Unknown

Dataset Information

0

Bifunctional Mesoporous Carbon Nitride: Highly Efficient Enzyme-like Catalyst for One-pot Deacetalization-Knoevenagel Reaction.


ABSTRACT: Recently, mesoporous carbon nitride (MCN) has aroused extensive interest for its potential applications in organocatalysis, photo- and electrochemistry and CO2 capture. However, further surface functionalization of MCN for advanced nanomaterials and catalysis still remains very challenging. Here we show that acidic carboxyl groups can be smoothly introduced onto the surface of well-ordered MCN without annihilation between the introduced acid groups and MCN's inherent basic groups through a facile UV light oxidation method. The functionalization generates a novel bifunctional nanocatalyst which offers an enzyme-like catalytic performance in the one-pot deacetalization-Knoevenagel reaction of benzaldehyde dimethylacetal and malononitrile with 100% conversion and more than 99% selectivity due to the cooperative catalysis between the acid and base groups separated on the surface of the catalyst. The results provide a general method to create multifunctional nanomaterials and open new opportunities for the development of high efficient catalyst for green organic synthesis.

SUBMITTER: Zhong L 

PROVIDER: S-EPMC4525375 | biostudies-literature | 2015 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Bifunctional Mesoporous Carbon Nitride: Highly Efficient Enzyme-like Catalyst for One-pot Deacetalization-Knoevenagel Reaction.

Zhong Lin L   Anand Chokkalingam C   Lakhi Kripal Singh KS   Lawrence Geoffrey G   Vinu Ajayan A  

Scientific reports 20150805


Recently, mesoporous carbon nitride (MCN) has aroused extensive interest for its potential applications in organocatalysis, photo- and electrochemistry and CO2 capture. However, further surface functionalization of MCN for advanced nanomaterials and catalysis still remains very challenging. Here we show that acidic carboxyl groups can be smoothly introduced onto the surface of well-ordered MCN without annihilation between the introduced acid groups and MCN's inherent basic groups through a facil  ...[more]

Similar Datasets

| S-EPMC6824099 | biostudies-literature
| S-EPMC8434330 | biostudies-literature
| S-EPMC3896229 | biostudies-literature
| S-EPMC10511422 | biostudies-literature
| S-EPMC5943943 | biostudies-literature
| S-EPMC6026460 | biostudies-literature
| S-EPMC8492782 | biostudies-literature
| S-EPMC9476541 | biostudies-literature
| S-EPMC9494687 | biostudies-literature
| S-EPMC9323834 | biostudies-literature