4.5 Article

Soluble and Stable Near-Infrared Dyes Based on Polycyclic Aromatics

Journal

CURRENT ORGANIC CHEMISTRY
Volume 14, Issue 18, Pages 2145-2168

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138527210793351616

Keywords

Near-infrared dye; polycyclic aromatic hydrocarbon; rylene; porphyrin; phthalocyanine

Funding

  1. Singapore DSTA DIRP [DSTA-NUS-DIRP/2008/03]
  2. NUS [R-143-000-356-101]
  3. NRF

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Currently, how to obtain near-infrared (NIR) dyes is intriguing and attractive but full of challenges. Although some cyanine dyes have been commercialized, near infrared dyes with intensive NIR absorption and/or emission, good chemical and photo-stability, and high solubility still remain as challenging targets. Certain polycyclic aromatic compounds such as rylenes, porphyrins, and phthalocyanines represent a key class of near-infrared dyes and also give rise to outstanding physical and chemical properties after appropriate chemical modification. This review highlights and updates the principal synthetic strategies used to obtain polycyclic aromatics-based soluble and stable near-infrared dyes. We will also summarize the physical properties of these newly developed NIR dyes, including absorption, emission, quantum yield, solubility and stability.

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