Synthesis of Calix[4]arene Derivatives with NLO Properties
✍ Scribed by Zhu Bai; Chao-Zhi Zhang; Guo-Yuan Lu; Fang Liu
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 78 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0256-7660
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The new chromophore compounds with NLO properties were prepared by Knoevenagel condensation from formyl or diformyl calix[4]arene and isophorone derivatives in the presence of piperidine and acetic acid, respectively. In these chromophore calix[4]arenes, the ring locked trienes were employed as the conjugation bridge and electron acceptor in D‐π‐A units. The NMR spectra demonstrated that they existed in a cone conformation and consequently non‐conjugated D‐π‐A units could be oriented at nearly the same direction.
📜 SIMILAR VOLUMES
## Abstract The synthesis of two new flavin substituted calix[4]arene derivatives, **9** and **10**, is described. The first flavin substituted calix[4]arene derivative **9** was synthesized by the reaction of 3‐methylalloxazine (**5**) with 25,27‐bis(3‐bromopropoxy)‐26,28‐dihydroxy‐5,11,17,23‐tetr
Two calix[4] arene derivatives (5 and 8) and their telomers are synthesized to estimate selective extraction of alkali and transition metal cations from the aqueous to the organic phase (chloroform). Compound 5 shows selectivity toward Hg 2ϩ . Compound 8 and telomers 6 and 9 are not selective but a