Activation and Deactivation of a Robust Immobilized Cp*Ir-Transfer Hydrogenation Catalyst: A Multielement in Situ X-ray Absorption Spectroscopy Study
- Submitting institution
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The University of Leeds
- Unit of assessment
- 12 - Engineering
- Output identifier
- CHEM-22
- Type
- D - Journal article
- DOI
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10.1021/ja512868a
- Title of journal
- Journal of the American Chemical Society
- Article number
- -
- First page
- 4151
- Volume
- 137
- Issue
- 12
- ISSN
- 0002-7863
- Open access status
- Out of scope for open access requirements
- Month of publication
- March
- Year of publication
- 2015
- URL
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-
- Supplementary information
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https://ndownloader.figstatic.com/files/3620775
- Request cross-referral to
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- Output has been delayed by COVID-19
- No
- COVID-19 affected output statement
- -
- Forensic science
- No
- Criminology
- No
- Interdisciplinary
- No
- Number of additional authors
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12
- Research group(s)
-
-
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- This is a fundamental study, using both in-situ and ex-situ, multi-element X-ray Absorption Spectroscopy, of deactivation mechanisms in an immobilised version of a homogenous catalyst, widely used in organic transfer hydrogenation reactions. Results were corroborated by catalyst poisoning and kinetic experiments and were critical in terms of commercial catalyst development, in collaboration with Yorkshire Process Technologies (now Apex Molecular Ltd). The work advances mechanistic understanding of changes around the catalytic centre, in both the immobilised and ubiquitous homogenous versions of the catalyst (e.g. doi.org/10.1002/chem.201603825). The approach has been cited in both catalyst (e.g. doi.org/10.1021/acs.chemrev.5b00203) and technique (e.g. doi.org/10.1007/978-3-319-43866-5_27) reviews.
- Author contribution statement
- -
- Non-English
- No
- English abstract
- -