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作 者:李金山[1,2] 冯乙巳[1,2] 门振宇[1,2]
机构地区:[1]南开大学元素有机化学研究所 [2]南开大学物理系
出 处:《高等学校化学学报》1998年第5期732-736,共5页Chemical Journal of Chinese Universities
基 金:国家自然科学基金
摘 要:合成了13个四芳基卟啉锰配离子的TCNQ电荷转移盐[TAPMn][TCNQ]n(TAPH2=α,β,γ,δ-四芳基卟啉;A=C6H5,4-CH3C6H4,4-CH3OC6H4,4-ClC6H4,3-ClC6H4,3-FC6H4,4-(CH3)2NC6H4,2,4-Cl2C6H3;TCNQ=7,7,8,8-四氰基对苯醌二甲烷;n=1,2).通过元素分析、IR、XPS、ESR、磁化率和电导率对其进行了表征.结果表明:这些电荷转移盐分子中存在TCNQ0和TCNQ-,且TCNQ0和TCNQ-之间存在相互作用,部分电荷从[TCNQ]-n向[TAPMn]+转移,导致化合物中的锰表现为混合价态.复合盐的室温电导率在10-7~10-10S·cm-1,属于有机半导体,简单盐的室温电导率小于10-11S·cm-1.Thirteen TCNQ charge transfer salts of tetraarylporphinatomanganese complex ions with the general formula TAPMn TCNQ n (TAPH 2=tetraarylporphyrin; A=C 6H 5, 4 CH 3C 6H 4, 4 CH 3OC 6H 4, 4 ClC 6H 4, 3 ClC 6H 4, 3 FC 6H 4, 2,4 Cl 2C 6H 3, 4 Me 2NC 6H 4; TCNQ =7,7,8,8 tetracyanoquinodimethane; n =1, 2) have been synthesized and characterized by elementary analyses, IR spectra, X ray photoelectron spectra, ESR spectra, magnetic susceptibilities and conductivities. The results indicate that there are TCNQ - and TCNQ 0 in the molecules of these charge transfer salts as well as interaction between TCNQ - and TCNQ 0. It leads manganese of these compounds to mixed valence state because partial electrons transfer from TCNQ - n to TAPMn +. The room temperature conductivities of the complex salts are between 10 -7 and 10 -10 S\5cm -1 , they belong to organic semiconductor. The conductivities of the simple salts are lower than 10 -11 S\5cm -1 .
分 类 号:TN304.53[电子电信—物理电子学] O614.711[理学—无机化学]
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