Alam Al-Mahmnur, Shon Young-Seok
Department of Chemistry and Biochemistry and the Keck Energy and Materials Program (KEMP), California State University, Long Beach, Long Beach, California 90840, United States.
ACS Appl Nano Mater. 2021 Apr 23;4(4):3294-3318. doi: 10.1021/acsanm.1c00335. Epub 2021 Apr 13.
This article recaps a variety of interesting catalytic studies based on solubilized and freely movable noble metal nanoparticle catalysts employed for organic reactions in either pure water or water-organic biphasic systems. Small organic ligand-capped metal nanoparticles are fundamentally attractive materials due to their enormous potential as a well-defined system that can provide spatial control near active catalytic sites. The nanoparticle catalysts are first grouped based on the synthetic method (direct reduction, phase transfer, and redispersion) and then again based on the type of reaction such as alkene hydrogenation, arene hydrogenation, nitroaromatic reduction, carbon-carbon coupling reactions, etc. The impacts of various ligands on the catalytic activity and selectivity of semi-heterogeneous nanoparticles in water are discussed in detail. The catalytic systems using polymers, dendrimers, and ionic liquids as supporting or protecting materials are excluded from the subject of this review.
本文概述了一系列有趣的催化研究,这些研究基于用于纯水或水-有机双相体系中有机反应的可溶解且可自由移动的贵金属纳米颗粒催化剂。带有小有机配体的金属纳米颗粒是极具吸引力的材料,因为它们作为一种定义明确的体系具有巨大潜力,能够在活性催化位点附近提供空间控制。纳米颗粒催化剂首先根据合成方法(直接还原、相转移和再分散)进行分类,然后再根据反应类型如烯烃氢化、芳烃氢化、硝基芳烃还原、碳-碳偶联反应等进行分类。详细讨论了各种配体对水中半均相纳米颗粒催化活性和选择性的影响。本综述主题不包括使用聚合物、树枝状大分子和离子液体作为支撑或保护材料的催化体系。