Evidence map›Paper›PMID 40880476›Full record

ArticleScience advances2025

Highly selective aldehyde coupling on the heterointerface of molybdenum selenide and graphdiyne.

Siao Chen, Yurui Xue, Yang Gao, Han Wu, Xuchen Zheng, Yuliang Li

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Metal Atoms and Quantum Dots Coexist for Water Electrolysis.Advanced materials (Deerfield Beach, Fla.) · 2026
    Article
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

6 authors.

Siao ChenKey Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.ORCID 0009-0005-6500-3194
Yurui XueKey Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.ORCID 0000-0002-9783-1753
Yang GaoKey Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.ORCID 0000-0002-4977-2680
Han WuKey Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
Xuchen ZhengKey Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
Yuliang LiKey Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.ORCID 0000-0001-5279-0399

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The highly negative reduction potential prevents the selective coupling of two aldehydes to construct C─C bonds and hinders the formation of ketyl radicals. However, this important comprehensive issue remains unsolved. Here, we report the efficient activation of aldehydes by the in situ growth of a molybdenum selenide-graphdiyne heterointerface structure, allowing an aldehyde molecule to be selectively coupled with another aldehyde at room temperature and ambient pressure. High-resolution transmission electron microscopy and scanning transmission electron microscopy (HAADF-STEM) images reveal the formation of high-density active sites at the interface structure. The synchrotron x-ray photoelectron spectroscopy, x-ray absorption spectroscopy, and electron paramagnetic resonance spectroscopy results confirmed the selective formation of ketyl radicals. The noninteger charge transfer between graphdiyne and metal atoms promotes the continuous selectivity and efficient activation of aldehydes and C─C coupling of ketyl radicals. The ultrahigh selectivity of 2-furaldehyde for hydrofurion reached 92 ± 2%, while the turnover frequency reached 57 ± 4 per second.

Identifiers

PMID40880476
PMCPMC12396337

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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.