Evidence map›Paper›PMID 32457820›Full record

ArticleACS catalysis2020

Mechanism of Cobalt-Catalyzed Heterodimerization of Acrylates and 1,3-Dienes. A Potential Role of Cationic Cobalt(I) Intermediates.

Montgomery Gray, Michael T Hines, Mahesh M Parsutkar, A J Wahlstrom, Nicholas A Brunelli, T V RajanBabu

Open access · greenAbstract read
In one paragraph

Article in ACS catalysis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 29 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

6 authors at 1 institution in 1 country.

Montgomery Gray151 W. Woodruff, Columbus, OH 43210 and the Department of Chemistry and Biochemistry, 100 W. 18th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0002-7902-2805
Michael T HinesThe Ohio State University, William G. Lowrie Department of Chemical and Biomolecular Engineering, 100 W. 18th Avenue, Columbus, Ohio 43210, United States.
Mahesh M Parsutkar151 W. Woodruff, Columbus, OH 43210 and the Department of Chemistry and Biochemistry, 100 W. 18th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0001-6320-2345
A J WahlstromThe Ohio State University, William G. Lowrie Department of Chemical and Biomolecular Engineering, 100 W. 18th Avenue, Columbus, Ohio 43210, United States.
Nicholas A BrunelliThe Ohio State University, William G. Lowrie Department of Chemical and Biomolecular Engineering, 100 W. 18th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0003-0712-8966
T V RajanBabu151 W. Woodruff, Columbus, OH 43210 and the Department of Chemistry and Biochemistry, 100 W. 18th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0001-8515-3740
The Ohio State University · US

Funding

New Alkene Chemistry for the Synthesis of Medicinally Relevant CompoundsR01GM108762 · NIGMS · OHIO STATE UNIVERSITY · PI RAJANBABU, T V · 2015 to 2018
$1.3M
NIGMS NIH HHS R01 GM108762
6 · The paper itself

Abstract

Coupling reactions of feedstock alkenes are promising, but few of these reactions are practiced industrially. Even though recent advances in the synthetic methodology have led to excellent regio- and enantioselectivies in the dimerization reactions between 1,3-dienes and acrylates, the efficiency as measured by the turnover numbers (TON) in the catalyst has remained modest. Through a combination of reaction progress kinetic analysis (RPKA) of a prototypical dimerization reaction, characterization of isolated low-valent cobalt catalyst precursors involved, several important details of the mechanism of this reaction have emerged. (i) The prototypical reaction has an induction period that requires at least two hours of stir time to generate the competent catalyst. (ii) Reduction of a Co(II) complex to a Co(I) complex, and subsequent generation of a cationic [Co

Indexed as

1,3-dienesacrylatescobalt catalysiscounterion effectsheterodimerizationkineticsmechanism

Identifiers

PMID32457820
PMCPMC7250405
OpenAlexW3009477660

What OpenQuestion holds

Textmetadata
LicenceTDM
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.