Literature DB >> 33094565

Fluorescent Chromophores Containing the Nitro Group: Relatively Unexplored Emissive Properties.

Meng-Chi Chen1, Deng-Gao Chen1, Pi-Tai Chou1.   

Abstract

Apart from numerous applications, for example in azo dye precursors, explosives, and industrial processes, the nitro group (-NO2 ) appears on countless molecules in photochemical research owing to its unique characteristics such as a strong electron-withdrawing ability and facile conversion to the reduced substituent. Although it is well known as a fluorescence quencher, fluorescent chromophores that contain the nitro group have also emerged, with 3-nitrophenothiazine being recently reported to have 100 % emission quantum yield in nonpolar solvents. The diverse characters of nitro-containing chromophores motivated us to systematically review those chromophores with nitro substituents, their associated photophysical properties, and applications. In this Review, we succinctly elaborate the advance of the fluorescent nitro chromophores in fields of intramolecular charge transfer, fluorescent probes and nonlinear properties. Special attention is paid to the rationalization of the associated emission spectroscopy, so that the readers can gain insights into the structure-photophysics relationship and hence gain insights for the strategic design of nitro chromophores.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  chromophores; fluorescence; nitro groups; photophysics; quantum yields

Year:  2020        PMID: 33094565     DOI: 10.1002/cplu.202000592

Source DB:  PubMed          Journal:  Chempluschem        ISSN: 2192-6506            Impact factor:   2.863


  6 in total

1.  Making Nitronaphthalene Fluoresce.

Authors:  Katarzyna Rybicka-Jasińska; Eli M Espinoza; John A Clark; James B Derr; Gregory Carlos; Maryann Morales; Mimi Karen Billones; Omar O'Mari; Hans Ågren; Glib V Baryshnikov; Valentine I Vullev
Journal:  J Phys Chem Lett       Date:  2021-10-15       Impact factor: 6.475

2.  Polarized, V-Shaped, and Conjoined Biscoumarins: From Lack of Dipole Moment Alignment to High Brightness.

Authors:  Łukasz Kielesiński; Irena Deperasińska; Olaf Morawski; Kateryna V Vygranenko; Erik T Ouellette; Daniel T Gryko
Journal:  J Org Chem       Date:  2022-04-12       Impact factor: 4.198

3.  Nitro-Substituted Dipyrrolyldiketone BF2 Complexes as Electronic-State-Adjustable Anion-Responsive π-Electronic Systems.

Authors:  Atsuko Kuno; Hiromitsu Maeda
Journal:  Molecules       Date:  2021-01-23       Impact factor: 4.411

4.  Potent strategy towards strongly emissive nitroaromatics through a weakly electron-deficient core.

Authors:  Bartłomiej Sadowski; Marzena Kaliszewska; Yevgen M Poronik; Małgorzata Czichy; Patryk Janasik; Marzena Banasiewicz; Dominik Mierzwa; Wojciech Gadomski; Trevor D Lohrey; John A Clark; Mieczysław Łapkowski; Bolesław Kozankiewicz; Valentine I Vullev; Andrzej L Sobolewski; Piotr Piatkowski; Daniel T Gryko
Journal:  Chem Sci       Date:  2021-09-29       Impact factor: 9.825

5.  Twisted intramolecular charge transfer of nitroaromatic push-pull chromophores.

Authors:  Sebok Lee; Myungsam Jen; Taehyung Jang; Gisang Lee; Yoonsoo Pang
Journal:  Sci Rep       Date:  2022-04-21       Impact factor: 4.996

6.  A Fluorescent Cage for Supramolecular Sensing of 3-Nitrotyrosine in Human Blood Serum.

Authors:  Lidia A Pérez-Márquez; Marcelle D Perretti; Raúl García-Rodríguez; Fernando Lahoz; Romen Carrillo
Journal:  Angew Chem Int Ed Engl       Date:  2022-05-23       Impact factor: 16.823

  6 in total

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