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Studies on Properties of p-Nitrophenylazo Calixarene Derivatives

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【作者】 金传明归敏芝陆国元郭勋张宏游效曾

【Author】 JIN, Chuan Ming a,b GUI, Min Zhi c LU, Guo Yuan , a GUO, Xun a ZHANG, Hong , c YOU, Xiao Zeng a aDepartment of Chemistry, State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing, Jiangsu 210093, China b Department of Chemistry and Environment Engineering, Hubei Normal University, Huangshi, Hubei 435002, China c National Laboratory of Molecular and Biomolecular Electronics, Southeast University, Nanjing, Jiangsu 210096, China

【机构】 Department of ChemistryState Key Laboratory of Coordination ChemistryNanjing UniversityNanjingJiangsu 210093ChinaNational Laboratory of Molecular and Biomolecular ElectronicsSoutheast UniversityJiangsu 210096ChinaChina Department of Chemistry and Environment EngineeringHubei Normal UniversityHuangshiHubei 435002China

【Abstract】 The p nitrophenylazo calixarene derivatives 1a-1d with nonlinear optical (NLO) properties were prepared by the diazo coupling reaction of calixarene with p nitrophenyl diazonium. The diazotization reaction of p nitroaniline was carried out with isoamyl nitrite as a source of nitrous acid in EtONa/EtOH under refluxing condition. X Ray crystallographic analysis and 1H NMR spectra reveal that they exist as cone conformation in crystal state or in solution. HRS measurements at 1064 nm in THF indicate that p nitrophenylazo calixarenes have higher hyperpolarizability β z values than the corresponding reference compound 4 (4 nitrophenylazo) 2,6 dimethyl phenol, without red shift of the charge transfer band. The tetrakis p nitrophenylazo calixarene (2) with longer alkyl chains can form monolayer at the air/water interface.

【基金】 ProjectsupportedbytheNationalNaturalScienceFoundationofChina (No .90 10 10 18)andtheCenterofMaterialsAnalysisofNanjingUniver sity .
  • 【文献出处】 Chinese Journal of Chemistry ,中国化学(英文版) , 编辑部邮箱 ,2003年02期
  • 【分类号】O625.6
  • 【被引频次】2
  • 【下载频次】6
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