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Development of fluorescent probes based on protection-deprotection of the key functional groups for biological imaging

Journal

CHEMICAL SOCIETY REVIEWS
Volume 44, Issue 15, Pages 5003-5015

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cs00103j

Keywords

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Funding

  1. NSFC [21172063, 21472067]
  2. University of Jinan
  3. National Creative Research Initiative programs of the National Research Foundation of Korea (NRF) - Korean government (MSIP) [2012R1A3A2048814]

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Recently, the strategy of protection-deprotection of functional groups has been widely employed to design fluorescent probes, as the protection-deprotection of functional groups often induces a marked change in electronic properties. Significant advances have been made in the development of analyte-responsive fluorescent probes based on the protection-deprotection strategy. In this tutorial review, we highlight the representative examples of small-molecule based fluorescent probes for bioimaging, which are operated via the protection-deprotection of key functional groups such as aldehyde, hydroxyl, and amino functional groups reported from 2010 to 2014. The discussion includes the general protection-deprotection methods for aldehyde, hydroxyl, or amino groups, as well as the design strategies, sensing mechanisms, and deprotection modes of the representative fluorescent imaging probes applied to bio-imaging.

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