Search results for "photor"

showing 10 items of 340 documents

Patterning of Conducting Polymers Using UV Lithography: The in-Situ Polymerization Approach

2012

We report on the in-situ polymerization of 3T with Cu(ClO4)2 inside several host polymers such as Novolak-based negative-tone photoresist, polystyrene (PS), poly(4-vinylphenol) (P4VP), poly(methyl methacrylate) (PMMA), and poly(4-vinylphenol)-co-(methyl methacrylate) (P4VP-co-MMA) to form an interpenetrating polymer network (IPN). Conducting IPN films in the order of 10–4–150 S/cm are obtained depending on the specific IPN composition. Moreover, the convenience of this synthetic approach has been demonstrated using a commercially available negative-tone photoresist based on Novolak as a host polymer. Novolak photoresist was properly formulated with 3T and Cu(ClO4)2 to preserve as far as pos…

chemistry.chemical_classificationConductive polymerMaterials sciencePolymerPhotoresistSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionGeneral EnergyChemical engineeringchemistryPolymerizationlawPolymer chemistryInterpenetrating polymer networkPhysical and Theoretical ChemistryPhotolithographyIn situ polymerizationLithographyThe Journal of Physical Chemistry C
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In-situ synthesis of thiophene-based multifunctional polymeric networks with tunable conductivity and high photolithographic performance

2017

Abstract Design of novel multifunctional polymeric materials combining electrically conducting properties with patterning capability is a significant challenge in materials science. Herein, we report on the synthesis of multifunctional interpenetrating polymer networks (IPN) by the in-situ oxidative polymerization of thiophene-based monomers with Cu(ClO 4 ) 2 inside a novolac-based photoresist. The resulting IPNs show conductivities up to 20 S/cm depending on the monomer properties. Among them, 3,3‴-Dihexyl-2,2’:5′,2’’:5″,2‴-quaterthiophene (DH4T) is chosen because it has the largest conjugation length and excellent solubility in organic solvents. Moreover, it renders a low percolation thre…

chemistry.chemical_classificationConductive polymerMaterials sciencePolymers and PlasticsOrganic ChemistryPercolation threshold02 engineering and technologyPolymerPhotoresist010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundTerthiopheneMonomerchemistryChemical engineeringPolymerizationPolymer chemistryMaterials ChemistryThiophene0210 nano-technologyPolymer
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Halogen-bonded photoresponsive materials

2015

The aim of the present review is to illustrate to the reader the state of the art on the construction of supramolecular azobenzene-containing materials formed by halogen bonding. These materials include several examples of polymeric, liquid crystalline or crystalline species whose performances are either superior to the corresponding performances of their hydrogen-bonded analogues or simply distinctive of the halogen-bonded species. submittedVersion Peer reviewed

chemistry.chemical_classificationHalogen bondAzobenzene; Halogen bonding; Liquid crystals; Photoresponsive materials; PolymersAzobenzeneLiquid crystallinePolymersLiquid crystals116 Chemical sciencesSupramolecular chemistryPolymerchemistry.chemical_compoundchemistryAzobenzeneLiquid crystalPhotoresponsive materialLiquid crystalPolymer chemistryHalogenSettore CHIM/07 - Fondamenti Chimici Delle TecnologieHalogen bondingta116Photoresponsive materials
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Photoresponsive ionic liquid crystals assembled: Via halogen bond: En route towards light-controllable ion transporters

2017

We demonstrate that halogen bonding (XB) can offer a novel approach for the construction of photoresponsive ionic liquid crystals. In particular, we assembled two new supramolecular complexes based on 1-ethyl-3-methylimidazolium iodides and azobenzene derivatives containing an iodotetrafluoro-benzene ring as XB donor, where the iodide anion acted as an XB acceptor. DSC and X-ray diffraction analyses revealed that the preferred stoichiometry between the XB donors and acceptors is 2 : 1, and that the iodide anions act as bidentate XB-acceptors, binding two azobenzene derivatives. Due to the high directionality of the XB, calamitic superanions are obtained, while the segregation occurring betw…

chemistry.chemical_classificationHalogen bondta114ChemistryInorganic chemistryIodideSupramolecular chemistryIonic bonding02 engineering and technologySupramolecular Chemistry Liquid Crystals Halogen Bonding Photoresponsive010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAcceptor0104 chemical sciencesCrystallographychemistry.chemical_compoundAzobenzeneIonic liquidMoleculeSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical Chemistry0210 nano-technology
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3D defect engineering in polymer opals

2006

The possibility to create defined structures inside a synthetic opal is a key step towards applications in optics, where control of the propagation of light inside a photonic crystal is necessary. Here we report different methods for realizing defined embedded defects in opaline structures. Monodisperse colloids are synthesized by surfactant free emulsion polymerization of the acid labile monomer t-butyl-methacrylate (tBMA). The PtBMA colloids can be filled with sensitizer and photo acid generator and it is possible to crystallize them into photosensitive polymer opals. One method for the introduction of defects is a multilayer build-up of photo-labile (filled with photo acid generator) and…

chemistry.chemical_classificationMaterials sciencebusiness.industryDispersityEmulsion polymerizationPolymerPhotoresistMultiphoton lithographylaw.inventionPolymerizationchemistrylawOptoelectronicsPhotolithographybusinessLithographySPIE Proceedings
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Use of gaseous 13NH3 administered to intact leaves of Nicotiana tabacum to study changes in nitrogen utilization during defence induction

