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Golden Age of Fluorenylidene Phosphaalkenes–Synthesis, Structures, and Optical Properties of Heteroaromatic Derivatives and Their Gold Complexes

[Image: see text] The substitution of 2,7-dibromo-9-fluorenyl phosphaalkenes with heteroaromatic substituents (bithiophene, benzothiophene, pyridine) offers access to interesting push–pull dye molecules. Steric shielding due to the bulky P-substituent gives marked different reactivities at the 2- an...

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Autores principales: Green, Joshua P., Morales Salazar, Daniel, Gupta, Arvind Kumar, Orthaber, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684575/
https://www.ncbi.nlm.nih.gov/pubmed/32830965
http://dx.doi.org/10.1021/acs.joc.0c01336
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author Green, Joshua P.
Morales Salazar, Daniel
Gupta, Arvind Kumar
Orthaber, Andreas
author_facet Green, Joshua P.
Morales Salazar, Daniel
Gupta, Arvind Kumar
Orthaber, Andreas
author_sort Green, Joshua P.
collection PubMed
description [Image: see text] The substitution of 2,7-dibromo-9-fluorenyl phosphaalkenes with heteroaromatic substituents (bithiophene, benzothiophene, pyridine) offers access to interesting push–pull dye molecules. Steric shielding due to the bulky P-substituent gives marked different reactivities at the 2- and 7-positions, allowing the synthesis of mixed/asymmetric derivatives. Further functionalization via gold(I) coordination was demonstrated and increased the acceptor character, concomitant with a red-shifted absorption.
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spelling pubmed-76845752020-11-24 Golden Age of Fluorenylidene Phosphaalkenes–Synthesis, Structures, and Optical Properties of Heteroaromatic Derivatives and Their Gold Complexes Green, Joshua P. Morales Salazar, Daniel Gupta, Arvind Kumar Orthaber, Andreas J Org Chem [Image: see text] The substitution of 2,7-dibromo-9-fluorenyl phosphaalkenes with heteroaromatic substituents (bithiophene, benzothiophene, pyridine) offers access to interesting push–pull dye molecules. Steric shielding due to the bulky P-substituent gives marked different reactivities at the 2- and 7-positions, allowing the synthesis of mixed/asymmetric derivatives. Further functionalization via gold(I) coordination was demonstrated and increased the acceptor character, concomitant with a red-shifted absorption. American Chemical Society 2020-08-24 2020-11-20 /pmc/articles/PMC7684575/ /pubmed/32830965 http://dx.doi.org/10.1021/acs.joc.0c01336 Text en This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Green, Joshua P.
Morales Salazar, Daniel
Gupta, Arvind Kumar
Orthaber, Andreas
Golden Age of Fluorenylidene Phosphaalkenes–Synthesis, Structures, and Optical Properties of Heteroaromatic Derivatives and Their Gold Complexes
title Golden Age of Fluorenylidene Phosphaalkenes–Synthesis, Structures, and Optical Properties of Heteroaromatic Derivatives and Their Gold Complexes
title_full Golden Age of Fluorenylidene Phosphaalkenes–Synthesis, Structures, and Optical Properties of Heteroaromatic Derivatives and Their Gold Complexes
title_fullStr Golden Age of Fluorenylidene Phosphaalkenes–Synthesis, Structures, and Optical Properties of Heteroaromatic Derivatives and Their Gold Complexes
title_full_unstemmed Golden Age of Fluorenylidene Phosphaalkenes–Synthesis, Structures, and Optical Properties of Heteroaromatic Derivatives and Their Gold Complexes
title_short Golden Age of Fluorenylidene Phosphaalkenes–Synthesis, Structures, and Optical Properties of Heteroaromatic Derivatives and Their Gold Complexes
title_sort golden age of fluorenylidene phosphaalkenes–synthesis, structures, and optical properties of heteroaromatic derivatives and their gold complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684575/
https://www.ncbi.nlm.nih.gov/pubmed/32830965
http://dx.doi.org/10.1021/acs.joc.0c01336
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