A theoretical study at the B3LYP/6-311++G(d,p) level has been carried out on 2,2 0 -, 3,3 0 -and 4,4 0 -bipyridines, as well as on their monoprotonated and diprotonated forms. The geometries, torsion angles, and the energies of the minima and transition states have been calculated with good agreemen
3,3′-Disubstitued 2,2′-Bipyridines as Carboxylate Receptors: Conformational Regulation of the Bipyridine Moiety
✍ Scribed by Ana M. Costero; Salvador Gil; Margarita Parra; Nuria Huguet; Zouhir Allouni; Rajae Lakhmiri; Ahmed Atlamsani
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 454 KB
- Volume
- 2008
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
Abstract
Two bipyridine derivatives were synthesized and characterized, and their ability to act as sensors for carboxylates was evaluated by UV/Vis and fluorescence studies. The influence of the substituents of the thiourea groups on the stoichiometry of the resulting dicarboxylate complexes was established. Conformational changes in the bipyridine moiety under different conditions were evaluated.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
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