Solid-state studies into the possible rearrangement mechanisms for the fluxional behaviour of the tetranuclear carbonyls M4(CO)12 and their derivativesSolid-State Studies into the Possible Rearregment Mechenisms for the Fluxional Behavior of the Tetranuclear Carbonyls M4 (CO)12 and Their Derivatives

Johnson, Brian F. G. and Roberts, Yvonne V. and Parisini, Emilio and Benfield, Robert E. (1994) Solid-state studies into the possible rearrangement mechanisms for the fluxional behaviour of the tetranuclear carbonyls M4(CO)12 and their derivativesSolid-State Studies into the Possible Rearregment Mechenisms for the Fluxional Behavior of the Tetranuclear Carbonyls M4 (CO)12 and Their Derivatives. Journal of Organometallic Chemistry, 478 (1-2). pp. 21-28. ISSN 0022-328X. (The full text of this publication is not available from this repository)

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Official URL
http://dx.doi.org/10.1016/0022-328X(94)88152-9

Abstract

The deformation from an idealised geometry, observed in the solid state for a given cluster species, may indicate the paths taken by the cluster in ligand fluxionality processes. A number of single-crystal X-ray structures of M4(CO)12-n(L)n clusters (M = Co, Rh, Ir; n = 1-5) have been examined in order to elucidate any geometric trends in their ligand envelope deformations. It has been revealed that the complementary geometries adopted by M4(CO)12-n(L)n species may be both metal- and ligand-dependent. Iridium species adopt T(d)-cubeoctahedral structures, but the available data provide no clear picture for the complementary geometry adopted by cobalt or rhodium species. Additionally, tripodal ligands have been shown to stabilise D3h (icosahedral) ligand polyhedra.

Item Type: Article
Uncontrolled keywords: MOLYBDENUM; RHODIUM; IRIDIUM; CRYSTAL STRUCTURE; FLUXIONALITY; CARBONYL
Subjects: Q Science > QD Chemistry
Divisions: Faculties > Science Technology and Medical Studies > School of Engineering and Digital Arts
Depositing User: P. Ogbuji
Date Deposited: 25 Jun 2009 10:14
Last Modified: 09 May 2014 08:36
Resource URI: http://kar.kent.ac.uk/id/eprint/20276 (The current URI for this page, for reference purposes)
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