Nicola, O. published the artcileCyclopentadienylmagnesium alkoxides derived from polyfunctional alcohols, Application of N2-(2-Hydroxyethyl)-N1,N1,N2-trimethyl-1,2-ethylenediamine, the main research area is cyclopentadienylmagnesium alkoxide; magnesium cyclopentadienyl alkoxide; magnesocene alc reaction; polymeric cyclopentadienylmagnesium alkoxide.
Magnesocene (1) reacts with polyfunctional alcs. (2a, N,N-dimethylethanolamine; 2b, 2-ethoxyethanol; 2c, 2-(2-ethoxyethoxy)ethanol; 2d, 2-[[(2-dimethylamino)ethyl]methylamino]ethanol) to yield polymeric cyclopentadienylmagnesium alkoxides [(η-C5H5)MgOR]x (3a-d). Compounds 3a-d dissolve in pyridine to yield solutions containing pyridine adducts of the corresponding monomers. These compounds all appear to contain formally 12-electron, pseudo-6-coordinate magnesium. Compound 1 reacts with 2,4-dimethyl-6-tert-butylphenol to form cyclopentadienyl (2,4-dimethyl-6-tert-butylphenoxy)magnesium, in which the steric bulk of the phenoxide ligand stabilizes the monomeric, 8-electron configuration.
Journal of Organometallic Chemistry published new progress about cyclopentadienylmagnesium alkoxide; magnesium cyclopentadienyl alkoxide; magnesocene alc reaction; polymeric cyclopentadienylmagnesium alkoxide. 2212-32-0 belongs to class alcohols-buliding-blocks, name is N2-(2-Hydroxyethyl)-N1,N1,N2-trimethyl-1,2-ethylenediamine, and the molecular formula is C7H18N2O, Application of N2-(2-Hydroxyethyl)-N1,N1,N2-trimethyl-1,2-ethylenediamine.
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