Literature DB >> 30474286

Tetra-Aza-Pentacenes by means of a One-Pot Friedländer Synthesis.

Narcisse Ukwitegetse1, Patrick J G Saris1, Jonathan R Sommer1, Ralf M Haiges1, Peter I Djurovich1, Mark E Thompson1.   

Abstract

Tetra-aza-pentacenes are attractive n-type small molecules for optoelectronic device applications, yet their syntheses are often laborious. Disclosed here is a one-pot Friedländer synthesis of 1,7,8,14-tetraazapentacece (tAP) derivatives (linear and/or bent), fully aromatized in situ despite the absence of an exogenous oxidant. The photophysics of linear tAPs resembles that of regular pentacene though their crystal structures differ. A LUMO energy of -3.71 eV for di-tert-butylanisole-substituted linear tAP is similar to that of the well-known acceptor, C60 .
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Friedländer reaction; acenes; n-type molecules; one-pot synthesis; tetra-aza-pentacene

Year:  2018        PMID: 30474286     DOI: 10.1002/chem.201805655

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Modular Two-Step Access to π-Extended Naphthyridine Systems-Potent Building Blocks for Organic Electronics.

Authors:  Fabian Stuck; Martin C Dietl; Maximilian Meißner; Finn Sebastian; Matthias Rudolph; Frank Rominger; Petra Krämer; A Stephen K Hashmi
Journal:  Angew Chem Int Ed Engl       Date:  2021-12-10       Impact factor: 16.823

2.  Tuning of Molecular Electrostatic Potential Enables Efficient Charge Transport in Crystalline Azaacenes: A Computational Study.

Authors:  Andrey Sosorev; Dmitry Dominskiy; Ivan Chernyshov; Roman Efremov
Journal:  Int J Mol Sci       Date:  2020-08-06       Impact factor: 5.923

  2 in total

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