fac-Tricarbonyl[hydroxybis(2-pyridyl)methanolato-kappa3N,O,N']rhenium(I).

Acta Crystallogr C

Department of Chemistry, The University of the West Indies, Mona Campus, Kingston 7, Jamaica, West Indies.

Published: February 2002

The Re(I) centre in the title compound, [Re(C(11)H(9)N(2)O(2))(CO)(3)] or fac-Re(CO)(3)(dpkO,OH) [dpkO,OH is hydroxybis(2-pyridyl)methanolato], (I), is in a pseudo-octahedral environment in which the major distortion is due to the constraints associated with the tridentate binding of the dpkO,OH anion. The carbonyl groups are orthogonal, with an average C-Re-C angle of 90.2(3) degree. The molecules pack in stacks of antiparallel tapes of (I) interlocked via a network of hydrogen bonds.

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http://dx.doi.org/10.1107/s0108270101019527DOI Listing

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A series of new (tricarbonyl)rhenium(I) complexes were synthesized using chiral bidentate ligands (+)/(-)-iminopyridines (L/L). The reaction yielded a mixture of mononuclear Re(I) diastereoisomers, formulated as -[Br(CO)ReL]. Each single diastereoisomer was isolated and fully characterized.

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fac-Tricarbonyl[hydroxybis(2-pyridyl)methanolato-kappa3N,O,N']rhenium(I).

Acta Crystallogr C

February 2002

Department of Chemistry, The University of the West Indies, Mona Campus, Kingston 7, Jamaica, West Indies.

The Re(I) centre in the title compound, [Re(C(11)H(9)N(2)O(2))(CO)(3)] or fac-Re(CO)(3)(dpkO,OH) [dpkO,OH is hydroxybis(2-pyridyl)methanolato], (I), is in a pseudo-octahedral environment in which the major distortion is due to the constraints associated with the tridentate binding of the dpkO,OH anion. The carbonyl groups are orthogonal, with an average C-Re-C angle of 90.2(3) degree.

View Article and Find Full Text PDF

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