Evidence map›Paper›PMID 42786186›Full record

ArticleNature chemistry2026

Programming semiconducting two-dimensional conjugated metal-organic frameworks via anisotropic reticular chemistry.

Jianjun Zhang, Guojun Zhou, Hio-Ieng Un, Jianbo Song, Petko St Petkov, Rashid Iqbal, Shuai Fu, Xing Huang, Geping Zhang, Yang Lu and 16 more

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

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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

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3 · Its place in the literature

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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

26 authors.

Jianjun Zhang *Center for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany.
Guojun Zhou *Wallenberg Initiative Materials Science for Sustainability, Department of Chemistry, Stockholm University, Stockholm, Sweden.
Hio-Ieng Un *Optoelectronics Group, Department of Physics, Cavendish Laboratory, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-4242-3573
Jianbo SongWallenberg Initiative Materials Science for Sustainability, Department of Chemistry, Stockholm University, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-5868-7269
Petko St PetkovFaculty of Chemistry and Pharmacy, University of Sofia, Sofia, Bulgaria.ORCID http://orcid.org/0000-0001-6315-8591
Rashid IqbalDepartment of Chemistry, The University of Hong Kong, Hong Kong, China.ORCID http://orcid.org/0000-0003-2953-6725
Shuai FuCenter for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0003-4038-2384
Xing HuangCenter for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0001-6807-7440
Geping ZhangDepartment of Chemistry, The University of Hong Kong, Hong Kong, China.
Yang LuCenter for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0001-9416-2198
Darius PohlDresden Center for Nanoanalysis, Center for Advancing Electronics Dresden, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-4859-4325
Renxiang LiuCenter for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany.
Yubin FuMax Planck Institute of Microstructure Physics, Halle, Germany.ORCID http://orcid.org/0000-0002-2613-394X
Xiaodong LiMax Planck Institute of Microstructure Physics, Halle, Germany.ORCID http://orcid.org/0000-0002-9628-329X
Wenjie ZhangMax Planck Institute of Microstructure Physics, Halle, Germany.
Bernd RellinghausDresden Center for Nanoanalysis, Center for Advancing Electronics Dresden, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-1367-8545
Alexey AlfonsovLeibniz Institute for Solid State and Materials Research, Dresden, Germany.
Volodymyr BonDepartment of Inorganic Chemistry I, Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-9851-5031
Jie DingMax Planck Institute of Microstructure Physics, Halle, Germany.ORCID http://orcid.org/0000-0002-1427-9618
Stuart S P ParkinMax Planck Institute of Microstructure Physics, Halle, Germany.
Thomas HeineCenter for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0003-2379-6251
Zhiyong WangCenter for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany. zhiyong.wang@mpi-halle.mpg.de.ORCID http://orcid.org/0000-0002-0909-9495
Zhehao HuangWallenberg Initiative Materials Science for Sustainability, Department of Chemistry, Stockholm University, Stockholm, Sweden. zhehaohuang@scut.edu.cn.ORCID http://orcid.org/0000-0002-4575-7870
Henning SirringhausOptoelectronics Group, Department of Physics, Cavendish Laboratory, University of Cambridge, Cambridge, UK. hs220@cam.ac.uk.ORCID http://orcid.org/0000-0001-9827-6061
Xinliang FengCenter for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany. xinliang.feng@mpi-halle.mpg.de.ORCID http://orcid.org/0000-0003-3885-2703
Renhao DongDepartment of Chemistry, The University of Hong Kong, Hong Kong, China. rhdong@hku.hk.ORCID http://orcid.org/0000-0002-4125-9284

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 417590517National Natural Science Foundation of China (National Science Foundation of China) 22272092National Natural Science Foundation of China (National Science Foundation of China) 22472085Shenzhen Science and Technology Innovation Commission JCYJ20250604190017022Svenska Forskningsrådet Formas (Swedish Research Council Formas) 2020-00831
6 · The paper itself

Abstract

Electrically conductive two-dimensional (2D) conjugated metal-organic frameworks (c-MOFs) are emerging electronic materials with tunable topologies and metal nodes. However, the uniform reactivity of conventional high-symmetry ligands typically leads to homogeneous linking, limiting the programmable construction of diverse topologies and metal nodes from a single-type ligand. Here we report an anisotropic reticular chemistry strategy using the 1,2,5,6,9,10,12,13-octahydroxydibenzo-[fg,op]naphthacene ligand with diverse catechol reactivities to construct seven distinct c-MOF crystals. Site-selective coordination of 1,2,5,6,9,10,12,13-octahydroxydibenzo-[fg,op]naphthacene yields three topologically distinct copper-based c-MOFs, including 2D square-arranged (Cu-2D-sql), 2D honeycomb-arranged (Cu-2D-hcb) and one-dimensional linear (Cu-1D) structures. Cu-1D could further react with metal ions to produce four bimetallic CuM-2D-sql (M = Ni, Co, Zn or Mn) with defined bimetal node arrangements. Theoretical modelling and single-crystal electrical measurements reveal that this structural programming effectively modulates the charge transport behaviour. The anisotropic reticular chemistry strategy thus provides a route towards atomic-level control over the structures and electronic properties of conductive frameworks.

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PMID42786186

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