کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1310533 | 975253 | 2007 | 9 صفحه PDF | دانلود رایگان |
The very sterically encumbered secondary chlorophosphines ArTrip2P(Ph)Cl(ArTrip2=C6H3-2,6(C6H2-2,4,6-Pri3)) and ArMes2P(Ph)Cl(ArMes2=C6H3-2,6(C6H2-2,4,6-Me3)) were prepared from the respective aryllithium precursors and PhPCl2. Subsequent reduction of the chlorophosphines with Li[AlH4] yielded the corresponding phosphines ArylP(Ph)H in high yield; these afforded the lithium salts ArylP(Ph)Li upon treatment with nBuLi, and the synthesis and structural characterization of the monomeric terphenyl phosphide {[ArMes2P(Ph)]Li(THF)2}{[ArMes2P(Ph)]Li(THF)2} are described. Reaction of two equivalents of the lithium phosphide with SnCl2 afforded a rare example of a monomeric Sn(II)-diphosphide, [ArMes2P(Ph)]2Sn[ArMes2P(Ph)]2Sn.
A series of very sterically encumbered secondary phosphines ArylP(Ph)H were prepared featuring bulky terphenyl substitutents. These species are promising synthons for the preparation of low-coordinate main group phosphido complexes.Figure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 360, Issue 4, 1 March 2007, Pages 1278–1286