dc.contributor.author |
Berestovitskaya V. |
|
dc.contributor.author |
Baichurin R. |
|
dc.contributor.author |
Islamov D. |
|
dc.contributor.author |
Kataeva O. |
|
dc.contributor.author |
Aboskalova N. |
|
dc.contributor.author |
Trukhin E. |
|
dc.date.accessioned |
2018-09-19T21:00:12Z |
|
dc.date.available |
2018-09-19T21:00:12Z |
|
dc.date.issued |
2016 |
|
dc.identifier.issn |
1070-3632 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/143494 |
|
dc.description.abstract |
© 2016, Pleiades Publishing, Ltd.X-ray diffraction analysis established that 3-(4-N,N-dimethylaminophenyl)-2-nitro-1-phenylprop-2-en-1-one has E configuration both in crystal and in solution. The benzoyl group deviates from the styrene plane by 89.83°. The elongation of the C=C bond and shortening of its surrounding single bonds points to a high polarization of the molecule, implying a great contribution of the bipolar structure to the ground state. |
|
dc.relation.ispartofseries |
Russian Journal of General Chemistry |
|
dc.subject |
13 С NMR spectroscopy |
|
dc.subject |
bipolar structure |
|
dc.subject |
X-ray diffraction analysis |
|
dc.subject |
zwitter ion |
|
dc.subject |
α-nitrochalcones |
|
dc.title |
3-(4-N,N-dimethylaminophenyl)-2-nitro-1-phenylprop-2-en-1-one by <sup>13</sup>C NMR spectroscopy and X-ray diffraction analysis |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
10 |
|
dc.relation.ispartofseries-volume |
86 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
2312 |
|
dc.source.id |
SCOPUS10703632-2016-86-10-SID84996802217 |
|