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Three carboxamidequinoline ligands were synthesized and their complexes with Eu 3+ were used for recognition and detection of organic/inorganic phosphates in water. The signal transduction process is based on an “On–Off–On” switch in the fluorescence signal utilizing changes in the intramolecular charge transfer (ICT). The fluorescence emission of ligands is quenched upon exposure to the Eu 3+ (Off signal). Following the addition of the phosphate analytes the ligand–Eu 3+ complex disassembles, which results in the regeneration of the original emission of the ligand (On signal). In general, the Eu 3+ complexes show higher affinity towards adenosine 5′-triphosphate (ATP) and lower affinity to other phosphates, namely adenosine 5′-diphosphate (ADP), adenosine 5′-monophosphate (AMP), pyrophosphate (H 2 P 2 O 7 2− , PPi), and dihydrogenphosphate (H 2 PO 4 − , Pi).
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Charge-Tagged DNA Radicals in the Gas Phase Characterized by UV/Vis Photodissociation Action Spectroscopy
Adenosine radicals tagged with a fixed-charge group were generated in the gas phase and structurally characterized by tandem mass spectrometry, deuterium labeling, and UV/Vis action spectroscopy. Experimental results in combination with Born–Oppenheimer molecular dynamics, ab initio, and excited-state calculations led to unambiguous assignment of adenosine radicals as N-7 hydrogen atom adducts. The chargetagged radicals were found to be electronically equivalent to natural DNA nucleoside radicals.
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- Award ID(s):
- 1951518
- PAR ID:
- 10225578
- Date Published:
- Journal Name:
- Angewandte Chemie
- Volume:
- 59
- ISSN:
- 0170-9046
- Page Range / eLocation ID:
- 7772-7772
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1002/ange.201916493
