Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/66622
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dc.contributor.authorM. Sinchowen_US
dc.contributor.authorThammanoon Chuasaarden_US
dc.contributor.authorBunlawee Yotnoien_US
dc.contributor.authorApinpus Rujiwatraen_US
dc.date.accessioned2019-09-16T12:49:19Z-
dc.date.available2019-09-16T12:49:19Z-
dc.date.issued2019-10-01en_US
dc.identifier.issn1095726Xen_US
dc.identifier.issn00224596en_US
dc.identifier.other2-s2.0-85070285339en_US
dc.identifier.other10.1016/j.jssc.2019.120902en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85070285339&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/66622-
dc.description.abstract© 2019 Elsevier Inc. New series of [Ln2 (pydc)2(SO4) (H2O)x]·yH2O (H2pydc = 2,5-pyridinedicarboxylic acid), differing in number of the coordinating (x) and the crystallizing (y) water, have been hydrothermally synthesized and characterized: (i) x = 2, y = 6, and Ln = La, Pr and Nd; (ii) x = 3, y = 2 and Ln = Pr and Nd; and (iii) x = y = 0 and Ln = Pr and Nd. Influences of the subtle change in reaction temperature (80–180 °C) and time (1–7 days) on x and y values, and structural diversity of the titled complexes are reported. The association between x and y values and the hydrogen bonding interactions facilitated by the water molecules, the aromatic π-π interactions of the pydc2− ligand, as well as the coordination modes of both pydc2− and sulfate is discussed. Dissimilar thermogravimetric behaviors and the framework stabilities are presented.en_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.subjectPhysics and Astronomyen_US
dc.titleDiversity in framework architecture of lanthanide-2,5-pyridinedicarboxylate-sulfate coordination polymersen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Solid State Chemistryen_US
article.volume278en_US
article.stream.affiliationsUniversity of Phayaoen_US
article.stream.affiliationsChiang Mai Universityen_US
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