Photocatalytic oxidative-coupling of 5-amino-1H-tetrazole for the synthesis of 5,5′-azotetrazolate energetic salts at mild conditions

被引:5
|
作者
Huang, Ji [1 ]
Du, Jinyan [1 ]
Wu, Bo [1 ]
Wang, Jun [1 ]
Yang, Long [1 ]
Zhou, Yong [2 ]
Dong, Faqin [1 ]
Wu, Yuting [1 ]
Li, Jie [1 ]
Sun, Xue [4 ]
Liu, Kun [3 ]
Yang, Dingming [1 ]
He, Huichao [1 ]
机构
[1] Southwest Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Sichuan, Peoples R China
[2] Nanjing Univ, Ecomat & Renewable Energy Res Ctr, Sch Phys, Nanjing 211102, Peoples R China
[3] Chongqing Res Acad Environm Sci, Chongqing 401147, Peoples R China
[4] Aux Air Conditioning Co Ltd, Qual Ctr, Ningbo 315000, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxidative-coupling; 5,5 '-azotetrazolate; g-C3N4; Photocatalysis; HETEROGENEOUS PHOTOCATALYSTS; DERIVATIVES; THIOUREA;
D O I
10.1016/j.catcom.2019.105923
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The conventional approach of 5-amino-1H-tetrazole (5AT) oxidative-coupling into 5,5'-azotetrazolate salts are confronted with several issues, including high energy consumption, insufficient security and inconvenient purification. A green photocatalytic method was demonstrated for the first time to achieve the selective oxidative-coupling of 5AT into 5,5'-azotetrazolate at mild conditions using g-C3N4. The oxidative-coupling of 5AT into 5,5'-azotetrazolate was mainly initiated by the photogenerated holes of g-C3N4, but center dot O-2(-) and center dot OH played important role in the activation of 5AT through capturing single hydrogen from the its amino. Under natural solar irradiation, the scaling-up photocatalytic synthesis of 5,5'-azotetrazolate energetic salt can be conveniently conducted.
引用
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页数:4
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