1-CF_Three, R¹-Te2-C≡C-Np3-Ph2-CF_Three, R¹-Te2-C≡C-N
p3-Ph3-CF_Three, R¹-Te2-C≡C-Np3-Np1-CF_Three, R¹-Te2-C≡C-N
p3-Np2-CF_Three, R¹-Te2-C≡C-Np3-Np3-CF_Three, R¹-Te2-C≡C-N
p3-Np4-CF_Three, R¹-Te1-C≡C-Np3-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1
-C≡C-Np3-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te1-C≡C-Np3-CH _TwoCH_Two-N
p1-CF_Three, R¹-Te1-C≡C-Np3-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-C≡
C-Np3-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-C≡C-Np3-CH_TwoCH_Two-Np4-C
F_Three, R¹-Te2-C≡C-Np3-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-C≡C-Np
3-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te2-C≡C-Np3-CH_TwoCH_Two-Ph3-CF_Three,
R¹-Te2-C≡C-Np3-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-C≡C-Np3-CH
_TwoCH_Two-Np2-CF_Three, R¹-Te2-C≡C-Np3-CH _TwoCH_Two-Np3-CF_Three, R¹-T
e2-C≡C-Np3-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-C≡C-Np3-C≡C-P
h2-CF_Three, R¹-Te1-C≡C-Np3-C≡C-Ph3-CF_Three, R¹-Te1-C≡C-
Np3-C≡C-Np1-CF_Three, R¹-Te1-C≡C-Np3-C≡C-Np2-CF_Three, R¹
-Te1-C≡C-Np3-C≡C-Np3-CF_Three, R¹-Te1-C≡C-Np3-C≡C-N
p4-CF_Three, R¹-Te2-C≡C-Np3-C≡C-Ph1-CF_Three, R¹-Te2-C≡C-
Np3-C≡C-Ph2-CF_Three, R¹-Te2-C≡C-Np3-C≡C-Ph3-CF_Three, R¹
-Te2-C≡C-Np3-C≡C-Np1-CF_Three, R¹-Te2-C≡C-Np3-C≡C-N
p2-CF_Three, R¹-Te2-C≡C-Np3-C≡C-Np3-CF_Three, R¹-Te2-C≡C-
Np3-C≡C-Np4-CF_Three,

R¹-Te1-C≡C-Np4-Ph1-CF_Three, R¹-Te1-C≡C-N
p4-Ph2-CF_Three, R¹-Te1-C≡C-Np4-Ph3-CF _Three, R¹-Te1-C≡C-N
p4-Np1-CF_Three, R¹-Te1-C≡C-Np4-Np2-CF_Three, R¹-Te1-C≡C-N
p4-Np3-CF_Three, R¹-Te1-C≡C-Np4-Np4-CF_Three, R¹-Te2-C≡C-N
p4-Ph1-CF_Three, R¹-Te2-C≡C-Np4-Ph2-CF_Three, R¹-Te2-C≡C-N
p4-Ph3-CF_Three, R¹-Te2-C≡C-Np4-Np1-CF_Three, R¹-Te2-C≡C-N
p4-Np2-CF_Three, R¹-Te2-C≡C-Np4-Np3-CF_Three, R¹-Te2-C≡C-N
p4-Np4-CF_Three, R¹-Te1-C≡C-Np4-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te1
-C≡C-Np4-CH_TwoCH_Two-Ph3-CF_Three, R¹-Te1-C≡C-Np4-CH _TwoCH_Two-N
p1-CF_Three, R¹-Te1-C≡C-Np4-CH_TwoCH_Two-Np2-CF_Three, R¹-Te1-C≡
C-Np4-CH_TwoCH_Two-Np3-CF_Three, R¹-Te1-C≡C-Np4-CH_TwoCH_Two-Np4-C
F_Three, R¹-Te2-C≡C-Np4-CH_TwoCH_Two-Ph1-CF_Three, R¹-Te2-C≡C-Np
4-CH_TwoCH_Two-Ph2-CF_Three, R¹-Te2-C≡C-Np4-CH_TwoCH_Two-Ph3-CF_Three,
R¹-Te2-C≡C-Np4-CH_TwoCH_Two-Np1-CF_Three, R¹-Te2-C≡C-Np4-CH
_TwoCH_Two-Np2-CF_Three, R¹-Te2-C≡C-Np4-CH _TwoCH_Two-Np3-CF_Three, R¹-T
e2-C≡C-Np4-CH_TwoCH_Two-Np4-CF_Three, R¹-Te1-C≡C-Np4-C≡C-P
h2-CF_Three, R¹-Te1-C≡C-Np4-C≡C-Ph3-CF_Three, R¹-Te1-C≡C-
Np4-C≡C-Np1-CF_Three, R¹-Te1-C≡C-Np4-C≡C-Np2-CF_Three, R¹
-Te1-C≡C-Np4-C≡C-Np3-CF_Three, R¹-Te1-C≡C-Np4-C≡C-N
p4-CF_Three, R¹-Te2-C≡C-Np4-C≡C-Ph1-CF_Three, R¹-Te2-C≡C-
Np4-C≡C-Ph2-CF_Three, R¹-Te2-C≡C-Np4-C≡C-Ph3-CF_Three, R¹
-Te2-C≡C-Np4-C≡C-Np1-CF_Three, R¹-Te2-C≡C-Np4-C≡C-N
p2-CF_Three, R¹-Te2-C≡C-Np4-C≡C-Np3-CF_Three, R¹-Te2-C≡C-
Np4-C≡C-Np4-CF_Three,

The compounds of the general formula (I) have m, n, R, V,
Depending on the selection of W, X, Y, Z, Q ¹ , Q ² , Q ³ , ring A, ring B and ring C, they can be produced by various synthetic methods. Representative examples thereof are shown below.

For example, m = n = 0, Y is a single bond, R may be substituted by 1 to 7 fluorine atoms or C 1 to C 7 alkoxyl groups, and may contain a branched chain. When Z is a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group or a hydrogen atom, it can be produced according to the following formula.

[0191]

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(Wherein V, Q ¹ , Q ² , Q ³ and ring C are represented by the general formula
Represents the same meaning as in (I), R ² may be substituted by 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms, and may have a saturated carbon number which may include a branched chain.
Represents an alkyl group of 1 to 20, Z ¹ is a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group,
Represents a difluoromethoxy group or a hydrogen atom, and Mtl ¹ is L
i represents a metal ion such as BrMg and IMg. That is, a ketone represented by the general formula (II-a)
The aryl lithium or magnesium reactant represented by II-a) is represented by the general formula (IV-a) by reacting in the presence or absence of a metal salt such as cerium chloride or manganese chloride or a Lewis acid. After obtaining an alcohol, the mixture is heated in the presence of an acid catalyst such as p-toluenesulfonic acid to obtain a dihydronaphthalene compound represented by the general formula (Va), which is converted to Pd-C, Rh-C, Pt By hydrogenation in the presence of a metal catalyst such as -C and Pd (OH) ₂ , the desired general formula (I
The compound represented by -a) can be obtained.

