Please use this identifier to cite or link to this item:
Title: 3,11,19-Trithia[3.3.3]pyridinophane: Structural diversity in its transition metal complexes
Authors: Vetrichelvan, M. 
Lai, Y.-H. 
Mok, K.F. 
Keywords: Coordination polymers
Structural diversity
Transition metals
Issue Date: 17-May-2004
Citation: Vetrichelvan, M., Lai, Y.-H., Mok, K.F. (2004-05-17). 3,11,19-Trithia[3.3.3]pyridinophane: Structural diversity in its transition metal complexes. European Journal of Inorganic Chemistry (10) : 2086-2095. ScholarBank@NUS Repository.
Abstract: The pyridine-containing aza-thia macrocycle 3,11,19-trithia-[3.3.3] pyridinophane (10) and its complexes with NiII, PdII, CuI, AgI and HgII were synthesised and their crystal structures were determined. The NiII and HgII complexes (11, 12) are mononuclear with 10 serving as an unusual quinquedentate ligand. The CuI complex 13 is also mononuclear with 10 being tetra-coordinated to a tetrahedral CuI. Palladium(II) forms a binuclear complex 14 which exists as an inorganic zwitterion and both Pd II metal ions adopt the expected square-planar geometry with facial coordination, Silver(I). forms one-dimensional coordination polymers (15 and 16) with 10 and these exhibit two different coordination modes, namely tetrahedral and trigonal planar. It was found that the macrocycle 10 did not show any selectivity among a series of metal ions. The electronic and redox properties of several complexes were studied. © Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
Source Title: European Journal of Inorganic Chemistry
ISSN: 14341948
DOI: 10.1002/ejic.200300835
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.