The Bis-Barium Complex of a Butterfly Crown Ether as a Phototunable Supramolecular Catalyst
- 1 February 2003
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 125 (8), 2224-2227
- https://doi.org/10.1021/ja029331x
Abstract
Reversible phototuning of the catalytic efficiency of the bis-barium complex of azobis(benzo-18-crown-6) in the basic ethanolysis of anilide derivatives has been achieved by light-induced cis right arrow over left arrow trans interconversion of the azobenzene spacer unit of the catalyst. The geometry of the productive catalyst-substrate complex is more favorable when the concave cis form of the catalyst is involved. Continuous photoregulation of the catalytic activity at any intermediate value between the "HIGH" and "LOW" levels was achieved by proper adjustment of the excitation wavelength or the irradiation time. The complete and relatively fast interconvertibility of photostationary states allowed the activity of the catalyst to be repeatedly photoswitched "HIGH" and "LOW" in the course of the same run.This publication has 8 references indexed in Scilit:
- Size-Selective Catalysis of Ester and Anilide Cleavage by the Dinuclear Barium(II) Complexes of cis- and trans-Stilbenobis(18-crown-6)The Journal of Organic Chemistry, 2001
- A Dinuclear Strontium(II) Complex as Substrate-Selective Catalyst of Ester CleavageThe Journal of Organic Chemistry, 2001
- Photochemical Biomolecular Switches: The Route to OptobioelectronicsPublished by Wiley ,2001
- Supramolecular Catalysis of Ester and Amide Cleavage by a Dinuclear Barium(II) ComplexAngewandte Chemie International Edition, 1999
- Photoswitchable Biomaterials: En Route to Optobioelectronic SystemsAccounts of Chemical Research, 1997
- Light‐Switchable Catalysis in Synthetic ReceptorsAngewandte Chemie International Edition in English, 1995
- Photoresponsive crown ethers. 5. Light-driven ion transport by crown ethers with a photoresponsive anionic capJournal of the American Chemical Society, 1982
- Minor and trace sterols in marine invertebrates. 19. Isolation, structure elucidation, and partial synthesis of 24-methylene-25-ethylcholesterol (mutasterol): first example of sterol side-chain bioalkylation at position 25Journal of the American Chemical Society, 1981