Carotenes are naturally abundant unsaturated hydrocarbon pigments, and their fascinating physical and chemical properties have been studied intensively not only for better understanding of the roles in biological processes but also for the use in artificial chemical systems. However, their metal-binding ability has been virtually unexplored. Here we report that β-carotene has the ability to assemble and align ten metal atoms to afford decanuclear homo- and heterometal chain complexes. The metallo–carotenoid framework shows reversible metalation–demetalation reactivity with multiple metals, which allows us to control the size of metal chains as well as the heterobimetallic composition and arrangement of the carotene-supported metal chains.
Metal clusters are effectively stabilized by bridging π-coordination of planar π-conjugated unsaturated hydrocarbons. However, the mechanism of π-envelopment of a metal cluster has been elusive. By employing 1,2-bis(4-aryl-1,3-butadienyl)benzene as the π-conjugated ligand, we found that the π-envelopment of a Pd4 cluster proceeded in a stepwise manner, where the sp(2)-carbon ligands initially envelop the Pd4 cluster through a bent binding mode, and then isomerized to a thermodynamically more stable planar mode under mild heating or visible light irradiation. The involvement of a bent binding mode indicates the kinetically preferred coordination at the axial coordination site trans to a metal-metal bond.
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