CN102443141B - Metalloporphyrin-quinoxaline organic semiconductor material and preparation method and application thereof - Google Patents

Metalloporphyrin-quinoxaline organic semiconductor material and preparation method and application thereof Download PDF

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CN102443141B
CN102443141B CN 201010509494 CN201010509494A CN102443141B CN 102443141 B CN102443141 B CN 102443141B CN 201010509494 CN201010509494 CN 201010509494 CN 201010509494 A CN201010509494 A CN 201010509494A CN 102443141 B CN102443141 B CN 102443141B
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quinoxaline
phenyl
porphyrin
semiconductor material
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周明杰
黄杰
刘贻锦
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Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Engineering Co Ltd
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Abstract

The invention belongs to the field of an optoelectronic material, and discloses a metalloporphyrin-quinoxaline organic semiconductor material and a preparation method and an application thereof. The metalloporphyrin-quinoxaline organic semiconductor material is shown in Formula (I), wherein n is an integer between 1 and 100, R1, R2, R3 and R4 are H, C1-C32 alkyl, phenyl and alkyl benzene or alkoxy benzene containing one or more C1-C32, and M is a metal ion. The metalloporphyrin-quinoxaline organic semiconductor material has a broad scope of light absorption, and the rate of utilization of sunlight can be increased. The metalloporphyrin-quinoxaline organic semiconductor material also has better thermal stability and environmental stability. In addition, the process of the preparation method is simple and is easy to operate and control.

Description

Metalloporphyrin-quinoxaline organic semiconductor material and its preparation method and application
Technical field
The present invention relates to a kind of organic semiconductor material, relate to a kind of metalloporphyrin-quinoxaline organic semiconductor material more specifically.
The invention still further relates to preparation method and the application thereof of metalloporphyrin-quinoxaline organic semiconductor material.
Background technology
Utilize cheap material preparation low cost, dynamical solar cell is research focus and the difficult point in photovoltaic field always.Be used for the silicon wafer battery on ground at present owing to complex manufacturing, cost height, its application is restricted.In order to reduce the battery cost, expand range of application, people are seeking novel solar cell material always for a long time.Organic semiconductor material with its raw material be easy to get, cheap, preparation technology is simple, environmental stability good, have good advantages such as photovoltaic effect to receive much concern.Go up report conjugated polymers and C from N.S.Sariciftci in 1992 etc. at SCIENCE (N.S Sariciftci, L. Smilowitz, A.J.Heeger, etal.Science, 1992,258,1474) 60Between photoinduction transfer transport phenomenon after, people have dropped into big quantity research aspect polymer solar battery, and have obtained development at full speed, but still much lower than the efficiency of conversion of inorganic solar cell.The main restricting factor that limiting performance improves has: the spectral response of organic semiconductor material and solar radiation spectrum do not match, the electrode collection effciency of the carrier mobility that organic semiconductor is relatively low and lower current carrier etc.In order to make polymer solar battery obtain actual application, the material of development of new increases substantially the top priority that its effciency of energy transfer is still this research field.
The porphyrin molecule is the general name that is connected with a substituent class macrocylc compound at porphin ring, and porphines is the big ring delocalized of the two dimensional structure conjugated system that is replaced by the Dan Shuanjian that four pyrrole rings and four methyne bridgings get up.The quantum yield of their charge transfer and energy transfer reaction is higher, has good electron resiliency and photoelectric magnetic property, good hard and soft property and better thermostability and environmental stability.Therefore, porphyrin class organic semiconductor material is the up-and-coming material of a class, and its application in the photovoltaic field has obtained broad research.Metal and some non-metallic elements nearly all in the periodic table of elements can form title complex with the porphyrin effect.In these compounds, comprised most main group and subgroup metallic element, some lanthanide series metals (Pr, Eu, Yb etc.) are also synthetic.Because porphyrin is the big rail system altogether with 18 πDian Zis, the electronics flowability is very good in its ring, and therefore, most of metal porphyrinses have photoelectric property preferably.
Quinoxaline is outstanding photoelectric material unit, has the electrophilic characteristic, and the electron transfer capacity that it has height mates itself and electron donor material, can reduce the energy gap of organic photovoltaic material, has wideer sunlight and absorbs.
Yet the organic semiconductor material that contains the metalloporphyrin-quinoxaline of silicon fluorenes does not still have document and patent report so far, and this has just limited the range of application of organic semiconductor material greatly.
Summary of the invention
The object of the present invention is to provide a kind of metalloporphyrin-quinoxaline organic semiconductor material, it can address the above problem.
The present invention also aims to provide preparation method and the application thereof of this metalloporphyrin-quinoxaline organic semiconductor material.
Metalloporphyrin involved in the present invention-quinoxaline organic semiconductor material has following structure (I):
In the formula: n is the integer between 1-100, R 1, R 2, R 3, R 4Be H identical or inequality, C 1-C 32Alkyl, phenyl, contain one or more C identical or inequality 1-C 32Alkylbenzene or alkoxy benzene; M is metal ion, can but be not limited to Zn 2+, Cu 2+, Fe 2+, Co 2+, Cd 2+, Pt 2+, Zr 2+, Mn 2+, Ni 2+, Pb 2+, Sn 2+Deng metal ion.
Metalloporphyrin of the present invention-quinoxaline organic semiconductor material is to adopt following steps to make:
Step S1: with two pyrroles's methane (A), the first silicon fluorene derivatives (B) and the second silicon fluorene derivatives (C) in molar ratio i: j: k be dissolved in first organic solvent that contains oxygenant and first catalyzer, and under 20-100 ℃, reacted 1-24 hour, obtain silicon fluorenes derivatives of porphyrin (D), reaction formula is as follows:
Wherein, i: j: k=1: 1~100: 1~100, and i=+k, i 〉=j>0; First catalyzer adopts organic acid, as propionic acid, trifluoroacetic acid; Oxygenant can adopt DDQ (DDQ), and first organic solvent can be in trichloromethane or the methylene dichloride one or both;
Step S2: be dissolved in the silicon fluorenes derivatives of porphyrin (D) and the bromizating agent that obtain among the step S1 in second organic solvent in 1: 2 in molar ratio~1: 5, reacted 1~72 hour down in 0~120 ℃, obtain dibromo silicon fluorenes derivatives of porphyrin (E), under 0-120 ℃ of condition, reacted 1~72 hour, obtain dibromo silicon fluorenes derivatives of porphyrin (structural formula is e); Reaction formula is as follows:
Figure BSA00000306799000041
Wherein, the consumption mol ratio of silicon fluorenes derivatives of porphyrin (structural formula is d) and bromizating agent is 1: 2~1: 5; Bromizating agent can be N-bromo-succinimide (NBS), and second organic solvent is tetrahydrofuran (THF) (THF), chloroform (CHCl 3), at least a in dimethylformamide (DMF) or the orthodichlorobenzene;
Step S3: the dibromo silicon fluorenes derivatives of porphyrin (E) that obtains among the step S2 is dissolved in the 3rd organic solvent, at least a as in methylene dichloride, trichloromethane, tetrahydrofuran (THF), benzene or the toluene, then add and contain the M metal ion solution, stirred 0.5-24 hour down in 0-30 ℃, obtain dibromo silicon fluorenes metal porphyrin derivative (F); Reaction formula is as follows:
Wherein, the mol ratio of described dibromo silicon fluorenes derivatives of porphyrin (E) and M metal ion is 1: 1~1: 5, the M metal ion can but be not limited to Zn 2+, Cu 2+, Fe 2+, Co 2+, Cd 2+, Pt 2+, Zr 2+, Mn 2+, Ni 2+, Pb 2+, Sn 2+Deng, the M metallic salt can comprise M (OAc) 2, MCl 2, MSO 4, M (NO 3) 2Deng;
Step S4: in oxygen-free environment, (comprise the protection of inert gas atmosphere that nitrogen and/or argon gas etc. constitute), with the dibromo silicon fluorenes metal porphyrin derivative (F) and 5 that obtains among the step S3,8-two (tributyl tin)-2, two (phenyl) quinoxalines (G) of 3-were dissolved in the 4th organic solvent that contains second catalyzer in 1: 2 in molar ratio~2: 1, under 50-120 ℃, carry out the Stille coupling reaction 12~72 hours, and obtained described metalloporphyrin-quinoxaline organic semiconductor material (I); Reaction formula is as follows:
Figure BSA00000306799000051
In the formula, n is the integer between 1-100;
Wherein, second catalyzer can for the mixture of organic palladium or organic palladium and organophosphor ligand (mol ratio of organic palladium and organophosphor ligand is 1: 1-20), as Pd 2(dba) 3/ P (o-Tol) 3, Pd (OAc) 2/ tricyclohexyl phosphine, Pd (PPh 3) 4Or Pd (PPh 3) 2Cl 2Deng; The mole dosage of second catalyzer is 5,8-two (tributyl tin)-2, the 0.01%-20% of two (phenyl) quinoxaline (G) molar weights of 3-; Described the 4th organic solvent is at least a in tetrahydrofuran (THF), methylene dichloride, chloroform, dioxane, dimethylformamide, dimethyl sulfoxide (DMSO), glycol dimethyl ether, chlorobenzene, benzene or the toluene etc.
