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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 861-871 
    ISSN: 0268-2605
    Keywords: diorganotin ; Pyrimidine ; complex ; Mössbauer ; IR ; NMR ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexes formed between the diorganotin(IV) moieties, R2Sn(IV), and the ligand 2-mercaptopyrimidine, (H)SPym, were investigated. Complexes R2SnHal(SPym) and R2Sn(SPym)2 [R = Me, iPr, nBu, iBu, tBu, cyclohexyl(Cy), Ph] were synthesized, and characterized by elemental analysis. In the solid state, chelation of SPym through S and N donors was established by IR spectroscopy, and the nature of the environment of tin centers was investigated by 119Sn Mössbauer spectroscopy. From the dynamics of 119Sn nuclei determined by variable-temperature measurements on representative compounds [Me2SnCl(SPym) and Cy2SnBr(SPym)], as well as by point-charge model treatment of nuclear quadrupole splitting parameters, it was inferred that Me2SnCl-­(SPym) may assume a trans-Me2 octahedral coordination geometry around tin in a monodimensional polymer, or a monomeric trigonal-bipyramidal structure (distorted). The latter type of structure was assigned to the other R2SnHal(SPym) species, while R2Sn(SPym)2 complexes assume a trans-octahedral, or skew trapezoidal, tin environment. In CHCl3-CDCl3 solutions, monomeric species occur (according to vapor-pressure osmometry), where 1H and 13C NMR spectroscopic parameters of SPym indicate the persistence of Sn chelation by S and N donor atoms. The Me2SnCl(SPym) species assume trigonal-bipyramidal structures with a chelating SPym ligand, in CDCl3 and C2H5OH solutions, according to the coupling constants 1J(119Sn,13C), as well as IR and 119Sn Mössbauer spectroscopic data. 119Sn NMR parameters fully correspond with data for the homologous complexes with 2-mercaptopyridine. Copyright © 1998 John Wiley & Sons, Ltd.
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  • 2
    ISSN: 0268-2605
    Keywords: Organotin ; 2-mercaptopyridine ; pyridine-2-thiolato complexes ; Mössbauer ; IR ; NMR ; crystal structure ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diorganotin(IV) derivatives of 2-mercaptopyridine (HSPy), R2Sn(SPy)2, R2SnCl(SPy) (R = Me, iPr, nBu, tBu, Cy, Ph) and Cy2SnBr(SPy), were obtained from R2SnX2 (X = Cl, Br) and NaSPy.Ph2SnCl(SPy) crystals, as determined by singlecrystal X-ray diffraction, are monoclinic in the space group P21/n. Tin forms with the bidentate SPy ligand a four-membered chelate ring with a short NSnS bite angle of 64.8(1)° leading to a heavily distorted trigonal-bipyramidal environment about tin. Apical Cl-Sn-N angle = 156.1(1)° equatorial C-Sn-C angle = 121.9(2)°. From 119Sn Mössbauer and IR data, analogous structures are inferred for the other solid compounds R2SnX(SPy), and distorted octahedral molecular structures for the solid compounds R2Sn(SPy)2 with R in the trans position, and sulfur atoms and nitrogen-donor atoms each in cis positions. According to IR and 1H, 13C and 119Sn NMR data, the solid-state molecular structures are retained in chloroform solution.
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  • 3
    ISSN: 0268-2605
    Keywords: organotin ; pyridine-2-thiolate complexes ; pyrimidine-2-thiolate complexes ; crystal structure ; Mössbauer ; IR ; NMR ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mono-organotin(IV) and tin(IV) derivatives of 2-mercaptopyridine (HSPy) and 2-mercaptopyrimidine (HSPym), RSnL3 (R=Me, n-Bu, Ph; L=SPy, SPym; R=Bz=benzyl, o-ClBz, o-ClC6H4, p-ClC6H4, o-tolyl, p-tolyl; L=SPy), RSnClL2 (R=Me, n-Bu, Ph; L=SPy, SPym), RSnCl2L (R=Me, n-Bu; L=SPy, SPym) and SnCl4-nLn (L=SPy, SPym; n=2, 4) were obtained from RSnCl3 or SnCl4 and NaL or by neutralization (R=Ph, p-tolyl; L=SPy, SPym). RSnClL2 and RSnCl2L were better prepared by comproportionation of RSnCl3 and RSnL3.MeSn(SPy)3 and PhSn(SPy)3·1.5CHCl3 crystals, as determined by single-crystal X-ray diffraction, are monoclinic. In the discrete monomeric RSn(SPy)3 units, three bidentate SPy ligands together with R form a distorted pentagonal bipyramid around tin. One S and the C(R) atom are in the axial positions. Two S atoms and three N atoms form the pentagonal plane.From 119Sn Mössbauer and IR data, analogous structures are inferred for the other solid RSnL3 compounds, except for R=Bz, o-ClBz, o-ClC6H4 and o-tolyl, in which tin would be hexacoordinated. In the compounds RSnClL2 and RSnCl2L, tin is at the center of an octahedron or a trigonal bipyramid, respectively. For Sn(SPym)4 and SnCl2(SPym)2, the same type of octahedral structure as was previously found for Sn(SPy)4·HSPy and SnCl2(SPy)2 is proposed.According to IR and 1H, 13C and 119Sn NMR data, the solid-state molecular structures are retained in chloroform and dimethyl sulfoxide solution. © 1997 John Wiley & Sons, Ltd.
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