Title of article :
Di-n-butyl­bis­­[N-(2-meth­­oxy­eth­yl)-N-methyl­di­thio­carbamato-κ2S,S′]tin(IV): crystal structure and Hirshfeld surface analysis
Author/Authors :
Mohamad, Rapidah Biomedical Science Programme - School of Diagnostic and Applied Health Sciences - Faculty of Health Sciences - Universiti Kebangsaan Malaysia - Malaysia , Awang, Normah Environmental Health and Industrial Safety Programme - School of Diagnostic and Applied Health Sciences - Faculty of Health Sciences - Universiti Kebangsaan Malaysia, Malaysia , Kamaludin, Nurul F. Environmental Health and Industrial Safety Programme - School of Diagnostic and Applied Health Sciences - Faculty of Health Sciences - Universiti Kebangsaan Malaysia, Malaysia , Jotani, Mukesh M. Department of Physics - Bhavan's Sheth R. A. College of Science, Ahmedabad, India , Tiekink, Edward R. T. Research Centre for Chemical Crystallography - School of Science and Technology, Sunway University, Malaysia
Pages :
11
From page :
1
To page :
11
Abstract :
The complete mol­ecule of the title compound, [Sn(C4H9)2(C5H10NOS2)2], is generated by a crystallographic mirror plane, with the SnIV atom and the two inner methyl­ene C atoms of the butyl ligands lying on the mirror plane; statistical disorder is noted in the two terminal ethyl groups, which deviate from mirror symmetry. The di­thio­carbamate ligand coordinates to the metal atom in an asymmetric mode with the resulting C2S4 donor set defining a skew trapezoidal bipyramidal geometry; the n-butyl groups are disposed to lie over the longer Sn—S bonds. Supra­molecular chains aligned along the a-axis direction and sustained by methyl­ene-C—H⋯S(weakly coordinating) inter­actions feature in the mol­ecular packing. A Hirshfeld surface analysis reveals the dominance of H⋯H contacts in the crystal
Keywords :
crystal structure , Hirshfeld surface analysis , di­thio­carbamate , organotin
Journal title :
Acta Crystallographica Section E: Crystallographic Communications
Serial Year :
2017
Full Text URL :
Record number :
2621313
Link To Document :
بازگشت