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dc.contributor.author | Safin D. | |
dc.contributor.author | Bolte M. | |
dc.contributor.author | Shakirova E. | |
dc.contributor.author | Babashkina M. | |
dc.date.accessioned | 2018-09-18T20:07:51Z | |
dc.date.available | 2018-09-18T20:07:51Z | |
dc.date.issued | 2009 | |
dc.identifier.issn | 0277-5387 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/136806 | |
dc.description.abstract | Two N-thiophosphorylated thiosemicarbazides of the common formula RC(S)NHP(S)(OiPr)2 [R = PhNHNH- (1); EtN(NH2)- (2)] have been synthesized and characterized by IR, 1H and 31P spectroscopy, and the single crystal X-ray diffraction method. Single crystal X-ray diffraction studies showed the thiosemicarbazides form both intra- and intermolecular hydrogen bonds, which in turn lead to polymeric chain formation. Moreover, according to the X-ray data of the phenylsubstituted thiosemicarbazide, the formation of intermolecular H⋯η6-phenyl interactions were established. © 2008 Elsevier Ltd. All rights reserved. | |
dc.relation.ispartofseries | Polyhedron | |
dc.subject | Crystal structures | |
dc.subject | Ethylhydrazine | |
dc.subject | Phenylhydrazine | |
dc.subject | Thiosemicarbazide | |
dc.title | The influence of the substituent [PhNHNH- and EtN(NH2)-] on the N-thiophosphorylated thiosemicarbazides RC(S)NHP(S)(OiPr)2 crystal design | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 3 | |
dc.relation.ispartofseries-volume | 28 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 501 | |
dc.source.id | SCOPUS02775387-2009-28-3-SID59349100824 |