Synthesis, Characterization and Thermal Study of some new Organochalcogenide compounds containing arylamide group | ||||
Egyptian Journal of Chemistry | ||||
Article 30, Volume 64, Issue 9, September 2021, Page 5009-5015 PDF (637.26 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/ejchem.2021.49176.3009 | ||||
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Authors | ||||
Attared Fadel Hassan![]() ![]() ![]() ![]() | ||||
1Department of chemistry, College of science, University of basrah, Basrah, Iraq | ||||
2Department of chemistry /college of science /university of Basrah / Basrah/Iraq | ||||
3Chemistry, Science , University of Basrah | ||||
4Department of Chemistry /college of Pharmacy/university of Basrah/Iraq | ||||
Abstract | ||||
Two Series of organochalcogen compounds were prepared. The first series was prepared by the reaction of 2-chloro-N-arylacetamide (where aryl is benzyl, phenyl, o-toluene, or p-toluene) with sodium hydrogen selenide (prepared in situ) to give diorganyl selenide compounds (R2Se). The second series was prepared by reaction of N-benzyl-2-chloro-N-(2-chloroacetyl)acetamide with sodium chalcogenate , Na2E (where E= S, Se, and Te) to give the corresponding cyclic chalcogenide compounds. Diiodo derivatives of cyclic selenide and telluride were also prepared. The thermal stability of the new selenium compounds (R2Se) were decomposed at 300oC. Thermogram showed a phase transfer point between 120-150oC indicating that these compounds may act as liquid crystal compounds. All new compounds were characterized by CHN elemental analysis, UV-Visible, FT-IR and 1H NMR spectroscopic data. | ||||
Keywords | ||||
2-chloro-N-arylacetamide; selenium; tellurium; organochalcogen compounds; heterocycles | ||||
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