Fifteen title compounds, e.g. (I)-(III), are prepared essentially as described previously. Evaluation of their absorption, emission and laser properties shows that N-allyl substituted derivatives (Ia) and (IIa) have high fluorescence quantum yields and laser efficiencies of 137 and 140%, respectivel
Studies on synthesis and anion recognition properties of (3′-nitrobenzo)[2,3-d]-(3″-nitrobenzo)[9,10-d]-1,4,8,11-tetraazacyclotetradecane-5,7,12,14-tetraone
✍ Scribed by Xue-Fang Shang; Xiu-Fang Xu; Hai Lin; Jie Shao; Hua-Kuan Lin
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 157 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0952-3499
- DOI
- 10.1002/jmr.816
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A novel artificial receptor, (3′‐nitrobenzo)[2,3‐d]‐(3″‐nitrobenzo)[9,10‐d]‐1,4,8,11‐tetraazacyclotetradecane‐5,7,12,14‐tetraone, was designed and synthesized. The interactions of this receptor with different anions were determined by UV‐vis and ^1^H NMR titration experiments, and their affinity constants to different anions were compared with those of other similar/different systems. The results indicated that this receptor showed a high selective and recognitive ability for F^−^ among F^−^, Cl^−^, Br^−^, I^−^, AcO^−^, OH^−^, and H~2~PO. Moreover, the low energy configuration of this receptor was further determined by means of theoretical investigations. Copyright © 2007 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract H~10~TTPR was prepared starting from terephthalaldehyde and characterized. Crystal structure of H~10~TTPR and an intermediate compound 11 were determined by X‐ray diffraction analysis. A quasi‐reversible redox wave at 1.15 V (vs. SCE) was observed for H~10~TTPR, indicating that it is a