The aryl lithium or magnesium reactant represented by the general formula (III-a) used here is commonly used in the production of liquid crystals, and can be easily prepared from the corresponding halide.

The compound represented by the general formula (II-a) can be produced by several methods, and a typical method is represented by the general formula (VI-a) as shown in the following formula. After converting the phenylacetic acid derivative into an acid chloride, it is reacted with ethylene in the presence of aluminum chloride.

[0195]

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(In the formula, R ² , V, Q ¹ , Q ² and Q ³ are the same as described above.) When Q ¹ , Q ² and Q ³ are all hydrogen, the following formula is used. In addition, the compound represented by the general formula (II-a ′) is represented by the general formula (VI
It can be synthesized by hydrogenating the naphthol derivative represented by Ia) in the presence of a transition metal catalyst such as palladium, rhodium, platinum and ruthenium, and further oxidizing as necessary.

[0197]

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(In the formula, R ² and V are the same as described above.) Further, as shown in the following formula, an amine such as pyrrolidine is allowed to act on 1,4-cyclohexadione monoacetal, and methyl vinyl ketone is further reacted. the octahydronaphthalene dione mono acetal can be synthesized by reacting, of reacted with organometallic reagents represented by R ² -Mtl ^1, further obtaining octahydro naphthalate Lennon acetal by dehydration reaction. To this, use a metal catalyst such as palladium, rhodium, ruthenium, platinum as a dehydrogenation catalyst, or 2,3-dichloromethane.
The compound of the general formula (II- The compound represented by a '') can be synthesized.

[0199]

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(In the formula, R ² is the same as above.) M = n = 0, Y is —CH ₂ CH ₂ —, R is 1 to 7 fluorine atoms or alkoxyl having 1 to 7 carbon atoms. A saturated alkyl group having 1 to 20 carbon atoms which may be substituted by a group and may include a branched chain, wherein Z is a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group or a hydrogen atom; When it is an atom, it can be produced according to the following formula

[0201]

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(Wherein V, Q ¹ , Q ² , Q ³ and ring C represent a general formula
Represents the same meaning as in (I), R ² may be substituted by 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms, and may have a saturated carbon number which may include a branched chain.
Represents an alkyl group of 1 to 20, Z ¹ is a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group,
Represents a difluoromethoxy group or a hydrogen atom, and Mtl ¹ is L
i represents a metal ion such as BrMg and IMg. That is, a ketone represented by the general formula (II-a)
The aryl lithium or magnesium reactant represented by II-b) is represented by the general formula (IV-b) by reacting in the presence or absence of a metal salt such as cerium chloride or manganese chloride or a Lewis acid. After obtaining an alcohol, the mixture is heated in the presence of an acid catalyst such as p-toluenesulfonic acid to obtain a dihydronaphthalene compound represented by the general formula (Vb). By hydrogenation in the presence of a metal catalyst such as -C, Pd (OH) ₂ or the like, the desired general formula (I
The compound represented by -b) can be obtained.

The ethynyllithium or magnesium reactant represented by the general formula (III-b) used here is commonly used in the production of liquid crystals, and is prepared by reacting an alkyllithium or alkylmagnesium halide on a corresponding acetylene compound. Can be easily prepared.

When (III-c) and (III-d) are used instead of (III-a) and (III-b) in the above formula, they can be represented by the general formulas (Ic) and (Id). Compounds can be prepared.

[0205]

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(Where V, Q¹, Q^Two, Q^Three, Ring B and ring C are
Represents the same meaning as in general formula (I), R ^Two, Z¹And Mtl¹
Has the same meaning as above, and Y¹Is a single bond or -CH_TwoCH_Two-
Represent. ) In addition, as shown in the following formula, represented by the general formula (II-a)
Compounds such as ylide compounds represented by the general formula (VIII-a)
And the obtained olefin compound (IX-a) is hydrogenated.
By adding, the compound represented by the general formula (I-b)
Can be manufactured.

[0207]

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(Wherein V, Z, Q ¹ , Q ² , Q ³ and ring C have the same meanings as in formula (I), and R ² and Y ¹ have the same meanings as described above). Then, by using (VIII-b) instead of (VIII-a), the compound represented by the general formula (Id) can be produced.

[0209]

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(Wherein V, Z, Q ¹ , Q ² , Q ³ , ring B and ring C
Has the same meaning as in general formula (I), and R ² and Y ¹ have the same meaning as described above. As further shown in the following formula, by reacting the tetrahydronaphthalenone represented by (II-a) with an ylide compound represented by (VIII-c), and treating with an acid, the general formula (Xa) Can be obtained. To this (VIII-
By reacting the ylide compound represented by d) and hydrogenating the obtained olefin (XI-a), a compound represented by the general formula (Ib)
Can be produced.

[0211]

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(In the formula, V, Z, Q ¹ , Q ² , Q ³ and ring C have the same meanings as in the general formula (I), and R ² and Y ¹ have the same meanings as described above.) Then, by using (VIII-e) instead of (VIII-d), a compound represented by the general formula (Id) can be produced.

[0213]

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(Wherein V, Z, Q ¹ , Q ² , Q ³ , ring B and ring C
Has the same meaning as in general formula (I), and R ² and Y ¹ have the same meaning as described above. In the above method, when (II-b) is used instead of (II-a), the compound represented by the general formula (XII-a) can be produced.

[0215]

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(Wherein n, Q¹, Q^Two, Q^Three, Ring B and ring C are
Represents the same meaning as in general formula (I), R ^Two, Z¹, Y¹Is above
Has the same meaning as X¹Is a single bond or -CH_TwoCH_Two-The table
You. ) By substituting bromine of this compound (XII-a),
Many of the compounds can be made. For example, (XII
The acetylene compound represented by I-a) is converted to PdCl_Two(PPh_Three)_TwoAnd Pd
(PPh_Three) _FourSuch as palladium catalyst and triethylamine
When reacted with (XII-a) in the presence of an amine of the general formula (I-e)
Can be obtained. In addition, metal touch
Hydrogenation in the presence of a medium to form an acetylenediyl group (-C≡C-)
Ethylene group (-CH_TwoCH_TwoYou can also convert to-).

[0219]

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(Wherein n, Q¹, Q^Two, Q^Three, Ring B and ring C are
Represents the same meaning as in general formula (I), Z ¹, Y¹And X¹Is
Represents the same meaning as above, R^TwoR is from 1 to 7 fluorine atoms
Or substituted by an alkoxyl group having 1 to 7 carbon atoms.
Saturated or unsaturated, which may be branched or branched
Represents an alkyl group having 1 to 18 carbon atoms. Further, by replacing (XIII-a) with (XIII-b), the general formula (I
The compound represented by -f) can be obtained. And this
In the presence of a metal catalyst to give an acetylenediyl group (-
C≡C-) with an ethylene group (-CH_TwoCH_TwoCan also be converted to-)
You.

[0219]

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(Wherein R, V, n, Q ¹ , Q ² , Q ³ , ring A, ring B and ring C have the same meanings as in formula (I), and Z ¹ , Y ¹
And X ¹ have the same meaning as described above. ) In addition, in the presence of a nickel or palladium catalyst, the organolithium or organomagnesium reagent represented by R-Mtl ¹ is converted to (XII-a)
To produce a compound represented by the general formula (Ig).

