Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/20487
Title: Methyl and vinyl substituted 1H-, 2H-, and 3H-phospholes and their Diels-Alder reactions with ethylene: A semiempirical AM1 study
Authors: Geetha, K
Sastry, G Narahari
Issue Date: Jan-2003
Publisher: NISCAIR-CSIR, India
Abstract: The equilibrium geometries and the relative stabilities of all the possible isomers of phospho le, methylphosphole and vinylphosphole have been estimated using the semiempirical AM1 method. The Diels-Alder transition states and products between each of these isomers, with ethylene as dienophile, have been located. AM1 results show that 2H-phosphole is more stable than 3H-phosphole by 3.6 kcal mol-1 which is in turn more stable than 1H-phosphole by about 6.0 kcal mol-1. The Diels-Alder activation energies of 2H-phospholes are much lower compared to those involving 1H- and 3H-phospholes. Either methyl or vinyl substitution does not alter the broad features in the activation and reaction energies compared to the parent compound.
Page(s): 11-18
URI: http://hdl.handle.net/123456789/20487
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.42A(01) [January 2003]

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