Reaktionen koordinierter Liganden, III [1]. Stabilisierung von Dimenthyldiphosphen und Menthylphosphiniden als Brückenliganden in Metallcarbonylkomplexen / Reaction of Coordinated Ligands, III [1]. Stabilization of Dim enthyldiphosphene and Menthylphosphinidene as Bridging Ligands in Metal Carbon... (original) (raw)
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Zeitschrift für Naturforschung B, 1988
Compounds RPBr2Cr(CO)5 (R = Me, Et, i-Pr. t-Bu, c-Hex. (-)Menthyl. Ph) and RPBr2W(CO)5 (R = (-)Menthyl, Ph) are obtained from M(CO)5THF and organodibromophosphane. Dehalogenation of the chromium complexes with magnesium in THF leads to (RP)3[Cr(CO)5]m (m = 1. 2, 3) with m depending on the bulkiness of R. When dissolved in THF the binuclear complexes (m = 2) are gradually converted into mononuclear compounds. The isomeric structure of the cyclotriphosphane complexes is deduced from their 31P{1H} NMR spectra.
Zeitschrift für anorganische und allgemeine Chemie, 2010
The transition metal complexes with the ligand 1,3bis(N,N,N',N'-tetramethylguanidino)propane (btmgp), [Mn(btmgp)Br 2 ] (1), [Co(btmgp)Cl 2 ] (2), [Ni(btmgp)I 2 ] (3), [Zn(btmgp)Cl 2 ] (4), [Zn(btmgp)(O 2 CCH 3) 2 ] (5), [Cd(btmgp)Cl 2 ] (6), [Hg(btmgp)Cl 2 ] (7) and [Ag 2 (btmgp) 2 ][ClO 4 ] 2 •2MeCN (8), were prepared and characterised for the first time. The stoichiometric reaction of the corresponding water-free metal salts with the ligand btmgp in dry MeCN or THF resulted in the straightforward formation of the mononuclear com
Zeitschrift für Naturforschung B, 1986
Zeitschrift für Naturforschung B, 2005
Reactions of L-tert-Leucine (tert-butylglycine), tert-leucine methyl ester, GlyValOMe, and Leu- AlaOMe with the chloro-bridged complexes [Cp*IrCl2]2, [(p-cymene)RuCl2]2 or [(C6Me6)RuCl2]2 in the presence of NaOMe give the complexes [Cp*Ir(Cl)NH2CH(R)CO2] (1), [(p-cymene)Ru(Cl)- NH2CH(R)CO2] (2), Cp*Ir(Cl2)[NH2CH(R)CO2Me] (5), {(C6Me6)Ru(Cl)[NH2CH2CONHCH(R)- CO2Me]}+Cl− (6), [Cp*Ir(Cl)NH2CH2CONCH(R)CO2Me] (7), [Cp*Ir(Cl)NH2CH(CH2CHMe2)- CONCH(R)CO2Me)] (8), and Cp*Ir(Cl2)[NH2CH2CONHCH(R)CO2Me) (9). With pentaglycine the complexes [Cp*Ir(Cl2)(pentaglycinate+Na+)] (10) and [(C6Me6)Ru(pentaglycineOMe- H+)] (11) could be isolated. Coordination of one equivalent of the S-protected tripeptide glutathione to [Cp*Ir(Cl)] and to [(C6Me6)Ru(Cl)] was observed. Some in situ prepared (p-cymene)Ru complexes with deprotonated dipeptide esters were tested as catalysts and the complex [(p-cymene)Ru(Cl)(NH2CH(CHMeEt)NCH (CHMe2)CO2tert-Bu)] gave a yield of 73% and moderate entantiomeric excess (36% ee)...
Zeitschrift für Naturforschung B, 1983
Carbene Transfer, Metal-Metal Multiple Bonds Carbene transfer from aliphatic diazoalkanes upon coordinatively unsaturated metal centers is a general synthetic concept that provides straightforward routes into organometallic hydrocarbon chemistry. A comparison focussing on several key reactions of general applicability demonstrates that mononuclear organometal substrates add carbenes that may act as bridging ligands (e.g., compound 6) if they arise from u>,co'-bisdiazoalkanes. By way of contrast, metal-metal double bonds cleanly form dimetallacyclopropane-type derivatives under very mild conditions (7-9). The broadest variety of structures is finally encountered with metal-metal triply bonded precursors such as the molybdenum compounds 3: here, the initial diazoalkane adducts are subject to further rearrangement processes commonly leading to metal-metal single bonds (11) or causing irreversible cleavage of the dinuclear metal systems (10).
Diels- Aider- Addukte des Diphosphens F3CP = PCF3 / Diels-Alder Adducts of the Diphosphene F3P =PCF3
Zeitschrift für Naturforschung B, 1985
The heterocycles 3 to 6 are formed in a one-pot procedure by reacting trifluoromethyl phosphorus diiodide F3CPI2 with tin dichloride SnCl2 in the presence of the corresponding 1,3-dienes. The reactions proceed via [2+4] cycloaddition of the diphosphene intermediate F3CP = PCF3 (1) as suggested by the high yields obtained (50 to 100%) and the formation of the cyclic tetraphosphane (F3CP)4 (2) as the only by-product. Cycloreversion occurs at moderate temperatures as demonstrated by the reaction of 6 with 2,3-dimethylbutadiene to give 3 and cyclohexadiene. The products have been characterized by NMR and mass spectra