Syntheses and structures of N, C, N-stabilized antimony chalcogenides

被引:7
|
作者
Ganesamoorthy, Chelladurai [1 ]
Woelper, Christoph [1 ]
Dostal, Libor [2 ]
Schulz, Stephan [1 ]
机构
[1] Univ Duisburg Essen, Fac Chem, Ctr Nanointegrat CENIDE, Univ Str 5-7, D-45117 Essen, Germany
[2] Univ Pardubice, Fac Chem Technol, Dept Gen & Inorgan Chem, Studentska 573, Pardubice 53210, Czech Republic
关键词
Pincer ligand; Chalcogens; Subvalent compounds; Oxidation; HEAVIER GROUP-15 ELEMENTS; SOLID-STATE STRUCTURES; MAIN-GROUP ELEMENTS; N; C; N-CHELATED ANTIMONY(III); ORGANOBISMUTH COMPOUNDS; BOND-CLEAVAGE; ORGANOANTIMONY; RINGS; SB; BI;
D O I
10.1016/j.jorganchem.2017.01.007
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The oxidation reactions of ArSb [Ar = 2,6-( HC=N-t- Bu)(2)C6H3] with S-8, grey Se and Te as well as E2Ph2 (E== S, Se, Te) are demonstrated. The reactions of ArSb with elemental sulfur and selenium occurred at elevated temperatures and yielded ArSbE (E== S, 1; Se 2), whereas the reactions with E2Ph2 proceeded at room temperature with subsequent formation of the corresponding insertion complexes ArSb(EPh) 2 (E==S 3; Se 4). In addition, ArSb(TePh)(2) (5) was formed at very low temperature and showed a temperature-dependent reversible equilibrium with ArSb and Te2Ph2 between -80 degrees C and 20 degrees C. The formation and structure of compounds 1-4, which were isolated in good yields, are assigned through multinuclear NMR (H-1, C-13, Se-77), IR spectroscopy and microanalyses data. In addition, the molecular structures of 2-4 are further confirmed by single crystal X-ray diffraction studies. (C) 2017 Elsevier B. V. All rights reserved.
引用
收藏
页码:38 / 43
页数:6
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