Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ulrich Schatzschneider"'
Publikováno v:
Organometallics. 40:2584-2593
Publikováno v:
Organometallics. 39:1423-1430
trans-[Pt(bodipy)(N3)(PEt3)2] (bodipy = 4,4-difluoro-4-bora-3a,4a-diaza-s-indacen-8-yl; Et = ethyl) reacts with dimethyl acetylenedicarboxylate (DMAD) or F3C–C≡C–COOEt in a catalyst-free room-tempe...
Autor:
Mario Löhr, Carsten Hagemann, Kun Peng, Ulrich Schatzschneider, Viviane Mawamba, Ellina Schulz
Publikováno v:
Inorganic Chemistry. 58:11508-11521
Two square-planar palladium(II) and platinum(II) azido complexes [M(N3)(L)] with L = N-phenyl-2-[1-(2-pyridinyl)ethylidene]hydrazine carbothioamide reacted with four different electron-poor alkynes R-C≡C-R' with R = R' = COOCH3, COOEt, COOCH2CH2OCH
Publikováno v:
European Journal of Inorganic Chemistry. 2017:3024-3029
Rhodium(III) azide half-sandwich complexes of general formula [Rh(Cp*)(N3)(bpyR,R)]CF3SO3 with R = H, OCH3 were prepared in three steps in an overall yield of 55–65 %. Their stability strongly depends on the 4,4′-substituent on the 2,2′-bipyrid
A series of photoactivatable CO‐releasing molecules (PhotoCORMs) was prepared from manganese pentacarbonyl bromide and 1H‐benzimidazol‐2‐ylmethyl‐(N‐phenyl)amine ligands (L) bearing different electron‐donating and electron‐withdrawing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04cc37ac09b60854b6717c412de8354d
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/21836
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/21836
Publikováno v:
Journal of Organometallic Chemistry. 782:116-123
Four NHC complexes of rhodium and iridium of the general structure [RhI(COD)(NHC)], [IrCl(COD)(NHC)], [IrCl(CO)2(NHC)], and [Ir(N3)(COD)(NHC)] (NHC = N-heterocyclic carbene) were synthesised and characterised, including X-ray structure determination
Publikováno v:
European Journal of Inorganic Chemistry. 2013:5547-5554
Four new N-heterocyclic carbene (NHC) rhodium and iridium complexes decorated with anionic or cationic pendant groups to increase their water solubility and biological activity have been synthesised and characterised. The lipophilicity of the complex
Autor:
P. Lauterjung, Florian Wittkamp, Bert Mallick, Ulf-Peter Apfel, Christoph Nagel, Ulrich Schatzschneider
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 45(25)
Here we present the syntheses and structural, spectroscopic, as well as electrochemical properties of four dinitrosyl iron complexes (DNICs) based on silicon- and carbon-derived di- and tripodal phosphines. Whereas CH3C(CH2PPh2)3 and Ph2Si(CH2PPh2)2
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 638:543-546
[MnBr(CO)5] reacts with one equivalent each of 1, 3, 5-triaza-7-phosphaadamantane (PTA) and sodium diethyldithiocarbamate to afford the yellow MnI complex fac-[Mn(S2CNEt2)(PTA)(CO)3]. Similarly, the same MnI precursor reacts with the sodium salt ofL-
Publikováno v:
Inorganic Chemistry. 50:4362-4367
Silicium dioxide nanoparticles of about 20 nm diameter containing azido groups at the surface were prepared by emulsion copolymerization of trimethoxymethylsilane and (3-azidopropyl)triethoxysilane and studied by transmission electron microscopy (TEM