Mohan, Hari ; Palit, D. K. ; Mittal, Jai P. ; Chiang, L. Y. ; Asmus, Klaus-Dieter ; Guldi, Dirk M. (1998) Excited states and electron transfer reactions of C60(OH)18 in aqueous solution Journal of the Chemical Society, Faraday Transactions, 94 (3). pp. 359-363. ISSN 0956-5000
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Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/1998...
Related URL: http://dx.doi.org/10.1039/A705293F
Abstract
Dynamic light scattering of fullerenol solutions [C60(OH)18] reveals evidence for the formation of fullerene aggregates at high solute concentration (up to 3.85×10-2 mol dm-3). This hydrophilic fullerene derivative emits very weak fluorescence regardless of its concentration. Photolysis (35 ps; λex=355 nm) of C60(OH)18 in aqueous solution yields the immediate formation of a transient singlet excited state with broad absorption in the 550–800 nm region with ε670nm=2130 d mol-1 cm-1. The energetically higher-lying singlet excited state transforms via intersystem crossing (i.e., with τ1/2=500 ps) to the also broadly absorbing (550-800 nm), triplet excited state. In contrast, at low solute concentration, the features of the (∗T1→∗Tn) absorption differ significantly exhibiting an absorption maximum at 650 nm concomitant to a shoulder at 570 nm. The π-radical anion of fullerenol, [C60(OH)18]·−, generated by electron transfer from hydrated electrons and (CH3)2C(OH) radicals, absorbs with λmax at 870, 980 and 1050 nm. Based on electron transfer studies with suitable electron donor/acceptor substrates, the reduction potential of the C60(OH)18/[C60(OH)18]·− couple was estimated to be in the range between -0.358 and -0.465 V vs. NHE.
Item Type: | Article |
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Source: | Copyright of this article belongs to Royal Society of Chemistry. |
ID Code: | 34085 |
Deposited On: | 31 Mar 2011 06:03 |
Last Modified: | 17 May 2016 16:59 |
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