Triplet Energy (triplet + energy)

Distribution by Scientific Domains
Distribution within Polymers and Materials Science

Kinds of Triplet Energy

  • high triplet energy

  • Terms modified by Triplet Energy

  • triplet energy gap
  • triplet energy level

  • Selected Abstracts


    Photopolymerization of 1,6-hexanedioldiacrylate initiated by three-component systems based on N -arylphthalimides

    JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 16 2004
    T. Brian Cavitt
    Abstract Three-component photoinitiators comprised of an N -arylphthalimide, a diarylketone, and a tertiary amine were investigated for their initiation efficiency of acrylate polymerization. The use of an electron-deficient N -arylphthalimide resulted in a greater acrylate polymerization rate than an electron-rich N -arylphthalimide. Triplet energies of each N -arylphthalimide, determined from their phosphorescence spectra, and the respective rate constants for triplet quenching by the N -arylphthalimide derivatives (acquired via laser flash photolysis) indicated that an electron,proton transfer from an intermediate radical species to the N -arylphthalimide (not energy transfer from triplet sensitization) is responsible for generating the initiating radicals under the conditions and species concentrations used for polymerization. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4009,4015, 2004 [source]


    Structure Variation and Luminescence Properties of Lanthanide Complexes Incorporating a Naphthalene-Derived Chromophore Featuring Salicylamide Pendant Arms

    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 11 2008
    Xue-Qin Song
    Abstract A new potentially bridging ligand containing two salicylamide pendant arms separated by a 2,3-dimethoxynaphthalene spacer has been prepared and its coordination chemistry with LnIII ions has been investigated. An analysis of the presented crystal structures indicates that the diversity of these supramolecular structures is mainly dictated by the nature of the metal ions. These compounds represent good examples of tuning crystal structures arising from the flexibility of the ligands and the Ln contraction effect. Luminescence studies showed that the introduction of the methoxyl substituents on the naphthalene backbone lowers the triplet energy and considerably changes the luminescent behaviors of the EuIII and TbIII complexes, which is very different from the literature data on similar compounds. In the emission spectra of the Tb complex the ligand fluorescence remains relatively important because of the back-energy transfer from the TbIII ion to the ligand, which to the best of our knowledge, may be the first example of salicylamide lanthanide complexes. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source]


    Tuning the Optoelectronic Properties of Carbazole/Oxadiazole Hybrids through Linkage Modes: Hosts for Highly Efficient Green Electrophosphorescence

    ADVANCED FUNCTIONAL MATERIALS, Issue 2 2010
    Youtian Tao
    Abstract A series of bipolar transport host materials: 2,5-bis(2-(9H -carbazol-9-yl)phenyl)-1,3,4-oxadiazole (o -CzOXD) (1), 2,5-bis(4-(9H -carbazol-9-yl)phenyl)-1,3,4-oxadiazole (p -CzOXD) (2), 2,5-bis(3-(9H -carbazol-9-yl)phenyl)-1,3,4-oxadiazole (m -CzOXD) (3) and 2-(2-(9H -carbazol-9-yl)phenyl)-5-(4-(9H-carbazol-9-yl)phenyl)-1,3,4-oxadiazole (op -CzOXD) (4) are synthesized through simple aromatic nucleophilic substitution reactions. The incorporation of the oxadiazole moiety greatly improves their morphological stability, with Td and Tg in the range of 428,464,°C and 97,133,°C, respectively. The ortho and meta positions of the 2,5-diphenyl-1,3,4-oxadiazole linked hybrids (1 and 3) show less intramolecular charge transfer and a higher triplet energy compared to the para-position linked analogue (2). The four compounds exhibit similar LUMO levels (2.55,2.59,eV) to other oxadiazole derivatives, whereas the HOMO levels vary in a range from 5.55,eV to 5.69,eV, depending on the linkage modes. DFT-calculation results indicate that 1, 3, and 4 have almost complete separation of their HOMO and LUMO levels at the hole- and electron-transporting moieties, while 2 exhibits only partial separation of the HOMO and LUMO levels possibly due to intramolecular charge transfer. Phosphorescent organic light-emitting devices fabricated using 1,4 as hosts and a green emitter, Ir(ppy)3 or (ppy)2Ir(acac), as the guest exhibit good to excellent performance. Devices hosted by o -CzOXD (1) achieve maximum current efficiencies (,c) as high as 77.9,cd A,1 for Ir(ppy)3 and 64.2,cd A,1 for (ppy)2Ir(acac). The excellent device performance may be attributed to the well-matched energy levels between the host and hole-transport layers, the high triplet energy of the host and the complete spatial separation of HOMO and LUMO energy levels. [source]


    Multifunctional Crosslinkable Iridium Complexes as Hole Transporting/Electron Blocking and Emitting Materials for Solution-Processed Multilayer Organic Light-Emitting Diodes

