ArticleNature communications2024
Ambient hydrogenation of solid aromatics enabled by a high entropy alloy nanocatalyst.
Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The trial behind it
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Who cites it
4 citing papers in PubMed.
- Temperature-Regulated N-Involved Ru Nucleation on Lignin-Derived Carbon for Enhanced Catalytic Transfer Hydrogenation of Levulinic Acid to γ-Valerolactone.ChemSusChem · 2026Article
- Iron Single-Atom Catalyzed N-Alkylation of Amines with Alcohols via Solvent-Free Borrowing Hydrogen Strategy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Tea-derived catalysts: a sustainable approach to organic transformations.RSC advances · 2025Review
- MoZn-based high entropy alloy catalysts enabled dual activation and stabilization in alkaline oxygen evolution.Science advances · 2024Article
Corrections and comments
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Authors and funding
14 authors.
Funding
Abstract
Hydrogenation is a versatile chemical process with significant applications in various industries, including food production, petrochemical refining, pharmaceuticals, and hydrogen carriers/safety. Traditional hydrogenation of aromatics, hindered by the stable π-conjugated phenyl ring structures, typically requires high temperatures and pressures, making ambient hydrogenation a grand challenge. Herein, we introduce a PdPtRuCuNi high entropy alloy (HEA) nanocatalyst, achieving an exceptional 100% hydrogenation of carbon-carbon unsaturated bonds, including alkynyl and phenyl groups, in solid 1,4-bis(phenylethynyl)benzene (DEB) at 25 °C under ≤1 bar H
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Registered trials
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.