A Titanium(IV)‐Based Metal–Organic Framework Featuring Defect‐Rich Ti‐O Sheets as an Oxidative Desulfurization Catalyst

While titanium‐based metal–organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few TiIV MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK‐47 is now presented, the first Ti carboxylate MOF based o...

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Vydané v:Angewandte Chemie International Edition Ročník 58; číslo 27; s. 9160 - 9165
Hlavní autori: Smolders, Simon, Willhammar, Tom, Krajnc, Andraž, Sentosun, Kadir, Wharmby, Michael T., Lomachenko, Kirill A., Bals, Sara, Mali, Gregor, Roeffaers, Maarten B. J., De Vos, Dirk E., Bueken, Bart
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Germany Wiley Subscription Services, Inc 01.07.2019
Vydanie:International ed. in English
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ISSN:1433-7851, 1521-3773, 1521-3773
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Abstract While titanium‐based metal–organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few TiIV MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK‐47 is now presented, the first Ti carboxylate MOF based on sheets of TiIVO6 octahedra, which can be synthesized with a range of different linkers. COK‐47 can be synthesized as an inherently defective nanoparticulate material, rendering it a highly efficient catalyst for the oxidation of thiophenes. Its structure was determined by continuous rotation electron diffraction and studied in depth by X‐ray total scattering, EXAFS, and solid‐state NMR. Furthermore, its photoactivity was investigated by electron paramagnetic resonance and demonstrated by catalytic photodegradation of rhodamine 6G. COK‐47, the first Ti carboxylate sheet‐based MOF, can be synthesized as pristine or inherently defective nanoparticulate material. Its structure was extensively characterized and its defects render it a highly efficient catalyst for the oxidation of thiophenes. The material also features photocatalytic activity.
AbstractList While titanium‐based metal–organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few Ti IV MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK‐47 is now presented, the first Ti carboxylate MOF based on sheets of Ti IV O 6 octahedra, which can be synthesized with a range of different linkers. COK‐47 can be synthesized as an inherently defective nanoparticulate material, rendering it a highly efficient catalyst for the oxidation of thiophenes. Its structure was determined by continuous rotation electron diffraction and studied in depth by X‐ray total scattering, EXAFS, and solid‐state NMR. Furthermore, its photoactivity was investigated by electron paramagnetic resonance and demonstrated by catalytic photodegradation of rhodamine 6G.
While titanium‐based metal–organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few TiIV MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK‐47 is now presented, the first Ti carboxylate MOF based on sheets of TiIVO6 octahedra, which can be synthesized with a range of different linkers. COK‐47 can be synthesized as an inherently defective nanoparticulate material, rendering it a highly efficient catalyst for the oxidation of thiophenes. Its structure was determined by continuous rotation electron diffraction and studied in depth by X‐ray total scattering, EXAFS, and solid‐state NMR. Furthermore, its photoactivity was investigated by electron paramagnetic resonance and demonstrated by catalytic photodegradation of rhodamine 6G. COK‐47, the first Ti carboxylate sheet‐based MOF, can be synthesized as pristine or inherently defective nanoparticulate material. Its structure was extensively characterized and its defects render it a highly efficient catalyst for the oxidation of thiophenes. The material also features photocatalytic activity.
While titanium-based metal-organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few Ti MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK-47 is now presented, the first Ti carboxylate MOF based on sheets of Ti O octahedra, which can be synthesized with a range of different linkers. COK-47 can be synthesized as an inherently defective nanoparticulate material, rendering it a highly efficient catalyst for the oxidation of thiophenes. Its structure was determined by continuous rotation electron diffraction and studied in depth by X-ray total scattering, EXAFS, and solid-state NMR. Furthermore, its photoactivity was investigated by electron paramagnetic resonance and demonstrated by catalytic photodegradation of rhodamine 6G.
While titanium-based metal-organic frameworks (MOFs) have been widely studied for their (photo) catalytic potential, only a few Ti-IV MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK-47 is now presented, the first Ti carboxylate MOF based on sheets of (TiO6)-O-IV octahedra, which can be synthesized with a range of different linkers. COK-47 can be synthesized as an inherently defective nanoparticulate material, rendering it a highly efficient catalyst for the oxidation of thiophenes. Its structure was determined by continuous rotation electron diffraction and studied in depth by X-ray total scattering, EXAFS, and solid-state NMR. Furthermore, its photoactivity was investigated by electron paramagnetic resonance and demonstrated by catalytic photodegradation of rhodamine 6G.