Among above-mentioned preparation method's the step S4,5,8-two (tributyl tin)-2, two (phenyl) quinoxalines (G) of 3-adopt following steps to make
Step S41, with diphenylthanedione (S) and 1, the dibromo O-Phenylene Diamine of 4-(X) adds in the 5th organic solvent with mol ratio 1: 5~5: 1, and in 20 ℃-120 ℃ reactions 1-24 hour down, obtain 5,8-dibromo 2,3-two (phenyl) quinoxaline (Y), reaction formula is as follows:
Figure BSA00000306799000061
Step S42: with above-mentioned 5,8-dibromo 2,3-hexichol quinoxaline (Y) is dissolved in the 6th organic solvent, is cooled to-30 ℃ with liquid nitrogen/Virahol subsequently, drips n-Butyl Lithium, at-30 ℃ of reaction 1-3h, adds SnBu more then 3Cl (three normal-butyl chlorination tin, down together) or SnMe 3Cl (trimethyltin chloride, down with) is at-30 ℃ of reaction 0.5-2h, and the room temperature of intensification naturally was reacted 3-36 hour then, obtain described 5,8-two (tributyl tin)-2,3-pair of (phenyl) quinoxalines (G); Reaction formula is as follows:
Figure BSA00000306799000062
Above-mentioned metalloporphyrin-quinoxaline organic semiconductor material can be widely used in organic solar batteries, organic electroluminescent, and organic field effect tube, organic optical storage is in the fields such as organic non-linear device and organic laser apparatus.
The organic semiconductor material of the metalloporphyrin-quinoxaline of the siliceous fluorenes of the present invention's exploitation, such material is by introducing the silicon fluorene group to the porphyrin framework, and the coordination by metal ion, adjusted the band gap of porphyrin polymer, and then the better stability of acquisition and good film-forming properties, widened the visible spectrum absorption region, make its absorption region extend to the near-infrared region, improve it to the utilization ratio of sunlight, improve carrier mobility simultaneously, enlarged them in the range of application in fields such as organic solar batteries.
Compared with prior art, the present invention has following advantage:
1. the silicon fluorenes unit that contains in the organic semiconductor material molecule among the present invention has good thermostability, and higher electron affinity and higher electronics injection and transmittability;
2. also contain the porphyrin unit simultaneously, have the big ring delocalized conjugated system of two dimensional structure, the quantum yield of charge transfer and energy transfer reaction is higher, has good hard and soft property and better thermostability and environmental stability.
3. also contain quinoxaline unit simultaneously, have very high electric transmission character and second-order transition temperature, excellent electrochemical reduction character etc., it also has strong electrophilic characteristic, it is a kind of good body unit that is subjected to, itself and electron donor material are mated, can reduce the energy gap of material, widen the absorption region to sunlight.
4. organic semiconductor material of the present invention is owing to comprised silicon fluorene structural units, porphyrin unit and quinoxaline unit simultaneously, taken into account their performance advantage, and expanded the absorption region of this organic semiconductor material to sunlight, increased the matching degree with solar radiation spectrum, thus effectively expanded this organic semiconductor material at polymer solar battery, organic electroluminescence device, organic field effect tube, organic light storage device or/and the application in the organic laser apparatus;
5. the preparation technology of described organic semiconductor material is simple, is easy to operate and control.
Description of drawings
Fig. 1 is with the structural representation of the organic semiconductor material among the present invention as the organic solar batteries device of active coating.
Fig. 2 is with the structural representation of the organic semiconductor material among the present invention as the organic electroluminescence device of luminescent layer.
Fig. 3 is with the structural representation of the organic semiconductor material among the present invention as the organic field effect tube device of organic semiconductor layer.
Embodiment
Metalloporphyrin involved in the present invention-quinoxaline organic semiconductor material has following structure (I):
Figure BSA00000306799000081
In the formula: n is the integer between 1-100, R 1, R 2, R 3, R 4Be H identical or inequality, C 1-C 32Alkyl, phenyl, contain one or more C identical or inequality 1-C 32Alkylbenzene or alkoxy benzene; M is metal ion, can but be not limited to Zn 2+, Cu 2+, Fe 2+, Co 2+, Cd 2+, Pt 2+, Zr 2+, Mn 2+, Ni 2+, Pb 2+, Sn 2+Deng metal ion.
The preparation method of metalloporphyrin-quinoxaline organic semiconductor material that the present invention is designed, step is as follows:
Step S1: with two pyrroles's methane (A), the first silicon fluorene derivatives (B) and the second silicon fluorene derivatives (C) in molar ratio i: j: k be dissolved in first organic solvent that contains oxygenant and first catalyzer, in described first organic solvent, add oxygenant, first catalyzer, and under 20-100 ℃, reacted 1-24 hour, obtain silicon fluorenes derivatives of porphyrin (D), reaction formula is as follows:
Figure BSA00000306799000082
Wherein, i: j: k=1: 1~100: 1~100, and i=j+k, i 〉=j>0; First catalyzer adopts organic acid, as propionic acid, trifluoroacetic acid; Oxygenant can adopt DDQ (DDQ), and first organic solvent can be in trichloromethane or the methylene dichloride one or both;
Step S2: the silicon fluorenes derivatives of porphyrin (D) and the bromizating agent that obtain among the step S1 were dissolved in second organic solvent in 1: 2 in molar ratio~1: 5, reacted 1~72 hour down in 0~120 ℃, obtain dibromo silicon fluorenes derivatives of porphyrin (E); Reaction formula is as follows:
Figure BSA00000306799000091
Wherein, the consumption mol ratio of silicon fluorenes derivatives of porphyrin (D) and bromizating agent is 1: 2~1: 5; Bromizating agent can be N-bromo-succinimide (NBS), and second organic solvent is tetrahydrofuran (THF) (THF), chloroform (CHCl 3), at least a in dimethylformamide (DMF) or the orthodichlorobenzene;
Step S3: the dibromo silicon fluorenes derivatives of porphyrin (E) that obtains among the step S2 is dissolved in the 3rd organic solvent, at least a as in methylene dichloride, trichloromethane, tetrahydrofuran (THF), benzene or the toluene, then add and contain the M metal ion solution, stirred 0.5-24 hour down in 0-30 ℃, obtain dibromo silicon fluorenes metal porphyrin derivative (F); Reaction formula is as follows:
Figure BSA00000306799000092
Wherein, the mol ratio of described dibromo silicon fluorenes derivatives of porphyrin (E) and M metal ion is 1: 1~1: 5, the M metal ion can but be not limited to Zn 2+, Cu 2+, Fe 2+, Co 2+, Cd 2+, Pt 2+, Zr 2+, Mn 2+, Ni 2+, Pb 2+, Sn 2+Deng, the M metallic salt can comprise M (OAc) 2, MCl 2, MSO 4, M (NO 3) 2Deng;
Step S4: in oxygen-free environment, (comprise the protection of inert gas atmosphere that nitrogen and/or argon gas etc. constitute), with the dibromo silicon fluorenes metal porphyrin derivative (F) and 5 that obtains among the step S3,8-two (tributyl tin)-2, two (phenyl) quinoxalines (G) of 3-were dissolved in the 4th organic solvent that contains second catalyzer in 1: 2 in molar ratio~2: 1, under 50-120 ℃, carry out the Stille coupling reaction 12~72 hours, and obtained described metalloporphyrin-quinoxaline organic semiconductor material (I); Reaction formula is as follows:
In the formula, n is the integer between 1-100;
Wherein, second catalyzer can for the mixture of organic palladium or organic palladium and organophosphor ligand (mol ratio of organic palladium and organophosphor ligand is 1: 1-20), as Pd 2(dba) 3/ P (o-Tol) 3, Pd (OAc) 2/ tricyclohexyl phosphine, Pd (PPh 3) 4Or Pd (PPh 3) 2Cl 2Deng; The mole dosage of second catalyzer is 5,8-two (tributyl tin)-2, the 0.01%-20% of two (phenyl) quinoxaline (G) molar weights of 3-; Described the 4th organic solvent is at least a in tetrahydrofuran (THF), methylene dichloride, chloroform, dioxane, dimethylformamide, dimethyl sulfoxide (DMSO), glycol dimethyl ether, chlorobenzene, benzene or the toluene etc.
