Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1210
Title: Appraisal of through-bond and through-space substituent effects via molecular electrostatic potential topography
Authors: Sayyed, F B
Suresh, C H
Gadre, S R
Keywords: Resonance
Quantitative assessment
Benzenes
Issue Date: 2010
Publisher: American Chemical Society
Citation: Journal of Physical Chemistry A 114(46):12330-12333;25 Nov 2010
Abstract: Through-bond (TB) and through-space (TS) substituent effects in substituted alkyl, alkenyl, and alkynyl arenes are quantified separately using molecular electrostatic potential (MESP) topographical analysis. The deepest MESP point over the aromatic ring (V(min)) is considered as a probe for monitoring these effects for a variety of substituents. In the case of substituted alkyl chains, the TS effect (79.6%) clearly dominates the TB effect, whereas in the unsaturated analogues the TB effect (similar to 55%) overrides the TS effect.
URI: http://ir.niist.res.in:8080/jspui/handle/123456789/1210
ISSN: 1089-5639
Appears in Collections:2010

Files in This Item:
File Description SizeFormat 
2010_ 0081.pdf
  Restricted Access
177.78 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.