Self-assembly of novel co-ordination polymers containing polycatenated molecular ladders and intertwined two-dimensional tilings

被引:138
作者
Carlucci, L
Ciani, G
Proserpio, DM
机构
[1] Dipartimento Chim Strutturale & Stereochim Inorga, I-20133 Milan, Italy
[2] Ctr CNR, I-20133 Milan, Italy
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1999年 / 11期
关键词
D O I
10.1039/a903107c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four novel co-ordination polymers have been obtained from the reactions of M-II(NO3)(2) salts (M-II = Zn, Co or Cd) and the bidentate spacer ligands 1,2-bis(4-pyridyl)ethyne (bpethy) and trans-4,4'-azobis(pyridine) (azpy), all exhibiting the same metal-to-ligand molar ratio of 2:3. Crystal structure analyses, however, have revealed two quite different polymeric motifs, in spite of the presence of similar co-ordination geometries of the metal ions, that are bound to three pyridyl groups, with a T-shaped disposition, and to the oxygen atoms of two eta(2)-nitrates, thus resulting in a distorted pentagonal-bipyramidal seven-co-ordination. The species [M-2(bpethy)(3)(NO3)(4)] (M = Zn or Co) consist of ladder-like polymers that interpenetrate in an unprecedented fashion to produce an overall three-dimensional array. On the other hand, the species [Cd-2(bpethy)(3)(NO3)(4)]. CH2Cl2 and [Cd-2(azpy)(3)(NO3)(4)] contain undulated two-dimensional layers with an unprecedented tiled pattern, that give threefold interpenetration in a parallel fashion.
引用
收藏
页码:1799 / 1804
页数:6
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