End-to-end intramolecular quenching of aromatic ketone triplets in aqueous solutions of 2,6-di-(O-methyl)-cyclodextrins
- 1 April 1991
- journal article
- Published by Elsevier in Journal of Photochemistry and Photobiology A: Chemistry
- Vol. 57 (1-3) , 97-109
- https://doi.org/10.1016/1010-6030(91)85009-6
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- A fine-tuning of photoreactivity of large ring 2-phenylcycloalkanones adsorbed in cyclodextrinsTetrahedron Letters, 1990
- Photochemistry and photophysics within cyclodextrin cavitiesAccounts of Chemical Research, 1988
- Modification of photochemical reactivity by cyclodextrin complexation: alteration of photochemical behavior via restriction of translational and rotational motions. AlkyldeoxybenzoinsThe Journal of Organic Chemistry, 1987
- Modification of photochemical reactivity by cyclodextrin: difference in photobehavior between short-chain and long-chain benzoin alkyl ethers: conformational effectThe Journal of Organic Chemistry, 1987
- Modification of photochemical reactivity by cyclodextrin complexation: consequences of restricted rotation of Norrish type II 1,4 diradicals from aryl alkyl ketonesThe Journal of Organic Chemistry, 1987
- Miniature organic models of enzymesAccounts of Chemical Research, 1987
- Organic photochemistry in organized mediaTetrahedron, 1986
- Excited-state reactivity changes induced by complexation with cyclodextrins: inclusion of 2,2-bis(.alpha.-naphthylmethyl)-1,3-dithiane into .beta.- and .gamma.-cyclodextrinsThe Journal of Physical Chemistry, 1983
- Cyclodextrin catalysis as a model for enzyme actionAccounts of Chemical Research, 1982
- Enhanced intramolecular excimer formation of guest molecules included in the cavity of γ-cyclodextrinJournal of the Chemical Society, Chemical Communications, 1981