Search results for "Bathochromic shift"

showing 10 items of 37 documents

Methylium Ions with OPV Chains − New NIR Dyes

2001

Carbinols, which contain three OPV chains, were generated in convergent syntheses. The extension of the conjugation leads to a bathochromic effect that shifts the absorption from the UV into the visible region. The carbinol series has a convergence limit of the absorption at λmax = 415 nm. The corresponding carbenium ions exhibit a stronger bathochromic shift with the increasing number of repeating units in each chain. Thus, NIR dyes were obtained which show a convergence limit at λmax = 879 nm. The charge distribution in the ground state of the carbocations is discussed on the basis of 13C NMR spectroscopic data.

ChemistryOrganic ChemistryBathochromic shiftAnalytical chemistryCharge densityPhysical and Theoretical ChemistryCarbon-13 NMRCarbocationAbsorption (chemistry)PhotochemistryGround stateIonEuropean Journal of Organic Chemistry
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Extension of Conjugation Leading to Bathochromic or Hypsochromic Effects in OPV Series

2004

Four OPV series 1-4 (a-d) with a terminal dialkylamino group as electron donor were prepared by Wittig-Horner reactions. To study the influence of the push-pull effect on the long-wavelength absorption, three of the four series contained terminal acceptor groups (CN, CHO, NO(2)). The length of the chromophores strongly affects the intramolecular charge transfer (ICT)-an effect which superimposes upon the extension of the conjugation. Increasing numbers n of repeat units cause an overall bathochromic shift for the purely donor-substituted series 1 a-4 a and the series 1 b-4 b with CN as weak acceptor. The two effects annihilate each other in the series 1 c-4 c with terminal CHO groups, so th…

ChemistryOrganic ChemistryElectron donorProtonationGeneral ChemistryChromophorePhotochemistryAcceptorCatalysischemistry.chemical_compoundAtomic electron transitionIntramolecular forceBathochromic shiftHypsochromic shiftChemistry - A European Journal
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Metallophilic interactions in stacked dinuclear rhodium 2,2'-biimidazole carbonyl complexes

2012

Non-covalent metallophilic interactions were studied by investigating the stacking of two neutral rhodium complexes [Rh2I(R2bim)Cl2(CO)4] (R = Et, ethyl or Pr, propyl) in the solid state. Both dinuclear complexes formed infinite arrays of square planar d8 rhodium centres with intramolecular Rh⋯Rh distances of 3.1781(5) A (R = Et) and 3.1469(3) A (R = Pr) and the intermolecular Rh⋯Rh distances of 3.4345(6) A (R = Et) and 3.4403(3) A (R = Pr) between the adjacent molecules. The crystalline solids were stable and did not contain any solvent of crystallization. The effect of the metallophilic interactions on the absorption properties were studied using TD-DFT methods. The computational results …

ChemistryStackingchemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsRhodiumlaw.inventionMetalCrystalCrystallographylawIntramolecular forcevisual_artBathochromic shiftvisual_art.visual_art_mediumMoleculeGeneral Materials ScienceCrystallizationta116CrystEngComm
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Dyes That Bear Thiazolylazo Groups as Chromogenic Chemosensors for Metal Cations

2011

A family of dyes (L 1-L 6) that contain a thiazolylazo group as signalling subunit and several macrocyclic cavities with different ring sizes and type and number of heteroatoms as binding sites has been synthesized and characterized. Solutions of L 1-L 6 in acetonitrile show broad and structureless absorption bands in the 554-577 nm range with typicalmolar absorption coefficients that range from 20000 to 32000 M -1 cm -1. A detailed protonation study was carried out with solutions of L 1, L 2 and L 5 in acetonitrile. Addition of one equivalent of protons to L 1 and L 2 resulted in the development of a new band at 425 and 370 nm, respectively, which was ascribed to protonation in the aniline…

ChemosensorsHeteroatomQUIMICA INORGANICAProtonationMercuryCation sensorsPhotochemistryInorganic ChemistryMetalchemistry.chemical_compoundAzodyesDensity functional calculationsQUIMICA ORGANICAchemistryLeadAbsorption bandvisual_artBathochromic shiftQUIMICA ANALITICAvisual_art.visual_art_mediumMoietyDensity functional theoryAcetonitrileDyes
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Ein optisch aktives Polyamid mit atropisomeren Binaphthyl-Grundbausteinen

1968

Zur Darstellung eines optisch aktiven Polyamids mit atropisomeren Grundbausteinen in der Hauptkette wurde (+)-2.2′-Diamino-binaphthyl-(1.1′) (II) hergestellt. Die Drehwerte in einigen Losungsmitteln sowie optische Rotationsdispersion (ORD), Circulardichroismus (CD) und UV-Spektrum werden angegeben. Durch Grenzflachenpolykondensation von II mit Terephthaloylchlorid wurde ein optisch aktives Polyamid (III) erhalten. Drehwerte, ORD und CD von III werden gemessen und mit denen des als Modellsubstanz dargestellten (+)-2.2′-Dibenzamido-binaphthyls-(1.1′) (IV) verglichen. Beide Substanzen zeigen mehrere COTTON-Effekte, die hinsichtlich ihres Vorzeichens ubereinstimmen. In ihrer Lage sind jedoch di…

Circular dichroismchemistry.chemical_compoundchemistryRotatory powerPolymer chemistryBathochromic shiftPolyamideTerephthaloyl chlorideOptically activeOptical rotatory dispersionDie Makromolekulare Chemie
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Monodisperse Dialkoxy-Substituted Oligo(phenyleneethenylene)s

2006

Individual but connected synthetic routes for the preparation of the all-E-configured 2,5-dipropoxy-substituted oligo(1,4-phenyleneethenylene)s 1a–g were developed. An increasing number of conjugated stilbene units from n = 1 to n = 11 led to a convergent bathochromic shift (Δλ = λ∞ − λ1 = 127 nm) in the UV/Vis absorption. An exponential function for the convergence of the absorption energies (wavelengths) in conjugated systems is proposed. By a simple extrapolation of this function the effective chain length may be determined.

