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超声条件下,磺化还原氧化石墨烯催化酰肼与二氧化碳环化合成 1,3,4-噁二唑。

Sulfonated reduced graphene oxide catalyzed cyclization of hydrazides and carbon dioxide to 1,3,4-oxadiazoles under sonication.

机构信息

Department of Chemical Engineering, National Chung Hsing University, 250 KuoKuang Raod, Taichung, Taiwan, R.O.C.

Department of Chemical Engineering, National Chung Hsing University, 250 KuoKuang Raod, Taichung, Taiwan, R.O.C..

出版信息

Sci Rep. 2017 Jul 5;7(1):4675. doi: 10.1038/s41598-017-04143-4.

Abstract

Acid catalysts facilitate many chemical reactions. Sulfonated reduced grapheneoxide (rGOPhSOH) has shown to be an encouraging solid acid catalyst because of its efficiency, cost-effectiveness and safety of use. In this study, we prepared the rGOPhSOH nano acid catalyst, with the introduction of aromatic sulfonic acid radicals onto GO by fractional removal of oxygenated functions. It was thoroughly characterized by FT-IR, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy, energy dispersive spectroscopy (EDS) and solid state C MAS NMR (SSNMR). Here we report the conversion of CO (1.0 atm pressure, at = 50 °C, the source of C carbon feed stock) with hydrazides and a catalytic amount rGOPhSOH, which through a cyclization reaction results in a new strategy for the synthesis of 5-substituted-3H-[1,3,4]-oxadiazol-2-ones (SOxdOs) under ultrasonic irradiation. Hence this concept of cyclization opens up for new insights.

摘要

酸催化剂促进了许多化学反应。磺化还原氧化石墨烯(rGOPhSOH)因其高效、经济实惠且使用安全而被证明是一种有前途的固体酸催化剂。在这项研究中,我们通过部分去除含氧官能团,将芳基磺酸基团引入 GO 上,制备了 rGOPhSOH 纳米酸催化剂。通过傅里叶变换红外光谱(FT-IR)、X 射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、拉曼光谱、能谱(EDS)和固态 C MAS NMR(SSNMR)对其进行了全面表征。在这里,我们报告了在超声辐射下,CO(1.0 大气压,= 50°C,C 碳源)与酰肼的转化,以及催化量的 rGOPhSOH,通过环化反应,为合成 5-取代-3H-[1,3,4]-恶二唑-2-酮(SOxdOs)提供了一种新策略。因此,这种环化概念为新的见解开辟了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b4a/5498654/95e7a8beaf71/41598_2017_4143_Fig1_HTML.jpg

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