中南民族大学学报(自然科学版)
中南民族大學學報(自然科學版)
중남민족대학학보(자연과학판)
JOURNAL OF SOUTH-CENTRAL UNIVERSITY FOR NATIONALITIES(NATURAL SCIENCE EDITION)
2014年
4期
20-25
,共6页
吴腊梅%何为%李志有%张涛%蔡烨
吳臘梅%何為%李誌有%張濤%蔡燁
오석매%하위%리지유%장도%채엽
水杨酸%氨基硫脲%1 ,3 ,4-噻二唑%光致发光%希夫碱
水楊痠%氨基硫脲%1 ,3 ,4-噻二唑%光緻髮光%希伕堿
수양산%안기류뇨%1 ,3 ,4-새이서%광치발광%희부감
salicylic acid%thiosemicarbazide%1,3,4-thiadiazole%luminescence%Schiff base
以水杨酸、氨基硫脲为原料,POCl3作为溶剂、催化剂、环合剂,合成了2-氨基-5-(2-羟基苯基)-1,3,4-噻二唑。通过其与相应的芳香醛反应,合成了3种含杂环1,3,4-噻二唑的希夫碱及其金属配合物。采用傅里叶红外光谱( FT-IR)和核磁共振(1 H-NMR)对目标产物及其中间体进行了表征,通过荧光光谱研究了其光学性能。结果表明:所用方法反应时间短、操作简单、产率高,这些化合物具有较强的荧光发射光谱,有望成为较好的有机光电材料。
以水楊痠、氨基硫脲為原料,POCl3作為溶劑、催化劑、環閤劑,閤成瞭2-氨基-5-(2-羥基苯基)-1,3,4-噻二唑。通過其與相應的芳香醛反應,閤成瞭3種含雜環1,3,4-噻二唑的希伕堿及其金屬配閤物。採用傅裏葉紅外光譜( FT-IR)和覈磁共振(1 H-NMR)對目標產物及其中間體進行瞭錶徵,通過熒光光譜研究瞭其光學性能。結果錶明:所用方法反應時間短、操作簡單、產率高,這些化閤物具有較彊的熒光髮射光譜,有望成為較好的有機光電材料。
이수양산、안기류뇨위원료,POCl3작위용제、최화제、배합제,합성료2-안기-5-(2-간기분기)-1,3,4-새이서。통과기여상응적방향철반응,합성료3충함잡배1,3,4-새이서적희부감급기금속배합물。채용부리협홍외광보( FT-IR)화핵자공진(1 H-NMR)대목표산물급기중간체진행료표정,통과형광광보연구료기광학성능。결과표명:소용방법반응시간단、조작간단、산솔고,저사화합물구유교강적형광발사광보,유망성위교호적유궤광전재료。
2-amino-5-(2-hydroxylphenyl)-1,3,4-thiadiazole was synthesized from salicylic acid and thiosemicarbazide with phosphorus oxychloride as solvent, cyclization reagent and catalyst.Then three schiff base compounds containing 1,3,4-thiadiazole and their metal complexes were formed by the reaction of 2-amino-5-(2-hydroxylphenyl)-1,3,4-thiadiazole and the corresponding aromatic aldehydes.These compounds were characterized by FT-IR and 1 H-NMR and the luminescence of the three schiff bases and their metal complexes were also studied.The results indicated that the synthesis was characterized by short reaction time, simple operation and high yield.The three schiff bases exhibited strong fluorescence emission spectrum and were expected to be of use as preferable organic photoelectric materials.