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Abstract: A series of new triorganotin(IV) complexes with 4-hydroxy-2-mercapto-6-methylpyrimidine (L1H2), 4-hydroxy-2-mercapto-pyrimidine (L2H2), 2,4(1H,3H)-pyrimidinedithione (L3H2) () of the type R3SnLSnR3 (R=Me 1, 4, 7; R=Ph 2, 5, 8; R=PhCH2 3, 6, 9) have been synthesized by reactions of triorganotin(IV) chloride and corresponding ligands. All complexes are characterized by elemental analyses, IR spectra and NMR spectra analyses. Among them, complexes 2, 5 and 8 are also characterized by X-ray crystallography diffraction analyses. Significant π⋯π stacking, C–H⋯π interactions and intramolecular hydrogen bonds stabilize these structures. [Copyright &y& Elsevier]

A series of organotin(IV) complexes with 2,5-dimercapto-1, 3, 4-thiodiazole (HHdmt) of the type (RnSnClm)2(dmt) (m=0, n=3, R=Ph 1, PhCH2 2, n-Bu 3; m=1, n=2, R=Ph 4) and [R2Sn(dmt) · L]n (L=0.5C6H6, R=CH3 5; L=0, n=5, R=n-Bu 6) have been synthesized. All complexes 1–6 were characterized by elemental analysis, IR, 1H and 13C NMR spectra. And except for 3, complexes 1, 2, 4, 5 and 6 were also determined by X-ray crystallography. The tin atoms of complexes 1, 2, 3 and 4 are all five-coordinated. The geometries at tin atoms of 1, 2, 3 and 4 are distorted trigonal bipyramidal. The tin atoms of complexes 5 and 6 are six-coordinated and their geometries are distorted octahedral. [Copyright &y& Elsevier]

The diorganotin(IV) dichloride reacts with sodium 2-pyridinethiolato-N-oxide in a 1:1 ratio to produce [Me2SnCl(2-SpyO)] (1), [Et2SnCl(2-SpyO)] (2), [Bu2SnCl(2-SpyO)] (3), [Ph2SnCl(2-SpyO)] (4), and [(PhCH2)2SnCl(2- SpyO)] (5). The new complexes have been characterized by elemental analysis and IR and NMR (1H, 119Sn, and 13C) spectroscopy. On the basis of 119Sn NMR data the effective coordination number in solution is five. The structures 1 and 4 have been confirmed by X-ray crystallography. Crystals of 1 are triclinic with space group Pbar over 1 and those of 4 are monoclinic, P21/n. The tin environment is a distorted trigonal bipyramid with the Cl and oxygen atoms in apical positions. Both complexes exhibit strong π–π stacking interactions. [ABSTRACT FROM AUTHOR]

Abstract: A series of organotin(IV) complexes with O,O-diethyl phosphoric acid (L1H) and O,O-diisopropyl phosphoric acid (L2H) of the types: [R3Sn·L] n (L=L1, R=Ph 1, R=PhCH2 2, R=Me 3, R=Bu 4; L=L2, R=Ph 9, R=PhCH2 10, R=Me 11, R=Bu 12), [R2Cl Sn·L] n (L=L1, R=Me 5, R=Ph 6, R=PhCH2 7, R=Bu 8; L=L2, R=Me 13, R=Ph 14, R=PhCH2 15, R=Bu 16), have been synthesized. All complexes were characterized by elemental analysis, TGA, IR and NMR (1H, 13C, 31P and 119Sn) spectroscopy analysis. Among them, complexes 1, 2, 3, 5, 8, 9 and 11 have been characterized by X-ray crystallography diffraction analysis. In the crystalline state, the complexes adopt infinite 1D infinite chain structures which are generated by the bidentate bridging phosphonate ligands and the five-coordinated tin centers. [Copyright &y& Elsevier]