New Organic Dyes from Phthalonitrile via Interesting Nucleophilic Reactions

Abstract

Phthalonitrile (PN) is regarded mostly as an important precursor for phthalocyanine (Pc). However, the presence of two ortho triple bonds also endow PN with significant potential to form novel conjugated systems. Based on several unexpected nucleophilic reactions, our group has discovered novel applications of PN for the synthesis of asymmetric benzo-fused aza-BOIDPYs and new fused-ring phthalorubines (Pr). This Synpacts highlights our recent advances in this field.

1 Introduction

2 Benzo-Fused Aza-BODIPYs

3 Phthalorubines

4 Conclusion

Key words

dyes - nucleophilic reactions - phthalonitrile - benzo-fused BODIPY - fused rings - phthalorubine

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