Eduardo Arias

Prof. Eduardo Arias

Advanced Materials, Centro de Investigación en Química Aplicada, Saltillo, Coahuila de Zaragoza, Mexico
orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2005 in European Polymer Journal
Verified
Journal Article
Closed access
Rodolfo Cruz-SilvaRodolfo Cruz-Silva
Rodolfo Cruz-Silva
JRJorge Romero-García
Jorge Romero-García
JAJose Luis Angulo-Sánchez
Jose Luis Angulo-Sánchez
ALAntonio Ledezma-Pérez
Antonio Ledezma-Pérez
Eduardo AriasEduardo Arias
Eduardo Arias
EFErika Flores-Loyola
Erika Flores-Loyola

1 July 2014 in Dyes and Pigments
Verified
Journal Article
Closed access
MGMaría C. García-López
María C. García-López
BMBlanca M. Muñoz-Flores
Blanca M. Muñoz-Flores
VPVíctor M. Jiménez Pérez
Víctor M. Jiménez Pérez
IMIvana Moggio
Ivana Moggio
Eduardo AriasEduardo Arias
Eduardo Arias
RSRosa Santillan
Rosa Santillan

8 June 2015 in Journal of Materials Chemistry B
Verified
Journal Article
Closed access
PDF file
VPVíctor M. Jiménez Pérez
Víctor M. Jiménez Pérez
MGMaría C. García-López
María C. García-López
BMBlanca M. Muñoz-Flores
Blanca M. Muñoz-Flores
RCRodrigo Chan-Navarro
Rodrigo Chan-Navarro
JBJessica C. Berrones-Reyes
Jessica C. Berrones-Reyes
ACArturo Chavez-Reyes
Arturo Chavez-Reyes
A series of eight new organotin compounds derived from Schiff bases has been prepared by a multicomponent reaction from 2-hydroxy-1-naphthaldehyde or 4-substituted-2-hydroxybenzalhedyde, benzhydrazine, and the corresponding diorganotin oxide (R2SnO, R = nBu or Ph). All of the compounds were fully characterized by NMR (1H, 13C, and 119Sn), IR, UV/vis, elemental analyses and fluorescence spectroscopy. The crystal structures for some organotin compounds were determined by single crystal X-ray diffraction analysis. All of the compounds display fluorescence at room temperature with quantum yields of about 2 × 10−4 to 0.56. The cytotoxic activity and cellular imaging studies were carried out with the newly synthesized compounds. To the best of our knowledge, this is the first report of organotin compounds with Schiff base ligands investigated for fluorescence bioimaging (FBI).

1 February 2006 in Polymer
Verified
Journal Article
Closed access
Rodolfo Cruz-SilvaRodolfo Cruz-Silva
Rodolfo Cruz-Silva
CRC. Ruiz-Flores
C. Ruiz-Flores
LAL. Arizmendi
L. Arizmendi
JRJ. Romero-García
J. Romero-García
Eduardo AriasEduardo Arias
Eduardo Arias
MFM.H. Farias
M.H. Farias

19 July 2018 in New Journal of Chemistry
Verified
Journal Article
Closed access
PDF file
ACArelly M. Cantón-Díaz
Arelly M. Cantón-Díaz
BMBlanca M. Muñoz-Flores
Blanca M. Muñoz-Flores
IMIvana Moggio
Ivana Moggio
Eduardo AriasEduardo Arias
Eduardo Arias
Arxel De LeónArxel De León
Arxel De León
VPVíctor M. Jiménez Pérez
Víctor M. Jiménez Pérez
Four organotin compounds bearing Schiff bases were prepared via a multicomponent microwave-assisted reaction among 2-hydroxy-1-naphthaldehyde, 2-aminophenol derivatives and the corresponding diorganotin oxide (R2SnO, R = nBu or Ph), with high yields and a low economic/environmental impact. All of the compounds were fully characterized by NMR (1H, 13C, and 119Sn) spectroscopy, high-resolution mass spectrometry, X-ray diffraction, cyclic voltammetry, UV/Vis spectroscopy, and fluorescence spectroscopy. All of the compounds absorb in the visible region around 480–490 nm, close to the maximum solar emission, with an optical band gap of around 2.3 eV and low fluorescence quantum yields. According to the electrochemical study, they present LUMO values close to that of [6,6]-phenyl-C61-butyric acid methyl ester (PCBM-C60), a typical electron acceptor organic photovoltaic material. Based on this combined optical/electrochemical study and as it allows the preparation of homogeneous spun films, the n-butyltin complex with carboxylic acid was selected for the investigation of its possible photovoltaic properties in organic solar cells. Charge photogeneration was obtained only using this organotin compound as an electron acceptor material with poly(3-hexylthiophene, P3HT) (typical electron donor material) with an open circuit voltage of 300 mV, a short-circuit current density of 0.11 mA cm−2 and an efficiency of 5.2 × 10−3%. Despite the fact that the efficiency is much lower with respect to the reference device P3HT/PCBM-C60, this preliminary result suggests that, after chemical and device processing optimization, tin complexes with Schiff bases could be applied as electron acceptor materials in organic photovoltaic devices.

25 March 2000 in Langmuir
Verified
Journal Article
Closed access
Eduardo AriasEduardo Arias
Eduardo Arias
JAJ. C. Arnault
J. C. Arnault
DGD. Guillon
D. Guillon
TMT. Maillou
T. Maillou
JMJ. Le Moigne
J. Le Moigne
Jean-Michel NunziJean-Michel Nunzi
Jean-Michel Nunzi