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Journal ArticleDOI

Photochemistry of matrix‐isolated norbornadiene

TLDR
The role of the rigid matrix environment on selectivity of the photochemical reaction is discussed in this article, where the photoproduct, representing a single species, was assigned to quadricyclane.
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This article is published in Journal of Physical Organic Chemistry.The article was published on 1989-07-01. It has received 2 citations till now. The article focuses on the topics: Norbornadiene & Quadricyclane.

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Journal ArticleDOI

Radical cations of quadricyclane and norbornadiene in polar ZSM-5 matrices: thermal retro Diels–Alder reaction

TL;DR: The radical cation of norbornadiene or quadricyclane (Q) produced by γ-radiolysis in polar ZSM-5 undergo a reverse Diels-Alder reaction as mentioned in this paper.
References
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Journal ArticleDOI

New molecular energy storage systems

TL;DR: In this paper, an outstanding molecular energy storage system A/B composed of a cycle of reactions including a direct sunlight-induced endoergic process and an energy-releasing reverse process was investigated on the basis of new concepts.
Journal ArticleDOI

Photochemical transformations—VIII: The isomerization of Δ2,5-bicyclo[2.2.1]heptadiene to quadricyclo[2.2.1.02,6·03,5]heptane (quadricyclene)☆☆☆★

TL;DR: In this article, the valence tautomeric quadricyclene (IV) was studied with hydrogen, with acetic acid and with bromine, and it was shown that IV can be reformulated with hydrogen.
Journal ArticleDOI

The infrared laser photoisomerization of HONO in solid N2 and Ar

TL;DR: In this paper, the IR induced photoisomerization of HONO in solid N2 and Ar is a single photon process and the reaction occurs at sites where the isomerization is least hindered by the cage.
Journal ArticleDOI

Vibrational relaxation of matrix‐isolated HCl and DCl

TL;DR: In this article, the authors measured lifetimes for HCl (v=1,2) in Ar as a function of concentration and temperature, and for dilute samples of DCl(v=2), and they were consistent with a relaxation process in which the rate determining step is intramolecular V→R transfer.
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