Citation: Xiaohang JIN, Qi LIU, Jianping LANG. Room‑temperature solid‑state synthesis, structure, and third‑order nonlinear optical properties of phosphine‑ligand‑protected silver thiolate clusters[J]. Chinese Journal of Inorganic Chemistry, ;2025, 41(8): 1505-1512. doi: 10.11862/CJIC.20250125 shu

Room‑temperature solid‑state synthesis, structure, and third‑order nonlinear optical properties of phosphine‑ligand‑protected silver thiolate clusters

Figures(5)

  • The cluster precursor [Ag9(Tab) 8(MeCN)8]2(PF6)18·4MeCN (Ag18, Tab=4-(trimethylammonio)benzenethio- late), MeCN=acetonitrile) was subjected to solid-state grinding reactions with two phosphine ligands, triphenylphos- phine (L1) and diphenyl- 2-pyridylphosphine (L2), respectively. The obtained solid powders were dissolved in DMF/ EtOH solvents, followed by centrifugal separation. Two silver thiolate clusters protected by phosphine ligands were obtained from the supernatant through Et2O diffusion crystallization: [Ag7(Tab)6(L1)6Cl] (PF6)6·8DMF (1) and [Ag17(Tab)20(L2) 2](PF 6)17·32DMF (2). Both compounds were thoroughly characterized via single-crystal X-ray diffrac- tion, powder X -ray diffraction, infrared spectroscopy, ultraviolet- visible spectroscopy, thermogravimetric, and ele- mental analysis. Single-crystal X-ray diffraction analysis revealed that both clusters are stabilized by a combination of phosphine and Tab ligands, with the diphenyl-2-pyridylphosphine ligand in 2 exhibiting simultaneous coordina- tion through both phosphorus and nitrogen atoms. Z-scan measurements demonstrated that both compounds in solu- tion exhibit notable third-order nonlinear optical responses.
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