Evidence map›Paper›PMID 36443531›Full record

ArticleNature chemistry2023

Recyclable cyclic bio-based acrylic polymer via pairwise monomer enchainment by a trifunctional Lewis pair.

Yanjiao Song, Jianghua He, Yuetao Zhang, Reid A Gilsdorf, Eugene Y-X Chen

Abstract read
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Article in Nature chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
7.6field-weighted citation impact, top 1% 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

10 citing papers in PubMed, 72 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Yanjiao SongState Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, Jilin, China.
Jianghua HeState Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, Jilin, China.
Yuetao ZhangState Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, Jilin, China. ytzhang2009@jlu.edu.cn.ORCID http://orcid.org/0000-0002-6406-1959
Reid A GilsdorfDepartment of Chemistry, Colorado State University, Fort Collins, CO, USA.ORCID http://orcid.org/0000-0003-4229-0678
Eugene Y-X ChenDepartment of Chemistry, Colorado State University, Fort Collins, CO, USA.ORCID http://orcid.org/0000-0001-7512-3484
Jilin University · CNColorado State University · US

Funding

National Natural Science Foundation of China (National Science Foundation of China) 21871107National Natural Science Foundation of China (National Science Foundation of China) 22071077National Science Foundation (NSF) NSF-1904962
6 · The paper itself

Abstract

The existing catalyst/initiator systems and methodologies used for the synthesis of polymers can access only a few cyclic polymers composed entirely of a single monomer type, and the synthesis of such authentic cyclic polar vinyl polymers (acrylics) devoid of any foreign motifs remains a challenge. Here we report that a tethered B-P-B trifunctional, intramolecular frustrated Lewis pair catalyst enables the synthesis of an authentic cyclic acrylic polymer, cyclic poly(γ-methyl-α-methylene-γ-butyrolactone) (c-PMMBL), from the bio-based monomer MMBL. Detailed studies have revealed an initiation and propagation mechanism through pairwise monomer enchainment enabled by the cooperative and synergistic initiator/catalyst sites of the trifunctional catalyst. We propose that macrocyclic intermediates and transition states comprising two catalyst molecules are involved in the catalyst-regulated ring expansion and eventual cyclization, forming authentic c-PMMBL rings and concurrently regenerating the catalyst. The cyclic topology of the c-PMMBL polymers imparts an ~50 °C higher onset decomposition temperature and a much narrower degradation window compared with their linear counterparts of similar molecular weight and dispersity, while maintaining high chemical recyclability.

Identifiers

PMID36443531
OpenAlexW4310157291

What OpenQuestion holds

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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.