Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/20046
Title: A series of new lanthanide fumarates displaying three types of 3-D frameworks
Author: Tan, Xiao-Feng
Zhou, Jian
Fu, Lianshe
Xiao, Hong-Ping
Zou, Hua-Hong
Tang, Qiuling
Keywords: METAL-ORGANIC FRAMEWORKS
SINGLE-MOLECULE MAGNET
COORDINATION POLYMERS
REVERSIBLE DEHYDRATION
FLUORESCENCE EMISSION
CRYSTAL-STRUCTURE
PHOTOLUMINESCENCE
COMPLEXES
ND
LN
Issue Date: 2016
Publisher: ROYAL SOC CHEMISTRY
Abstract: A series of lanthanide fumarates [Sm-2(fum)(3)(H(2)fum)(H2O)(2)] (1, H(2)fum = fumaric acid), [Ln(2)(fum)(3)-(H2O)(4)]center dot 3H(2)O {Ln = Tb (2a), Dy (2b)} and [Ln(2)(fum)(3)(H2O)(4)] {Ln = Y (3a), Ho (3b), Er (3c), Tm (3d)} were prepared by the hydrothermal method and their structures were classified into three types. The 3-D framework of compound 1 contains a 1-D infinite [Sm O Sm](n) chain built up from the connection of SmO8(H2O) polyhedra sharing edges via three -COO group bridges of fumarate ligands, which is further constructed into a 3-D network structure with three kinds of fumarate ligands. Compounds 2a-b are isostructural and consist of a 3-D porous framework with 0-D cavities for the accommodation of chair-like hexameric (H2O)(6) clusters. Compounds 3a-d are isostructural and have a 3-D network structure remarkably different from those of 1 and 2a-b, due to the different coordination numbers for the Ln(3+) ions and distinct fumarate ligand bridging patterns. A systematic investigation of seven lanthanide fumarates and five reported compounds revealed that the well-known lanthanide contraction has a significant influence on the formation of lanthanide fumarates. The magnetic properties of compounds 1, 2b and 3b-3d were also investigated.
Peer review: yes
URI: http://hdl.handle.net/10773/20046
DOI: 10.1039/c6dt00205f
ISSN: 1477-9226
Publisher Version: 10.1039/c6dt00205f
Appears in Collections:CICECO - Artigos

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