Evidence map›Paper›PMID 38998707›Full record

ArticleNanomaterials (Basel, Switzerland)2024

URJC-1: Stable and Efficient Catalyst for O-Arylation Cross-Coupling.

Elena García-Rojas, Pedro Leo, Jesús Tapiador, Carmen Martos, Gisela Orcajo

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Elena García-RojasChemical and Environmental Engineering Group, ESCET, Rey Juan Carlos University, C/Tulipán s/n, 28933 Móstoles, Spain.ORCID 0000-0001-8879-5669
Pedro LeoChemical and Environmental Engineering Group, ESCET, Rey Juan Carlos University, C/Tulipán s/n, 28933 Móstoles, Spain.ORCID 0000-0002-6888-4215
Jesús TapiadorChemical and Environmental Engineering Group, ESCET, Rey Juan Carlos University, C/Tulipán s/n, 28933 Móstoles, Spain.ORCID 0000-0003-1731-6514
Carmen MartosChemical and Environmental Engineering Group, ESCET, Rey Juan Carlos University, C/Tulipán s/n, 28933 Móstoles, Spain.ORCID 0000-0001-7733-0997
Gisela OrcajoChemical and Environmental Engineering Group, ESCET, Rey Juan Carlos University, C/Tulipán s/n, 28933 Móstoles, Spain.

Funding

Spanish Ministry of Science and Innovation ECOCAT Project (PID2022-136321OA-C22)
6 · The paper itself

Abstract

The design of metal-organic frameworks (MOFs) allows the definition of properties for their final application in small-scale heterogeneous catalysis. Incorporating various catalytic centers within a single structure can produce a synergistic effect, which is particularly intriguing for cross-coupling reactions. The URJC-1 material exhibits catalytic duality: the metal centers act as Lewis acid centers, while the nitrogen atoms of the organic ligand must behave as basic centers. The impact of reaction temperature, catalyst concentration, and basic agent concentration was evaluated. Several copper-based catalysts, including homogeneous and heterogeneous MOF catalysts with and without the presence of nitrogen atoms in the organic ligand, were assessed for their catalytic effect under optimal conditions. Among the catalysts tested, URJC-1 exhibited the highest catalytic activity, achieving complete conversion of 4-nitrobenzaldehyde with only 3% mol copper concentration in one hour. Furthermore, URJC-1 maintained its crystalline structure even after five reaction cycles, demonstrating remarkable stability in the reaction medium. The study also examined the impact of various substituents of the substrate alcohol on the reaction using URJC-1. The results showed that the reaction had high activity when activating substituents were present and for most cyclic alcohols rather than linear ones.

Indexed as

aldehydecopper MOFsfine chemistryMOF catalystO-arylationphenol

Identifiers

PMID38998707
PMCPMC11243573

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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.