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首页> 外文期刊>Journal of mass spectrometry: JMS >ESI activity of Br-, BF4-, ClO4 (-) and BPh4- anions in the presence of Li+ and NBu4+ counter-ions
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ESI activity of Br-, BF4-, ClO4 (-) and BPh4- anions in the presence of Li+ and NBu4+ counter-ions

机译:在Li+和NBu4+反离子存在下,Br-、BF4-、ClO4(-)和BPh4-阴离子的ESI活性

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摘要

To improve our understanding of the electrospray ionization (ESI) process, we have subjected equimolar mixtures of salts A(+) X- (A(+) = Li+, NBu4+; X-= Br (-), ClO4-, BF4-, BPh4-))in different solvents (CH3CN, tetrahydrofuran, CH3OH, H2O) to negative-ion mode ESI and analyzed the relative ESI activity of the different anionic model analytes. The ESI activity of the large and hydrophobic BPh(4)(-)ion greatly exceeds that of the smaller and more hydrophilic anions Br-, ClO4- and BF4-, which we ascribe to its higher surface activity. Moreover, the ESI activity of the anions is modulated by the action of the counter-ions and their different tendency toward ion pairing. The tendency toward ion pairing can be reduced by the addition of the chelating ligands 12-crown-4 and 2.2.1 cryptand and is, although to a smaller degree, further influenced by the variation of the solvent. Complementary electrical conductivity measurements afford additional information on the interactions of the ionic constituents of the sample solutions. Copyright (C) 2017 John Wiley Sons, Ltd.
机译:为了提高我们对电喷雾电离 (ESI) 过程的理解,我们进行了等摩尔盐 A(+) X- (A(+) = Li+, NBu4+;X-= Br (-), ClO4-, BF4-, BPh4-))在不同溶剂(CH3CN、四氢呋喃、CH3OH、H2O)中对负离子模式ESI进行分析,并分析了不同阴离子模型分析物的相对ESI活性。大而疏水的BPh(4)(-)离子的ESI活性大大超过更小和更亲水的阴离子Br-、ClO4-和BF4-,我们将其归因于其更高的表面活性。此外,阴离子的ESI活性受到反离子的作用及其不同的离子对趋势的调节。通过添加螯合配体 12-crown-4 和 2.2.1 cryptand 可以减少离子配对的趋势,并且尽管程度较小,但受溶剂变化的进一步影响。互补电导率测量提供了有关样品溶液中离子成分相互作用的额外信息。版权所有 (C) 2017 John Wiley & Sons, Ltd.

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