While titanium-based metal-organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few TiIV MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK-47 is now presented, the first Ti carboxylate MOF based on sheets of TiIV O6 octahedra, which can be synthesized with a range of different linkers. COK-47 can be synthesized as an inherently defective nanoparticulate material, rendering it a highly efficient catalyst for the oxidation of thiophenes. Its structure was determined by continuous rotation electron diffraction and studied in depth by X-ray total scattering, EXAFS, and solid-state NMR. Furthermore, its photoactivity was investigated by electron paramagnetic resonance and demonstrated by catalytic photodegradation of rhodamine 6G.While titanium-based metal-organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few TiIV MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK-47 is now presented, the first Ti carboxylate MOF based on sheets of TiIV O6 octahedra, which can be synthesized with a range of different linkers. COK-47 can be synthesized as an inherently defective nanoparticulate material, rendering it a highly efficient catalyst for the oxidation of thiophenes. Its structure was determined by continuous rotation electron diffraction and studied in depth by X-ray total scattering, EXAFS, and solid-state NMR. Furthermore, its photoactivity was investigated by electron paramagnetic resonance and demonstrated by catalytic photodegradation of rhodamine 6G.
While titanium‐based metal–organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few TiIV MOFs have been reported owing to the high reactivity of the employed titanium precursors. The synthesis of COK‐47 is now presented, the first Ti carboxylate MOF based on sheets of TiIVO6 octahedra, which can be synthesized with a range of different linkers. COK‐47 can be synthesized as an inherently defective nanoparticulate material, rendering it a highly efficient catalyst for the oxidation of thiophenes. Its structure was determined by continuous rotation electron diffraction and studied in depth by X‐ray total scattering, EXAFS, and solid‐state NMR. Furthermore, its photoactivity was investigated by electron paramagnetic resonance and demonstrated by catalytic photodegradation of rhodamine 6G.
Author Wharmby, Michael T.
De Vos, Dirk E.
Willhammar, Tom
Sentosun, Kadir
Bueken, Bart
Lomachenko, Kirill A.
Roeffaers, Maarten B. J.
Mali, Gregor
Krajnc, Andraž
Smolders, Simon
Bals, Sara
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  organization: University of Antwerp
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  givenname: Michael T.
  surname: Wharmby
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  organization: Deutsches Elektronen-Synchrotron
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  givenname: Kirill A.
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  fullname: Mali, Gregor
  organization: National Institute of Chemistry
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  givenname: Maarten B. J.
  surname: Roeffaers
  fullname: Roeffaers, Maarten B. J.
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  givenname: Dirk E.
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  surname: De Vos
  fullname: De Vos, Dirk E.
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Issue 27
Keywords Ti-oxo sheets
photocatalysis
titanium
metal-organic frameworks
oxidative desulfurization
Language English
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Snippet While titanium‐based metal–organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few TiIV MOFs have been reported...
While titanium‐based metal–organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few Ti IV MOFs have been reported...
While titanium-based metal-organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few Ti MOFs have been reported owing...
While titanium-based metal-organic frameworks (MOFs) have been widely studied for their (photo)catalytic potential, only a few TiIV MOFs have been reported...
While titanium-based metal-organic frameworks (MOFs) have been widely studied for their (photo) catalytic potential, only a few Ti-IV MOFs have been reported...
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SubjectTerms Catalysis
Catalysts
Electron diffraction
Electron paramagnetic resonance
Metal-organic frameworks
Nanoparticles
NMR
Nuclear magnetic resonance
Oxidation
oxidative desulfurization
photocatalysis
Photodegradation
Rhodamine 6G
Sheets
Synthesis
Thiophenes
Ti-oxo sheets
Titanium
Title A Titanium(IV)‐Based Metal–Organic Framework Featuring Defect‐Rich Ti‐O Sheets as an Oxidative Desulfurization Catalyst
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201904347
https://www.ncbi.nlm.nih.gov/pubmed/31059170
https://www.proquest.com/docview/2253674616
https://www.proquest.com/docview/2232113191
https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-171793
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