Among above-mentioned preparation method's the step S4,5,8-two (tributyl tin)-2, two (phenyl) quinoxalines (G) of 3-adopt following steps to make
Step S41, with diphenylthanedione (S) and 1, the dibromo O-Phenylene Diamine of 4-(X) adds in the 5th organic solvent with mol ratio 1: 5~5: 1, and in 20 ℃-120 ℃ reactions 1-24 hour down, obtain 5,8-dibromo 2,3-two (phenyl) quinoxaline (Y), reaction formula is as follows:
Figure BSA00000306799000111
Step S42: with above-mentioned 5,8-dibromo 2,3-hexichol quinoxaline (Y) is dissolved in the 6th organic solvent, is cooled to-30 ℃ with liquid nitrogen/Virahol subsequently, drips n-Butyl Lithium, at-30 ℃ of reaction 1-3h, adds SnBu more then 3Cl or SnMe 3Cl is at-30 ℃ of reaction 0.5-2h, and the room temperature of intensification naturally was reacted 3-36 hour then, obtain described 5,8-two (tributyl tin)-2,3-pair of (phenyl) quinoxalines (G); Reaction formula is as follows:
Figure BSA00000306799000112
2-bromo-9-replaces the silicon fluorenes and makes (reference: Macromolecules 2002 by 2-bromine silicon fluorenes and corresponding bromide under the catalyst/solvent condition, 35,3474), 2-aldehyde-9-replaces the silicon fluorenes and makes (reference: Macromolecules 2006 by 2-bromo-9-replacement silicon fluorenes in n-Butyl Lithium/dimethyl formamide/tetrahydrofuran (THF) system, 39,456), two pyrroles's methane make (reference: Tetrahedron 1994 by formaldehyde and pyrroles under catalyst action, 39,11427).
Above-mentioned metalloporphyrin-quinoxaline organic semiconductor material can be widely used in organic solar batteries, organic electroluminescent, and organic field effect tube, organic optical storage is in the fields such as organic non-linear device and organic laser apparatus.
The organic semiconductor material of the metalloporphyrin-quinoxaline of the siliceous fluorenes of the present invention's exploitation, such material is by introducing the silicon fluorene group to the porphyrin framework, and the coordination by metal ion, adjusted the band gap of porphyrin polymer, and then the better stability of acquisition and good film-forming properties, widened the visible spectrum absorption region, make its absorption region extend to the near-infrared region, improve it to the utilization ratio of sunlight, improve carrier mobility simultaneously, enlarged them in the range of application in fields such as organic solar batteries.
Below in conjunction with accompanying drawing, preferred embodiment of the present invention is described in further detail.
Embodiment 1
Present embodiment discloses the following silicon fluorenes zinc protoporphyrin-quinoxaline organic semiconductor material of a kind of structure
Figure BSA00000306799000121
In the following formula, n=10;
Above-mentioned organic semiconductor material preparation process is as follows:
One, 5,8-two bromo-2, two (phenyl) quinoxalines of 3-synthetic
Figure BSA00000306799000122
(1.01g, (0.39g is in 20ml acetic acid solution 1.8mmol) 3.7mmol) to join the compound diphenylthanedione with 3,6-, two bromo-O-Phenylene Diamines at 120 ℃.Backflow is spent the night, and reaction solution is poured in the water, and sodium bicarbonate is neutralized to neutrality.Chloroform extraction, saturated common salt water washing, anhydrous sodium sulfate drying.The rotary evaporation desolventizing, thick product column chromatography gets white solid.Chloroform/normal hexane recrystallization obtains the white solid powder then, productive rate 86%.
GC-MS(EI-m/z):440(M +)
Two, 5,8-two (tributyl tin)-2, two (phenyl) quinoxalines of 3-synthetic
Figure BSA00000306799000131
In the 500ml there-necked flask, add 5,8-, two bromo-2, two (phenyl) quinoxaline (1.32g of 3-, 3mmol), the 300ml tetrahydrofuran (THF) is cooled to system-30 ℃, the n-Butyl Lithium (2.5ml of dropping, 2.5M, 6.3mmol), then at-30 ℃ of reactions 1h, property adding SnBu again 3(2.08g 6.4mmol), at-30 ℃ of reaction 30min, is warming up to room temperature to Cl then naturally, and stirring reaction spends the night.Reactant is poured in the frozen water, used extracted with diethyl ether, anhydrous magnesium sulfate drying, the underpressure distillation desolventizing is carried out column chromatography for separation with silica gel/sherwood oil (30~60 ℃), obtains product, productive rate 80%.
GC-MS(EI-m/z):860(M +)
Three, 5,15-two (9 ', 9 '-dioctyl) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000132
Put up the anhydrous and oxygen-free device, take by weighing intermediate 2-aldehyde-9, (0.44g is 1mmol) with two pyrroles's methane (0.15g for 9-dioctyl silicon fluorenes, 1mmol), be dissolved in the 250ml methylene dichloride, feed nitrogen 30min, syringe adds propionic acid 1ml, 20 ℃ are stirred 24h down, (0.91g 4mmol), continues at room temperature to stir 30min to add DDQ (DDQ) then, add 1ml triethylamine cancellation reaction then, concentrated solvent filters, and collects filtrate and is spin-dried for solvent, with methylene dichloride drip washing fast on silicagel column, be spin-dried for solvent, to product, productive rate is about 85% with ether/recrystallizing methanol.
GC-MS(EI-m/z):1120(M +)
Four, 5,15-two bromo-10,20-two (9 ', 9 '-dioctyl) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000141
Put up the anhydrous and oxygen-free device, take by weighing 10,20-two (9 ', 9 '-dioctyl) (0.23g 0.2mmol) is dissolved in the 80ml chloroform silicon fluorenes porphyrin, adds the 1ml pyridine, reactant is dropped to 0 ℃, and adding N-bromo-succinimide (0.07g, 0.4mmol), after stirring 72h, mixture returns to room temperature, continues to stir 4h then, add 5ml acetone termination reaction, desolventizing is carried out recrystallization with ether/methyl alcohol and is obtained product, productive rate 81%.
GC-MS(EI-m/z):1278(M +)
Five, 5,15-two bromo-10,20-two (9 ', 9 '-dioctyl) silicon fluorenes zinc protoporphyrin synthetic
Figure BSA00000306799000142
Take by weighing intermediate 5,15-two bromo-10,20-two (9,9-dioctyl fluorene) porphyrin (0.25g, 0.2mmol) be dissolved in the 50ml methylene dichloride, add contain zinc acetate (0.11g, methanol solution 0.5mmol) (5ml) stirs 5h under the room temperature, be spin-dried for solvent, use methylene dichloride/sherwood oil (1/1) drip washing on silicagel column then, collect and be spin-dried for solvent and obtain product, productive rate 94%.
