TY - JOUR
T1 - Mössbauer, 13C NMR and infrared spectroscopic studies of aryliron derivatives [Fe(Ar)(Co)L(η5-C5H5)]
AU - Butler, I. R.
AU - Lindsell, W. E.
AU - Thomas, M. J K
PY - 1984/2/7
Y1 - 1984/2/7
N2 - 57Fe Mössbauer, 13C{1H} NMR and IR spectroscopic investigations have been carried out on the aryliron derivatives [Fe(Ar)(CO)L(?5-C5H5)] (L = CO, Ar = C6H5, C6F5, 2-FC6H4, 2-ClC6H4 2-IC6H4, 2-CH3C6H4, 2-(C6H5CH2)C6H4 and C6H5CO; L = PPh3, Ar = C6H5, 2-FC6H4). Mössbauer isomer shifts and quadrupole splittings, 13C NMR chemical shifts and IR ?(CO) stretching force constants are presented. These data are discussed in relation to variation of the aryl ligand, Ar, and the FeC bonds. Evidence is presented for some ortho interactions between the iron and the 2-phenyl substituent and is discussed. © 1984.
AB - 57Fe Mössbauer, 13C{1H} NMR and IR spectroscopic investigations have been carried out on the aryliron derivatives [Fe(Ar)(CO)L(?5-C5H5)] (L = CO, Ar = C6H5, C6F5, 2-FC6H4, 2-ClC6H4 2-IC6H4, 2-CH3C6H4, 2-(C6H5CH2)C6H4 and C6H5CO; L = PPh3, Ar = C6H5, 2-FC6H4). Mössbauer isomer shifts and quadrupole splittings, 13C NMR chemical shifts and IR ?(CO) stretching force constants are presented. These data are discussed in relation to variation of the aryl ligand, Ar, and the FeC bonds. Evidence is presented for some ortho interactions between the iron and the 2-phenyl substituent and is discussed. © 1984.
UR - http://www.scopus.com/inward/record.url?scp=0042651001&partnerID=8YFLogxK
M3 - Article
SN - 0022-328X
VL - 262
SP - 59
EP - 68
JO - Journal of Organometallic Chemistry
JF - Journal of Organometallic Chemistry
IS - 1
ER -