Diving into UnknownWaters: Water-Soluble ClickableAu<sub>13</sub> Nanoclusters Protected with N‑HeterocyclicCarbenes for Bio-Medical Applications

The use of gold nanoclusters in biomedical applications has been steadily increasing in recent years. However, water solubility is a key factor for these applications, and water-soluble gold nanoclusters are often difficult to isolate and susceptible to exchange or oxidation in vivo. Herein, we report the isolation of N-heterocyclic carbene (NHC)-protected atomically precise gold nanoclusters functionalized with triethylene glycol monomethyl ether groups. These clusters are highly luminescent and water soluble and are shown to be stable in biological media. Importantly, the core structure, stability, and high quantum yield of the nanoclusters were conserved after backbone modification. Depending on the nature of the halide group, clusters have high stability in simulated biofluids and resist attack by glutathione. In vivo studies show that no abnormal cellular morphology is introduced in the kidney, liver, or spleen of mice treated with [Au<sub>13</sub>(NHC)<sub>5</sub>Br<sub>2</sub>]­Br<sub>3</sub> nanoclusters protected by 1,8-dimethylnaphthyl-linked NHCs. This cluster has a blood elimination half-life of 0.68 h. Functionalization of the wingtip groups of the cluster with azide groups is demonstrated, and complete reaction of all 10 azide groups with strained alkynes is shown, highlighting the potential of these clusters in biological settings.

Publication Details

Journal
Figshare
Published
2025-01-22
DOI
https://doi.org/10.1021/jacs.4c14240.s001
Primary Topic
Nanocluster Synthesis and Applications
Type
article
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article

Diving into UnknownWaters: Water-Soluble ClickableAu13 Nanoclusters Protected with N‑HeterocyclicCarbenes for Bio-Medical Applications

Figshare
Nanocluster Synthesis and Applications
article

Diving into UnknownWaters: Water-Soluble ClickableAu13 Nanoclusters Protected with N‑HeterocyclicCarbenes for Bio-Medical Applications

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Abstract

The use of gold nanoclusters in biomedical applications has been steadily increasing in recent years. However, water solubility is a key factor for these applications, and water-soluble gold nanoclusters are often difficult to isolate and susceptible to exchange or oxidation in vivo. Herein, we report the isolation of N-heterocyclic carbene (NHC)-protected atomically precise gold nanoclusters functionalized with triethylene glycol monomethyl ether groups. These clusters are highly luminescent and water soluble and are shown to be stable in biological media. Importantly, the core structure, stability, and high quantum yield of the nanoclusters were conserved after backbone modification. Depending on the nature of the halide group, clusters have high stability in simulated biofluids and resist attack by glutathione. In vivo studies show that no abnormal cellular morphology is introduced in the kidney, liver, or spleen of mice treated with [Au<sub>13</sub>(NHC)<sub>5</sub>Br<sub>2</sub>]­Br<sub>3</sub> nanoclusters protected by 1,8-dimethylnaphthyl-linked NHCs. This cluster has a blood elimination half-life of 0.68 h. Functionalization of the wingtip groups of the cluster with azide groups is demonstrated, and complete reaction of all 10 azide groups with strained alkynes is shown, highlighting the potential of these clusters in biological settings.

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Clean water and sanitation
Openalex Percentile: Top 63%
Nanocluster Synthesis and Applications
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