Determination of alkali metal ion binding selectivities of calixarenes by matrix-assisted laser desorption ionization and electrospray ionization in a quadrupole ion trap

被引:52
作者
Goolsby, BJ
Brodbelt, JS [1 ]
Adou, E
Blanda, M
机构
[1] Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
[2] SW Texas State Univ, Dept Chem, San Marcos, TX 78666 USA
基金
美国国家科学基金会;
关键词
MALDI; electrospray ionization; calixarene; quadrupole ion trap; binding selectivity;
D O I
10.1016/S1387-3806(99)00163-3
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) and electrospray ionization mass spectrometry (ESI-MS) are used to evaluate the alkali metal ion binding selectivities of a series of calixarenes. Each calixarene of interest is mixed with one or more alkali metal salts (1:100 ratio of calixarene to metal), either in the: ESI solution or on the MALDI probe surface, and the relative binding selectivities are directly determined from the intensities of the calixarene/metal complexes in the mass spectra. For t-butylcalix[4]arene-tetraacetic acid tetraethyl ester (calixarene 1), complexation of Na+ is favored over complexation of K+, in agreement with prior solution results obtained by conventional methods. For the three calixarenes that do not have t-butyl groups on the upper rims, the calixarenes preferentially bind K+ over Na+, thus demonstrating that size selective complexation can be probed with both the ESI and MALDI methods. Collision-activated dissociation results indicate that the phenyl oxygens, but not necessarily the ethoxy ethyl oxygens of the lower rims, are the primary binding sites for the alkali metal ions. (C) 1999 Elsevier Science B.V.
引用
收藏
页码:197 / 204
页数:8
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