Synthesis of a new macrocyclic compound and its self-assembly
β Scribed by Pan Zhi-Quan; Luo Qin-Hui; Long De-Liang; Chen Jiu-Tong
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 258 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0256-7660
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
A new macrocyclic compound has been synthesized by condensation of pyridineβlβoxideβ2, 6βdialdehyde with diethylenetriamine. The selfβassembly behaviours were studied by Xβray diffraction. The results show that the selfβassembly were controlled by intermolecular hydrogen bonds and ΟβΟ stacking effects.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract A novel amphiphilic starch piperinic ester (SPE) has been synthesized by coupling a carboxyl group on the piperic acid and a hydroxyl group on the starch backbone. The synthetic process includes three steps. Firstly, piperic acid was obtained by hydrolyzing piperine that was extracted f
A convienent one-pot synthesis of macrocycles containing a bis(thiocarbamoyl) derivatives 3. In the final step, a ringclosure reaction using a large number of Ξ±,Ο-dielectrophilic tetraaminoethene substructure is described. Starting from oxalic amidines 1, reduction with lithium and subsequent buildi