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Transition metal NMR chemical shifts and polarizability effect in organometallic complexes
Authors:Alexey N Egorochkin  Olga V Kuznetsova  Nadiya M Khamaletdinova  Yury A Kurskii  Lada G Domratcheva‐Lvova  Georgy A Domrachev
Institution:1. G. A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, 49 Tropinin Str., 603950 Nizhny Novgorod, Russia;2. Universidad Michoacana de San Nicolas de Hidalgo, Ciudad Universitaria, 58030 Morelia, Michoacán, Mexico
Abstract:The literature data on substituent influence on the 51V, 55Mn, 57Fe, 59Co, 61Ni, 95Mo, 103Rh, 183W, 187Os and 195Pt NMR chemical shifts (δ) and on J (M, P; M = Mn, Fe, Mo, Rh, W, Os) coupling constants have been analyzed for 30 series of the organometallic complexes. It has been established for the first time that the δ and J values depend on the inductive, resonance and polarizability effects of substituents. The polarizability effect is caused by the partial charge on the central M atom. The contribution of this effect ranges from 3 to 86%. Copyright © 2009 John Wiley & Sons, Ltd.
Keywords:NMR  transition metal nuclei  organometallic complexes  inductive effects  conjugation  polarizability effects
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