Evidence map›Paper›PMID 35310507›Full record

ArticleChemical science2022

Mechanism of diastereoisomer-induced chirality of BiOBr.

Kun Ding, Jing Ai, Yingying Duan, Lu Han, Zhibei Qu, Shunai Che

Abstract read
In one paragraph

Article in Chemical science, 2022. 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. 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.

Kun DingSchool of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, State Key Laboratory of Composites Materials, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 P. R. China chesa@sjtu.edu.cn.
Jing AiSchool of Chemical Science and Engineering, Tongji University 1239 Siping Road Shanghai 200092 P. R. China yyduan@tongji.edu.cn luhan@tongji.edu.cn.
Yingying DuanSchool of Chemical Science and Engineering, Tongji University 1239 Siping Road Shanghai 200092 P. R. China yyduan@tongji.edu.cn luhan@tongji.edu.cn.ORCID https://orcid.org/0000-0001-6549-2446
Lu HanSchool of Chemical Science and Engineering, Tongji University 1239 Siping Road Shanghai 200092 P. R. China yyduan@tongji.edu.cn luhan@tongji.edu.cn.ORCID https://orcid.org/0000-0002-6119-4895
Zhibei QuSchool of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, State Key Laboratory of Composites Materials, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 P. R. China chesa@sjtu.edu.cn.ORCID https://orcid.org/0000-0003-1517-0822
Shunai CheSchool of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, State Key Laboratory of Composites Materials, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 P. R. China chesa@sjtu.edu.cn.ORCID https://orcid.org/0000-0001-7831-1552

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chiral molecule-driven asymmetric structures are known to be elusive because of the intriguing chirality transfer from chiral molecules to achiral species. Here, we found that the chiral assembly of BiOBr is independent of the chirality of the organic molecular inducer but dependent on geometric structural matching between the inducer and inorganic species. Diastereoisomeric sugar alcohols (DSAs) with identical numbers of carbon chiral centers and functional groups but with different

Identifiers

PMID35310507
PMCPMC8864704

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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.