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Design and constructions of three novel metal–organic frameworks based on pillared-layer motifsElectronic supplementary information (ESI) available: Details of the structures of 1–3, PXRD and TG curves of complexs 1–3. CCDC reference numbers 714763–714765. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b909053c

Authors :
Yan-Yan Xu
Yan-Yan Xing
Xian-Ying Duan
Yi-Zhi Li
Hui-Zhen Zhu
Qing-Jin Meng
Source :
CrystEngComm. Feb2010, Vol. 12 Issue 2, p567-572. 6p.
Publication Year :
2010

Abstract

Three novel 3D metal–organic frameworks, [Co2(butca)(o-bix)2·8H2O]n(1), [Co2(butca)(m-bix)2·2H2O]n(2) and [Co2(butca)(p-bix)2·3H2O]n(3) (butca = 1,2,3,4-butane-tetracarboxylic acid; o-bix = 1,2-bis(imidazol-1-ylmethyl)-benzene; m-bix = 1,3-bis(imidazol-1-ylmethyl)-benzene; and p-bix = 1,4-bis(imidazol-1-ylmethyl)-benzene), have been successfully synthesized from a 2D layer compound [Co2(butca)(H2O)5·2H2O]n(0) employing a three isomer pillars insertion reaction, and their structures were determined by single-crystal X-ray diffraction studies. Complexes 1and 2are isostructural. Interestingly, there exist metal-bix double-helical chains in these two 3D frameworks, which are arranged left- and right-handed alternately. Different from 1and 2which have only one coordination model, Co atoms in 3have two types of different coordination enviroments. The Co1 ions are exclusively bridged by cis-bix ligands to give one 26-number ring through spontaneous resolution. At the same time, the Co2 ions are wholely connected with tran-bix ligands to form a 1-D zigzag chain. Moreover, the relationship between a 2D layer structure and 3D metal–organic frameworks based on the pillared-layer motifs is discussed. This work has significant potential for the study of crystal engineering of transition metal coordination networks. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14668033
Volume :
12
Issue :
2
Database :
Academic Search Index
Journal :
CrystEngComm
Publication Type :
Academic Journal
Accession number :
47737119
Full Text :
https://doi.org/10.1039/b909053c