34989-06-5

Upstream product

• 57137-55-0 3-(diphenylphosphino)propyl chloride 
• 57322-05-1 Diphenyl<3-(phenylphosphino)propyl>phosphin 
• 638-21-1 phenylphosphane 
• 829-85-6 diphenylphosphane 
• 644-97-3 Dichlorophenylphosphine 

Downstream Products

• 69069-21-2 Rh(OH)(ttp) 
• 5259-72-3 cyclo-octa-1,5-diene 
• 78505-56-3 {chloro(bis(3-diphenylphosphinopropyl)phenylphosphine)iridium(I)} 
• 84623-51-8 Ru(CO)2(bis(3-(diphenylphosphino)propyl)phenylphosphine) 
• 96445-03-3 (C₂H₅)4N⁽¹⁺⁾*V(CO)3P(C₆H₅)(CH₂CH₂CH₂P(C₆H₅)2)2^(1-) 
• 96445-02-2 (C₂H₅)4N⁽¹⁺⁾*V(CO)4P(C₆H₅)(CH₂CH₂CH₂P(C₆H₅)2)2^(1-) 
• 96445-00-0 (C₂H₅)4N⁽¹⁺⁾*V(CO)5P(C₆H₅)(CH₂CH₂CH₂P(C₆H₅)2)2^(1-) 
• 95144-47-1 Ir(CO)(CH₂C(CH₃)3)(C₆H₅P((CH₂)3P(C₆H₅)2)2) 
• 95144-48-2 Ir(CO)(CH₂Si(CH₃)3)(C₆H₅P((CH₂)3P(C₆H₅)2)2) 
• 82581-44-0 C₅H₅V(CO)2(C₆H₅)2PCH₂CH₂CH₂PC₆H₅CH₂CH₂CH₂P(C₆H₅)2 
• 82581-44-0 cis-(η5-C5H5)V(CO)2(Ph2P(CH2)3)2PPh 
• 35096-66-3 Rh((C₆H₅)P(CH₂CH₂CH₂P(C₆H₅)2)2)Cl(SO₂) 
• 35235-57-5 Rh((C₆H₅)P(CH₂CH₂CH₂P(C₆H₅)2)2)Cl(BF₃) 
• 51018-53-2 Rh⁽¹⁺⁾*(C₆H₅)P(CH₂CH₂CH₂P(C₆H₅)2)2*Cl^(1-)*S₂=Rh((C₆H₅)P(CH₂CH₂CH₂P(C₆H₅)2)2)Cl(S₂) 

Relevant academic research and scientific papers

Novel tridentate phosphines and method of forming aldehyde hydrogenation catalysts

This invention comprises a process for hydrogenation of aldehydes to alcohols using novel homogeneous catalysts. The catalysts are generated in situ under hydrogen and carbon monoxide gases in a suitable solvent, by mixing a rhodium catalyst precursor, such as Rh(CO)2 acetoacetonate and a defined ligand.

Oligophosphine Ligands, I Convenient Syntheses of the Trimethylene-linked Triphosphines RP2 and their Precursors Ph2P(CH2)3P(H)R (R=Ph, Me)

The secondary-tertiary diphosphines Ph2P(CH2)3P(H)Ph (2) and Ph2P(CH2)3P(H)Me (3) have been prepared from Ph2P(CH2)3Cl (1) and NaP(H)Ph or LiP(H)Me, respectively.Metallation of 2 and 3 with n-butyl lithium and further reaction of the lithio-derivatives with one equivalent of 1 yields PhP2 (4) and MeP2 (5).The tritertiary phosphines 4 and 5 have likewise been obtained from RPLi2 (R=Ph, Me) and two equivalents of 1.The synthesis of 4 from PhPCl2 and two equivalents of the Grignard reagent of 1 is also reported.Each of the phosphines 1-5 was characterized by NMR and mass spectroscopy. - Keywords: Secondary-tertiary Diphosphines, Tritertiary Phosphines, Preparation, NMR Spectra, Mass Spectra