Mass spectrometric characterization of polyhedral oligosilsesquioxanes and heterosilsesquioxanes
β Scribed by Ray Bakhtiar; Frank J. Feher
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 142 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0951-4198
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β¦ Synopsis
Silsesquioxanes constitute a diverse range of Si-O frameworks with a wide variety of intriguing possibilities as models for catalysis. These topologically interesting molecules are formed by the hydrolytic condensation of trifunctional organosilanes. Heterosilsesquioxanes are formally derived by substitution of a main-group, transition-metal, or f-element atom for one or more Si atoms in a silsesquioxane. A number of silsesquioxanes and their metal-containing derivatives, metallasilsesquioxanes (Si-O-M), were characterized using atmospheric pressure chemical ionization (APCI) and turbo ion-spray (TISP) mass spectrometry. The use of n-hexane or n-hexane/ethanol (90:10, v/v) allowed the techniques to be utilized to characterize a large number of complexes. In some cases addition of trace amounts of ammonium acetate, sodium chloride, or sodium acetate to the ethanolic portion of the solvent allowed the detection of [M NH 4 ] or [M Na] ions.
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18-Hydroxy-11-deoxycorticosterone forms a non-polar dimer under acidic conditions. The dimer was purified by high performance liquid chromatography and further analysed by electrospray mass spectrometry. The purified dimer has a molecular weight of 656 Da with two free ketone groups and no free hydr