Synthesis, spectral characterization, electrochemical studies and catalytic properties in Suzuki–Miyaura coupling reactions of the mononuclear PdII, trinuclear PdII(BPh2)2 and RuIIPdIIRuII type complexes containing 4‐amino‐1‐benzyl piperidine and phenyl groups
Makaleler > Tam Makale · 2008
Yazarlar: Ahmet Kilic, Ismail Yilmaz, Mahmut Ulusoy, Esref Tas
Applied Organometallic Chemistry, Uluslararası, Wos, 2008, cilt 22, ss 494-502
DOI: 10.1002/aoc.1430
Özet
Abstract The ligand containing the 4‐amino‐1‐benzyl piperidine group, N, N′‐(4‐amino‐1‐benzyl piperidine)‐glyoxime, (LH2) (1) was prepared from 4‐amino‐1‐benzyl piperidine with anti‐dichloroglyoxime at − 15 °C in absolute Tetrahydrofuran (THF). In the trinuclear [Pd(L)2Ru2(phen)4](ClO4)2 (4) and [Pd(L)2Ru2(bpy)4](ClO4)2 (5) metal complexes, the PdII ion centered into the main oxime core by the coordination of the imino groups while the two RuII ions coordinated dianionic oxygen donors of the oxime groups and linked to the ligands of 1,10‐phenanthroline and 2,2′‐bipyridine. The mono and trinuclear metal complexes were characterized by elemental analyses, FT‐IR, UV–vis, 1H and 13C‐NMR spectra, magnetic susceptibility measurements, molar conductivity, cyclic voltammetry, mass spectra, X‐ray powder techniques and their morphology by SEM measurements. The cyclic voltammetric results show that the cathodic peak (Epc) potential of (3) shifts towards more positive values compared with that of (2) as a result of the BPh2+‐bridged complex formation. The Suzuki–Miyaura reaction was used to investigate their activity as catalyst either prepared in‐situ or from well‐defined complexes. Copyright © 2008 John Wiley & Sons, Ltd.