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trans-Fe(CO)3(PPh2Et)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36870-06-1

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36870-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36870-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,7 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36870-06:
(7*3)+(6*6)+(5*8)+(4*7)+(3*0)+(2*0)+(1*6)=131
131 % 10 = 1
So 36870-06-1 is a valid CAS Registry Number.

36870-06-1Downstream Products

36870-06-1Relevant academic research and scientific papers

A Facile, high-yield synthesis of trans-Fe(CO)3(PR3)2 from Fe(CO)5, Fe(CO)4CHO-, HFe(CO)4-, or HFe(CO)3PR3-

Keiter, Richard L.,Keiter, Ellen A.,Hecker, Karl H.,Boecker, Carol A.

, p. 2466 - 2469 (2008/10/08)

The reaction of Fe(CO)5 with PR3 and NaBH4 in refluxing n-butyl alcohol affords high yields of trans-Fe(CO)3(PR3)2. It has been shown that Fe(CO)4PR3, which does not appear in the collected product, is also not a significant intermediate in the reaction. The reaction proceeds by initial formation of H2 gas and Fe(CO)4CHO-. The formyl complex decomposes to HFe(CO)4- which reacts with PR3 to give the disubstituted product. The principal intermediate for this substitution is believed to be HFe(CO)3PR3-, although polynuclear species may also be important. The substitution of HFe(CO)4- by PR3 is favorable when the counterion is Na+ but not when it is PPN+. The overall reaction is very sensitive to choice of solvent; substitution of ethanol for n-butyl alcohol leads to greatly reduced yields.

Olefin replacement on cyclooctatetraeneiron tricarbonyl by neutral ligands

Faraone, Felice,Zingales, Franco,Uguagliati, Paolo,Belluco, Umberto

, p. 2362 - 2364 (2007/12/02)

Kinetic data are reported on reactions of cyclooctatetraeneiron tricarbonyl with tertiary phosphines (L) and 1,2-bis(diphenylphosphino)ethane (L-L) in decalin at various temperatures. The reactions involve replacement of cyclooctatetraene leading to trans-Fe(CO)3L2 and cis-Fe(CO)3(L-L). Reaction rates depend on the nature and concentration of the entering ligand. Results are interpreted in terms of a mechanism consisting of a slow coordination of L on the substrate followed by fast elimination of cyclooctatetraene from the resulting labile intermediate. Activation parameters are discussed to support this mechanism.

Some tertiary phosphine-iron carbonyl compounds

Manuel

, p. 854 - 858 (2008/10/08)

Derivatives of iron pentacarbonyl containing 1,2-bis-(diphenylphosphino)-ethane are described, as well as related compounds containing halide and perfluoroalkyl groups. Stereoisomers of dichlorodicarbonyl-[1,2-bis-(diphenylphosphino)-ethane]-iron(II) have been observed. A modified synthesis of tertiary phosphine-iron carbonyl compounds is described.

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