RESUMEN
Three prototypes of the remarkable new class of compound referred to in the title have been synthesised by treating ferrocene with the same mixed lithium (or sodium)-magnesium amide recipes as those used previously to make s-block metal inverse crowns.
RESUMEN
More usually thought of as a base, the sodium zincate [(TMEDA)·Na(µ-TMP)(µ-(t)Bu)Zn((t)Bu)] 1 can undergo single electron transfer with TEMPO to give [(TMEDA)·Na(µ-TMP)(µ-TEMPO(-))Zn((t)Bu)] 2 and [(TMEDA)·Na(µ-TEMPO(-))(2)Zn((t)Bu)] 3; and with chalcone [PhCOCH=CHPh] gives [{(TMEDA)·Na(µ-TMP)Zn((t)Bu)}(2)(µ-OCPhCH=CHPhCHPhCH=CPh-µ-O)] which contains two chalcone units C-C coupled though their benzylic C atoms.
Asunto(s)
Chalcona/química , Óxidos N-Cíclicos/química , Compuestos Organometálicos/química , Sodio/química , Zinc/química , Transporte de Electrón , Estructura MolecularRESUMEN
The metallation reaction between dibutylmagnesium and 2,6-diisopropyl-N-(trimethylsilyl)aniline gives the unusual monomeric three-coordinate complex (diethyl ether-kappa O)bis[2,6-diisopropyl-N-(trimethylsilyl)anilido-kappa N]magnesium(II), [Mg(C(15)H(26)NSi)(2)(C(4)H(10)O)] or [Mg[(Me(3)Si)(2,6-(i)Pr(2)C(6)H(3))N](2)(Et(2)O)]. This low-coordinate species has a distorted trigonal-planar coordination environment, with an additional short Mg-C(ipso) contact of 2.799 (2) A.
RESUMEN
The title complex, [ZrCl2(C4H8O)2(C14H14N)2].0.5C7H8, was prepared in an unusual manner by utilizing [Mg[N(CH2Ph)2]2] as a ligand transfer reagent. The Zr atom lies in a distorted octahedral environment where steric repulsion from the large dibenzylamino ligands leads to a widening of the N-Zr-N angle [99.95 (9) degrees ] and corresponding compression of other angles [Cl-Zr-Cl 160.95 (3) degrees and O-Zr-O 78.22 (7) degrees ]. This distortion is compared with those found in the previously determined structures of the dimethylamino and diethylamino analogues.