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Two [Au(CN)2]−-bridged heterometallic coordination polymers directed by different 2,2′-bipyridyl-like ligandsElectronic supplementary information (ESI) available: Perspective view of the pseudo-hexagonal channel in 1(a) and of the phen ligands in the network of 1(b) along the caxis (Fig. S1); view of the supramolecular structure of 2showing AuAu and two kinds of hydrogen bonds (Fig. S2); distances and angles of hydrogen bonds for complex 2(Table S1); . CCDC reference numbers 290064 and 291090. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b809381d

Authors :
Yang Guo
Zhan-Quan Liu
Bin Zhao
Yu-Hua Feng
Gong-Feng Xu
Shi-Ping Yan
Peng Cheng
Qing-Lun Wang
Dai-Zheng Liao
Source :
CrystEngComm; Jan2009, Vol. 11 Issue 1, p61-66, 6p
Publication Year :
2009

Abstract

Two new cyanide-bridged heterobimetallic coordination polymers constructed by using the [Au(CN)2]−building block, {Cd(bipy)[Au(CN)2]2}n(1) and {{Cd(phen)[Au(CN)2]2(H2O)}·iPrOH}n(2) (bipy = 2,2′-bipyridine, phen = 1,10-phenanthroline), have been synthesized and characterized. Complex 1with chiral P3112 space group exhibits a novel three-fold interpenetrating quartz-like 3-D network, which is completely unsupported by aurophilic interactions, while complex 2with the replacement of bipy by phen shows C2/cspace group and features the 1-D zigzag chain structure and an extended supramolecular 2-D array in which aurophilic interactions may play an important role in sustaining the supramolecular solid-state architectures. 1and 2feature various networks most likely due to the different steric hindrances of the bipy and phen ligands. In addition, the solid state photoluminescence spectrum of complex 2exhibits a strong green emission band (λmax= 524 nm) at room temperature. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14668033
Volume :
11
Issue :
1
Database :
Complementary Index
Journal :
CrystEngComm
Publication Type :
Academic Journal
Accession number :
35747073
Full Text :
https://doi.org/10.1039/b809381d