Evidence map›Paper›PMID 34447548›Full record

ArticleChemical science2021

Reversible redox controlled acids for cationic ring-opening polymerization.

Michael J Supej, Elizabeth A McLoughlin, Jesse H Hsu, Brett P Fors

Abstract read
In one paragraph

Article in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Tuning Electrode Reactivity through Organometallic Complexes.ACS applied materials & interfaces · 2023
    Review
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

4 authors.

Michael J SupejDepartment of Chemistry and Chemical Biology, Cornell University Ithaca New York 14853 USA bpf46@cornell.edu.ORCID https://orcid.org/0000-0002-2441-0536
Elizabeth A McLoughlinDepartment of Chemistry and Chemical Biology, Cornell University Ithaca New York 14853 USA bpf46@cornell.edu.
Jesse H HsuDepartment of Chemistry and Chemical Biology, Cornell University Ithaca New York 14853 USA bpf46@cornell.edu.
Brett P ForsDepartment of Chemistry and Chemical Biology, Cornell University Ithaca New York 14853 USA bpf46@cornell.edu.ORCID https://orcid.org/0000-0002-2222-3825

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advancements in externally controlled polymerization methodologies have enabled the synthesis of novel polymeric structures and architectures, and they have been pivotal to the development of new photocontrolled lithographic and 3D printing technologies. In particular, the development of externally controlled ring-opening polymerization (ROP) methodologies is of great interest, as these methods provide access to novel biocompatible and biodegradable block polymer structures. Although ROPs mediated by photoacid generators have made significant contributions to the fields of lithography and microelectronics development, these methodologies rely upon catalysts with poor stability and thus poor temporal control. Herein, we report a class of ferrocene-derived acid catalysts whose acidity can be altered through reversible oxidation and reduction of the ferrocenyl moiety to chemically and electrochemically control the ROP of cyclic esters.

Identifiers

PMID34447548
PMCPMC8356742

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.