合成了纳米尺度氧化石墨烯(NGO)层,用作碳催化剂高效催化苄醇与芳香醛的氧化反应.对于醇氧化反应,当80℃时H2O2存在下,NGOs(20 wt％)可高效催化醇选择性生成醛,其反应速率和产率取决于醇上取代基的性质.对于4-硝基苄醇,反应24 h后,只有10％可转换为相应羧酸.相反,4-甲氧基苄醇和二苯基甲醇分别反应仅9和3h则可完全转化为对应的羧酸和酮.NGO碳催化剂上芳香醛氧化速率高于醇氧化速率.对于所有的醛,采用7 wt％ NGO作催化剂,在70℃反应2-3 h后,就可完全转化为相应羧酸.我们讨论了NGO催化剂结构对苄醇和芳香醛氧化反应影响的可能机理.
Nanoscale graphene oxide (NGO) sheets were synthesized and used as carbocatalysts for effective oxidation of benzylic alcohols and aromatic aldehydes.For oxidation of alcohols in the presence of H202 at 80 ℃,the NGOs (20％ mass fraction) as carbocatalysts showed selectivity toward aldehyde.The rate and yield of this reaction strongly depended on the nature of substituents on the alcohol.For 4-nitrobenzyl alcohol,＜10％ of it was converted into the corresponding carboxylic acid after 24 h.By contrast,4-methoxybenzyl alcohol and diphenylmethanol were completely converted into the corresponding carboxylic acid and ketone after only 9 and 3 h,respectively.The conversion rates for oxidation of aromatic aldehydes by NGO carbocatalysts were higher than those for alcohol oxidation.For all the aldehydes,complete conversion to the corresponding carboxylic acids was achieved using 7％ (mass fraction) of NGO at 70 ℃ within 2-3 h.Possible mechanisms for NGO carbocatalyst structure-dependent oxidation of benzyl alcohols and structure-independent oxidation of aromatic aldehydes are discussed.
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