期刊文献+

Synthesis,spectroscopic properties and applications of novel N-heterocycle-containing benzotriazoles as UV absorbers 被引量:4

Synthesis,spectroscopic properties and applications of novel N-heterocycle-containing benzotriazoles as UV absorbers
原文传递
导出
摘要 Two novel N-heterocycle-containing benzotriazole compounds, 5-(5-chloro-2-benzotriazolyl)-6-hydroxy-l,4-dimethyl-3-car- bonitrile-2-pyddone (2) and 4-(5-chloro-2-benzotdazolyl)-5-methyl-2-phenyl-3-pyrazolone (4), were synthesized from reactant 4- chloro-2-nitroaniline via diazotization, azo coupling, reductive cyclization and acidification. Their structures were confirmed by Fr-IR, 1H NMR, mass spectroscopy and elemental analysis. Their spectral properties were investigated and compared with that of a common commercial benzotriazole UV absorber Tinuvin 326. It is found that the novel N-heterocycle-containing benzotriazole compounds exhibit sharp single peak in the range of 280-400 nm and have much higher molar extinction coefficients than that of Tinuvin 326. Their anti-UV protection properties on polyester fabric were also evaluated and compound 4 was much superior to compound 2 due to its higher exhaustion. Two novel N-heterocycle-containing benzotriazole compounds, 5-(5-chloro-2-benzotriazolyl)-6-hydroxy-l,4-dimethyl-3-car- bonitrile-2-pyddone (2) and 4-(5-chloro-2-benzotdazolyl)-5-methyl-2-phenyl-3-pyrazolone (4), were synthesized from reactant 4- chloro-2-nitroaniline via diazotization, azo coupling, reductive cyclization and acidification. Their structures were confirmed by Fr-IR, 1H NMR, mass spectroscopy and elemental analysis. Their spectral properties were investigated and compared with that of a common commercial benzotriazole UV absorber Tinuvin 326. It is found that the novel N-heterocycle-containing benzotriazole compounds exhibit sharp single peak in the range of 280-400 nm and have much higher molar extinction coefficients than that of Tinuvin 326. Their anti-UV protection properties on polyester fabric were also evaluated and compound 4 was much superior to compound 2 due to its higher exhaustion.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2012年第9期1019-1022,共4页 中国化学快报(英文版)
基金 supported by the National Natural Science Foundation of China(Nos.21106135 and 51173168) Zhejiang Provincial Natural Science Foundation of China(Nos.Y4090227 and Y5080021) Zhejiang Provincial Key Innovation Team(No.2010R50038)
关键词 BENZOTRIAZOLE UV absorber PYRAZOLONE PYRIDONE Anti-UV protection Benzotriazole UV absorber Pyrazolone Pyridone Anti-UV protection
  • 相关文献

参考文献8

  • 1R.R. Cordero, E Roth, A. Georgiev, Energy Convers. Manage. 46 (2005) 2907.
  • 2D. Rosu, L. Rosu, C.N. Cascaval, J. Photochem. Photobiol. A: Chem. 194 (2008) 275.
  • 3N. Gandra, A.T. Frank, O.L. Gendre, Tetrahedron 62 (2006) 10771.
  • 4M. Zayat, P. Garaia-Parejo, D. Levy, Chem. Soc. Rev. 36 (2007) 1270.
  • 5E Waiblinger, J. Keck, M. Stein, J. Phys. Chem. A 104 (2000) 1100.
  • 6J. Pospisil, S. Nespurek, Prog. Polym. Sci. 25 (2000) 1261.
  • 7N.A. Evans, J. Rosevcar, P.J. Waters, Polym. Degrad. Stab. 14 (1986) 263.
  • 8A.I. Vogel, B.S. Furniss, Vogel's Textbook of Practical Organic Chemistry, 4th ed., Longman, London, 1978, p. 715.

同被引文献10

引证文献4

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部