Ordered Mesoporous Carbon Nitrides with Tuneable Nitrogen Contents and Basicity for Knoevenagel Condensation

Knoevenagel冷凝 催化作用 丙二腈 介孔材料 化学 煅烧 三嗪 碳纤维 有机化学 无机化学 高分子化学 材料科学 复合数 复合材料
作者
Sujanya Maria Ruban,C. I. Sathish,Kavitha Ramadass,Stalin Joseph,Sungho Kim,Venkata D. B. C. Dasireddy,In Young Kim,Ala’a H. Al‐Muhtaseb,Yoshihiro Sugi,Ajayan Vinu
出处
期刊:Chemcatchem [Wiley]
卷期号:13 (1): 468-474 被引量:30
标识
DOI:10.1002/cctc.202001434
摘要

Abstract We report on the preparation of ordered mesoporous carbon nitrides (MCN) with a 3D porous structure, tuneable nitrogen contents and basicity and their basic catalytic activities on the Knoevenagel condensation of benzaldehyde with malononitrile. The chemical structure and the nitrogen contents of the materials are finely tuned with the simple adjustment of the calcination temperature from 350 to 550 °C. The samples prepared at 350 and 400 °C exhibit C 3 N 5 structures with 1‐amino/imino‐1,2,4‐triazole moieties, whereas the samples synthesised at 450, 500, and 550 °C possess C 3 N 4 structures with 2‐amino/imino‐1,3,5‐triazine moieties. The materials prepared at the temperature lower than 400 °C show much higher activity than those of the samples prepared at 450, 500 and 550 °C. The change in the catalytic activities of these materials is linked with the change of the structure, nitrogen contents and the functional groups on the surface of the materials prepared at different temperatures. CO 2 temperature programme desorption study reveals that 1‐amino/imino‐1,2,4‐triazole moieties in C 3 N 5 samples provide high basicity due to the strain in 5‐membered 1,2,4‐triazole rings; however, the samples with 1,3,5‐triazine moieties have limited basicity which significantly affects the catalytic activity of the material. The optimised C 3 N 5 catalyst shows an enhanced catalytic activity when compared to other mesoporous basic catalysts and C 3 N 4 . It is also found that the optimised catalysts are highly stable and can be recycled several times and no major change in the activity is observed.
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