Abstract
Two Ru-porphyrin-linked β-cyclodextrin units form the supramolecular system, which as an enzyme mimic for β,β-carotene 15,15'-dioxgenase binds two substrates of the enzyme with K(a) > 106 M-1 and selectively catalyzes the cleavage of the central carotinoid bond in the presence of tert- butylhydroperoxide (see picture). Mechanistic aspects of this unusual cleavage of E-configured, conjugated double bonds are discussed.
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French, R. R., Holzer, P., Leuenberger, M. G., & Woggon, W. D. (2000). A supramolecular enzyme mimic that catalyzes the 15,15’ double bond scission of β,β-carotene. Angewandte Chemie - International Edition, 39(7), 1267–1269. https://doi.org/10.1002/(SICI)1521-3773(20000403)39:7<1267::AID-ANIE1267>3.0.CO;2-7
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