His primary scientific interests are in Ferrocene, Redox, Photochemistry, Inorganic chemistry and Electrochemistry. As part of the same scientific family, Pedro Molina usually focuses on Ferrocene, concentrating on Combinatorial chemistry and intersecting with Organic chemistry, Stereochemistry, Ring, Nitramarine and Fascaplysin. His studies in Redox integrate themes in fields like Imidazole, Crystallography, Receptor and Metal ions in aqueous solution, Metal.
His work carried out in the field of Photochemistry brings together such families of science as Pyrene, Excimer, Transition metal, Ion and Aqueous solution. His Inorganic chemistry study incorporates themes from Hydrogen, Molecule, Naked eye and Absorption spectroscopy. His Electrochemistry research incorporates elements of Pyridine, Intramolecular force, Proton NMR and Click chemistry.
His primary areas of study are Organic chemistry, Medicinal chemistry, Stereochemistry, Ring and Bicyclic molecule. His work deals with themes such as Combinatorial chemistry and Polymer chemistry, which intersect with Organic chemistry. His Medicinal chemistry research includes themes of Intramolecular force and Triphenylphosphine.
His research on Stereochemistry also deals with topics like
His main research concerns Ferrocene, Photochemistry, Redox, Electrochemistry and Inorganic chemistry. His Ferrocene research includes elements of Crystallography, Receptor, Ion, Triazole and Absorption spectroscopy. His study in Photochemistry is interdisciplinary in nature, drawing from both Proton NMR, Metal and Solvent.
His work carried out in the field of Redox brings together such families of science as Molecule, Staudinger reaction and Ion pairs. His Electrochemistry research is multidisciplinary, incorporating elements of Pyridine and Guanidine. His Combinatorial chemistry research focuses on Organic chemistry and how it relates to Chemical synthesis.
His primary areas of investigation include Ferrocene, Redox, Photochemistry, Inorganic chemistry and Electrochemistry. Pedro Molina has included themes like Thiourea and Moiety, Stereochemistry in his Ferrocene study. The Redox study combines topics in areas such as Receptor, Imidazole and Absorption spectroscopy.
His Photochemistry research integrates issues from Ion, Metal and Pyrene. His Inorganic chemistry study incorporates themes from Mercury and Aqueous solution. His Electrochemistry study combines topics from a wide range of disciplines, such as Crystallography, Pyridine, Proton NMR and Click chemistry.
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Highly selective chromogenic and redox or fluorescent sensors of Hg2+ in aqueous environment based on 1,4-disubstituted azines.
Antonio Caballero;Rosario Martínez;Vega Lloveras;Imma Ratera.
Journal of the American Chemical Society (2005)
Iminophosphoranes: Useful Building Blocks for the Preparation of Nitrogen-Containing Heterocycles
Pedro Molina;Maria Jesús Vilaplana.
New Hg2+ and Cu2+ Selective Chromo- and Fluoroionophore Based on a Bichromophoric Azine
Rosario Martínez;Arturo Espinosa;and Alberto Tárraga;Pedro Molina.
Organic Letters (2005)
Imidazole derivatives: a comprehensive survey of their recognition properties.
Pedro Molina;Alberto Tárraga;Francisco Otón.
Organic and Biomolecular Chemistry (2012)
Anion Recognition Strategies Based on Combined Noncovalent Interactions.
Pedro Molina;Fabiola Zapata;Antonio Caballero.
Chemical Reviews (2017)
Cation Coordination Induced Modulation of the Anion Sensing Properties of a Ferrocene−Imidazophenanthroline Dyad: Multichannel Recognition from Phosphate-Related to Chloride Anions
Fabiola Zapata;Antonio Caballero;Arturo Espinosa;Alberto Tárraga.
Journal of Organic Chemistry (2008)
2-Aza-1,3-butadiene Derivatives Featuring an Anthracene or Pyrene Unit: Highly Selective Colorimetric and Fluorescent Signaling of Cu2+ Cation
Rosario Martínez;Fabiola Zapata;Antonio Caballero;Arturo Espinosa.
Organic Letters (2006)
Application of Iminophosphorane-Based Methodologies for the Synthesis of Natural Products
Pilar M. Fresneda;Pedro Molina.
One-pot preparation of derivatives of the unknown 1,9-diazaphenalene ring by a consecutive electrocyclic ring-closure/Claisen rearrangement/intramolecular amination process
Pedro Molina;Mateo Alajarín;Angel Vidal.
Journal of The Chemical Society, Chemical Communications (1990)
A Click-Generated Triazole Tethered Ferrocene−Pyrene Dyad for Dual-Mode Recognition of the Pyrophosphate Anion
Tomás Romero;Antonio Caballero;Alberto Tárraga;Pedro Molina.
Organic Letters (2009)
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