Radical cyclopolymerization of 3-phenyl[5] ferrocenophane-1,5-dimethylene (2) and copolymerization with styrene gave polymers (3 and 4) with [3]ferrocenophane moieties pendant to the backbone. Cyclic voltammetry (CV) on polymer 3 in CH 2 Cl 2 showed two oxidation waves at 00.13 and /0.05 V (versus
Synthesis and Properties of 1,2-Dimethylene-3,5-cycloheptadiene
✍ Scribed by Mitsunori Oda; Shigeyasu Kuroda; Ichiro Shimao; Noboru Morita; Toyonobu Asao
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 166 KB
- Volume
- 113
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
The regioselective synthesis of dimethyl 1,3,5‐cyloheptatriene‐1,2‐dicarboxylate (4) was achieved by a ring expansion method, starting from dimethyl 1,3‐cyclohexadiene‐2,3‐dicarboxylate (5). The title compound 3 was obtained as an air‐sensitive oil by zinc‐copper reduction of 1,2‐bis(bromomethyl)cyclohepta‐1,3,5‐triene (10) to which the diester 4 was transformed.
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