Journal of the American Chemical Society, ISSN 0002-7863, 11/2012, Volume 134, Issue 47, pp. 19401 - 19408
An endohedral metallofullerene, La2@C80, is covalently linked to the strong electron acceptor 11,11,12,12-tetracyano-9,10-anthra-p-quinodimethane (TCAQ) by...
Models, Molecular | Molecular Structure | Fullerenes - chemistry | Anthraquinones - chemistry | Electrons | Lanthanum - chemistry | Methane | Thermal properties | Usage | Spin coupling | Quantum chemistry | Analysis | Nuclear magnetic resonance spectroscopy | Chemical properties | Electron transport | Methods
Models, Molecular | Molecular Structure | Fullerenes - chemistry | Anthraquinones - chemistry | Electrons | Lanthanum - chemistry | Methane | Thermal properties | Usage | Spin coupling | Quantum chemistry | Analysis | Nuclear magnetic resonance spectroscopy | Chemical properties | Electron transport | Methods
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 01/2015, Volume 80, Issue 2, pp. 980 - 987
Pd-catalyzed direct arylation (DA) reaction conditions have been established for unsubstituted furan (Fu) and thiophene (Th) with three popular acceptor...
CHAIN | ROUTE | ACTIVATION | SERIES | CONJUGATED POLYMERS | COUPLING REACTIONS | PALLADIUM-CATALYZED ARYLATION | CHEMISTRY, ORGANIC | POLYMERIZATION | NAPHTHALENE DIIMIDE | COPOLYMER | Naphthalenes - chemistry | Acetamides - chemistry | Hydrogen Bonding | Furans - chemistry | Bromides - chemistry | Benzothiazoles - chemistry | Molecular Structure | Fluorobenzenes - chemistry | Thiophenes - chemistry | Alkylation | Electrons | Thermal properties | Arylation | Analysis | Benzene | Bromides | Chemical properties | Catalysis
CHAIN | ROUTE | ACTIVATION | SERIES | CONJUGATED POLYMERS | COUPLING REACTIONS | PALLADIUM-CATALYZED ARYLATION | CHEMISTRY, ORGANIC | POLYMERIZATION | NAPHTHALENE DIIMIDE | COPOLYMER | Naphthalenes - chemistry | Acetamides - chemistry | Hydrogen Bonding | Furans - chemistry | Bromides - chemistry | Benzothiazoles - chemistry | Molecular Structure | Fluorobenzenes - chemistry | Thiophenes - chemistry | Alkylation | Electrons | Thermal properties | Arylation | Analysis | Benzene | Bromides | Chemical properties | Catalysis
Journal Article
ChemSusChem, ISSN 1864-5631, 06/2016, Volume 9, Issue 12, pp. 1433 - 1441
Two donor–acceptor–acceptor (D–A–A)‐type molecules incorporating nitrobenzoxadiazole (NBO) as the A–A block and ditolylamine as the D block bridged through a...
