Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Kevin M, Szkop"'
Autor:
Piers St. Onge, Zheng-Wang Qu, Stefan Grimme, Douglas W. Stephan, David A. Petrone, Linkun Miao, Kevin M. Szkop
Publikováno v:
Angewandte Chemie International Edition. 60:18547-18551
Primary acyl-phosphines are scarce in the literature. Here we show that the reaction of Ph3 GePCO with the ylide Ph3 PCH2 proceeds to give the species Ph3 PCHC(O)PH(GePh3 ) 1. Deprotonation of 1 with Na[N(SiMe3 )2 ] generates the salt [Na(THF)2 ][Ph3
Publikováno v:
Dalton Transactions. 49:885-890
Reactions of Ph3GePCO with KP(t-Bu)2 and Ph3SiCl, or direct reaction with Ph3SiP(t-Bu)2 provides the (Z)- and (E)-isomers of the phosphaalkene (t-Bu2)PC(OSiPh3)P(GePh3) 2, respectively. These isomers interconvert thermally and photochemically, while
Publikováno v:
Chemistry – A European Journal. 25:10084-10087
The phosphaketene Ph3 GePCO is shown to react with the phosphide KP(tBu)2 to generate the anion [Ph3 GePC(O)P(tBu)2 ]- 1. This species reacts with CH3 I or ClGePh3 to give the dissymmetric diphospha-ureas (tBu)2 PC(O)P(GePh3 )(CH3 ) 2 and (Ph3 Ge)2 P
Publikováno v:
Chemical Science
Acyl(chloro)phosphines RC(O)P(Cl)(t-Bu) have been prepared by formal insertion of tert-butyl phosphinidene (t-Bu–P) from t-BuPA (A = C14H10 or anthracene) into the C–Cl bond of acyl chlorides.
Acyl(chloro)phosphines RC(O)P(Cl)(t-Bu) have bee
Acyl(chloro)phosphines RC(O)P(Cl)(t-Bu) have bee
Autor:
Farah E. Farinha, Douglas W. Stephan, Shawn Postle, James H. W. LaFortune, Kevin M. Szkop, Timothy C. Johnstone
Publikováno v:
Dalton Transactions. 47:11411-11419
The electrophilic phosphonium cation (EPC) salt [(3,5-(CF3)2C6H3)3PF][B(C6F5)4] (2) is prepared via oxidation of the precursor phosphine with XeF2 and subsequent abstraction of fluoride with [Et3Si(tol)][B(C6F5)4]. The Lewis acidity of 2 is evaluated
Publikováno v:
Dalton Transactions. 47:8933-8939
Phosphine oxidation by MesCNO is rapid; however, an FLP strategy intercepts the 1,3 addition products including [MesC(R3P)NOB(C6F5)3] (R = Ph 1, p-tol 2), [MesC(Mes2PH)NOB(C6F5)3] 3 (MesC(NOB(C6F5)3)Ph2P)2(CH2)n (n = 2: 4, 3: 5) and [MesC(Ph3P)NOB(C6
Publikováno v:
Angewandte Chemie International Edition. 56:14174-14177
The reactions of the phosphaethynolate anion ([PCO]- ) with a range of boranes were explored. BPh3 and [PCO]- form a dimeric anion featuring P-B bonds and is prone to dissociation at room temperature. The more Lewis acidic borane B(C6 F5 )3 yields a
Autor:
Kevin M. Szkop, Douglas W. Stephan
Publikováno v:
Dalton Transactions. 46:3921-3928
Oxidation of 2,6-bis(diphenylphosphine)methyl pyridine with MeO3SCF3, yields the dication [2,6-(CH2PMePh2)2C5H3N][CF3SO3]22, while subsequent treatment with two equivalents of [K(THF)n][B(C6F5)4] (n = 1.3–1.5) afforded [2,6-(CH2PMePh2)2C5H3N][B(C6F
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(43)
The phosphaketene Ph
Publikováno v:
Journal of Solid State Chemistry. 242:126-132
The reduction and oxidation of the solid solution Y2−xPrxO3+δ (0.0≤x ( I a 3 ¯ ) . The oxidized solid solution Y2−xPrxO3+δ (0.0≤x ( I a 3 ¯ ) whereas Y2−xPrxO3+δ (1.4≤x ( F m 3 ¯ m ) with variable oxide defect concentrations. The tw