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Spectroscopic characterization of meso-tetrakis(1-methylpyridinium-4-yl)porphyrins, ((TMpyP)H sub 2 ) sup 4+ and ((TMpyP)M) sup 4+ , in aqueous micellar media, where M = VO sup 2+ , Cu(II), and Zn(II)

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100154a075· OSTI ID:5774806

Spectroscopic characterization of ((TMpyP)H{sub 2}){sup 4+} and ((TMpyP)M){sup 4+}, where M = Cu(II), Zn(II), or VO{sup 2+} and TMpyP = meso-tetrakis(1-methylpyridinium-4-yl)porphyrin, was carried out in water and in aqueous solutions containing the anionic surfactant sodium dodecyl sulfate (SDS), the cationic surfactant cetyltrimethylammonium bromide (CTAB), or the neutral surfactant Triton X-100 (TX-100). UV-visible, {sup 1}H NMR, and ESR spectra data indicate that these tetracationic porphyrins interact with and exist as monomeric entities in the anionic SDS micelle. In contrast, neither the cationic nor the neutral micelle shows an interaction with the investigated porphyrins. Comparisons are made between the data for tetracationic and tetraanionic porphyrins in different micellar media and it is suggested that intercalation of the positively charged porphyrins in SDS is due to Coulombic rather than hydrophobic interactions.

OSTI ID:
5774806
Journal Information:
Journal of Physical Chemistry; (USA), Journal Name: Journal of Physical Chemistry; (USA) Vol. 95:1; ISSN 0022-3654; ISSN JPCHA
Country of Publication:
United States
Language:
English

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