Mass spectrometry studies on the complexation of several organometallic complexes by α- and β-cyclodextrins
✍ Scribed by R. Bakhtiar; A. E. Kaifer
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 87 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0951-4198
No coin nor oath required. For personal study only.
✦ Synopsis
The complexation of ferrocene and several ferrocene derivatives with the hosts a-cyclodextrin (a-CD) and b-cyclodextrin (b-CD) was investigated by electrospray mass spectrometry. A 2:1 complex was detected between a-CD and ferrocene while a 1:1 complex was observed with b-CD and this organometallic guest. All the remaining ferrocene derivatives surveyed in this work exhibited mass spectrometry signals corresponding to 1:1 complexes with either host. In contrast to previous electrochemical and proton NMR spectroscopic studies, no evidence was found for ternary or quaternary complexes in these host-guest systems. These results demonstrate for the first time that complexes between cyclodextrins and organometallic compounds are detected in the gas phase.
📜 SIMILAR VOLUMES
Naturally occurring nucleosides and nucleobases form inclusion complexes with b-cyclodextrin. These host-guest complexes could be detected by fast atom bombardment mass spectrometry. The collision-induced dissociation spectra of the protonated complexes showed mainly ions related to the guest molecu
The multicomponent non-covalent associations of fbcyclodextrin (p-CD)-drug host-guest complexes with appropriate molecules are of current interest to the pharmaceutical industry, as they can increase dramatically the solubility in water of scarcely soluble guest drugs. The present study by ionspray
The particle beam liquid chromatography/mass spectrometry (PB LC/MS) characterization of diphosphine-substituted selenido iron and ruthenium clusters is reported. The clusters considered result from the reaction between the diphosphine diselenides (Ph 2 PSe) 2 R [R = CH 2 , dppmSe 2 ; R = CH 2 CH 2
The formation of complexes and the mode of binding to macrocyclic host molecules (a-and bcyclodextrins, CDs) of the nootropic drug CI-844 (3-phenoxypyridine sulphate, Warner-Lambert/Parke-Davis) were studied using NMR techniques (T-ROESY) complemented by molecular dynamics (MD) protocols which allow