2010

Nitrogen-13 (t(1/2) 9.97 m), a radioactive isotope of nitrogen, offers unique opportunities to explore plant nitrogen utilization over short time periods. Here we describe a method for administering (13)N as gaseous (13)NH(3) to intact leaves of Nicotiana tabacum L. (cv Samsun), and measuring the labelled amino acids using radio high-performance liquid chromatography (HPLC) on tissue extract. We used this method to study the effects of defence induction on plant nitrogen utilization by applying treatments of methyl jasmonate (MeJA), a potent defence elicitor. MeJA caused a significant increase relative to controls in key [(13)N]amino acids, including serine, glycine and alanine by 4 h post-…

chemistry.chemical_classificationMethyl jasmonatePhysiologyNicotiana tabacumPlant ScienceMetabolismBiologybiology.organism_classificationElicitorchemistry.chemical_compoundchemistryBiochemistryGlutamate synthaseGlycinebiology.proteinPhotorespirationAmino acid synthesisPlant, Cell & Environment
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The Quest for Mononuclear Gold(II) and Its Potential Role in Photocatalysis and Drug Action.

2017

The chemistry of gold strongly focuses on the ubiquitous oxidation states +I and +III. The intermediate oxidation state +II is generally avoided in mononuclear gold species. In recent years, gold(II) has been increasingly suggested as a key intermediate in artificial photosynthesis systems, with gold(III) moieties acting as electron acceptors, as well as in gold-catalyzed photoredox catalysis and radical chemistry. This Minireview provides a concise summary of confirmed and characterized mononuclear open-shell gold(II) complexes. Recent findings on structural motifs and reactivity patterns will be discussed. Exciting developments in the fields of photosynthesis, photocatalysis, and potentia…

chemistry.chemical_classificationMolecular Structure010405 organic chemistryChemistryRadicalChemistry PharmaceuticalPhotoredox catalysisElectronsGeneral ChemistryElectron acceptor010402 general chemistryPhotochemical Processes01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesArtificial photosynthesisElectron transferOxidation statePhotocatalysisOrganic chemistryReactivity (chemistry)Organogold CompoundsAngewandte Chemie (International ed. in English)
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Design and Optimization of Chromophores for Liquid Crystal and Photorefractive Applications

1999

ABSTRACTOrganic chromophores have been exploited for a wide range of discrete optical and electronic functions as well as a growing number of combined opto-electronic functions. We are pursuing development of organic and polymer materials for a range of applications that require properties including liquid crystallinity, second order optical nonlinearity, photorefractivity and, more recently, special nonlinear optical behavior involving molecular chirality.

chemistry.chemical_classificationMolecular dynamicsCrystallinityMaterials sciencechemistryLiquid crystalPhysics::OpticsNonlinear opticsNanotechnologyPhotorefractive effectPolymerChromophoreChirality (chemistry)MRS Proceedings
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The synergy between the CsPbBr3 nanoparticle surface and the organic ligand becomes manifest in a demanding carbon–carbon coupling reaction

2020

We demonstrate here the suitability of CsPbBr3nanoparticles as photosensitizers for a demanding photoredox catalytic homo- and cross-coupling of alkyl bromides at room temperature by merely using visible light and an electron donor, thanks to the cooperative action between the nanoparticle surface and organic capping. Fil: Rosa-Pardo, Ignacio. Instituto de Ciencia Molecular; España. Universidad de Valencia; España Fil: Casadevall, Carla. Barcelona Institute Of Science And Technology. Institut Català D'investigació Química.; España Fil: Schmidt, Luciana Carina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigac…

chemistry.chemical_classificationPEROVSKITE CsPbBr3LigandChemistryMetals and AlloysReinforced carbon–carbonNanoparticleElectron donorGeneral ChemistryPhotochemistryCatalysisCoupling reactionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysis//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCARBON-CARBON COUPLING//purl.org/becyt/ford/1.4 [https]Materials ChemistryCeramics and CompositesPHOTOREDOXAlkylVisible spectrumChemical Communications
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2021

Ruthenium(II) polypyridine complexes are among the most popular sensitizers in photocatalysis, but they face some severe limitations concerning accessible excited-state energies and photostability that could hamper future applications. In this study, the borylation of heteroleptic ruthenium(II) cyanide complexes with alpha-diimine ancillary ligands is identified as a useful concept to elevate the energies of photoactive metal-to-ligand charge-transfer (MLCT) states and to obtain unusually photorobust compounds suitable for thermodynamically challenging energy transfer catalysis as well as oxidative and reductive photoredox catalysis. B(C6F5)(3) groups attached to the CN- ligands stabilize t…

chemistry.chemical_classificationPhotoisomerization010405 organic chemistryChemistryPinacolPhotoredox catalysischemistry.chemical_elementContext (language use)010402 general chemistryPhotochemistry01 natural sciencesBorylation0104 chemical sciencesCoordination complexRutheniumCatalysischemistry.chemical_compoundJACS Au
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