NMR spectra of oriented biologically important molecules. The structure of and the internal rotation in N,N'-dimethyluracil

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DC Field	Value	Language
dc.contributor.author	Khetrapal, C.L.	-
dc.contributor.author	Kunwar, A.C.	-
dc.date.accessioned	2007-06-28T08:45:55Z	-
dc.date.available	2007-06-28T08:45:55Z	-
dc.date.issued	1982	-
dc.identifier.citation	Journal of Physical Chemistry, 1982, Vol. 86, p4815-4817.	en
dc.identifier.uri	http://hdl.handle.net/2289/3194	-
dc.description	Restricted Access.	en
dc.description.abstract	From the proton NMR spectra of Nfl-dimethyluracil oriented in two different nematic solvents, the internal rotation of the methyl groups about the N-C bonds is studied. It has been observed that the preferred conformation of the methyl group having one carbonyl in the vicinity is the one where a C-H bond is in the ring plane pointing toward the carbonyl group. The results are not sensitive to the mode of rotation of the other methyl group. These data are interpreted in terms of the bond polarizations.	en
dc.format.extent	392680 bytes	-
dc.format.mimetype	application/pdf	-
dc.language.iso	en	en
dc.publisher	American Chemical Society	en
dc.relation.uri	http://dx.doi.org	en
dc.rights	1982 American Chemical Society	en
dc.title	NMR spectra of oriented biologically important molecules. The structure of and the internal rotation in N,N'-dimethyluracil	en
dc.type	Article	en
Appears in Collections:	Research Papers (SCM)

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