Visible light-driven photocatalytic benzoyl azides formation from benzotrichlorides using rhodium ion modified TiO2

Keita Shichijo, Hisashi Shimakoshi
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Abstract

Visible light-driven benzoyl azides formation catalyzed by a rhodium ion modified TiO2 (Rh3+/TiO2) is reported. The Rh3+/TiO2 was prepared as a visible light responsive photocatalyst by a simple procedure from TiO2 and RhCl3・3H2O. The Rh3+/TiO2 exhibited a broaden visible light absorption from 400 nm to 600 nm. Benzoyl azide formation from a benzotrichloride and a trimethylsilyl azide (TMS-N3) was performed catalyzed by the Rh3+/TiO2 under visible light irradiation (λ ≥ 420 nm) in air at room temperature. In this reaction, the benzotrichloride was effectively reduced by the single electron transfer (SET) from the Rh3+/TiO2, and the benzoyl azide was produced in 71% yield via the reaction between the benzoyl chloride and TMS-N3. In addition, several benzotrichloride derivatives were applied to this reaction and the corresponding benzoyl azide derivatives were formed in up to 71% yield. A kinetic analysis was also performed on these reactions, and it was suggested that the SET is the rate determining step in this reaction.

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铑离子修饰TiO2在可见光下催化苯并三氯化物生成苯甲酰叠氮化物
报道了铑离子修饰TiO2 (Rh3+/TiO2)在可见光下催化苯甲酰叠氮化物的生成。以TiO2和RhCl3 - 3H2O为原料,通过简单的工艺制备了Rh3+/TiO2作为可见光响应光催化剂。Rh3+/TiO2对可见光的吸收范围从400 nm扩大到600 nm。采用Rh3+/TiO2在可见光(λ≥420 nm)照射下,在室温条件下由苯并三氯和三甲基硅基叠氮化物(TMS-N3)催化生成苯甲酰叠氮化物。在该反应中,通过Rh3+/TiO2的单电子转移(SET),苯甲酰氯被有效还原,并通过苯甲酰氯与TMS-N3的反应,以71%的产率生成了苯甲酰叠氮化物。此外,在该反应中加入了几种苯并三氯衍生物,生成了相应的苯甲酰叠氮衍生物,收率高达71%。对这些反应进行了动力学分析,认为SET是该反应的速率决定步骤。
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