GC-MS(EI-m/z):1340(M +)
Six, silicon fluorenes zinc protoporphyrin-quinoxaline organic semiconductor material is synthetic
Figure BSA00000306799000151
Under nitrogen protection; add 5; 8-two (tributyl tin)-2, and two (phenyl) quinoxalines of 3-(172mg, 0.2mmol), 5; 15-two bromo-10; (268mg is 0.2mmol) with toluene solvant 50ml for 20-two (9 ', 9 '-dioctyl) silicon fluorenes zinc protoporphyrin; vacuumize deoxygenation and charge into nitrogen, add 5mg Pd (PPh then 3) 2Cl 2With 2ml NaHCO 3(50%) solution is heated to 100 ℃ of reaction 56h.Be cooled to after the room temperature mixed solution is added drop-wise to and carry out sedimentation in the 300ml methyl alcohol.Suction filtration, methanol wash, drying.With the toluene dissolving, join in the aqueous solution of Thiocarb then, then mixed solution is heated to 80 ℃ of stirrings and spends the night.With the column chromatography of organic phase by aluminum oxide, chlorobenzene drip washing.Organic solvent, methyl alcohol sedimentation are removed in decompression.Suction filtration, the gained solid extracted three days with the acetone apparatus,Soxhlet's.The methyl alcohol sedimentation, suction filtration.Taking out under the vacuum pump spends the night obtains product, and productive rate 70%.Molecular weight (GPC, THF, R.I): Mn=14600, Mw/Mn=2.62; )
Embodiment 2
Present embodiment discloses the following silicon fluorenes iron porphyrin-quinoxaline organic semiconductor material of a kind of structure
Figure BSA00000306799000161
In the following formula, n=28;
Above-mentioned organic semiconductor material preparation process is as follows:
One, 5,8-two (tributyl tin)-2, two (phenyl) quinoxalines of 3-synthetic
Its preparation sees embodiment 1. for details
Two, 5-(9 '-methyl-9 '-hexadecyl) silicon fluorenes-15-(9 '-dotriacontyl) silicon fluorenes porphyrin is synthetic
Put up the anhydrous and oxygen-free device, take by weighing intermediate 2-aldehyde-9-methyl-9-hexadecyl silicon fluorenes (0.45g, 1mmol), 2-aldehyde-9-dotriacontyl silicon fluorenes (0.66g, 1mmol), two pyrroles's methane (0.30g, 2mmol), be dissolved in the 250ml methylene dichloride, feed nitrogen 30min, syringe adds trifluoroacetic acid 2ml, 100 ℃ are stirred 1h down, (1.82g 8mmol), continues at room temperature to stir 30min to add DDQ (DDQ) then, add 2ml pyridine cancellation reaction then, concentrated solvent filters, and collects filtrate and is spin-dried for solvent, with methylene dichloride drip washing fast on silicagel column, be spin-dried for solvent, to product, productive rate is about 71% with ether/recrystallizing methanol.
GC-MS(EI-m/z):1359(M +)
Three, 5,15-two bromo-10-(9 '-methyl-9 '-hexadecyl) silicon fluorenes-20-(9 '-dotriacontyl) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000171
Put up the anhydrous and oxygen-free device, (0.27g 0.2mmol) is dissolved in the 80ml chloroform to take by weighing 5-(9 '-methyl-9 '-hexadecyl) silicon fluorenes-15-(9 '-dotriacontyl) silicon fluorenes porphyrin, add the 1ml pyridine, reactant is dropped to 0 ℃, add N-bromo-succinimide (0.07g, 0.4mmol), after stirring 0.5h, mixture is warming up to 120 ℃, after continuing then to stir 1h, add 5ml acetone termination reaction, desolventizing is carried out recrystallization with ether/methyl alcohol and is obtained product, productive rate 72%.
GC-MS(EI-m/z):1516(M +)
Four, 5,15-two bromo-10-(9 '-methyl-9 '-hexadecyl) silicon fluorenes-20-(9 '-dotriacontyl) silicon fluorenes iron porphyrin synthetic
Figure BSA00000306799000172
N 2Under the condition, take by weighing intermediate 5, (0.31g 0.2mmol) is dissolved in the 50ml methylene dichloride 15-two bromo-10-(9 '-methyl-9 '-hexadecyl) silicon fluorenes-20-(9 '-dotriacontyl) silicon fluorenes porphyrin, adds to contain the ferrous (0.12g of chlorination, methanol solution 1mmol) (5ml), stir 8h under the room temperature, be spin-dried for solvent, use methylene dichloride/sherwood oil (1/1) drip washing on silicagel column then, collect and be spin-dried for solvent and obtain product, productive rate 95%.
GC-MS(EI-m/z):1569(M +)
Five, silicon fluorenes iron porphyrin-quinoxaline organic semiconductor material is synthetic
Figure BSA00000306799000181
Under nitrogen protection; add 5; 8-two (tributyl tin)-2; two (phenyl) quinoxaline (172mg of 3-; 0.2mmol), 5,15-two bromo-10-(9 '-methyl-9 '-hexadecyl) silicon fluorenes-20-(9 '-dotriacontyl) silicon fluorenes iron porphyrin (314mg, 0.2mmol) and toluene solvant 120ml; vacuumize deoxygenation and charge into nitrogen, add Pd (OAc) then 2(2.5mg)/tricyclohexyl phosphine (6.5mg) and 2ml 20% (wt) Et 4NOH solution is heated to 120 ℃ of reaction 24h.Be cooled to after the room temperature mixed solution is added drop-wise to and carry out sedimentation in the 200ml methyl alcohol.Suction filtration, methanol wash, drying.With the toluene dissolving, join in the aqueous solution of Thiocarb then, then mixed solution is heated to 80 ℃ of stirrings and spends the night.With the column chromatography of organic phase by aluminum oxide, chlorobenzene drip washing.Organic solvent, methyl alcohol sedimentation are removed in decompression.Suction filtration, the gained solid extracted three days with the acetone Soxhlet.The methyl alcohol sedimentation, suction filtration.Taking out under the vacuum pump spends the night obtains product, and productive rate 81%.Molecular weight (GPC, THF, R.I): Mn=47300, Mw/Mn=2.94; )
Embodiment 3
It is following that present embodiment discloses a kind of structure) silicon fluorenes copper porphyrin-quinoxaline organic semiconductor material
Figure BSA00000306799000191
In the following formula, n=40;
Above-mentioned organic semiconductor material preparation process is as follows:
One, 5,8-two (tributyl tin)-2, two (phenyl) quinoxalines of 3-synthetic
Its preparation sees embodiment 1. for details
Two, 10,20-two (9 '-hexadecyl-9 '-(3 "-hexadecyl-4 "-n-Hexadecane oxygen base) benzene) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000192
Put up the anhydrous and oxygen-free device, take by weighing intermediate 2-aldehyde-9-hexadecyl-9-(3 '-hexadecyl-4 '-n-Hexadecane oxygen base) benzene) silicon fluorenes (1.95g, 2mmol) (0.30g 2mmol), is dissolved in the 300ml methylene dichloride with two pyrroles's methane, feed nitrogen 30min, syringe adds trifluoroacetic acid 2ml, stirs 3h under the room temperature, adds DDQ (DDQ) (1.82g then, 8mmol), continue at room temperature to stir 30min, add 2ml triethylamine cancellation reaction then, concentrated solvent, filter, collect filtrate and be spin-dried for solvent, with methylene dichloride drip washing fast on silicagel column, be spin-dried for solvent, to product, productive rate is about 85% with ether/recrystallizing methanol.
GC-MS(EI-m/z):2201(M +)
Three, 5,15-two bromo-10,20-two (9 '-hexadecyl-9 '-(3 "-hexadecyl-4 "-n-Hexadecane oxygen base) benzene) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000201
Put up the anhydrous and oxygen-free device, take by weighing 10,20-two (9 '-hexadecyl-9 '-(3 "-hexadecyl-4 "-n-Hexadecane oxygen base) benzene) silicon fluorenes porphyrin (0.44g, 0.2mmol) be dissolved in the 80ml chloroform, add the 1ml pyridine, reactant is dropped to 0 ℃, adding N-bromo-succinimide (0.07g, 0.4mmol), behind the stirring 0.5h, mixture is warming up to 30 ℃, continue to stir 48h then, add 5ml acetone termination reaction, desolventizing, carry out recrystallization with ether/methyl alcohol and obtain product, productive rate 72%.