[0221]

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Wherein R, n, Q ¹ , Q ² , Q ³ , ring B and ring C
Has the same meaning as in the general formula (I), and Z ¹ , Y ¹ , X ¹ and Mtl ¹ have the same meanings as described above. ) In addition, in the presence of a nickel or palladium catalyst, the organolithium or organomagnesium reagent represented by (XIV-a) is converted to (XII-
a) or after converting the organolithium or organomagnesium reactant represented by (XIV-a) to boron, tin, silicon compounds, in the presence of a nickel or palladium catalyst, to (XII-a) General formula by reacting
The compound represented by (Ih) can be produced.

[0223]

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Wherein R, n, Q ¹ , Q ² , Q ³ , ring B and ring C
Has the same meaning as in general formula (I), Z ¹ , Y ¹ , X ¹ and Mtl ¹ have the same meaning as described above, V ¹ represents a single bond or an oxygen atom, and ring A ¹ represents one or two Represents a 1,4-phenylene group which may be substituted with two fluorine atoms or a naphthalene-2,6-diyl group which may be substituted with two fluorine atoms. (XII-a) is reacted with magnesium, lithium, alkyl lithium, etc., and converted to (XV-a), and then reacted with a halide represented by (XVI-a) in the presence of nickel or a palladium catalyst. Or by converting (XIV-a) into boron, tin, and a silicon compound, and then reacting with a halide represented by (XVI-a) in the presence of a nickel or palladium catalyst to obtain a compound represented by the general formula (Ii). Can be produced.

[0225]

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(Wherein, R, V, n, Q ¹ , Q ² , Q ³ , ring B and ring C have the same meanings as in formula (I), and Z ¹ , Y ¹ , X ¹
And Mtl ¹ represent the same meaning as described above, and the ring A ² is a 1,4-phenylene group which may be substituted with one or two fluorine atoms, a pyridine-2,5-diyl group, a pyrimidine-2,5- A diyl group, a pyrazine-2,5-diyl group, a pyridazine-3,6-diyl group and a naphthalene-2,6-diyl group which may be substituted with one or two fluorine atoms, wherein Hal is a chlorine atom, Represents a bromine or iodine atom. The compound represented by (XV-a) is reacted with the cyclohexane derivative represented by (XVII-a) to give an alcohol (X
VII-a). This is dehydrated by heating in the presence of an acid catalyst to give compound (XVIII-a). Further, the compound represented by (Ij) can be obtained by hydrogenation in the presence of a transition metal catalyst.

[0227]

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Wherein V, n, Q ¹ , Q ² , Q ³ , ring B and ring C
Has the same meaning as in general formula (I), and R ² , Z ¹ , Y ¹ , X
¹ and Mtl ¹ represent the same meaning as described above. In the above method, when (II-c) is used instead of (II-a), the compound represented by the general formula (Ik) can be produced.

[0229]

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(Wherein n, Q¹, Q^Two, Q^Three, Ring B and ring C are
Represents the same meaning as in general formula (I), R ^Two, Z¹, X¹, Y¹Is
Represents the same meaning as above. ) (I-k), hydrobromic acid, boron tribromide
Demethylation by the action of aluminum or aluminum chloride
And (XIX-a)

[0231]

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(Wherein n, Q¹, Q^Two, Q^Three, Ring B and ring C are
Represents the same meaning as in general formula (I), Z ¹, X¹, Y¹Is above
Has the same meaning as ) Is obtained. This is represented by the general formula (XX-
a) and (XX-b)

[0233]

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(Wherein R, V and ring A have the same meanings as in formula (I)), or are reacted with a dehydrating condensing agent such as dicyclohexylcarbodiimide, or (XX-a ) And (XX-b) are converted to acid halides using thionyl chloride or the like, and then reacted in the presence of an amine to obtain the compounds represented by the general formulas (Il) and (Im).

[0235]

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(Wherein R, n, Q ¹ , Q ² , Q ³ , ring A, ring B and ring C have the same meanings as in formula (I), and Z ¹ , X ¹ ,
Y ¹ has the same meaning as described above. ) Can be obtained.

(XIX-a) is represented by the general formulas (XXI-a) and (XXI-b)

[0238]

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(In the formula, R, V and ring A have the same meanings as in the general formula (I), and R ³ represents 1 to 7 fluorine atoms or carbon atoms unless the 1,2-position is unsaturated. A saturated or unsaturated alkyl group having 1 to 20 carbon atoms which may be substituted by an alkoxyl group having 1 to 7 atoms and which may contain a branched chain), and sodium hydride And in the presence of a base such as sodium hydroxide, the general formulas (In) and (Io)

[0240]

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(In the formula, R, n, Q ¹ , Q ² , Q ³ , ring A, ring B and ring C have the same meanings as in formula (I), and R ³ , Z ¹ ,
X ¹ and Y ¹ represent the same meaning as described above. ) Can be obtained.

Further, the compound of the general formula (XXII-a) obtained by reacting (XIX-a) with trifluoromethanesulfonic acid chloride or anhydride in the presence of a base

[0243]

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(Wherein n, Q¹, Q^Two, Q^Three, Ring B and ring C are
Represents the same meaning as in general formula (I), Z ¹, X¹, Y¹Is above
Has the same meaning as ) Represented by (XIII-a),
(XIII-b), R-Mtl¹And the same conditions as (XIV-a) and (XII-a)
(I-e), (I-f), (I-g) and (I-h)
Obtainable.

As shown in the following formula, an octahydronaphthalenone derivative which can be synthesized by reacting an amine such as pyrrolidine with the cyclohexanone derivative represented by the general formula (XXIII-a) and further reacting with methyl vinyl ketone has R ² -Mtl ¹
An octahydronaphthalenone derivative is obtained by the action of an organometallic reactant represented by
To this, palladium as a dehydrogenation catalyst, rhodium, ruthenium, using a metal catalyst such as platinum, or by allowing an oxidizing agent such as 2,3-dichloro-5,6-dicyano-1,4-benzoquinone to act, or The compound represented by the general formula (Ip) can be synthesized by aromatization using sulfur, bromine, iodine, or the like.

[0246]

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(In the formula, n, X, Y, Z, ring B and ring C have the same meanings as in formula (I), and R ² and Mtl ¹ have the same meanings as described above.) The cyclohexanone derivative represented by the general formula (XXIII-a) is commonly used in the production of liquid crystals, and is easily available.

Further, instead of R ² -Mtl ¹ , (XIV-a), (XIV-a)
-b) and (XIV-c)

[0249]

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(Wherein R has the same meaning as in general formula (I), and V ¹ , ring A ¹ and Mtl ¹ have the same meanings as described above).

[0251]

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(Wherein R, n, X, Y, Z, ring B and ring C are
Represents the same meaning as in general formula (I), ¹, R^TwoAnd ring A¹
Has the same meaning as above, and W¹Is a single bond, -C≡C- or
Is -CH_TwoCH_Two-Represents ) Can be manufactured.

