Microwave assisted synthesis of bithiophene based donor-acceptor-donor oligomers and their optoelectronic performances

被引:4
|
作者
Bathula, Chinna [1 ,2 ]
Buruga, Kezia [3 ]
Lee, Sang Kyu [4 ]
Khazi, Imtiyaz Ahmed M. [5 ]
Kang, Youngjong [1 ,2 ]
机构
[1] Hanyang Univ, Res Inst Nat Sci, Dept Chem, Seoul 133791, South Korea
[2] Hanyang Univ, Inst Nanosci & Technol, Seoul 133791, South Korea
[3] Natl Inst Technol, Dept Chem Engn, Surathkal 575025, Karnataka, India
[4] Korea Res Inst Chem Technol, Energy Mat Res Ctr, 141 Gajeong Ro, Daejeon 305600, South Korea
[5] Karnatak Univ, Dept Chem, Dharwad 580003, Karnataka, India
关键词
Thiadiazolo [3,4-cjpyridine; Bithiophene; Optoelectronics; Suzuki reaction; UV-visible studies; ORGANIC SOLAR-CELLS; NON-FULLERENE; SMALL MOLECULES; EFFICIENT; PHOTOVOLTAICS;
D O I
10.1016/j.molstruc.2017.03.033
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this article we present the synthesis of two novel bithiophene based symmetrical pi conjugated oligomers with donor-acceptor-donor (D-A-D) structures by microwave assisted PdCl2(dppf) catalyzed Suzuki coupling reaction. These molecules contain electron rich bithiophene as a donor, dithienothiadiazole[3,4-c]pyridine and phthalic anhydride units as acceptors. The shorter reaction time, excellent yields and easy product isolation are the advantages of this method. The photophysical prerequisites for electronic application such as strong and broad optical absorption, thermal stability, and compatible energy levels were determined for synthesized oligomers. Optical band gap for the oligomers is found to be 1.72-1.90 eV. The results demonstrated the novel oligomers to be promising candidates in organic optoelectronic applications. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 129
页数:5
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