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|Title:||12,13,25,26-Tetraaza-2,15-dithia[3.3]phenanthrolinophane. Synthesis, conformational study and complexation reactions||Authors:||Lai, Y.-H.
|Issue Date:||Mar-1996||Citation:||Lai, Y.-H., Ma, L., Mok, K.F. (1996-03). 12,13,25,26-Tetraaza-2,15-dithia[3.3]phenanthrolinophane. Synthesis, conformational study and complexation reactions. Tetrahedron 52 (13) : 4673-4678. ScholarBank@NUS Repository. https://doi.org/10.1016/0040-4020(96)00138-X||Abstract:||12,13,25,26-Tetraaza-2,15-dithia[3.3]phenanthrolinophane 7 was prepared from a cyclization reaction of 2,9-bis(bromomethyl)phenanthroline 3. The syn isomer of 7 was kinetically favoured while the anti isomer was the thermodynamically more stable product isolated. The macrocycle 7 formed 1:1 complexes, namely 10 and 11, respectively, with zinc(II) and cadmium(II) ions. A tetragonal-pyrimidal configuration is proposed for these complexes. A comparison of the 1H NMR spectral data of 7, 10 and 11 suggests that the complexation results in a symmetrical structure through the four nitrogen donor atoms. The sulfur atoms in the bridges do not seem to coordinate strongly to the metal ions.||Source Title:||Tetrahedron||URI:||http://scholarbank.nus.edu.sg/handle/10635/92901||ISSN:||00404020||DOI:||10.1016/0040-4020(96)00138-X|
|Appears in Collections:||Staff Publications|
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