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.
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http://dx.doi.org/10.1021/acsnano.1c10905 | DOI Listing |
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