多座β-チオキセミナート配位子を有する一塩化銅(I)錯体におけるスペーサー長依存的な核性および銅親和性調節

This study explores the impact of alkyl spacer length in multidentate β-thioketiminate ligands (H₂²L-H₂⁴L, H₂⁶L, and H₂⁸L) on the nuclearity and structural properties of copper(I) complexes. Ligands, synthesized thiation of β-ketoiminate precursors, were characterized by ¹H, ¹³C NMR, FT-IR, UV-vis spectroscopy, and ESI-MS. Reaction with CuO^tBu led to the formation of tetranuclear ([LCu₂]₂, C2-C4 spacers) and bis-trinuclear ([LCu₂]₃, C6 and C8 spacers) complexes, analyzed by ¹H, ¹³C NMR, FT-IR, UV-vis, Raman, and single-crystal X-ray diffraction. Each Cu(I) center adopts a distorted trigonal planar geometry, coordinated by one nitrogen and two sulfur atoms through chelating and bridging modes. Shorter spacers favor tetranuclear clusters with stronger cuprophilic interactions (Cu···Cu: 2.58-3.43 Å), while longer spacers promote bis-trinuclear clusters, including a previously unreported triple-helicate with asymmetric Cu···Cu distances (2.76-2.87 Å). Importantly, coordination of 2,4,6-trimethylphenyl isocyanide induces fragmentation of these clusters into dinuclear [L(Cu-CNR)₂] complexes, as confirmed by single-crystal X-ray diffraction and FT-IR (νC≡N blue shift), revealing a spacer-dependent susceptibility to isocyanide-driven S-Cu bridge cleavage. These findings demonstrate spacer length as a key modulator of Cu(I) cluster nuclearity and metal-metal interactions, advancing bioinspired metallosupramolecular design.