Skip to content
DraconiticResearch
Search Sources API
201,683 studies31 sourcesUpdated 1 h ago
PreprintCC BYChemRxiv

eHydrogenation 2.0: Pd/C-Catalysed Hydrogenation of Alkenes and Alkynes without Externally Supplied H₂

5 affiliations
  1. 1School of Science, Faculty of Engineering and Science
  2. 2University of Greenwich
  3. 3École Nationale Supérieure de Chimie de Mulhouse (ENSCMu)
  4. 4Université de Haute-Alsace
  5. 5Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, London, UK, W12 0BZ

Abstract

We report an electrochemically driven Pd/C-catalysed method for the exhaustive hydrogenation of alkenes and alkynes without externally supplied H2. In an undivided cell, commercially available Pd/C in EtOH converts terminal and internal unsaturated substrates under mild constant-current conditions. Standard carbon-electrode/TFA conditions and a complementary Mg-anode/Et4NBF4 protocol furnish saturated products in up to quantitative yield while tolerating alcohols, ethers, esters, amides, sulfonamides, nitriles, phosphates, heterocycles, and carbon–halogen bonds. Most alkenes react at 4 F mol-1, whereas alkynes generally require 6 F mol-1. Coupling heterogeneous catalysis with electrochemical generation of reducing equivalents provides an operationally simple alternative to conventional hydrogenation with externally supplied H2.

Related

  1. Iron- versus ruthenium-catalysed oxidation of unprotected polyols via transfer hydrogenation: direct and tunable access to diverse poly-hydroxy-heterocycles and diamidopolyols
    David Branquet, Antoine Lancien, Yassine El Ouafi +3
    RSC SustainabilityPeer-reviewedCC BY-NC 4.0Full textInorganic & organometallic chemistryHAL
  2. Asymmetric Anti-Hydrogenation of Tetrasubstituted Alkenes
    Justin Manoff, Kyle Schultz, Julian Morales +7
    ChemRxivPreprintCC BY-NC-NDInorganic & organometallic chemistryChemRxiv
  3. Selective Adsorption Processes in Mordenite-Catalysed Ethanol Dehydration
    Matthew T. Robinson, Ben France, Glenn J. Sunley +3
    ChemRxivPreprintLicence not statedGeneral chemistryChemRxiv
  4. Chemoselective Ni-catalysed directed C(sp2)–H alkylation at low temperature using alkyl sulfonylhydrazides
    Shuanghu Wang, David A. Cagan, Yilin Cao +5
    Nature SynthesisPeer-reviewedLicence not stated12 citedOrganic chemistryOpenAlex
  5. A focus on double borane-catalysed sulfenylation of alkynes: two B's or not two B's?
    Natalia A F Atherley, Andrew R Jupp
    Chemical sciencePeer-reviewedCC BYFull textOrganic chemistryEurope PMCPMC
BibTeX
@misc{salehzadeh2026ehydrogenation,
  title = {{eHydrogenation 2.0: Pd/C-Catalysed Hydrogenation of Alkenes and Alkynes without Externally Supplied H₂}},
  author = {Hamid Salehzadeh and Feba T. Pulikkottil and Romain Ogier and Jack Brennan and Zhixuan He and Kevin Lam},
  howpublished = {ChemRxiv},
  year = {2026},
  month = sep,
  doi = {10.26434/chemrxiv.15008455/v1},
  url = {https://chemrxiv.org/doi/full/10.26434/chemrxiv.15008455/v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - eHydrogenation 2.0: Pd/C-Catalysed Hydrogenation of Alkenes and Alkynes without Externally Supplied H₂
AU  - Hamid Salehzadeh
AU  - Feba T. Pulikkottil
AU  - Romain Ogier
AU  - Jack Brennan
AU  - Zhixuan He
AU  - Kevin Lam
PY  - 2026
DA  - 2026/09/07
PB  - ChemRxiv
DO  - 10.26434/chemrxiv.15008455/v1
UR  - https://chemrxiv.org/doi/full/10.26434/chemrxiv.15008455/v1
AB  - We report an electrochemically driven Pd/C-catalysed method for the exhaustive hydrogenation of alkenes and alkynes without externally supplied H2. In an undivided cell, commercially available Pd/C in EtOH converts terminal and internal unsaturated substrates under mild constant-current conditions. Standard carbon-electrode/TFA conditions and a complementary Mg-anode/Et4NBF4 protocol furnish saturated products in up to quantitative yield while tolerating alcohols, ethers, esters, amides, sulfonamides, nitriles, phosphates, heterocycles, and carbon–halogen bonds. Most alkenes react at 4 F mol-1, whereas alkynes generally require 6 F mol-1. Coupling heterogeneous catalysis with electrochemical generation of reducing equivalents provides an operationally simple alternative to conventional hydrogenation with externally supplied H2.
ER  -