This is an excerpt from the following book*1) as a memo of what I found interesting. Oxidation and reduction can proceed simultaneously in the same reaction field (on a photocatalyst), a characteristic unique to photocatalytic reactions that cannot be realized in other reaction systems.
When L-lysine, a kind of essential amino acid, is used as a raw material for photocatalytic reactions in aqueous solution in an oxygen-free atmosphere, pipecolic acid is generated. The photocatalytic synthesis of pipecolinic acid is the only synthetic pathway known to date that does not require any special reagents and does not produce any byproducts because the reaction involves redox reactions with excited electrons and holes.
The only photochemical reaction currently used for industrial production is probably the PNC method of ε-caprolactam synthesis by photo-nitrosation, developed by Toray Industries, Inc. ε-caprolactam is the raw material for 6-nylon, which is probably synthesized in hundreds of thousands of tons per year worldwide. Organic synthesis reactions using photocatalysis also have many basic advantages over other reactions, but in order to actually industrialize them, it is necessary to start from scratch, i.e., to create equipment that has never been used before.
*1) Mechanism Illustration: Photocatalyst at its Best by Mai Takashima and Fumiaki Otani, 2019, 1st printing, p68, 170

コメント
コメントを投稿