Functionalization of pentacene-5,7,12,14-tetraone with geminal enediyne and 1,3-dithiole groups

文献信息

发布日期 2017-03-21

DOI 10.1039/C7QO00041C

影响因子 5.281

作者

Eyad A. Younes, Yuming Zhao

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摘要

Pentacene-5,7,12,14-tetraone was subjected to selective olefination and cross-coupling reactions to yield a new class of pentacene-based π-conjugated systems functionalized with geminal enediyne and 1,3-dithiole groups. The electron donating and accepting effects of enediyne and dithiole groups render these compounds intriguing structural, electronic properties, and redox activities which were systematically investigated by UV-Vis absorption and cyclic voltammetric analyses in conjunction with density functional theory (DFT) calculations. The bis(enediyne)-substituted pentacenedione showed potential application in the preparation of carbon-rich polymeric materials.

期刊推荐

Helvetica Chimica Acta

Israel Journal of Chemistry

Journal of Heterocyclic Chemistry

Russian Chemical Reviews

Molecular Pharmacology

Journal of Organometallic Chemistry

Pure and Applied Chemistry

Science

Journal of Medicinal Chemistry

Nature

来源期刊

Organic Chemistry Frontiers

CiteScore: 7.8

自引率: 8.7%

年发文量: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Functionalization of pentacene-5,7,12,14-tetraone with geminal enediyne and 1,3-dithiole groups

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