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Metal Organic Frameworks Assembled from Y(III), Na(I), and Chiral Flexible-Achiral Rigid Dicarboxylates

Autor(es) y otros:
Amghouz, ZakariaeAutoridad Uniovi; Roces Fernández, LauraAutoridad Uniovi; García-Granda, SantiagoAutoridad Uniovi; García Menéndez, José RubénAutoridad Uniovi; Souhail, Badredine; Mafra, Luís Miguel Monteiro; Shi, Fha-Nian; Rocha, João Carlos Matias Celestino Gomes da
Fecha de publicación:
2010
Versión del editor:
http://dx.doi.org/10.1021/ic100867w
Citación:
Inorganic Chemistry, 49(17), p. 7917-7926 (2010); doi:10.1021/ic100867w
Descripción física:
p. 7917-7926
Resumen:

New chiral metal organic frameworks, assembled from Y(III), Na(I), and chiral flexible-achiral rigid dicarboxylate ligands, formulated as [NaY(Tart)(BDC)(H2O)2] (1) and [NaY(Tart)(biBDC)(H2O)2] (2) (H2Tart = Tartaric acid; H2BDC = Terephthalic acid; H2biBDC = Biphenyl-4,4′-dicarboxylic acid), were obtained as single phases under hydrothermal conditions. Their structures were solved by single-crystal X-ray diffraction (XRD), and characterized by 13C CPMAS NMR, thermal analyses (thermogravimetry-mass spectrometry (TG-MS) and differential scanning calorimetry (DSC)), and X-ray thermodiffractometry. Both compounds crystallize in the orthorhombic chiral space group C2221 with a = 6.8854(2) Å, b = 30.3859(7) Å, c = 7.4741(2) Å for 1, and a = 6.8531(2) Å, b = 39.0426(8) Å, c = 7.4976(2) Å for 2. 1 and 2 are layered structures whose three-dimensional stability is ensured by strong hydrogen bond interactions. The dehydration of both compounds is accompanied by phase transformation, while the spontaneous rehydration process is characterized by different kinetics, fast in the case of 1 and slow for 2.

New chiral metal organic frameworks, assembled from Y(III), Na(I), and chiral flexible-achiral rigid dicarboxylate ligands, formulated as [NaY(Tart)(BDC)(H2O)2] (1) and [NaY(Tart)(biBDC)(H2O)2] (2) (H2Tart = Tartaric acid; H2BDC = Terephthalic acid; H2biBDC = Biphenyl-4,4′-dicarboxylic acid), were obtained as single phases under hydrothermal conditions. Their structures were solved by single-crystal X-ray diffraction (XRD), and characterized by 13C CPMAS NMR, thermal analyses (thermogravimetry-mass spectrometry (TG-MS) and differential scanning calorimetry (DSC)), and X-ray thermodiffractometry. Both compounds crystallize in the orthorhombic chiral space group C2221 with a = 6.8854(2) Å, b = 30.3859(7) Å, c = 7.4741(2) Å for 1, and a = 6.8531(2) Å, b = 39.0426(8) Å, c = 7.4976(2) Å for 2. 1 and 2 are layered structures whose three-dimensional stability is ensured by strong hydrogen bond interactions. The dehydration of both compounds is accompanied by phase transformation, while the spontaneous rehydration process is characterized by different kinetics, fast in the case of 1 and slow for 2.

URI:
http://hdl.handle.net/10651/7076
ISSN:
0020-1669
Identificador local:

20100277

DOI:
10.1021/ic100867w
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