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Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au(13) and heart-shaped Au(8) clusters

Due to distinctive quantum confinement effects, ultrasmall gold nanoparticles usually exhibit interesting electronic structure and molecular-like properties. However, the lack of atomically-precise structural information makes the understanding of them almost impossible, such as understanding the re...

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Autores principales: Zhang, Shan-Shan, Feng, Lei, Senanayake, Ravithree D., Aikens, Christine M., Wang, Xing-Po, Zhao, Quan-Qin, Tung, Chen-Ho, Sun, Di
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885941/
https://www.ncbi.nlm.nih.gov/pubmed/29675171
http://dx.doi.org/10.1039/c7sc03566g
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author Zhang, Shan-Shan
Feng, Lei
Senanayake, Ravithree D.
Aikens, Christine M.
Wang, Xing-Po
Zhao, Quan-Qin
Tung, Chen-Ho
Sun, Di
author_facet Zhang, Shan-Shan
Feng, Lei
Senanayake, Ravithree D.
Aikens, Christine M.
Wang, Xing-Po
Zhao, Quan-Qin
Tung, Chen-Ho
Sun, Di
author_sort Zhang, Shan-Shan
collection PubMed
description Due to distinctive quantum confinement effects, ultrasmall gold nanoparticles usually exhibit interesting electronic structure and molecular-like properties. However, the lack of atomically-precise structural information makes the understanding of them almost impossible, such as understanding the relationships between their compositions and unique properties. Herein, by reducing a diphosphine Au(I) precursor (Au(2)(dppm)(2)Cl(2); dppm = Ph(2)PCH(2)PPh(2)) with or without a S(2–) releasing reagent, we enriched our knowledge of the members in the families of Au(13) and Au(8) by the structural determinations of two new dppm-protected gold nanoclusters, [Au(13)(dppm)(6)](5+) (SD/Au1) and [Au(8)(dppm)(4)S(2)](2+) (SD/Au2), respectively. Within SD/Au1, the Au(13) kernel significantly deviates from the ideal I(h) icosahedron by the elongation of three surface Au–Au bonds to ∼3.5 Å, giving it C(3) symmetry, whereas SD/Au2 has a novel heart-shaped C(2) symmetric Au(8)S(2) core (central Au(4) tetrahedron + two Au(2)S units) protected by four μ(2)-dppm ligands in the outer shell. Of note, SD/Au1 represents a rare Au(13) nanocluster with an opened icosahedral geometry, and SD/Au2 shows a new edge-shared “core + 4exo” structure type that has never been observed before. The electronic structures and optical absorption spectra of these systems are correlated with time-dependent density functional theory (TDDFT) calculations. Based on the spherical jellium model, the stability of the Au(13) and Au(8) nanoclusters can be ascribed to 8- and 2-electron superatoms with 1S(2)1P(6) and 1S(2) configurations, respectively. Interestingly, the cluster SD/Au2 exhibits bright yellow luminescence with an emission maximum at 591 nm that slightly hypsochromically shifts to 581 nm upon cooling to 93 K. Our findings not only enrich the family of diphosphine-protected ultrasmall gold nanoclusters, but also demonstrate the rich variations of gold kernels during the transformation from a simple Au(I) precursor to Au nanoclusters.
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spelling pubmed-58859412018-04-19 Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au(13) and heart-shaped Au(8) clusters Zhang, Shan-Shan Feng, Lei Senanayake, Ravithree D. Aikens, Christine M. Wang, Xing-Po Zhao, Quan-Qin Tung, Chen-Ho Sun, Di Chem Sci Chemistry Due to distinctive quantum confinement effects, ultrasmall gold nanoparticles usually exhibit interesting electronic structure and molecular-like properties. However, the lack of atomically-precise structural information makes the understanding of them almost impossible, such as understanding the relationships between their compositions and unique properties. Herein, by reducing a diphosphine Au(I) precursor (Au(2)(dppm)(2)Cl(2); dppm = Ph(2)PCH(2)PPh(2)) with or without a S(2–) releasing reagent, we enriched our knowledge of the members in the families of Au(13) and Au(8) by the structural determinations of two new dppm-protected gold nanoclusters, [Au(13)(dppm)(6)](5+) (SD/Au1) and [Au(8)(dppm)(4)S(2)](2+) (SD/Au2), respectively. Within SD/Au1, the Au(13) kernel significantly deviates from the ideal I(h) icosahedron by the elongation of three surface Au–Au bonds to ∼3.5 Å, giving it C(3) symmetry, whereas SD/Au2 has a novel heart-shaped C(2) symmetric Au(8)S(2) core (central Au(4) tetrahedron + two Au(2)S units) protected by four μ(2)-dppm ligands in the outer shell. Of note, SD/Au1 represents a rare Au(13) nanocluster with an opened icosahedral geometry, and SD/Au2 shows a new edge-shared “core + 4exo” structure type that has never been observed before. The electronic structures and optical absorption spectra of these systems are correlated with time-dependent density functional theory (TDDFT) calculations. Based on the spherical jellium model, the stability of the Au(13) and Au(8) nanoclusters can be ascribed to 8- and 2-electron superatoms with 1S(2)1P(6) and 1S(2) configurations, respectively. Interestingly, the cluster SD/Au2 exhibits bright yellow luminescence with an emission maximum at 591 nm that slightly hypsochromically shifts to 581 nm upon cooling to 93 K. Our findings not only enrich the family of diphosphine-protected ultrasmall gold nanoclusters, but also demonstrate the rich variations of gold kernels during the transformation from a simple Au(I) precursor to Au nanoclusters. Royal Society of Chemistry 2017-12-04 /pmc/articles/PMC5885941/ /pubmed/29675171 http://dx.doi.org/10.1039/c7sc03566g Text en This journal is © The Royal Society of Chemistry 2018 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Zhang, Shan-Shan
Feng, Lei
Senanayake, Ravithree D.
Aikens, Christine M.
Wang, Xing-Po
Zhao, Quan-Qin
Tung, Chen-Ho
Sun, Di
Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au(13) and heart-shaped Au(8) clusters
title Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au(13) and heart-shaped Au(8) clusters
title_full Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au(13) and heart-shaped Au(8) clusters
title_fullStr Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au(13) and heart-shaped Au(8) clusters
title_full_unstemmed Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au(13) and heart-shaped Au(8) clusters
title_short Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au(13) and heart-shaped Au(8) clusters
title_sort diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral au(13) and heart-shaped au(8) clusters
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885941/
https://www.ncbi.nlm.nih.gov/pubmed/29675171
http://dx.doi.org/10.1039/c7sc03566g
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