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光异构化的中等依赖双机制情况:一键翻转和呼啦圈扭转。

The case of medium-dependent dual mechanisms for photoisomerization: one-bond-flip and hula-twist.

作者信息

Liu R S, Hammond G S

机构信息

Department of Chemistry, University of Hawaii, 2545 The Mall, Honolulu, HI 96822, USA.

出版信息

Proc Natl Acad Sci U S A. 2000 Oct 10;97(21):11153-8. doi: 10.1073/pnas.210323197.

Abstract

This paper critically reviews examples in the literature of photochemical cis-trans isomerization paying particular attention to the medium effect and accompanied conformational changes. A case is made that the Hula-Twist mechanism, postulated in 1985 as a photochemical reaction pathway for a polyene chromophore imbedded in a protein binding cavity such as those of rhodopsin and bacteriorhodopsin, is also a dominant reaction pathway for a diene, or a longer polyene confined in a rigid (relative to isomerization rate) medium. The conventional one-bond-flip process is the preferred reaction pathway in a fluid medium. While defining experiments are proposed, this dual mechanistic approach successfully accounts for all examples in the literature on photoisomerization reactions whether involving conformational changes or not.

摘要

本文批判性地回顾了文献中光化学顺反异构化的实例,特别关注介质效应和伴随的构象变化。有证据表明,1985年提出的“呼啦圈扭转”机制,作为嵌入蛋白质结合腔(如视紫红质和细菌视紫红质的结合腔)中的多烯发色团的光化学反应途径,对于限制在刚性(相对于异构化速率)介质中的二烯或更长的多烯也是主要的反应途径。传统的一键翻转过程是流体介质中首选的反应途径。虽然提出了确定性实验,但这种双重机制方法成功地解释了文献中所有关于光异构化反应的实例,无论是否涉及构象变化。

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本文引用的文献

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Low-Temperature Photochemistry of Previtamin D: A Hula-Twist Isomerization of a Triene.前维生素D的低温光化学:三烯的扭摆异构化
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Key issues in the photochemistry and signalling-state formation of photosensor proteins.
J Photochem Photobiol B. 2000 Feb;54(2-3):94-102. doi: 10.1016/s1011-1344(00)00004-x.

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