Abstract
Hydrothermal treatment of halide mono-substituted complex of (Me4N)2[Cd4(SPh)9Cl] (1) afforded three-dimensional framework [Cd4(SPh)8]n (2), its three-dimensional framework can be destroyed by coordination with PPh3 ligand, forming a polymeric complex of [Cd4(SPh)8(PPh3)]n (3) with one-dimensional zig–zig chain structure. Complexes 1, 2 and 3 were structurally characterized by single crystal X-ray structure analysis. Their diffuse reflectance spectra and photoluminescence properties were also investigated at room temperature.
Graphical Abstract
Insert of tertiary phosphine ligands into the three-dimensional framework of [Cd4(SPh)8]n reduced its dimensionality and afforded a one-dimensional polymeric chain of [Cd4(SPh)8(PPh3)]n.
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Acknowledgments
This project was supported by the Natural Science Foundation of China (90922008). Q. F. Zhang thanks State Key Laboratory of Coordination Chemistry of Nanjing University for the assistance.
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Xu, C., Shi, HT., Xin, ZF. et al. Ligand-Participated Formation of Covalent Superlattices Containing [Cd4(μ-SPh)6] Cores with Adamantane-Like Stereochemistry. J Clust Sci 25, 1353–1361 (2014). https://doi.org/10.1007/s10876-014-0713-5
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DOI: https://doi.org/10.1007/s10876-014-0713-5