4.8 Article

Switching of C-C and C-N Coupling/Cleavage for Hypersensitive Detection of Cu2+ by a Catalytically Mediated 2-Aminoimidazolyl-Tailored Six-Membered Rhodamine Probe

Journal

ORGANIC LETTERS
Volume 22, Issue 21, Pages 8234-8239

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c02814

Keywords

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Funding

  1. National Natural Science Foundation of China [21702037, 21662009, 31860516, 21877021]
  2. Research Project of the Ministry of Education of China [20135201110005, 213033A]
  3. Key Technologies RD Program [2014BAD23B01]
  4. Guizhou Provincial ST Program [[2017]5788]
  5. Program of Introducing Talents of Discipline to Universities of China (111 Program) [D20023]

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A robust six-membered rhodamine spirocyclic probe 1 containing a versatile 2-aminoimidazolyl moiety was elaborately designed and synthesized via an attractive C-C and C-N coupling strategy to improve the performance in the detection of ultralow transition metal ions. Probe 1 allowed the highly hypersensitive detection of Cu2+ with a superior picomolar limit of detection (35 pM) and nanomolar naked-eye performance (80 nM) via the switching of C-C and C-N cleavage by a catalytic hydrolysis mode.

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