Thieno[2,3-f]benzofuran compounds and their polymers and applications of polymers

A technology of benzofuran and 3-f, which is applied in the field of organic optoelectronic material synthesis, can solve problems such as few reports, achieve great commercial prospects, good thermal stability, and improve solubility

Inactive Publication Date: 2016-01-13
CENT SOUTH UNIV
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Benzo[1,2-b; 3,4-b]difuran (BDF) is an important electron-donor unit, but its application as a donor unit in organic electronics after polymerization with other fused heterocyclic acceptor units There are not many reports in the field

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Thieno[2,3-f]benzofuran compounds and their polymers and applications of polymers
  • Thieno[2,3-f]benzofuran compounds and their polymers and applications of polymers
  • Thieno[2,3-f]benzofuran compounds and their polymers and applications of polymers

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] a) Thionyl chloride (65.3mL, 0.9mol) was added dropwise into a 500ml dry round-bottomed flask of furan-3-carboxylic acid (25.1g, 0.224mol), stirred and refluxed for 4 hours, then cooled to room temperature Finally, the solvent was spin-dried to obtain compound 1 as a colorless oil, which was used in the next step without further purification.

[0052] b) Compound 1 (29.24g, 224mmol) was added dropwise to a solution of diethylamine (92.6mL) in dichloromethane (100mL) at 0°C, and then the reaction mixture was warmed to room temperature and stirred for 1 hour. After cooling to room temperature, the mixture was poured into ice water, extracted with dichloromethane, the organic phase was washed twice with water, dried over anhydrous magnesium sulfate, and the solvent was spin-dried, and the crude product was passed through a silica gel column (eluted with ethyl acetate / petroleum ether (2:1 , V / V) is the eluent) to obtain compound 2 (7.5 g, 85%) as an orange-red oil. 1 HNMR ...

Embodiment 2

[0058] The synthesis method of thieno[2,3-f]benzofuran compound is as in Example 1.

[0059] Polymer (PTBFDTBTz) was prepared by Stille reaction: under nitrogen protection, M1 (0.134g, 0.151mmol) and N-octyl-4,7-dithienyl-benzotriazole dibromide (0.0838g, 0.151g) Add to 10mL of anhydrous toluene and 2ml of DMF, then add Pd(PPh 3 ) 4 (10mg), stirred and reacted at 110°C for 24 hours, cooled to room temperature, poured into 100mL methanol for precipitation, filtered, extracted with methanol, n-hexane, and chloroform sequentially in a Soxhlet extractor, recovered the chloroform solution, and spin-dried Add a small amount of chloroform to dissolve the excess solvent, pour it into a centrifuge tube, add methanol to make it chromatographically, pour off the upper clear night after high-speed centrifugation, and repeat several times to obtain the target polymer PTBFDTBTz (91mg, 62%). m n = 2.8 kDa; M w = 21.88 kDa; PDI = 7.8. Anal. Calcdfor (C 58 h 69 N 3 OS 5 )n (%): C, 70....

Embodiment 3

[0061] The synthesis method of thieno[2,3-f]benzofuran polymer is as in Example 1.

[0062] Polymer (PTBFDTBO) was prepared by Stille reaction: under nitrogen protection, M1 (0.1359g, 0.153mmol) and 5,6-dioctyloxy-4,7-dithienyl-benzoxadiazole dibromide (0.1068 g, 0.153mmol) was added to 10mL of anhydrous toluene and 2 ml of DMF, and then Pd (PPh 3 ) 4 (10mg), stirred and reacted at 110°C for 24 hours, cooled to room temperature, poured into 100mL methanol for precipitation, filtered, extracted with methanol, n-hexane, and chloroform sequentially in a Soxhlet extractor, recovered the chloroform solution, and spin-dried Add a small amount of chloroform to dissolve the excess solvent and pour it into a centrifuge tube, add methanol to make it chromatographically come out, pour off the upper layer after high-speed centrifugation, and repeat several times to obtain the target polymer PTBFDTBO (89mg, yield 52%) . m n = 524.1 kDa; M w = 1011.5 kDa; PDI = 1.9. Anal. Calcdfor (C ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
energy conversion efficiencyaaaaaaaaaa
Login to view more

Abstract

The invention discloses a thieno[2,3-f]benzofuran compound and its polymer and the application of the polymer. The thieno[2,3-f]benzofuran compound is combined with benzothiadiazole, benzofuran Monomers such as triazole and benzoxadiazole synthesized a series of polymers with thieno[2,3-f]benzofuran compound unit structure through Stille coupling polymerization method, the thermal stability and electrical stability of the polymers With good chemical properties, it can be mixed with commonly used fullerene and organic acceptor substances to prepare polymer solar cells with high photoelectric conversion efficiency. The photoelectric conversion efficiency of single-layer polymer solar cell devices is as high as 6.4%. The polymer material is used in solar cells There are huge commercial prospects in the application of .

Description

technical field [0001] The invention relates to a thieno[2,3-f]benzofuran compound and its polymer and the application of the polymer, and belongs to the field of organic photoelectric material synthesis. Background technique [0002] In recent years, conjugated polymers containing benzo[1,2-b; 3,4-b]dithiophene (BDT) groups as donors have shown excellent photovoltaic performance. Yang Yang, Wu Hongbin, Hou Jianhui and others synthesized a series of conjugated polymers based on BDT. These polymers have very good photoelectric properties. The highest power conversion efficiency (PCE) of the reported tandem device solar cell is 10.6%, but based on The stability of BDT material is slightly lacking, and there are many layers of stacked devices, and the process is relatively complicated. [(1) Z.He, C.Zhong, S.Su, M.Xu, H.Wu, Y.Cao, Nature Photonics2012, 6, 591; (2) L.Dou, J.You, J.Yang, C.- C. Chen, Y. He, S. Murase, T. Moriarty, K. Emery, G. Li, Y. Yang, Nature Photonics 2012,...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): C07D495/04C08G61/12H01L51/46
CPCC07D495/04C08G61/123C08G61/125C08G61/126C08G2261/3246C08G2261/3245C08G2261/3242C08G2261/3241C08G2261/3243C08G2261/91H10K85/113Y02E10/549Y02P70/50
Inventor 邹应萍樊令郭秀萍崔锐利蒋历辉江文辉
Owner CENT SOUTH UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap