Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6681
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dc.contributor.authorRao, Bojja Rajeshwar-
dc.date.accessioned2009-11-19T04:26:41Z-
dc.date.available2009-11-19T04:26:41Z-
dc.date.issued2006-09-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6681-
dc.description2083-2090en_US
dc.description.abstractThe geometry and electronic structures of uracil, uridine and uridylic acid involving [1,3] sigmatropic hydrogen migration in the formation of tautomers have been fully optimized and evaluated by semi-empirical molecular orbital AM1 method. In this connection, the heats of formation (Hf°), dipole moments (), full atomic charges, and energies of frontier molecular orbitals (EHOMO and ELUMO) have been calculated and discussed. The mechanistic investigation of [1,3] sigmatropic rearrangement in uracil affected in the conformational changes of uridine and uridylic acid has been studied by the comparison of net charges of atoms in different positions of the molecule. All tautomers exist with in the energy of 20.569 kcal/mol. Furthermore, dipole moment and atomic charges of all tautomers indicated that the dipole-dipole interactions play a vital role during the synthesis of proteins and enzymes.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl.8 C07Den_US
dc.sourceIJC-B Vol.45B(09) [September 2006]en_US
dc.subjectFrontier molecular orbitalen_US
dc.subject[1,3] sigmatropic rearrangementen_US
dc.subjecttautomersen_US
dc.subjectconformationsen_US
dc.titleStudy of [1,3] sigmatropic hydrogen migration in uracil, uridine and uridylic acid by AM1 methoden_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(09) [September 2006]

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