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Title: | Identification of Intermediate Au22(SR)4(SR′)14 Cluster on Ligand-Induced Transformation of Au25(SR)18 Nanocluster |
Authors: | Nair, Akhil S. Pathak, Biswarup |
Keywords: | Extended X ray absorption fine structure spectroscopy;Mass spectrometry;X ray absorption;Aromatic ligands;Extended X-ray absorption fine structures;Highly stables;Intermediate specie;Ligand exchange mechanism;Ligand exchanges;Optical spectroscopy;Theoretical calculations;Ligands |
Issue Date: | 2019 |
Publisher: | American Chemical Society |
Citation: | George, A., Sundar, A., Nair, A. S., Maman, M. P., Pathak, B., Ramanan, N., & Mandal, S. (2019). Identification of intermediate Au22(SR)4(SR′)14 cluster on ligand-induced transformation of Au25(SR)18 nanocluster. Journal of Physical Chemistry Letters, 10(16), 4571-4576. doi:10.1021/acs.jpclett.9b01856 |
Abstract: | We report the ligand-exchange-induced transformation from an icosahedral Au25(SR)18 cluster (where SR = 2-phenylethanethiol (PET)) to a bitetrahedral Au22(SR)4(SR′)14 cluster (where SR′ = 4-tert-butylbenzenethiol (TBBT)). This partial exchange of the ligands was achieved by controlling the concentration of the incoming TBBT ligand. Being a bulky and aromatic ligand, TBBT can efficiently distort the atomic structure of the Au25PET18 cluster, resulting in Au22(PET)4(TBBT)14, which is highly stable and considered to be an intermediate with a bitetrahedral structure. Time-dependent mass spectrometry and optical spectroscopy revealed the dissociation of the parent cluster and gave a deep insight on the ligand-exchange mechanism. Theoretical calculations and extended X-ray absorption fine structure studies confirm the formation of the Au22 structure. Identifying the atomic structure of the intermediate species opens a new avenue to study the transformation of one cluster to another. © 2019 American Chemical Society. |
URI: | https://doi.org/10.1021/acs.jpclett.9b01856 https://dspace.iiti.ac.in/handle/123456789/8886 |
ISSN: | 1948-7185 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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