    ADVANCED FUNCTIONAL MATERIALS, Issue 7 2009
    Biwu Ma
    Abstract Here, a new series of crosslinkable heteroleptic iridium (III) complexes for use in solution processed phosphorescent organic light emitting diodes (OLEDs) is reported. These iridium compounds have the general formula of (PPZ-VB)2Ir(C,N), where PPZ-VB is phenylpyrazole (PPZ) vinyl benzyl (VB) ether; and the C,N ligands represent a family of four different cyclometallating ligands including 1-phenylpyrazolyl (PPZ) (1), 2-(4,6-difluorophenyl)pyridyl (DFPPY) (2), 2-(p-tolyl)pyridyl (TPY) (3), and 2-phenylquinolyl (PQ) (4). With the incorporation of two crosslinkable VB ether groups, these compounds can be fully crosslinked after heating at 180,°C for 30,min. The crosslinked films exhibit excellent solvent resistance and film smoothness which enables fabrication of high-performance multilayer OLEDs by sequential solution processing of multiple layers. Furthermore, the photophysical properties of these compounds can be easily controlled by simply changing the cyclometallating C,N ligand in order to tune the triplet energy within the range of 3.0,2.2,eV. This diversity makes these materials not only suitable for use in hole transporting and electron blocking but also as emissive layers of several colors. Therefore, these compounds are applied as effective materials for all-solution processed OLEDs with (PPZ-VB)2IrPPZ (1) acting as hole transporting and electron blocking layer and host material, as well as three other compounds, (PPZ-VB)2IrDFPPY (2), (PPZ-VB)2IrTPY(3), and (PPZ-VB)2IrPQ(4), used as crosslinkable phosphorescent emitters. [source]


    Solution-Processed Solid Solution of a Novel Carbazole Derivative for High-Performance Blue Phosphorescent Organic Light-Emitting Diodes

    ADVANCED MATERIALS, Issue 37 2010
    Shanghui Ye
    Blue light: Incorporation of two fluorenyl rings into a phenyl group at the C9 position of fluorene builds a bulky and rigidly tetrahedral framework, which is functionalized by two carbazole groups. This molecule possesses excellent thermal and morphological stability, miscibility to the phosphorescent dopant, and high triplet energy, leading to narrow blue phosphorescent emission. [source]


    Solution-Processable Carbazole-Based Conjugated Dendritic Hosts for Power-Efficient Blue-Electrophosphorescent Devices

    ADVANCED MATERIALS, Issue 48 2009
    Junqiao Ding
    A novel class of hosts suitable for solution processing has been developed based on a conjugated dendritic scaffold. By increasing the dendron generation, the highest occupied molecular orbital (HOMO) energy level can be tuned to facilitate hole injection, while the triplet energy remains at a high level, sufficient to host high-energy-triplet emitters. A power-efficient blue-electrophosphorescent device based on H2 (see figure) is presented. [source]


    New Host Containing Bipolar Carrier Transport Moiety for High-Efficiency Electrophosphorescence at Low Voltages

    ADVANCED MATERIALS, Issue 6 2009
    Zhi Qiang Gao
    A new host material for use in phosphorescent OLEDs with desirable electronic properties has been synthesized. The material exhibits superior carrier-transport properties, a narrow optical band gap, relatively high triplet energy, and high thermal stability. It is synthesized by integrating hole-transporting carbazole groups into an electron-transporting phenanthroline core (see figure), and is demonstrated to be an excellent host for phosphorescent dopant emitters. [source]


    High-Triplet-Energy Poly(9,9,-bis(2-ethylhexyl)-3,6-fluorene) as Host for Blue and Green Phosphorescent Complexes,

    ADVANCED MATERIALS, Issue 12 2008
    Zhonglian Wu
    A novel polyfluorene with high triplet energy level the soluble conjugated homopolymer poly(9,9,-bis(2-ethylhexyl)-3,6-fluorene)) (P36EHF) is successfully synthesized and characterized. Preliminary results indicate that P36EHF could be a good host material for green and blue phosphorescent complexes (see figure), making it a wide-bandgap conjugated polymer host suitable for blue- or green-phosphorescent polymer LEDs. [source]


    Harvesting Triplet Excitons from Fluorescent Blue Emitters in White Organic Light-Emitting Diodes,

    ADVANCED MATERIALS, Issue 21 2007
    G. Schwartz
    A novel concept for white organic light emitting diodes (OLEDs) enabling the utilization of all electrically generated excitons for light generation is introduced. The key feature is a fluorescent blue emitter with high triplet energy, rendering it possible to harvest its triplet excitons by letting them diffuse to an orange phosphorescent iridium complex. [source]


    Computational study of the cooperative effects of nitrogen and silicon atoms on the singlet,triplet energy spacing in 1,3-diradicals and the reactivity of their singlet states

