PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
September 28, 2025ChemCatChem2 citations

Z‐Selective Semihydrogenation of Internal Alkynes Catalyzed by Phenanthroline‐Based PNNP‐Fe(II) Complexes

View Full Paper
TWTao WangYKYoshihito KayakiHFHiroto Fujisaki

Key Points

  • The catalysts produced Z-alkenes effectively through semihydrogenation of internal alkynes using atmospheric H2, achieving selectivity.
  • Good functional group compatibility was exhibited towards various substituents, including polar esters and cyano groups.
  • Catalyst loading of 2-5 mol%/Fe enabled efficient reactions with various substrates, enhancing overall yield.
  • The study emphasizes the importance of metal–ligand cooperation in catalysis for selective reactions.

Abstract

Abstract Fe(II) complexes bearing a phenanthroline‐based tetradentate PNNP ligand (2,9‐bis(diphenylphosphino)methyl‐1,10‐phenanthroline, 2,9‐bis(dicyclohexylphosphino)methyl‐1,10‐phenanthroline) were applied as metal–ligand cooperative catalysts to promote semihydrogenation of internal alkynes. The reaction proceeded with atmospheric H 2 at a catalyst loading of 2–5 mol%/Fe to selectively produce the corresponding Z ‐alkenes. The reactions exhibited good functional group compatibility toward substrates with various substituents, including polar ester and cyano groups, as well as a coordinating sulfur‐containing thiophene moiety.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Wang et al. (2025) studied this question.

synapsesocial.com/papers/68d90a0f41e1c178a14f6b00https://doi.org/10.1002/cctc.202500785
Ask AI
Helpful
Bookmark
Share
View Full Paper