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Au10(SG)10: A Chiral Gold Catenane Nanocluster with Zero Confined Electrons. Optical Properties and First-Principles Theoretical Analysis
Author(s) -
Franck Bertorelle,
Isabelle RussierAntoine,
Nathalie Calin,
Clothilde CombyZerbino,
Amina BensalahLedoux,
Stéphan Guy,
Philippe Dugourd,
PierreFrançois Brevet,
Željka Sanader Maršić,
Marjan Krstić,
Vlasta BonačićKoutecký,
Rodolphe Antoine
Publication year - 2017
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.7b00611
Subject(s) - nanoclusters , homoleptic , catenane , electron , circular dichroism , materials science , molecular physics , metal , crystallography , chemistry , nanotechnology , physics , molecule , quantum mechanics , organic chemistry , metallurgy
We report facile synthesis of the Au 10 (SG) 10 nanoclusters, where SG stands for glutathione, found to be promising as a new class of radiosensitizers for cancer radiotherapy. The homoleptic catenane structure with two Au 5 SG 5 interconnected rings, among different isomer structures, gives the best agreement between theoretical and experimental optical spectra and XRD patterns. This catenane structure exhibits a centrosymmetry-broken structure, resulting in enhanced second harmonic response and new characteristic circular dichroism signals in the spectral region of 250-400 nm. This is the first determination of the nonlinear optical properties of a ligated cluster with an equal Au-to-ligand ratio, thus without a metallic core and therefore zero confined electrons. Insight into the nonlinear and chiroptical efficiencies arising from interplay between structural and electronic properties is provided by the TD-DFT approach.

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