The primary photochemical reaction step of unsubstituted indolino-spiropyrans
- 1 January 1990
- journal article
- Published by Walter de Gruyter GmbH in Pure and Applied Chemistry
- Vol. 62 (8) , 1483-1488
- https://doi.org/10.1351/pac199062081483
Abstract
The photochem. ring-opening of unsubstituted indolino-spiropyrans to the corresponding merocyanines in pentane, was followed by transient absorption spectroscopy. The temporal resoln. was better than 0.4 ps. During the pump pulse, an ultrafast unstructured absorption covered the entire measurement range 380-680 nm. From it emerged the structured absorption spectrum of a 1st merocyanine isomer, with typical time consts. in the range 0.9-1.4 ps. The transient merocyanine spectra are compared to the spectra which are obtained when the spiropyrans are irradiated at low temp. in argon. In conjunction with semiempirical calcns., the 1st merocyanine isomer is assigned a trans-trans-cis structureKeywords
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