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选择性还原氧化石墨烯(英文) 被引量:19
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作者 徐超 员汝胜 汪信 《新型炭材料》 SCIE EI CAS CSCD 北大核心 2014年第1期61-66,共6页
还原氧化石墨烯已被广泛用于制备基于石墨烯的材料。目前,还原处理方法均是尽可能地将氧化石墨烯中的功能团去除,恢复石墨烯的电子结构。由于氧化石墨烯中氧基功能团(如羟基、羧基及环氧基)不同的反应活性,氧化石墨烯是可能通过分步的... 还原氧化石墨烯已被广泛用于制备基于石墨烯的材料。目前,还原处理方法均是尽可能地将氧化石墨烯中的功能团去除,恢复石墨烯的电子结构。由于氧化石墨烯中氧基功能团(如羟基、羧基及环氧基)不同的反应活性,氧化石墨烯是可能通过分步的方法进行还原。利用醇溶剂如乙醇、乙二醇、丙三醇还原氧化石墨烯,并采用不同分析手段对样品进行表征。结果发现,在一定条件下这些醇可选择性地还原氧化石墨烯。经这些醇的处理后,氧化石墨烯中环氧功能团被大部分去除,而其他的功能团如羟基和羧基仍被保留。这种选择性去除氧化石墨烯表面功能团的方法可利于有效地控制氧化石墨烯的还原程度、获得具有特定功能团的石墨烯衍生物,从而扩大这类材料的使用范围。 展开更多
关键词 氧化石墨烯 氧化功能团 选择性还原
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Electrolytic reduction of Nantong coal and model compounds with oxygenic functional groups in an aqueous NaCl solution 被引量:1
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作者 ZHAO Wei YAO Li-ping LIN Juan ZONG Zhi-min 《Journal of China University of Mining and Technology》 EI 2008年第1期112-115,共4页
Electrolytic reductions of oxygenic functional groups (OFGs) on coal surface and coal model compounds with OFGs in an aqueous NaCl solution are studied by electrochemical methods combined with GC/MS, GC and FFIR ana... Electrolytic reductions of oxygenic functional groups (OFGs) on coal surface and coal model compounds with OFGs in an aqueous NaCl solution are studied by electrochemical methods combined with GC/MS, GC and FFIR analyses. Different electrode reactions, their corresponding potentials and dynamic equations during the processes are investigated. The results show that benzoic acid, benzaldehyde, benzalcohol and hypnone are reduced to benzaldehyde and benzalcohol, methoxybenzene and benzal- cohol, toluene and styrene, respectively, at the cathode. The corresponding electrode potentials and dynamic equations are deter- mined. The.electrolytic reduction also leads to an increase in the contents of hydroxyl groups and aliphatic moieties and a corresponding decrease in those of carboxyl and carbonyl groups in Nantong coal, a high-sulfur coal, an enhancement in the flotation desulfurization of the coal. ER also reduces organic sulfur and FeS2 in the coal. 展开更多
关键词 COAL model compounds electrolytic reduction dynamic equations
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Copper-catalyzed direct acyloxylation of C(sp^2)–H bonds with Benzoic acids 被引量:1
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作者 Sheng Zhao Fa-Jie Chen +1 位作者 Bin Liu Bing-Feng Shi 《Science China Chemistry》 SCIE EI CAS CSCD 2015年第8期1302-1309,共8页
A copper-catalyzed acyloxylation of C(sp2)–H bond with sterically bulky benzoic acids was achieved.This protocol is compatible with a broad range of functional groups and could proceed in gram scale,providing an effi... A copper-catalyzed acyloxylation of C(sp2)–H bond with sterically bulky benzoic acids was achieved.This protocol is compatible with a broad range of functional groups and could proceed in gram scale,providing an efficient and practical protocol for the synthesis of aryl esters. 展开更多
关键词 COPPER C-H activation acyloxylation ESTER BIDENTATE
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Effect of oxygen and nitrogen functionalization on the physical and electronic structure of graphene 被引量:3
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作者 Alexander J. Marsden Peter Brommer +9 位作者 James J. Mudd M. Adam Dyson Robert Cook Maria Asensio Jose Avila Ana Levy Jeremy Sloan David Quigley Gavin R. Bell Neil R. Wilson 《Nano Research》 SCIE EI CAS CSCD 2015年第8期2620-2635,共16页
Covalent functionalization of graphene offers opportunities for tailoring its properties and is an unavoidable consequence of some graphene synthesis techniques. However, the changes induced by the functionalization a... Covalent functionalization of graphene offers opportunities for tailoring its properties and is an unavoidable consequence of some graphene synthesis techniques. However, the changes induced by the functionalization are not well understood. By using atomic sources to control the extent of the oxygen and nitrogen functionalization, we studied the evolution in the structure and properties at the atomic scale. Atomic oxygen reversibly introduces epoxide groups whilst, under similar conditions, atomic nitrogen irreversibly creates diverse functionalities including substitutional, pyridinic, and pyrrolic nitrogen. Atomic oxygen leaves the Fermi energy at the Dirac point (i.e., undoped), whilst atomic nitrogen results in a net n-doping; however, the experimental results are consistent with the dominant electronic effect for both being a transition from delocalized to localized states, and hence the loss of the signature electronic structure of graphene. 展开更多
关键词 GRAPHENE FUNCTIONALIZATION chemical vapor deposition density functional theory
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