The new preparative synthesis and the characterisation of l',l'-dibromo-1,2-methano[60]fullerene l a using a Seyferth reagent and the mass spectrometric evidence of the novel dumb-bell shaped molecular carbon allotropes C121 2 and ClZ2 3 obtained via a proposed intermediate C&: carbene generated from l a are reported.
An experimental comparison of product ion spectra produced by matrix-assisted laser desorption/ionization (MALDI) and electrospray ion-trap MS( n) for a group of small drug molecules is presented in this paper. The goal of the study was to demonstrate the usefulness of MALDI-MS with post-source decay (PSD) and collision-induced dissociation (CID) for the structural analysis of small drug molecules in the drug discovery process, where traditionally electrospray LC/MS methods are used. PSD and PSD/CID gave diverse product ions that were highly indicative of the structure of the drugs investigated (a group of 4-quinolone antibiotics and oleandomycin). In addition, the number of different product ions generated with MALDI-MS was always higher than with electrospray ion-trap MS( n) (with n < or =4) for the drug molecules studied. This investigation also showed that the choice of a suitable MALDI matrix for the analysis of low molecular weight compounds is quite important. It was found that of the three matrices examined, alpha-cyano-4-hydroxycinnamic acid (alpha-CHCA) produced the most intense fragmentation levels while TiO2, with its advantage of virtually no low mass background signals, did not generate quite the same amount of information.
Due to their octahedral symmetry, otherwise not available for carbon based chemistry, hypervalent sulfur fluorides are very attractive as structural building blocks for functional organic materials. Direct fluorination offers a convenient access to multigram quantities of highly stable bis(4-nitrophenyl)tetrafluorosulfurane. Guided by molecular modeling, a novel catalytic process was devised to isomerize the predominantly formed cis isomer to the pure trans isomer.
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