In the compound represented by formula (I), Z is a chlorine atom (Ir)

[0254]

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(Where m, n, R, V, W, X, Y, Q ¹ , Q ² , Q
³ , ring A, ring B and ring C have the same meanings as in formula (I). ) With copper cyanide, the general formula (Is)

[0256]

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(Where m, n, R, V, W, X, Y, Q ¹ , Q ² , Q
³ , ring A, ring B and ring C have the same meanings as in formula (I). ) Can be obtained.

Representative examples of the compound represented by the general formula (I) thus produced are shown below.

[0259]

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The present invention also provides a liquid crystal composition containing at least one compound represented by the general formula (I) as a component.

At least one of the compounds represented by the general formula (I)
In the liquid crystal composition containing the type as a component, any compound other than the compound represented by the general formula (I) may be included as long as the composition exhibits liquid crystallinity. As the first component, at least one compound represented by the general formula (I) is contained, and as the other components, it is particularly preferable to contain at least one of the following second to fourth components.

That is, the second component is a so-called fluorine-based (halogen-based) p-type liquid crystal compound and has the following general formula (A1)
It consists of the compound represented by (A3).

[0263]

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[0264] In the formula, Alk ^a represents an alkyl group having 1 to 12 carbon atoms, which may have a methyl or ethyl branches may be linear, of 3-6 membered cyclic May have a structure, and any -CH _2- present in the group is -O-, -C
H = CH-, -CH = CF-, -CF = CH-, -CF = CF- or -C≡C- may be exchanged, and any hydrogen atom present in the group may be a fluorine atom or a tri atom. Although it may be substituted by a fluoromethoxy group, a linear alkyl group having 2 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms, a linear chain having 4 to 7 carbon atoms 3-alkenyl group, terminal has 1-3 carbon atoms
Is preferably an alkyl group having 1 to 5 carbon atoms substituted by an alkoxyl group. When an asymmetric carbon is generated by branching, the compound may be optically active or racemic.

Ring Fa, ring Fb and ring Fc are each independently substituted by trans-1,4-cyclohexylene group, transdecahydronaphthalene-trans-2,6-diyl group and one or more fluorine atoms. 1,4-phenylene group,
A naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, a tetrahydronaphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, substituted by a fluorine atom 1,4-cyclohexenylene, 1,3-dioxane-trans-2,5-diyl, pyrimidine-2,5-diyl or pyridine-2,5-diyl which may be -1,4-cyclohexylene group, transdecahydronaphthalene-trans-2,6-diyl group,
Naphthalene-2,6 which may be substituted by a fluorine atom
-Diyl groups or 1,4-phenylene groups which may be substituted by one or two fluorine atoms are preferred. Particularly when the ring Fb is a trans-1,4-cyclohexylene group or a transdecahydronaphthalene-trans-2,6-diyl group,
Ring Fa is preferably a trans-1,4-cyclohexylene group, a ring Fb when the ring Fc is a trans-1,4-cyclohexylene group or a transdecahydronaphthalene-trans-2,6-diyl group And ring Fa is preferably a trans-1,4-cyclohexylene group. In (A3), the ring Fa is preferably a trans-1,4-cyclohexylene group. L ^a , L ^b and L ^c are linking groups, each independently being a single bond, an ethylene group (-CH ₂ CH _2- ), a 1,2-propylene group (-CH (CH ₃ ) CH ₂ -and -CH ₂ CH (CH ₃ )-), 1,4-butylene group, -COO-, -OCO-, -OCF _2- , -CF ₂ O-, -CH = CH-, -CH
= CF-, -CF = CH-, -CF = CF-, -C≡C- or -CH = NN = CH-, but a single bond, an ethylene group, a 1,4-butylene group, -COO
-, -OCF _2- , -CF ₂ O-, -CF = CF- or -C≡C- are preferred,
A single bond or an ethylene group is particularly preferred. In (A2), at least one of them preferably represents a single bond in (A3).

The ring Fz is an aromatic ring represented by the following general formulas (Ga) to (G
It can be represented by c).

[0267]

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[0268] In the formula, it represents a J ^a through J ^j each independently a hydrogen atom or fluorine atom, in (Ga), J ^a and
At least one of J ^b is preferably a fluorine atom, in (Gb), it is preferable that at least one of J ^d through J ^f is a fluorine atom, and more preferably, especially J ^d is a fluorine atom .

[0269] end group P ^a represents a fluorine atom, a chlorine atom, trifluoromethoxy group, difluoromethoxy group, trifluoromethyl group or difluoromethyl group or 2 or more carbon atoms substituted by fluorine atoms 2 or 3 of alkoxylation Represents a group, an alkyl group, an alkenyl group or an alkenyloxy group, preferably a fluorine atom, a trifluoromethoxy group or a difluoromethoxy group, particularly preferably a fluorine atom.

In the compounds (A1) to (A3), the compound of the general formula (I) of the present invention is excluded.

The third component is a so-called cyano-based p-type liquid crystal compound, which is a compound represented by the following general formulas (B1) to (B3).

[0272]

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[0273] In the above formula, Alk ^b represents an alkyl group having 1 to 12 carbon atoms, which may have a methyl or ethyl branches may be linear, of 3-6 membered cyclic May have a structure, and any -CH _2- present in the group is -O-, -C
H = CH-, -CH = CF-, -CF = CH-, -CF = CF- or -C≡C- may be exchanged, and any hydrogen atom present in the group may be a fluorine atom or a tri atom. Although it may be substituted by a fluoromethoxy group, a linear alkyl group having 2 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms, a linear chain having 4 to 7 carbon atoms 3-alkenyl group, terminal has 1-3 carbon atoms
Is preferably an alkyl group having 1 to 5 carbon atoms substituted by an alkoxyl group. When an asymmetric carbon is generated by branching, the compound may be optically active or racemic.

Ring Fd, ring Fe and ring Ff are each independently substituted by trans-1,4-cyclohexylene group, transdecahydronaphthalene-trans-2,6-diyl group, and one or more fluorine atoms. 1,4-phenylene group,
A naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, a tetrahydronaphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, substituted by a fluorine atom 1,4-cyclohexenylene, 1,3-dioxane-trans-2,5-diyl, pyrimidine-2,5-diyl or pyridine-2,5-diyl which may be -1,4-cyclohexylene group, transdecahydronaphthalene-trans-2,6-diyl group,
Naphthalene-2,6 which may be substituted by a fluorine atom
-Diyl groups or 1,4-phenylene groups which may be substituted by one or two fluorine atoms are preferred. Particularly when the ring Fe is a trans-1,4-cyclohexylene group or a transdecahydronaphthalene-trans-2,6-diyl group,
Ring Fd is preferably a trans-1,4-cyclohexylene group, and when the ring Ff is a trans-1,4-cyclohexylene group or a transdecahydronaphthalene-trans-2,6-diyl group, the ring Fd And ring Fe is preferably a trans-1,4-cyclohexylene group. In (B3), the ring Fd is preferably a trans-1,4-cyclohexylene group.

