Synthesis, structure determination and characterization by UV-Vis and IR spectroscopy of bis(diisopropylammonium) cis-dichloridobis-(oxalato-κ2O1,O2)stannate(IV)

被引:0
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作者
Sarr, Bougar [1 ]
Mbaye, Abdou [2 ]
Diop, Cheikh Abdoul Khadir [1 ]
Sidibe, Mamadou [1 ]
Rousselin, Yoann [3 ]
机构
[1] Univ Cheikh Anta Diop, Fac Sci & Tech, Dept Chim, Lab Chim Minerale & Analyt, Dakar, Senegal
[2] UASZ, LCPM, BP 523, Ziguinchor, Senegal
[3] ICMUB, UMR 6302, 9 Ave Alain Savary, F-21000 Dijon, France
关键词
crystal structure; tin(IV) oxalate derivative; spectroscopic studies; hydrogen bonding; CRYSTAL-STRUCTURE; COMPLEXES;
D O I
10.1107/S2056989019006030
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The organic-inorganic title salt, (C6H16N)(2)[Sn(C2O4)(2)Cl-2] or ((Pr2NH2)-Pr-i)(2)-[Sn(C2O4)(2)Cl-2], was obtained by reacting bis(diisopropylammonium) oxalate with tin(IV) chloride dihydrate in methanol. The Sn-IV atom is coordinated by two chelating oxalate ligands and two chloride ions in cis positions, giving rise to an [Sn(C2O4)(2)Cl-2](2-) anion (point group symmetry 2), with the Sn-IV atom in a slightly distorted octahedral coordination. The cohesion of the crystal structure is ensured by the formation of N-H center dot center dot center dot O hydrogen bonding between ((Pr2NH2)-Pr-i)(+) cations and [SnCl2(C2O4)(2)](2-) anions. This gives rise to an infinite chain structure extending parallel to [101]. The main inter-chain interactions are van der Waals forces. The electronic spectrum of the title compound displays only one high intensity band in the UV region assignable to ligand-metal ion charge-transfer (LMCT) transitions. An IR spectrum was also recorded and is discussed.
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页码:742 / +
页数:8
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