The inclusion complex formation of a water-soluble beta(1)-selective adrenoreceptor antagonist Metoprolol (Met) with alpha-cyclodextrin (alpha-CyD), beta-cyclodextrin (beta-CyD), gamma-cyclodextrin (gamma-CyD), and 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CyD) in aqueous solution was studied by ul
Synthesis and Spectroscopic Characterizations of an Insulinomimetic Peroxovanadate Complex in Aqueous Solution
โ Scribed by Shu-Hui Cai; Xian-Yong Yu; Zhong Chen; Hui-Lin Wan
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 417 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0256-7660
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract The structure of inclusion complexes of ฮณโcyclodextrin (ฮณโCD), (โ)โgallocatechin gallate (GCg), and (โ)โepigallocatechin gallate (EGCg) in D~2~O was investigated using several NMR techniques. GCg formed a 1:1 inclusion complex with ฮณโCD in which the A and C rings of GCg were inserted de
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
We present additional spectroscopic evidence for the formation of low-barrier hydrogen bonds (LBHBs) within vicinal and geminal dicarboxylic acid monoanions. Hydrogen ciscyclohexane 1,2-dicarboxylate, displays low-field 1 H NMR signals in aprotic solvents at 19.3 to 19.7 ppm, depending on the solven