## Abstract For Abstract see ChemInform Abstract in Full Text.
N,N′-Disubstituted Ureas: Influence of Substituents on the Formation of Supramolecular Polymers
✍ Scribed by Frédéric Lortie; Sylvie Boileau; Laurent Bouteiller
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 190 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0947-6539
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Symmetrical N,N′‐disubstituted ureas have been synthesized and characterized. Among them, the branched dialkylureas prepared are highly soluble in organic media. Moreover, the solutions obtained are very viscous in heptane, if the branched alkyl groups are not too bulky (i.e. a methyl group on the α carbon, or an ethyl group on the β carbon). Due to the strong, bifurcated hydrogen bonds between the urea moieties, linear supramolecular polymers are formed. The degree of association of these supramolecular polymers has been determined by FTIR spectroscopy.
📜 SIMILAR VOLUMES
The influence of protonation at N 1 on the conformational preferences Ž . 6 Ž . of the N 6 substituent in the modified nucleic acid base N -N-glycylcarbonyl adenine, gc 6 Ade, was investigated by the quantum chemical perturbative configuration interaction Ž . using localized orbitals PCILO method.