Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kai Helmdach"'
Publikováno v:
Dalton Transactions. 52:326-337
Variation of a single ligand in the W(ii) alkyne complexes of bis(diphenylphosphino)acetylene leads to W(ii)/W(iii) redox potentials spanning a window of 850 mV. The corresponding dinuclear complexes with PdCl2 show differing catalytic activity.
Autor:
Mareike Hüttenschmidt, Alexander Villinger, Elisabeth Oberem, Stephan Ludwig, Jabor Rabeah, Wolfram W. Seidel, Ralf Ludwig, Kai Helmdach
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
A pair of diastereomeric dinuclear complexes, [Tp′(CO)BrW{μ‐η2‐C,C′‐κ2‐S,P‐C2(PPh2)S}Ru(η5‐C5H5)(PPh3)], in which W and Ru are bridged by a phosphinyl(thiolato)alkyne in a side‐on carbon P,S‐chelate coordination mode, were syn
Publikováno v:
Organometallics. 36:4844-4853
The terminal phosphine groups at the tungsten bisphosphine alkyne complex [Tp*W(CO)(I)(η2-C,C′-Ph2PC2PPh2)] (2) {Tp* = hydridotris(3,4,5-trimethylpyrazolyl)borate} were selectively oxidized by common methods to form the alkyne complexes 2EE (E = O
Autor:
Wolfram W. Seidel, Alexander Villinger, Dirk Hollmann, Stephan Ludwig, Kai Helmdach, Jutta Kösters
Publikováno v:
Chemical Communications. 53:5894-5897
A paramagnetic WIII alkyne complex bearing free terminal diphenylphosphino groups at the side-on coordinated alkyne was synthesized using a stepwise template strategy. This moderately stable metal supported open shell diphosphine shows an unprecedent
Publikováno v:
Dalton Transactions. 46:11140-11144
We present the synthesis and coordination chemistry of a series of WII alkyne complexes with symmetric and asymmetric acetylene diphosphines. Chelate-like P,P'-coordination of PtCl2 cause a drastic potential change of the W centered oxidation proving
Publikováno v:
Chemical Communications. 52:2616-2619
The synthesis and reactivity of a W(ii) C2I2 complex towards various nucleophiles are described. Soft, aprotic nucleophiles like 4-dimethylaminopyridine (DMAP) lead to substitution of one CO at tungsten, whereas reaction with an excess of benzylamine
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 641:2300-2305
The oxo tungsten(IV) alkyne complexes [Tp′W(O)(I)(η2-C2Ph2)] (1), [Tp′W(O)(I){η2-C2(SC2H4SiMe3)2}] (2), and [Tp′W(O)(I){η2-C2(SBn)2}] (3) [Tp′ = hydridotris(3, 5-dimethylpyrazolyl)borate, Bn = benzyl] were synthesized from [Tp′W(O)(CO)(I
Autor:
Steffen Kleinschmidt, David Schallenberg, Kai Helmdach, Alexander Villinger, Alexander Hinz, Wolfram W. Seidel
Publikováno v:
Organometallics. 34:1091-1097
The C/C coupling activity of the cationic Re(III) species [(C5H5)ReBr]+ with different heteroatom-substituted alkynes was investigated. By using the sulfide-substituted bis(benzylsulfanyl)acetylene...
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 46(34)
We present the synthesis and coordination chemistry of a series of W