Artifact-free matrix-assisted laser desorption ionization time-of-flight mass spectra of tert.-butyldimethylsilyl ether derivatives of cyclodextrins used for the synthesis of single-isomer, chiral resolving agents for capillary electrophoresis

Artifact-free, high-resolution matrix-assisted laser desorption ionization (MALDI) time-of-flight mass spectra have been obtained for the labile, sing le-isomer, tert.-butyldimethylsilyl ether derivatives of alpha-, beta- and gamma -cyclodextrins by optimizing the MALDI sample preparation method. 2,5 -Dihydroxybenzoic acid, a 3:1 mixture of 2,5-dihydroxybenzoic acid and 1-hy droxyisoquinoline, and 2,4,6-trihydroxyacetophenone were investigated as MA LDI matrices with methanol and acetonitrile as matrix solvents. Partial-to- complete loss of the tert.-butyldimethylsilyl groups was observed when the commonly used 3,5-dihydroxybenzoic acid was the MALDI matrix and/or methano l was the solvent, both with and without trifluoroacetic acid as additive. Loss of the labile tert.-butyldimethylsilyl groups was avoided with 2,4,6-t rihydroxyacetophenone as MALDI matrix and acetonitrile as matrix solvent. G ood ion intensities were achieved for the (M+Na)(+) and (M+K)(+) quasimolec ular ions in the positive-ion mode. Minor byproducts were observed in some of the samples and the information was used to aid the optimization of the synthetic work. (C) 2001 Elsevier Science B.V. All rights reserved.