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Triorganotin Pseudohalides

By rxn. of MeaSnOH with NH4SCN in c.MeCeHn under reflux, in 75 yield (266O). Prop.t m. 107-110° (2027) 105-108° (far) IR spectra and assignment (2027, [Pg.562]

with MSCN Complex formation and dissocn. by electrophoresis and anion exchange paper chromatography M Na, K (2585)  [Pg.563]

MegSnNCS-Py, m. 112-1 (266O), IIO-I3 and assignment, struct. (2IO3) [SnC9Hi4N2S]. [Pg.563]

Me3SnNCS Et4NSCN, from components in EtOH, m. 120-121° (dec.), complex formation by paper chromatography and electrophoresis (72) [SnCx3H29N3S2l  [Pg.563]

By rxn. of Me3SnCl with aq. HN3 and extraction with EtsO, in 58% yield (556-7)- [Pg.563]

Ionization of tin-halogen bonds can occur in triorganotin halides containing two intramolecular donor groups, e.g. (18). Diorganotin dUialides and bis-pseudohalides also exhibit strong tendencies to form aggregated species with... [Pg.4883]

See other pages where Triorganotin Pseudohalides is mentioned: [Pg.562]    [Pg.566]    [Pg.567]    [Pg.562]    [Pg.566]    [Pg.567]    [Pg.208]    [Pg.1102]    [Pg.10]    [Pg.2047]   


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Pseudohalide

Pseudohalides

Triorganotins

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