Di‐ and Tetracyano‐Substituted Pyrene‐Fused Pyrazaacenes: Aggregation in the Solid State

Five di‐ and tetracyano‐substituted pyrene‐fused pyrazaacenes were synthesized and studied as potential electron acceptors in the solid state. Single crystals of all compounds were grown and the crystal packing studied by DFT calculations (transfer integrals and reorganization energies) to get insig...

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Detalles Bibliográficos
Autores principales: Ueberricke, Lucas, Ciubotaru, Ioana, Ghalami, Farhad, Mildner, Felix, Rominger, Frank, Elstner, Marcus, Mastalerz, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Full Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540477/
https://www.ncbi.nlm.nih.gov/pubmed/32459010
http://dx.doi.org/10.1002/chem.202002382
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author Ueberricke, Lucas
Ciubotaru, Ioana
Ghalami, Farhad
Mildner, Felix
Rominger, Frank
Elstner, Marcus
Mastalerz, Michael
author_facet Ueberricke, Lucas
Ciubotaru, Ioana
Ghalami, Farhad
Mildner, Felix
Rominger, Frank
Elstner, Marcus
Mastalerz, Michael
author_sort Ueberricke, Lucas
collection PubMed
description Five di‐ and tetracyano‐substituted pyrene‐fused pyrazaacenes were synthesized and studied as potential electron acceptors in the solid state. Single crystals of all compounds were grown and the crystal packing studied by DFT calculations (transfer integrals and reorganization energies) to get insight into possible use for semiconducting charge transport.
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spelling pubmed-75404772020-10-09 Di‐ and Tetracyano‐Substituted Pyrene‐Fused Pyrazaacenes: Aggregation in the Solid State Ueberricke, Lucas Ciubotaru, Ioana Ghalami, Farhad Mildner, Felix Rominger, Frank Elstner, Marcus Mastalerz, Michael Chemistry Full Papers Five di‐ and tetracyano‐substituted pyrene‐fused pyrazaacenes were synthesized and studied as potential electron acceptors in the solid state. Single crystals of all compounds were grown and the crystal packing studied by DFT calculations (transfer integrals and reorganization energies) to get insight into possible use for semiconducting charge transport. John Wiley and Sons Inc. 2020-07-30 2020-09-04 /pmc/articles/PMC7540477/ /pubmed/32459010 http://dx.doi.org/10.1002/chem.202002382 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Ueberricke, Lucas
Ciubotaru, Ioana
Ghalami, Farhad
Mildner, Felix
Rominger, Frank
Elstner, Marcus
Mastalerz, Michael
Di‐ and Tetracyano‐Substituted Pyrene‐Fused Pyrazaacenes: Aggregation in the Solid State
title Di‐ and Tetracyano‐Substituted Pyrene‐Fused Pyrazaacenes: Aggregation in the Solid State
title_full Di‐ and Tetracyano‐Substituted Pyrene‐Fused Pyrazaacenes: Aggregation in the Solid State
title_fullStr Di‐ and Tetracyano‐Substituted Pyrene‐Fused Pyrazaacenes: Aggregation in the Solid State
title_full_unstemmed Di‐ and Tetracyano‐Substituted Pyrene‐Fused Pyrazaacenes: Aggregation in the Solid State
title_short Di‐ and Tetracyano‐Substituted Pyrene‐Fused Pyrazaacenes: Aggregation in the Solid State
title_sort di‐ and tetracyano‐substituted pyrene‐fused pyrazaacenes: aggregation in the solid state
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540477/
https://www.ncbi.nlm.nih.gov/pubmed/32459010
http://dx.doi.org/10.1002/chem.202002382
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