<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>64(38)</volume><submitter>Thomas SR</submitter><pubmed_abstract>A series of gold nanoparticles (AuNPs) stabilized by bidentate acyclic diamino carbenes (ADCs) were synthesized via the reduction of dimeric gold(I) complexes. The resulting ADC-AuNPs were characterized by NMR spectroscopy, UV-vis spectroscopy, X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA), revealing nanoparticles with a narrow size distribution and sizes ranging from 1.7 to 3.3 nm. This synthetic approach was extended to an asymmetric dinuclear ADC-gold(I) complex, affording slightly larger AuNPs (∼4 nm) upon reduction. The ADC-AuNPs with shorter linkers exhibited significant catalytic activity for the reduction of 4-nitrophenol, demonstrating a versatile and efficient route to catalytically active gold nanoparticles stabilized by both symmetric and asymmetric ADC ligands.</pubmed_abstract><journal>Inorganic chemistry</journal><pagination>19316-19324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12486202</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Bidentate Acyclic Diamino Carbene-Stabilized Gold Nanoparticles from Symmetric and Asymmetric Gold(I) Complexes: Synthesis, Characterization, and Catalytic Activity.</pubmed_title><pmcid>PMC12486202</pmcid><pubmed_authors>Chalermnon M</pubmed_authors><pubmed_authors>Reithofer MR</pubmed_authors><pubmed_authors>Thomas SR</pubmed_authors><pubmed_authors>Tan TTY</pubmed_authors><pubmed_authors>Rubio GMDM</pubmed_authors><pubmed_authors>Chin JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bidentate Acyclic Diamino Carbene-Stabilized Gold Nanoparticles from Symmetric and Asymmetric Gold(I) Complexes: Synthesis, Characterization, and Catalytic Activity.</name><description>A series of gold nanoparticles (AuNPs) stabilized by bidentate acyclic diamino carbenes (ADCs) were synthesized via the reduction of dimeric gold(I) complexes. The resulting ADC-AuNPs were characterized by NMR spectroscopy, UV-vis spectroscopy, X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA), revealing nanoparticles with a narrow size distribution and sizes ranging from 1.7 to 3.3 nm. This synthetic approach was extended to an asymmetric dinuclear ADC-gold(I) complex, affording slightly larger AuNPs (∼4 nm) upon reduction. The ADC-AuNPs with shorter linkers exhibited significant catalytic activity for the reduction of 4-nitrophenol, demonstrating a versatile and efficient route to catalytically active gold nanoparticles stabilized by both symmetric and asymmetric ADC ligands.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-04T00:23:55.738Z</modification><creation>2026-05-03T03:12:35.759Z</creation></dates><accession>S-EPMC12486202</accession><cross_references><pubmed>40939637</pubmed><doi>10.1021/acs.inorgchem.5c03050</doi></cross_references></HashMap>