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A novel design for porphyrin based D–s–A systems as molecular rectifiers

Two Si-based hybrid self-assembled monolayers of porphyrin based on a D–s–A system were synthesized by electro-grafting. The monolayers showed a stable and reversible rectification at room temperature. The monolayer fabricated using a porphyrin with an eleven-carbon alkyl chain linker was comparativ...

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Autores principales: Garg, Kavita, Majumder, Chiranjib, Gupta, Shiv K., Aswal, Dinesh Kumar, Nayak, Sandip Kumar, Chattopadhyay, Subrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964962/
https://www.ncbi.nlm.nih.gov/pubmed/29899898
http://dx.doi.org/10.1039/c5sc03590b
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author Garg, Kavita
Majumder, Chiranjib
Gupta, Shiv K.
Aswal, Dinesh Kumar
Nayak, Sandip Kumar
Chattopadhyay, Subrata
author_facet Garg, Kavita
Majumder, Chiranjib
Gupta, Shiv K.
Aswal, Dinesh Kumar
Nayak, Sandip Kumar
Chattopadhyay, Subrata
author_sort Garg, Kavita
collection PubMed
description Two Si-based hybrid self-assembled monolayers of porphyrin based on a D–s–A system were synthesized by electro-grafting. The monolayers showed a stable and reversible rectification at room temperature. The monolayer fabricated using a porphyrin with an eleven-carbon alkyl chain linker was comparatively more compact and exhibited a 10(5) times higher rectification ratio (RR) relative to another similar system that had a six-carbon alkyl chain linker, possibly because of the compact packing.
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spelling pubmed-59649622018-06-13 A novel design for porphyrin based D–s–A systems as molecular rectifiers Garg, Kavita Majumder, Chiranjib Gupta, Shiv K. Aswal, Dinesh Kumar Nayak, Sandip Kumar Chattopadhyay, Subrata Chem Sci Chemistry Two Si-based hybrid self-assembled monolayers of porphyrin based on a D–s–A system were synthesized by electro-grafting. The monolayers showed a stable and reversible rectification at room temperature. The monolayer fabricated using a porphyrin with an eleven-carbon alkyl chain linker was comparatively more compact and exhibited a 10(5) times higher rectification ratio (RR) relative to another similar system that had a six-carbon alkyl chain linker, possibly because of the compact packing. Royal Society of Chemistry 2016-02-01 2015-11-16 /pmc/articles/PMC5964962/ /pubmed/29899898 http://dx.doi.org/10.1039/c5sc03590b Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Garg, Kavita
Majumder, Chiranjib
Gupta, Shiv K.
Aswal, Dinesh Kumar
Nayak, Sandip Kumar
Chattopadhyay, Subrata
A novel design for porphyrin based D–s–A systems as molecular rectifiers
title A novel design for porphyrin based D–s–A systems as molecular rectifiers
title_full A novel design for porphyrin based D–s–A systems as molecular rectifiers
title_fullStr A novel design for porphyrin based D–s–A systems as molecular rectifiers
title_full_unstemmed A novel design for porphyrin based D–s–A systems as molecular rectifiers
title_short A novel design for porphyrin based D–s–A systems as molecular rectifiers
title_sort novel design for porphyrin based d–s–a systems as molecular rectifiers
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964962/
https://www.ncbi.nlm.nih.gov/pubmed/29899898
http://dx.doi.org/10.1039/c5sc03590b
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