The Comparison of the Orientation of Sodium 3-Hydroxy-2-Naphthalenecarboxylate in the Cavity ofβ-Cyclodextrin and Heptakis-(2,3,6-Tri-O-Methyl)-β-Cyclodextrin
✍ Scribed by Zheng-Ping Yi; Jun Hu; Hui-Lan Chen
- Book ID
- 110432620
- Publisher
- Springer Netherlands
- Year
- 2003
- Tongue
- English
- Weight
- 124 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0923-0750
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The complexation of three guests containing 4,4'-bipyridinium redoxactive residues by p-cyclodextrin (p-CD) and its heptakis-(2,6-O-dimethyl) analogue (DM-b-CD) was investigated by means of voltammetric techniques. The three 4,4'-bipyridinium (viologen) derivatives used as guests were designed to be
The crystal of the 1: 1 complex of ethyl laurate with heptakis(2,3,6-tri-0-methyl)cyclomaltoheptaose (ThI-@CD, permethyIated &cyclodextrin) is orthorombic, P&2,2,, with a = 14.796(Z), b m 22.444(6), c = 27.720@) A; V = 9~5(4) k3; and Z = 4. The macrocycles have a distorted ~nfo~ation due to the abse