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Journal ArticleDOI

Photophysics, photochemistry and kinetics of photochromic 2H-pyrans and chromenes

Christian Lenoble, +1 more
- 01 May 1986 - 
- Vol. 33, Iss: 2, pp 187-197
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TLDR
In this paper, photochromism of coumarin-substituted chromenes (xanthyletin and seselin) was observed in about 800 ns.
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This article is published in Journal of Photochemistry.The article was published on 1986-05-01. It has received 86 citations till now. The article focuses on the topics: Triplet state.

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Citations
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Journal ArticleDOI

Photoprocesses in Spiropyran-Derived Merocyanines

TL;DR: The photophysical and photochemical properties of a series of spiro[2H-1-benzopyran-2,2‘-indoline] compounds were studied by nanosecond laser photolysis in solution as discussed by the authors.
Journal ArticleDOI

Kinetic and structural studies of the photochromic process of 3H-naphthopyrans by UV and NMR spectroscopy

TL;DR: The photomerocyanines resulting from the UV irradiation of closed colourless 3,3-diphenyl-3H-naphtho[2,1-b]pyran and its 3, 3-bis(4-fluorophenyl) derivative have been studied by UV-VIS and NMR spectroscopy as discussed by the authors.
Journal ArticleDOI

NMR Kinetic Investigations of the Photochemical and Thermal Reactions of a Photochromic Chromene

TL;DR: The photochromic behavior of 2,2-di(4-fluorophenyl)-6-methoxy-2H-1-chromene has been investigated by 19F NMR spectroscopy and it has been shown that, among the 12 possible isomerization processes, only some paths were active.
Journal ArticleDOI

Spectrokinetic study of 2,2-diphenyl-5,6-benzo(2H)chromene: a thermoreversible and photoreversible photochromic system

TL;DR: In this article, the photochromic reaction of the 2,2-diphenyl-5,6-benzo(2H)chromene is investigated by spectrophotometric methods using monochromatic irradiation wavelengths in the UV and visible ranges.
References
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Journal ArticleDOI

The spectroscopy and photochemistry of naturally occurring and synthetic chromenes.

TL;DR: All naturally occurring and synthetic chromenes studied exhibit photochromism at — 196°C and in some cases at room temperature, and Lapachenole (a 7,8‐benzochromene) shows the most rapid and highest percentage conversion to the colored form and no emission.
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