Please use this identifier to cite or link to this item: https://elar.usfeu.ru/handle/123456789/8887
Title: X-ray diffraction investigation of 1-phenyl-3-isopropyl-5-(benzothiazol-2- yl)formazan
Authors: Slepukhin, P. A.
Pervova, I. G.
Rezinskikh, Z. G.
Lipunova, G. N.
Gorbatenko, Y. A.
Lipunov, I. N.
Issue Date: 2008
Publisher: Pleiades Publishing
Citation: Slepukhin, P. A. X-ray diffraction investigation of 1-phenyl-3-isopropyl-5-(benzothiazol-2- yl)formazan / P. A. Slepukhin, I. G. Pervova, Z. G. Rezinskikh [et al.] // Crystallography Reports. – 2008. – Vol. 53. – Iss. 1. – P. 88-91.
Abstract: The crystal structure of 1-phenyl-3-isopropyl-5-(benzothiazol-2-yl)formazan is investigated using X-ray diffraction. The compound crystallizes in the form of two crystallographically independent molecules (A and B) in identical conformations that are stabilized by intermolecular hydrogen bonds. The intermolecular hydrogen bonds N-H ⋯ N (N⋯N, 2.892 and 2.939 Å) link molecules into AB dimers. Both molecules have a flattened structure, except for the isopropyl fragment. The bonds in the formazan chains are delocalized. Molecules A and B have close geometric characteristics. © 2008 Pleiades Publishing, Inc.
Keywords: CRYSTAL STRUCTURE
HYDROGEN BONDS
MOLECULAR STRUCTURE
X RAY DIFFRACTION
COMPOUND CRYSTALLIZES
FORMAZAN CHAINS
IDENTICAL CONFORMATIONS
BENZENE
URI: https://elar.usfeu.ru/handle/123456789/8887
DOI: 10.1134/S1063774508010112
SCOPUS: 2-s2.0-38749110402
WoS: WOS:000252797600011
RSCI: 13590581
Appears in Collections:Научные публикации, проиндексированные в SCOPUS и WoS CC

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