Synthesis, reactivity, and optoelectronic properties of poly(3-alkenylthiophene) diblock copolymers

被引:20
作者
Bhatt, Mahesh P. [1 ]
Huynh, Martin K. [1 ]
Sista, Prakash [1 ]
Nguyen, Hien Q. [1 ]
Stefan, Mihaela C. [1 ]
机构
[1] Univ Texas Dallas, Dept Chem, Richardson, TX 75080 USA
基金
美国国家科学基金会;
关键词
atomic force microscopy (AFM); conjugated polymers; copolymerization; diblock copolymers; organic field-effect transistors; poly(3-alkenylthiophene); poly(3-hexylthiophene); semiconducting polymers; REGIOREGULAR POLY(3-HEXYLTHIOPHENE); BLOCK-COPOLYMERS; ELECTRICAL-CONDUCTIVITY; POLYTHIOPHENE; POLY(3-ALKYLTHIOPHENES); MOBILITY; POLYMERIZATION; ELECTROLUMINESCENCE; PERFORMANCE; CELLS;
D O I
10.1002/pola.26095
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(3-hexylthiophene)-b-poly(3-pentenylthiophene) and poly(3-hexylthiophene)-b-poly(3-undecenylthiophene) diblock copolymers have been synthesized by McCullough method. X-ray diffraction analysis of the diblock copolymers displayed all the reflection peaks specific to regioregular poly(3-hexylthiophene), indicating that the presence of poly(3-alkenylthiophene) block does not affect the packing of the polymer in the solid state. The synthesized diblock copolymers were subjected to hydroboration/oxidation and hydrosilation to demonstrate the reactivity of the alkenyl substituents. Furthermore, poly(3-hexylthiophene)-b-poly(3-pentenylthiophene) was used as a chain transfer agent for the ruthenium-catalyzed ring-opening metathesis polymerization of cyclooctene to generate a polycyclooctene graft copolymer, which was hydrogenated to give poly(3-hexylthiophene)-b-poly(3-pentenylthiophene-g-polyethylene). The opto-electronic properties and the morphology of the synthesized polymers have been investigated. (c) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012
引用
收藏
页码:3086 / 3094
页数:9
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