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Density functional theory study of the canthaxanthin and other carotenoid radical cations
KTH, Superseded Departments, Biotechnology.ORCID iD: 0000-0003-0007-0394
KTH, Superseded Departments, Biotechnology.
2002 (English)In: Chemical Physics Letters, ISSN 0009-2614, E-ISSN 1873-4448, Vol. 366, no 02-jan, 73-81 p.Article in journal (Refereed) Published
Abstract [en]

B3LYP hybrid density functional theory method is employed to study the five carotenoid radical cations of canthaxanthin (1), 7',7'-dimethyl-7'-apo-beta-carotene (2), 8'-apo-beta-carotene-8'-al hydrazone (3), 7',7'-dicyano-7'-apo-beta-carotene (4), and 8'-apo-beta-carotene-8'-al (5). The radicals are characterized by means of their geometries, spin populations, and isotropic hyperfine coupling constants. It is shown that for all the systems, the unpaired spin is delocalized over the whole pi-conjugated system in an odd-alternant pattern. As a result of this, the hyperfine coupling constants are rather low. The radical cations of 1, 2, and 3, have very similar properties to the unsubstituted P-carotene radical, while the dicyano- and aldehyde-substitutions result in significantly different electronic structures.

Place, publisher, year, edition, pages
2002. Vol. 366, no 02-jan, 73-81 p.
Keyword [en]
photosystem-ii, beta-carotene, pulsed endor, epr, chlorophyll, photooxidation, oxidation, exchange, spectra
Identifiers
URN: urn:nbn:se:kth:diva-22048ISI: 000179253000012OAI: oai:DiVA.org:kth-22048DiVA: diva2:340746
Note
QC 20100525Available from: 2010-08-10 Created: 2010-08-10 Last updated: 2017-12-12Bibliographically approved

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