97940-81-3Relevant academic research and scientific papers
Organyl Complexes of (ν5-Cyclopentadienyl)(triorganophosphano)iron
Lehmkuhl, Herbert,Mehler, Gerlinde,Benn, Reinhard,Rufinska, Anna,Schroth, Gerhard,et al.
, p. 1987 - 2002 (2007/10/02)
A series of organyliron complexes of the type Cp(L)2Fe-R (Cp = C5H5, C5H4Me, C5Me5; L = PhnMe3-nP, N = 0-3; R = Me, Et, Bu, Ph, CH2CH2Ph, CH=CH3) have been prepared either from the corresponding iron chlorides (1-7) and organomagnesium compounds or from Cp(COD)FeLi (8, 9), organic halide, and phosphane.The thermal stability of the ethyliron complexes 17 - 24 towards β-H elimination (to give the ν2-ethylene)iron hydrides 37 - 39 or the Cp(L)2FeH compounds 40 - 48) increases with the basicity of the phosphane ligand and decreases with increasing methyl-substitution of the Cp ligand.The vinyliron compounds 29 - 32, 54, and 55 react with ethylene with insertion into the vinyl-Fe bond to give the (ν3-crotyl)iron complexes 56 - 61 as the result of isomerization.The (ν1,ν2-alkenyl)iron compounds (62), C5Me5 (63) and (67) were isolated and are stable at 20 deg C.
Organyliron Complexes of the Type Cp(Ph2PnPPh2)Fe-R
Lehmkuhl, Herbert,Mehler, Gerlinde
, p. 2407 - 2417 (2007/10/02)
The preparation of the (η5-cyclopentadienyl)bis(triorganophosphane)iron halide complexes 6 - 10 involving Me3P, Me2PhP, MePh2P, (Ph2PCH2)2, and (Ph2PCH2CH2)2 is described.Reaction with organomagnesium halides RMgHal leads in the case of 9 (Ligand L-L = (Ph2PCH2)2) to complexes 13 - 19 of the type Cp(L-L)Fe-R (R = Me, Et, Bu, i-Bu, cyclopropyl, vinyl, 2-butenyl) and in the case of 10 (L-L = (Ph2PCH2CH2)2) to 21 (R = Bu).The hydridoiron complexes 12 and 20 are formed as side products in cases where the group R contains β-H-atoms and are the sole product where R = i-Pr or t-Bu.Thermolysis of the organoiron complexes 14 - 16 as well as 19 and 21 between 50 and 100 deg C also leads to 12 or 20.The Fe-β-H-elimination is reversible in the case of the (2-butenyl)iron complex 19.
