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Heterobimetallic Pd(0) complexes with Pd→Ln (Ln = Sc, Y, Yb, Lu) dative bonds: rare-earth metal-dominated frustrated
Jun Du1, Yanan Zhang, Zeming Huang
1Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecule-Based Materials, College of Chemistry and Materials Science, Anhui Normal University, S 189, Jiuhua Road, Wuhu, Anhui 241002, P. R. China. pcui@ahnu.edu.cn slzhou@ahnu.edu.cn.
Abstract:
A series of heterobimetallic Pd-Ln complexes with Pd→Ln (Ln = Sc, Y, Yb, Lu) dative bonds were synthesized via sequential reactions of phosphinoamine Ph2PNHAd with (Me3SiCH2)3Ln(THF)2 and (Ph3P)4Pd or (COD)Pd(CH2SiMe3)2. These complexes were characterized by NMR spectroscopy, X-ray diffractions, and computational as well as electrochemical studies, which revealed Pd→Ln dative interactions that vary according to the ionic radii of Ln3+. Furthermore, the notable dynamic structural features of the Pd-Ln complexes in solution and their unexpected frustrated Lewis pair-like reactivity toward aryl halides and ketene were also studied.
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