L^d, L^eAnd L^fIs a linking group,
Independently a single bond, an ethylene group (-CH _TwoCH_Two-), 1,2-Propylene
Len group (-CH (CH_Three) CH_Two-And-CH_TwoCH (CH_Three)-), 1,4-butyl
Group, -COO-, -OCO-, -OCF_Two-, -CF_TwoO-, -CH = CH-, -CH = C
F-, -CF = CH-, -CF = CF-, -C≡C-, -OCH_Two-, -CH_TwoO-, again
Represents -CH = N-N = CH-, but a single bond, an ethylene group, -COO-,
-OCF_Two-, -CF_TwoO-, -CF = CF- or -C≡C- is preferable, and
A bond, an ethylene group or -COO- is particularly preferred. Also,
At least one of them in (B2), and in (B3)
Preferably, at least two of them represent a single bond.

The ring Fy is an aromatic ring and has the following general formula (Gd) to (G
f).

[0277]

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[0278] In the formula, J ^k through J ^q are each independently represent a hydrogen atom or a fluorine atom, in (Ge), J ⁿ and
J ^o is preferably a hydrogen atom. The terminal group Pa represents ^a cyano group (—CN), a cyanato group (—OCN) or —C≡CCN, and a cyano group is preferable.

The compounds of the general formula (I) of the present invention are excluded from (B1) to (B3).

The fourth component is a so-called n-type liquid crystal having a dielectric anisotropy of about 0 or less.
It consists of the compounds represented by (C1) to (C3).

[0281]

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In the above formula, Alk ^c and Alk ^d each independently represent an alkyl group having 1 to 12 carbon atoms, which may be linear or have a methyl or ethyl branch, may have a cyclic structure having 3 to 6-membered ring, any -CH ₂ present in the group - is -O -, - CH = CH - , - CH = CF -, - CF = CH
-, -CF = CF- or -C≡C- may be exchanged,
Any hydrogen atom present in the group may be substituted by a fluorine atom or a trifluoromethoxy group, but may be a linear alkyl group having 1 to 7 carbon atoms, a linear alkyl group having 2 to 7 carbon atoms. -An alkenyl group, a linear 3-alkenyl group having 4 to 7 carbon atoms, a linear alkoxyl group having 1 to 3 carbon atoms or a carbon atom having a terminal substituted by an alkoxyl group having 1 to 3 carbon atoms A linear alkyl group having 1 to 5 is preferable, and at least one is a linear alkyl group having 1 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms or 4 to 7 carbon atoms. Particularly preferred is a linear 3-alkenyl group of

Ring Fg, ring Fh, ring Fi and ring Fj each independently represent a trans-1,4-cyclohexylene group, a transdecahydronaphthalene-trans-2,6-diyl group, 1-2 fluorine atoms 1,4-phenylene group which may be substituted by an atom or a methyl group, naphthalene-2,6-diyl group which may be substituted by one or more fluorine atoms, which is substituted by 1 to 2 fluorine atoms Optionally tetrahydronaphthalene-2,6-diyl group, 1,4-cyclohexenylene group optionally substituted by 1 to 2 fluorine atoms, 1,3-
Dioxane-trans-2,5-diyl group, pyrimidine-2,5-
Represents a diyl group or a pyridine-2,5-diyl group, but in each compound, transdecahydronaphthalene-trans-2,6-diyl group, naphthalene-2, which may be substituted with one or more fluorine atoms, 6-diyl group, tetrahydronaphthalene-2,6-diyl group optionally substituted by 1 to 2 fluorine atoms, 1,4-cyclohexenylene group optionally substituted by fluorine atom, 1,3 -Dioxane-trans-2,5-diyl group, pyrimidine-2,5-diyl group or pyridine-2,5-diyl group is preferably one or less, and the other ring is trans-1,4-cyclohexyl. It is preferably a silene group or a 1,4-phenylene group which may be substituted by one or two fluorine atoms or methyl groups.

L^g, L^hAnd LⁱIs a linking group,
Independently a single bond, an ethylene group (-CH _TwoCH_Two-), 1,2-Propylene
Len group (-CH (CH_Three) CH_Two-And-CH_TwoCH (CH_Three)-), 1,4-butyl
Group, -COO-, -OCO-, -OCF_Two-, -CF_TwoO-, -CH = CH-, -CH = C
F-, -CF = CH-, -CF = CF-, -C≡C- or -CH = N-N = CH-
However, single bond, ethylene group, 1,4-butylene group, -COO-,-
OCO-, -OCF_Two-, -CF_TwoO-, -CF = CF-, -C≡C- or -CH = N-N
= CH- is preferable, and in (C2), at least one of
However, in (C3), at least two of them represent a single bond
Is preferred.

The more preferable form of (C1) can be represented by the following formulas (C1a) to (C1h).

[0286]

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[0287] In the above formulas, a linear alkyl group of Alk ^e and Alk ^f each independently from 1 to 7 carbon atoms, carbon atoms
2-7 linear 1-alkenyl group, 4-7 carbon atoms linear
A 3-alkenyl group, a linear alkoxyl group having 1 to 3 carbon atoms or a linear alkyl group having 1 to 5 carbon atoms substituted at the terminal with an alkoxyl group having 1 to 3 carbon atoms, One represents a linear alkyl group having 1 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms or a linear 3-alkenyl group having 4 to 7 carbon atoms. However, the ring
If Fg1~ ring Fg3 are aromatic rings, the corresponding Alk ^e except the 1-alkenyl group and an alkoxyl group, when the ring Fh1~ ring Fh3 the aromatic ring, the corresponding Alk ^f excludes 1-alkenyl groups and alkoxyl groups .

Ring Fg1 and ring Fh1 are each independently substituted by trans-1,4-cyclohexylene group, transdecahydronaphthalene-trans-2,6-diyl group, 1-2 fluorine atoms or methyl groups. 1,4-phenylene group which may be substituted, naphthalene-2,6-diyl group which may be substituted by one or more fluorine atoms, tetrahydronaphthalene which may be substituted by one or two fluorine atoms
2,6-diyl group, 1,4-cyclohexenylene group optionally substituted by 1 to 2 fluorine atoms, 1,3-dioxane-
Represents a trans-2,5-diyl group, a pyrimidine-2,5-diyl group or a pyridine-2,5-diyl group.In each compound, a trans-decahydronaphthalene-trans-2,6-diyl group, one Naphthalene-2,6-diyl group which may be substituted by the above fluorine atoms, tetrahydronaphthalene-2,6- which may be substituted by 1 to 2 fluorine atoms
1,4-diyl group which may be substituted by a fluorine atom
Cyclohexenylene group, 1,3-dioxane-trans-2,5-
Diyl group, pyrimidine-2,5-diyl group or pyridine-2,
It is preferable that the number of 5-diyl groups is one or less, in which case the other ring may be substituted with a trans-1,4-cyclohexylene group or one or two fluorine atoms or methyl groups, 4-phenylene group. Ring Fg2 and Ring Fh2
Are each independently a trans-1,4-cyclohexylene group, a transdecahydronaphthalene-trans-2,6-diyl group, and may be substituted with 1 to 2 fluorine atoms or 1,4- A phenylene group, a naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, a tetrahydronaphthalene-2,6-diyl group optionally substituted by one or two fluorine atoms Is, in each compound, a transdecahydronaphthalene-trans-2,6-diyl group, a naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, The number of the optionally substituted tetrahydronaphthalene-2,6-diyl group is preferably one or less, in which case the other ring is a trans-1,4-cyclohexylene group or one to two fluorine atoms or By methyl group Optionally substituted 1,4-phenylene group. Ring Fg3 and ring Fh3 are each independently a 1,4-phenylene group which may be substituted by 1 to 2 fluorine atoms or methyl groups, a naphthalene-2 which may be substituted by one or more fluorine atoms. , 6-diyl group, represents a tetrahydronaphthalene-2,6-diyl group which may be substituted by 1 to 2 fluorine atoms, but in each compound, naphthalene which may be substituted by 1 or more fluorine atoms It is preferable that the number of -2,6-diyl groups and the number of tetrahydronaphthalene-2,6-diyl groups which may be substituted by one or two fluorine atoms is one or less.

