Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ulrich Schatzschneider"'
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
Autor:
Paul Schmid, Matthias Maier, Hendrik Pfeiffer, Alexandra Friedrich, Anja Belz, Ulrich Schatzschneider, Katharina Edkins, Lucas Henry, Fabian Schönfeld
Publikováno v:
Schmid, P, Maier, M, Pfeiffer, H, Belz, A, Henry, L, Friedrich, A, Schonfeld, F, Edkins, K & Schatzschneider, U 2017, ' Catalyst-free room-temperature iClick reaction of molybdenum(II) and tungsten(II) azide complexes with electron-poor alkynes: Structural preferences and kinetic studies ', Dalton Transactions . https://doi.org/10.1039/C7DT03096G
Two isostructural and isoelectronic group VI azide complexes of the general formula [M([small eta]3-allyl)(N3)(bpy)(CO)2] with M = Mo, W and bpy = 2,2'-bipyridine were prepared and fully characterized, including X-ray structure analysis. Both reacted
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