Chinese Journal of Catalysis ›› 2026, Vol. 87: 386-395.DOI: 10.1016/S1872-2067(26)65103-0

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Boehmite lattice hydroxyl-mediated selective hydrogenation of cinnamaldehyde via water as hydrogen source

Wenxin Hea,b,1, Yuanhong Lua,b,1, Chenxi Guana,b,1, Xiaohui Houa,b, Rui Huanga,b,*(), Dehui Denga,b,*()   

  1. a School of Chemistry, Dalian University of Technology, Dalian 116024, Liaoning, China
    b State Key Laboratory of Catalysis, iChEM, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China
  • Received:2025-07-28 Accepted:2026-03-13 Online:2026-08-18 Published:2026-06-24
  • About author:1Contributed equally to this work.
  • Supported by:
    National Natural Science Foundation of China(2225204);National Natural Science Foundation of China(22372019);National Natural Science Foundation of China(U24A20487);National Natural Science Foundation of China(22588201);National Key R&D Program of China(2022YFA1504500);National Key R&D Program of China(2024YFA1510103);State Key Laboratory of Catalysis in DICP(2024SKL-A-002);State Key Laboratory of Catalysis in DICP(N-22-02);Innovation Fund of Dalian Institute of Chemical Physics, Chinese Academy of Sciences(DICP I202506)

Abstract:

Selective hydrogenation of cinnamaldehyde (CAL) to cinnamyl alcohol (COL) using water as the hydrogen source offers a promising route to eliminate traditional H2 preparation. However, this approach faces a trade-off between concurrently crating abundant active hydroxyls for hydrogenation and readily removing residual oxygen under mild conditions, restricting current development. Here, we report a naturally abundant lattice hydroxyl-mediated selective hydrogenation process over a boehmite-supported gold catalyst (Au/AlOOH), using H2O as the hydrogen source and CO as the oxygen acceptor. This process achieves 79% CAL conversion and 84% COL selectivity at 90 °C, doubling the efficiency of H2-based hydrogenation counterpart. In contrast, the OH-free Au/Al2O3 shows no activity. Mechanistic studies indicate that the Au/AlOOH boundary provides unsaturated Al3+ sites for selective C=O adsorption and lattice hydroxyls for hydrogenation, which are continuously replenished from water. CO adsorbed on Au facilitates oxygen removal, regenerating Al3+ sites. This work presents a practical hydrogen transfer strategy that leverages the unique lattice hydroxyls of boehmite to efficiently extract hydrogen from water.

Key words: Selective hydrogenation, α,β-Unsaturated aldehydes, Boehmite, Gold catalyst, Water as a hydrogen source