𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.

✦ 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)


📜 SIMILAR VOLUMES


A theoretical study of the conformation,
✍ Ibon Alkorta; José Elguero; Christian Roussel 📂 Article 📅 2011 🏛 Elsevier 🌐 English ⚖ 553 KB

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

DNA Interactions of the Functionalized (
✍ Li-Feng Tan; Fang Wang; Hui Chao; Sheng Zhang; Jun-Jie Fei; Liang-Nian Ji 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 German ⚖ 320 KB

## Abstract A novel polypyridine ligand, dipyrido[3,2‐__a:__2′,3′‐__c__]phenazine‐11‐carboxylic acid methyl ester (=dppz‐11‐CO~2~Me), and its ruthenium(II) complex, [Ru(bpy)~2~(dppz‐11‐CO~2~Me)]^2+^ (**1**), were synthesized and characterized. The binding properties of this complex to calf‐thymus D

Structural and conformational analysis b
✍ N. Platzer; J. P. Bouchet; J. P. Volland 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 571 KB

Structural and Conformational Analysis by lH NMR and 13C NMR of a New Angiotensin I Converting Enzyme Inhibitor, the tert-Butylamine Salt of (2S)-2-[ (1S)-l-Carbethoxybutylamino]-loxopropyl-(2S,3aSJaS) perhydroindole-2-carboxylic acid (Perindopril)