Probing the Lewis Acidity and Catalytic Activity of the Metal-Organic Framework [Cu3(btc)2] (BTC=Benzene-1,3,5-tricarboxylate)

An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu3(btc)2] (BTC=benzene‐1,3,5‐tricarboxylate). The crystalline material was characterized by X‐ray diffraction, optical microscopy, SEM, X‐ray photoelectron spectroscopy, N2 sorption, thermograv...

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Vydáno v:Chemistry : a European journal Ročník 12; číslo 28; s. 7353 - 7363
Hlavní autoři: Alaerts, Luc, Séguin, Etienne, Poelman, Hilde, Thibault-Starzyk, Frédéric, Jacobs, Pierre A., De Vos, Dirk E.
Médium: Journal Article
Jazyk:angličtina
Vydáno: Weinheim WILEY-VCH Verlag 25.09.2006
WILEY‐VCH Verlag
Wiley
Wiley-VCH Verlag
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ISSN:0947-6539, 1521-3765
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Abstract An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu3(btc)2] (BTC=benzene‐1,3,5‐tricarboxylate). The crystalline material was characterized by X‐ray diffraction, optical microscopy, SEM, X‐ray photoelectron spectroscopy, N2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number of Cu2O impurities, and particularly on the free CuII coordination sites in the framework. [Cu3(btc)2] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of α‐pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2‐bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu3(btc)2] are hard Lewis acids. Catalyst stability, re‐usability, and heterogeneity are critically assessed. A systematic study of the catalytic properties of a metal‐organic framework: [Cu3(btc)2] is a very selective catalyst for specific isomerizations of terpenes, terpene epoxides, and ketals (see scheme). Together with IR spectroscopic measurements on adsorbed probe molecules, this proves the hard Lewis acid properties of the material.
AbstractList An optimized procedure was designed for the preparation of the microporous metal-organic framework (MOF) [Cu3(btc)2] (BTC=benzene-1,3,5-tricarboxylate). The crystalline material was characterized by X-ray diffraction, optical microscopy, SEM, X-ray photoelectron spectroscopy, N2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number of Cu2O impurities, and particularly on the free CuII coordination sites in the framework. [Cu3(btc)2] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of alpha-pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2-bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu3(btc)2] are hard Lewis acids. Catalyst stability, re-usability, and heterogeneity are critically assessed.
An optimized procedure was designed for the preparation of the microporous metal-organic framework (MOF) [Cu-3(btc),] (BTC=benzene-1,3,5-tricarboxylate). The crystalline material was characterized by X-ray diffraction, optical microscopy, SEM, X-ray photoelectron spectroscopy, N-2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number Of Cu2O impurities, and particularly on the free Cu-II coordination sites in the framework. [Cu-3(btC)(2)] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of a-pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2-bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu-3(btC)(2)] are hard Lewis acids. Catalyst stability, re-usability, and heterogeneity are critically assessed.
An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu3(btc)2] (BTC=benzene‐1,3,5‐tricarboxylate). The crystalline material was characterized by X‐ray diffraction, optical microscopy, SEM, X‐ray photoelectron spectroscopy, N2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number of Cu2O impurities, and particularly on the free CuII coordination sites in the framework. [Cu3(btc)2] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of α‐pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2‐bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu3(btc)2] are hard Lewis acids. Catalyst stability, re‐usability, and heterogeneity are critically assessed. A systematic study of the catalytic properties of a metal‐organic framework: [Cu3(btc)2] is a very selective catalyst for specific isomerizations of terpenes, terpene epoxides, and ketals (see scheme). Together with IR spectroscopic measurements on adsorbed probe molecules, this proves the hard Lewis acid properties of the material.
An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu 3 (btc) 2 ] (BTC=benzene‐1,3,5‐tricarboxylate). The crystalline material was characterized by X‐ray diffraction, optical microscopy, SEM, X‐ray photoelectron spectroscopy, N 2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number of Cu 2 O impurities, and particularly on the free Cu II coordination sites in the framework. [Cu 3 (btc) 2 ] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of α‐pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2‐bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu 3 (btc) 2 ] are hard Lewis acids. Catalyst stability, re‐usability, and heterogeneity are critically assessed.
