| 摘要: | 
	         
			 
		     | 通过邻胺基苯酚与二醛或二酮反应制备了4种新型的N,N′,O,O′-Salen配体,再利用配体与Mn(Ac)2·2H2O配位反应合成新型Salen-Mn催化剂C1,C2,C3,C4,用FT-IR,UV-Vis和配位滴定法等方法对催化剂进行了表征;利用高斯03软件(Hartree-Fock/3-21G)对各种配体的结构进行了优化;考察了4种催化剂在环氧化反应中的催化性能.从催化结果可以看出:新型催化剂的催化活性与结构有关,其中新型催化剂C1与传统催化剂C5结构相似,在环氧化反应中都具有良好的催化活性,而新型催化剂C2,C3,C4的催化活性相对弱很多. | 
	         
			
	         
				| 关键词:  新型Salen Mn  邻氨基苯酚  二醛  二酮  环氧化反应 | 
	         
			 
                | DOI: | 
           
            
                | 分类号:0621.25+1 | 
             
			 
             
                | 基金项目:湖南省教育厅资助项目(16C0154); 湖南省大学生研究性学习和创新性实验计划资助项目(湘教通〔2016〕283号) | 
             
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                | Study on the preparation of new-type homogeneous N,N′,O,O′-Salen Mn(III) catalysts and the catalytic performance inepoxidation of olefins | 
           
           
			
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				Zhou Jianbo, Xiong Donglu, Fu Zaihui, Zou Shuai, Cui Xiaoying, Xu Chao
						
				
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				Department of Basic Medical Science, Changsha Medical University, Changsha 410219, China
				
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                | Abstract: | 
              
			
                | Four new-type N,N′,O,O′-Salen ligands were synthesized by the condensation of o-aminophenol with dialdehyde or diketone, and new-type Salen-Mn catalysts (C1, C2, C3, C4) were synthesized by ligand coordination reaction with Mn(Ac)2·2H2O. The catalysts were characterized by FT-IR, UV-Vis and coordination titration and the structure of the ligands was optimized by using Hartree-Fork/3-21G. The catalytic performance of the catalysts was investigated by epoxidation. The results indicated that the catalytic activity of the new-type Salen-Mn catalysts is related to the structure, the new-type catalyst C1 and the traditional catalyst C5 have considerable catalytic activity in the epoxidation reactions due to their similar structure, but the catalytic activity of the new-type catalysts C2, C3, C4 is weaker than that of C1 because of the different structure with C1 and C5. | 
            
	       
                | Key words:  new-type Salen Mn  o-aminophenol  dialdehyde  diketone  epoxidation reaction |