Fluorescent chemosensors based on spiroring-opening of xanthenes and related derivatives

  • Xiaoqiang Chen
  • , Tuhin Pradhan
  • , Fang Wang
  • , Jong Seung Kim*
  • , Juyoung Yoon
  • *Corresponding author for this work

    Research output: Contribution to journalReview articlepeer-review

    Abstract

    Different xanthene derivatives according to their analytes with mechanistic schemes published from 1997 to February 2011 are introduced. Kim and co-workers reported the design and synthesis of a new rhodamine-based derivative, bearing an N-butyl-1,8-naphthalimide group. Huang's and Li's groups reported a rhodamine B derivative, containing a highly electron-rich S atom as a fluorescence turn-on chemodosimeter for Cu 2+ in an aqueous medium. Peng et al. reported a rhodamine-based chemodosimeter, via a mechanism of Hg 2+-promoted hydrolysis. Lin et al. presented a rhodamine-based probe, composed of a sulfur atom and an alkyne moiety for the irreversible detection of Hg 2+. Shang et al. synthesized molecule, composed of a fluorescein fluorophore and a rhodamine B hydrazide linked together by a thiourea spacer. Nagano and co-workers have synthesized a series of symmetric and asymmetric rhodamine derivatives,using rhodamine as scaffolds.

    Original languageEnglish
    Pages (from-to)1910-1956
    Number of pages47
    JournalChemical reviews
    Volume112
    Issue number3
    DOIs
    Publication statusPublished - 2012 Mar 14

    ASJC Scopus subject areas

    • General Chemistry

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