• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Symmetrical imines having a molecular structure according to Formula (1): wherein the core (X) is a five-membered thiadiazole ring; andwherein the side chains (R) are triphenylamine derivatives.
    公开号:EP3689856A1
    申请号:EP19182458.0
    申请日:2019-06-26
    公开日:2020-08-05
    发明作者:Krzysztof Artur Bogdanowicz；Agnieszka Iwan
    申请人:Wojskowy Instytut Techniki Inzynieryjnej Im Profesora Jozefa Kosackiego；
    IPC主号:C07D285-00
    专利说明:
    [0001] The present invention relates to symmetrical imines and a method of synthesizing symmetrical imines. The symmetrical imines can be applied in particular in photovoltaic devices and solar cells. BACKGROUND
    [0002] Compounds containing imine groups exhibit properties that make them applicable in organic photovoltaic cells (also called solar cells). Organic solar cells are an alternative to the most prevalent silicon-based solar cells.
    [0003] The structure of a solar cell is built via application of thin films made of polymers and block copolymers, such as poly(3-hexylthiophene-2,5-diyl), poly(3,4-ethylenedioxythiophene), doped poly(styrene sulfonate) or poly(3,4-ethylenedioxythiophene) as conductors and semiconductors. Other small-molecule compounds, such as fullerenes or their derivatives, can be added to these layers.
    [0004] Various publications, including: "Synthesis, spectroscopy, and electrochemical investigation of new conjugated polymers containing thiophene and 1,3,4-thiadiazole in the main chain" (by P.S. Patil et al. J Appl Polymer Sci 2012, Vol. 125, 1882-1889) "Bent Shaped 1,3,4-Oxadiazole/Thiadiazole heterocyclic rings containing liquid crystals" (by C. Selvarasu et al. J. Chem. Sci. 2015, Vol. 127, No. 10, pp. 1831-1838) "SYNTHESIS, CHARACTERIZATION AND EVALUATION OF ANTICANCER ACTIVITY OF SOME NEW SCHIFF BASES OF 1, 3, 4-THIADIAZOLE DERIVATIVES" (by A. Naskar et al. Int J Pharm Pharm Sci 2015, Vol 7, Issue 3, 397-402) "Synthesis and Characterization of Novel 1,3,4-Oxadiazole- or 1,3,4-Thiadiazole-Containing Wholly Conjugated Polyazome-thines" (by Y. Saegusa et al. J. Appl. Polym. Sci. Part A: Polym. Chem. 1990, Vol. 28, pp. 3647-3659) present methods of obtaining asymmetric azomethines or systems containing thiadiazole structures via multi-stage reactions. However, that prior art does not provide examples of the use of these compounds in photovoltaic devices. There are no known examples of symmetrical imines containing thiadiazole groups and the method of obtaining thereof.SUMMARY
    [0005] The present invention relates to symmetrical imines having a molecular structure according to Formula (1)
    [0006] The core (X) may have the formula:
    [0007] The side chains (R) may have the formula:
    [0008] The substituent (Y) can be H or CH3.
    [0009] The present invention also relates to a method of synthesizing symmetrical imines according to Formula (1), the method comprising the steps of: in an inert gas atmosphere, adding a five-membered thiadiazole ring compound (X) to a dimethylacetamide solution comprising triphenylamine derivatives (R), in a presence of acidic catalyst; conducting a reaction in a temperature range from 140°C to 185°C for a period from 24 to 72 hours; pouring the obtained mixture to water; washing the obtained raw product first with ethanol and afterwards with acetone; recrystalising the washed product in a cold mixture of acetone and hexane; filtering off and drying the recrystalized product.
    [0010] The five-membered thiadiazole ring compound (X) may a form of a diamine.
    [0011] The triphenylamine derivatives (R) may have a form of an aldehyde.
    [0012] The inert gas can be nitrogen or argon.
    [0013] The temperature of acetone and hexane is preferably from 1°C to 4°C and the ratio of acetone: hexane is preferably from 1:10 to 7:10.
