摘要
研究了异丙基桥连的希夫碱及其锰(Ⅲ)络合物催化剂的红外光谱(3800~150cm-1),对一些主要吸收谱带进行了经验归属。配体内氢键谱带出现在3446cm-1附近(以LH为例),νC-O谱带在1724cm-1附近(以LC为例,下同),νC=N谱带在1649和1629cm-1附近,苯环的特征谱带在1601,1470和753cm-1附近,νMn-N为主的复合振动在363cm-1附近,δMn-N为主的复合振动在248cm-1附近,νMn-O为主的复合振动在330cm-1附近,δMn-O为主的复合振动在275cm-1附近,νMn-Cl特征谱带在302cm-1附近。与苯基锰(Ⅲ)卟啉络合物相比,νMn-N特征谱带向高波数发生了位移,而νMn-Cl特征谱带向低波数发生了较大的位移。
The FTIR spectra(3 800~150 cm -1 ) of Schiff base ligands and their Mn(Ⅲ) complexes with isopropyl bridge were measured and investigated.The major bands were empirically assigned in comparison with a large number of previous results.It was found that the characteristic absorption bands of intra_molecular hydrogen bond of ligands are at ca 3 446 cm -1 ;in the ligands and complexes ν C-O is at ca 1 724 cm -1 , the ν C=N at ca 1 649 and 1 629 cm -1 ;the characteristic absorption bands of the phenyl ring at ca 1 601,1 470 and 753 cm -1 ;the vibrations coupling between the Mn—N stretching modes and the phenyl ring deformation at ca 363 cm -1 ,between the Mn—N and the phenyl ring deformation modes at ca 248 cm -1 ,between the Mn—O stretching modes and the phenyl ring deformation at ca 330 cm -1 ,between the Mn—N and the phenyl ring deformation modes at ca 275 cm -1 ;the ν Mn—Cl of the complexes were found at ca 302 cm -1 ;the ν Mn—N of the complexes shifted to higher wavenumbers and the ν Mn—Cl to lower wavenumbers than of the phenylporphyrin Mn(Ⅲ) complexes.
出处
《分析测试学报》
CAS
CSCD
1998年第6期9-12,共4页
Journal of Instrumental Analysis
基金
国家自然科学基金