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Synthesis and characterization of amino-capped oligothiophene-based hole-transport materials

机译:氨基封端的低聚噻吩基空穴传输材料的合成与表征

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摘要

A series of seven thiophene-based oligomers were prepared as hole transport materials.The DBATn series is composed of six oligothiophenes(n =1-6)capped with two dibutylaminostyryl electron donating moieties.The band gaps for these compounds range from 2.47 to 2.19 eV.It was found that the bis(amino)substituents control the ionization potential,while the electron affinity and energy gap depend directly on the oligothiophene chain length.The bulk crystalline properties of these materials depend strongly on whether the number of thiophene rings in the bridge is even or odd.This results in the compounds that have an odd number of thiophene units in the bridge to exhibit depressed melting points with respect to the structures with an even number of rings.X-Ray structure determination was obtained from single crystals of DBAT1 and-2.Good solubility,thermal stability and film forming properties were found throughout the series of compounds.A seventh compound,DH2E4T,was also prepared.This molecule is comparable to alpha,omega-dihexylsexithiophene but with greater solubility and reduced optical band gap(2.32 eV).
机译:制备了一系列七个以噻吩为基的低聚物作为空穴传输材料.DBATn系列由六个低聚噻吩(n = 1-6)覆盖有两个二丁基氨基苯乙烯基给电子部分,这些化合物的带隙范围为2.47至2.19 eV。发现双(氨基)取代基控制着电离势,而电子亲和力和能隙直接取决于寡聚噻吩的链长。这些材料的整体晶体性质强烈取决于桥中噻吩环的数量偶数或奇数。这导致在桥中具有奇数个噻吩单元的化合物相对于偶数环的结构表现出较低的熔点。从DBAT1单晶获得X射线结构测定和-2。在该系列化合物中均发现良好的溶解性,热稳定性和成膜性。还制备了第七种化合物DH2E4T。 cule可与α,ω-二己基环己基噻吩媲美,但具有更高的溶解度和减小的光学带隙(2.32 eV)。

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