Evidence map›Paper›PMID 35657101›Full record

ArticleJournal of the American Chemical Society2022

Cobalt-Carbon Bonding in a Salen-Supported Cobalt(IV) Alkyl Complex Postulated in Oxidative MHAT Catalysis.

Conner V Wilson, Dongyoung Kim, Ajay Sharma, Reagan X Hooper, Rinaldo Poli, Brian M Hoffman, Patrick L Holland

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
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  8. Article
  9. Evaluating Diazene to NChemistry (Weinheim an der Bergstrasse, Germany) · 2024
    Article
  10. Article
  11. Article
  12. 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

7 authors.

Conner V WilsonDepartment of Chemistry, Yale University, New Haven, Connecticut 06520, United States.
Dongyoung KimDepartment of Chemistry, Yale University, New Haven, Connecticut 06520, United States.
Ajay SharmaDepartment of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.ORCID 0000-0002-0829-6753
Reagan X HooperDepartment of Chemistry, Yale University, New Haven, Connecticut 06520, United States.
Rinaldo PoliCNRS, Laboratoire de Chimie de Coordination, Université de Toulouse, F-31077 Toulouse Cedex, France.ORCID 0000-0002-5220-2515
Brian M HoffmanDepartment of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.ORCID 0000-0002-3100-0746
Patrick L HollandDepartment of Chemistry, Yale University, New Haven, Connecticut 06520, United States.ORCID 0000-0002-2883-2031

Funding

Coboglobins-Cobalt-Substituted Hemoglobins and MyoglobinR01GM111097 · NIGMS · NORTHWESTERN UNIVERSITY · PI HOFFMAN, BRIAN M · 2014 to 2025
$6.7M
Mechanistically guided improvement in radical alkene coupling by base metal catalystsR01GM129081 · NIGMS · YALE UNIVERSITY · PI HOLLAND, PATRICK L · 2019 to 2022
$1.2M
NIGMS NIH HHS R01 GM111097NIGMS NIH HHS R01 GM129081
6 · The paper itself

Abstract

The catalytic hydrofunctionalization of alkenes through radical-polar crossover metal hydrogen atom transfer (MHAT) offers a mild pathway for the introduction of functional groups in sterically congested environments. For M = Co, this reaction is often proposed to proceed through secondary alkylcobalt(IV) intermediates, which have not been characterized unambiguously. Here, we characterize a metastable (salen)Co(isopropyl) cation, which is capable of forming C-O bonds with alcohols as proposed in the catalytic reaction. Electron nuclear double resonance (ENDOR) spectroscopy of this formally cobalt(IV) species establishes the presence of the cobalt-carbon bond, and accompanying DFT calculations indicate that the unpaired electron is localized on the cobalt center. Both experimental and computational studies show that the cobalt(IV)-carbon bond is stronger than the analogous bond in its cobalt(III) analogue, which is opposite of the usual oxidation state trend of bond energies. This phenomenon is attributable to an inverted ligand field that gives the bond Co

Indexed as

CobaltHydrogenCarbonCatalysisEthylenediaminesMetalsOxidation-ReductionOxidative StressOxygenCarbonCobaltdisalicylaldehyde ethylenediamineEthylenediaminesHydrogenMetalsOxygen

Identifiers

PMID35657101
PMCPMC9206546

What OpenQuestion holds

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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.