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Trovacenchemie. 13 [1] Weg und Irrweg zu Di([5]trovacenyl)keton
Authors:Christoph Elschenbroich,J  rn Plackmeyer,Klaus Harms,Olaf Burghaus,Jü  rgen Pebler
Affiliation:Christoph Elschenbroich,Jörn Plackmeyer,Klaus Harms,Olaf Burghaus,Jürgen Pebler
Abstract:Trovacene Chemistry. 13 [1] On Being Lead and Mislead in the Synthesis of Di([5]trovacenyl)ketone Di([5]trovacenyl)ketone ( 3¨ ) has been prepared from lithio‐[5]trovacene and dimethylcarbamoyl chloride and studied by X‐ray diffraction, cyclic voltammetry, magnetic susceptometry and EPR spectroscopy. Slight variation of the synthetic protocol affords an unusual trinuclear complex 5 ? that is also fully characterized. Spin‐spin exchange interaction is smaller in 3¨ than in 1,1‐di([5]trovacenylethene ( 2¨ ), which differs from 3¨ by a replacement of O for CH2. The novel trinuclear complex 5 ? , however, displays exchange coupling very similar to that observed in 1‐methoxy‐2,5,6‐tri([5]trovacenyl)benzene ( 7 ? ). In both cases, an unsymmetrical triangular arrangement of S = 1/2 centers is encountered. These findings are discussed in terms of the nature of the respective spacers.
Keywords:Oligonuclear sandwich complexes  Vanadium  Electronspin exchange‐coupling  Redox potentials
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