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Investigation of the structure variation of metal diphosphonates with the changing of N-donor auxiliary ligands and their properties
Tang, Si-Fu1; Li, Liang-Jun2; Wang, Chao1; Zhao, Xue-Bo2
2014
发表期刊CRYSTENGCOMM
卷号16期号:38页码:9104-9115
摘要

Nine metal diphosphonates, [Co(H2L)(pyz)(H2O)][(H2O)(0.3)] (1), [Ni(H2L)(pyz)(H2O)(2)] (2), [Ni(H2L)(2,2'-bipy)(2)][(H2O)(2)] (3), [Ni(H2L)(4,4'-bipy)(H2O)][(H2O)(2)] (4), [Ni(H2L)(dpe)(H2O)(2)][(H2O)(2)] (5), [Cu(H2L)(pyz)(H2O)(2)] (6), [Cu(H2L)(4,4'-bipy)][(H2O)(2)] (7), [Zn(H2L)(2,2'-bipy)(H2O)(2)] (8) and [Cd(H2L)(pyz)(H2O)(2)] (9), have been synthesized from a diphosphonate ligand 2,5-dimethyl-1,4-phenylenediphosphonic acid (H4L) and four N-donor auxiliary ligands (pyz = pyrazine, 2,2'-bipy = 2,2'-bipyridine, 4,4'-bipy = 4,4'-bipyridine, dpe = 1,2-di(4-pyridyl)ethylene). In compound 1, pyrazine molecules behave as pillars which connect the Co(H2L) layers into a 3D network structure. Compounds 2, 6 and 9 are isostructural and also show 3D framework structures, in which metal centers are linked by the bidentate diphosphonate ligands into 1D infinite chains and are connected by the pyrazine linkers. In compounds 3 and 8, the diphosphonate ligands, showing bidentate or tetradentate coordination modes, bridge the respective metal ions (Ni2+ and Zn2+) into a 1D infinite chain or 2D layer structure, respectively, in which the 2,2'-bipy ligands chelate to the central metal ions and complete the coordination spheres. In compound 4, the 4,4'-bipy molecules also behave as pillars between the 2D layers, which are constructed from tridentate bridging diphosphonate ligands and six-coordinated Ni2+ ions. Compounds 5 and 7 have similar square grid layered structures which are constructed from bridging bidentate diphosphonate ligands and 4,4'-bipy or dpe linkers. Photophysical measurements indicate that compounds 8 and 9 display ligand centered emissions. Magnetic studies reveal that dominant antiferromagnetic interactions are propagated in compounds 1-3 between the magnetic centers.

文章类型Article
WOS标题词Science & Technology ; Physical Sciences
DOI10.1039/c4ce01266f
关键词[WOS]AROMATIC POLYCARBOXYLATE ACIDS ; COORDINATION POLYMERS ; ORGANIC FRAMEWORKS ; LUMINESCENT PROPERTIES ; CRYSTAL-STRUCTURES ; MAGNETIC-PROPERTIES ; PHOSPHONATE ; CLUSTERS ; TRANSFORMATIONS ; TETRANUCLEAR
收录类别SCI
语种英语
WOS研究方向Chemistry ; Crystallography
WOS类目Chemistry, Multidisciplinary ; Crystallography
WOS记录号WOS:000342070400023
引用统计
文献类型期刊论文
条目标识符http://ir.qibebt.ac.cn/handle/337004/6365
专题多相催化转化研究组
作者单位1.Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Key Lab Biofuel, Qingdao 266101, Peoples R China
2.China Univ Petr East China, Inst Unconvent Hydrocarbon & New Energy Sources, Qingdao 266580, Peoples R China
推荐引用方式
GB/T 7714
Tang, Si-Fu,Li, Liang-Jun,Wang, Chao,et al. Investigation of the structure variation of metal diphosphonates with the changing of N-donor auxiliary ligands and their properties[J]. CRYSTENGCOMM,2014,16(38):9104-9115.
APA Tang, Si-Fu,Li, Liang-Jun,Wang, Chao,&Zhao, Xue-Bo.(2014).Investigation of the structure variation of metal diphosphonates with the changing of N-donor auxiliary ligands and their properties.CRYSTENGCOMM,16(38),9104-9115.
MLA Tang, Si-Fu,et al."Investigation of the structure variation of metal diphosphonates with the changing of N-donor auxiliary ligands and their properties".CRYSTENGCOMM 16.38(2014):9104-9115.
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