GC-MS(EI-m/z):2360(M +)
Four, 5,15-two bromo-10,20-two (9 '-hexadecyl-9 '-(3 "-hexadecyl-4 "-n-Hexadecane oxygen base) benzene) silicon fluorenes copper porphyrin synthetic
Figure BSA00000306799000211
Take by weighing intermediate 5,15-two bromo-10,20-two (9 '-hexadecyl-9 '-(3 "-hexadecyl-4 "-n-Hexadecane oxygen base) benzene) (0.47g 0.2mmol) is dissolved in the 50ml methylene dichloride silicon fluorenes porphyrin, adds CuSO 45H 2(0.05g, 0.2mmol) solution (5ml) stirs 5h under the room temperature to O, is spin-dried for solvent, uses methylene dichloride/sherwood oil (1/1) drip washing on silicagel column then, collects and is spin-dried for solvent and obtain product, productive rate 93%.
GC-MS(EI-m/z):2416(M +)
Five, silicon fluorenes copper porphyrin-quinoxaline organic semiconductor material is synthetic
Figure BSA00000306799000212
Under nitrogen protection; add 5; 8-two (tributyl tin)-2; two (phenyl) quinoxalines of 3-(172mg, 0.2mmol), 5,15-two bromo-10; 20-two (9 '-hexadecyl-9 '-(3 "-hexadecyl-4 "-n-Hexadecane oxygen base) benzene) silicon fluorenes copper porphyrin (483mg; 0.2mmol) and toluene solvant 100ml, vacuumize deoxygenation and charge into nitrogen, add 10mg Pd (PPh then 3) 2Cl 2With 2ml KHCO 3(30%) solution is heated to 50 ℃ of reaction 72h.Be cooled to after the room temperature mixed solution is added drop-wise to and carry out sedimentation in the 300ml methyl alcohol.Suction filtration, methanol wash, drying.With the toluene dissolving, join in the aqueous solution of Thiocarb then, then mixed solution is heated to 80 ℃ of stirrings and spends the night.With the column chromatography of organic phase by aluminum oxide, chlorobenzene drip washing.Organic solvent, methyl alcohol sedimentation are removed in decompression.Suction filtration, the gained solid extracted three days with the acetone Soxhlet.The methyl alcohol sedimentation, suction filtration.Taking out under the vacuum pump spends the night obtains product, productive rate 72%.Molecularweight(GPC,THF,R.I):Mn=101600,Mw/Mn=3.41;)
Embodiment 4
Present embodiment discloses the following silicon fluorenes cadmium porphyrin-quinoxaline organic semiconductor material of a kind of structure
Figure BSA00000306799000221
In the following formula, n=56;
Above-mentioned organic semiconductor material preparation process is as follows:
One, 5,8-two (tributyl tin)-2, two (phenyl) quinoxalines of 3-synthetic
Its preparation sees embodiment 1. for details
Two, 5-(9 '-to eicosyl benzene-9 '-(3 ", 5 "-two dodecyloxy benzene)) silicon fluorenes-15-(9 '-to n-Hexadecane oxygen base benzene-9 '-decyl benzene) silicon fluorenes porphyrin synthetic
Put up the anhydrous and oxygen-free device, take by weighing the eicosyl benzene-9-(3 ' of intermediate 2-aldehyde-9-, 5 '-two dodecyloxy benzene) silicon fluorenes (1.02g, 1mmol), decyl benzene silicon fluorenes (0.74g between the n-Hexadecane oxygen of 2-aldehyde-9-base benzene-9-, 1mmol) (0.30g 2mmol), is dissolved in the 250ml methylene dichloride with two pyrroles's methane, feed nitrogen 30min, syringe adds acetic acid 1ml, and 20 ℃ are stirred 24h down, add DDQ (DDQ) (0.91g then, 4mmol), continue at room temperature to stir 30min, add 1ml triethylamine cancellation reaction then, concentrated solvent, filter, collect filtrate and be spin-dried for solvent, with methylene dichloride drip washing fast on silicagel column, be spin-dried for solvent, to product, productive rate is about 83% with ether/recrystallizing methanol.
GC-MS(EI-m/z):2205(M +)
Three, 5,15-two bromo-10-(9 '-to eicosyl benzene-9 '-(3 ", 5 "-two dodecyloxy benzene)) silicon fluorenes-20-(9 '-to n-Hexadecane oxygen base benzene-9 '-decyl benzene) silicon fluorenes porphyrin synthetic
Put up the anhydrous and oxygen-free device, take by weighing 5,15-two bromo-10-(9 '-to eicosyl benzene-9 '-(3 "; 5 "-two dodecyloxy benzene)) silicon fluorenes-20-(9 '-to n-Hexadecane oxygen base benzene-9 '-decyl benzene) silicon fluorenes porphyrin (0.44g, 0.2mmol) be dissolved among the 80ml DMF, reactant is dropped to 0 ℃, adding N-bromo-succinimide (0.07g, 0.4mmol), behind the stirring 72h, mixture returns to room temperature, continue to stir 4h then, add 5ml acetone termination reaction, desolventizing, carry out recrystallization with ether/methyl alcohol and obtain product, productive rate 82%.
GC-MS(EI-m/z):2162(M +)
Four, 5,15-two bromo-10-(9 '-to eicosyl benzene-9 '-(3 ", 5 "-two dodecyloxy benzene)) silicon fluorenes-20-(9 '-to n-Hexadecane oxygen base benzene-9 '-decyl benzene) silicon fluorenes cadmium porphyrin synthetic
Figure BSA00000306799000241
Take by weighing intermediate 5,15-two bromo-10-(9 '-to eicosyl benzene-9 '-(3 "; 5 "-two dodecyloxy benzene)) (0.43g 0.2mmol) is dissolved in the 50ml methylene dichloride silicon fluorenes-20-(9 '-to n-Hexadecane oxygen base benzene-9 '-decyl benzene) silicon fluorenes porphyrin, adds Cd (NO 3) 24H 2(0.31g, methanol solution 1mmol) (5ml) stirs 5h under the room temperature to O, is spin-dried for solvent, uses methylene dichloride/sherwood oil (1/1) drip washing on silicagel column then, collects and is spin-dried for solvent and obtain product, productive rate 94%.
