Abstract
Photoreversible reactions of 1,4‐butanediol dicinnamylideneacetate(BCA) and its photocyclized compound (BCD), the model compounds for poly(vinyl cinnamylideneacetate), were studied. They exhibited an excellent photoreversibility in a rigid medium at 77°K. The quantum yield of dimerization in the rigid medium is much larger than that in the solution and approximately equal to that in polymer film. Poly(vinyl esters) of substituted cinnamylideneacetic acids also showed photoreversibility to various extents, depending on the substituent. Poly(vinyl α‐cyanocinnamylideneacetate) showed the best photoreversibility among the series, reflecting the least amount of side reaction upon the photodimerization.