Ju, SY Kwon, DI Min, SJ Ahn, KD Park, KH Kim, JM 2024-01-21T08:15:28Z 2024-01-21T08:15:28Z 2021-09-03 2003-08-21 1010-6030 https://pubs.kist.re.kr/handle/201004/138311 Acrylate- and styrene-derived polymers having pendant phenoxyquinones for photochromism were prepared by 2,2'-azoisobutyronitrile (AIBN)-initiated radical polymerization. Synthesis of the monomers were straightforward and the polymers were obtained in high yields in spite of the quinone moieties presented in the monomers, which usually can function as radical scavengers and/or catalysts poison. Photo-induced rearrangement from the "trans"-quinone forms to the "ana"-quinone forms readily occurred when the polymer films were irradiated with UV light. (C) 2003 Elsevier Science B.V. All rights reserved. English ELSEVIER SCIENCE SA AMPEROMETRIC TRANSDUCTION MONOLAYER-ELECTRODE Synthesis and photochromism of polymer-bound phenoxyquinone derivatives Article 10.1016/S1010-6030(03)00211-9 1 JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, v.160, no.3, pp.151 - 157 JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY 160 3 151 157 scie scopus 000184848400002 2-s2.0-0041302238 Chemistry, Physical Chemistry Article AMPEROMETRIC TRANSDUCTION MONOLAYER-ELECTRODE photochromism 1-phenoxynaphthacenequinone polymer radical polymerization