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一种石墨烯结构的二维聚苯的合成及性能研究 被引量:1

Synthesis and properties of two-dimensional polyphenylene with graphene structure
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摘要 以四苯基环戊二烯酮和1,4-二苯乙炔基苯为原料,通过Diels-Alder加成反应合成了1,4-二(2,3,4,5,6-五苯基苯基)苯,进一步在CuCl2/AlCl3作用下脱氢环化制备了石墨烯结构的二维聚苯,并通过红外光谱、紫外光谱、核磁共振氢谱和元素分析对其结构进行了表征。研究了上述化合物的热稳定性和发光特性,结果表明,这两种化合物的分解温度都大于450℃,热稳定性较好。1,4-二(2,3,4,5,6-五苯基苯基)苯和石墨烯结构的二维聚苯的荧光发光波长分别在349.2 nm和487 nm处。 1,4-( 2,3,4,5,6 -Pentaphenylphenyl)benzene was synthesized by Diels-Alder reaction with tetraphenylcyclopentadienone and 1,4- bis(phenylethynyl) benzene. Two-dimensional polyphenylene with graphene structure was prepared through the dehydroeyelization of 1,4 -( 2,3,4,5,6 - Pentaphenylphenyl) benzene at presence of CuCl2 and AlCl3. The as-synthesized compounds were characterized by FT-IR, UV-Vis, ^1H NMR spectroscopy and elemental analysis. Thermogravimetric analysis shows that the as-synthesized compounds have excellent thermal stability with the decomposition temperature being above 450 ℃. Fluorescence spectra show that the maximum fluorescence wavelength of 1,4 - ( 2,3,4,5,6 - Pentaphenylphenyl) benzene and two-dimensional polyphenylene is 349.2 nm and 487 nm respectively.
出处 《阜阳师范学院学报(自然科学版)》 2013年第2期35-38,共4页 Journal of Fuyang Normal University(Natural Science)
基金 国家自然科学基金项目(50903018) 阜阳师范学院科研项目(2011CXY04 2009FSKJ03) 阜阳师范学院博士科研启动项目 安徽省教育厅教学研究重点项目(20100642)资助
关键词 石墨烯 二维聚苯 脱氢环化 DIELS-ALDER反应 荧光 graphene two-dimensional polyphenylene cyclodehydrogenation Diels-Alder reaction fluorescence
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参考文献9

  • 1Geim A K. Graphene : status and prospects [ J ]. Sci- ence, 2009, 324(5934): 1530-1534.
  • 2顾盾寅,黄美荣,李新贵.二维多环全苯芳烃的合成、性能及应用[J].化学进展,2010,22(12):2309-2315. 被引量:3
  • 3Wu J, Pisula W, Miillen K. Graphenes as potential ma- terial for electronlcs[J]. Chemical Reviews, 2007, 107 (3) : 718-747.
  • 4Rao C N R, Sood A K, Subrahmanyam K S, et al. Gra- phene : the new two-dimensional nanomaterial [ J ]. An- gewandte Chemic International Edition, 2009, 48 (42) : 7752-7777.
  • 5Fechtenkotter A, Saalwachter K, Harbison M A, et al. Highly ordered columnar structures from hexa-peri- hexabenzocoronense-synthesis, X-raydiffraetion, and solid-state heteronuclear multiple-quantum NMR investi- gations [ J ]. Angewandte Chemic International Edition, 1999, 38(20) : 3039-3042.
  • 6S, Wehmeier M, Brand J D, et al. Synthesis and self-assembly of funetionalized hexa-peri-hexabenzocoro- nenes [ J ]. Chemistry-A European Journal, 2000, 6 (23) : 4327-4342.
  • 7Herwig P, Kayser C W, Mtillen K, et al. Columnar me- sophases of alkylated hexa-perihexabenzocoronenes with remarkably large phase widths [ J ]. Advanced Materials, 1996, 8(6) : 510-513.
  • 8Mtiller M, Iyer V S, Kttbel C, et al. From Hexa-peri- hexabenzocoronene to "Superacenes" [ J ]. Angewandte Chemie Intemational Edition in English, 1997, 36 (15) : 1604-1607.
  • 9董秋静,罗春华.1,4-二苯乙炔基苯衍生物的合成和发光性能研究[J].化学试剂,2008,30(9):672-674. 被引量:3

二级参考文献50

  • 1Li X G, Liu Y W, Huang M R, Peng S, Gong L Z, Moloney M G. Chem. Eur. J., 2010, 16(16): 4803-4813.
  • 2Sergei A A, Valefii M K. Chem. Phys. , 2000, 201:809-814.
  • 3Miller T M, Neenan T X. Chem. Mater. , 1990, 2(4) : 346- 349.
  • 4Muller M, Kubel C, Mullen K. Chem. Eur. J. , 1998,4(11) : 2099-2109.
  • 5Watson M D, Fechtenktter A, Mullen K. Chem. Rev. , 2001, 101 : 1267-1300.
  • 6Mullen K, Rabe J P. Ann. N. Y. Acad. Sci. , 1998, 852: 205 -218.
  • 7Berresheim A J, Muller M, Mullen K. Chem. Rev. , 1999, 99: 1747-1785.
  • 8Shen X, Ha D M, Pascal R A. Org. Lett. , 2003,5(3) : 369- 371.
  • 9Hyatt J A. Org. Prep. Proe. Int. , 1991, 23(4) : 460-463.
  • 10Wu J H, Watson M D, Mullen K. Angew. Chem. , 2003, 115: 5487-5491.

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