Volume 20, Issue 18
Organoelement Compounds
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ChemInform Abstract: Synthesis, Electrochemistry, and Electron Spin Resonance Spectra of Some Seventeen-Electron Complexes Containing the (Mo(NO))2+ Core and the Molecular Structure of (Mo(NO)(HB(Me2pz)3)(pyr)2).

N. AL OBAIDI

N. AL OBAIDI

Sch. Chem., Univ. Birmingham, Edgbaston, Birmingham B15 2TT, UK

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A. J. EDWARDS

A. J. EDWARDS

Sch. Chem., Univ. Birmingham, Edgbaston, Birmingham B15 2TT, UK

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C. J. JONES

C. J. JONES

Sch. Chem., Univ. Birmingham, Edgbaston, Birmingham B15 2TT, UK

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J. A. MCCLEVERTY

J. A. MCCLEVERTY

Sch. Chem., Univ. Birmingham, Edgbaston, Birmingham B15 2TT, UK

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B. D. NEAVES

B. D. NEAVES

Sch. Chem., Univ. Birmingham, Edgbaston, Birmingham B15 2TT, UK

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F. E. MABBS

F. E. MABBS

Sch. Chem., Univ. Birmingham, Edgbaston, Birmingham B15 2TT, UK

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D. COLLISON

D. COLLISON

Sch. Chem., Univ. Birmingham, Edgbaston, Birmingham B15 2TT, UK

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First published: May 2, 1989

Abstract

The reactions between the 16-electron complex (I) and several neutral, unsaturated N-heterocyclic ligands (II) are investigated in order to establish the nature of the paramagnetic cationic 17-electron complexes (III).

ChemInform Abstract

The reactions between the 16-electron complex (I) and several neutral, unsaturated N-heterocyclic ligands (II) are investigated in order to establish the nature of the paramagnetic cationic 17-electron complexes (III). These complexes exhibit room-temp. ESR signals in which hyperfine coupling to MO isotopes is apparent. The complexes with Py or N-methylimidazole as ligand exhibit a reversible one-electron reduction process in their cyclic voltammograms. However, where an exchangeable proton is bound to an N atom in L, irreversible reduction is observed. The neutral diamagnetic complex (V) (space group P1, Z=2) undergoes a reversible one-electron reduction at more anodic potentials than the complexes (III).

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