structure–property relationships | electrochemistry | electron transfer | photochemistry | organic photovoltaics | Electrochemistry | Electron transfer | Organic photovoltaics | Structure-property relationships | Photochemistry | POWER CONVERSION EFFICIENCY | MEROCYANINE DYES | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | DESIGN | SEMICONDUCTORS | PERFORMANCE | CHEMISTRY, MULTIDISCIPLINARY | structure-property relationships | CHEMISTRY | SYSTEMS | PHOTOVOLTAIC PROPERTIES | CHARGE-TRANSFER | COPOLYMER | Electric Power Supplies | Electron Transport | Quantum Theory | Solar Energy | Temperature | Molecular Conformation | Nitrogen Dioxide - chemistry | Benzene - chemistry | Models, Molecular | Thiophenes - chemistry | Thermal properties | Solar cells | Electrochemical reactions | Solar batteries | Analysis | Thiophene | Nitrogen dioxide | Photovoltaic cells | Efficiency
structure–property relationships | electrochemistry | electron transfer | photochemistry | organic photovoltaics | Electrochemistry | Electron transfer | Organic photovoltaics | Structure-property relationships | Photochemistry | POWER CONVERSION EFFICIENCY | MEROCYANINE DYES | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | DESIGN | SEMICONDUCTORS | PERFORMANCE | CHEMISTRY, MULTIDISCIPLINARY | structure-property relationships | CHEMISTRY | SYSTEMS | PHOTOVOLTAIC PROPERTIES | CHARGE-TRANSFER | COPOLYMER | Electric Power Supplies | Electron Transport | Quantum Theory | Solar Energy | Temperature | Molecular Conformation | Nitrogen Dioxide - chemistry | Benzene - chemistry | Models, Molecular | Thiophenes - chemistry | Thermal properties | Solar cells | Electrochemical reactions | Solar batteries | Analysis | Thiophene | Nitrogen dioxide | Photovoltaic cells | Efficiency
Journal Article
RSC Advances, 01/2018, Volume 8, Issue 38, pp. 21252 - 21264
Indolocarbazole bearing donor–acceptor type polymers have rarely been reported in the electrochromic field despite them having considerable development in the...
Organic chemistry | Scanning electron microscopy | Carbazoles | Thermogravimetric analysis | Oxidation | Electrochromism | Photoelectricity | Polymers | Chemical synthesis | Thermal stability
Organic chemistry | Scanning electron microscopy | Carbazoles | Thermogravimetric analysis | Oxidation | Electrochromism | Photoelectricity | Polymers | Chemical synthesis | Thermal stability
Journal Article
Journal of Electronic Materials, ISSN 0361-5235, 12/2017, Volume 46, Issue 12, pp. 6784 - 6794
Development of nonfullerene acceptors plays an important role in the commercial availability of plastic solar cells. We report herein synthesis of...
Solid State Physics | Suzuki coupling | perylene | Materials Science | bulk heterojunction | Optical and Electronic Materials | Electronics and Microelectronics, Instrumentation | Characterization and Evaluation of Materials | Organic solar cells | acceptors | PHYSICS, APPLIED | UNIT | DEVICE PERFORMANCE | MATERIALS SCIENCE, MULTIDISCIPLINARY | ELECTRON-ACCEPTOR | ENGINEERING, ELECTRICAL & ELECTRONIC | PHOTOVOLTAIC PERFORMANCE | POLYMER ACCEPTORS | DERIVATIVES | MORPHOLOGY | Solar cells | Solar batteries | Technology application | Electrochemical analysis | Fourier transforms | Nuclear magnetic resonance--NMR | Energy levels | Nuclear electric power generation | Agglomeration | Thermal stability | Diimide | Coupling (molecular) | Photovoltaic cells | Spectrum analysis | Optical properties | Heterojunctions | Samarium | Polymers | Chemical synthesis | Energy conversion efficiency
Solid State Physics | Suzuki coupling | perylene | Materials Science | bulk heterojunction | Optical and Electronic Materials | Electronics and Microelectronics, Instrumentation | Characterization and Evaluation of Materials | Organic solar cells | acceptors | PHYSICS, APPLIED | UNIT | DEVICE PERFORMANCE | MATERIALS SCIENCE, MULTIDISCIPLINARY | ELECTRON-ACCEPTOR | ENGINEERING, ELECTRICAL & ELECTRONIC | PHOTOVOLTAIC PERFORMANCE | POLYMER ACCEPTORS | DERIVATIVES | MORPHOLOGY | Solar cells | Solar batteries | Technology application | Electrochemical analysis | Fourier transforms | Nuclear magnetic resonance--NMR | Energy levels | Nuclear electric power generation | Agglomeration | Thermal stability | Diimide | Coupling (molecular) | Photovoltaic cells | Spectrum analysis | Optical properties | Heterojunctions | Samarium | Polymers | Chemical synthesis | Energy conversion efficiency
Journal Article
Journal of Electronic Materials, ISSN 0361-5235, 6/2015, Volume 44, Issue 6, pp. 1606 - 1613
Donor–acceptor–donor conjugated polymers are superior to other thermoelectric organic materials because it is much easier to modify their structure to reduce...
