Gold Single‐Atom Catalysts Enable Selective Shuttle Hydrochlorination of Alkynes

Shuttle catalysis enables the transfer of reactive functional groups without relying on highly corrosive reagents. However, it remains largely confined to homogeneous systems, where catalyst recovery and reuse are often challenging. Here, we report a recyclable gold single-atom catalyst (SAC) supported on activated carbon (AC) for the selective shuttle hydrochlorination of terminal alkynes to vinyl chlorides, which are key intermediates in pharmaceutical synthesis. Spectroscopic and catalytic studies indicate that the combination of Au(I) single atoms with the AC carrier is essential for the unique chemo- and stereoselectivity observed. This heterogeneous system displays broad substrate compatibility, including sterically hindered alkynes, heterocycles, acid-labile groups, and drug-derived substrates. Upon reuse, gradual aggregation of gold single atoms into nanoparticles leads to activity losses, but the associated speciation changes are reversible by oxidative redispersion, while quantitative metal retention ensures recoverability. Overall, this study demonstrates how to extend heterogeneous SACs to shuttle catalysis, highlighting the complementary reactivity and distinct catalyst design requirements for developing recoverable, safer, and more sustainable heterogeneous transfer reactions.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-10-12
DOI
https://doi.org/10.1002/anie.1983055
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Gold Single‐Atom Catalysts Enable Selective Shuttle Hydrochlorination of Alkynes

Eva J. Meeus, Javier Pérez‐Ramírez, Sharon Mitchell, Aram L. Bugaev et al.
Angewandte Chemie International Edition
Catalytic Alkyne Reactions
article

Gold Single‐Atom Catalysts Enable Selective Shuttle Hydrochlorination of Alkynes

Eva J. Meeus, Javier Pérez‐Ramírez, Sharon Mitchell, Aram L. Bugaev, Milivoj Plodinec, Marc‐Eduard Usteri, Bill Morandi, S Choi, Christian Zachau
article en

Abstract

Shuttle catalysis enables the transfer of reactive functional groups without relying on highly corrosive reagents. However, it remains largely confined to homogeneous systems, where catalyst recovery and reuse are often challenging. Here, we report a recyclable gold single-atom catalyst (SAC) supported on activated carbon (AC) for the selective shuttle hydrochlorination of terminal alkynes to vinyl chlorides, which are key intermediates in pharmaceutical synthesis. Spectroscopic and catalytic studies indicate that the combination of Au(I) single atoms with the AC carrier is essential for the unique chemo- and stereoselectivity observed. This heterogeneous system displays broad substrate compatibility, including sterically hindered alkynes, heterocycles, acid-labile groups, and drug-derived substrates. Upon reuse, gradual aggregation of gold single atoms into nanoparticles leads to activity losses, but the associated speciation changes are reversible by oxidative redispersion, while quantitative metal retention ensures recoverability. Overall, this study demonstrates how to extend heterogeneous SACs to shuttle catalysis, highlighting the complementary reactivity and distinct catalyst design requirements for developing recoverable, safer, and more sustainable heterogeneous transfer reactions.

Angewandte Chemie International Edition
Paul Scherrer Institute (CH), ETH Zurich (CH), Scientific Center for Optical and Electron Microscopy (CH), Institute for Chemical and Bioengineering (CH)
Openalex Percentile: Top 25%
Catalytic Alkyne Reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.