A new application about 2-(Diphenylphosphino)benzaldehyde

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.50777-76-9, you can also check out more blogs about50777-76-9

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 50777-76-9, 50777-76-9, Name is 2-(Diphenylphosphino)benzaldehyde, molecular formula is C19H15OP.

Syntheses and structures of tungsten o-(Diphenylphosphino)benzaldehyde complexes bearing pi-bonded aldehyde groups

Reaction of the bidentate ligand Ph2P(o-C6H4)C(=O)H (abbreviated as PCHO) with W(CO)3(eta3-(MeNCH2)3) at room temperature affords W(CO)3(eta1-PCHO) (eta3-PCHO) (1), which subsequently loses a carbonyl ligand to give W(CO)2(eta3-PCHO)2 (2). Further treatment of 2 with PCHO in refluxing benzene results in carbon – carbon coupling of the PCHO ligands to produce W(CO)(eta3-PCHO)(eta3-(PCHO)2) (3). The structures of 1-3 have been determined by an X-ray diffraction study. The PCHO ligands in these compounds act as chelating phosphine-aldehydes with the aldehyde groups coordinating in a pi fashion.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.50777-76-9, you can also check out more blogs about50777-76-9

Reference£º
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate