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Metal Nanoparticles Confronted with Foreign Ligands: Mere Ligand Exchange or Further Structural Transformation?
Author(s) -
Yan Nan,
Xia Nan,
Wu Zhikun
Publication year - 2021
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.202000609
Subject(s) - nanoclusters , ligand (biochemistry) , nanoparticle , metal , chemistry , crystallography , nucleophile , crystal structure , nanotechnology , materials science , catalysis , organic chemistry , receptor , biochemistry
Ligand exchange reactions have attracted extensive interest due to their utility in tailoring the properties and applications of metal nanoparticles, but these techniques are not well understood due to the unclearness of metal nanoparticles at an atomic level. The emerging ultrasmall metal nanoparticles (metal nanoclusters) provide excellent opportunities for investigating this challenging issue. Herein, it is revealed that structurally similar Au 25 (SC 2 H 4 Ph) 18 , Au 24 Cd(SC 2 H 4 Ph) 18, and Au 24 Hg(SC 2 H 4 Ph) 18 transform to Au 24 (SCH 2 Ph‐ t Bu) 20 , Au 24 Cd(SCH 2 Ph‐ t Bu) 18 and ≈5 nm gold nanoparticles after reacting with HSCH 2 Ph‐ t Bu, respectively. Based on this and some other facts, it is suggested that the intrinsic stability is one key factor that determines the ligand exchange direction, whether by mere ligand exchange or further structure transformation (including aggregation). Single crystal X‐ray crystallography further reveals that the partial surface ligand configuration reverses after ligand exchange, providing structure evidence for the unimolecular nucleophilic substitution (S N 1)‐like mechanism.