D. A. Bardonov, K. A. Lysenko, I. E. Nifantiev, M. E. Minyaev, D. M. Roitershtein
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引用次数: 0
Abstract
The reaction of di-, tri-, and tetraphenylcyclopentadienylpotassium with yttrium chloride tetrahydrofuranate in the presence of 1,3,5-trimethyl-1,3,5-triazacyclohexane (Me3tach) gives complexes of the type [Cp'Y(Me3tach)Cl2] (Cp' = Ph2C5H3 (CpPh2) (I), Ph3C5H2 (CpPh3) (II), Ph4C5H (CpPh4) (III). The molecular structure of complexes I–III was established by X-ray diffraction (CCDC nos. 2406644 (I), 2406645 (II), 2406646 (III)). The main structural parameters of all of the obtained monocyclopentadienyl complexes were similar, irrespective of the number of phenyl substituents in the cyclopentadienyl ligand. According to NMR spectroscopy data, compounds I and III retained their structure in THF solution.
期刊介绍:
Russian Journal of Coordination Chemistry is a journal that publishes reviews, original papers, and short communications on all aspects of theoretical and experimental coordination chemistry. Modern coordination chemistry is an interdisciplinary science that makes a bridge between inorganic, organic, physical, analytical, and biological chemistry.