A Convenient Synthesis of Diketopyrrolopyrrole Dyes.

IF 4.6 2区 化学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecules Pub Date : 2021-08-06 DOI:10.3390/molecules26164758
Vitor A S Almodôvar, Augusto C Tomé
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Abstract

Diketopyrrolo[3,4-c]pyrroles (DPP) are high-performance organic optoelectronic materials. They have applications in solar cells, fluorescent probes, bioimaging, photodynamic/photothermal therapy, and in many other areas. This article reports a convenient two-step synthesis of various DPP dyes from Pigment Red 254, an inexpensive commercial pigment. The synthesis includes a Suzuki-Miyaura cross-coupling reaction of a bis(4-chlorophenyl)DPP derivative with aryl and hetaryl boronic acids under mild reaction conditions. The new dyes show large Stokes shifts and high fluorescence quantum yields, important features for their potential use in technical and biological applications.

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二酮吡咯染料的便捷合成。
二酮吡咯并[3,4-c]吡咯(DPP)是一种高性能有机光电材料。它们可应用于太阳能电池、荧光探针、生物成像、光动力/光热疗法以及许多其他领域。本文报告了一种以廉价的商业颜料颜料红 254 为原料,分两步合成各种 DPP 染料的简便方法。合成过程包括双(4-氯苯基)DPP 衍生物与芳基和正十八烷基硼酸在温和的反应条件下进行的 Suzuki-Miyaura 交叉偶联反应。新染料显示出较大的斯托克斯偏移和较高的荧光量子产率,这些都是它们可能用于技术和生物应用的重要特征。
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来源期刊
Molecules
Molecules 化学-有机化学
CiteScore
7.40
自引率
8.70%
发文量
7524
审稿时长
1.4 months
期刊介绍: Molecules (ISSN 1420-3049, CODEN: MOLEFW) is an open access journal of synthetic organic chemistry and natural product chemistry. All articles are peer-reviewed and published continously upon acceptance. Molecules is published by MDPI, Basel, Switzerland. Our aim is to encourage chemists to publish as much as possible their experimental detail, particularly synthetic procedures and characterization information. There is no restriction on the length of the experimental section. In addition, availability of compound samples is published and considered as important information. Authors are encouraged to register or deposit their chemical samples through the non-profit international organization Molecular Diversity Preservation International (MDPI). Molecules has been launched in 1996 to preserve and exploit molecular diversity of both, chemical information and chemical substances.
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