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All-Calixarene-Protected Silver Nanocluster with All Silver Atoms in a Face-Centered Cubic Arrangement.

Authors :
Zheng LM
Shi WQ
Hu F
Guan ZJ
Wang QM
Source :
Journal of the American Chemical Society [J Am Chem Soc] 2024 Sep 11; Vol. 146 (36), pp. 25101-25107. Date of Electronic Publication: 2024 Aug 28.
Publication Year :
2024

Abstract

Tailoring the surface ligands of metal nanoclusters is important for engineering unique configurations of metal nanoclusters. Thiacalix[4]arene has found extensive applications in the construction of metal nanoclusters. In this investigation, we present the synthesis and characterization of the first all-calixarene-protected silver nanoclusters, [Ag(CH <subscript>3</subscript> CN) <subscript>4</subscript> ] <subscript>2</subscript> [Ag <subscript>44</subscript> (BTCA) <subscript>6</subscript> ] ( Ag <subscript> 44 </subscript> , H <subscript>4</subscript> BTCA = p-tert -butylthiacalix[4]arene). Single-crystal X-ray structural analysis reveals that all silver atoms are in a face-centered cubic ( fcc ) arrangement. The formation of such an fcc structure is attributed to the selectively passivation on {100} facets by BTCA <superscript>4-</superscript> . Thiacalixarene substantially facilitates the stability of Ag <subscript> 44 </subscript> due to its multiple coordination sites and bulkiness. Mass spectrometry and theoretical calculations reveal that Ag <subscript> 44 </subscript> is a superatomic silver nanocluster with 22 free electrons in the following configuration: 1S <superscript>2</superscript> 1P <superscript>6</superscript> 1D <superscript>6</superscript> 1F <superscript>2</superscript> 2S <superscript>2</superscript> 1D <superscript>4</superscript> . This work not only elucidates the impact of macrocyclic ligands on the stabilization of silver clusters but also furnishes an approach for assembling atomically precise fcc nanoclusters.

Details

Language :
English
ISSN :
1520-5126
Volume :
146
Issue :
36
Database :
MEDLINE
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
39196903
Full Text :
https://doi.org/10.1021/jacs.4c08094