Multiple Stimuli-Responsive Conformational Exchanges of Biphen[3]arene Macrocycle.

Yiliang Wang, Liu-Pan Yang, Xiang Zhao, Lei Cui, Jian Li, Xueshun Jia, Jianhui Fang, Chunju Li

Abstract read

In one paragraph

Article in Molecules (Basel, Switzerland), 2020. 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

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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.

Controlled interconversion of macrocyclic atropisomers via defined intermediates.Nature communications · 2024
Article

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Yiliang WangCenter for Supramolecular Chemistry and Catalysis and Department of Chemistry, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China.ORCID 0000-0002-6557-7412

Liu-Pan YangAcademy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Xueyuan Blvd 1088, Shenzhen 518055, China.

Xiang ZhaoCenter for Supramolecular Chemistry and Catalysis and Department of Chemistry, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China.

Lei CuiCenter for Supramolecular Chemistry and Catalysis and Department of Chemistry, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China.

Jian LiCenter for Supramolecular Chemistry and Catalysis and Department of Chemistry, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China.

Xueshun JiaCenter for Supramolecular Chemistry and Catalysis and Department of Chemistry, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China.

Jianhui FangCenter for Supramolecular Chemistry and Catalysis and Department of Chemistry, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China.

Chunju LiCenter for Supramolecular Chemistry and Catalysis and Department of Chemistry, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China.

Funding

National Natural Science Foundation of China 21971192, 21801125 and 21772118

6 · The paper itself

Abstract

Conformational exchanges of synthetic macrocyclic acceptors are rather fast, which is rarely studied in the absence of guests. Here, we report multiple stimuli-responsive conformational exchanges between two preexisting conformations of 2,2',4,4'-tetramethoxyl biphen[3]arene (MeBP3) macrocycle. Structures of these two conformations are both observed in solid state, and characterized by

Indexed as

Models, MolecularMolecular ConformationHydrogen-Ion ConcentrationMacrocyclic CompoundsMagnetic Resonance SpectroscopyMolecular StructureSolventsTemperatureMacrocyclic CompoundsSolventsconformational exchangemacrocyclemultiple stimuli-responsive

Identifiers

PMID33302382

DOI10.3390/molecules25245780

PMCPMC7762528

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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.