Search results for "oligomeeri"

showing 10 items of 11 documents

Dithiol-Induced Oligomerization of Thiol-Protected Gold Nanoclusters

2018

Controlled synthesis of nanostructure oligomers requires detailed understanding of their wet chemistry and the forces driving the polymerization process. In this paper, we report the main factors affecting the reaction yields of a dithiol-induced synthesis of covalently bound nanocluster dimers and oligomers and present a detailed analysis of possible reaction mechanisms. We synthesize the nanocluster oligomers using monodisperse para-mercaptobenzoic acid (p-MBA)-protected gold nanoclusters with a nominal composition of Au∼250(p-MBA)n to minimize ensemble effects on size, shape, and surface structure. Ligand exchange was performed on the nanoclusters with five different dithiol linkers: 5,5…

Reaction mechanismNanostructureDispersity02 engineering and technology010402 general chemistry01 natural sciencesOligomeroligomerNanoclusterschemistry.chemical_compoundPolymer chemistryPhysical and Theoretical Chemistryta116ta114LigandDithiol021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsoligomeeriGeneral EnergychemistryPolymerizationnanohiukkasetnanoparticles0210 nano-technologyJournal of Physical Chemistry C
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The Role of Orbital Symmetries in Enforcing Ferromagnetic Ground State in Mixed Radical Dimers

2018

One of the first steps in designing ferromagnetic (FM) molecular materials of p-block radicals is the suppression of covalent radical–radical interactions that stabilize a diamagnetic ground state. In this contribution, we demonstrate that FM coupling between p-block radicals can be achieved by constructing mixed dimers from different radicals with differing symmetries of their singly occupied molecular orbitals. The applicability of this approach is demonstrated by studying magnetic interactions in organic radical dimers built from different derivatives of the well-known phenalenyl radical. The calculated enthalpies of dimerization for different homo- and heterodimers show that the formati…

oligomeerimagneettiset ominaisuudetvapaat radikaalit
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Efficient stabilisation of a dihydrogenphosphate tetramer and a dihydrogenpyrophosphate dimer by a cyclic pseudopeptide containing 1,4-disubstituted …

2017

A cyclic pseudooctapeptide 2 is described containing 1,4-disubstituted 1,2,3-triazole moieties. This compound features eight converging hydrogen bond donors along the ring, namely four amide NH and four triazole CH groups, which enable 2 to engage in interactions with anions. While fully deprotonated sulfate anions exhibit only moderate affinity for 2, protonated anions such as dihydrogenpyrophosphate and dihydrogenphosphate anions are strongly bound. Complexation of the phosphate-derived anions involves sandwiching of a dihydrogenpyrophosphate dimer or a dihydrogenphosphate tetramer between two pseudopeptide rings. X-ray crystallography provided structural information, while 1H NMR spectro…

fosfaatit010405 organic chemistryStereochemistryChemistryHydrogen bondDimerTriazoleIsothermal titration calorimetryProtonationGeneral Chemistry010402 general chemistry01 natural sciencesphosphate oligomers0104 chemical sciencesoligomeeriCrystallographychemistry.chemical_compoundDeprotonationpseudopeptidesTetramerAmidestabilisationta116orgaaniset yhdisteetChemical Science
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Spatial localization of hotspots in Fano-resonant plasmonic oligomers for surface-enhanced coherent anti-Stokes Raman scattering

2020

AbstractRealization of Fano resonance in plasmonic oligomers is often exploited to design efficient plasmonic substrates for surface-enhanced coherent anti-Stokes Raman scattering. Disk-type Fano-resonant plasmonic oligomers are widely used to enhance the Raman signal of the probe material. Generally, hot spots are generated in those oligomers at different spatial locations at different wavelengths and only a few spatially overlapping hot spots at multiple wavelengths can be achieved with oblique incidence of excitation light. In this work, we proposed hexagonal gold nanoparticle based Fano-resonant plasmonic oligomers that can yield higher number of spatially overlapped hot spots compared …

