Evidence map›Paper›PMID 42129155›Full record

ArticleNature communications2026

Organocatalytic atom transfer radical polymerization with light and pH dual-gated regulation.

Yu Jiang, Qiang Ma, Jianxu Chen, Xue Yang, Liuyin Jiang, Jinshuai Song, Saihu Liao

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Yu Jiang *State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China.ORCID http://orcid.org/0009-0001-9036-753X
Qiang Ma *State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China.ORCID http://orcid.org/0000-0002-6320-8955
Jianxu Chen *State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China.
Xue YangState Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China.
Liuyin JiangState Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China. lyjiang@xmu.edu.cn.
Jinshuai SongCollege of Chemistry, and Pingyuan Laboratory, Zhengzhou University, Zhengzhou, China. jssong@zzu.edu.cn.ORCID http://orcid.org/0000-0002-1909-9253
Saihu LiaoState Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China. shliao@xmu.edu.cn.ORCID http://orcid.org/0000-0002-0251-8757

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22371240, 22361132535, 22173083
6 · The paper itself

Abstract

To improve the control and precision in polymer synthesis, the development of polymerization with logical control by multiple stimuli has attracted considerable attention in recent years. Herein, we describe the introduction of a dual regulation by light and pH to organocatalytic atom transfer radical polymerization (O-ATRP), which features mild pH conditions, visible light irradiation, transition metal-free products, and excellent on/off control by both pH and light. 1,1-Binaphthol (BINOL) was successfully identified as a class of pH-responsive photoredox catalysts for O-ATRP, and show readily tunable photophysical properties and highly reversible chromic shift of maximum absorption (up to 60 nm) by very mild pH-mediation (pH 5/7). Moreover, the unique pH-responsive feature of BINOL also inspires the discovery of simple phenols like naphthol and pyrenol that could also drive the radical polymerization under light and afford higher catalytic efficiency and better control upon basic mediation. Given the widespread presence of phenols in natural compounds, we anticipate this work could also draw greater attention to their potential pH-responsive photophysical properties or other roles in catalysis or life systems.

Identifiers

PMID42129155
PMCPMC13376173

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.