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首页> 外文期刊>Organic letters >Dithiophene-Fused Tetracyanonaphthoquinodimethanes (DTTNAPs): Synthesis and Characterization of π-Extended Quinoidal Compounds for n-Channel Organic Semiconductor
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Dithiophene-Fused Tetracyanonaphthoquinodimethanes (DTTNAPs): Synthesis and Characterization of π-Extended Quinoidal Compounds for n-Channel Organic Semiconductor

机译:二噻吩融合的四氰基萘醌二甲烷(DTTNAPs):用于n通道有机半导体的π扩展醌型化合物的合成与表征

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摘要

Dithiophene-fused tetracyanonaphthoquinodimethanes (DTTNAPs) were synthesized and evaluated as n-channel organic semiconductors. DTTNAPs, regardless of isomeric structures and substituents, have low-lying LUMO energy levels (~4.6 eV below the vacuum level), suitable for stable n-channel field-effect transistors (FETs) under ambient conditions. In fact, α-DTTNAP derivatives afforded solution-processed FETs showing an electron mobility of 10~(-3) cm~2 V~(-1) s~(-1), indicating that DTTNAPs are a potential molecular framework for nchannel organic semiconductors.
机译:合成了二噻吩稠合的四氰基萘醌二甲烷(DTTNAP),并将其评估为n通道有机半导体。 DTTNAP不论异构体结构和取代基如何,都具有较低的LUMO能级(比真空度低约4.6 eV),适合在环境条件下稳定的n沟道场效应晶体管(FET)。实际上,α-DTTNAP衍生物提供了溶液处理的FET,其电子迁移率为10〜(-3)cm〜2 V〜(-1)s〜(-1),表明DTTNAPs是n通道有机物的潜在分子框架。半导体。

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