Effect of peripheral hydrophobic alkoxy substitution on the organic field effect transistor performance of amphiphilic tris(phthalocyaninato) europium triple-decker complexes
Effect of peripheral hydrophobic alkoxy substitution on the organic field effect transistor performance of amphiphilic tris(phthalocyaninato) europium triple-decker complexes
复制标题
外围疏水烷氧基取代对两亲性三(酞菁)铕三层配合物有机场效应晶体管性能的影响
DOI:
10.1021/la701512r
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发表时间:
2007-12-04
期刊:
影响因子:
3.9
通讯作者:
Jiang, Jianzhuang
中科院分区:
文献类型:
--
作者:
Chen, Yanli;Li, Renjie;Jiang, Jianzhuang
A series of four amphiphilic heteroleptic tris(phthalocyaninato) europium complexes with different lengths of hydrophobic alkoxy substituents on one outer phthalocyanine ligand [Pc(15C5)(4)]Eu[Pc(15C5)(4)]Eu[Pc(OCnH2n+1)(8)] (n = 4, 6, 10,12) (1, 2, 4, and 5) was designed and prepared. Their film forming and organic field effect transistor properties have been systematically studied in comparison with analogous [Pc(15C5)(4)]Eu[Pc(15C5)(4)]Eu[Pc(OC8H17)(8)] (3). Experimental results showed that all these typical amphiphilic sandwich triple-decker molecules have been fabricated into highly ordered films by the Langmuir-Blodgett (LB) technique, which displays carrier mobility in the direction parallel to the aromatic phthalocyanine rings in the range of 0.0032-0.60 cm(2) V-1 s(-1) depending on the length of the hydrophobic alkoxy substituents. This is rationalized on the basis of comparative morphology analysis results of the LB films by the atomic force microscopy technique.