Silyl-substituted poly(thienylenevinylene) via heteroaromatic dehydrohalogenation polymerization
A long alkylsilyl group was attached to a thiophene ring system to overcome the instability of 2.5 bis(halomethyl) thiophene monomers, by imparting steric hindrance and electronic delocalization. The resulting stable monomer could be used directly to prepare low band gap poly(thienylenevinylene) (1.57 eV) through heteroaromatic dehydrohalogenation polymerization.
- Publisher
- WILEY-V C H VERLAG GMBH
- Issue Date
- 2003-05
- Language
- English
- Article Type
- Article
- Citation
MACROMOLECULAR RAPID COMMUNICATIONS, v.24, pp.522 - 526
- ISSN
- 1022-1336
- Appears in Collection
- CH-Journal Papers(저널논문)
- Files in This Item
- There are no files associated with this item.
This item is cited by other documents in WoS
| ⊙ Detail Information in WoSⓡ | Click to see |  |
| ⊙ Cited 8 items in WoS | Click to see citing articles in |  |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.