Safety of Nickel(II) chloride ethylene glycol dimethyl ether complex. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: Nickel(II) chloride ethylene glycol dimethyl ether complex, is researched, Molecular C4H10Cl2NiO2, CAS is 29046-78-4, about Cu(I) coordination by N,N,N’,N’-tetra(di-ortho-anisylphosphanylmethyl) ethylene and propylene diamine: First example of a sandwiched CuCl-tetramer. Author is Pann, Johann; Ehrmann, Katharina; Pehn, Richard; Roithmeyer, Helena; Viertl, Wolfgang; Kopacka, Holger; Brueggeller, Peter; Oberhauser, Werner.
New chelating α-aminophosphanes were obtained by Mannich-type reactions between formaldehyde, bis(2-methoxyphenyl)phosphine and aliphatic primary diamines bearing either a C2 or C3 carbon bridge between the amine functionalities. The reaction conditions, and in particular, the reaction sequence was found to significantly depend on the length of the carbon bridge of the diamine. Both obtained α-aminophosphines (i.e. N,N,N’,N’-tetra(di-ortho-anisylphosphanylmethyl)-1,2-diaminoethane (L1) and N,N,N’,N’-tetra(di-ortho-anisylphosphanylmethyl)-1,3-diaminopropane (L2)) gave along with neocuproine cationic dinuclear Cu(I) complexes. The Cu(I) complex with L2 as ligand was further converted by the aid of NiCl2(DME) (DME = 1,2-dimethoxyethane) into a tetranuclear copper cluster showing a new type of CuCl-tetramer mol. structure. All synthesized compounds were characterized in solution by multinuclear NMR-, UV/Vis-spectroscopy, mass spectrometry and in the solid state by elemental anal. and some of them by single crystal structure anal.
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