3-D lanthanide coordination polymers with the flexible 1,3-phenylenediacetate linker: Spectroscopic, structural and thermal investigations

被引:8
作者
Lyszczek, Renata [1 ]
Rusinek, Iwona [1 ]
Sienkiewicz-Gromiuk, Justyna [1 ]
Iwan, Mariola [1 ]
Pavlyuk, Oleksiy [2 ]
机构
[1] Marie Curie Sklodowska Univ, Dept Gen & Coordinat Chem, Fac Chem, MC Sklodowska Sq 2, PL-20031 Lublin, Poland
[2] Ivan Franko Natl Univ Lviv, Dept Inorgan Chem, Fac Chem, Kyryla & Mefodiya St 6, UA-79005 Lvov, Ukraine
关键词
Coordination polymers; 1,3-Phenylenediacetate; Lanthanides; X-ray structures; TG-DSC; METAL-ORGANIC FRAMEWORKS; LUMINESCENT; RELIABILITY; COMPLEXES; CRITERION; SERIES;
D O I
10.1016/j.poly.2018.11.049
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four isostructural lanthanide coordination polymers of the formula [Ln(2)(1,3-pda)(3)(H2O)]center dot H2O where Ln = Gd(1), Dy(2), Er(3), Lu(4) and 1,3-pda = 1,3-phenylenediacetate were hydrothermally synthesized and characterized by vibrational spectroscopy, thermal analysis, powder and single-crystal X-ray diffraction methods. All 1,3-phenylenediacetates act as mu(4)-linkers and connect the eight-coordinate lanthanide ions into the 3-D coordination networks. Carboxylate groups in the ligands molecules exhibit diverse conformations: both trans or trans and cis. Changes of Ln-O bond lengths among the investigated compounds point out to the lanthanide contraction. Infrared and Raman spectra confirmed that both carboxylic groups of ligand were deprotonated. The presence of the band of non-hydrogen bonded hydroxyl group from water molecule in the infrared spectra was discussed. Thermal behaviour of the complexes was investigated by the TG-DSC and TG-FTIR methods. The investigated complexes are thermally stable in air and nitrogen atmosphere up to 106-135 degrees C. Further heating of the complexes leads to dehydration and decomposition. Water, carbon oxides, m-xylene and methane are main volatile products of complexes thermal decomposition in nitrogen. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:93 / 101
页数:9
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