Synthesis of novel porphyrin-based biscalix[4]arenes
✍ Scribed by Miroslav Dudicˇ; Pavel Lhota´k; Vladimi´r Kra´l; Kamil Lang; Ivan Stibor
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 250 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A novel method for the preparation of porphyrin-based biscalix[4]arenes has been developed, starting from appropriate aryldipyrrolylmethane and calix[4]arene monoaldehyde. The condev~tion reaction in the presence of BF3"Et20 leads to the title compounds in good yields (30-54%). Novel derivatives represent the first example of porphyrin-based calix[4]areaes with directly connected aromatic subsystems of both moieties. The photophysical properties of biscalix[4]arenes are presented.
📜 SIMILAR VOLUMES
The biscalix[4]arene showed remarkably enhanced inclusion ability for the N-methylpyridinium ion due to the increasing p-basicity of the benzene rings, which interact with the guest in an edge-to-face manner, in calix[4]arene skeletons.
A biscalixarene bearing tert-butylated and de-tert-butylated calix[4]arene unit connected by four ethylenoxy bridges has been prepared. This compound adopts the pinched cone conformation (C 2v symmetry) and hence, is suitably preorganised for Ag + complexation. X-ray crystallography showed that the
## Abstract **Summary:** A new calix[4]arene‐based periodic mesoporous organosilica has been synthesized using tetraethoxysilane (TEOS) and a calix[4]arene‐based silane monomer as the precursors and cetyltrimethylammonium bromide (CTAB) surfactant as the structure‐directing template, and is shown t