Synthesis and aggregation behavior of a novel water-soluble porphyrin platinum(II) terpyridine complex

Author:

Plutino Maria Rosaria1,Castriciano Maria Angela1,Mazzaglia Antonino1,Saporita Maria2,Romeoa Andrea12,Scolaro Luigi Monsù12

Affiliation:

1. CNR-ISMN Istituto per lo Studio dei Materiali Nanostrutturati, c/o Dipartimento di Chimica, Inorganica, Chimica, Analitica e Chimica Fisica, Università di Messina, V.le Ferdinando Stagno D'Alcontres 31, 98166 Vill. S. Agata, Messina, Italy

2. Dipartimento di Chimica Inorganica, Chimica Analitica e Chimica Fisica, Università di Messina, and C.I.R.C.M.S.B. V.le Ferdinando Stagno D'Alcontres 31, 98166 Vill.S.Agata, Messina, Italy

Abstract

A new water soluble tetranuclear platinum(II) porphyrin complex cation has been synthesized through the coordination of four [ Pt (2,2′:6′,2″-terpyridine)] moieties to the pyridyl groups of 5,10,15,20-tetrakis(4-pyridyl)-21H,23H-porphine (TPyP). The porphyrin derivative has been fully characterized by a combination of spectroscopic techniques. The high positive charge of the complex cation (8+) inhibits the aggregation in aqueous solution at low concentrations. By increasing the ionic strength, the electrostatic repulsion is screened leading to the formation of large unstable aggregates. The formation of microsized globular objects still emissive on the solid state is easily achieved by simple evaporation from diluted solutions. The solubilization of the complex in anionic aqueous surfactant solutions (sodium dodecyl sulfate, SDS) has revealed the inclusion of the complex ion in the hydrophobic region of the micelles as a monomeric species. Kinetics of Cu(II) insertion into the free-base tetranuclear Pt(II) porphyrin complex have been carried out in micellar media and the rate constants have been determinated.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

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