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Charge interactions of water soluble oxo-titanium(IV) porphyrins with CTAC and SDS micelles

Authors
Kim, Yong HeeJung, Sang DonJang, Yoon JungIm, ChanKim, Seog K.Cho, Dae Won
Issue Date
15-10월-2013
Publisher
ELSEVIER SCIENCE SA
Keywords
Oxo-titanium(IV) porphyrin; Micelle; Surfactant; Raman spectroscopy; Transient absorption spectroscopy
Citation
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, v.270, pp.7 - 13
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Volume
270
Start Page
7
End Page
13
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/101869
DOI
10.1016/j.jphotochem.2013.07.003
ISSN
1010-6030
Abstract
The interactions of anionic oxo-titanium (IV) meso-tetrakis(4-sulfonatophenyl)porphyrin and cationic oxo-titanium(IV) meso-tetrakis(1-methylpyridium-4-yl)porphyrin with anionic and cationic micelles were examined by Raman spectroscopy and transient absorption spectroscopy. The Raman bands of O=Ti-IV porphyrins in the presence of surfactants with same charge were similar to those observed in a pure water solution. The characteristic Raman band was observed at 915 cm(-1), which was assigned to the O=Ti stretching mode of the 6-coordinated complex, O=Ti-(H2O) porphyrins. On the other hand, in the presence of oppositely charged surfactants, a markedly up-shifted Raman band was observed at 945 cm-1, which was assigned to the O=Ti stretching mode of a 5-coordinated complex, O=Ti porphyrins. O=Ti porphyrins interact with oppositely charged surfactant micelles by losing the sixth axial ligand (H2O). The 5-coordinate complexes showed a shorter lifetime of the exited triplet state due to the lower lying quenching state. (C) 2013 Elsevier B.V. All rights reserved.
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