Synthesis and structural study of triphenylbismuth bis (salicylate)

Chouaih, Abdelkader; Feham, Kheira; Benkadari, Abdelkarim; Miloudi, Abdellah; Boyer, Gérard; El Abed, Douniazed

dc.contributor.author	Chouaih, Abdelkader
dc.contributor.author	Feham, Kheira
dc.contributor.author	Benkadari, Abdelkarim
dc.contributor.author	Miloudi, Abdellah
dc.contributor.author	Boyer, Gérard
dc.contributor.author	El Abed, Douniazed
dc.date.accessioned	2019-07-02T09:00:18Z
dc.date.available	2019-07-02T09:00:18Z
dc.date.issued	2013-03-29
dc.identifier.uri	http://e-biblio.univ-mosta.dz/handle/123456789/11321
dc.description.abstract	The crystal of triphenylbismuth bis (Salicylate) pentavalent was synthesized from the reaction of triphenylbismuth di-chloride with salicylic acid dissolved in methylene chloride at room temperature. The molecular and crystal structures of triphenylbismuth bis (Salicylate) were determined by X-ray diffraction analysis. This compound crystallizes in the triclinic space group 1P with crystallographic parameters: a = 11.2937 (3) Å, b = 14.6516 (3) Å, c = 17.8253 (4) Å, α = 78.2958 (7)°, β = 76.232 (6)°, γ = 85.351 (6)°,6.332mm, V = 2803.59 (11) Å, 2Z, 31.693gcmDc, . The final residual factor is 0.0602 for 5806 reflexions with 0001392,F2932KT2II. The bismuth atom of the compound has a distorted trigonal-bipyramidal configuration.	en_US
dc.publisher	Cryst Struct Theory Appl	en_US
dc.subject	Organobismuth	en_US
dc.subject	Structure	en_US
dc.subject	X-Ray Diffraction	en_US
dc.subject	Salicylate	en_US
dc.subject	Synthesis	en_US
dc.title	Synthesis and structural study of triphenylbismuth bis (salicylate)	en_US
dc.type	Article	en_US