Strongly Polarized π-Extended 1,4-Dihydropyrrolo[3,2-<i>b</i>]pyrroles Fused with Tetrazolo[1,5-<i>a</i>]quinolines-Reference-Cited by-同舟云学术

Strongly Polarized π-Extended 1,4-Dihydropyrrolo[3,2-b]pyrroles Fused with Tetrazolo[1,5-a]quinolines

Published:2024-03-26 Issue:7 Volume:89 Page:4657-4672
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Teimouri Mohammad B.¹²^ORCID,Deperasińska Irena³,Rammo Matt⁴,Banasiewicz Marzena³^ORCID,Stark Charles W.⁴^ORCID,Dobrzycki Łukasz⁵^ORCID,Cyrański Michał K.⁵,Rebane Aleksander⁴⁶^ORCID,Gryko Daniel T.¹^ORCID

Affiliation:

1. Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, Warsaw 01-224, Poland

2. Faculty of Chemistry, Kharazmi University, Mofateh Ave, Tehran 15719-14911, Iran

3. Institute of Physics of Polish Academy of Sciences, Polish Academy of Sciences, Al. Lotników 32/46, Warsaw 02-668, Poland

4. National Institute for Chemical Physics and Biophysics, Akadeemia tee 23, Tallinn 12618, Estonia

5. Faculty of Chemistry, University of Warsaw, Pasteura 1, Warsaw 02-093, Poland

6. Department of Physics, Montana State University, Bozeman, Montana 59717, United States

Funder

Narodowe Centrum Nauki

HORIZON EUROPE Marie Sklodowska-Curie Actions

Fundacja na rzecz Nauki Polskiej

Kharazmi University

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02916

Reference65 articles.

1. Aromaticity Competition in Differentially Fused Borepin-Containing Polycyclic Aromatics

2. Tetrazolo[1,5-a]pyridine-Containing π-Conjugated Systems: Synthesis, Properties, and Semiconducting Characteristics

3. Recent Advances in Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds

4. Synthesis, Structures, and Properties of Core-Expanded Azacoronene Analogue: A Twisted π-System with Two N-Doped Heptagons

5. Modular Nitrogen‐Doped Concave Polycyclic Aromatic Hydrocarbons for High‐Performance Organic Light‐Emitting Diodes with Tunable Emission Mechanisms**