Abstract An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu 3 (btc) 2 ] (BTC=benzene‐1,3,5‐tricarboxylate). The crystalline material was characterized by X‐ray diffraction, optical microscopy, SEM, X‐ray photoelectron spectroscopy, N 2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number of Cu 2 O impurities, and particularly on the free Cu II coordination sites in the framework. [Cu 3 (btc) 2 ] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of α‐pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2‐bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu 3 (btc) 2 ] are hard Lewis acids. Catalyst stability, re‐usability, and heterogeneity are critically assessed.
Author Séguin, Etienne
Thibault-Starzyk, Frédéric
Jacobs, Pierre A.
Poelman, Hilde
Alaerts, Luc
De Vos, Dirk E.
Author_xml – sequence: 1
  givenname: Luc
  surname: Alaerts
  fullname: Alaerts, Luc
  organization: Centre for Surface Chemistry and Catalysis K.U.Leuven, Kasteelpark Arenberg 23, 3001 Heverlee, Belgium, Fax: (+32) 16-321-998
– sequence: 2
  givenname: Etienne
  surname: Séguin
  fullname: Séguin, Etienne
  organization: Laboratoire Catalyse & Spectrochimie CNRS-UMR 6506, ENSICAEN, Boulevard Maréchal Juin 6 14050 Caen CEDEX, France
– sequence: 3
  givenname: Hilde
  surname: Poelman
  fullname: Poelman, Hilde
  organization: Department of Solid State Sciences Ghent University, Krijgslaan 281 S1, 9000 Gent, Belgium
– sequence: 4
  givenname: Frédéric
  surname: Thibault-Starzyk
  fullname: Thibault-Starzyk, Frédéric
  organization: Laboratoire Catalyse & Spectrochimie CNRS-UMR 6506, ENSICAEN, Boulevard Maréchal Juin 6 14050 Caen CEDEX, France
– sequence: 5
  givenname: Pierre A.
  surname: Jacobs
  fullname: Jacobs, Pierre A.
  organization: Centre for Surface Chemistry and Catalysis K.U.Leuven, Kasteelpark Arenberg 23, 3001 Heverlee, Belgium, Fax: (+32) 16-321-998
– sequence: 6
  givenname: Dirk E.
  surname: De Vos
  fullname: De Vos, Dirk E.
  email: dirk.devos@biw.kuleuven.be
  organization: Centre for Surface Chemistry and Catalysis K.U.Leuven, Kasteelpark Arenberg 23, 3001 Heverlee, Belgium, Fax: (+32) 16-321-998
BackLink https://www.ncbi.nlm.nih.gov/pubmed/16881030$$D View this record in MEDLINE/PubMed
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Issue 28
Keywords DESIGN
heterogeneous catalysis
STABILITY
ISOMERIZATION
carbon monoxide
Lewis acids
IR spectroscopy
metal-organic frameworks
REARRANGEMENT
(+)CITRONELLAL
ALPHA-PINENE OXIDE
SITES
ZEOLITES
COORDINATION POLYMERS
2-BROMOPROPIOPHENONE
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Snippet An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu3(btc)2] (BTC=benzene‐1,3,5‐tricarboxylate). The...
An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu 3 (btc) 2 ] (BTC=benzene‐1,3,5‐tricarboxylate)....
An optimized procedure was designed for the preparation of the microporous metal-organic framework (MOF) [Cu-3(btc),] (BTC=benzene-1,3,5-tricarboxylate). The...
An optimized procedure was designed for the preparation of the microporous metal-organic framework (MOF) [Cu3(btc)2] (BTC=benzene-1,3,5-tricarboxylate). The...
Abstract An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu 3 (btc) 2 ]...
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SubjectTerms carbon monoxide
Chemical Sciences
Chemistry
Chemistry, Multidisciplinary
heterogeneous catalysis
IR spectroscopy
Lewis acids
metal-organic frameworks
Physical Sciences
Science & Technology
Title Probing the Lewis Acidity and Catalytic Activity of the Metal-Organic Framework [Cu3(btc)2] (BTC=Benzene-1,3,5-tricarboxylate)
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