The multichromophoric character of two sulfonylurea herbicides, SMT and BNS, has been investigated in its manifestations in the electronic absorption spectra and in some fluorescence properties through a combined experimental and theoretical approach. After a theoretical analysis of the most stable structures of these flexible systems, the UV absorption spectra of the two multichromophoric compounds have been analysed both experimentally and theoretically, and most transitions have been assigned to individual chromophores, also by comparison with four suitable reference compounds (5-8). Finally, some experimental information concerning the fluorescence spectra and quantum yields have been analysed with reference to the contributions from single fluorophores and the role of low-lying n -> pi* states. (c) 2006 Elsevier B.V. All rights reserved.
Electronic spectra and fluorescence properties of multichromophoric sulfonylureas / Baraldi, Ivan; Caselli, Monica; Ponterini, Glauco; Vanossi, Davide. - In: INORGANICA CHIMICA ACTA. - ISSN 0020-1693. - STAMPA. - 360:3(2007), pp. 931-937. [10.1016/j.ica.2006.06.040]
Electronic spectra and fluorescence properties of multichromophoric sulfonylureas
BARALDI, Ivan;CASELLI, Monica;PONTERINI, Glauco;VANOSSI, Davide
2007
Abstract
The multichromophoric character of two sulfonylurea herbicides, SMT and BNS, has been investigated in its manifestations in the electronic absorption spectra and in some fluorescence properties through a combined experimental and theoretical approach. After a theoretical analysis of the most stable structures of these flexible systems, the UV absorption spectra of the two multichromophoric compounds have been analysed both experimentally and theoretically, and most transitions have been assigned to individual chromophores, also by comparison with four suitable reference compounds (5-8). Finally, some experimental information concerning the fluorescence spectra and quantum yields have been analysed with reference to the contributions from single fluorophores and the role of low-lying n -> pi* states. (c) 2006 Elsevier B.V. All rights reserved.Pubblicazioni consigliate
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