Abstract
Silylene-phenylene and silylene-thienylene copolymers were prepared by the reactions of α,ω-dichloropermethylated oligosilanes with 1,4-dilithiobenzene and 2,5-dilithiothiophene respectively. All the copolymers were soluble in a wide range of organic solvents. The influence of the chain length of the dimethylsilylene unit in the copolymer backbone on the electronic absorption spectra was investigated. The enhancement of σ-π conjugations between the dimethylsilylene units and the π-conjugated units with increasing dimethylsilylene chain length was suggested by the thermochromism.
Original language | English |
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Pages (from-to) | 15-22 |
Number of pages | 8 |
Journal | Journal of Organometallic Chemistry |
Volume | 489 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 1995 Mar 8 |
Keywords
- Conjugation
- Lithium
- Silicon
- Silylene-phenylene
- Silylene-thienylene
- Thermochromism
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry