Evidence map›Paper›PMID 42424644›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2026

Guiding the De Novo Synthesis of Open Metal Frameworks Through Low-Symmetry Bent Linker for Hydrogen Isotope Separation.

Guo-Ying Han, Zhiye Zhong, Yong-Sheng Wang, Tian-Yi Li, Yu Gai, Qin-Yi Cheng, Pascal Van Der Voort, Yanhang Ma, Guang-Ping Hao, Xiao Feng

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 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

10 authors.

Guo-Ying HanSchool of Chemistry, Dalian University of Technology, Dalian, China.
Zhiye ZhongSchool of Physical Science and Technology & Shanghai Key Laboratory of High-resolution Electron Microscopy, Shanghai Tech University, Shanghai, China.
Yong-Sheng WangState Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, Liaoning Key Laboratory for Catalytic Conversion of Carbon Resources, and School of Chemical Engineering, Dalian University of Technology, Dalian, China.
Tian-Yi LiState Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, Liaoning Key Laboratory for Catalytic Conversion of Carbon Resources, and School of Chemical Engineering, Dalian University of Technology, Dalian, China.
Yu GaiSchool of Chemistry, Dalian University of Technology, Dalian, China.
Qin-Yi ChengSchool of Chemistry, Dalian University of Technology, Dalian, China.
Pascal Van Der VoortCenter For Ordered Materials, Organometallics and Catalysis (COMOC), Department of Chemistry, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0002-1248-479X
Yanhang MaSchool of Physical Science and Technology & Shanghai Key Laboratory of High-resolution Electron Microscopy, Shanghai Tech University, Shanghai, China.ORCID https://orcid.org/0000-0003-4814-3740
Guang-Ping HaoState Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, Liaoning Key Laboratory for Catalytic Conversion of Carbon Resources, and School of Chemical Engineering, Dalian University of Technology, Dalian, China.ORCID https://orcid.org/0000-0001-5849-9965
Xiao FengSchool of Chemistry, Dalian University of Technology, Dalian, China.ORCID https://orcid.org/0000-0002-3055-0172

Funding

Foundation of State Key Laboratory of Coal Conversion J24-25-611Fundamental Research Funds for the Central Universities DUT24LK004Liaoning Provincial Science and Technology Program 2025JH2/101900044National Natural Science Foundation of China 22101039National Natural Science Foundation of China 22311530679National Natural Science Foundation of China 22471027Open Research Fund of Guangdong Advanced Carbon Materials Co., Ltd Kargen-2024A0102Science Fund for Creative Research Groups of the National Natural Science Foundation of China 22021005State Key Laboratory of Catalysis 2024SKL-A-006State Key Laboratory of Catalysis N-23-01
6 · The paper itself

Abstract

Open metal sites (OMS) serve as crucial active sites in numerous applications, including hydrogen isotope separation, highlighting the importance of developing targeted synthesis strategies for OMS-containing frameworks. Unlike defect-engineered approaches that generate disordered OMS, synthesizing frameworks with an ordered distribution of OMS remains highly challenging yet is essential for efficient separation. Guided by the topological simplification process-which abstracts connectivity while overlooking coordination geometry-this study introduces a strategy to construct metal-organic frameworks (MOFs) with ordered OMS by reducing linker symmetry. By employing bent linkers with lower axial symmetry, rather than linear linkers of equivalent topological connectivity, OMF-2 (OMF = Open-Metal Framework) was synthesized, a pcu 8-connected framework featuring four OMS per cluster, thereby validating the approach. Remarkably, OMF-2 demonstrates exceptional hydrogen isotope separation performance, with an ideal adsorbed solution theory (IAST) selectivity of 7.7, a cryogenically programmed desorption (CPD) selectivity of 6.6, and a breakthrough test selectivity of 2.3 for D

Indexed as

hydrogen isotope separationlinker designMOFsopen metal sites

Identifiers

PMID42424644
PMCPMC13549031

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Registered trials

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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.