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作 者:Ali Reza Kiasat Roya Mirzajani Fakhri Ataeian Mehdi Fallah-Mehrjardi
机构地区:[1]Chemistry Department,College of Science,Shahid Chamran University [2]Marine Chemistry Department,Khoramshahr Marine Science and Technology University
出 处:《Chinese Chemical Letters》2010年第9期1015-1019,共5页中国化学快报(英文版)
基 金:supports for this work by Shahid Chamran University Research Council
摘 要:Nanoparticles have properties that can be fine-tuned by their size as well as shape.Hence,there is significant current interest in preparing nano-materials of small size dispersity and to arrange them in close-packed aggregates.This letter describes a way of synthesising silver nanoparticles and their protection to aggregate by silica gel.The combination of catalytic quantities of immobilized silver nanoparticles with reductive ability of NaBH_4 efficiently reduces aromatic nitroarenes to the corresponding amines in aqueous medium.Noteworthy is that highly chemoselective reactions were achieved in the presence of other functional groups such as halogen and carboxylic acid groups.The silver particles immobilized on silica gel are stable in the presence of oxygen for several months.Nanoparticles have properties that can be fine-tuned by their size as well as shape.Hence,there is significant current interest in preparing nano-materials of small size dispersity and to arrange them in close-packed aggregates.This letter describes a way of synthesising silver nanoparticles and their protection to aggregate by silica gel.The combination of catalytic quantities of immobilized silver nanoparticles with reductive ability of NaBH_4 efficiently reduces aromatic nitroarenes to the corresponding amines in aqueous medium.Noteworthy is that highly chemoselective reactions were achieved in the presence of other functional groups such as halogen and carboxylic acid groups.The silver particles immobilized on silica gel are stable in the presence of oxygen for several months.
关 键 词:Silver nanoparticle REDUCTION Aromatic nitro compounds Aromatic amines Sodium borohydride
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