The stability constants I( of the 1:l host to guest complexes formed between eight phenols and the cyclis tetramer, cyclotetr chromotropylene, 't in an aqueous solution at pD 7.0 at 25 C were determined b H nmr spectroscopy. They vary from -0 (p-sodium sulfonatophenol) to 400 M \_y (pnitrophenol).
Complexation of aromatic hydrocarbons with cyclotetrachromotropylene in aqueous solution
β Scribed by Bo-Long Poh; Leeng-Sze Koay
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 138 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
The stability constants K of the 1:l host to guest complexes formed between the cyclic tetramer, cyclotetrachromotropytene, and amino acids in water atpD 7.0 and 25' C were determined by H nmr spectroscopy. The results indicate that the interactions between the aromatic u-bonds of the host and the C
The phosphorescence spectra of several simple arenes, pyrene, naphthahne, biphenyl and their bfiminated derivatives have been observed in aqueous micellar solutions at room temperature. The success of these experiments is due to the protective screening of the arene triplet state by solubilization i