Direct access to 4,8-functionalized benzo[1,2-b:4,5-b′]dithiophenes with deep low-lying HOMO Levels and high mobilities

被引:36
作者
Zhu, Enwei [1 ]
Ge, Guidong [1 ]
Shu, Jingkun [2 ]
Yi, Mingdong [2 ]
Bian, Linyi [1 ]
Hai, Jiefeng [1 ]
Yu, Jiangsheng [1 ]
Liu, Yun [1 ]
Zhou, Jie [1 ]
Tang, Weihua [1 ]
机构
[1] Nanjing Univ Sci & Technol, Key Lab Soft Chem & Funct Mat, Nanjing 210094, Jiangsu, Peoples R China
[2] Nanjing Univ Posts & Telecommun, Inst Adv Mat, Key Lab Organ Elect & Informat Displays, Nanjing 210046, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
BANDGAP CONJUGATED POLYMERS; DITHIOPHENE-BASED POLYMERS; OPEN-CIRCUIT VOLTAGE; SOLAR-CELLS; PHOTOVOLTAIC PERFORMANCE; SEMICONDUCTING POLYMERS; COPOLYMERS; DESIGN; BENZODITHIOPHENE; UNITS;
D O I
10.1039/c4ta01226g
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
A general methodology has been proposed for the straightforward access to 4,8-functionalized benzo[1,2-b:4,5-b']dithiophenes (BDTs) via Pd mediated coupling reactions including Suzuki-Sonogashira coupling and carbon-sulfur bond formation reactions. This versatile platform can be used to construct a library of BDT core centred conjugated systems, featuring large fused-ring structure and good charge mobility, where a hole mobility of 0.061 cm(2) V-1 s(-1) is demonstrated. With the energy level fine-tuned with functionalization, the charge transporting BDTs show great potential for donor-acceptor polymers.
引用
收藏
页码:13580 / 13586
页数:7
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