Pentakoordiniertes Silicium: Intramolekulare Koordination bei O-Fluorsilylderivaten von N.N-disubstituierten Aminoethanolen bzw. N-fluorsilylsubstituierten Derivaten des Trimethylethylendiamins/Penta-co-ordinate Silicon: Intramolecular Coordination of O-Fluorosilyl Derivatives of N.N-Disubstituted Aminoethanols and of N-Fluorosilyl Substituted Derivatives of Trimethylethylenediamine

Abstract

Abstract Tetrafluorosilane and phenyltrifluorosilane react with the O-trimethylsilyl derivatives of N.N-disubstituted aminoethanols and with the N-trimethylsilyl derivative of N.N.N′-trimethylethylene diamine to give the corresponding monosubstituted fluorosilyl compounds in which, on the basis of 19F NMR spectroscopic studies, intramolecular N -Si bonding raises the coordination number of silicon from four to five (i.e. λ4Si -> λ5Si). The low temperature 19F NMR data suggest a trigonal-bipyramidal configuration at λ5 Si with an axial N -Si coordinate bond.