    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 4 2010
    Takeshi Nakamura
    Abstract Quantum chemical calculations were performed to investigate the cooperative effect of the nitrogen and silicon atoms on the singlet,triplet energy spacing and the reactivity of the singlet state in 1,2-diazacyclopentane-3,5-diyls and 1,2-diaza-4-silacyclopentane-3,5-diyls. The largest singlet,triplet energy gap (,=,,36.1,kcal/mol) found so far in localized 1,3-diradicals was in the C2v symmetry of 4,4-difluoro-1,2-diaza-4-silacyclopentane-3,5-diyl at the UB3LYP/6-31G(d) level of theory. The cooperative effect was also found in the energy differences of singlet diradicals with the corresponding ring-closing compounds, bicyclo[2.1.0]pentane derivatives. The singlet state of the 1,2-diaza-4-silacyclopentane-3,5-diyls was calculated to be energetically more stable than the ring-closing compound. The notable finding on the stability of the singlet diradicals may be attributed to the resonance structures that specifically stabilize the singlet state of diradicals. The computational studies predict that the singlet 1,2-diaza-4-silacyclopentane-3,5-diyl is a persistent molecule under conditions without intermolecular-trapping reagents. Copyright © 2010 John Wiley & Sons, Ltd. [source]


    Design and Synthesis of Phosphorescent Iridium Containing Dendrimers for Potential Applications in Organic Light-Emitting Diodes,

    MACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 18 2008
    Qin-De Liu
    Abstract Three phosphorescent dendrimers (IrC1, IrC3, and IrF2) with an iridium complex core and oligocarbazole or oligofluorene substituted ligands were synthesized and characterized. The structures of the oligocarbazole were designed to maintain high triplet energy of the ligands so that phosphorescence quenching in the resulting dendrimers can be prevented, while the oligofluorene in IrF2 resulted in undesired phosphorescence quenching. Best performance was obtained from an IrC3 based electrophosphorescent light-emitting device with a maximum luminance of 13,060 cd,·,m,2 at a driving voltage of 11.5 V and a peak current-efficiency of 4.3 cd,·,A,1 at a luminance of 3,400 cd,·,m,2, owing to its high PL efficiency, and efficient energy transfer between the iridium complex core and the ligands. [source]


    Designing Simple Tridentate Ligands for Highly Luminescent Europium Complexes

    CHEMISTRY - A EUROPEAN JOURNAL, Issue 41 2009

    Abstract A series of tridentate benzimidazole-substituted pyridine-2-carboxylic acids have been prepared with a halogen, methyl or alkoxy group in the 6-position of the benzimidazole ring, which additionally contains a solubilising N -alkyl chain. The ligands form neutral homoleptic nine-coordinate lanthanum, europium and terbium complexes as established from X-ray crystallographic analysis of eight structures. The coordination polyhedron around the lanthanide ion is close to a tricapped trigonal prism with ligands arranged in an up,up,down fashion. The coordinated ligands serve as light-harvesting chromophores in the complexes with absorption maxima in the range 321,341,nm (,=(4.9,6.0)×104,M,1,cm,1) and triplet-state energies between 21,300 and 18,800,cm,1; the largest redshifts occur for bromine and electron-donor alkoxy substituents. The ligands efficiently sensitise europium luminescence with overall quantum yields () and observed lifetimes (,obs) reaching 71,% and 3.00,ms, respectively, in the solid state and 52,% and 2.81,ms, respectively, in CH2Cl2 at room temperature. The radiative lifetimes of the Eu(5D0) level amount to ,rad=3.6,4.6,ms and the sensitisation efficiency ,sens=(,rad/,obs) is close to unity for most of the complexes in the solid state and equal to approximately 80,% in solution. The photophysical parameters of the complexes correlate with the triplet energy of the ligands, which in turn is determined by the nature of the benzimidazole substituent. Facile modification of the ligands makes them promising for the development of brightly emissive europium-containing materials. [source]


    Primary Photophysical Processes in Photosystem II: Bridging the Gap between Crystal Structure and Optical Spectra

    CHEMPHYSCHEM, Issue 6 2010
    Thomas Renger Prof. Dr.
    Abstract This Minireview summarizes our current knowledge of the optical properties of photosystem II (PS-II) and how these properties are related to the photosynthetic function, that is, excitation energy transfer from the antenna complexes to the reaction center (RC) and the subsequent transmembrane charge separation in the latter. Interpretation of the optical spectra of PS-II is much more difficult than for the RC of purple bacteria, due to the "spectral congestion" problem, namely, the strong spectral overlap of optical bands in PS-II. Recent developments in deciphering the optical properties of the pigments in PS-II, the identification of functional states, and the kinetic details of the primary excitation energy and charge-transfer reactions are summarized. The spectroscopic term P680 that is generally used in the literature no longer indicates the same entity in its cationic and singlet excited form but different subsets of the six innermost pigments of the RC. The accessory chlorophyll ChlD1 forms a sink for singlet excitation and triplet energy and most likely represents the primary electron donor in PS-II. In this respect, a special chlorophyll monomer in PS-II plays the role of the special pair in purple bacteria. Evidence that exciton transfer between the core antenna complexes CP43 and CP47 and the RC is the bottleneck for the overall photochemical trapping of excitation energy in PS-II is discussed. A short summary is provided of PS-II of Acaryochloris marina, which mainly contains chlorophyll d instead of the usual chlorophyll a. This system does not suffer from the spectral congestion problem and, therefore, represents an interesting model system. The final part of this Minireview provides a discussion of challenging problems to be solved in the future. [source]