lcsh:Applied optics. PhotonicsNanostructureMaterials sciencespektroskopiaPhysics::OpticsNear and far field02 engineering and technologyresonanssi01 natural sciences010309 opticssymbols.namesakenanorakenteet0103 physical scienceslcsh:QC350-467sirontaCoherent anti-Stokes Raman scatteringPlasmonPlasmonic oligomersbusiness.industrylcsh:TA1501-1820Fano resonance021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsplasmonitoligomeeriWavelengthpintailmiötsymbolsFano resonanceOptoelectronicsplasmonic oligomerscoherent anti-Stokes Raman scattering0210 nano-technologyRaman spectroscopybusinesslcsh:Optics. LightExcitationRaman scatteringJournal of the European Optical Society-Rapid Publications
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Influence of Fano resonance on SERS enhancement in Fano-plasmonic oligomers

2019

Plasmonic oligomers can provide profound Fano resonance in their scattering responses. The sub-radiant mode of Fano resonance can result in significant near-field enhancement due to its light trapping capability into the so-called hotspots. Appearance of these highly localized hotspots at the excitation and/or Stokes wavelengths of the analytes makes such oligomers promising SERS active substrates. In this work, we numerically and experimentally investigate optical properties of two disk-type gold oligomers, which have different strength and origin of Fano resonance. Raman analysis of rhodamine 6G and adenine with the presence of the fabricated oligomers clearly indicates that an increment …

Materials sciencePhysics::Optics02 engineering and technologyFano planeresonanssioptiset ominaisuudet01 natural sciencesLight scattering010309 opticsRhodamine 6Gchemistry.chemical_compoundsymbols.namesakeOptics0103 physical sciencessirontaPlasmonQuantitative Biology::Biomoleculesbusiness.industryScatteringfood and beveragesFano resonance021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsoligomeerichemistrysymbolsOptoelectronicsplasmonic oligomersvalokemia0210 nano-technologybusinessRaman spectroscopyExcitationOptics Express
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The Role of Orbital Symmetries in Enforcing Ferromagnetic Ground State in Mixed Radical Dimers

2018

One of the first steps in designing ferromagnetic (FM) molecular materials of p-block radicals is the suppression of covalent radical-radical interactions that stabilize a diamagnetic ground state. In this contribution, we demonstrate that FM coupling between p-block radicals can be achieved by constructing mixed dimers from different radicals with differing symmetries of their singly occupied molecular orbitals. The applicability of this approach is demonstrated by studying magnetic interactions in organic radical dimers built from different derivatives of the well-known phenalenyl radical. The calculated enthalpies of dimerization for different homo- and heterodimers show that the formati…

magneettiset ominaisuudetMaterials scienceRadicalDimerfree radicalsvapaat radikaalit010402 general chemistry01 natural sciencesoligomerchemistry.chemical_compound0103 physical sciencesGeneral Materials ScienceMolecular orbitalPhysics::Chemical PhysicsPhysical and Theoretical Chemistryta116Coupling010304 chemical physics0104 chemical sciencesoligomeeriFerromagnetismchemistryChemical physicsCovalent bondDiamagnetismGround stateThe Journal of Physical Chemistry Letters
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Selective Synthesis of Z -Silyl Enol Ethers via Ni-Catalyzed Remote Functionalization of Ketones

2021

Journal of the American Chemical Society : JACS 143(22), 8375-8380 (2021). doi:10.1021/jacs.1c01797

ketonesSilylationDimerketonit010402 general chemistry01 natural sciencesBiochemistrytransition metalsCatalysisCatalysischemistry.chemical_compoundkatalyytitColloid and Surface ChemistryPolymer chemistryhydrocarbonsoligomerseetteritkemiallinen synteesiOlefin fiberGeneral ChemistrySilyl enol ether540Enolhiilivedyt3. Good health0104 chemical sciencesoligomeerietherschemistryChain walkingddc:540nikkeliSelectivityJournal of the American Chemical Society
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Efficient stabilisation of a dihydrogenphosphate tetramer and a dihydrogenpyrophosphate dimer by a cyclic pseudopeptide containing 1,4-disubstituted …

