1999
DOI: 10.1016/s0021-9673(99)00444-6
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Macrocyclic polyamine as a selective modifier in a bonded-phase capillary column for the electrophoretic separation of aromatic acids

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Cited by 26 publications
(9 citation statements)
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References 27 publications
(21 reference statements)
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“…Thus, there is a need to improve the reproducibility of migration times for analytes by CE. For this purpose, capillary walls have been modifi ed by applying a sulfonated polymer [12] or noncovalent anionic polymer [13], and by covalently linking a macrocyclic polyamine [14] or sulfonated groups [15,16]. Better 1 3 reproducibility in CE can be achieved by the relatively constant EOF.…”
Section: Introductionmentioning
confidence: 99%
“…Thus, there is a need to improve the reproducibility of migration times for analytes by CE. For this purpose, capillary walls have been modifi ed by applying a sulfonated polymer [12] or noncovalent anionic polymer [13], and by covalently linking a macrocyclic polyamine [14] or sulfonated groups [15,16]. Better 1 3 reproducibility in CE can be achieved by the relatively constant EOF.…”
Section: Introductionmentioning
confidence: 99%
“…We have demonstrated that 24-and 28-membered macrocyclic polyamines are highly selective as the receptor for anions such as oxyanions, polycarboxylates and polyphosphates in the CEC separation [27][28][29][30][31][32][33][34][35]. This highly selective property has been attributed to anion coordination, anion exchange, and reversal of the EOF provided by the wall-bonded functional groups.…”
Section: Introductionmentioning
confidence: 99%
“…4A). and (Ph) 4 As + mixture, it was found that increasing the applied voltage from 0, −10, −15, −20 and −25 kV, a better resolution and higher intensity was obtained. Meanwhile faster mobility was indicated, except for the positive ion, (Ph) 4 As + .…”
Section: Sample Injectionmentioning
confidence: 96%
“…The interaction between analyte and the bonded phase was expected to be predominantly anion complexation [3,4]. Taking account of having higher fraction of protonated bonded phase and higher effective charge of the analyte, pH value of the background electrolyte was kept at 6.0-6.5.…”
Section: Nature Of the Electrolyte Buffermentioning
confidence: 99%
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