    [0014] Consequently, the method allows for a single-stage synthesis of symmetric imines, short reaction time and simple purification process, which significantly reduces the production cost, when compared to other imines. The method also allows to obtain symmetric imines that have layer-forming properties. Another advantage of the method is a simplified production process for solar cells due to the symmetric imines being applied directly from the solution, forming a thin film. Typically, solar cells that comprise organic compounds acting as electron donor or acceptor materials are made using various printing methods, i.e. roll-to-roll printing process. For this reason, active organic compounds are processed in form of inks capable of forming continuous coatings. Hence, the new organic compounds need to meet this requirement. DETAILED DESCRIPTION
    [0015] The invention will be presented by means of detailed embodiments. First embodiment
    [0016] 0.005 mole of 4-(diphenylamino)benzaldehyde was added to 12 cm3 of dimethylacetamide solution containing 0.002 mole of 3,5-diamino-1,2,4-thiadiazole and 10 mol% of p-Tolueneosulfonic acid in an argon atmosphere. The reaction was carried out at a temperature of 170°C for 24 hours. Then, the obtained mixture was poured into 100 cm3 of water. The formed product was filtered off and first washed with 30 cm3 of ethanol and then with 5 cm3 of acetone. Next, the product was recrystalized in a cold mixture of acetone and hexane (having a temperature of 4°C), in a volumetric proportion of acetone:hexane of 3:10. Following the recrystallisation, the product was filtered off and dried for 24 hours at a temperature of 60°C. Second embodiment
    [0017] 0.005 mole of 4-(ditolylamino)benzaldehyde was added to 12 cm3 dimethylacetamide solution containing 0.002 mole of 3,5-diamino-1,2,4-thiadiazole and 10 mol% of p-Tolueneosulfonic acid in an argon atmosphere. The reaction was carried out at a temperature of 170°C for 48 hours. Then, the obtained mixture was poured into 100 cm3 of water. The formed product was filtered off and first washed with 30 cm3 of ethanol and then with 5 cm3 of acetone. Next, the product was recrystalized in a cold mixture of acetone and hexane (having a temperature of 4°C), in a volumetric proportion of acetone:hexane of 3:10. Following the recrystallisation, the product was filtered off and dried for 24 hours at the temperature of 60°C. Third embodiment
    [0018] 0.005 mole of 4-(diphenylamino)benzaldehyde was added to 12 cm3 of dimethylacetamide solution containing 0.002 mole of 3,5-diamino-1,3,4-thiadiazole and 10 mol% of p-Tolueneosulfonic acid in an argon atmosphere. The reaction was carried out at a temperature of 170°C for 72 hours. Then, the obtained mixture was poured into 100 cm3 of water. The formed product was filtered off and first washed with 30 cm3 of ethanol and then with 5 cm3 of acetone. Next, the product was recrystalized in a cold mixture of acetone and hexane (having a temperature of 4°C), in a volumetric proportion of acetone:hexane of 3:10. Following the recrystallisation, the product was filtered off and dried for 24 hours at the temperature of 60°C. Fourth embodiment
    [0019] 0.005 mole of 4-(ditolylamino)benzaldehyde was added to 12 cm3 of dimethylacetamide solution containing 0.002 mole of 3,5-diamino-1,3,4-thiadiazole and 10 mol% of p-Tolueneosulfonic acid in an argon atmosphere. The reaction was carried out at a temperature of 175°C for 24 hours. Then, the obtained mixture was poured into 100 cm3 of water. The formed product was filtered off and first washed with 30 cm3 of ethanol and then with 5 cm3 of acetone. Next, the product was recrystalized in a cold mixture of acetone and hexane (having a temperature of 4°C), in a volumetric proportion of acetone:hexane of 3:10. Following the recrystallisation, the product was filtered off and dried for 24 hours at the temperature of 60°C.
    [0020] Table 1 presents a molecular formula, molecular mass and reaction yield for the obtained symmetric imines with the thiadiazole core having the Formula (1), wherein the side chains (R) contain triphenylamine-derivatives. Table 1 Core (X) R Substituent (Y) Yield [%] Molecular formula (molecular mass) 1,2,4-thiadiazole 4-(diphenylamino)fenylo- -H 33 C40H30N6S 626.77 1,2,4-thiadiazole 4-(ditolylamino) fenylo- -CH3 44 C44H38N6S 682.88 1,3,4-thiadiazole 4-(diphenylamino)fenylo- -H 31 C40H30N6S 626.77 1,3,4-thiadiazole 4-(ditolylamino) fenylo- -CH3 34 C44H38N6S 682.88
    [0021] Table 2 presents examples of 1H NMR spectra for symmetric imines with thiadiazole core with the Formula (1), wherein the side chains (R) contain triphenylamine-derivatives. Table 2 Core (X) R Substituent (Y) Signals 1H NMR [δ, ppm] 1,2,4-thiadiazole 4-(diphenylamino) fenylo- -H 8.31 (2H, d, -HC=N-); 7.65-7.55 (8H, m, arom. -Ph-); 7.4-7.0 (20 H, arom. -Ph) 1,2,4-thiadiazole 4-(ditolylamino) phenylo- -CH3 8.31 (2H, d, -HC=N-); 7.65-755 (8H, m, arom. -Ph-); 7.4-7.0 (16 H, arom. -Ph-); 2.35 (12H, t, -CH3) 1,3,4-thiadiazole 4-(diphenylamino) phenylo- -H 8.56 (2H, s, -HC=N-); 7.65-7.55 (8H, m, arom. -Ph-); 7.4-7.0 (20 H, arom. -Ph) 1,3,4-thiadiazole 4-(ditolylamino) phenylo- -CH3 8.55 (2H, s, -HC=N-); 7.75-7.55 (8H, m, arom. -Ph-); 7.2-6.90 (16 H, arom. -Ph-); 2.35 (12H, s, -CH3)
    权利要求:
    Claims (6)
    [0001] Symmetrical imines having a molecular structure according to Formula (1):
    [0002] A method of synthesizing symmetrical imines according to Formula (1):
    [0003] The method according to claim 2, wherein the five-membered thiadiazole ring compound (X) has a form of a diamine.
    [0004] The method according to any of claims 2-3, wherein the triphenylamine derivatives (R) have a form of an aldehyde.
    [0005] The method according to any of claims 2-4, wherein the inert gas is nitrogen.
    [0006] The method according to any of claims 2-4, wherein the inert gas is argon.
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    PL428808A1|2020-08-10|
    EP3689856B1|2021-06-02|
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