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Complexation of aromatic hydrocarbons with cyclotetrachromotropylene in aqueous solution

✍ 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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πŸ“œ SIMILAR VOLUMES


1H NMR study on the complexation of phen
✍ Bo-Long Poh; Cho Hoon Lim; Chi Ming Tan; Wai Mung Wong πŸ“‚ Article πŸ“… 1993 πŸ› Elsevier Science 🌐 French βš– 322 KB

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).

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✍ Poh Bo-Long; Ming Tan Chi πŸ“‚ Article πŸ“… 1994 πŸ› Elsevier Science 🌐 French βš– 486 KB

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

Room temperature phosphorescence of arom
✍ K. Kalyanasundaram; F. Grieser; J.K. Thomas πŸ“‚ Article πŸ“… 1977 πŸ› Elsevier Science 🌐 English βš– 451 KB

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