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Electrochemical hydrogenation (ECH) of unsaturated carbon-heteroatom bonds is essential for chemical transformations but is often limited by a barrier-intensive surface hydrogen transfer process. The interfacial hydrogen bond (HB) network offers a promising pathway for proton transfer but requires addressing the challenge of nondirectional proton shuttling in three-dimensional space. Here, we create hydrophilic CuO islands on Cu foam (CF) and load electron-enriched Pd (Pd) single atoms as proton traps (Pd-CuO/CF) to guide a fast proton transfer along a modified HB network to enhance ECH efficiency. During ECH, hydrophilic CuO islands dissociate HO into protons and reconstruct the interfacial HB network for facile proton transfer, while the Pd single atoms reorient HO molecules to electrostatically attract and reduce protons to active hydrogen, enabling efficient substrate hydrogenation. With guided proton transfer, Pd-CuO/CF achieves 99% hydrogenation efficiency for C─Cl bonds, outperforming Pd-CF (69%) and CuO/CF (57%), and demonstrates high selectivity and Faradaic efficiency in hydrogenating C═O and C≡N bonds to produce valuable chemicals.
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http://dx.doi.org/10.1126/sciadv.adu1602 | DOI Listing |
Chem Res Toxicol
September 2025
Maseeh Department of Civil, Architectural and Environmental Engineering, University of Texas at Austin, Austin, Texas 78712, United States.
Exposure to air pollution plays a significant role in human health. Current methods of measuring human exposure are often limited to outdoor measurements, are time intensive, or are unable to accurately measure certain classes of compounds. This study proposes human hair as a promising indicator of pollution exposure.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemical Sciences, Tezpur University, Napaam 784028, Sonitpur, Assam, India.
Reaction of [Mn(salophen)Cl] {salophen = -phenylenediamine bis(salicylidenaminato)} with a tricyano Fe(III) precursor complex, [Fe(bbp)(CN)] {Hbbp = bis(2-benzimidazolyl)pyridine}, affords a dinuclear cyano-bridged heterometallic Mn-(μ-NC)-Fe fragment in the complex salt [Mn(salophen)(HO)][Mn(salophen)(HO)(μ-NC)Fe(bbp)(CN)]·4HO (1). The title compound shows field-induced slow relaxation of magnetization below 2.8 K.
View Article and Find Full Text PDFFEBS J
September 2025
Neutron Scattering Division, Oak Ridge National Laboratory, USA.
Serine hydroxymethyltransferase (SHMT) is a critical enzyme in the one-carbon (1C) metabolism pathway catalyzing the reversible conversion of L-Ser into Gly and concurrent transfer of 1C unit to tetrahydrofolate (THF) to give 5,10-methylene-THF (5,10-MTHF), which is used in the downstream syntheses of biomolecules critical for cell proliferation. The cellular 1C metabolism is hijacked by many cancer types to support cancer cell proliferation, making SHMT a promising target for the design and development of novel small-molecule antimetabolite chemotherapies. To advance structure-assisted drug design, knowledge of SHMT catalysis is crucial, but can only be fully realized when the atomic details of each reaction step governed by the acid-base catalysis are elucidated by visualizing active site hydrogen atoms.
View Article and Find Full Text PDFOrg Lett
September 2025
State Key Laboratory of Precision and Intelligent Chemistry, Department of Chemistry, University of Science and Technology of China, Hefei 230026, P. R. China.
A novel palladium-catalyzed asymmetric aminomethylative pyridonation of conjugated dienes with -acetals and 2-hydroxypyridines was established, which provided a direct and reliable method for the synthesis of a wide range of γ-aminated N-substituted 2-pyridones with good to excellent enantioselectivities. The simple BF was identified as an effective cocatalyst to improve the reaction efficiency, and DFT calculations revealed that proton transfer between the aminomethylated allylic palladium species and 2-hydroxypyridine promoted by BF is crucial for obtaining good reactivity.
View Article and Find Full Text PDFOrg Lett
September 2025
School of Pharmaceutical and Chemical Engineering and Institute for Advanced Studies, Taizhou University, 1139 Shifu Road, Taizhou, Zhejiang 318000, China.
Here, intramolecular hydrogen bond (IMHBs)-induced rigidity is used for the first time to synthesize macrocyclic arenes. Calix[]azanediyldibenzoates (C[]A, where = 3, 4, or 5) are synthesized through a one-step condensation reaction between dimethyl 2,2'-azanediyldibenzoate and paraformaldehyde. Compared to the monomer, the macrocycles exhibit a fast and significant acidochromic response due to the intramolecular charge transfer that is boosted by the synergistic effect of their adsorption and protonation.
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