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Eduardo Arias

Publications -  79
Citations -  691

Eduardo Arias is an academic researcher. The author has contributed to research in topics: Fluorescence spectroscopy & Liquid crystal. The author has an hindex of 13, co-authored 73 publications receiving 564 citations.

Papers
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Synthesis and photophysical characterization of organotin compounds derived from Schiff bases for organic light emitting diodes

TL;DR: In this paper, the multicomponent reaction of the 2-hydroxynaphthaldehyde with 2-aminophenol derivatives and their in situ complexation with diphenyltin oxide in acetonitrile provided, in high yield, the products: (((E)-12-nitro-8,8-diphenylbenzo[d]naphtho[1,2-h][1,3,6,2]dioxazastannonine and (E)-11-nitrogen-8-8-,dipphen
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New application of fluorescent organotin compounds derived from Schiff bases: synthesis, X-ray structures, photophysical properties, cytotoxicity and fluorescent bioimaging

TL;DR: To the best of the knowledge, this is the first report of organotin compounds with Schiff base ligands investigated for fluorescence bioimaging (FBI) and the crystal structures for someorganotin compounds were determined by single crystal X-ray diffraction analysis.
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On the Influence of Silver Nanoparticles Size in the Electrical Conductivity of PEDOT: PSS

TL;DR: In this paper, the influence of the size of the nanoparticles on the electrical conductivity of PEDOT:PSS in Ag(PEDOT PSS) films was studied.
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Synthesis, optical properties and supramolecular order of π-conjugated 2,5-di(alcoxy)phenyleneethynylene oligomers

TL;DR: In this paper, two series of 2,5-di(alkoxy)phenyleneethynylene oligomers were synthesized by Sonogashira-Heck coupling reaction and the chemical structure was corroborated by 1H, 13C, APT, DEPT-135 NMR, Raman, FTIR and MALDI-TOF mass spectrometry.
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One-pot microwave-assisted synthesis of organotin Schiff bases: an optical and electrochemical study towards their effects in organic solar cells

TL;DR: In this paper, 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.