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Synthesis and structural characterization of metal-organic frameworks with the mellitate linker M2(OH)2[C12O12H2].2H2O (M = Al, Ga, In) MIL-116

Identifieur interne : 000406 ( Main/Repository ); précédent : 000405; suivant : 000407

Synthesis and structural characterization of metal-organic frameworks with the mellitate linker M2(OH)2[C12O12H2].2H2O (M = Al, Ga, In) MIL-116

Auteurs : RBID : Pascal:14-0019972

Descripteurs français

English descriptors

Abstract

A new series of isostructural MOF-type carboxylates called MIL-116 (M2(OH)2[C12O12H2].2H2O), was synthesized from the combination of mellitic acid and trivalent p cations M = Al3+, Ga3+ or In3+. Their structures were analyzed either by single-crystal microdiffraction using the synchrotron radiation beamline (ID13 station at ESRF, Grenoble) or solved from powder X-ray diffraction. The 3D hybrid framework is built up from the connection of infinite straight chains of metal-centered octahedra sharing trans corners linked to each other through the mellitate ligands. Here the ligand acts as octadentate linker with four of the carboxylic groups involved in the M-O-C bondings. The two other carboxylate arms remain non-bonded under their protonated form. This represents a rare case of the occurrence of both non-bonding and bonding organic functionalities in a MOF-type solid. Within the tunnels are located water species that interact with the non-coordinated -COOH groups pointing towards the channel.

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Pascal:14-0019972

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<title xml:lang="en" level="a">Synthesis and structural characterization of metal-organic frameworks with the mellitate linker M
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(OH)
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[C
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O
<sub>12</sub>
H
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O (M = Al, Ga, In) MIL-116</title>
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<div type="abstract" xml:lang="en">A new series of isostructural MOF-type carboxylates called MIL-116 (M
<sub>2</sub>
(OH)
<sub>2</sub>
[C
<sub>12</sub>
O
<sub>12</sub>
H
<sub>2</sub>
]
<sub>.</sub>
2H
<sub>2</sub>
O), was synthesized from the combination of mellitic acid and trivalent p cations M = Al
<sup>3+</sup>
, Ga
<sup>3+</sup>
or In
<sup>3+</sup>
. Their structures were analyzed either by single-crystal microdiffraction using the synchrotron radiation beamline (ID13 station at ESRF, Grenoble) or solved from powder X-ray diffraction. The 3D hybrid framework is built up from the connection of infinite straight chains of metal-centered octahedra sharing trans corners linked to each other through the mellitate ligands. Here the ligand acts as octadentate linker with four of the carboxylic groups involved in the M-O-C bondings. The two other carboxylate arms remain non-bonded under their protonated form. This represents a rare case of the occurrence of both non-bonding and bonding organic functionalities in a MOF-type solid. Within the tunnels are located water species that interact with the non-coordinated -COOH groups pointing towards the channel.</div>
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<sub>12</sub>
O
<sub>12</sub>
H
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]
<sub>.</sub>
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<sup>3+</sup>
, Ga
<sup>3+</sup>
or In
<sup>3+</sup>
. Their structures were analyzed either by single-crystal microdiffraction using the synchrotron radiation beamline (ID13 station at ESRF, Grenoble) or solved from powder X-ray diffraction. The 3D hybrid framework is built up from the connection of infinite straight chains of metal-centered octahedra sharing trans corners linked to each other through the mellitate ligands. Here the ligand acts as octadentate linker with four of the carboxylic groups involved in the M-O-C bondings. The two other carboxylate arms remain non-bonded under their protonated form. This represents a rare case of the occurrence of both non-bonding and bonding organic functionalities in a MOF-type solid. Within the tunnels are located water species that interact with the non-coordinated -COOH groups pointing towards the channel.</s0>
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