Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/15734
Title: Dioxo derivatives of benzenoid hydrocarbons: Part IV - Dioxo-bisanthrenes
Authors: Gutman, Ivan
Markovic, Zoran
Issue Date: May-1999
Publisher: NISCAIR-CSIR, India
Abstract: Depending on the position of the two oxo groups, isomeric dioxo derivatives of benzenoid hydrocarbons drastically differ in the extent and mode of π-electron conjugation. We report here the results of AMI studies of the 14 Kekulean dioxo derivatives of bisanthrene (phenanthro-( 1,10,9,8-o,p,q,r,a]perylene). Our calculations indicate that in this case also the relative stabilities and the geometries of the dioxo derivatives are predominantly determined by π -electron conjugation and to a lesser extent by steric repulsion of the oxo groups in positions 3,4,10 and/or 11 , and by electrostatic repulsion of near-lying oxo groups.
Page(s): 407-410
Appears in Collections:IJC-A Vol.38A(05) [May 1999]

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