Metallo‐Supramolecular Helicates as Surface‐Enhanced Raman Scattering (SERS) Substrates with High Tailorability

The exploration of novel functionalized supramolecular coordination complexes (SCCs) can enable new applications in domains that include purification and sensing. In this study, employing a coordination-driven self-assembly strategy, we designed and prepared a series of benzochalcogenodiazole-based metallohelicates as high-efficiency charge-transfer surface-enhanced Raman scattering (SERS) substrates, expanding the range of applications for these metallohelicates. Through structural modifications, including the substitution of single heteroatoms on ligands, replacement of coordinating metals, and alteration of ligand framework linkages, the Raman performance of these metallohelicates as substrates were systematically optimized. Notably, the SERS enhancement factors (EFs) of the metallohelicate-based SERS substrates were significantly enhanced to levels as high as 1.03×10<sup>7</sup>, which rivals the EFs of noble metals devoid of "hot spots". Additionally, the underlying Raman enhancement mechanisms of these metallohelicates have been investigated through a combination of control experiments and theoretical calculations. This study not only demonstrates the utility of metallohelicates as SERS substrates but also offers insights and materials for the development of high-efficiency new charge-transfer SERS substrates.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2024-09-02
DOI
https://doi.org/10.1002/anie.202414089
Citations
10
Primary Topic
Gold and Silver Nanoparticles Synthesis and Applications
Type
article
Field-Weighted Citation Impact
1.18
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article

Metallo‐Supramolecular Helicates as Surface‐Enhanced Raman Scattering (SERS) Substrates with High Tailorability

Bo Song, Xiao‐Li Zhao, Jonathan R. Nitschke, Hai‐Bo Yang et al.
10 citations
Angewandte Chemie International Edition
Gold and Silver Nanoparticles Synthesis and Applications
1.18
article

Metallo‐Supramolecular Helicates as Surface‐Enhanced Raman Scattering (SERS) Substrates with High Tailorability

Bo Song, Xiao‐Li Zhao, Jonathan R. Nitschke, Hai‐Bo Yang, Wei‐Tao Dou, Zhonghui Zhang, Yang Tian, Lin Xu, Chen Wang, Chunchun Li, Yanfei Niu
article en
10 citations

Abstract

The exploration of novel functionalized supramolecular coordination complexes (SCCs) can enable new applications in domains that include purification and sensing. In this study, employing a coordination-driven self-assembly strategy, we designed and prepared a series of benzochalcogenodiazole-based metallohelicates as high-efficiency charge-transfer surface-enhanced Raman scattering (SERS) substrates, expanding the range of applications for these metallohelicates. Through structural modifications, including the substitution of single heteroatoms on ligands, replacement of coordinating metals, and alteration of ligand framework linkages, the Raman performance of these metallohelicates as substrates were systematically optimized. Notably, the SERS enhancement factors (EFs) of the metallohelicate-based SERS substrates were significantly enhanced to levels as high as 1.03×10<sup>7</sup>, which rivals the EFs of noble metals devoid of "hot spots". Additionally, the underlying Raman enhancement mechanisms of these metallohelicates have been investigated through a combination of control experiments and theoretical calculations. This study not only demonstrates the utility of metallohelicates as SERS substrates but also offers insights and materials for the development of high-efficiency new charge-transfer SERS substrates.

Angewandte Chemie International EditionVol. 64(2)
University of Shanghai for Science and Technology (CN), University of Cambridge (GB), East China Normal University (CN)
Openalex Percentile: Top 23%
Gold and Silver Nanoparticles Synthesis and Applications
1.18
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Metallo‐Supramolecular Helicates as Surface‐Enhanced Raman Scattering (SERS) Substrates with High Tailorability — Bo Song, Xiao‐Li Zhao, et al. · Angewandte Chemie International Edition (2024) | TGRS Research Map | TGRS