ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

The central region of meso-3,4-diphenylhexane-2,5-dione

Balasubrahmanyam, SN and Kulkarni, GU and Gopalan, RS and Kumar, AS and Hiremath, US (2003) The central region of meso-3,4-diphenylhexane-2,5-dione. In: Journal of Molecular Structure, 645 (2-3). 159-169 .

[img] PDF
The_central_region.pdf - Published Version
Restricted to Registered users only

Download (237kB) | Request a copy
Official URL: http://dx.doi.org/10.1016/S0022-2860(02)00537-9


As with 1,2-diphenylethane (dpe), X-ray crystallographic methods measure the central bond in meso-3,4-diphenylhexane-2,5-done (dphd) as significantly shorter than normal for an sp(3)-sp(3) bond. The same methods measure the benzylic (ethane C-Ph) bonds in dphd as unusually long for sp(3)-sp(2) liaisons. Torsional motions of the phenyl rings about the C-Ph bonds have been proposed as the artifacts behind the result of a 'short' central bond in dpe. While a similar explanation can, presumably, hold for the even 'shorter' central bond in dphd, it cannot account for the 'long' C-Ph bonds. The phenyl groups, departing much from regular hexagonal shape, adopt highly skewed conformations with respect to the plane constituted by the four central atoms. It is thought that-the thermal motions of the phenyl rings, conditioned by the potential wells in which they are ensconced in the unit cell, are largely libratory around their normal axes. In what appears to be a straightforward explanation under the 'rigid-body' concept, it appears that these libratory motions of the phenyl rings, that account, at the same time, for the 'short' central bond, are the artifacts behind the 'long' measurement of the C-Ph bonds. These motions could be superimposed on torsional motions analogous to those proposed in the case of dpe. An inspection of the ORTEP diagram from the 298 K data on dphd clearly suggests these possibilities. Supportive evidence for these qualitative explanations from an analysis of the differences between the mean square displacements of C(1) and C(7)/C(1a) and C(7a) based on the 'rigid-body model' is discussed. (C) 2002 Elsevier Science B.V. All rights reserved.

Item Type: Journal Article
Publication: Journal of Molecular Structure
Publisher: Elsevier Science
Additional Information: Copyright of this article belongs to Elsevier Science.
Keywords: Diphenylethanes;X-ray crystallography;Short and long measured bond distances;Calculated bond distances;Rigid-bond/rigidbody model;TLS analysis
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 24 Aug 2011 07:08
Last Modified: 24 Aug 2011 07:08
URI: http://eprints.iisc.ac.in/id/eprint/40264

Actions (login required)

View Item View Item