A more preferred embodiment of (C2) can be represented by the following formulas (C2a) to (C2m).

[0290]

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In the above formula, ring Fg1, ring Fg2, ring Fg3, ring Fh1, ring
Fh2 and ring Fh3 represent the above-mentioned meaning, ring Fi1 is ring Fg1,
Ring Fi2 has the same meaning as ring Fg2, and ring Fi3 has the same meaning as ring Fg3. In each of the above compounds, transdecahydronaphthalene-trans-2,6-diyl group, naphthalene-2,6-diyl group optionally substituted with one or more fluorine atoms, 1-2 fluorine atoms A tetrahydronaphthalene-2,6-diyl group which may be substituted by a 1,4-cyclohexenylene group which may be substituted by a fluorine atom,
1,3-dioxane-trans-2,5-diyl group, pyrimidine-
It is preferred that the number of 2,5-diyl groups or pyridine-2,5-diyl groups is one or less, in which case the other ring is trans-
A 1,4-cyclohexylene group or a 1,4-phenylene group which may be substituted by one or two fluorine atoms or methyl groups.

Next, more preferred embodiments of (C3) can be represented by the following general formulas (C3a) to (C3f).

[0293]

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In the above formula, ring Fg1, ring Fg2, ring Fh1, ring Fh2, ring
Fi1 and ring Fi2 represent the same meaning as described above, ring Fj1 represents the same meaning as ring Fg1 and ring Fj2 represents the same meaning as ring Fg2. In each of the above compounds, transdecahydronaphthalene-trans-2,6-diyl group, naphthalene-2,6-diyl group optionally substituted with one or more fluorine atoms, 1-2 fluorine atoms Tetrahydronaphthalene-2,6-diyl group optionally substituted by 1,4-cyclohexenylene group optionally substituted by fluorine atom, 1,3-dioxane-
The trans-2,5-diyl group, pyrimidine-2,5-diyl group or pyridine-2,5-diyl group is preferably one or less, in which case the other ring is trans-1,4-cyclohexyl. It is a 1,4-phenylene group which may be substituted by a silene group or one or two fluorine atoms or a methyl group.

A liquid crystal composition having a maximum temperature of a nematic phase of 117 ° C. was actually prepared using the above compound, and the liquid crystal composition (I-2) was prepared.
When the compound represented by the formula (1) was added in an amount of 20% by weight, the maximum temperature of the nematic phase was 74 ° C., and no precipitation occurred even after storage at 0 ° C. for 1 week. As a compound having a similar structure, the maximum temperature of the nematic phase when trans-4-propyl- (3,4,5-trifluorophenyl) cyclohexane is added is 70.
It is found that the compound represented by the formula (I-2) has excellent solubility in the host liquid crystal composition and can exhibit a liquid crystal phase in an extremely wide temperature range.

Further, when the voltage holding ratio of this composition was measured, it showed a sufficiently high value at the time of preparation, after heating and after irradiation with ultraviolet rays, similarly to the host liquid crystal composition.

As described above, the compound of the present invention has excellent liquid crystallinity and excellent compatibility with currently used liquid crystal compounds and liquid crystal compositions. In addition, it can be seen that the compound has an effect superior to conventional compounds in preparing a liquid crystal composition having a wide temperature range showing a liquid crystal phase, a low threshold voltage, and a high-speed response.

Therefore, the compound of the general formula (I) can be used as a mixture with another nematic liquid crystal compound in a TN or ST mode.
It can be suitably used as a liquid crystal material having a wide temperature range and capable of being driven at a low voltage, particularly for an N-type or other field effect display cell. Further, among the compounds of (I), those which do not contain a cyano group or an ester bond can easily obtain a large specific resistance and a high voltage holding ratio, and can be used as a component of an active matrix driving liquid crystal material. It is possible. Furthermore, it is expected that ferroelectric liquid crystals and antiferroelectric liquid crystals are not limited to nematic liquid crystals but can be used as low viscosity agents indispensable for realizing high-speed response.

[0299]

EXAMPLES Hereinafter, the tetrahydronaphthalene derivative of the present invention and its production method, and the advantages of the liquid crystal composition obtained by using the tetrahydronaphthalene derivative of the present invention as a component will be described in more detail with specific examples. The gist and scope of the invention are not limited by these examples.

Example 1 6-propyl-2- (3,4,5-trifluorophenyl) -1,2,3,4-tetrahydronaphthalene (I-2)
Synthesis of

[0301]

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To magnesium (4.0 g) was added 3,4,5-trifluorobromobenzene (30 g) in tetrahydrofuran (100 m
l) The solution was added dropwise to prepare a Grignard reagent. Toluene (150 ml) was added thereto, and the solvent was evaporated at room temperature under reduced pressure.
100 ml were distilled off. Heat this to 60 ° C and add 6-propyl-
A solution of 1,2,3,4-tetrahydronaphthalen-2-one (25 g) in toluene (50 ml) was added dropwise over 20 minutes. After stirring for another 30 minutes, the temperature was returned to room temperature, and the reaction solution was poured into 10% hydrochloric acid. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane: ethyl acetate = 6: 1) to give 2-hydroxy-6-propyl-2- (3,4,5-trifluorophenyl) -1,
2,3,4-tetrahydronaphthalene (29 g) was obtained. To this, toluene (100 ml) and p-toluenesulfonic acid (3 g) were added, and 1
The mixture was heated and stirred for an hour. After cooling, the reaction solution was concentrated, and the residue was purified by silica gel column chromatography (hexane) to give 6-propyl-2- (3,4,5-trifluorophenyl) -3,4-
Dihydronaphthalene (26 g) was obtained. To this, ethanol
(50 ml), ethyl acetate (50 ml) and 5% palladium-carbon (3 g)
Was added and stirred at room temperature for 2 hours under a hydrogen atmosphere. The reaction solution was filtered through Celite, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (hexane) to obtain 6-propyl-2- (3,4,5-trifluorophenyl) -1,2,3,4-tetrahydronaphthalene (26 g). This compound is 99% pure by gas chromatography and, by mass spectrometry,
The molecular weight was 304.

