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2000
Volume 28, Issue 17
  • ISSN: 1385-2728
  • E-ISSN: 1875-5348

Abstract

A luminescent calix[5]arene with a covalently linked dansyl chromophore substituent has been successfully used, both in solution and in the gas phase (ESI-MS), for the recognition of biogenic amines that contain linear alkylammonium structural unit. Binding constant values, determined by fluorescence spectroscopy, revealed a greater affinity for cadaverine, spermidine, and L-lysine, in which the terminal ammonium group allows for additional stabilizing interactions with the dansyl moiety.

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/content/journals/coc/10.2174/0113852728313438240429052927
2024-10-01
2024-12-29
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