Wang Zhi, Su Hai-Feng, Zhang Li-Ping, Dou Jian-Min, Tung Chen-Ho, Sun Di, Zheng Lansun
School of Chemistry and Chemical Engineering, State Key Laboratory of Crystal Materials, Shandong University, Ji'nan 250100, People's Republic of China.
State Key Laboratory for Physical Chemistry of Solid Surfaces and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China.
ACS Nano. 2022 Mar 22;16(3):4500-4507. doi: 10.1021/acsnano.1c10905. Epub 2022 Mar 1.
Metalloligand strategy has been well recognized in the syntheses of heterometallic coordination polymers; however, such a strategy used in the assembly of silver nanoclusters is not broadly available. Herein, we report the stepwise syntheses of a family of halogen-templated Ag nanoclusters (-) based on Mo-anchored --butylthiacalix[4]arene (HTC4A) as a metalloligand (hereafter named MoO-TC4A). X-ray crystallography demonstrates that they are similar -symmetric silver-organic nanocalices capped by six MoO-TC4A metalloligands, which are evenly distributed up and down the base of 42 silver atoms. These nanoclusters can be disassembled to six bowl-shaped [Ag(MoO-TC4A)(RS)] secondary building units (SBUs, R = Et or Pr), which are fused together in a face-sharing fashion surrounding Cl or Br as a central anion template. The electrospray mass spectrometry (ESI-MS) indicates their high stabilities in solution and verifies the formation of the MoO-TC4A metalloligand, thereby rationalizing the overall stepwise assembly process for them. Moreover, shows lower cytotoxicity and better activity against the HepG-2 cell line than MCF-7 and BGC-823. These results not only exemplify the effectiveness of a thiacalix[4]arene-based metalloligand in the assembly of silver nanoclusters but also give us profound insight about the step-by-step assembly process in silver nanoclusters.
金属配体策略在异金属配位聚合物的合成中已得到广泛认可;然而,这种策略在银纳米团簇组装中的应用并不广泛。在此,我们报告了基于钼锚定的对叔丁基硫杂杯[4]芳烃(HTC4A)作为金属配体(以下简称MoO-TC4A)逐步合成一系列卤素模板化的Ag纳米团簇(-)。X射线晶体学表明,它们是由六个MoO-TC4A金属配体封端的类似对称的银-有机纳米杯,这些配体在由42个银原子组成的底部上下均匀分布。这些纳米团簇可以分解为六个碗状的[Ag(MoO-TC4A)(RS)]二级结构单元(SBUs,R = Et或Pr),它们以面共享的方式围绕作为中心阴离子模板的Cl或Br融合在一起。电喷雾质谱(ESI-MS)表明它们在溶液中具有高稳定性,并验证了MoO-TC4A金属配体的形成,从而合理化了它们的整体逐步组装过程。此外,[具体物质未给出名称]对HepG-2细胞系的细胞毒性低于MCF-7和BGC-823,且活性更好。这些结果不仅例证了基于硫杂杯[4]芳烃的金属配体在银纳米团簇组装中的有效性,也为我们深入了解银纳米团簇的逐步组装过程提供了深刻见解。