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用于在露天条件下选择性形成C-N键的功能化无金属碳纳米球催化剂

Functionalized Metal-Free Carbon Nanosphere Catalyst for the Selective C-N Bond Formation under Open-Air Conditions.

作者信息

Krishan Kumar, Swapna Bhattu, Chourasia Ankit Kumar, Sharma Chandra S, Sudarsanam Putla

机构信息

Department of Chemistry, Indian Institute of Technology Hyderabad, Kandi, Telangana 502284, India.

Department of Chemical Engineering, Indian Institute of Technology Hyderabad, Kandi, Telangana 502284, India.

出版信息

ACS Omega. 2024 Aug 8;9(33):35676-35685. doi: 10.1021/acsomega.4c03987. eCollection 2024 Aug 20.

Abstract

A versatile shape-controlled carbon nanomaterial that can efficiently catalyze the selective C-N coupling reactions under metal-free and open-air conditions was developed by applying N-doping and KOH activation strategies in candle soot (ANCS). The TEM and elemental mapping results showed the formation of sphere-shaped carbon particles as well as the uniform distribution of nitrogen species in the carbon framework. KOH activation enhanced the specific surface area of carbon, whereas N-doping enriched the electron-deficient nature by introducing functional N-based pyrrolic/graphitic structures in the carbon framework. The synergistic effect of N-doping and KOH activation significantly improved the catalytic efficiency of the carbon catalyst (ANCS), giving a 96% conversion of -phenylenediamine (OPD) with a good selectivity to 2-phenylbenzimidazole (97%). In contrast, the pristine carbon exhibited very low activity (48% conversion of the OPD and 36% selectivity to 2-phenylbenzimidazole). Besides, the ANCS nanomaterial provided a facile catalytic approach for the homo- and cross-C-N condensation of various aromatic amines and diamines to produce diverse functional imines and benzimidazoles at mild conditions. This work provided promising insights into developing advanced, metal-free carbon-based catalysts for selective C-N coupling reactions to produce valuable drug motifs.

摘要

通过在蜡烛烟灰(ANCS)中应用氮掺杂和KOH活化策略,开发了一种多功能形状可控的碳纳米材料,该材料能够在无金属和露天条件下高效催化选择性C-N偶联反应。透射电子显微镜(TEM)和元素映射结果表明形成了球形碳颗粒,并且氮物种在碳骨架中均匀分布。KOH活化提高了碳的比表面积,而氮掺杂通过在碳骨架中引入基于氮的吡咯/石墨功能结构,丰富了缺电子性质。氮掺杂和KOH活化的协同效应显著提高了碳催化剂(ANCS)的催化效率,对苯二胺(OPD)的转化率达到96%,对2-苯基苯并咪唑的选择性良好(97%)。相比之下,原始碳的活性非常低(OPD转化率为48%,对2-苯基苯并咪唑的选择性为36%)。此外,ANCS纳米材料为各种芳香胺和二胺的均相和交叉C-N缩合提供了一种简便的催化方法,可在温和条件下生成多种功能性亚胺和苯并咪唑。这项工作为开发用于选择性C-N偶联反应以生产有价值药物基序的先进无金属碳基催化剂提供了有前景的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecef/11339823/faadee19ee1e/ao4c03987_0001.jpg

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