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Ultrafast dynamics of hydrophilic carbonyl carotenoids - Relation between structure and excited-state properties in polar solvents
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SYSNO ASEP 0355284 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Ultrafast dynamics of hydrophilic carbonyl carotenoids - Relation between structure and excited-state properties in polar solvents Tvůrce(i) Chábera, P. (CZ)
Fuciman, M. (CZ)
Naqvi, K.R. (NO)
Polívka, Tomáš (BC-A) RID, ORCIDZdroj.dok. Chemical Physics. - : Elsevier - ISSN 0301-0104
Roč. 373, 1-2 (2010), s. 56-64Poč.str. 9 s. Jazyk dok. eng - angličtina Země vyd. NL - Nizozemsko Klíč. slova hydrophilic carotenoids ; excited-state dynamics ; charge-transfer state Vědní obor RIV BO - Biofyzika CEZ AV0Z50510513 - UMBR-M, BC-A (2005-2011) UT WOS 000280065100010 DOI 10.1016/j.chemphys.2010.01.007 Anotace A study of excited-state dynamics of water-soluble carbonyl carotenoids, crocin, norbixin, and astalysine in solvents with different polarity. While no polarity effects were observed in 2-propanol and methanol, polarity-induced lifetime shortening has been detected in water. For crocin and astalysine the S1 lifetime decreases from 135 ps to 61 ps (crocin), and from 4 ps to 2.2 ps (astalysine) when going from methanol to water. The S1 lifetime of norbixin is within the 15-18 ps range in all solvents, an effect attributed to its carboxylic group, which isolates the carbonyl group from the rest of conjugation. No spectral bands attributable to the intramolecular charge transfer (ICT) state have been found in any transient absorption spectra. The ICT-Sn transition is made forbidden, we suggest, by the symmetric location of the conjugated carbonyl groups. In astalysine, we have found a clear signature of the S* state with a life-time of 7 ps (methanol) and 6.1 ps (water). Pracoviště Biologické centrum (od r. 2006) Kontakt Dana Hypšová, eje@eje.cz, Tel.: 387 775 214 Rok sběru 2012
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