The infrared spectra of metal carbonyl compounds. Part IV. [13C]-and [18O]-substitution in metal carbonyls

Author(s):  
G. Bor ◽  
B. F. G. Johnson ◽  
J. Lewis ◽  
P. W. Robinson
1982 ◽  
Vol 37 (2) ◽  
pp. 201-208 ◽  
Author(s):  
Hartmut Menzel ◽  
Wolf Peter Fehlhammer ◽  
Wolfgang Beck

Abstract Polyisocyanides with the groups -CH2N ≡ C and -C(O)O(CH2)2N≡C attached to polystyrene have been prepared and reacted with various metal carbonyl compounds resulting in the fixation on the polymeric supports of-M(CO)5, -M(CO)4 (M = Cr, Mo, W), -MO(Cl)(η-C5H5)(CO)2, -Mn2(CO)η -Mn(CO)ηX (N = 3, 4; X = Cl, Br), -Fe(CO)4, -Fe3(CO)11, -FeI2(CO)2, -FeX(η-C5H5)(CO) (X = Cl, Br, I), -Ru(CO)4, -Ru3(CO)9, ,,-Os3H2(CO)10", and -RhCl(CO)2. The cyano complexes [Fe(CN)2(η-C5H5)CO]- and [Mo(CN)2(η-C5H5)(CO)2]- have been immobilized by alkylation with chloromethylated polystyrene


1970 ◽  
Vol 48 (19) ◽  
pp. 3089-3094 ◽  
Author(s):  
P. J. Craig

Raman and infrared spectra of a series of complexes RCOMo(CO)2[L]π-C5H5 (R = Me, Et, σ-C3H5, CH2Ph; L = PPh3, P(OCH2)3CCH3) and of ClMo(CO)2[PPh3]π-C5H5 and HW(CO)2[P(OPh)3]π-C5H5 have been recorded. In this complementary study of complex metal carbonyl compounds, assignments are suggested for metal–carbon–oxygen deformation, metal–carbon stretching, metal–ring, and metal–phosphorus stretching vibrations. It is thought that the latter occur in the range 240–200 cm−1, frequencies for phosphite complexes being lower than for the corresponding phosphine derivatives.


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