54294-46-1

Upstream product

• 5055-11-8 (2-chloroethyl)diphenylphosphane 
• 60778-67-8 dilithium salt of 1,2-bis(phenylphosphino)ethane 
• 1663-45-2 1,2-bis-(diphenylphosphino)ethane 

Downstream Products

• 134649-06-2 C₄₂H₄₂P₄S₄ 
• 134649-05-1 C₄₂H₄₂P₄Se₄ 
• 121072-91-1 {BrNb(CO)2(Ph₂PCH₂CH₂PPhCH₂)2} 
• 121072-89-7 {BrNb(CO)3(CH₂PPhCH₂CH₂PPh₂)2} 
• 126900-29-6 PtCl(P(C₆H₅)2((CH₂)2P(C₆H₅))2(CH₂)2P(C₆H₅)2)⁽¹⁺⁾*BF₄^(1-)={PtCl(P(C₆H₅)2((CH₂)2P(C₆H₅))2(CH₂)2P(C₆H₅)2)}(BF₄) 
• 121072-90-0 {ClNb(CO)2(Ph₂PCH₂CH₂PPhCH₂)2} 
• 111834-55-0 cis-{(C₂H₅)4N}{Ta(CO)4{(C₆H₅)2PCH₂CH₂P(C₆H₅)2}2} 
• 111532-99-1 Ta(H)(CO)3{(C₆H₅)2PCH₂CH₂P(C₆H₅)CH₂}2} 
• 131296-50-9 Mo₂Cl₄(tetraphos-1) 
• 148508-92-3 meso-Mo₂Cl₄(tetraphos-1) 
• 151989-08-1 {(η3-1,1,4,7,10,10-hexaphenyl-1,4,7,10-tetraphosphadecane)Pt(η2-S2CO)} 

Relevant academic research and scientific papers

New dihydrogen complexes: the synthesis and spectroscopic properties of iron(II), ruthenium(II), and osmium(II) complexes containing the meso-tetraphos-1 ligand

The synthesis and properties of dihydrogen complexes trans-+, M = Fe, Ru, Os, which contain the ligand meso-tetraphos-1, S,R-Ph2PCH2CH2P(Ph)CH2CH2P(Ph)CH2CH2PPh2 (L) are described.There are interesting possibilities of isomerism in such trans complexes because the axial binding sites at the metal are different, one being surrounded by four phenyl groups and the other by two phenyl groups.The osmium complex is prepared in an unusual reaction of cis-β-Os(Cl)2L with H2 (1 atm) and NaBPh4 (1 mol) in THF or by the reaction of trans-OsH(Cl)L with NaBPh4 and H2.The iron and ruthenium complexes were made by a reaction of HBF4 with complexes trans-M(H)2L that have inequivalent trans hydrides.The ruthenium complex was also prepared starting from isomers of trans-RuH(Cl)L.The H-H distance in the rapidly spinning dihydrogen ligand has been calculated from T1(min) data to be 0.88, 0.89, and 0.99 Angstroem for the complexes of Fe, Ru, Os, respectively.The presence of the H-D bond in the isotopomers trans-+ and trans-+ is also confirmed by the observation of 1JHD coupling constants of 32, 33.5, and 26.4 Hz for Fe, Ru, and Os, respectively.There is no rapid intramolecular H atom exchange in these complexes in contrast to those with di-tert-phosphine ligands like + or to the trihydride Re(H)3L.Described also are the properties of the precursor complexes including cis-β- and trans-Ru(Cl)2L and derivatives of the dihydrogen complexes trans-+, L' = CH3CN (on Ru and Os), PMe2Ph (on Ru), and CO (on Os).Trends in the NMR properties of isostructural complexes are reported.