Reactions of sterically demanding phosphinimines R3PNH [R=i-Pr (1), t-Bu (2)] were examined. Reactions with B(C6F5)3 formed the adducts (R3PNH)B(C6F5)3 [R=i-Pr (3), t-Bu (4)] in high yield. On the other hand, 2 reacts with HB(OBu)2, evolving H2 to give t-Bu3PNB(OBu)2 (5).
View Article and Find Full Text PDFThe reaction of the phosphine oxides, OPEt31 and OPn-Bu32 with pinacolborane (HBpin) results in phosphine oxide reduction and the formation of O(Bpin)23. In contrast, the phosphine oxide OPn-Bu3 reacts with HB(C6F5)2 or B(C6F5)3 to give only the donor-acceptor adducts. Compound 3 reacts with HNPt-Bu3 to give the phosphinimonium borate salt, [t-Bu3PNH2][(Bpin(OBpin)2]6, while reaction with Cp2ZrMe2 affords the species Cp2Zr(OBpin)27.
View Article and Find Full Text PDFA series of catecholboryl-phosphinimide complexes with the general formula (mu-(R(3)PN)Bcat)(x)() (cat = O(2)C(6)H(4)) have been synthesized via associative metathetical reactions. For R = Et, n-Bu, Ph, and i-Pr and R(3) = n-Bu t-Bu(2) X-ray crystallography as well as solution NMR spectroscopy and reactivity studies reveal that these species are dimeric. In the case of R = t-Bu, the steric congestion results in the monomeric species, t-Bu(3)PNBcat.
View Article and Find Full Text PDFSynthetic routes to vanadium(V)-phosphinimide derivatives are addressed. Initial synthetic efforts afforded the known compound formulated as VCl(2)(NPPh(3))(3) which was crystallographically determined to be the salt [VCl(NPPh(3))(3)]Cl (1). Reactions of the vanadium-imide precursors VCl(3)(NAr) (Ar = Ph, C(6)H(3)-2,6-iPr(2)) with R(3)PNSiMe(3) (R = Ph, iPr, tBu) afforded VCl(2)(NPh)(NPPh(3)) (4), VCl(2)(NPh)(NPiPr(3)) (5), VCl(2)(NPh)(NPtBu(3)) (6), VCl(2)(NC(6)H(3)-2,6-iPr(2))(NPPh(3)) (7), VCl(2)(NC(6)H(3)-2,6-iPr(2))(NPiPr(3)) (8), and VCl(2)(NC(6)H(3)-2,6-iPr(2))(NPtBu(3)) (9) in yields ranging from 72% to 84%.
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