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Comparison of Two Phosphinidenes Binding to Silicon(IV)dichloride as well as to Silylene.
Kundu, Subrata; Sinhababu, Soumen; Siddiqui, Mujahuddin M; Luebben, Anna V; Dittrich, Birger; Yang, Tao; Frenking, Gernot; Roesky, Herbert W.
Afiliación
  • Kundu S; Institut für Anorganische Chemie , Universität Göttingen , Tammannstrasse 4 , D-37077 Göttingen , Germany.
  • Sinhababu S; Institut für Anorganische Chemie , Universität Göttingen , Tammannstrasse 4 , D-37077 Göttingen , Germany.
  • Siddiqui MM; Institut für Anorganische Chemie , Universität Göttingen , Tammannstrasse 4 , D-37077 Göttingen , Germany.
  • Luebben AV; Institut für Anorganische Chemie , Universität Göttingen , Tammannstrasse 4 , D-37077 Göttingen , Germany.
  • Dittrich B; Anorganische und Strukturchemie II , Heinrich Heine-Universität Düsseldorf , Gebäude 26.42.01.21, Universitätsstrasse 1 , 40225 Düsseldorf , Germany.
  • Yang T; Fachbereich Chemie , Philipps-Universität Marburg , Hans-Meerweinstrasse 4 , 35032 Marburg , Germany.
  • Frenking G; Fachbereich Chemie , Philipps-Universität Marburg , Hans-Meerweinstrasse 4 , 35032 Marburg , Germany.
  • Roesky HW; Institut für Anorganische Chemie , Universität Göttingen , Tammannstrasse 4 , D-37077 Göttingen , Germany.
J Am Chem Soc ; 140(30): 9409-9412, 2018 08 01.
Article en En | MEDLINE | ID: mdl-30011193
ABSTRACT
The cyclic alkyl(amino) carbene (cAAC) anchored silylene with two phosphinidenes was isolated as (cAAC)Si{P(cAAC)}2 (3) at room temperature, which was synthesized from the reduction of (Cl2)Si{P(cAAC)}2 (2) using 2 equiv of KC8. Compound 2 resulted from the reaction of 2 equiv of (cAAC)PK (1) with 1 equiv of SiCl4. Compounds 2 and 3 are the first examples where two terminal phosphinidenes are binding each to a silicon center characterized by single crystal X-ray structural analysis. Furthermore, the structure and bonding of compounds 2 and 3 have been investigated by theoretical methods for comparison.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2018 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2018 Tipo del documento: Article País de afiliación: Alemania