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9 results for “Molecular catalyst”

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zenodo40/100

Heterogenized Molecular Rhodium Phosphine Catalysts within Metal–Organic Frameworks for Alkene Hydroformylation

<p>Supplementary information for associated publication</p>

opencc-by-4.0Sep 2023View details →
dryad32/100

Data for: Immobilization of molecular catalysts on electrode surfaces using host–guest interactions

<p>Anchoring molecular catalysts on electrode surfaces combines the high selectivity and activity of molecular systems with the practicality of heterogeneous systems. Molecular catalysts, however, are far less stable than traditional heterogeneous electrocatalysts, and therefore a method to easily replace anchored molecular catalysts that have degraded could make such electrosynthetic systems more attractive. Here, we apply a non-covalent 'click' chemistry approach to reversibly bind molecular electrocatalysts to electrode surfaces through host–guest complexation with surface-anchored cyclodextrins. The host–guest interaction is remarkably strong and enables the flow of electrons between the electrode and the guest catalyst. Electrosynthesis in both organic and aqueous media was demonstrated on metal oxide electrodes, with stability on the order of hours. The catalytic surfaces can be recycled by controlled release of the guest from the host cavities and readsorption of fresh guest. </p>

opencc-zeroJan 2021View details →
zenodo32/100

Dataset for the paper: "Using molecular oxygen and Fe-N/C heterogeneous catalysts to achieve Mukaiyama epoxidations via in situ produced organic peroxy acids and acylperoxy radicals"

<p>The data in this spreadsheet was used to produce the figures in the paper&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</p> <p>Authors:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; M. Gong, Y. Guo, D. Malko, G. J.P. Britovsek, J. Rubio-Garcia, J. Dawson and A. Kucernak</p> <p>Title:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Using molecular oxygen and Fe-N/C heterogeneous catalysts to achieve Mukaiyama epoxidations via in situ produced organic peroxy acids and acylperoxy radicals</p> <p>Journal: Catalysis Science &amp; Technology</p> <p>DOI:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 10.1039/D2CY00356B</p> <p>Please cite the above reference if you wish to use this data&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</p> <p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;</p> <p>DOI of data:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 10.5281/zenodo.6384017</p>

opencc-by-4.0Mar 2022View details →
zenodo32/100

Data used for the paper Daniel Malko, Yanjun Guo, Pip Jones, George Britovsek, and Anthony Kucernak, "Heterogeneous iron containing carbon catalyst (Fe-N/C) for epoxidation with molecular oxygen|", Journal of Catalysis, 2019, DOI:10.1016/j.jcat.2019.01.008

<p>The data in this spreadsheet was used to produce the figures in the paper</p> <p>Daniel Malko, Yanjun Guo, Pip Jones, George Britovsek, and Anthony Kucernak</p> <p>Heterogeneous iron containing carbon catalyst (Fe-N/C) for epoxidation with molecular oxygen</p> <p>Journal of Catalysis</p> <p>DOI:10.1016/j.jcat.2019.01.008</p> <p>Please cite the above reference if you wish to use this data<br> DOI of this data file is: 10.5281/zenodo.2539183</p>

opencc-by-4.0Jan 2019View details →
zenodo32/100

Unravelling the Molecular Structure and Confining Environment of an Organometallic Catalyst Heterogenized within Amorphous Porous Polymers

<p>Raw data corresponding to Figure 4c of the following publicaiton:&nbsp;</p> <div> <div> <div>Jabbour, R.; Ashling, C. W.; Robinson, T. C.; Khan, A. H.; Wisser, D.; Berruyer, P.; Ghosh, A. C.; Ranscht, A.; Keen, D. A.; Brunner, E.; Canivet, J.; Bennett, T. D.; Mellot-Draznieks, C.; Lesage, A.; Wisser, F. M. Unravelling the Molecular Structure and Confining Environment of an Organometallic Catalyst Heterogenized within Amorphous Porous Polymers. <em>Angewandte Chemie International Edition</em> <strong>2023</strong>, <em>62</em> (44), e202310878. <a href="https://doi.org/10.1002/anie.202310878">https://doi.org/10.1002/anie.202310878</a>.</div> </div> </div>

opencc-by-4.0Oct 2024View details →
zenodo32/100

Molecular and structural insights into H2 indicator supraparticles: lowering the limit of detection by tuning incorporated catalyst nanoparticles

<p>Raw data from DRIFTS experiments, TEM and SEM microscopy, Zeta potential measurements, and TGA measurements for the article&nbsp;&quot;Molecular and structural insights into H2 indicator supraparticles: lowering the limit of detection by tuning incorporated catalyst nanoparticles&quot; published in Chemistry of Materials&nbsp;<a href="https://doi.org/10.1021/acs.chemmater.3c01105">https://doi.org/10.1021/acs.chemmater.3c01105</a>.</p>

opencc-by-4.0Jul 2023View details →
dryad32/100

Data for: Immobilization of molecular catalysts on electrode surfaces using host–guest interactions

Open the record for dataset details and reuse information.

publicJan 2021View details →
zenodo28/100

RECOVERY OF HIGH MOLECULAR HYDROCARBONS FROM SYNTHESIS GAS AND PHYSICO-CHEMICAL CHARACTERISTICS OF THE CATALYST

Open the record for dataset details and reuse information.

opencc-by-4.0Mar 2024View details →
zenodo24/100

Dataset of the article 'Charge accumulation kinetics in multi-redox molecular catalysts immobilised on TiO2'

<p>Data published in&nbsp;the article &#39;Charge accumulation kinetics in multi-redox molecular catalysts immobilised on TiO<sub>2</sub>&#39;, available at&nbsp;<a href="https://doi.org/10.1039/D0SC04344C">https://doi.org/10.1039/D0SC04344C</a>.</p> <p>Abstract: Multi-redox catalysis requires the accumulation of more than one charge carrier and is crucial for solar energy conversion into fuels and valuable chemicals. In photo(electro)chemical systems, however, the necessary accumulation of multiple, long-lived charges is challenged by recombination with their counterparts. Herein, we investigate charge accumulation in two model multi-redox molecular catalysts for proton and CO<sub>2</sub> reduction attached onto mesoporous TiO<sub>2</sub> electrodes. Transient absorption spectroscopy and spectroelectrochemical techniques have been employed to study the kinetics of photoinduced electron transfer from the TiO<sub>2</sub> to the molecular catalysts in acetonitrile, with triethanolamine as the hole scavenger. At high light intensities, we detect charge accumulation in the millisecond timescale in the form of multi-reduced species. The redox potentials of the catalysts and the capacity of TiO<sub>2</sub> to accumulate electrons play an essential role in the charge accumulation process at the molecular catalyst. Recombination of reduced species with valence band holes in TiO<sub>2</sub> is observed to be faster than microseconds, while electron transfer from multi-reduced species to the conduction band or the electrolyte occurs in the millisecond timescale. Finally, under light irradiation, we show how charge accumulation on the catalyst is regulated as a function of the applied bias and the excitation light intensity.</p>

opencc-by-4.0Nov 2020View details →

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Last verified 2026-04-29Open record