Literature DB >> 32598137

Amphiphilic Carbon Quantum Dots as a Bridge to a Pseudohomogeneous Catalyst for Selective Oxidative Cracking of Alkenes to Aldehydes: A Nonmetallic Oxidation System.

Leila Hadian-Dehkordi1, Aram Rezaei1, Ali Ramazani2, Mehdi Jaymand1, Hadi Samadian1, Lingxia Zheng3,4, Xiaolei Deng3,4, Huajun Zheng3,4.   

Abstract

The oxidative cleavage of alkenes to the corresponding aldehydes using new amphiphilic carbon quantum dots (A-CQDs) as a pseudohomogeneous carbocatalyst is achieved for the first time through green and sustainable chemical processes. In this work, we successfully design a recyclable pseudohomogeneous catalyst based on A-CQDs, which is decorated with 1-aminopropyl-3-methyl-imidazolium chloride and stearic acid. The functionalization is conducted to introduce a hydrophilic/hydrophobic functionality on the surface of the catalyst to achieve high catalyst availability in polar and nonpolar media with the green goal of eliminating organic (co)solvents and additives. This amphiphilic carbocatalyst provides high mass transferability to the biphasic system, which is beneficial to promoting the oxidative cracking of a variety of olefins into corresponding aldehydes with a substrate/A-CQD ratio of 150. Around 87% of the substrates are converted to the related aldehydes using the carbocatalyst in the presence of H2O2, in pure water, without using a phase-transfer catalyst or any additives and organic solvents, which is comparable with the current metal-based cleavage systems. Surprisingly, A-CQDs exhibit high catalytic activity for the scission of electron-deficient C═C bond of coumarin derivatives, accompanied by the cleavage of C-O bonds to produce the corresponding salicylaldehyde derivatives without overoxidation to acid. As a brief conclusion, A-CQDs exhibit high conversion efficiency without significant loss of activity even after six catalytic cycles. The conversion of alkenes into aldehydes is fast and high-throughput without overoxidation to acids and is accompanied by excellent solubility and stability in various solvents. Moreover, the product and the catalyst are recoverable from the reaction medium by simple extraction. So, this pseudohomogeneous carbocatalyst promises new horizons in imminent "catalytic age". All in all, this paper provides a significant and novel advancement in carbocatalyst chemistry.

Entities:  

Keywords:  alkene oxidative cleavage; amphiphilic carbon quantum dots; green chemistry; metal-free carbocatalyst; pseudohomogeneous catalyst

Year:  2020        PMID: 32598137     DOI: 10.1021/acsami.0c05025

Source DB:  PubMed          Journal:  ACS Appl Mater Interfaces        ISSN: 1944-8244            Impact factor:   9.229


  3 in total

1.  Ultrasound-assisted pseudohomogeneous tungstate catalyst for selective oxidation of alcohols to aldehydes.

Authors:  Aram Rezaei; Yasaman Mohammadi; Ali Ramazani; Huajun Zheng
Journal:  Sci Rep       Date:  2022-03-01       Impact factor: 4.379

2.  A pseudohomogeneous nanocarrier based on carbon quantum dots decorated with arginine as an efficient gene delivery vehicle.

Authors:  Aram Rezaei; Ehsan Hashemi
Journal:  Sci Rep       Date:  2021-07-02       Impact factor: 4.379

3.  Pseudohomogeneous metallic catalyst based on tungstate-decorated amphiphilic carbon quantum dots for selective oxidative scission of alkenes to aldehyde.

Authors:  Aram Rezaei; Leila Hadian-Dehkordi; Hadi Samadian; Mehdi Jaymand; Homa Targhan; Ali Ramazani; Hadi Adibi; Xiaolei Deng; Lingxia Zheng; Huajun Zheng
Journal:  Sci Rep       Date:  2021-02-24       Impact factor: 4.379

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.