Propane Dehydrogenation Catalyzed by Supported Group IV (Ti, Zr, Hf) Organometallics on Silicon Nitride

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Authors: Meaghan A. Bruening, Jacklyn N. Hall, Yu Lim Kim, Vitor F. Grizzi, Frédéric A. Perras, Jens Niklas, Oleg G. Poluektov, A. Jeremy Kropf, Cong Liu, David M. Kaphan, Massimiliano Delferro
Cited by: 4
References: 53

Abstract

Mesoporous silicon nitride (Si 3 N 4 ) enables access to chemisorbed group IV organometallics catalysts active for propane dehydrogenation (PDH) compared to the organometallic analogues on mesoporous silica under the same reaction conditions. The series of Si 3 N 4 -supported materials are active catalysts, (Zr > Hf > Ti k f = 290, 232, and 162 mol mol Metal –1 h –1 at 450 °C with 2% C 3 H 8 in Ar, respectively) with selectivity above 95%, demonstrating additional examples of Ti and Hf systems for PDH. However, the underlying mechanism of the improved performance relative to oxide supported homologues is not well-understood. Characterization of thermally treated samples (DRIFTS, XAS and SSNMR) and computational modeling of this catalyst series was utilized to differentiate between potential amido - (C–H activation along the M-N bond) and imido - (C–H activation along the M=N bond) mechanisms. Due to remaining mechanistic ambiguity, a Ga analogue was synthesized and evaluated for PDH activity as an indirect probe to experimentally differentiate pathways. An inversion of the oxide/nitride performance trend is observed for the Ga congener which does not form a Ga=N bond, most consistent with different mechanisms dictating the performance of the group IV/Si 3 N 4 catalysts vs Ga/Si 3 N 4 .

Fields of Study & Subjects

Catalysis and Oxidation Reactions Carbon dioxide utilization in catalysis Organometallic Complex Synthesis and Catalysis

Publication details

Journal / source
ACS Catalysis
Publisher
American Chemical Society (ACS)
Volume
16
Issue
7
Pages
6841–6850
Publication date
11 March 2026
Language
EN