about
Electroluminescent materials for white organic light emitting diodes.Synthetic Aspects and Electro-Optical Properties of Fluorinated Arylenevinylenes for Luminescence and Photovoltaics.Electrowetting of nitro-functionalized oligoarylene thiols self-assembled on polycrystalline gold.Tailoring density and optical and thermal behavior of gold surfaces and nanoparticles exploiting aromatic dithiols.The correct assignment of stereochemistry in di-μ-dichlorido-bis{bis[2-(5-benzylsulfonyl)-3-fluoro-2-(pyridin-2-yl)phenyl-κ2N,C1]iridium(III)} toluene monosolvate.A synthetic strategy leading to monodisperse PPV oligomers by coupling reactions of vinyltrimethylsilanes.Synthesis of poly(aryleneethynylene)s bearing glucose units as substituents.Langmuir-Schaefer films for aligned carbon nanotubes functionalized with a conjugate polymer and photoelectrochemical response enhancement.Raman spectra of poly(p-phenylenevinylene)s with fluorinated vinylene units: evidence of inter-ring distortion.Iridium(III) complexes with sulfonyl and fluorine substituents: synthesis, stereochemistry and effect of functionalisation on their photophysical properties.Multiple Routes to Smart Nanostructured Materials from Diatom Microalgae: A Chemical Perspective.Large blue-shift in the optical spectra of fluorinated polyphenylenevinylenes. A combined theoretical and experimental study.Synthesis of S-acetyl oligoarylenedithiols via Suzuki-Miyaura cross-coupling.Photochemical tuning of light emission in a conjugated polymer containing norbornadiene units in the main chain.Pd-Catalyzed Thiophene-Aryl Coupling Reaction via C-H Bond Activation in Deep Eutectic Solvents.Self-assembly of mono- and bidentate oligoarylene thiols onto polycrystalline AuSingle white light emitting hybrid nanoarchitectures based on functionalized quantum dotsDiscrimination of Mercuric Ions in Piezoelectric Sensors with a Conjugated Polymeric Active LayerA sensitivity-enhanced field-effect chiral sensorA novel cyclization reaction between 2,3-bis(trimethylsilyl)buta-1,3-diene and acyl chlorides with straightforward formation of polysubstituted furansThin Film Construction and Characterization and Gas-Sensing Performances of a Tailored Phenylene−Thienylene CopolymerA Novel Regio- and Stereoselective Formal Cross-Coupling Reaction of Unsaturated Silanes with Arenediazonium TetrafluoroboratesInfluence of electronic and steric effects of substituted ligands coordinated to Ir(iii) complexes on the solution processed OLED propertiesSynthesis and Structure of Conjugated Molecules with the Benzofulvene CoreMono/bidentate thiol oligoarylene-based self-assembled monolayers (SAMs) for interface engineeringPhotoactive film by covalent immobilization of a bacterial photosynthetic protein on reduced graphene oxide surfaceAligning Single-Walled Carbon Nanotubes By Means Of Langmuir-Blodgett Film Deposition: Optical, Morphological, and Photo-electrochemical StudiesFluoro-functionalization of vinylene units in a polyarylenevinylene for polymer solar cellsSolvent-Free Pd-Catalyzed Heteroaryl–Aryl Coupling via C–H Bond Activation for the Synthesis of Extended Heteroaromatic Conjugated MoleculesEnhancing the Light Harvesting Capability of a Photosynthetic Reaction Center by a Tailored Molecular FluorophoreExcited-state switching by per-fluorination of para-oligophenylenesSurface Immobilized His-tagged Azurin as a Model Interface for the Investigation of Vectorial Electron Transfer in Biological Systems1,5-Diaminonaphtalene is a Highly Performing Electron-Transfer Secondary-Reaction Matrix for Laser Desorption Ionization Mass Spectrometry of Indolenine-Based CroconainesSynthesis and Computational Study of Semicroconaines and Nonsymmetric CroconainesMelanin Layer on Silicon: an Attractive Structure for a Possible Exploitation in Bio-Polymer Based Metal-Insulator-Silicon Devices
P50
Q37857713-8965AD3A-9C22-4127-87BD-815BA83F642AQ38624464-E8A6185F-2017-48ED-BB42-C6CFEECE30BAQ40254475-D1877B8C-6B16-42B5-AA30-9D62F18D59FFQ43078358-909E711B-EC6B-4410-BDA5-D9247E8B90D5Q43574745-1F8E0AE1-940E-4A84-A499-B2264D67EF22Q43618713-98E30C34-153A-45EE-8E5D-FE0627E68C4EQ44335071-0D840596-E9BF-41BD-AA78-0E4F1838E79AQ45797342-7EC383E1-834B-44D0-983A-7D3776E9F33EQ46030878-E8CB371D-4961-40F2-8850-0B75FD890956Q46236593-71A33ADB-8FF3-4FA3-8AFF-46DB919FFD04Q46253597-46C0148E-CF1C-4B24-89DA-DB7CAAA0E6A0Q46751008-F5173093-9060-4647-BB18-C1278FF78965Q46877411-091D56FC-3EC8-433D-9148-2964ECD64762Q51032920-A3C9315A-9EA6-4CDB-B213-657908B83ED3Q53083822-F2D3C7E8-49BE-4CB0-80E3-616189748250Q56977075-A5E200B7-D461-420A-A89E-7B32AB15C26AQ57351814-2A92EFFF-FAA1-481C-814C-B981AAC9C089Q57718444-B2FC0E85-8458-4D20-84A9-594814809C6EQ57718515-E5C92E0B-61E6-4C61-AB4F-3FE907462D69Q57718553-682B13A0-CC11-4F05-AC31-0E73829CEAB5Q57718670-9E2A79F8-6415-4E60-A6D7-5CCD1AB04550Q57718692-5300F53D-C6AA-4017-8839-05394C7B9413Q57853444-0F87B347-2886-4AE7-9220-49A4FDFD8FE4Q57853466-D6D1F1D1-C7E4-455D-B643-6E8BB6C7D5B3Q58237068-A09271B0-F41B-40C7-B575-CB87BAB17E21Q58560862-2879B42D-026C-4546-B58F-92B411430F13Q60164547-3131B1E1-2ACD-4913-B8B6-7C98B5955B2AQ60319477-E73D38FE-7FBC-4764-A85E-A824695B0A20Q60668033-A02029F6-C44B-465D-92AE-BA2CD6A9EE6CQ60668066-92973556-F16F-420D-9171-D3189A439AE8Q60668067-44B6A8CF-D60D-4923-B18A-62053D69E09FQ61700304-CA3F7EEB-6F2F-493D-A2A8-1E7D502CE75BQ62396258-2360508A-163F-4617-9265-C478DC85916AQ62396259-5CCC2DDB-977F-4EBC-B1C7-D90A5D2F18D8Q62396288-9EC00C31-439D-424E-BBD5-2A8D8ECF1010
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Gianluca M Farinola
@fr
Gianluca M Farinola
@sl
Gianluca M. Farinola
@en
Gianluca M. Farinola
@es
Gianluca M. Farinola
@nl
type
label
Gianluca M Farinola
@fr
Gianluca M Farinola
@sl
Gianluca M. Farinola
@en
Gianluca M. Farinola
@es
Gianluca M. Farinola
@nl
prefLabel
Gianluca M Farinola
@fr
Gianluca M Farinola
@sl
Gianluca M. Farinola
@en
Gianluca M. Farinola
@es
Gianluca M. Farinola
@nl
P106
P1153
6701749462
P21
P31
P496
0000-0002-1601-2810