Major, Mate M’s team published research in Journal of Coordination Chemistry in 2021 | 699-12-7

Journal of Coordination Chemistry published new progress about Amino acids Role: SPN (Synthetic Preparation), PREP (Preparation). 699-12-7 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H10OS, Safety of 2-(Phenylthio)ethanol.

Major, Mate M.; Balogh, Szabolcs; Simon, Jozsef; Bakos, Jozsef; Farkas, Gergely published the artcile< New chiral thioether-phosphite ligands and their rhodium-coordination chemistry: steric and electronic properties, dynamic processes and application in catalysis>, Safety of 2-(Phenylthio)ethanol, the main research area is rhodium thioether phosphite chiral BINOL ester complex preparation; asym hydrogenation catalyst rhodium thioether BINOL phosphite cyclooctadiene complex.

Thioether-phosphite ligands (S)-BINOL-PO(CH2)nSPh (SP’s, n = 2, 3; BINOL-H2 = 1,1′-binaphthyl-2,2′-diol, H8-1,1′-binaphthyl-2,2′-diol) with axially chiral binaphthyl or 5,5′,6,6′,7,7′,8,8′-octahydrobinaphthyl moiety and their [Rh(COD)(SP)]BF4 complexes have been synthesized to study their coordination chem. and catalytic features and to compare them to those of the structurally analogous phosphine-phosphites (S)-BINOL-PO(CH2)nPPh2 (PP’s). NMR exchange studies on [Rh(COD)(SP)]BF4 complexes showed selective 1,5-cyclooctadiene dynamics. Firm evidence has been found that this fluxional process involves dissociation of the Rh-sulfur bond. Based on in situ NMR studies, SP ligands can form two types of bis-ligated species at ligand-to-metal ratio higher than 1. Unlike bis-ligated phosphine-phosphite complexes, bis-ligated thioether-phosphite Rh-complexes can efficiently catalyze asym. hydrogenation reactions due to their distinct coordination chem.

Journal of Coordination Chemistry published new progress about Amino acids Role: SPN (Synthetic Preparation), PREP (Preparation). 699-12-7 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H10OS, Safety of 2-(Phenylthio)ethanol.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts