Heptakis-6-(5-methylene-thioureido-5′-methyl-2,2′-bipyridyl)-β-cyclodextrin: synthesis and metal complexation study
✍ Scribed by Romain Heck; Alain Marsura
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 210 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A new heptapode heptakis-6-(5-methylene-thioureido-5%-methyl-2,2%-bipyridyl)-b-cyclodextrin was prepared and its complexation properties towards metal cations were investigated. Substituting the urea functions by the corresponding thioureas promoted the inversion of the metal coordination selectivity. Preliminary results showed the heptapode unable to complex lanthanides but authorise selective complexation of 'soft' and 'borderline' metal cations.
📜 SIMILAR VOLUMES
The potentially trinucleating ligands H4L were synthesized in situ by reacting 2,6-dipicolinoyl-hydrazine with 4-acyl-l-phenyl-3-methyl-pyrazolones-5 (acyl= benzoyl, acetyl, iso-butyryl or iso-valeroyl) in a 1:2 molar ratio. These ligands react with an excess of uranyl acetate dihydrate to yield tri