Catalyst-FreeThiol–yne Nucleophilic PhotoclickChemistry

Abstract X-yne nucleophilic addition reactions are essential and powerful tools in a range of synthetic routes for realizing functional and stimuli-responsive materials. Unfortunately, the lack of spatiotemporal control and the requirement for catalyst addition in these reactions limit their full potential in synthetic and materials-based applications, including in light-driven 3D printing. Herein, we close this critical gap and exploit a spirothiopyran (STP) photoswitch as a synthon for photoinduced and catalyst-free thiol–yne click reactions, an important class of X-yne click chemistries. We further employ our photoswitch-based entity for rapid and facile postpolymerization modification as well as photopolymerization under very mild and aerobic conditions.

Authors

Institutions

Publication Details

Journal
Journal of the American Chemical Society
Published
2026-08-14
DOI
https://doi.org/10.1021/jacs.6c09543
Primary Topic
Photochromic and Fluorescence Chemistry
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Catalyst-FreeThiol–yne Nucleophilic PhotoclickChemistry

Christopher Barner‐Kowollik, Linh Duy Thai, S. Roth, Frank Kirschhöfer
Journal of the American Chemical Society
Photochromic and Fluorescence Chemistry
article

Catalyst-FreeThiol–yne Nucleophilic PhotoclickChemistry

Christopher Barner‐Kowollik, Linh Duy Thai, S. Roth, Frank Kirschhöfer
article en

Abstract

Abstract X-yne nucleophilic addition reactions are essential and powerful tools in a range of synthetic routes for realizing functional and stimuli-responsive materials. Unfortunately, the lack of spatiotemporal control and the requirement for catalyst addition in these reactions limit their full potential in synthetic and materials-based applications, including in light-driven 3D printing. Herein, we close this critical gap and exploit a spirothiopyran (STP) photoswitch as a synthon for photoinduced and catalyst-free thiol–yne click reactions, an important class of X-yne click chemistries. We further employ our photoswitch-based entity for rapid and facile postpolymerization modification as well as photopolymerization under very mild and aerobic conditions.

Journal of the American Chemical Society
Karlsruhe Institute of Technology (DE), Queensland University of Technology (AU)
Alexander von Humboldt-Stiftung
Openalex Percentile: Top 22%
Photochromic and Fluorescence Chemistry
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.