## Abstract 2‐(2‐Thienyl)ethyl methacrylate (2TEMA, 1), 2‐(3‐thienyl)ethyl methacrylate (3TEMA,2) and 2‐(__N__‐pyrrolyl)ethyl methacrylate (PEMA, 3) were synthesized and copolymerized with methyl methacrylate (MMA) by radical initiation with AIBN. The reactivity ratios for the system MMA/2TEMA were
Polythiophene-graft-Styrene and Polythiophene-graft-(Styrene-graft-C60) Copolymers
✍ Scribed by Xiwen Chen; Bobak Gholamkhass; Xu Han; George Vamvounis; Steven Holdcroft
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 205 KB
- Volume
- 28
- Category
- Article
- ISSN
- 1022-1336
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Poly(3‐hexylthiophene) was quantitatively brominated and subsequently used in the Suzuki cross‐coupling with a boronic ester of a nitroxide to form a macroinitiator bearing a TEMPO group on each thienyl ring. This macroinitiator initiated the nitroxide‐mediated radical polymerization of styrene and 4‐chloromethylstyrene (CMS), and subsequently reacted with C~60~ to yield soluble graft, rod‐coil polymers. Films of the polymers display a bi‐continuous phase structure as revealed by AFM. Similar polymers, in which only a fraction of the thienyl units boasted C~60~‐bearing side chains, displayed optical properties representative of extensive π‐delocalization. The potential application of this methodology for the synthesis of graft polymers for photovoltaic devices is discussed.
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