Example 2 2- (3,4-difluorophenyl) -6-
Synthesis of propyl-1,2,3,4-tetrahydronaphthalene (I-1) Under the same conditions as in Example 1, using 3,4-difluorobromobenzene instead of 3,4,5-trifluorobromobenzene To give 2- (3,4-difluorophenyl) -6-propyl-1,2,3,4-
Tetrahydronaphthalene was synthesized. 99% purity, molecular weight 2
86.

Example 3 6-propyl-2- (4-trifluoromethoxyphenyl) -1,2,3,4-tetrahydronaphthalene (I
Synthesis of -3) Under the same conditions as in Example 1, using 4-trifluoromethoxybromobenzene instead of 3,4,5-trifluorobromobenzene, 6-propyl-2- (4-trifluoromethoxy Phenyl) -1,2,3,4-tetrahydronaphthalene was synthesized.
Purity 99%, molecular weight 334.

Example 4 2- (3,4-difluorophenyl) -6
Synthesis of-(trans-4-propylcyclohexyl) -1,2,3,4-tetrahydronaphthalene (I-4)

[0306]

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A solution of 3,4-difluorobromobenzene (25 g) in tetrahydrofuran (100 ml) was added dropwise to magnesium (3.5 g) to prepare a Grignard reagent. This was filtered through a glass filter, toluene (150 ml) was added to the filtrate, and about 100 ml of the solvent was distilled off at room temperature under reduced pressure. This was heated to 60 ° C., and a solution of 6-bromo-1,2,3,4-tetrahydronaphthalen-2-one (27 g) in toluene (50 ml) was added dropwise over 20 minutes. After stirring for another 30 minutes, the temperature was returned to room temperature, and the reaction solution was poured into 10% hydrochloric acid. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated. The residue was subjected to silica gel column chromatography (hexane: ethyl acetate =
6: 1), 6-bromo-2- (3,4-difluorophenyl)
2-hydroxy-1,2,3,4-tetrahydronaphthalene (29 g)
I got Toluene (100 ml) and p-toluenesulfonic acid (3 g) were added thereto, and the mixture was stirred with heating for 1 hour. After cooling the reaction solution,
Concentrate and concentrate the residue on silica gel column chromatography.
(Hexane) to give 6-bromo-2- (3,4-difluorophenyl) -3,4-dihydronaphthalene (26 g). to this,
Ethanol (50 ml), ethyl acetate (50 ml) and 5% rhodium-
Carbon (3 g) was added, and the mixture was stirred at room temperature under a hydrogen atmosphere for 2 hours. The reaction solution was filtered through Celite, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (hexane) to give 6-bromo-2- (3,4-difluorophenyl) -1,2,3,4-
Tetrahydronaphthalene (26 g) was obtained. magnesium
(2.3 g), 6-bromo-2- (3,4-difluorophenyl) -1,
A solution of 2,3,4-tetrahydronaphthalene (26 g) in tetrahydrofuran (70 ml) was added dropwise to prepare a Grignard reagent. To this was added dropwise a solution of 4-propylcyclohexanone (13.5 g) in tetrahydrofuran (30 ml). After stirring for another 30 minutes, the reaction solution was poured into 10% hydrochloric acid. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated.
The residue was purified by silica gel column chromatography (hexane: ethyl acetate = 6: 1) to give 2- (3,4-difluorophenyl) -2-hydroxy-6- (trans-4-propylcyclohexyl) -1,2, 3,4-Tetrahydronaphthalene (23 g) was obtained. To this, toluene (80 ml) and p-toluenesulfonic acid (2
g) was added and the mixture was stirred with heating for 1 hour. After cooling, the reaction mixture was concentrated, and the residue was purified by silica gel column chromatography (hexane) to give 2- (3,4-difluorophenyl) -6- (trans-4-propylcyclohexyl) -3,4-dihydronaphthalene. (26 g) was obtained. Ethanol (30 ml), ethyl acetate (50 ml) and 5% palladium-carbon (2 g) were added thereto, and the mixture was stirred under a hydrogen atmosphere at room temperature for 2 hours. The reaction solution was filtered through Celite, and the filtrate was concentrated. Dimethylformamide in the residue
(50 ml) and potassium t-butoxide (5.5 g).
Stirred for hours. 10% hydrochloric acid was added to the reaction solution, and the mixture was extracted with toluene. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane) and further recrystallized from ethanol to give 2- (3,4-difluorophenyl) -6- (trans-4-
(Propylcyclohexyl) -1,2,3,4-tetrahydronaphthalene (20 g) was obtained. This compound had a purity of 99.8% by gas chromatography and a molecular weight of 368 by mass spectrometry.

Example 5 2- (3,4-difluorophenyl) -6
Synthesis of-(4-propylphenyl) -1,2,3,4-tetrahydronaphthalene (I-5)

[0309]

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A Grignard reagent prepared from 4-propylbromobenzene and magnesium was reacted with trimethylboric acid, and then hydrolyzed with dilute hydrochloric acid to obtain 4-propylphenylboric acid (4.5 g). 6-bromo-2- (3,4-difluorophenyl) -1,2,
3,4-tetrahydronaphthalene (5.0 g), tetrakis (triphenylphosphine) palladium (0) (0.3 g) and potassium phosphate (3.0 g) in dimethylformamide (30 ml),
Stirred at 80 ° C. for 8 hours. After cooling the reaction to room temperature,
Water was added and extracted with toluene. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane) and further recrystallized from ethanol to give 2- (3,4-difluorophenyl) -6- (4-propylphenyl) -1,2,3,4-tetrahydronaphthalene (4 g) was obtained. This compound had a purity of 99.7% by gas chromatography and a molecular weight of 362 by mass spectrometry.

Example 6 Preparation of Liquid Crystal Composition A general-purpose host liquid crystal (H) having a wide temperature range, low viscosity and usable for active matrix driving was prepared. This (H)
Shows a nematic phase at 116.7 ° C or less, and its melting point is 11 ° C.
It is. The measured values of the physical properties of this composition and the threshold voltage (Vth) at 20 ° C. of the TN cell (cell thickness 4.5 μm) prepared using the composition were as follows.

Nematic phase upper limit temperature (T _NI ) 116.7 ° C. Dielectric anisotropy (Δε) 4.80 Threshold voltage (Vth) 1.88 V Response time (τ) 21.5 msec Next, 80% of this host liquid crystal (H) was used. When a liquid crystal composition (M-1) comprising 20% of the compound (I-2) of the present invention obtained in Example 1 was prepared, the maximum liquid crystal phase temperature (T _NI ) was 74 ° C. After leaving this (M-1) at 150 ° C. for 20 hours, its _TNI was measured. As a result, no change was observed from that before heating. Although the ultraviolet irradiation for 20 hours, changes in T _NI was observed. Next, when the voltage holding ratio of this composition was measured, it showed a sufficiently high value at the time of preparation, after heating and after irradiation with ultraviolet light, similarly to the host liquid crystal (H).

Next, a liquid crystal device was prepared by filling (M-1) into a TN cell having a cell thickness of 4.5 μm, and its electro-optical characteristics were measured. The results were as follows.

