Solution and solid state conformation of Fischer carbene complexes vis-a-vis conformation of aryl carboxamides: complexation of the aromatic ring by tricarbonylchromium makes a difference
Kn. Jayaprakash et al., Solution and solid state conformation of Fischer carbene complexes vis-a-vis conformation of aryl carboxamides: complexation of the aromatic ring by tricarbonylchromium makes a difference, J ORGMET CH, 617(1), 2001, pp. 709-722
Crystallography and proton NMR spectroscopy were used to compare the confor
mations of aryl amino Fischer carbene complexes with structurally analogous
aryl carboxamides. The similarity disappears when the aromatic rings were
complexed with tricarbonylchromium groups. Details of synthesis, spectral a
nd analytical data for all new compounds are provided. (C) 2001 Elsevier Sc
ience B.V. All rights reserved.