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dc.contributor.authorAcharjee, Nivedita-
dc.contributor.authorBanerji, Avijit-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.description.abstractThe preferred configurations and conformations of C-aryl-N-phenyl nitrones have been predicted theoretically by detailed comparison of DFT/B3LYP/6-311+G(2d,p) calculated gauge invariant atomic orbital nuclear magnetic shielding tensors and experimentally recorded chemical shift values. The frontier molecular orbital energies, electronic chemical potentials, chemical hardness, chemical softness and global electrophilicity indices of C-aryl-N-phenyl nitrones have been calculated at DFT/B3LYP/ 6-31+G(d,p) level of theory. Condensed Fukui functions and local electrophilicity indices have been computed to characterize the reactive sites and predict the preferred interactions of C-aryl-N-phenyl nitrones to methyl and ethyl crotonates. The softness matching indices have been evaluated to determine the regioselectivity of the cycloaddition reactions. The theoretical predictions were found to be in complete agreement with the experimental results implying that the DFT based reactivity indices correctly predict the regioselectivities of 1,3-dipolar cycloadditions of C-aryl-N-phenyl nitrones to methyl and ethyl crotonates.en_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.49A(11) [November 2010]en_US
dc.subjectTheoretical chemistryen_US
dc.subjectDensity functional calculationsen_US
dc.subjectDipolar cycloadditionsen_US
dc.subjectElectrophilicity indexen_US
dc.subjectChemical shiftsen_US
dc.subjectNMR shielding tensorsen_US
dc.subjectAryl phenyl nitronesen_US
dc.title1,3-dipolar cycloadditions. Part XX. DFT study of the configuration and conformation of C-aryl-N-phenyl nitrones and their reactivities as 1,3-dipoles to methyl and ethyl crotonatesen_US
Appears in Collections:IJC-A Vol.49A(11) [November 2010]

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