Exciton coupling of tetra(p-hydroxyphenyl)porphyrin controlled by substituents of counterions in Triton X-100 micellar solution

The interactions of nonionic meso-tetra(p-hydroxyphenyl)porphyrin (THPP) with CX3COOH (X = F, Cl, Br) in Triton X-100 (TX) micellar solution have been investigated by optical absorption, resonance light-scattering, and fluorescence spectroscopies. The double red-shifted absorption bands and strong resonance light scattering (RLS) signal imply that the assemblies induced by trihalo acetic acids belong to J-aggregates. The fluorescence of porphyrin is quenched due to the aggregate formation. The kinetics of assemblies trigged by CBr3COOH is studied via stopped-flow techniques. No characteristics of autocatalyzed reactions are observed, and there is only a log phase. The nature of the exciton coupling of transition dipole moment can be systematically changed by the haloid substituents of the organic counteranion.

Medienart:

Artikel

Erscheinungsjahr:

2007

Erschienen:

2007

Enthalten in:

Zur Gesamtaufnahme - volume:111

Enthalten in:

The journal of physical chemistry. B - 111(2007), 6 vom: 15. Feb., Seite 1502-6

Sprache:

Englisch

Beteiligte Personen:

Li, Xiwen [VerfasserIn]
Li, Deijia [VerfasserIn]
Zeng, Wenfeng [VerfasserIn]
Zou, Guolin [VerfasserIn]
Chen, Zhangping [VerfasserIn]

Themen:

9002-93-1
Acetic Acid
Hydrocarbons, Halogenated
Ions
Journal Article
Micelles
Octoxynol
Porphyrins
Q40Q9N063P
Research Support, Non-U.S. Gov't
Solutions
Surface-Active Agents
Tetraphenylporphyrin

Anmerkungen:

Date Completed 01.06.2007

Date Revised 21.11.2013

published: Print-Electronic

Citation Status MEDLINE

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM167944215