Complex organic molecules are of great importance to research and industrial chemistry and typically synthesized from smaller building blocks by multistep reactions. The ability to perform multiple (distinct) transformations in a single reactor would greatly reduce the number of manipulations required for chemical manufacturing, and hence the development of multifunctional catalysts for such one-pot reactions is highly desirable. Here we report the synthesis of a hierarchically porous framework, in which the macropores are selectively functionalized with a sulfated zirconia solid acid coating, while the mesopores are selectively functionalized with MgO solid base nanoparticles. Active site compartmentalization and substrate channelling protects base-catalysed triacylglyceride transesterification from poisoning by free fatty acid impurities (even at 50 mol%), and promotes the efficient two-step cascade deacetalization-Knoevenagel condensation of dimethyl acetals to cyanoates.
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Nature Communications Open Access 08 October 2022
Dual metal nanoparticles within multicompartmentalized mesoporous organosilicas for efficient sequential hydrogenation
Nature Communications Open Access 17 August 2021
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We thank the Australian Research Council for support (LP180100116, IC150100019, DP 200100204 and DP200100313). Electron microscopy access was provided through the Leeds EPSRC Nanoscience and Nanotechnology Research Equipment Facility (EP/K023853/1), the University of Birmingham Nanoscale Physics Laboratory and the Durham University G.J. Russell Microscopy Facility.
The authors declare no competing interests.
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(a) SEM micrograph, and (b) macropore size distribution from Hg intrusion porosimetry of SZ/MgO/MM-SBA-15. Corresponding normal and cumulative size distributions from SEM of (c) macropore diameter, and (d) macropore window diameter. Note that Hg intrusion measures macropore window size and not macropore diameter64.
(a) DRIFT spectra of saturated chemisorbed pyridine adlayers, (b) reactively-formed propene mass spectra following temperature-programmed desorption of chemisorbed propylamine and associated acid site loadings determined from accompanying TGA mass losses, and (c) CO2 mass spectra following temperature-programmed desorption of chemisorbed CO2 with base site loadings from CO2 pulse chemisorption over MM-SBA-15 materials.
Extended Data Fig. 3 Imaging of acid and base sites within spatially orthogonal acid–base catalyst using funtionalised Pt nanoparticles.
(a) HAADF-STEM, and (b) bright-field micrographs of SZ/MgO/MM-SBA-15 treated with 3-mercaptopropionic acid functionalised Pt NPs, and (c) corresponding area-averaged Pt concentrations determined by EDX within highlighted regions of HAADF-STEM image. Analogous (d) HAADF-STEM, (e) bright-field, and (f) corresponding area-averaged Pt concentrations determined by EDX for SZ/MgO/MM-SBA-15 treated with 4-aminothiophenol functionalised Pt NPs. (g) and (h) Raw EDX spectra associated with mesopore and macropore domains in images (c) and (f) respectively.
Extended Data Fig. 4 Catalytic performance of bifunctional nanoparticle catalyst containing co-located acid–base sites.
Tributyrin transesterification (TAG) with methanol in the absence or presence of hexanoic acid (FFA) over MgO/SZ and SZ nanoparticle catalysts, and simultaneous FFA esterification. Error bars represent S.D. of the mean (n = 3). Reaction conditions: 100 mg catalyst, 5 mmol tributyrin or a mixture of 5 mmol tributyrin/5 mol hexanoic acid, 60 cm3 methanol, 0.1 mmol dihexylether as an internal standard, 60 °C under air, 3 h reaction.
Extended Data Fig. 5 Catalytic performance of hierarchical porous catalysts in the cascade deacetalisation and condensation of dimethyl acetals.
Cyanoester yield from cascade deacetalisation and Knoevenagel condensation of benzaldehyde dimethyl acetal (BDMA), 2-furaldehyde dimethyl acetal (FDMA) or anisaldehyde dimethyl acetal (ADMA) with ethyl cyanoacetate after 6 h reaction over SZ/MgO/MM-SBA-15, a 1:1 by weight physical mixture of SZ/MM-SBA-15 and MgO/MM-SBA-15, or without catalyst. Reaction conditions: 25 mg catalyst (except for physical mixture where 25 mg each of monofunctional catalyst was used), 5 mmol dimethyl acetal, 50 mmol ethyl cyanoacetate, 5 mmol deionised water, 5 cm3 toluene, 1 mmol nonane as an internal standard, 50 °C under N2. Error bars represent S.D. of the mean (n = 2).
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Isaacs, M.A., Parlett, C.M.A., Robinson, N. et al. A spatially orthogonal hierarchically porous acid–base catalyst for cascade and antagonistic reactions. Nat Catal 3, 921–931 (2020). https://doi.org/10.1038/s41929-020-00526-5
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