Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Olga Ekkert"'
Publikováno v:
Chemistry-A European Journal
The first bis(σ-zincane) complexes, heterotri- metallic species [M(CO)4 (η2 -HZnBDI)2 ], have been prepared (BDI=κ2 -{2,6-(iPr)2 C6 H3 NCMe}2 CH). For M=Cr, a single stereoisomer is observed in solution and the solid-state. For M=Mo and W, cis and
Publikováno v:
Organometallics. 33:7027-7030
[Cp*RhCl(μ-Cl)]2 is reported as a highly efficient and selective precatalyst for the hydrodefluorination of perfluoroarenes using a hydrocarbon-soluble aluminum dihydride as the terminal reductant. Reactions are directed to cleave a C–F bond adjac
Autor:
Juri Möbus, Constantin G. Daniliuc, Thomas Wiegand, Gerald Kehr, Hellmut Eckert, Olga Ekkert, Gerhard Erker, Melanie Siedow
Publikováno v:
Solid State Nuclear Magnetic Resonance. :8-14
A solid state NMR method is described for measuring the angle Θ specifying the orientation of the principal component of the 11 B electric field gradient tensor relative to the 11 B … 31 P internuclear vector of 11 B– 31 P spin pairs. It is base
Autor:
Roland Fröhlich, Jeffrey L. Petersen, Constantin G. Daniliuc, Birgit Wibbeling, Gerhard Erker, Olga Ekkert, Gerald Kehr
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 639:2455-2462
Diarylphosphino-substituted alkynes undergo a 1, 1-carboboration reaction with tris(pentafluorophenyl)borane to yield 2-diarylphosphino-substituted alkenylboranes. These unsaturated systems show a P/B interaction. Nevertheless, they feature a limited
Publikováno v:
Angew. Chem., Int. Ed.
Through a dramatic advance in the coordination chemistry of the zinc-hydride bond, we describe the trajectory for the approach of this bond to transition metals. The dynamic reaction coordinate was interrogated through analysis of a series of solid s
Autor:
Stefan Grimme, Gerhard Erker, Roland Fröhlich, Olga Ekkert, Hellmut Eckert, Gerald Kehr, Thomas Wiegand
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Covalent bonding interactions between the Lewis acid and Lewis base functionalities have been probed in a series of "frustrated Lewis pairs" (FLPs) (mainly substituted vinylene linked intramolecular phosphane-borane adducts), using solid-state nuclea
Publikováno v:
Journal of the American Chemical Society. 133:4610-4616
A series of diarylphosphinyl-substituted acetylenes of the type (aryl)(2)P-C≡C-R (aryl = phenyl or mesityl, R = Ph or n-propyl) react with the strongly Lewis acid reagent B(C(6)F(5))(3) in toluene at elevated temperatures (70-105 °C) to give the 1
Autor:
Conor Pranckevicius, Douglas W. Stephan, Gerald Kehr, Christopher B. Caputo, Olga Ekkert, Gerhard Erker, Constantin G. Daniliuc
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 20(36)
The reactions of the intramolecular frustrated Lewis pair-adduct Ph(2) PC(p-Tol)=C(C(6) F(5))B(C(6)F(5))2 (CNtBu) with XeF(2) gave Ph(2)P(F)C(p-Tol)=C(C(6)F(5))B(F)(C(6)F(5))(2)(3). This species reacts with two equivalents of Al(C(6)F(5))(3)⋅C(7)H(
Publikováno v:
ChemInform. 44
The title reaction affords phosphane-borane Lewis pairs (III) with a conjugated diene backbone.
Publikováno v:
Chemical communications (Cambridge, England). 49(62)
Simple alkenylbis(pentafluorophenyl)boranes undergo 1,1-alkenylboration with phosphanylacetylenes to give phosphane–borane Lewis pairs with a conjugated diene backbone.