Evidence map›Paper›PMID 40405454›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Hydrogen Bond-Assisted PCET and Formation of W

Wonjung Lee, Daeyong Um, Yujin Baek, Sugyeong Hong, Youngseob Lee, Jaeheon Lee, Jin Kim, Sun Hee Kim, Kyung-Bin Cho, Junhyeok Seo

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Hydrogen Bond-Assisted PCET and Formation of WAngewandte Chemie (International ed. in English) · 2025
    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

10 authors.

Wonjung LeeDepartment of Chemistry, Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.
Daeyong UmDepartment of Chemistry, Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.
Yujin BaekDepartment of Chemistry, Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.
Sugyeong HongWestern Seoul Center, Korea Basic Science Institute (KBSI), Seoul, 03759, Republic of Korea.
Youngseob LeeDepartment of Chemistry and Research Institute for Materials and Energy Sciences, Jeonbuk National University, Jeonju, 54896, Republic of Korea.
Jaeheon LeeDepartment of Chemistry, Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.
Jin KimDepartment of Chemistry, Sunchon National University, Suncheon, 57922, Republic of Korea.
Sun Hee KimWestern Seoul Center, Korea Basic Science Institute (KBSI), Seoul, 03759, Republic of Korea.
Kyung-Bin ChoDepartment of Chemistry and Research Institute for Materials and Energy Sciences, Jeonbuk National University, Jeonju, 54896, Republic of Korea.
Junhyeok SeoDepartment of Chemistry, Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.ORCID https://orcid.org/0000-0002-9436-6964

Funding

Korea Basic Science Institute (KBSI) grant A412560Ministry of Education of the Republic of Korea (MoE) LAMP Program RS-2024-00443714National Research Foundation of Korea 2023R1A2C2004733National Research Foundation of Korea RS-2021-NR058689National Research Foundation of Korea RS-2021-NR060081
6 · The paper itself

Abstract

The redox non-innocent nature of dithiolene ligands is well known for stabilizing high-valent metal ions and facilitating proton-coupled electron transfer (PCET) processes. Until now, proton reactivity at the dithiolene site has been primarily associated with low-valent metal centers, as high-valent metal-dithiolene complexes were not considered viable for such reactivity. This study introduces high-valent bis(dithiolene) tungsten (W)-oxo complexes featuring hydrogen-bonding interactions, unveiling a novel proton reduction mechanism mediated by the dithiolene moiety. The process begins with a nucleophilic W-oxo, forming a hydrogen bond, followed by a second hydrogen bond at the dithiolene-sulfur (S) site. These hydrogen-bonding interactions significantly modulate the molecular orbital energy levels, enabling the W

Indexed as

DithioleneHydrogen bondPCETWIII─OHW‐oxo

Identifiers

PMID40405454
PMCPMC12304848

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.