Synthesis and structural study of triphenylbismuth bis (salicylate)
| 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.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,F2932KT2II. The bismuth atom of the compound has a distorted trigonal-bipyramidal configuration. | en_US |
| dc.identifier.uri | http://e-biblio.univ-mosta.dz/handle/123456789/11321 | |
| 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 |