GC-MS(EI-m/z):2271(M +)
Five, silicon fluorenes cadmium porphyrin-quinoxaline organic semiconductor material is synthetic
Figure BSA00000306799000251
Under nitrogen protection; add 5; 8-two (tributyl tin)-2; two (phenyl) quinoxalines of 3-(172mg, 0.2mmol), 5,15-two bromo-10-(9 '-to eicosyl benzene-9 '-(3 "; 5 "-two dodecyloxy benzene)) silicon fluorenes-20-(9 '-to n-Hexadecane oxygen base benzene-9 '-decyl benzene) silicon fluorenes porphyrin (454mg; 0.2mmol) and dioxane solvent 60ml, vacuumize deoxygenation and charge into nitrogen, add Pd then 2(dba) 3(5mg)/P (o-Tol) 3(8mg) with 15% Na 2CO 3(3ml) solution is heated to 80 ℃ of reaction 36h.Be cooled to after the room temperature mixed solution is added drop-wise to and carry out sedimentation in the 250ml methyl alcohol.Suction filtration, methanol wash, drying.With the toluene dissolving, join in the aqueous solution of Thiocarb then, then mixed solution is heated to 80 ℃ of stirrings and spends the night.With the column chromatography of organic phase by aluminum oxide, chlorobenzene drip washing.Organic solvent, methyl alcohol sedimentation are removed in decompression.Suction filtration, the gained solid extracted three days with the acetone apparatus,Soxhlet's.The methyl alcohol sedimentation, suction filtration.Taking out under the vacuum pump spends the night obtains product, and productive rate 74%.Molecularweight (GPC, THF, R.I): Mn=134800, Mw/Mn=3.77;
Embodiment 5
Present embodiment discloses the following silicon fluorenes cobalt porphyrin-quinoxaline organic semiconductor material of a kind of structure
In the following formula, n=78;
Above-mentioned organic semiconductor material preparation process is as follows:
One, 5,8-two (tributyl tin)-2, two (phenyl) quinoxalines of 3-synthetic
Its preparation sees embodiment 1. for details
Two, 5-(9 '-(3 ", 4 ", 5 "-three the last of the ten Heavenly stems alkoxyl group) benzene-9 '-to hexadecyl benzene) silicon fluorenes-15-(9 '-(3 "-dodecyl-5 "-eicosane oxygen base) benzene-9 '-(3 "-dotriacontyl-4 "-laccerane oxygen base) benzene) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000262
Put up the anhydrous and oxygen-free device, take by weighing intermediate 2-aldehyde-9-(3 ', 4 ', 5 '-three the last of the ten Heavenly stems alkoxyl group) the hexadecyl benzene of benzene-9-silicon fluorenes (and 1.06g, 1mmol), 2-aldehyde-9-(3 '-dodecyl-5 '-eicosane oxygen base)-9-(3 '-dotriacontyl-4 '-laccerane oxygen base) benzene silicon fluorenes (1.74g, 1mmol), two pyrroles's methane (0.30g, 2mmol), be dissolved in the 250ml methylene dichloride, feed nitrogen 30min, syringe adds propionic acid 2ml, 100 ℃ are stirred 1h down, (1.82g 8mmol), continues at room temperature to stir 30min to add DDQ (DDQ) then, add 2ml pyridine cancellation reaction then, concentrated solvent filters, and collects filtrate and is spin-dried for solvent, with methylene dichloride drip washing fast on silicagel column, be spin-dried for solvent, to product, productive rate is about 74% with ether/recrystallizing methanol.
GC-MS(EI-m/z):3047(M +)
Three, 5,15-two bromo-10-(9 '-(3 "; 4 ", 5 "-three the last of the ten Heavenly stems alkoxyl group) benzene-9 '-to hexadecyl benzene) silicon fluorenes-20-(9 '-(3 "-dodecyl-5 "-eicosane oxygen base) benzene-9 '-(3 "-dotriacontyl-4 "-laccerane oxygen base) benzene) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000271
Put up the anhydrous and oxygen-free device, take by weighing 5-(9 '-(3 "; 4 "; 5 "-three the last of the ten Heavenly stems alkoxyl group) benzene-9 '-to hexadecyl benzene) silicon fluorenes-15-(9 '-(3 "-dodecyl-5 "-eicosane oxygen base) benzene-9 '-(3 "-dotriacontyl-4 "-laccerane oxygen base) benzene) silicon fluorenes porphyrin (0.61g, 0.2mmol) be dissolved in the 40ml tetrahydrofuran (THF), add the 0.5ml triethylamine, reactant is dropped to 0 ℃, add N-bromo-succinimide (0.07g, 0.4mmol), after stirring 0.5h, mixture is warming up to backflow, after continuing then to stir 1h, add 5ml acetone termination reaction, desolventizing is carried out recrystallization with ether/methyl alcohol and is obtained product, productive rate 82%.
GC-MS(EI-m/z):3204(M +)
Four, 5-(9 '-(3 "; 4 ", 5 "-three the last of the ten Heavenly stems alkoxyl group) benzene-9 '-to hexadecyl benzene) silicon fluorenes-15-(9 '-(3 "-dodecyl-5 "-eicosane oxygen base) benzene-9 '-(3 "-dotriacontyl-4 "-laccerane oxygen base) benzene) silicon fluorenes cobalt porphyrin synthetic
Figure BSA00000306799000281
Take by weighing intermediate 5-(9 '-(3 "; 4 "; 5 "-three the last of the ten Heavenly stems alkoxyl group) benzene-9 '-to hexadecyl benzene) silicon fluorenes-15-(9 '-(3 "-dodecyl-5 "-eicosane oxygen base) benzene-9 '-(3 "-dotriacontyl-4 "-laccerane oxygen base) benzene) silicon fluorenes porphyrin (0.64g, 0.2mmol) be dissolved in the 50ml methylene dichloride, add CoCl 26H 2(0.12g, 0.5mmol) solution (5ml) stirs 12h under the room temperature to O, is spin-dried for solvent, uses methylene dichloride/sherwood oil (1/1) drip washing on silicagel column then, collects and is spin-dried for solvent and obtain product, productive rate 96%.
GC-MS(EI-m/z):3257(M +)
Five, silicon fluorenes cobalt porphyrin-quinoxaline organic semiconductor material is synthetic
Figure BSA00000306799000282
Under nitrogen protection; add 5; 8-two (tributyl tin)-2; two (phenyl) quinoxaline (172mg of 3-; 0.2mmol), 5; 15-two bromo-10-(9 '-(3 "; 4 "; 5 "-three the last of the ten Heavenly stems alkoxyl group) benzene-9 '-to hexadecyl benzene) silicon fluorenes-20-(9 '-(3 "-dodecyl-5 "-eicosane oxygen base) benzene-9 '-(3 "-dotriacontyl-4 "-laccerane oxygen base) benzene) silicon fluorenes cobalt porphyrin (650mg; 0.2mmol) and DMF solvent 80ml; vacuumize deoxygenation and charge into nitrogen, add Pd (OAc) then 2(2.5mg)/tricyclohexyl phosphine (6.5mg) and 2ml 20% (wt) Et 3NOH solution is heated to 80 ℃ of reaction 48h.Be cooled to after the room temperature mixed solution is added drop-wise to and carry out sedimentation in the 250ml methyl alcohol.Suction filtration, methanol wash, drying.With the toluene dissolving, join in the aqueous solution of Thiocarb then, then mixed solution is heated to 80 ℃ of stirrings and spends the night.With the column chromatography of organic phase by aluminum oxide, chlorobenzene drip washing.Organic solvent, methyl alcohol sedimentation are removed in decompression.Suction filtration, the gained solid extracted three days with the acetone Soxhlet.The methyl alcohol sedimentation, suction filtration.Taking out under the vacuum pump spends the night obtains product, and productive rate 80%.Molecular weight (GPC, THF, R.I): Mn=263700, Mw/Mn=4.02;
Embodiment 6
Present embodiment discloses the following silicon fluorenes tin porphyrin-quinoxaline organic semiconductor material of a kind of structure
Figure BSA00000306799000291
In the following formula, n=100;
Above-mentioned organic semiconductor material preparation process is as follows:
One, 5,8-two (tributyl tin)-2, two (phenyl) quinoxalines of 3-synthetic
Its preparation sees embodiment 1. for details
Two, 5-(9 '-hexadecyl-9 '-(3 "-methyl-4 "-laccerane oxygen base) benzene) silicon fluorenes-15-(9 '-(3 ", 5 "-two decyls) benzene-9 '-(3 "-octyl group-4 "-dodecyloxy) benzene) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000301
Put up the anhydrous and oxygen-free device, take by weighing intermediate 2-aldehyde-9-hexadecyl-9-(3 '-methyl-4 '-laccerane oxygen base) benzene silicon fluorenes (0.99g, 1mmol), 2-aldehyde-9-(3 ', 5 '-two decyls) benzene-9-(3 '-octyl group-4 '-dodecyloxy) benzene silicon fluorenes (0.94g, 1mmol), (0.30g 2mmol), is dissolved in the 250ml methylene dichloride two pyrroles's methane, feed nitrogen 30min, syringe adds trifluoroacetic acid 2ml, and 100 ℃ are stirred 1h down, add DDQ (DDQ) (1.82g then, 8mmol), continue at room temperature to stir 30min, add 2ml triethylamine cancellation reaction then, concentrated solvent, filter, collect filtrate and be spin-dried for solvent, with methylene dichloride drip washing fast on silicagel column, be spin-dried for solvent, to product, productive rate is about 74% with ether/recrystallizing methanol.
