Article in Chemical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
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
5 citing papers in PubMed, 20 citations in OpenAlex.
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
12 authors at 4 institutions in 5 countries.
Chengjie LiKey Laboratory for Advanced Materials, Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science & Technology Shanghai 200237 China yshxie@ecust.edu.cn.ORCID https://orcid.org/0000-0001-5602-6566
Kai ZhangKey Laboratory for Advanced Materials, Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science & Technology Shanghai 200237 China yshxie@ecust.edu.cn.
Masatoshi IshidaDepartment of Chemistry and Biochemistry, Graduate School of Engineering, Center for Molecular Systems, Kyushu University Fukuoka 819-0395 Japan hfuruta@cstf.kyushu-u.ac.jp.ORCID https://orcid.org/0000-0002-1117-2188
Qizhao LiKey Laboratory for Advanced Materials, Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science & Technology Shanghai 200237 China yshxie@ecust.edu.cn.
Keito ShimomuraDepartment of Chemistry and Biochemistry, Graduate School of Engineering, Center for Molecular Systems, Kyushu University Fukuoka 819-0395 Japan hfuruta@cstf.kyushu-u.ac.jp.
Xin-Yan WuKey Laboratory for Advanced Materials, Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science & Technology Shanghai 200237 China yshxie@ecust.edu.cn.ORCID https://orcid.org/0000-0002-6942-7067
Hiroyuki FurutaDepartment of Chemistry and Biochemistry, Graduate School of Engineering, Center for Molecular Systems, Kyushu University Fukuoka 819-0395 Japan hfuruta@cstf.kyushu-u.ac.jp.ORCID https://orcid.org/0000-0002-3881-8807
Yongshu XieKey Laboratory for Advanced Materials, Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science & Technology Shanghai 200237 China yshxie@ecust.edu.cn.ORCID https://orcid.org/0000-0001-8230-7599
East China University of Science and Technology · CNKyushu University · JPStockholm Environment Institute · SEUniversity of Manchester · GB
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itself
Abstract
Oxidative ring closure of linear oligopyrroles is one of the synthetic approaches to novel porphyrinoids with dinuclear coordination sites and helical chirality. The spatial arrangement of the pyrrolic groups of octapyrrole (
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.
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion. · full record | OpenQuestion