Reactivity of CuI and CuBr toward Et2S: a Reinvestigation on the Self-Assembly of Luminescent Copper(I) Coordination Polymers

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Abstract
CuI reacts with SEt2 in hexane to afford the known strongly luminescent 1D coordination polymer [(Et2S)3{Cu4(μ3-I)4}]n (1). Its X-ray structure has been redetermined at 115, 235, and 275 K in order to address the behavior of the cluster-centered emission and is built upon Cu4(μ3-I)4 cubane-like clusters as secondary building units (SBUs), which are interconnected via bridging SEt2 ligands. However, we could not reproduce the preparation of a coordination polymer with composition [(Et2S)3{Cu4(μ3-Br)4}]n as reported in Inorg. Chem.1975, 14, 1667. In contrast, the autoassembly reaction of SEt2 with CuBr results in the formation of a novel 1D coordination polymer of composition [(Cu3Br3)(SEt2)3]n (2). The crystal structure of 2 has been solved at 115, 173, 195, and 235 K. The framework of the luminescent compound 2 consists of a corrugated array with alternating Cu(μ2-Br)2Cu rhomboids, which are connected through two bridging SEt2 ligands to a tetranuclear open-cubane Cu4Br4 SBU, ligated on two external Cu atoms with one terminal SEt2. The solid-state luminescence spectra of 1 and 2 exhibit intense halide-to-metal charge-transfer emissions centered at 565 and 550 nm, respectively, at 298 K. A correlation was also noted between the change in the full width at half-maximum of the emission band between 298 and 77 K and the relative flexibility of the bridging ligand. The emission properties of these materials are also rationalized by means of density functional theory (DFT) and time-dependent DFT calculations performed on 1.

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