Crystal structure of the 1:1 complex of heptakis(2,3,6-tri-O-methyl)cyclomaltoheptaose (permethylated β-cyclodextrin) with ethyl laurate
✍ Scribed by Dimitri Mentzafos; Irene M. Mavridis; Henk Schenk
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 714 KB
- Volume
- 253
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
✦ Synopsis
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 absence of intramolecular hydrogen bonds and are stacked in a head-to-tail mode to form channels parallel to the b axis of the crystal. In the interior of the channel, the guest molecules are acconunodated in extended conformation. fro water molecules have been located near the secondary rim of each TM-@CD molecule, forming hydrogen bonds with the oxygen atoms of the' guest.
📜 SIMILAR VOLUMES
Acylated ]3-o-xylopyranose derivatives are known to exist as a mixture of the 1C 4 and 4C I conformers in rapid equilibrium in solution [3]. Several conformations have also been reported for/3-D-xylopyranose derivatives in the solid state [4]. In the course of our study to investigate the functions
## Abstract The inclusion complex of heptakis(2,6‐di‐__O__‐methyl)‐β‐cyclodextrin (DIMEB) with euplotin C (EC), a cytotoxic metabolite isolated from the protistan strains composing the marine ciliate __Euplotes crassus,__ has been investigated by ^1^H NMR techniques, electrospray ionization mass sp
The title compound, C28H27O5, is triclinic, space group P1 with unit cell dimensions a = 12.763(2), b = 11.130(2), c = 4.764(3) A, alpha = 73.78(3), beta = 82.89(3), gamma = 62.16(1) degrees, V = 574.8(4) A3, and Z = 1. The pyranose ring has an 4H5 conformation with some flattening at C-4. Molecular