Solid State Physics | Seebeck coefficient | donor–acceptor–donor conjugated polymers | Optical and Electronic Materials | Electronics and Microelectronics, Instrumentation | Characterization and Evaluation of Materials | Material Science | Thermoelectric | electrical conductivity | power factor | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | POWER | CONDUCTIVE POLYMERS | ELECTROPOLYMERIZATION | GREEN | ENGINEERING, ELECTRICAL & ELECTRONIC | donor-acceptor-donor conjugated polymers | POLY(3,4-ETHYLENEDIOXYTHIOPHENE) | Measurement | Thermal properties | Polymeric composites | Azo compounds | Thermoelectricity | Electric properties | Conductivity | Materials science | Polymers | Heat conductivity
Solid State Physics | Seebeck coefficient | donor–acceptor–donor conjugated polymers | Optical and Electronic Materials | Electronics and Microelectronics, Instrumentation | Characterization and Evaluation of Materials | Material Science | Thermoelectric | electrical conductivity | power factor | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | POWER | CONDUCTIVE POLYMERS | ELECTROPOLYMERIZATION | GREEN | ENGINEERING, ELECTRICAL & ELECTRONIC | donor-acceptor-donor conjugated polymers | POLY(3,4-ETHYLENEDIOXYTHIOPHENE) | Measurement | Thermal properties | Polymeric composites | Azo compounds | Thermoelectricity | Electric properties | Conductivity | Materials science | Polymers | Heat conductivity
Journal Article
Dyes and Pigments, ISSN 0143-7208, 03/2018, Volume 150, pp. 89 - 96
Two series of donor–acceptor (D–A)-type azobenzene dyes with a tertiary amine as the donor were synthesized, and their photophysical and thermal properties...
Thermal stability | Hammett constant | Donor–acceptor | Azobenzene | STORAGE | MATERIALS SCIENCE, TEXTILES | ORGANIC-DYES | LIQUID-CRYSTALLINE POLYMERS | THERMAL-ANALYSIS | Donor-acceptor | ENGINEERING, CHEMICAL | SUBSTITUENT | CHEMISTRY, APPLIED | DERIVATIVES | PHOTOCHEMICAL PHASE-TRANSITION
Thermal stability | Hammett constant | Donor–acceptor | Azobenzene | STORAGE | MATERIALS SCIENCE, TEXTILES | ORGANIC-DYES | LIQUID-CRYSTALLINE POLYMERS | THERMAL-ANALYSIS | Donor-acceptor | ENGINEERING, CHEMICAL | SUBSTITUENT | CHEMISTRY, APPLIED | DERIVATIVES | PHOTOCHEMICAL PHASE-TRANSITION
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2019, Volume 58, Issue 17, pp. 5712 - 5717
The functionalization of MoS2 is of paramount importance for tailoring its properties towards optoelectronic applications and unlocking its full potential....
functionalization | phthalocyanines | spectroelectrochemistry | transition-metal dichalcogenides | charge transfer | MONOLAYER MOS2 | DYNAMICS | CHEMISTRY, MULTIDISCIPLINARY | Fluorescence | Phthalocyanins | Femtosecond | Optoelectronics | Imaging techniques | Electron transfer | Photochemicals | Energy harvesting | Zinc | Molybdenum disulfide | Excitons | Microscopy | Thermal imaging | Charge transfer
functionalization | phthalocyanines | spectroelectrochemistry | transition-metal dichalcogenides | charge transfer | MONOLAYER MOS2 | DYNAMICS | CHEMISTRY, MULTIDISCIPLINARY | Fluorescence | Phthalocyanins | Femtosecond | Optoelectronics | Imaging techniques | Electron transfer | Photochemicals | Energy harvesting | Zinc | Molybdenum disulfide | Excitons | Microscopy | Thermal imaging | Charge transfer
Journal Article
Dyes and Pigments, ISSN 0143-7208, 10/2018, Volume 157, pp. 143 - 150
This study involves the electrochemical, thermal and photophysical profiling of new pyromellitic diimide (PMDI) derivatives containing alkyl chains of...
