Synthesis of reactive 1,3-diphenyl-6-aryl-substituted fulvene chromophores

This data article describes a detailed synthetic strategy and experimental data for the synthesis of brominated fulvene chromophores as reactive precursors/monomers for conjugated organic materials. Metal-mediated coupling reactions of brominated fulvenes would result in conjugated small molecules o...

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Main Authors: Stephen M. Budy, David Y. Son, Gary J. Balaich, Scott T. Iacono
Format: Article
Language:English
Published: Elsevier 2018-08-01
Series:Data in Brief
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340918306772
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author Stephen M. Budy
David Y. Son
Gary J. Balaich
Scott T. Iacono
author_facet Stephen M. Budy
David Y. Son
Gary J. Balaich
Scott T. Iacono
author_sort Stephen M. Budy
collection DOAJ
description This data article describes a detailed synthetic strategy and experimental data for the synthesis of brominated fulvene chromophores as reactive precursors/monomers for conjugated organic materials. Metal-mediated coupling reactions of brominated fulvenes would result in conjugated small molecules or polymers that would find application as organic light emitting diodes (OLEDs) and photovoltaic (PV) applications.
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spelling doaj.art-23b2493e12d7433ea4fa0967c762e5552022-12-21T18:59:17ZengElsevierData in Brief2352-34092018-08-011916381642Synthesis of reactive 1,3-diphenyl-6-aryl-substituted fulvene chromophoresStephen M. Budy0David Y. Son1Gary J. Balaich2Scott T. Iacono3Department of Chemistry, Southern Methodist University, Dallas, TX 75275, USADepartment of Chemistry, Southern Methodist University, Dallas, TX 75275, USADepartment of Chemistry, Chemistry Research Center, United States Air Force Academy, Colorado Springs, CO 80919, USADepartment of Chemistry, Chemistry Research Center, United States Air Force Academy, Colorado Springs, CO 80919, USA; Corresponding author.This data article describes a detailed synthetic strategy and experimental data for the synthesis of brominated fulvene chromophores as reactive precursors/monomers for conjugated organic materials. Metal-mediated coupling reactions of brominated fulvenes would result in conjugated small molecules or polymers that would find application as organic light emitting diodes (OLEDs) and photovoltaic (PV) applications.http://www.sciencedirect.com/science/article/pii/S2352340918306772
spellingShingle Stephen M. Budy
David Y. Son
Gary J. Balaich
Scott T. Iacono
Synthesis of reactive 1,3-diphenyl-6-aryl-substituted fulvene chromophores
Data in Brief
title Synthesis of reactive 1,3-diphenyl-6-aryl-substituted fulvene chromophores
title_full Synthesis of reactive 1,3-diphenyl-6-aryl-substituted fulvene chromophores
title_fullStr Synthesis of reactive 1,3-diphenyl-6-aryl-substituted fulvene chromophores
title_full_unstemmed Synthesis of reactive 1,3-diphenyl-6-aryl-substituted fulvene chromophores
title_short Synthesis of reactive 1,3-diphenyl-6-aryl-substituted fulvene chromophores
title_sort synthesis of reactive 1 3 diphenyl 6 aryl substituted fulvene chromophores
url http://www.sciencedirect.com/science/article/pii/S2352340918306772
work_keys_str_mv AT stephenmbudy synthesisofreactive13diphenyl6arylsubstitutedfulvenechromophores
AT davidyson synthesisofreactive13diphenyl6arylsubstitutedfulvenechromophores
AT garyjbalaich synthesisofreactive13diphenyl6arylsubstitutedfulvenechromophores
AT scotttiacono synthesisofreactive13diphenyl6arylsubstitutedfulvenechromophores