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5,15-二苯基-10,20-二(4-N-咪唑基)苯基卟啉的合成与表征 被引量:2

Synthesis and Characterization of 5,15-Di(pheny)-10,20-di-[(4-N-imidazolyl) phenyl]porphyrin
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摘要 采用丙酸法合成了新的标题化合物,并对该化合物进行了EA、FT-IR、~1HNMR、MS、UV-Vis等表征,确定了所合成卟啉的分子结构。探讨了反应中催化剂的用量、反应温度、反应物比例及反应时间对目标化合物产率的影响。结果表明,合成目标化合物的适宜反应时间为1 h,反应温度为140℃。在该条件下,目标化合物的产率可高达36.6%。在400nm的光激发下,于666 nm处出现最强发射峰,目标化合物可用作潜在的光学材料。 The novel porphyrin 5,15-di(pheny)-10,20-di-[(4-N-imidazolyl) phenyl]porphyrin(H_2Pp) was synthesized by the Alder method and confirmed by elemental analyses,FT-IR,-1HNMR,MS and UV-Vis,etc. The effects of the dosage of catalyst,the appropriate ratio of reactants,reaction temperature and time on the yield of the target compound were investigated. The results show that the yield of the target compound reaches 36. 6% when the suitable reaction time is 1 h and the temperature is 140 ℃.It shows intense fluorescence emission with maximum at 666 nm upon 400 nm excitation at room temperature,indicating that it may be candidate for luminescent material.
作者 徐维霞 李维维 李小博 刘焕婷 孟凡洋 李珺 XU Wei-xia LI Wei- wei L LIU Huan-ting MENG Fan-yang LI Jun(College of Chemistry and Chemical Engineering, Xianyang Nor- mal University, Xianyang 712000, China Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry and Material Science, Northwest University, Xi'an 710069, China)
出处 《化学试剂》 CAS 北大核心 2017年第2期129-133,共5页 Chemical Reagents
基金 国家自然科学基金资助项目(21271148) 咸阳师范学院省级大学生创新创业训练计划资助项目(2104) 咸阳师范学院科研专项基金项目(14XSYK012 12XSYK029 12XSYK025) 咸阳师范学院校级大学生创新创业训练计划项目(2015017)
关键词 5 15-二苯基-10 20-二(4-N-咪唑基)苯基卟啉 合成 表征 5 15-di(pheny)-10 20-di-[(4-N-imidazolyl) phenyl]porphyrin synthesis characterization
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  • 1张燕慧,佘远斌,钟儒刚,周贤太,纪红兵.钴卟啉催化剂的前线轨道能级与其催化活性的相关性研究[J].化学学报,2004,62(22):2228-2232. 被引量:21
  • 2周贤太,纪红兵,裴丽霞,佘远斌,徐建昌,王乐夫.金属卟啉催化剂应用于均相氧化反应的研究进展[J].有机化学,2007,27(9):1039-1049. 被引量:24
  • 3乔刚.咪唑斯汀治疗慢性荨麻疹,有效性与安全性评估[J].国外医学:皮肤性病学分册,2001,27(3):180-180.
  • 4乔刚,国外医学.皮肤性病学分册,2001年,27卷,3期,180页
  • 5Colbum DE, Giles FJ, Oladovich D, et al, In vitro evalutation of cytochrome P450 mediated drug interactions between cytarabine, idarubicine, itraconazole and caspofungin [J]. Hematology, 2004, 9(3): 217-10.
  • 6Guengerich FP. Cytochrome P450: what have we learned and what are the future issues [ J ]. Drug Metab Rev, 2004, 36(2): 159-62.
  • 7Le Cluyse EL. Human hepatocyte microsome culture systems for the in vitro evaluation of cytochrome P450 expression and regulation [J]. Eur J Pharm Sci, 2001, 13(4): 343-7.
  • 8Jerdi MC, Daali Y, Oestreicher MK, et al. A simplified analytical method for a phenotyping cocktail of major CYP450 biotransformation routes [ J ]. J Pharm Biomed Anal, 2004, 35(5): 1203-12.
  • 9LEWIS J C, COELHO P S, ARNOLD F H. Enzymaticfunctionalization of carbon-hydrogen bonds [ J ]. Chem.Soc. Rev. ,2011,40(4) :2003-2021.
  • 10RAMIREZ T A,ZHAO Bao-guo,SHI Y. Recent advancesin transition metal-catalyzed sp3 C—H amination adjacentto double bonds and carbonyl groups [ J ]. Chem. Soc.Rev. ,2012,41(2) :931-942.

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