Cycloreversion performance of coumarin and hetero-coumarin dimers under aerobic conditions: unexpected behavior triggered by UV-A light-Reference-Cited by-同舟云学术

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Cycloreversion performance of coumarin and hetero-coumarin dimers under aerobic conditions: unexpected behavior triggered by UV-A light

Published:2021 Issue:32 Volume:23 Page:17703-17712
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Bieniek Nikolai¹^ORCID,Inacker Sebastian¹^ORCID,Hampp Norbert¹^ORCID

Affiliation:

1. Department of Chemistry, University of Marburg, Hans-Meerwein-Straße 4, D-35032 Marburg, Germany

Abstract

Photochemical [2+2]-cycloadditions of coumarin-like monomers are the textbook paradigms of photo-formation and photo-cleavage reactions.

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CP/D1CP01919H

Reference25 articles.

1. Das directe Ueberführen der Zimmtsäure in α‐Truxillsäure

2. Photo‐C 4 ‐Cyclodimerisation von Cumarin

3. Symmetric and asymmetric photocleavage of the cyclobutane rings in head-to-head coumarin dimers and their lactone-opened derivatives

4. Photocleavage of coumarin dimers studied by femtosecond UV transient absorption spectroscopy

5. Substituting Coumarins for Quinolinones: Altering the Cycloreversion Potential Energy Landscape

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