Copper Complexes of Silicon Pyridine-2-olates RSi(pyO)₃ (R = Me, Ph, Bn, Allyl) and Ph₂Si(pyO)₂

The organosilicon pyridine-2-olates 1a–1d (RSi(pyO)₃, R = Me (a), Ph (b), Bn (c), Allyl (d); pyO = pyridine-2-olate) may serve as tripodal ligands toward CuCl with formation of complexes of the type RSi(μ²-pyO)₃CuCl (2a–2d). In addition, for R = Allyl, formation of the more stable isomer 2d′ (κO-pyO)Si(μ²-pyO)₂(μ²-Allyl)CuCl was observed. In the presence of dry air (as a source of oxygen), reactions of 1a–1d and CuCl afforded Cu(II) complexes RSi(μ²-pyO)₄CuCl (3a–3d); 3a–3c in good yield, and 3d only as a side product. Reaction of Ph₂Si(pyO)₂ (4) and CuCl in equimolar ratio afforded, depending on reaction conditions, a series of (CuCl)n-ladder-type oligonuclear Cu(I) complexes Ph₂Si(μ2-pyO)₂(CuCl)n(μ²-pyO)₂SiPh₂ (n = 2 (52), 3 (53), 4 (54)). In all of the above compounds, the pyO group is Si–O bound and, in the case of μ² coordination, Cu–N bound. All new compounds (1c, 1d, 2b, 2c, 2d, 2d′, 3b, 3c, 3d, 52, 53, 54) were characterized by single-crystal X-ray diffraction, and further characterization includes solution ¹H, ¹³C, ²⁹Si NMR spectroscopy (1c, 1d, 2b, 2c, 2d’, 53, 54), solid-state ²⁹Si (2b, 2c, 2d′, 53, 54) and ⁶³Cu NMR spectroscopy (2c, 2d′) as well as computational analyses of the isomerization of the couple 2d, 2d′.