Novel organotin(IV) compounds derived from bis(organostannyl)methanes: Synthesis and crystal structures of bis[diphenyl(pyridin-2-onato)stannyl]methane and bis[bromophenyl(pyrimidine-2-thionato)stannyl]methane · C7H8

Reaction between bis(chlorodiphenylstanyl)methane and the sodium salt of 2-hydroxypyridine (pyONa) in the molar ratio of 1:2 provides the organotin hydroxide derivative [Ph2(pyO)SnCH2Sn(OH)Ph2]2 (1) (where pyO = anion of 2-hydroxypyridine), while reaction of bis(dibromophenylstanyl)methane with the sodium salt of pyrimidine-2-thione (pmtNa) in molar ratio of 1:4 gives the corresponding organotin thiolate derivative, as its toluene solvate [BrPh(pmt)Sn]2CH2 · C7H8 (2) (where pmt = anion of pyrimidine-2-thione). Both compounds were characterized by single crystal X-ray diffraction analysis and contain five-coordinate tin atoms. Compound 1 is a centrosymmetric head-to-tail dimmer with almost symmetrical Sn(1)–O(H)–Sn(2A) bridges.

Reaction between bis(chlorodiphenylstanyl)methane and the sodium salt of 2-hydroxypyridine (pyONa) provides the organotin hydroxide derivative [Ph2(pyO)SnCH2Sn(OH)Ph2]2 (1), while reaction of bis(dibromophenylstanyl)methane with the sodium salt of pyrimidine-2-thione (pmtNa) gives the organotin thiolate derivative, [BrPh(pmt)Sn]2CH2 · C7H8 (2). Compound (1) is a centrosymmetric head-to-tail dimmer with almost symmetrical Sn(1)–O(H)–Sn(2A) bridges.Figure optionsDownload as PowerPoint slide