CrystallographyChain lengthChemistryOrganic ChemistryBathochromic shiftDispersityPolymer chemistryExtrapolationGeneral ChemistryPhysical and Theoretical ChemistryAbsorption (chemistry)Conjugated systemExponential functionLiebigs Annalen
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Addressing subphthalocyanines and subnaphthalocyanines features relevant to fluorescence imaging

2018

International audience; A series of new synthetic subphthalocyanines bear structural features aimed at allowing either fluorescence activation or a bathochromic shift of the absorption band towards the near-infrared window, relevant to optical imaging. X-ray diffraction studies of four subphthalocyanines are reported. Spectrofluorimetric studies on subnaphthalocyanines and activatable subphthalocyanine pro-fluorophores are reported.

DiffractionFluorescence-lifetime imaging microscopyOptical window02 engineering and technologyFluorogenicphthalocyanines010402 general chemistry01 natural sciencesBiochemistryOptical imagingDrug DiscoveryBathochromic shiftanalogs[CHIM]Chemical SciencesPro-fluorophoreSubnaphthalocyaninebusiness.industryChemistrySubphthalocyanine[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistry021001 nanoscience & nanotechnologyFluorescence0104 chemical sciences3. Good healthAbsorption bandOptoelectronicsTurn-ON fluorescence0210 nano-technologybusiness
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Carbazole-based green and blue-BODIPY dyads and triads as donors for bulk heterojunction organic solar cells.

2020

Two BODIPY derivatives with one (B2) and two (B3) carbazole moieties were synthesized and applied as electron-donor materials in organic photovoltaic cells (OPV). Their optical and electrochemical properties were systematically investigated. These BODIPY dyes exhibit excellent solubility in organic solvents and present high molar extinction coefficients (1.37–1.48 × 105 M−1 cm−1) in solutions with absorption maxima at 586 nm for mono-styryl groups and at 672 nm for di-styryl groups. The introduction of the styryl moieties results in a large bathochromic shift and a significant decrease in the HOMO–LUMO energy-gaps. The BODIPY dyes show relatively low HOMO energies ranging from −4.99 to −5.1…

Inorganic Chemistrychemistry.chemical_compoundMaterials sciencechemistryOrganic solar cellCarbazoleBathochromic shiftMolecular orbitalCyclic voltammetryBODIPYPhotochemistryAcceptorPolymer solar cellDalton transactions (Cambridge, England : 2003)
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Spectral and microscopic study of self-assembly of novel cationic spermine amides of betulinic acid

2016

Supramolecular characteristics of two spermine amides of betulinic acid (1 and 2) were studied by measuring and evaluating their UV-VIS-NIR spectra in aqueous acetonitrile and DOSY-NMR spectra in tetradeuteromethanol, accompanied by atomic force microscopy (AFM) images, scanning electron microscopy (SEM) micrographs, and transmission electron microscopy (TEM) micrographs. Fibrous supramolecular self-assembly of 1 and 2 was observed by AFM images, as well as by the SEM and TEM micrographs. Bathochromic shifts of the absorbance maximum at 870nm to 1015-970nm in the UV-VIS-NIR spectra were observed with increasing water content in the acetonitrile/water systems, indicating formation of fibrous…

Magnetic Resonance SpectroscopyScanning electron microscopeClinical BiochemistrySupramolecular chemistrymacromolecular substancesDOSY-NMRMicroscopy Atomic Force010402 general chemistry01 natural sciencesBiochemistryAbsorbancechemistry.chemical_compoundEndocrinologyMicroscopy Electron TransmissionBathochromic shiftBetulinic AcidAcetonitrileta116Molecular BiologyPharmacologyAqueous solutionMolecular Structure010405 organic chemistryChemistryOrganic Chemistryta1182technology industry and agricultureAmidesTriterpenes0104 chemical sciencesCrystallographyTransmission electron microscopySEMTEMSpermineMicroscopy Electrochemical ScanningAFMPentacyclic TriterpenesChirality (chemistry)Steroids
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Tailoring the Emission of Fluorinated Bipyridine-Chelated Iridium Complexes

2018

New functionalized tris(2′,6′-difluoro-2,3′-bipyridinato-N,C4′)iridium(III) ((dfpypy)3Irs) complexes, including small molecules and their dendrimer embedded analogoues, were synthesized and characterized. It is demonstrated that both the fac-(dfpypy)3Ir-based polyphenylene dendrimers and (triisopropylsilyl)ethynyl (TIPSE)-substituted (dfpypy)3Ir complexes induce large bathochromic shifts (∼50 nm) of emission bands compared with fac-(dfpypy)3Ir. This is due to the pronounced 3π–π* character of emissive excited states and the extended conjugation. A further remarkable feature is the small bathochromic shift of the emissions of fac-tris(2-phenylpyridine)iridium (fac-(ppy)3Ir)-based polyphenyle…

Materials science010405 organic chemistryGeneral Chemical Engineeringchemistry.chemical_elementGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesSmall moleculeArticle0104 chemical scienceslcsh:ChemistryBipyridinechemistry.chemical_compoundchemistrylcsh:QD1-999Excited stateDendrimerBathochromic shiftChelationIridiumPhosphorescenceACS Omega
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