Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/21643
Title: 1H NMR spectral study of some 2,6 -diphenylthian-4-ones and their 1,1-dioxides
Authors: Pandiarajan, K
Benny, J Christophor Newton
Issue Date: Jul-2003
Publisher: NISCAIR-CSIR, India
Abstract: 1H NMR spectra have been recorded for r(2),c(6)diphenylthian-4-one 1, t(3)-methyl-r(2),c(6)-diphenylthian-4-one 2, c(3)-methyl-r(2),t(6)-diphenylthian-4-one 3 and their 1,1-dioxides 4-6 at 270 MHz. For 3 NOESY spectrum also has been recorded. AMI calculations have been performed on 1, 3 and 4. It seems that conformation 3AC with one axial methyl group and one axial phenyl group should contribute to some extent to 3 in solution. AM1 calculations suggest that conformation 3AC and boat conformation 3B have almost same energy and lie 1 kcal mol-1 above the chair conformation 3C. The calculations suggest that boat form could at best contribute to the extent of 4% to 1. In the sulphones the Jaa values are unusually large. The torsional angles are calculated using DAERM method and Altona's equatIOn. The results suggest that both methods are equally successful for sulphides but Altona's equation is not statisfactory in calculating ϕaa values in sulphones. Comparison of the results with those obtained from X-ray crystallographic studies suggests that proton-proton torsional angles in the solid state may considerably differ from those in solution. The 1H chemical shifts of 1-6 are analysed in some detail. It is found that an axial phenyl group deshields an adjacent axial proton by 0.6 ppm.
Page(s): 1711-1715
URI: http://hdl.handle.net/123456789/21643
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.42B(07) [July 2003]

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