Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/38890
Title: Fluorescence analysis of iodinated acetophenone derivatives
Authors: Crivelaro, F.
Oliveira, M. R. S.
Lima, S. M.
Andrade, L. H. C.
Casagrande, G. A.
Raminelli, C. [UNIFESP]
Caires, A. R. L.
Fundacao Univ Fed Grande Dourados
Universidade Estadual de Mato Grosso do Sul (UEMS)
Universidade Federal de Mato Grosso do Sul (UFMS)
Universidade Federal de São Paulo (UNIFESP)
Keywords: Fluorescence
Fluorescence quantum yield
Acetophenone
Iodine
Issue Date: 15-Mar-2015
Publisher: Elsevier B.V.
Citation: Spectrochimica Acta Part A-molecular and Biomolecular Spectroscopy. Oxford: Pergamon-Elsevier B.V., v. 139, p. 63-67, 2015.
Abstract: In the present paper the synthesis and optical characterization of iodinated acetophenone, 4-hydroxy-3-iodoacetophenone and 4-hydroxy-3,5-diiodoacetophenone obtained from 4-hydroxyacetophenone, were carried out. the optical features of iodinated molecules were determined by performing the UV-Vis absorption, fluorescence and thermal lens spectroscopies. the results showed that the optical properties of the 4-hydroxyacetophenone is altered when the iodine atom is inserted, as substituent, in the aromatic ring. Although it was determined that the optical feature was changed when one iodine atom was inserted in the aromatic ring (4-hydroxy-3-iodoacetophenone), the results revealed that emission behavior was strongly altered when two iodine atoms (4-hydroxy-3,5-diiodoacetophenone) were acting as substituents: the fluorescence quantum efficiency increases approximately 60%. (C) 2014 Elsevier B.V. All rights reserved.
URI: http://repositorio.unifesp.br/handle/11600/38890
ISSN: 1386-1425
Other Identifiers: http://dx.doi.org/10.1016/j.saa.2014.12.037
Appears in Collections:Em verificação - Geral

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