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Synthese amino- und silylsubstituierter Triphosphane – Struktur des 1.1.3.3-Tetrakis(di-iso-propylamino)-2-trimethylsilyl- und des 1.1.3.3-Tetraphenyl-2-tri-iso-propylsilyl-triphosphans / Synthesis of Amino- and Silyl-Substituted Triphosphines – Structure of 1,1,3,3-Tetrakis(di-iso-propylamino)-2-trimethylsilyl- and 1,1,3,3-Tetraphenyl-2-tri-iso-propylsilyl-triphosphine
1993
Zeitschrift für Naturforschung. B, A journal of chemical sciences
A variety of triphosphines [(Et2N)2P]2PR 4a–h, [(iPr2N)2P]2PR 5a–e and [Ph2P]2PR 9e–g [R = Cy (a), tBu (b), Mes (c), Me3Si (d), tBuMe2Si (e), ThexMe2Si (f), iPr3Si (g), Ad (h), H (i)] has been obtained by the reaction of the dilithiated primary phosphines RPH2 la–h with 2 equiv. of the chlorophosphines (Et2N)2PCl 2, (iPr2N)2PCl 3 or Ph2PCl 8. Methanolysis of the trimethylsilyl substituted derivative [(iPr2N)2P]2P(SiMe3) 5d yields the hydrogen substituted triphosphine [(iPr2N)2P]2PH 5i. The
doi:10.1515/znb-1993-1209
fatcat:mc65tkn7yrgjhjbcccscyio3ni