2D Sheet-like architectures constructed from main-group metal ions, 4,4′-bpno and 1,2-alternate p-sulfonatothiacalix[4]arene

被引:11
作者
Xiong, Kecai [1 ,2 ]
Jiang, Feilong [1 ]
Yang, Ming [1 ,2 ]
Wu, Mingyan [1 ]
Feng, Rui [1 ,2 ]
Xu, Wentao [1 ,2 ]
Hong, Maochun [1 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
ACID N-OXIDE; CRYSTAL-STRUCTURES; COORDINATION POLYMER; INCLUSION; COMPLEXES; LEAD(II); CAPSULE; SULFONATOCALIXARENES; CONFINEMENT; CALIXARENE;
D O I
10.1039/c1dt11239b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two novel 2D sheet-like complexes 1 and 2 have been prepared by reaction of p-sulfonatothiacalix[4] arene (TC4AS) with main-group metal ions (lead(II) or barium(II)) and 4,4'-bipyridine-N, N'-dioxide (4,4'-bpno). In both complexes 1 and 2, TC4AS molecules prefer 1,2-alternate conformation, forming 2D sheet-like layers in the presence of divalent ions and 4,4'-bpno ligand. The layers extend to 3D architectures via strong hydrogen bonding interactions. In addition, complexes 1 and 2 are thermally stable up to ca. 335 and 305 degrees C, respectively. It seems that the strong hydrogen bonds between the sheet-like layers impart the extraordinarily high degrees of stability to the structures. Further analysis indicates that complexes 1 and 2 are significantly different: (a) the divalent ions have different coordination environments due to the nature of the different ions; (b) TC4AS within complexes 1 and 2 connects to four Pb(II) or six Ba(II) ions, respectively; (c) 4,4'-bpno shows different connection modes; (d) in the solid state, complex 1 exhibits intense orange luminescence with triexponential decays, while complex 2 does not exhibit any obvious luminescence at cryogenic temperatures.
引用
收藏
页码:540 / 545
页数:6
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