Aza-BODIPY dyes with enhanced hydrophilicity

Author:

Kamkaew Anyanee1234,Burgess Kevin12345

Affiliation:

1. Department of Chemistry

2. Texas A&M University

3. College Station

4. USA

5. Department of Pharmacology

Abstract

Direct sulfonation of an aza-BODIPY dye gave products that were unstable relative to loss of the BF2 fragment, but hydrophilic fluors with peripheral cysteic acid groups were accessible.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Reference16 articles.

1. 156. 2 : 4-Diarylpyrroles. Part I. Synthesis of 2 : 4-diarylpyrroles and 2 : 2′ : 4 : 4′-tetra-arylazadipyrromethines

2. In Vitro Demonstration of the Heavy-Atom Effect for Photodynamic Therapy

3. A Modular Synthesis of Unsymmetrical Tetraarylazadipyrromethenes

4. Design and Synthesis of Alkyne-Substituted Boron in Dipyrromethene Frameworks

5. A. Loudet and K.Burgess, in Handbook of Porphyrin Science: With Applications to Chemistry, Physics, Materials Science, Engineering, Biology and Medicine, ed. K. Kadish, K. Smith and R. Guilard, World Scientific, 2010, p. 203

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