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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 |