Literature DB >> 24961807

Strategies for the synthesis of functional naphthalene diimides.

Sabin-Lucian Suraru1, Frank Würthner.   

Abstract

Naphthalene diimides, which have for a long time been in the shadow of their higher homologues the perylene diimides, currently belong to the most investigated classes of organic compounds. This is primarily due to the initial synthetic studies on core functionalization that were carried out at the beginning of the last decade, which facilitated diverse structural modifications of the naphthalene scaffold. Compounds with greatly modified optical and electronic properties that can be easily and effectively modulated by appropriate functionalization were made accessible through relatively little synthetic effort. This resulted in diverse interesting applications. The electron-deficient character of these compounds makes them highly valuable, particularly in the field of organic electronics as air-stable n-type semiconductors, while absorption bands over the whole visible spectral range through the introduction of core substituents enabled interesting photosystems and photovoltaic applications. This Review provides an overview on different approaches towards core functionalization as well as on synthetic strategies for the core expansion of naphthalene diimides that have been developed mainly in the last five years.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  annulation; dyes/pigments; naphthalene diimides; organic semiconductors

Year:  2014        PMID: 24961807     DOI: 10.1002/anie.201309746

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  17 in total

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2.  Molecular Encapsulation of Naphthalene Diimide (NDI) Based π-Conjugated Polymers: A Tool for Understanding Photoluminescence.

Authors:  Jeroen Royakkers; Kunping Guo; Daniel T W Toolan; Liang-Wen Feng; Alessandro Minotto; Daniel G Congrave; Magda Danowska; Weixuan Zeng; Andrew D Bond; Mohammed Al-Hashimi; Tobin J Marks; Antonio Facchetti; Franco Cacialli; Hugo Bronstein
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3.  Radical-mediated dehydrative preparation of cyclic imides using (NH4)2S2O8-DMSO: application to the synthesis of vernakalant.

Authors:  Dnyaneshwar N Garad; Subhash D Tanpure; Santosh B Mhaske
Journal:  Beilstein J Org Chem       Date:  2015-06-12       Impact factor: 2.883

4.  Core-Substituted Naphthalenediimides: LUMO Levels Revisited, in Comparison with Preylenediimides with Sulfur Redox Switches in the Core.

Authors:  François N Miros; Stefan Matile
Journal:  ChemistryOpen       Date:  2016-02-03       Impact factor: 2.911

5.  Generation of Low-Dimensional Architectures through the Self-Assembly of Pyromellitic Diimide Derivatives.

Authors:  Chiara Musumeci; Monika Wałe Sa-Chorab; Adam Gorczyński; Grzegorz Markiewicz; Andrzej Bogucki; Roman Świetlik; Zbigniew Hnatejko; Wojciech Jankowski; Marcin Hoffmann; Emanuele Orgiu; Artur R Stefankiewicz; Violetta Patroniak; Artur Ciesielski; Paolo Samorì
Journal:  ACS Omega       Date:  2017-04-26

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Journal:  Chem Sci       Date:  2016-11-04       Impact factor: 9.825

7.  Tailoring Colors by O Annulation of Polycyclic Aromatic Hydrocarbons.

Authors:  Tanja Miletić; Andrea Fermi; Ioannis Orfanos; Aggelos Avramopoulos; Federica De Leo; Nicola Demitri; Giacomo Bergamini; Paola Ceroni; Manthos G Papadopoulos; Stelios Couris; Davide Bonifazi
Journal:  Chemistry       Date:  2017-01-23       Impact factor: 5.236

8.  Pyridinium-Functionalized Pyromellitic Diimides with Stabilized Radical Anion States.

Authors:  Andrew J Greenlee; Charles K Ofosu; Qifan Xiao; Mohammed M Modan; Daron E Janzen; Dennis D Cao
Journal:  ACS Omega       Date:  2018-01-09

9.  Selective acceleration of disfavored enolate addition reactions by anion-π interactions.

Authors:  Yingjie Zhao; Sebastian Benz; Naomi Sakai; Stefan Matile
Journal:  Chem Sci       Date:  2015-08-25       Impact factor: 9.825

10.  A NIR dye with high-performance n-type semiconducting properties.

Authors:  Jiajun Xie; Ke Shi; Kang Cai; Di Zhang; Jie-Yu Wang; Jian Pei; Dahui Zhao
Journal:  Chem Sci       Date:  2015-10-06       Impact factor: 9.825

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