Search results for "PHI"

showing 10 items of 28259 documents

Marlies Jansegers, Hacia un enfoque múltiple de la polisemia. Un estudio empírico del verbo multimodal “sentir” desde una perspectiva sincrónica y di…

2019

This article reviews Hacia un enfoque multiple de la polisemia. Un estudio empirico del verbo multimodal “sentir” desde una perspectiva sincronica y diacronica 978 3 11 047470 1

010309 optics050101 languages & linguisticsLinguistics and LanguagePhilosophy0103 physical sciences05 social sciences0501 psychology and cognitive sciences01 natural sciencesHumanitiesLinguisticsLanguages in Contrast
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Sensitive Assays by Nucleophile-Induced Rearrangement of Photoactivated Diarylethenes.

2018

Upon light-induced isomerization, diarylethenes (DAEs) equipped with reactive aldehyde moieties rearrange selectively in the presence of amines, accompanied by decoloration. In a comprehensive study, the probe structure was optimized with regard to its inherent reactivity in the nucleophile-triggered rearrangement reaction. Detailed structure−reactivity relationships could be derived, in particular with regard to the type of integrated (het)aryl moieties as well as the location of the formyl residue, and the probes’ intrinsic reactivity with primary and secondary amines was optimized. Utilizing an ancillary base, the initially formed rearrangement product can engage in a subsequent catalyti…

010402 general chemistry01 natural sciencesBiochemistryAldehydeCatalysischemistry.chemical_compoundPhotochromismColloid and Surface ChemistryNucleophile541 Physikalische ChemieReactivity (chemistry)Rearrangement reactionsensingchemistry.chemical_classification010405 organic chemistryArylGeneral ChemistryphotochromismCombinatorial chemistry0104 chemical sciences540 Chemie und zugeordnete WissenschaftenaminechemistryCatalytic cycleddc:540diaryletheneddc:541547 Organische ChemieIsomerizationddc:547Journal of the American Chemical Society
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The Taming of Redox‐Labile Phosphidotitanocene Cations

2019

International audience; Tame d0 phosphidotitanocene cations stabilized with a pendant tertiary phosphane arm are reported. These compounds were obtained by one-electron oxidation of d1 precursors with [Cp2Fe][BPh4]. The electronic structure of these compounds was studied experimentally (EPR, UV/Vis, and NMR spectroscopy, X-ray diffraction analysis) and through DFT calculations. The theoretical analysis of the bonding situation by using the electron localization function (ELF) shows the presence of π-interactions between the phosphido ligand and Ti in the d0 complexes, whereas dπ–pπ repulsion prevents such interactions in the d1 complexes. In addition, CH–π interactions were observed in seve…

010402 general chemistry01 natural sciencesRedoxTransition metal phosphidesCatalysisFrustrated Lewis pairlaw.inventionchemistry.chemical_compoundFrustrated Lewis Pair (FLP)[CHIM.ANAL]Chemical Sciences/Analytical chemistrylaw[CHIM.COOR]Chemical Sciences/Coordination chemistryPhosphorus LigandsElectron paramagnetic resonanceDiphenylacetyleneComputingMilieux_MISCELLANEOUSTitanium[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryLigandOrganic Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyElectron localization function0104 chemical sciencesHomolysis[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryDensity Functional Theory (DFT)Crystallographychemistry[CHIM.CHEM]Chemical Sciences/CheminformaticsChemistry – A European Journal
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Nucleophilic iodonium interactions (NIIs) in 2-coordinate iodine(i) and silver(i) complexes

2021

The generality of nucleophilic iodonium interactions (NIIs) has been demonstrated by preparing a range of silver(i) and iodonium (I+) complexes and studying their 15N NMR chemical shifts, with the first example of a NII-complex involving a 2-coordinate silver(i) complex being confirmed by X-ray crystallography, and its nucleophilicity studied by DFT calculations.

010405 organic chemistryChemistryChemical shiftMetals and Alloyschemistry.chemical_elementGeneral Chemistry010402 general chemistryIodine01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNucleophileComputational chemistryMaterials ChemistryCeramics and CompositesChemical Communications
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Kinetic control in the temperature-dependent sequential growth of surface-confined supramolecular copolymers

2017

We report the sequential growth of supramolecular copolymers on gold surfaces, using oppositely charged dendritic peptide amphiphiles. By including water-solubilising thermoresponsive chains in the monomer design, we observed non-linear effects in the temperature-dependent sequential growth. The step-wise copolymerisation process is characterised using temperature dependent SPR and QCM-D measurements. At higher temperatures, dehydration of peripheral oligoethylene glycol chains supports copolymer growth due to more favourable comonomer interactions. Both monomers incorporate methionine amino acids but remarkably, desorption of the copolymers via competing sulphur gold interactions with the …

010405 organic chemistryChemistryComonomerSupramolecular chemistryQuartz crystal microbalance010402 general chemistry01 natural sciences0104 chemical sciencesMetalchemistry.chemical_compoundMonomerChemical engineeringDesorptionvisual_artAmphiphilePolymer chemistryCopolymervisual_art.visual_art_mediumPhysical and Theoretical ChemistryFaraday Discussions
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2020

