dc.contributor.author |
Vereshchagin A. |
|
dc.contributor.author |
Timosheva A. |
|
dc.contributor.author |
Vul'fson S. |
|
dc.contributor.author |
Remizov A. |
|
dc.contributor.author |
Arbuzov B. |
|
dc.date.accessioned |
2018-09-14T20:26:45Z |
|
dc.date.available |
2018-09-14T20:26:45Z |
|
dc.date.issued |
1973 |
|
dc.identifier.issn |
0568-5230 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132486 |
|
dc.description.abstract |
1. According to the data of the dipole moments, Kerr effects, light scattering, and IR spectra, 1,3-dihalopropanes symmetrically substituted in the 2-position are represented in CCl4 by conformers with trans-gauche and gauche-gauche (with an arrangement of the halogen atoms on different sides of the plane of the carbon atoms) orientations of the X-C-C-C-X chain. 2. 1, 2,3-Trihalopropanes exist chiefly in a gauche-gauche conformation. © 1974 Consultants Bureau. |
|
dc.relation.ispartofseries |
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
|
dc.title |
Conformation of compounds with two geminal halomethyl groups |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
11 |
|
dc.relation.ispartofseries-volume |
22 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
2363 |
|
dc.source.id |
SCOPUS05685230-1973-22-11-SID34250435067 |
|