The redox chemistry of copper tetraphenylporphyrin revisited

Author:

Saphier Magal12,Yifrah Tova3,Zilbermann Israel13,Saphier Oshra2,Shames Alexander I.4,Froumin Natalya5,Meyerstein Dan36,Guldi Dirk M.7

Affiliation:

1. Chemistry Dept., Nuclear Research Centre Negev, Beer-Sheva, Israel

2. Sami Shamoon College of Engineering, Beer-Sheva, Israel

3. Chemistry Dept., Ben-Gurion University of the Negev, Beer-Sheva, Israel

4. Physics Dept., Ben-Gurion University of the Negev, Beer-Sheva, Israel

5. Materials Engineering Dept., Ben-Gurion University of the Negev, Beer-Sheva, Israel

6. Biological Chemistry Dept., Ariel University Center of Samaria, Ariel, Israel

7. Chemistry and Pharmaceutical Dept., Friedrich-Alexander-Universitat Erlangen-Nuernberg-Germany, Germany

Abstract

Mixing Cu(II)Cl2 with free base tetraphenylporphyrin (( H2 (TPP)) in dry deaerated 1,2-dichloroethane surprisingly yields a mixture of Cu(II) (TPP) and Cu(III) (TPP). The later is long-lived in the absence of water and slowly decomposes within days to yield Cu(II) (TPP). Furthermore, in the presence of air, a slightly different CuIII porphyrin species forms, presumably, Cu(III) (TPP)•+, in which the Q-band is subject to a 10 nm red shift. The new Cu(III) (TPP) and Cu(III) (TPP)•+ differ in terms of absorption, fluorescence, electron paramagnetic resonance (EPR), and X-ray photoemission spectroscopy (XPS) when compared to the well-characterized Cu(II) (TPP), Cu(II) (TPP)•+, and Cu(II) (TPP)2+ species.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

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