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bis{phenyl(2-picolyl)phosphine}propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1491145-99-3

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1491145-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1491145-99-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,9,1,1,4 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1491145-99:
(9*1)+(8*4)+(7*9)+(6*1)+(5*1)+(4*4)+(3*5)+(2*9)+(1*9)=173
173 % 10 = 3
So 1491145-99-3 is a valid CAS Registry Number.

1491145-99-3Downstream Products

1491145-99-3Relevant academic research and scientific papers

Configurational isomerization of dinuclear iridium and rhodium complexes with a series of NPPN ligands, 2-PyCH2(Ph)P(CH2) nP(Ph)CH2-2-Py (Py = Pyridyl, n = 2-4)

Nakajima, Takayuki,Fukushima, Yuki,Tsuji, Minori,Hamada, Naoko,Kure, Bunsho,Tanase, Tomoaki

, p. 7470 - 7477 (2013)

New heterodonor NPPN tetradentate ligands, 2-PyCH2(Ph)P(CH 2)nP(Ph)CH2-2-Py (meso- and rac-Ln; n = 2-4, Py = pyridyl), were prepared and reacted with [CpMCl2] 2 (M = Ir, Rh; Cp* is pentamethylcyclopentadienyl) in the presence of NH4BF4 to afford a series of dinuclear complexes [(CpMCl)2(meso-Ln)](BF4)2 (M = Ir, n = 2 (2a), 3 (3a), 4 (4a); M = Rh, n = 2 (2c), 3 (3c), 4 (4c)) and [(CpMCl)2(rac-Ln)](BF4)2 (M = Ir, n = 2 (2b), 3 (3b), 4 (4b); M = Rh, n = 2 (2d), 3 (3d), 4 (4d)), which were characterized by IR, 1H and 31P{1H} NMR, and ESI mass spectroscopic techniques and X-ray crystallography. The configurations around the two metal centers were controlled by the configuration of the coordinated P atoms so as to avoid repulsive interaction between the phenyl group on P and the chloride ligand, resulting in the formation of stereospecific isomers; a meso configuration of the metal centers is induced from meso-L n (abbreviated as meso-P2/meso-M2), and in contrast, a rac configuration is induced from rac-Ln (rac-P 2/rac-M2). Furthermore, inversion of metal centers for the Ir2 complexes occurred in DMSO at higher temperatures (60-100 C), generating equilibrium mixtures of minor diastereomers (meso-P 2/rac-M2 or rac-P2/meso-M2) in low ratios together with the major isomers (meso-P2/meso-M2 or rac-P2/rac-M2). The equilibrium constants, K = [minor isomer]/[major isomer], varied appreciably depending on the lengths of the methylene chains as well as configurations of the NPPN ligands; the overall propensity for the K values was observed to be L2 3 4 and meso-Ln n, while rac-L3, rac-L4, and meso-L4 showed almost identical equilibrium constants, presumably resulting from no steric influence between the two metal centers.

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