Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Christian Schulte to Brinke"'
Hydrogen Activation by an Iridium(III) Complex Bearing a Bidentate Protic NH,NR-NHC∧Phosphine Ligand
Publikováno v:
Organometallics. 34:5454-5460
Benzimidazole 2 bearing an N1-(biscyclohexylphosphine)ethyl tether cleaves [IrCp*Cl2]2 to yield the mononuclear phosphine complex [3]. Heating of [3] yields via a formal C/N tautomerization complex [4]Cl with a protic NHC. Complex [4]Cl can be N3-dep
Publikováno v:
European Journal of Inorganic Chemistry. 2015:3227-3231
A series of trinuclear heterobimetallic AuI/M2 (M = RhIII, IrIII, RuII) complexes were prepared by the stepwise and selective metalation of a rigid cyclic tetraimidazolium salt. Reaction of the tetraimidazolium salt with exactly 1 equivalent of silve
Autor:
Alexander Hepp, F. Ekkehardt Hahn, Christian Schulte to Brinke, Hannah Koppetz, Sergei Krupski
Publikováno v:
Organometallics. 34:2624-2631
The monoalkylated or monoarylated o-phenylenediamines 1a–d (1a, R = t-Bu; 1b, R = adamantyl; 1c, R = phenyl; 1d, R = mesityl) react via transamination with Ge[N(SiMe3)2]2 or Sn[N(SiMe3)2]2 to give the protic benzimidazolin-2-germylenes 2a–d or th
Publikováno v:
Zeitschrift für Naturforschung B. 69:1248-1252
The 5,5′-bibenzimidazolium dibromide salts 2 and 3 have been prepared by fourfold N-alkylation of 5,5′-bibenzimidazole (2: R=Pr; 3: R=Bu). The diazolium salts were treated with silver oxide, and the in situ-formed silver complexes were subsequent
Publikováno v:
Organometallics. 33:4471-4478
Reaction of 2 equiv of 2-azidoethyl isocyanide and the tetraphosphine platinum(II) complexes [1a–c](X)2 (a, PR3 = PMe3; b, PR3 = PMe2Ph; c, PR3 = PMePh2) yielded via phosphine substitution and template-controlled cyclization of the isocyanide ligan
Autor:
F. Ekkehardt Hahn, Mareike C. Jahnke, Dirk Brackemeyer, Alexandre Hervé, Christian Schulte to Brinke
Publikováno v:
Journal of the American Chemical Society. 136:7841-7844
Purine nucleobases are excellent ligands for metal ions, forming normally coordinative Werner-type bonds by utilizing the N donor atoms of the nucleobase skeleton. Here we show that purines such as 8-chlorocaffeine and 8-bromo-9-methyladenine react w
Benzodicarbene-bridged dinuclear complexes as building blocks for metalosupramolecular architectures
Publikováno v:
Journal of Organometallic Chemistry. 751:620-627
Dinuclear benzodicarbene-bridged iridium(III) and rhodium(III) complexes [Cp*(Cl)2M(benzodicarbene)M(Cl)2Cp*] [3]–[5] have been synthesized from N,N′,N″,N″-tetraalkylbenzobisimidazolium salts and [MCp*(Cl)2]2 via the Ag2O method. Molecular st
Publikováno v:
Organometallics. 32:6174-6177
The bisimidazolium salt H2-1(PF6)2 featuring a bridging 1,4-phenylene group reacts with 0.5 equiv of [PdCl(allyl)]2 in the presence of Cs2CO3 to give the dinuclear complex [2](PF6)2, whereas the reaction of the same bisimidazolium salt with 0.5 equiv
Publikováno v:
Zeitschrift für Naturforschung B. 68:551-556
As a siderophore analog, the tripodal tris(benzene-o-dithiol)-functionalized ligand H6-5, has been synthesized in four steps including the reaction of 1,3,5-(triaminomethyl)-2,4,6-triethylbenzene and 2,3-bis(isopropylmercapto)benzoyl chloride followe
Autor:
Christian Schulte to Brinke, Jutta Kösters, Tania Pape, Kai-Oliver Feldmann, A. Carolin Dumke, F. Ekkehardt Hahn
Publikováno v:
Organometallics. 32:289-299
Reaction of 2-azidoethyl isocyanide 1, 2-azidophenyl isocyanide 2, or 2-nitrophenyl isocyanide 3 with complexes [Mo(CO)3(dppe)(py)] [4] or [W(CO)3(dppe)(N≡CCH3)] [5] yields the isocyanide complexes [Mo(CO)3(dppe)(C≡NR)] ([6]: C≡NR = 1; [12]: C