Solvent Induced Transformation of Homoleptic Alkynyl‐Protected Large Silver Nanoclusters

L Lu‐Ming Zheng (Department of Chemistry Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education) Tsinghua University Beijing 100084 P.R. China) Z Zhen‐Chao Long (Department of Chemistry Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education Tsinghua University Beijing 100084 P.R. China) F Feng Hu (Department of Chemistry, Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education)) J Jiangtao Chan (Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry) W Wan‐Qi Shi (Department of Chemistry Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education Tsinghua University Beijing 100084 P.R. China) B Ben Zhang (Department of Chemistry, Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education)) Z Zhaohui Wang (Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry) Q Quan‐Ming Wang (Department of Chemistry Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education Tsinghua University Beijing 100084 P.R. China)

Abstract

Abstract Structural transformation of high‐nuclearity nanoclusters is of significant interest because of its relevance to the formation mechanisms and stability of metal clusters. Herein, we report three large homoleptic alkynyl‐protected silver nanoclusters, [Ag 98 (2‐CH 3 C 6 H 4 C≡C) 52 ](BF 4 ) 2 , [Ag 86 (2‐CH 3 C 6 H 4 C≡C) 50 ](BF 4 ) 4 , and [Ag 74 (2‐CH 3 C 6 H 4 C≡C) 44 ](BF 4 ) 2 , synthesized from the same precursor 2‐CH 3 C 6 H 4 C≡CAg via fine‐tuning the reduction rate. X‐ray crystallography demonstrates that Ino decahedral Ag 13 units serve as building blocks in all three nanoclusters. Remarkably, Ag 98 undergoes an intercluster transformation in methanol. It initially converts into Ag 74 , then Ag 74 reacts with Ag 98 to form Ag 86 , which eventually is transformed into the thermodynamically stable Ag 74 . Time‐dependent electrospray ionization mass spectrometry (ESI‐MS) confirms such a multi‐step reaction process during the transformation, identifying Ag 86 as the key intermediate. Our findings not only provide new insights into the structural transformation pathways of nanoclusters but also enhance the understanding of transformation mechanisms, contributing to the rational synthesis of high‐nuclearity nanoclusters.

Article Details

Volume / Issue Vol. 64, Issue 26
Published June 24, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

L

Lu‐Ming Zheng

Department of Chemistry Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education) Tsinghua University Beijing 100084 P.R. China

Z

Zhen‐Chao Long

Department of Chemistry Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education Tsinghua University Beijing 100084 P.R. China

F

Feng Hu

Department of Chemistry, Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education)

J

Jiangtao Chan

Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry

W

Wan‐Qi Shi

Department of Chemistry Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education Tsinghua University Beijing 100084 P.R. China

B

Ben Zhang

Department of Chemistry, Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education)

Z

Zhaohui Wang

Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry

Q

Quan‐Ming Wang

Department of Chemistry Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education Tsinghua University Beijing 100084 P.R. China