1691-36-7

Upstream product

• 460-00-4 1-Bromo-4-fluorobenzene 
• 352-34-1 4-fluoro-1-iodobenzene 
• 352-13-6 4-flourophenylmagnesium bromide 
• 13272-84-9 (4-fluorophenyl)silane 

Downstream Products

• 850-60-2 Brom-tris-<4-fluor-phenyl>-silan 
• 850-61-3 (tris-(4-fluorophenyl))chlorosilane 
• 2287-68-5 tri-(p-fluorophenyl)-silanol 
• 189193-66-6 Rh(H)(Cl)(P(iPr)3)2(Si(C₆H₄F-p)3) 
• 204637-57-0 Rh₂(P(CH(CH₃)2)3)2(H)3(Si(C₆H₄F)3)2(Cl) 
• 2287-69-6 Hexakis-<4-fluor-phenyl>-disiloxan 

Relevant academic research and scientific papers

Organocalcium Complex-Catalyzed Selective Redistribution of ArSiH3or Ar(alkyl)SiH2to Ar3SiH or Ar2(alkyl)SiH

Calcium is an abundant, biocompatible, and environmentally friendly element. The use of organocalcium complexes as catalysts in organic synthesis has had some breakthroughs recently, but the reported reaction types remain limited. On the other hand, hydrosilanes are highly important reagents in organic and polymer syntheses, and redistribution of hydrosilanes through C-Si and Si-H bond cleavage and reformation provides a straightforward strategy to diversify the scope of such compounds. Herein, we report the synthesis and structural characterization of two calcium alkyl complexes supported by β-diketiminato-based tetradentate ligands. These two calcium alkyl complexes react with PhSiH3 to generate calcium hydrido complexes, and the stability of the hydrido complexes depends on the supporting ligands. One calcium alkyl complex efficiently catalyzes the selective redistribution of ArSiH3 or Ar(alkyl)SiH2 to Ar3SiH and SiH4 or Ar2(alkyl)SiH and alkylSiH3, respectively. More significantly, this calcium alkyl complex also catalyzes the cross-coupling between the electron-withdrawing substituted Ar(R)SiH2 and the electron-donating substituted Ar′(R)SiH2, producing ArAr′(alkyl)SiH in good yields. The synthesized ArAr′(alkyl)SiH can be readily transferred to other organosilicon compounds such as ArAr′(alkyl)SiX (where X = OH, OEt, NEt2, and CH2SiMe3). DFT investigations are carried out to shed light on the mechanistic aspects of the redistribution of Ph(Me)SiH2 to Ph2(Me)SiH and reveal the low activation barriers (17-19 kcal/mol) in the catalytic reaction.

Selective homo- And cross-desilacoupling of aryl and benzyl primary silanes catalyzed by a barium complex

Under mild conditions (25 °C, 5 mol% cat.), highly selective homo- and cross-desilacoupling of aryl and benzyl primary silanes to secondary silanes was achieved by the use of the heteroleptic barium aminobenzyl complex [(TpAd,iPr)Ba(CH2C6H4NMe2-o)] (TpAd,iPr = hydrotris(3-adamantyl-5-isopropyl-pyrazolyl)borate) (1) as a catalyst. Dihydrosilanes originating from catalytic redistribution and cross-desilacoupling reactions were isolated in fine yields, which demonstrates the feasible application of the barium complex in the syntheses of secondary aryl- and benzylsilanes. This journal is

Magnesium-containing electrolytic solution

It is an object of the present invention to provide an electrolytic solution having high oxidation decomposition potential, where dissolution and deposition of magnesium proceed repeatedly and stably, using a non-nucleophilic alkoxide-type magnesium salt.

Linear free-energy relationship and rate study on a silylation-based kinetic resolution: Mechanistic insights

The substituent effect of different p-substituted triphenylsilyl chlorides on silylation-based kinetic resolutions was explored. Electron-donating groups slow down the reaction rate and improve the selectivity, while electron-withdrawing groups increase the reaction rate and decrease the selectivity. Linear free-energy relationships were found correlating both selectivity factors and initial rates to the σpara Hammett parameters. A weak correlation of selectivity factors to Charton values was also observed when just alkyl substituents were employed but was nonexistent when substituents with more electronic effects were incorporated. The rate data suggest that a significant redistribution of charge occurs in the transition state, with an overall decrease in positive charge. The linear free-energy relationship derived from selectivity factors is best understood by the Hammond postulate. Early and late transition states describe the amount of substrate participation in the transition state and therefore the difference in energy between the diastereomeric transition states of the two enantiomers. This work highlights our efforts toward understanding the mechanism and origin of selectivity in our silylation-based kinetic resolution.

Hypervalent hydridosilicates: Synthesis, structure and hydride bridging

A range of hydridosilicate anions has been prepared and characterised by spectroscopic, structural and computational methods. The general approach involved reaction of KH with a neutral silane precursor in the presence of [18]crown-6. In this manner, [K([