6199-33-3Relevant academic research and scientific papers
Studies in aryltin chemistry. X 1. Synthesis and NMR spectra (119Sn and 13C) of some meta-and ortho-substituted tetra-and triaryltin compounds. The crystal and molecular structures of tris(m-tolyl)-and tris(3,5-dimethylphenyl) tin(IV) chloride
Wharf, Ivor,Simard, Michel G.
, p. 1 - 9 (2007/10/03)
Several new tetra-aryltin compounds, Ar4Sn [Ar = 3,5-(CH3)2C6H3, 3,5-Z2C6H3, and m-ZC6H4 (Z = F, Cl)] and Ar3SnX [X = Cl, Br, I: Ar = 3,5-(CH3)2C6H3, m-and o-CH3OC6H4; X = Br; Ar = m-ZC6H4 (Z = F, Cl)] have been synthesized by literature methods and complete solution NMR data (119Sn, 13C) are reported for these and other meta-and ortho-substituted aryltins. Meta-substituents appear to exert electronic effects on chemical shifts and coupling constants, but for ortho-substituents steric effects appear to predominate. Crystal data show that meta-substituted Ar3SnX have trigonal unit cells in contrast to the monoclinic unit cells adopted by para-and ortho-substituted Ar3SnX. Complete crystal structures are reported for (m-CH3C6H4)3SnCl: R3, a= 14.9262(15), c = 7.3482(12)A, Z=3 and (3,5-(CH3)2C6H3)3SnCl: R3c, a = 15.779(8), c = 15.593(4)A, Z = 6. In both cases, all molecules have trigonal symmetry, the first such examples to be reported.
TRIARYL-SILYL, -GERMYL, AND -STANNYL RADICALS MAr3 (M=Si, Ge, OR Sn AND Ar=2,4,6-Me3C6H2) AND Ge(2,6-Me2C6H3)3: SYNTHESIS AND ESR STUDIES
Gynane, Michael J. S.,Lappert, Michael F.,Riley, Paul I.,Riviere, Pierre,Riviere-Baudet, Monique
, p. 5 - 12 (2007/10/02)
The triarylmetal-centred radicals MAr3 (M=Si, Ge, or Sn: Ar=2,6-Me2C6H3 or 2,4,6-Me3C6H2) have been prepared from the appropriate triarylmetal chloride, MAr3Cl, and an electron-rich olefin >2 (R=Me or Et) under UV irradiation in toluene at low
