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Hydrogen‐Bonding Donor‐Acceptor Stenhouse Adducts.

Authors :
Mallo, Neil
Tron, Arnaud
Andréasson, Joakim
Harper, Jason B.
Jacob, Lorrie S. D.
McClenaghan, Nathan D.
Jonusauskas, Gediminas
Beves, Jonathon E.
Source :
ChemPhotoChem. Jun2020, Vol. 4 Issue 6, p407-412. 6p.
Publication Year :
2020

Abstract

The binding of donor‐acceptor Stenhouse adducts (DASAs) bearing hydrogen‐bond recognition groups by Hamilton‐type receptors significantly influenced their photoswitching properties by altering thermal barriers to isomerization. The thermal barrier between the most stable linear isomer and the photogenerated isomer is lowered on binding to a receptor, and this barrier is crucial for switching properties. The thermal isomerization was shown to proceed via a stepwise linear‐enol‐keto mechanism in DMSO where the tautomerisation barrier is within 2 kJ ⋅ mol−1 of that of the rate‐determining step, which may be important for analyzing switching properties. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23670932
Volume :
4
Issue :
6
Database :
Academic Search Index
Journal :
ChemPhotoChem
Publication Type :
Academic Journal
Accession number :
143704010
Full Text :
https://doi.org/10.1002/cptc.201900295