Volume 20, Issue 2
Organoelement Compounds
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ChemInform Abstract: Dioxygen-Copper Reactivity: Generation, Characterization, and Reactivity of a Hydroperoxo-Dicopper(II) Complex.

K. D. KARLIN

K. D. KARLIN

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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P. GHOSH

P. GHOSH

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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R. W. CRUSE

R. W. CRUSE

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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A. FAROOQ

A. FAROOQ

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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Y. GULTNEH

Y. GULTNEH

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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R. R. JACOBSON

R. R. JACOBSON

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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N. J. BLACKBURN

N. J. BLACKBURN

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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R. W. STRANGE

R. W. STRANGE

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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J. ZUBIETA

J. ZUBIETA

Dep. Chem., State Univ. N. Y., Albany, NY 12222, USA

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First published: January 10, 1989

Abstract

The title complex (III) can be formed by three different routes.

ChemInform Abstract

The title complex (III) can be formed by three different routes. By direct protonation of (II), by a displacement reaction from (IV) with H2O2 and by reaction of protonated forms such as (Va) of the complex (I) with O2. Instead of (V) an analogous complex without the axial ligands can be used and gives a yield of 85% for (III). The syntheses of (V) are described. (Vb) is characterized by a crystal structure determination (P1, Z=1). (III) is investigated by EXAFS and electronic spectral measurements. The reactivity of (III) with organic substrates is studied. With in situ generated (III) (from (Vc)) a clean oxygen transfer reaction with PPh3 (VI) or tetrahydrothiophene (VIII) takes place in a stoichiometric reaction. Olefins are not oxygenated.

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