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CMP
Credit: Jack Hobhouse

David Keen

Visiting Professor

Sub department

  • Condensed Matter Physics

Research groups

  • X-ray and neutron scattering
david.keen@physics.ox.ac.uk
Telephone: 01865 (2)72310
Clarendon Laboratory, room 106
  • About
  • Publications

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

Angewandte Chemie (International ed. in English) 62:44 (2023) e202310878

Authors:

Ribal Jabbour, Ribal Jabbour, Christopher W Ashling, Thomas C Robinson, Arafat Hossain Khan, Dorothea Wisser, Pierrick Berruyer, Ashta C Ghosh, Alisa Ranscht, David A Keen, Eike Brunner, Jérôme Canivet, Thomas D Bennett, Caroline Mellot-Draznieks, Anne Lesage, Florian M Wisser

Abstract:

The catalytic activity of multifunctional, microporous materials is directly linked to the spatial arrangement of their structural building blocks. Despite great achievements in the design and incorporation of isolated catalytically active metal complexes within such materials, a detailed understanding of their atomic-level structure and the local environment of the active species remains a fundamental challenge, especially when these latter are hosted in non-crystalline organic polymers. Here, we show that by combining computational chemistry with pair distribution function analysis, 129 Xe NMR, and Dynamic Nuclear Polarization enhanced NMR spectroscopy, a very accurate description of the molecular structure and confining surroundings of a catalytically active Rh-based organometallic complex incorporated inside the cavity of amorphous bipyridine-based porous polymers is obtained. Small, but significant, differences in the structural properties of the polymers are highlighted depending on their backbone motifs.
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Barriers to infection prevention and control in long-term care/assisted living settings in British Columbia during the COVID-19 pandemic: a cross-sectional survey.

Antimicrobial resistance and infection control 12:1 (2023) 84

Authors:

Jocelyn A Srigley, Brooke Cheng, Jun Chen Collet, Tara Donovan Towell, Guanghong Han, Dave Keen, Ka Wai Leung, Julie Mori, R Ayesha Ali

Abstract:

Background

The COVID-19 pandemic disproportionately impacted long-term care and assisted living (LTC/AL) facilities in Canada, where infection prevention and control (IPAC) programs had been suboptimal. We aimed to identify barriers affecting healthcare workers' (HCW) adherence to IPAC practices during the pandemic in British Columbia in LTC/AL compared to acute care settings.

Methods

We conducted a web-based survey of direct care providers and IPAC professionals across BC from August to September 2021, focused on knowledge and attitudes toward IPAC within the context of the COVID-19 pandemic, and barriers that affected respondents' abilities to follow IPAC practices throughout the pandemic.

Results

The final analysis included 896 acute care respondents and 441 from LTC/AL. More LTC/AL respondents reported experiencing the following barriers: following IPAC guidance was of lower priority compared to other tasks (29.1% vs. 14.7%, FDR = 0.001) and not their responsibility (28.0% vs. 11.2%, FDR = 0.001); limited supplies for personal protective equipment (PPE) (49.0% vs. 33.6%, FDR = 0.001), hand hygiene products (42.2% vs. 28.8%, FDR = 0.001), and cleaning/disinfection products (44.1% vs. 30.3%, FDR = 0.001); deficits in IPAC leadership support (46.2% vs. 38.9%, FDR = 0.012), IPAC education and training (46.9% vs. 32.0%, FDR = 0.001), and patient care knowledge for managing COVID-19 infections (46.6% vs. 36.0%, FDR = 0.001).

Conclusions

This survey found that barriers to HCWs' adherence to IPAC practices during the COVID-19 pandemic were different in LTC/AL settings compared to acute care. Improvement efforts should focus on strengthening IPAC programs in LTC/AL, particularly enhanced IPAC staffing/leadership, increased training and education, and improving access to PPE, hand hygiene, and cleaning products.
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Survival of Zirconium-Based Metal-Organic Framework Crystallinity at Extreme Pressures.

Inorganic chemistry 62:26 (2023) 10092-10099

Authors:

Georgina P Robertson, Sara Mosca, Celia Castillo-Blas, Florencia A Son, Omar K Farha, David A Keen, Simone Anzellini, Thomas D Bennett

Abstract:

Recent research on metal-organic frameworks (MOFs) has shown a shift from considering only the crystalline high-porosity phases to exploring their amorphous counterparts. Applying pressure to a crystalline MOF is a common method of amorphization, as MOFs contain large void spaces that can collapse, reducing the accessible surface area. This can be either a desired change or indeed an unwanted side effect of the application of pressure. In either case, understanding the MOF's pressure response is extremely important. Three such MOFs with varying pore sizes (UiO-66, MOF-808, and NU-1000) were investigated using in situ high-pressure X-ray diffraction and Raman spectroscopy. Partial crystallinity was observed in all three MOFs above 10 GPa, along with some recovery of crystallinity on return to ambient conditions if the frameworks were not compressed above thresholds of 13.3, 14.2, and 12.3 GPa for UiO-66, MOF-808, and NU-1000, respectively. This threshold was marked by an unexpected increase in one or more lattice parameters with pressure in all MOFs. Comparison of compressibility between MOFs suggests penetration of the pressure-transmitting oil into MOF-808 and NU-1000. The survival of some crystallinity above 10 GPa in all of these MOFs despite their differing pore sizes and extents of oil penetration demonstrates the importance of high-pressure characterization of known structures.
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Meltable, Glass-Forming, Iron Zeolitic Imidazolate Frameworks.

Journal of the American Chemical Society 145:20 (2023) 11258-11264

Authors:

Luis León-Alcaide, Rasmus S Christensen, David A Keen, José L Jordá, Isaac Brotons-Alcázar, Alicia Forment-Aliaga, Guillermo Mínguez Espallargas

Abstract:

We describe the first meltable iron-based zeolitic imidazolate framework (ZIF), denoted MUV-24. This material, elusive from direct synthesis, is obtained from the thermal treatment of [Fe3(im)6(Him)2], which yields Fe(im)2 upon loss of the neutral imidazole molecules. Different crystalline phase transformations are observed upon further heating, until the material melts at 482 °C. Vitrification upon cooling of the liquid phase gives rise to the first Fe-metal-organic framework glass. X-ray total scattering experiments show that the tetrahedral environment of the crystalline solids is maintained in the glass, whereas nanoindentation measurements reveal an increase in Young's modulus, in agreement with stiffening upon vitrification.
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Which phonons contribute most to negative thermal expansion in ScF3?

APL Materials AIP Publishing 11:4 (2023) 041130

Authors:

Martin T Dove, Zhongsheng Wei, Anthony E Phillips, David A Keen, Keith Refson
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