Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/2085
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dc.contributor.authorSun, Hai-tao-
dc.contributor.authorTang, Ke-
dc.contributor.authorWang, Zhi-zhong-
dc.contributor.authorZhou, Zheng-yu-
dc.date.accessioned2008-09-23T11:03:58Z-
dc.date.available2008-09-23T11:03:58Z-
dc.date.issued2008-04-
dc.identifier.issn0376-4710-
dc.identifier.urihttp://hdl.handle.net/123456789/2085-
dc.description542-547en_US
dc.description.abstractThe hydrogen bonding of complexes formed between formamide and adenine molecules has been investigated using density functional theory method at 6-311++G(d, p) level. Nine stable cyclic structures with two hydrogen bonds being involved in the interaction have been found on the potential energy surface. According to the different hydrogen donors offered by formamide molecules, the nine complexes can be divided into two groups. For AF1-AF5, the hydrogen donors are carbon atoms of the formamide molecules, while the nitrogen atoms act as the hydrogen donors in AF6-AF9. The complex AF6 is most stable amongst all the complexes and N8 atom and N9-H15 group form the strongest hydrogen bonds. The hydrogen bonds with the participation of C3-H11 group are the weakest. The vibrational frequency shifts and IR intensities shifts are also reported.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCA Vol.47A(4) [April 2008]en_US
dc.titleDensity functional theory study on the interaction between formamide and adenineen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.47A(04) [April 2008]

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