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A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications
The synthesis and characterization of a family of [60]fullerocurcuminoids obtained via Bingel reactions is reported. The new C(60) derivatives include curcumin and curcuminoids with a variety of end groups. Preliminary biological experiments show the potential activity of the compound containing a c...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754101/ https://www.ncbi.nlm.nih.gov/pubmed/31543960 http://dx.doi.org/10.1039/c8ra08334g |
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author | Castro, Edison Cerón, Maira R. Garcia, Andrea Hernandez Kim, Quentin Etcheverry-Berríos, Alvaro Morel, Mauricio J. Díaz-Torres, Raúl Qian, Wenjie Martinez, Zachary Mendez, Lois Perez, Frank Santoyo, Christy A. Gimeno-Muñoz, Raquel Esper, Ronda Gutierrez, Denisse A. Varela-Ramirez, Armando Aguilera, Renato J. Llano, Manuel Soler, Monica Aliaga-Alcalde, Núria Echegoyen, Luis |
author_facet | Castro, Edison Cerón, Maira R. Garcia, Andrea Hernandez Kim, Quentin Etcheverry-Berríos, Alvaro Morel, Mauricio J. Díaz-Torres, Raúl Qian, Wenjie Martinez, Zachary Mendez, Lois Perez, Frank Santoyo, Christy A. Gimeno-Muñoz, Raquel Esper, Ronda Gutierrez, Denisse A. Varela-Ramirez, Armando Aguilera, Renato J. Llano, Manuel Soler, Monica Aliaga-Alcalde, Núria Echegoyen, Luis |
author_sort | Castro, Edison |
collection | PubMed |
description | The synthesis and characterization of a family of [60]fullerocurcuminoids obtained via Bingel reactions is reported. The new C(60) derivatives include curcumin and curcuminoids with a variety of end groups. Preliminary biological experiments show the potential activity of the compound containing a curcumin addend, which exhibits moderate anti-HIV-1 and radical scavenger properties, but no anti-cancer activity. In addition, the new fullerocurcuminoids exhibit HOMO/LUMO energy levels that are reasonably matched with those of perovskites and when they were tested in perovskite solar cells (PSCs) as the electron transporting material (ETM), photoconversion efficiencies ranging from 14.04–14.95% were obtained, whereas a value of 16.23% was obtained for [6,6]-phenyl-C(61)-butyric acid methyl ester (PC(61)BM) based devices. |
format | Online Article Text |
id | pubmed-6754101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-67541012019-10-02 A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications Castro, Edison Cerón, Maira R. Garcia, Andrea Hernandez Kim, Quentin Etcheverry-Berríos, Alvaro Morel, Mauricio J. Díaz-Torres, Raúl Qian, Wenjie Martinez, Zachary Mendez, Lois Perez, Frank Santoyo, Christy A. Gimeno-Muñoz, Raquel Esper, Ronda Gutierrez, Denisse A. Varela-Ramirez, Armando Aguilera, Renato J. Llano, Manuel Soler, Monica Aliaga-Alcalde, Núria Echegoyen, Luis RSC Adv Chemistry The synthesis and characterization of a family of [60]fullerocurcuminoids obtained via Bingel reactions is reported. The new C(60) derivatives include curcumin and curcuminoids with a variety of end groups. Preliminary biological experiments show the potential activity of the compound containing a curcumin addend, which exhibits moderate anti-HIV-1 and radical scavenger properties, but no anti-cancer activity. In addition, the new fullerocurcuminoids exhibit HOMO/LUMO energy levels that are reasonably matched with those of perovskites and when they were tested in perovskite solar cells (PSCs) as the electron transporting material (ETM), photoconversion efficiencies ranging from 14.04–14.95% were obtained, whereas a value of 16.23% was obtained for [6,6]-phenyl-C(61)-butyric acid methyl ester (PC(61)BM) based devices. The Royal Society of Chemistry 2018-12-13 /pmc/articles/PMC6754101/ /pubmed/31543960 http://dx.doi.org/10.1039/c8ra08334g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Castro, Edison Cerón, Maira R. Garcia, Andrea Hernandez Kim, Quentin Etcheverry-Berríos, Alvaro Morel, Mauricio J. Díaz-Torres, Raúl Qian, Wenjie Martinez, Zachary Mendez, Lois Perez, Frank Santoyo, Christy A. Gimeno-Muñoz, Raquel Esper, Ronda Gutierrez, Denisse A. Varela-Ramirez, Armando Aguilera, Renato J. Llano, Manuel Soler, Monica Aliaga-Alcalde, Núria Echegoyen, Luis A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications |
title | A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications |
title_full | A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications |
title_fullStr | A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications |
title_full_unstemmed | A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications |
title_short | A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications |
title_sort | new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754101/ https://www.ncbi.nlm.nih.gov/pubmed/31543960 http://dx.doi.org/10.1039/c8ra08334g |
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