Single‐Pd‐Site Catalyst Induced by Different Dimensional Nitrogen of N‐Doping Carbon for Efficient Hydroaminocarbonylation of Alkynes

Abstract The unsaturated amides are traditionally synthesized by acylation of carboxylic acids or hydration of nitrile compounds but are rarely investigated by hydroaminocarbonylation of alkynes using heterogeneous single‐metal‐site catalysts (HSMSCs). Herein, single‐Pd‐site catalysts supported on N‐doping carbon (NC) with different nitrogen dimensions inherited from corresponding metal‐organic‐framework precursors are successfully synthesized. 2D NC‐supported single‐Pd‐site (Pd 1 /NC‐2D) exhibited the best performance with near 100% selectivity and 76% yield of acrylamide for acetylene hydroaminocarbonylation with better stability, superior to those of Pd 1 /NC‐3D, single‐metal‐site/nanoparticle coexisting catalyst, and nanoparticle catalyst. The coordination environment and molecular evolution of the single‐Pd‐site during the process of acetylene hydroaminocarbonylation on Pd 1 /NC‐2D are detailly illuminated by various characterizations and density functional theoretical calculations (DFT). DFT also showed the energy barrier of rate‐determining step on Pd 1 /NC‐2D is lower than that of Pd 1 /NC‐3D. Furthermore, Pd 1 /NC‐2D catalyst illustrated the general applicability of the hydroaminocarbonylation for various alkynes.