GC-MS(EI-m/z):2179(M +)
Three, 5,15-two bromo-10-(9 '-hexadecyl-9 '-(3 "-methyl-4 "-laccerane oxygen base) benzene) silicon fluorenes-20-(9 '-(3 ", 5 "-two decyls) benzene-9 '-(3 "-octyl group-4 "-dodecyloxy) benzene) silicon fluorenes porphyrin synthetic
Figure BSA00000306799000302
Put up the anhydrous and oxygen-free device, take by weighing 5-(9 '-hexadecyl-9 '-(3 "-methyl-4 "-laccerane oxygen base) benzene) silicon fluorenes-15-(9 '-(3 "; 5 "-two decyls) benzene-9 '-(3 "-octyl group-4 "-dodecyloxy) benzene) silicon fluorenes porphyrin (0.44g, 0.2mmol) be dissolved in the 80ml orthodichlorobenzene, add the 1ml pyridine, reactant is dropped to 0 ℃, adding N-bromo-succinimide (0.07g, 0.4mmol), behind the stirring 0.5h, mixture is warming up to 120 ℃, after continuing then to stir 1h, add 5ml acetone termination reaction, desolventizing, carry out recrystallization with ether/methyl alcohol and obtain product, productive rate 85%.
GC-MS(EI-m/z):2337(M +)
Four, 5,15-two bromo-10-(9 '-hexadecyl-9 '-(3 "-methyl-4 "-laccerane oxygen base) benzene) silicon fluorenes-20-(9 '-(3 ", 5 "-two decyls) benzene-9 '-(3 "-octyl group-4 "-dodecyloxy) benzene) silicon tin porphyrin synthetic
Figure BSA00000306799000311
N 2Under the atmosphere, take by weighing intermediate 5,15-two bromo-10-(9 '-hexadecyl-9 '-(3 "-methyl-4 "-laccerane oxygen base) benzene) silicon fluorenes-20-(9 '-(3 "; 5 "-two decyls) benzene-9 '-(3 "-octyl group-4 "-dodecyloxy) benzene) silicon fluorenes porphyrin (0.47g, 0.2mmol) be dissolved in the 50ml methylene dichloride, add and contain SnCl 2(0.11g, ethanolic soln 0.6mmol) (5ml) stirs 24h under the room temperature, is spin-dried for solvent, uses methylene dichloride/sherwood oil (1/1) drip washing on silicagel column then, collects and is spin-dried for solvent and obtain product, productive rate 95%.
GC-MS(EI-m/z):2451(M +)
Five, silicon fluorenes tin porphyrin-quinoxaline organic semiconductor material is synthetic
Figure BSA00000306799000321
Under nitrogen protection; add 5; 8-two (tributyl tin)-2; two (phenyl) quinoxalines of 3-(172mg, 0.2mmol), 5,15-two bromo-10-(9 '-hexadecyl-9 '-(3 "-methyl-4 "-laccerane oxygen base) benzene) silicon fluorenes-20-(9 '-(3 "; 5 "-two decyls) benzene-9 '-(3 "-octyl group-4 "-dodecyloxy) benzene) silicon fluorenes tin porphyrin (490mg; 0.2mmol) and glycol dinitrate ether solvents 80ml, vacuumize deoxygenation and charge into nitrogen, add 10mg Pd (PPh then 3) 4With 4ml K 2CO 3(5%) solution is heated to 80 ℃ of reaction 24h.Be cooled to after the room temperature mixed solution is added drop-wise to and carry out sedimentation in the 250ml methyl alcohol.Suction filtration, methanol wash, drying.With the toluene dissolving, join in the aqueous solution of Thiocarb then, then mixed solution is heated to 80 ℃ of stirrings and spends the night.With the column chromatography of organic phase by aluminum oxide, chlorobenzene drip washing.Organic solvent, methyl alcohol sedimentation are removed in decompression.Suction filtration, the gained solid extracted three days with the acetone Soxhlet.The methyl alcohol sedimentation, suction filtration.Taking out under the vacuum pump spends the night obtains product, and productive rate 72%.Molecular weight (GPC, THF, R.I): Mn=257400, Mw/Mn=3.98;
The present invention also provides structural formula to be
Figure BSA00000306799000322
(in the formula: n is the integer between 1-100, R 1, R 2, R 3, R 4Be H identical or inequality, C 1-C 32Alkyl, phenyl, contain one or more C 1-C 32Alkylbenzene or alkoxy benzene; M is metal ion, can but be not limited to Zn 2+, Cu 2+, Fe 2+, Co 2+, Cd 2+, Pt 2+, Zr 2+, Mn 2+, Ni 2+, Pb 2+, Sn 2+Deng) metalloporphyrin-quinoxaline organic semiconductor material at organic solar batteries, organic electroluminescent, organic field effect tube, organic optical storage, Application for Field such as organic non-linear device and organic laser apparatus.
Following examples be metalloporphyrin-quinoxaline organic semiconductor material at organic solar batteries, organic field effect tube, the application in the organic electroluminescence device.
Embodiment 7
Be the organic solar batteries device of active layer material with the metalloporphyrin among the embodiment 1-quinoxaline organic semiconductor material
A kind of organic solar batteries device, its structure as shown in Figure 1.Wherein, the substrate in the present embodiment adopts ito glass, and glass is as substrate, and ITO is as conductive layer.
The structure of this organic solar batteries device is: glass 11/ITO layer 12/PEDOT:PSS layer 13/ active coating 14/Al layer 15; Wherein, the material of active coating is mixture, comprises electron donor material, and PCBM is electron acceptor material; Electron donor material is material with the metalloporphyrin among the embodiment 1-quinoxaline organic semiconductor material, and electron acceptor material is [6,6] phenyl-C 61-methyl-butyrate (being called for short PCBM); ITO is that square resistance is the tin indium oxide of 10-20 Ω/mouth, and PEDOT is poly-(3,4-Ethylenedioxy Thiophene), and PSS is poly-(styrene sulfonic acid); Preferred square resistance is the ITO of 18 Ω/mouths.
This organic solar batteries preparation of devices process is: ito glass is through after the ultrasonic cleaning, handle with oxygen-Plasma, being coated with last layer at the ITO layer is the decorative layer of material with PEDOT:PSS, to be coated on the decorative layer after the organic semiconductor material among the present invention and the PCBM dissolving blend then, form active coating, evaporating Al layer on active coating again, obtain solar cell device, at last with after the epoxy encapsulation, place under 110 ℃ of air tight conditions and annealed 1.5 hours, drop to room temperature again, obtain the organic solar batteries device.Because after device was annealed, the chemical structure of material was more regular in order, has improved transmission speed and the efficient of current carrier, thereby has improved the photoelectric transformation efficiency of device.The thickness of preferred ITO, PEDOT:PSS layer, active coating, Al layer is respectively 140nm, 40nm, 140nm, 120nm.
Embodiment 8
Be the organic electroluminescence devices of material with the metalloporphyrin among the embodiment 1-quinoxaline organic semiconductor material
A kind of organic electroluminescence device, its structure is as shown in Figure 2; Substrate in the present embodiment adopts ito glass, and glass is as substrate, and ITO is as conductive layer.
The structure of this organic electroluminescence device is: glass 21/ITO layer 22/ luminescent layer 23/LiF buffer layer 24/Al layer 25; Wherein: luminescent layer is material with the metalloporphyrin among the embodiment 1-quinoxaline organic semiconductor material.
The preparation process of this organic electroluminescence device is:
Tin indium oxide (ITO) layer 22 in that surface deposition one deck square resistance of glass substrate 21 is 10-20 Ω/mouth forms the conductive layer as anode, and thickness is 50-300nm; Preferred square resistance is the ITO of 10 Ω/mouths.
Be the luminescent layer 23 of material at ITO surface preparation one deck with the metalloporphyrin among the embodiment 1-quinoxaline organic semiconductor material by spin coating technique, thickness is about 50-300nm;
Vacuum evaporation LiF on luminescent layer, as buffer layer 14, thickness is about 0.3-2nm;
Vacuum evaporation metallic aluminium on described luminescent layer forms the metal aluminium lamination 25 as negative electrode, obtains described organic electroluminescence device.