Nematic phase upper limit temperature (T _NI ) 74.0 ° C. Dielectric anisotropy (Δε) 5.50 Threshold voltage (Vth) 1.55 V Response time (τ) 30.5 ms Therefore, 20% of (I-2) is added. As a result, the threshold voltage (Vth) could be reduced by 0.33 V while the drop of the maximum temperature of the nematic phase (T _NI ) was suppressed to 46 °. The response time was also reduced to 9 ms. Further, no crystals were precipitated even after being left at 0 ° C. for one week. Further quenched and crystallized, its melting point (T _CN ) measured 12 ° C
In this case, there was almost no change from the host liquid crystal (H), indicating that (I-2) was well dissolved in the host liquid crystal.

Next, the voltage holding ratio of this device at room temperature and at 80 ° C. was measured, and it was found that all were extremely good and could be used sufficiently for driving an active matrix.

(Comparative Example 1) In Example 6, trans-4-propyl- (3,4,5-trifluorophenyl) cyclohexane was used in the same amount as the host liquid crystal (H) instead of (I-2). 20%) to prepare a liquid crystal composition (M-2). The maximum temperature of the nematic phase (T _NI ) of this composition was 70 ° C., indicating that the liquid crystallinity was lower than that of (I-2).

The other physical properties of this composition and the electro-optical properties of the device fabricated in the same manner are as follows.

Nematic phase upper limit temperature (T _NI ) 70.0 ° C. Dielectric anisotropy (Δε) 5.60 Threshold voltage (Vth) 1.58 V Response time (τ) 30.0 ms Refractive index anisotropy (Δn): 0.080 Nematic phase upper limit temperature (T _NI ) compared to I-2)
, The threshold voltage (Vth) hardly changes, and the response time hardly changes.

[0319]

The tetrahydronaphthalene derivative provided by the present invention is excellent in liquid crystallinity and compatibility with currently used liquid crystal compounds or compositions. Further, the addition thereof can greatly reduce the threshold voltage without substantially deteriorating the response. Furthermore, it is easy to produce industrially, is colorless and chemically stable. Therefore, a liquid crystal composition containing the same is extremely useful as a practical liquid crystal, particularly for a liquid crystal display requiring a low temperature drive and a high-speed response over a wide temperature range.

Continued on the front page F-term (reference) 4H006 AA01 AA03 AB64 BJ20 BM10 BM71 FC56 FC78 FC80 FE71 FE74 4H027 BA01 BA06 BA07 BB03 BB04 BC04 BD01 BD02 BD04 BD05 BD08 BD24 DK01 DK02 DK03 DK04 DK05 DM05 DM05 DM05 DM05

Claims (15)

[Claims] 1. A compound of the general formula (I)(Wherein R is 1 to 7 fluorine atoms or 1 to 7 carbon atoms
May be substituted with a lucoxyl group,
Saturated or unsaturated alkyl having 1 to 20 carbon atoms which may be contained
Represents a single bond, an oxygen atom, a sulfur atom
Represents -COO-, -OCO-, -OCOO-, -COS- or -SCO-,
The linking groups W, X and Y are each independently a single bond, -CH_TwoC
H_Two-, -CH = CH-, -CH (CH_Three) CH_Two-, -CH_TwoCH (CH_Three)-, -CH (CH_Three)
CH (CH_Three)-, -CF _TwoCF_Two-, -CF = CF-, -CH_TwoO-, -OCH_Two-, -OCH
(CH_Three)-, -CH (CH_Three) O-, -C≡C-, -CF_TwoO-, -OCF_Two-, -COO
-, -OCO-, -COS- or -SCO-, wherein Z is a fluorine atom,
Chlorine atom, cyano group, cyanato group, trifluoromethyl
Group, trifluoromethoxy group, difluoromethoxy group
Or hydrogen atom, Q¹, Q^TwoAnd Q^ThreeAre independent
Represents a hydrogen atom or a fluorine atom, and ring A and ring B are
Trans-1,4-cyclohexylene,
Lance-decahydronaphthalene-2,6-diyl group, trans
-1,3-dioxane-2,5-diyl group or one or two
1,4-phenylene group which may be substituted with a fluorine atom,
Gin-2,5-diyl group, pyrimidine-2,5-diyl group, pyrazine
2,5-diyl group, pyridazine-3,6-diyl group and one
Or naphthalene optionally substituted by two fluorine atoms
Represents a -2,6-diyl group, and ring C is one or two fluorine atoms
1,4-phenylene group which may be substituted with
Is naphthalene-2,6 which may be substituted by two fluorine atoms
-Diyl group, m and n are each independently 0 or
Represents 1. However, when Z is a hydrogen atom, there is one ring C
Or a 1,4-phenylene group substituted by two fluorine atoms
Or may be substituted with one or two fluorine atoms
Represents a naphthalene-2,6-diyl group, Q¹, Q^TwoAnd Q^ThreeTo go
All are hydrogen atoms, and m and n are both 0,
And when Y is -COO- and Z is a fluorine atom,
Ring C is 1,4-phenyl substituted with one or two fluorine atoms.
Substituted with a phenylene group or one or two fluorine atoms
Represents a naphthalene-2,6-diyl group which may be¹, Q^TwoYou
And Q^ThreeAre all hydrogen atoms, and m and n are both
0, Y is a single bond or -COO-, and Z is
When it is an ano group, ring C is one or two fluorine atoms
1,4-phenylene group or one or two
Naphthalene-2,6-diyl which may be substituted by fluorine atom
Represents a group. The tetrahydronaphthalene derivative represented by)
body. 2. The compound according to claim 1, wherein m is 0 in the general formula (I). 3. The compound according to claim 1, wherein n is 0 in the general formula (I). 4. The compound according to claim 1, wherein Q ¹ and Q ² in the formula (I) are both hydrogen atoms. 5. The compound according to claim 1, wherein in formula (I), the linking groups W, X and Y are each independently selected from a single bond or —CH ₂ CH ₂ —. 6. In the formula (I), ring A and ring B are each independently a trans-1,4-cyclohexylene group, a trans-decahydronaphthalene-2,6-diyl group or one or two fluorine atoms The compound according to any one of claims 1 to 5, wherein the compound is selected from a 1,4-phenylene group and a naphthalene-2,6-diyl group which may be substituted with an atom. 7. A compound according to claim 1, wherein ring C in formula (I) is selected from a 1,4-phenylene group or a naphthalene-2,6-diyl group substituted by one or two fluorine atoms.
A compound as described. 8. The compound according to claim 1, wherein in the general formula (I), Z is selected from a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group and a hydrogen atom. 9. The method according to claim 8, wherein in the general formula (I), Z is selected from a fluorine atom or a trifluoromethoxy group.
A compound as described. 10. The compound according to claim 1, wherein V in formula (I) represents a single bond. 11. The compound according to claim 1, wherein R is selected from a linear alkyl group having 1 to 10 carbon atoms in the general formula (I). 12. A liquid crystal composition comprising at least one compound of the general formula (I) according to claim 1. 13. The liquid crystal composition according to claim 12, which is used for driving an active matrix. 14. A liquid crystal device comprising the liquid crystal composition according to claim 13 as a constituent. 15. An active matrix driven liquid crystal display device using the liquid crystal composition according to claim 14.