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Ernsting, N. P. ; Dick, Bernhard ; Arthen-Engeland, T.

The primary photochemical reaction step of unsubstituted indolino-spiropyrans

Ernsting, N. P., Dick, Bernhard and Arthen-Engeland, T. (1990) The primary photochemical reaction step of unsubstituted indolino-spiropyrans. Pure and Applied Chemistry 62 (8), pp. 1483-1488.

Date of publication of this fulltext: 05 Aug 2009 13:50
Article
DOI to cite this document: 10.5283/epub.5539


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, ...

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 structure.



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Details

Item typeArticle
Journal or Publication TitlePure and Applied Chemistry
Publisher:International Union of Pure and Applied Chemistry
Volume:62
Number of Issue or Book Chapter:8
Page Range:pp. 1483-1488
Date1990
Additional Information (public)CAN 113:181179 74-1 Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes 2016-67-3; 51870-76-9 Role: USES (Uses) (MNDO calcns. of, in ground state, primary photochem. processes of photochromic indolino-spiropyrans in relation to); 1485-92-3; 1592-43-4 Role: RCT (Reactant), RACT (Reactant or reagent) (photochem. reactions of, primary processes in)
InstitutionsChemistry and Pharmacy > Institut für Physikalische und Theoretische Chemie > Chair of Chemistry III - Physical Chemistry (Molecular Spectroscopy and Photochemistry) > Prof. Dr. Bernhard Dick
Identification Number
ValueType
1990:581179Other
10.1351/pac199062081483DOI
KeywordsPhotochromism (of indolino-spiropyrans, primary photochem. reactions in); Ultraviolet and visible spectra (of transient products, in primary processes of photolysis of indolino-spiropyrans); Photolysis (laser-induced, of unsubstituted indolino-spiropyrans, primary processes in); photolysis indolino spiropyran merocyanine formation; photochromism indolino spiropyran
Dewey Decimal Classification500 Science > 540 Chemistry & allied sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgNo
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-55391
Item ID5539

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