Embodiment 9
Be the organic field effect tube of material with metalloporphyrin-quinoxaline organic semiconductor material of containing among the embodiment one among the embodiment one
A kind of organic field effect tube, its structure is as shown in Figure 3; Substrate in the present embodiment adopts doped silicon wafer (Si) as substrate.
The structure of this organic field effect tube is: the SiO that Si 31/450nm is thick 2Insulation layer 32/ is used for modifying SiO 2Octadecyl trichlorosilane (OTS) layer 33/ organic semiconductor layer 34/ be source electrode (S) 35 and the drain electrode (D) 36 of material with the gold; Wherein, organic semiconductor layer is material with the metalloporphyrin among the embodiment 1-quinoxaline organic semiconductor material; Wherein, source electrode (S) and drain electrode (D) material also can be selected copper material for use.
The preparation process of this organic field effect tube is:
At first, apply the thick SiO of one deck 450nm on a surface cleaning doped silicon wafer 31 later 2Insulation layer 32; Secondly, at described SiO 2Apply the octadecyl trichlorosilane layer 33 that one deck plays modification on the insulation layer, thickness is 10-200nm; Then, spin coating one deck is the organic semiconductor layer 34 of material with the metalloporphyrin among the embodiment 1-quinoxaline organic semiconductor material on described octadecyl trichlorosilane layer, and thickness is about 50-300nm; At last, described organic semiconductor layer be arranged at intervals with the gold but be not limited only to source electrode (S) 35 and the drain electrode (D) 36 that gold is material, obtain described organic field effect tube.
Should be understood that above-mentioned statement at preferred embodiment of the present invention is comparatively detailed, can not therefore think the restriction to scope of patent protection of the present invention, scope of patent protection of the present invention should be as the criterion with claims.

Claims (9)

1. metalloporphyrin-quinoxaline organic semiconductor material with following general formula (I):
Figure FDA00003010450400011
In the formula: n is the integer between 1-100, R 1, R 2, R 3, R 4Be H identical or inequality, C 1-C 32Alkyl, phenyl or contain one or more C 1-C 32The phenyl of alkyl or the phenyl of alkoxyl group; M is configuration metal ions Zn 2+, Cu 2+, Fe 2+, Co 2+, Cd 2+, Pt 2+, Zr 2+, Mn 2+, Ni 2+, Pb 2+Or Sn 2+In a kind of.
2. the preparation method of metalloporphyrin-quinoxaline organic semiconductor material is characterized in that, described preparation method comprises the steps:
Step S1, with two pyrroles's methane (A), the first silicon fluorene derivatives (B) and the second silicon fluorene derivatives (C) in molar ratio i:j:k be dissolved in first organic solvent that contains oxygenant and first catalyzer, and under 20-100 ℃, reacted 1-24 hour, obtain silicon fluorenes derivatives of porphyrin (D), wherein, i:j:k=2:1:1; Reaction formula is as follows:
Figure DEST_PATH_FDA00002934748800021
In the formula, R 1, R 2, R 3, R 4Be H identical or inequality, C 1-C 32Alkyl, phenyl or contain one or more C 1-C 32The phenyl of alkyl or the phenyl of alkoxyl group;
Step S2, with the silicon fluorenes derivatives of porphyrin (D) that obtains among the step S1 and bromizating agent in molar ratio 1:2~1:5 be dissolved in second organic solvent, in 0~120 ℃ of reaction 1~72 hour down, obtain dibromo silicon fluorenes derivatives of porphyrin (E); Reaction formula is as follows:
Figure FDA00003010450400022
Step S3, the dibromo silicon fluorenes derivatives of porphyrin (E) that obtains among the step S2 is dissolved in the 3rd organic solvent, then add and contain the M metal ion solution, stirred 0.5-24 hour down in 0-30 ℃, obtain dibromo silicon fluorenes metal porphyrin derivative (F), wherein, the mol ratio of described dibromo silicon fluorenes derivatives of porphyrin (E) and M metal ion is 1:1~1:5; The M metal ion is Zn 2+, Cu 2+, Fe 2+, Co 2+, Cd 2+, Pt 2+, Zr 2+, Mn 2+, Ni 2+, Pb 2+Or Sn 2+In a kind of; Reaction formula is as follows:
Figure FDA00003010450400031
In step S4, the oxygen-free environment, with the dibromo silicon fluorenes metal porphyrin derivative (F) and 5 that obtains among the step S3,8-two (tributyl tin)-2, two (phenyl) quinoxalines (G) of 3-1:2~2:1 in molar ratio are dissolved in the 4th organic solvent that contains second catalyzer, under 50-120 ℃, carry out the Stille coupling reaction 12~72 hours, and obtained described metalloporphyrin-quinoxaline organic semiconductor material (I); Reaction formula is as follows:
Figure FDA00003010450400032
In the formula, n is the integer between 1-100.
3. preparation method according to claim 2 is characterized in that, among the described step S1, described first catalyzer is propionic acid, trifluoroacetic acid; Described oxygenant is DDQ; Described first organic solvent is one or both in trichloromethane, the methylene dichloride.
4. preparation method according to claim 2 is characterized in that, among the described step S2, described bromizating agent is the N-bromo-succinimide; Described second organic solvent is at least a in tetrahydrofuran (THF), chloroform or the orthodichlorobenzene.
5. preparation method according to claim 2 is characterized in that, among the described step S3, described the 3rd organic solvent is at least a in methylene dichloride, trichloromethane, tetrahydrofuran (THF), benzene or the toluene; The solvent that contains the M metal ion solution is at least a in methyl alcohol, ethanol or the water.
6. preparation method according to claim 2 is characterized in that, among the described step S4, described second catalyzer is the mixture of organic palladium or organic palladium and organophosphorus ligand; The mole dosage of described second catalyzer is 5,8-two (tributyl tin)-2, the 0.01%-20% of two (phenyl) quinoxaline (G) mole dosage of 3-;
Described organic palladium is Pd 2(dba) 3, Pd (PPh 3) 4, Pd (OAc) 2Or Pd (PPh 3) 2Cl 2
Described organophosphorus ligand is P (o-Tol) 3, tricyclohexyl phosphine;
Described the 4th organic solvent is at least a in tetrahydrofuran (THF), methylene dichloride, chloroform, dioxane, glycol dimethyl ether, dimethyl sulfoxide (DMSO), benzene, chlorobenzene or the toluene.
7. preparation method according to claim 2 is characterized in that, and is described 5 among the described step S4,8-two (tributyl tin)-2, and two (phenyl) quinoxalines (G) of 3-adopt following steps to make:
Step S41, with diphenylthanedione (S) and 1, the dibromo O-Phenylene Diamine of 4-(X) adds in the 5th organic solvent with mol ratio 1:5~5:1, and under 20 ° of C-120 ° of C the reaction 1-24 hour, obtain 5,8-dibromo 2,3-two (phenyl) quinoxaline (Y), reaction formula is as follows:
Figure FDA00003010450400041
Step S42: with above-mentioned 5,8-dibromo 2,3-hexichol quinoxaline (Y) is dissolved in the 6th organic solvent, is cooled to-30 ℃ with liquid nitrogen/Virahol subsequently, drips n-Butyl Lithium, at-30 ℃ of reaction 1-3h, adds SnBu more then 3Cl is warming up to room temperature then naturally at-30 ℃ of reaction 0.5-2h, reacts 3-36 hour, obtain described 5,8-two (tributyl tin)-2,3-pair of (phenyl) quinoxalines (G); Reaction formula is as follows:
8. preparation method according to claim 7, it is characterized in that, be at least a in acetic acid, m-cresol, tosic acid, chloroform, methyl alcohol, ethanol or the butanols in described the 5th organic solvent, the 6th organic solvent is at least a in tetrahydrofuran (THF), ether or the dioxane; Described 5,8-dibromo 2,3-hexichol quinoxaline (Y) and SnBu 3The mol ratio 1:1-10 of Cl.
9. metalloporphyrin-quinoxaline the organic semiconductor material that has following general formula (I) according to claim 1 is at organic solar batteries, organic electroluminescence device, organic field effect tube, organic optical storage, organic non-linear device and organic laser apparatus Application for Field.
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