Evidence map›Paper›PMID 38979687›Full record

ArticleChemSusChem2024

A Heterogeneous Acid-Base Organocatalyst For Cascade Deacetalisation-Knoevenagel Condensations.

Ashis Chhetri, Ashakiran Maibam, Subashani Maniam, Ravichandar Babarao, Karen Wilson, Adam F Lee, Joyee Mitra

Abstract read
In one paragraph

Article in ChemSusChem, 2024. 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. 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.

Ashis ChhetriInorganic Materials & Catalysis Division, CSIR-Central Salt & Marine Chemicals Research Institute, Bhavnagar, Gujarat, 364002, India.
Ashakiran MaibamAcademy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
Subashani ManiamSchool of Science, STEM College, RMIT University, Melbourne VIC, 3000, Australia.
Ravichandar BabaraoCentre for Advanced Materials and Industrial Chemistry (CAMIC), RMIT University, Melbourne, VIC, 3001, Australia.
Karen WilsonCentre for Catalysis and Clean Energy, School of Environment and Science, Griffith University, Gold Coast, QLD 4222, Australia.
Adam F LeeCentre for Catalysis and Clean Energy, School of Environment and Science, Griffith University, Gold Coast, QLD 4222, Australia.ORCID https://orcid.org/0000-0002-2153-1391
Joyee MitraInorganic Materials & Catalysis Division, CSIR-Central Salt & Marine Chemicals Research Institute, Bhavnagar, Gujarat, 364002, India.

Funding

Australian Research Council DP200100204Australian Research Council DP200100313Australian Research Council LE200100Australian Research Council LP190100849National Computing Infrastructure CSMCRI PRIS No. 19/2024Science and Engineering Research Board SPG/2021/004430
6 · The paper itself

Abstract

Multifunctional heterogeneous catalysts are an effective strategy to drive chemical cascades, with attendant time, resource and cost efficiencies by eliminating unit operations arising in normal multistep processes. Despite advances in the design of such catalysts, the fabrication of proximate, chemically antagonistic active sites remains a challenge for inorganic materials science. Hydrogen-bonded organocatalysts offer new opportunities for the molecular level design of multifunctional structures capable of stabilising antagonistic active sites. We report the catalytic application of a charge-assisted, hydrogen-bonded crystalline material, bis(melaminium)adipate (BMA), synthesised from melamine and adipic acid, which possesses proximate acid-base sites. BMA exhibits high activity for the cascade deacetalisation-Knoevenagel condensation of dimethyl acetals to form benzylidenemalononitriles under mild conditions in water; BMA is amenable to large-scale manufacture and recycling with minimal deactivation. Computational modelling of the melaminium cation in protonated BMA explains the observed catalytic reactivity, and identifies the first demethoxylation step as rate-limiting, which is in good agreement with time-dependent

Indexed as

Antagonistic acid-base sitesCharge-assisted hydrogen bondingChemical cascadeOrganocatalysisSustainable catalysis

Identifiers

PMID38979687
PMCPMC11660745

What OpenQuestion holds

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LicenceCC BY
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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.