12213-19-3Relevant articles and documents
ACETYLATION OF DICARBONYL(η4-CYCLOHEXADIENE)TRIPHENYLPHOSPHINEIRON
Birch, Arthur J.,Raverty, Warwick D.,Hsu, Shih-Ying,Pearson, Anthony J.
, p. C59 - C62 (1984)
Friedel-Crafts acetylation of dicarbonyl(η4-cyclohexadiene)triphenylphosphineiron is accomplished in 96percent yield under mild conditions to give dicarbonyl-(η4-5-endo-acetylcyclohexa-1,3-diene)triphenylphosphineiron.The structure o
Replacement of CO by R3P in the cyclohexa-1,3-dienetricarbonyliron series
Birch,Kelly
, p. c5-c7 (2007/10/02)
Reaction of tricarbonylcyclohexa-1,3-dieneiron complexes with trimethylamine-N-oxide in the presence of trivalent phosphorus donor ligands gives the corresponding (R3P)(OC)2Fe(cyclohexa-1,3-diene).
DIENE-METAL ? BONDING. SOME UNEXPECTED EFFECTS OF GROUP 5 DONOR LIGANDS ON CARBON-13 NUCLEAR MAGNETIC RESONANCE PARAMETERS AND X-RAY CRYSTAL STRUCTURES
Pearson, Anthony J.,Raithby, Paul R.
, p. 884 - 891 (2007/10/02)
A number of η4-cyclohexadiene-Fe(CO)2L and η4-2-methoxycyclohexadiene-Fe(CO)2L complexes have been prepared and their 13C n.m.r. spectra recorded.Methoxy-substituent effects suggest a depopulation rather than the expected enhanced population of the diene l.u.m.o. (lowest unoccupied molecular orbital) as the ?-acceptor strength of L decreases.X-Ray crystal-structure determinations for L = PPh3 were in agreement, and an explanation is proposed.Complexes (7) and (8) both crystallise in the monoclinic space group P21/c with Z = 4.The cell parameters are a = 10.289(4), b =24.651(10), c = 9.282(4) Angstroem, and β = 109.37(3)deg for (7) and a = 14.444(7), b =18.052(10), c = 9.229.(4) Angstroem and β = 100.57(4)deg for (8).The structures were solved by a combination of Patterson and Fourier-difference techniques, and refined by blocked-cascade least squares to R = 0.053 for 3 325 unique observed reflections (7) and to R = 0.062 for 2 952 reflections (8).