The course of organic chemical reactions is efficiently modelled through the concepts of “electrophiles” and “nucleophiles” (meaning electron-seeking and nucleus-seeking reactive species). On the one hand, an advanced approach of the correlation of the nucleophilicity parameters N and electrophilicity E has been delivered from the linear free energy relationship log k (20 °C) = s(N + E). On the other hand, the general influence of the solvent mixtures, which are very often employed in preparative synthetic chemistry, has been poorly explored theoretically and experimentally, to date. Herein, we combined experimental and theoretical studies of the solvent influence on pyrrolidine nucleophili…

010405 organic chemistryChemistryGeneral Chemical EngineeringSolvationGeneral ChemistryFree-energy relationship010402 general chemistry01 natural sciencesPyrrolidine0104 chemical sciencesSolventchemistry.chemical_compoundComputational chemistryNucleophilic substitutionDensity functional theorySolvent effectsAcetonitrileRSC Advances
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TiO2 Nanoparticles Functionalized with Non-innocent Ligands Allow Oxidative Photocyanation of Amines with Visible/Near-Infrared Photons

2018

Photosynthesis is an efficient mechanism for converting solar light energy into chemical energy. We report on a strategy for the aerobic photocyanation of tertiary amines with visible and near-infrared (NIR) light. Panchromatic sensitization was achieved by functionalizing TiO2 with a 2-methylisoquinolinium chromophore, which captures essential features of the extended π-system of 2,7-diazapyrenium (DAP2+) dications or graphitic carbon nitride. Two phenolic hydroxy groups make this ligand highly redox-active and allow for efficient surface binding and enhanced electron transfer to the TiO2 surface. Non-innocent ligands have energetically accessible levels that allow redox reactions to chang…

010405 organic chemistryChemistryGraphitic carbon nitrideGeneral ChemistryCyanationChromophore010402 general chemistryPhotochemistry01 natural sciencesBiochemistryRedoxCatalysisNon-innocent ligand0104 chemical sciencesCatalysisElectron transferchemistry.chemical_compoundColloid and Surface ChemistryPhotocatalysisJournal of the American Chemical Society
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On the Road to MM′X Polymers: Redox Properties of Heterometallic Ni···Pt Paddlewheel Complexes

2014

On the quest of heterometallic mixed-valence MM'X chains, we have prepared two stable discrete bimetallic compounds: the reduced (PPN)[ClNi(μ-OSCPh)4Pt] (PPN = bis(triphenylphosphine)iminium; OSCPh = benzothiocarboxylato) and the oxidized [(H2O)Ni(μ-OSCPh)4PtCl] species. The role of the aqua and chlorido axial ligands is crucial to facilitate oxidation of the {Ni(μ-OSCPh)4Pt} core. Experimental and theoretical analyses indicate that a NiPt-Cl/Cl-NiPt isomerization process occurs in the oxidized species. The electronic structure of the reduced system shows two unpaired electrons, one located in a d(x(2)-y(2)) orbital of the Ni(II) ion and a second in the antibonding d(z(2)-dz(2)) combination…

010405 organic chemistryChemistryIminium010402 general chemistryPhotochemistryAntibonding molecular orbital01 natural sciencesRedox0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundUnpaired electron[CHIM]Chemical SciencesMolecular orbitalPhysical and Theoretical ChemistryTriphenylphosphineBimetallic stripIsomerizationComputingMilieux_MISCELLANEOUS
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An Entry to Mixed NHC-Fischer Carbene Complexes and Zwitterionic Group 6 Metal Alkenyls

2016

The addition of NHCs to α,β-unsaturated Cr(0) and W(0) (Fischer) carbene complexes is strongly dependent on the electrophilicity of the carbene carbon. Electrophilic alkoxy-carbene complexes quantitatively react with NHCs to yield stable zwitterionic (racemic) Cr(0) - and W(0) -alkenyls with total regio- and E-stereoselectivity. Less electrophilic aminocarbenes react with NHCs to promote the displacement of a CO ligand and yield "mixed" NHC/Fischer biscarbenes in a process that is unprecedented in group 6 metal-carbene chemistry. In fact, the compounds prepared, are some of the scarce examples of Fischer bisylidenes reported in the literature. The electrochemistry of the zwitterionic Cr(0) …

010405 organic chemistryChemistryLigandTransition metal carbene complexOrganic ChemistryCationic polymerizationGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesMetalchemistry.chemical_compoundvisual_artYield (chemistry)Electrophilevisual_art.visual_art_mediumOrganic chemistryCarbeneChemistry - A European Journal
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A Molecular Electron Density Theory Study of the Role of the Copper Metalation of Azomethine Ylides in [3 + 2] Cycloaddition Reactions.

2018

The copper metalation of azomethine ylides (AYs) in [3 + 2] cycloaddition (32CA) reactions with electron-deficient ethylenes has been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d,p) level, in order to shed light on the electronic effect of the metalation in the course of the reaction. Analysis of the Conceptual Density Functional Theory reactivity indices indicates that the metalation of AYs markedly enhances the nucleophilicity of these species given the anionic character of the AY framework. These 32CA reactions take place through stepwise mechanisms characterized by the formation of a molecular complex. Both nonmetalated and metalated 32CA reactions …

010405 organic chemistryChemistryMetalationOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesMedicinal chemistryCycloaddition0104 chemical sciencesNucleophileElectronic effectSingle bondDensity functional theoryReactivity (chemistry)The Journal of organic chemistry
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