Title

Properties and Structures of Five-coordinated Cobalt(II) and Copper(II) Complexes of N,N′-bis[(5-chloro-2-hydroxyphenyl)phenylmethylene]-4-oxaheptane-1,7- Diamine

Abstract

The title complexes, [Co(cbpO)] and (Cu(cbpO)], have been synthesized and studied by single-crystal X-ray diffraction. The copper complex contains the metal atom in a distorted square pyramid whose apex is formed by the Cu-O bond to the ether oxygen atom. The O 2N 2 base of the square pyramid is distorted so as to give some trigonal-bipyramidal character to the geometry, the N atoms being raised above (0.35 Å) the base and the Cu atom and the O atoms below it (0.06 and 0.35 Å, respectively). The Cu-O bond to the ether oxygen is markedly elongated (2.575 Å), indicating a rather weak linkage. This compares with apical bond elongations of 2.374 (10) and 2.686 (1) Å, respectively, in the related five-coordinated [Cu(mbpN)] and [Cu(cbpS)]. If the long Cu-O bond were absent, the copper environment would approximate a flattened tetrahedron. The metal environment in [Co(cbpO)] is distorted trigonal bipyramidal with the two Co-N bonds axial and the three Co-O bonds equatorial. The Co-O bond to the ether oxygen is relatively strong (2.124 (3) Å) in contrast with the [Cu(cbpO)] analogue. The observation of metal to ether oxygen bonding at all in these complexes contrasts with the apparent absence of such bonds in a series of related salicylaldimine complexes. (Co(cbpO)] readily forms a six-coordinated pyridine adduct, while [Cu(cbpO)] appears not to do so, even in pyridine solution. Crystal data for [Cu(cbpO)]: space group C2/c, Z = 8, a = 13.993 (5) Å, b = 13.652 (8) Å, c = 29.40 (1) Å, β = 91.46 (3)°, V = 5615 Å 3, R = 5.8% for 1840 reflections. Crystal data for [Co(cbpO)]: space group C2/c, Z = 8, a = 13.914 (7) Å, b = 13.477 (4) Å, c = 29.86 (1) Å, β = 90.57 (3)°, V = 5599 Å 3, R = 6.1% for 3397 reflections. © 1981 American Chemical Society.

Department(s)

Chemistry

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 1981 American Chemical Society (ACS), All rights reserved.


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