Literature DB >> 26689154

Thionated perylene diimides with intense absorbance in the near-IR.

Ben A Llewellyn1, E Stephen Davies1, Constance R Pfeiffer1, Mick Cooper1, William Lewis1, Neil R Champness1.   

Abstract

A synthetic strategy involving a combination of tetra-thionation and amine substitution in the bay region of a perylene diimide (PDI) leads to remarkable examples of neutral PDIs with intense absorption maxima in the near infrared. Generation of the corresponding monoanions red shifts the absorption profile to give short-wavelength infrared bands.

Entities:  

Year:  2016        PMID： 26689154     DOI： 10.1039/c5cc09962e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 in total

1.  Bay Functionalized Perylenediimide with Pyridine Positional Isomers: NIR Absorption and Selective Colorimetric/Fluorescent Sensing of Fe3+ and Al3+ Ions.

Authors:  Anu Kundu; Jayaraman Pitchaimani; Vedichi Madhu; Pachagounder Sakthivel; Ramasamy Ganesamoorthy; Savarimuthu Philip Anthony
Journal:  J Fluoresc       Date:  2016-11-17       Impact factor: 2.217

2.  Novel Conjugated Polymers Prepared by Direct (Hetero) arylation: An Eco-Friendly Tool for Organic Electronics.

Authors:  Fuchuan Liu; Yangqian Zhang; Hang Wang; Shiming Zhang
Journal:  Molecules       Date:  2018-02-13       Impact factor: 4.411

3.  Preparation of substituted triphenylenes via nickel-mediated Yamamoto coupling.

Authors:  Zachary W Schroeder; Joshua LeDrew; Vanessa M Selmani; Kenneth E Maly
Journal:  RSC Adv       Date:  2021-12-13       Impact factor: 4.036
  3 in total

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