Coexistence of cyclic (CH3OH)2(H2O)8 heterodecamer and acyclic water trimer in the channels of silver-azelate framework

► One Ag(I) complex built from azelaic acid and 1,3-bis(4-pyridyl)propane was ultrasonically synthesized and characterized. ► Discrete (CH3OH)2(H2O)8 heterodecameric and acyclic water trimeric clusters were accommodated in the channels. ► The complex exhibits strong photoluminescence maximized at 50...

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Veröffentlicht in:Journal of molecular structure 2012-08, Vol.1021, p.84-88
Hauptverfasser: Luo, Geng-Geng, Zhu, Rui-Min, He, Wei-Jun, Li, Ming-Zhi, Zhao, Qing-Hua, Li, Dong-Xu, Dai, Jing-Cao
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container_title Journal of molecular structure
container_volume 1021
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Zhu, Rui-Min
He, Wei-Jun
Li, Ming-Zhi
Zhao, Qing-Hua
Li, Dong-Xu
Dai, Jing-Cao
description ► One Ag(I) complex built from azelaic acid and 1,3-bis(4-pyridyl)propane was ultrasonically synthesized and characterized. ► Discrete (CH3OH)2(H2O)8 heterodecameric and acyclic water trimeric clusters were accommodated in the channels. ► The complex exhibits strong photoluminescence maximized at 500nm upon 350nm excitation. ► CIE chromaticity ordinate of the emission is close to that of edge of green component. Flexible azelaic acid (H2aze) and 1,3-bis(4-pyridyl)propane) (bpp) react ultrasonically with silver(I) oxide, generating a new metal–organic framework [Ag2(bpp)2(aze)·7H2O·CH3OH]n (1) that forms a 3D supramolecular structure through H-bonding interactions between solvent molecules and carboxylate O atoms with void spaces. Two kinds of solvent clusters, discrete cyclic (CH3OH)2(H2O)8 heterodecameric and acyclic water trimeric clusters occupy the channels in the structure. Furthermore, 1 exhibits strong photoluminescence maximized at 500nm upon 350nm excitation at room temperature, of which CIE chromaticity ordinate (x=0.28, y=0.44) is close to that of edge of green component.
doi_str_mv 10.1016/j.molstruc.2012.04.050
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Flexible azelaic acid (H2aze) and 1,3-bis(4-pyridyl)propane) (bpp) react ultrasonically with silver(I) oxide, generating a new metal–organic framework [Ag2(bpp)2(aze)·7H2O·CH3OH]n (1) that forms a 3D supramolecular structure through H-bonding interactions between solvent molecules and carboxylate O atoms with void spaces. Two kinds of solvent clusters, discrete cyclic (CH3OH)2(H2O)8 heterodecameric and acyclic water trimeric clusters occupy the channels in the structure. 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Flexible azelaic acid (H2aze) and 1,3-bis(4-pyridyl)propane) (bpp) react ultrasonically with silver(I) oxide, generating a new metal–organic framework [Ag2(bpp)2(aze)·7H2O·CH3OH]n (1) that forms a 3D supramolecular structure through H-bonding interactions between solvent molecules and carboxylate O atoms with void spaces. Two kinds of solvent clusters, discrete cyclic (CH3OH)2(H2O)8 heterodecameric and acyclic water trimeric clusters occupy the channels in the structure. 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Flexible azelaic acid (H2aze) and 1,3-bis(4-pyridyl)propane) (bpp) react ultrasonically with silver(I) oxide, generating a new metal–organic framework [Ag2(bpp)2(aze)·7H2O·CH3OH]n (1) that forms a 3D supramolecular structure through H-bonding interactions between solvent molecules and carboxylate O atoms with void spaces. Two kinds of solvent clusters, discrete cyclic (CH3OH)2(H2O)8 heterodecameric and acyclic water trimeric clusters occupy the channels in the structure. Furthermore, 1 exhibits strong photoluminescence maximized at 500nm upon 350nm excitation at room temperature, of which CIE chromaticity ordinate (x=0.28, y=0.44) is close to that of edge of green component.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.molstruc.2012.04.050</doi><tpages>5</tpages></addata></record>
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subjects Atomic structure
Azelate
CIE chromaticity diagram
hydrogen bonding
Methanol–water binary cluster
Photoluminescence
propane
silver
temperature
Water trimer
title Coexistence of cyclic (CH3OH)2(H2O)8 heterodecamer and acyclic water trimer in the channels of silver-azelate framework
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