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Syntheses, Structures, and Complexation Studies of Tris(organostannyl)methane Derivatives.
Wendji, Anicet Siakam; Lutter, Michael; Stratmann, Lukas M; Jurkschat, Klaus.
Afiliação
  • Wendji AS; Lehrstuhl für Anorganische Chemie II Fakultät für Chemie und Chemische Biologie Technische Universität Dortmund 44221 Dortmund Germany.
  • Lutter M; Lehrstuhl für Anorganische Chemie II Fakultät für Chemie und Chemische Biologie Technische Universität Dortmund 44221 Dortmund Germany.
  • Stratmann LM; Lehrstuhl für Anorganische Chemie II Fakultät für Chemie und Chemische Biologie Technische Universität Dortmund 44221 Dortmund Germany.
  • Jurkschat K; Lehrstuhl für Anorganische Chemie II Fakultät für Chemie und Chemische Biologie Technische Universität Dortmund 44221 Dortmund Germany.
ChemistryOpen ; 5(6): 554-565, 2016 Dec.
Article em En | MEDLINE | ID: mdl-28032025
ABSTRACT
The syntheses of tris(organostannyl)methanes HC(SnX n Ph(3-n))3 (1, n=0; 2, n=1, X=I; 3, n=1, X =F; 4, n=1, X=Cl; 5, n=1, X=OAc; 6, n=2, X=I; 7, n=2, X=Cl) and the organostannate complexes Et4N[HC(SnIPh2)3⋅F] (8), Ph4P[HC(SnClPh2)3⋅Cl] (9), and [Ph4P]2[HC(SnCl2Ph)3⋅2 Cl] (10) are reported. The compounds were characterized by 1H, 13C, 19F, and 119Sn NMR spectroscopy, IR spectroscopy, electrospray mass spectrometry, and (with the exception of 3) single-crystal X-ray diffraction analysis. From the reaction between 2 and AgClO4 resulted the unprecedented hexanuclear organotin oxocluster [HC{Sn(ClO4)2Ph2}2Sn(OH)2Ph]2 (11), the molecular structure of which was elucidated by using X-ray crystallography.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ChemistryOpen Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ChemistryOpen Ano de publicação: 2016 Tipo de documento: Article