Novel Synthetic Approach towards Amino‐Substituted Polycyclic Aromatic Hydrocarbons through Electrocyclization of Keteniminium Salts

Author:

Yoshimura Masahiko12ORCID,Quinodoz Pierre3ORCID,Reyes Méndez Lucía3,Kolleth Amandine3,Sulzer‐Mossé Sarah3,Vent‐Schmidt Thomas4,Karadeniz Yezer Ulfet5,Catak Saron5ORCID,De Mesmaeker Alain3ORCID

Affiliation:

1. Kyoto University iCeMS, Yoshida Ushinomiya-cho, Sakyo-ku Kyoto 606-8501 Japan

2. Laboratorium für Organische Chemie Department of Chemistry and Applied Biosciences ETH Zürich CH-8093 Zürich Switzerland

3. Syngenta Crop Protection AG Chemical Research Schaffhauserstrasse 101 CH-4332 Stein Switzerland

4. Syngenta Crop Protection AG Syngenta Chemical Development Breitenloh 5 CH-4333 Münchwilen Switzerland

5. Bogazici University Department of Chemistry Bebek 34342 Istanbul Turkey

Abstract

AbstractPolycyclic aromatic hydrocarbons (PAHs) are an important family of molecules in science and technology. Amino‐substituted PAHs are promising building blocks to create attractive molecules for materials science. However, the synthetic limitations have hampered to produce diverse structures of amino‐substituted PAHs. Here we describe a novel efficient synthetic method to access amino‐substituted PAHs through the electrocyclization of highly reactive keteniminium species. We demonstrated the synthesis of various amino‐substituted PAHs and disclosed some of their photophysical properties. Furthermore, combination with theoretical calculation revealed that the multiple electrocyclization reactions of keteniminium species is a stepwise process and the fusion of additional aromatic ring to the substrate accelerates the electrocyclization.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

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