2017

A cyclic pseudooctapeptide 2 is described containing 1,4-disubstituted 1,2,3-triazole moieties. This compound features eight converging hydrogen bond donors along the ring, namely four amide NH and four triazole CH groups, which enable 2 to engage in interactions with anions. While fully deprotonated sulfate anions exhibit only moderate affinity for 2, protonated anions such as dihydrogenpyrophosphate and dihydrogenphosphate anions are strongly bound. Complexation of the phosphate-derived anions involves sandwiching of a dihydrogenpyrophosphate dimer or a dihydrogenphosphate tetramer between two pseudopeptide rings. X-ray crystallography provided structural information, while 1 H NMR spectr…

oligomeeripseudopeptidesfosfaatitstabilisationorgaaniset yhdisteetphosphate oligomers
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Self-Complementary Dimers of Oxalamide-Functionalized Resorcinarene Tetrabenzoxazines

2018

Self‐complementarity is a useful concept in supramolecular chemistry, molecular biology and polymeric systems. Two resorcinarene tetrabenzoxazines decorated with four oxalamide groups were synthesized and characterized. The oxalamide groups possessed self‐complementary hydrogen bonding sites between the carbonyls and amide groups. The self‐complementary nature of the oxalamide groups resulted in self‐included dimeric assemblies. The hydrogen bonding interactions within the tetrabenzoxazines gave rise to the formation of dimers, which were confirmed by single‐crystal X‐ray diffractions analysis and supported by NMR spectroscopy and mass spectrometry. The self‐included dimers were connected b…

massaspektrometriaspectroscopyNoncovalent interactionsobligaatiotspektroskopiaSupramolecular chemistrycarbonylsdimers ; noncovalent interactions ; resorcinarenes ; supramolecular chemistry ; X-ray diffraction010402 general chemistry01 natural sciencesBiochemistryoligomerchemistry.chemical_compounddimersAmidePolymer chemistryNon-covalent interactionsresorcinarenesta116mass spectrometrychemistry.chemical_classificationbondsta114010405 organic chemistryHydrogen bondOrganic ChemistryIntermolecular forceGeneral ChemistryNuclear magnetic resonance spectroscopyPolymerResorcinareneX-ray diffraction0104 chemical sciencesoligomeeriamideschemistryvetyamidithydrogenself-complementaritySupramolecular chemistrykarbonyylitChemistry: An Asian Journal
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Non-Innocent Base Properties of 3- and 4-Pyridyl-dithia- and Diselenadiazolyl Radicals : The Effect of N-Methylation

2018

International audience; Condensation of persilylated nicotinimideamide and isonicotinimideamide with sulfur monochloride affords double salts of the 3-, 4-pyridyl-substituted 1,2,3,5-dithiadiazolylium DTDA cations of the general formula [3-, 4-pyDTDA][Cl][HCl] in which the pyridyl nitrogen serves as a noninnocent base. Reduction of these salts with triphenylantimony followed by deprotonation of the intermediate-protonated radical affords the free base radicals [3-, 4-pyDTDA], the crystal structures of which, along with those of their diselenadiazolyl analogues [3-, 4-pyDSDA], have been characterized by powder or single-crystal X-ray diffraction. The crystal structures consist of “pancake” π…

Base (chemistry)Radicalsuolat (yhdisteet)free radicals02 engineering and technologyCrystal structure010402 general chemistryMetathesistriflate saltsvapaat radikaalit01 natural sciencesMedicinal chemistryChlorideInorganic ChemistrydimersDeprotonationrikkiyhdisteetmedicinePhysical and Theoretical Chemistryta116dithiadiazoleschemistry.chemical_classificationIntermolecular forceFree base[CHIM.MATE]Chemical Sciences/Material chemistryN-methylation021001 nanoscience & nanotechnology0104 chemical sciencesoligomeerichemistry0210 nano-technologymedicine.drug
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