Fluorescence | Organic sensitizers | Thermal stability | PMDI | QUANTUM YIELDS | MATERIALS SCIENCE, TEXTILES | PERYLENE BISIMIDES | ENGINEERING, CHEMICAL | DSSCS | SENSITIZED SOLAR-CELLS | FLUORESCENT | POLYMER | BASIS-SETS | CHEMISTRY, APPLIED | EFFICIENCY | Thermal properties | Analysis
Fluorescence | Organic sensitizers | Thermal stability | PMDI | QUANTUM YIELDS | MATERIALS SCIENCE, TEXTILES | PERYLENE BISIMIDES | ENGINEERING, CHEMICAL | DSSCS | SENSITIZED SOLAR-CELLS | FLUORESCENT | POLYMER | BASIS-SETS | CHEMISTRY, APPLIED | EFFICIENCY | Thermal properties | Analysis
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 01/2015, Volume 80, Issue 2, pp. 882 - 896
A convergent, multistep protocol was employed for the synthesis of a Janus-type multivalent donor–acceptor system. The synthetic approach is based on a...
CONVENIENT SYNTHESIS | AMPHIPHILIC DIBLOCK DENDRIMERS | MACROMOLECULES | DENDRONS | MOLECULAR ARCHITECTURES | CHROMOPHORES | CHEMISTRY, ORGANIC | CRYSTAL-STRUCTURES | 2+2 CYCLOADDITION | CHARGE-TRANSFER INTERACTIONS | SHAPE-PERSISTENT | Thermal properties | Dendrimers | Usage | Analysis | Spectrum analysis | Ring formation (Chemistry) | Chemical properties | Electron transport | Methods
CONVENIENT SYNTHESIS | AMPHIPHILIC DIBLOCK DENDRIMERS | MACROMOLECULES | DENDRONS | MOLECULAR ARCHITECTURES | CHROMOPHORES | CHEMISTRY, ORGANIC | CRYSTAL-STRUCTURES | 2+2 CYCLOADDITION | CHARGE-TRANSFER INTERACTIONS | SHAPE-PERSISTENT | Thermal properties | Dendrimers | Usage | Analysis | Spectrum analysis | Ring formation (Chemistry) | Chemical properties | Electron transport | Methods
Journal Article
Solar Energy Materials and Solar Cells, ISSN 0927-0248, 10/2016, Volume 155, pp. 348 - 355
A donor-acceptor-donor (D-A-D) molecule has been designed and synthesized for use as the electron-donating material in solution-processed small-molecule...
Fullerene acceptor | High open-circuit voltage | Organic solar cell | Solution processing | Small-molecule donor | Thermal stability | POWER CONVERSION EFFICIENCY | PHYSICS, APPLIED | OPEN-CIRCUIT VOLTAGE | ENERGY & FUELS | PERFORMANCE | MATERIALS SCIENCE, MULTIDISCIPLINARY | BLENDS | CONJUGATED POLYMERS | PHOTOVOLTAIC APPLICATIONS | ARYLENEVINYLENE | EXCHANGE | PHENOTHIAZINE | MORPHOLOGY | Solar cells | Acrylonitrile | Solar batteries | Saturated fatty acids | Nitriles | Annealing | Fysik | Physical Sciences | Naturvetenskap | Atom- och molekylfysik och optik | Atom and Molecular Physics and Optics | Natural Sciences | High open-circuit ltage
Fullerene acceptor | High open-circuit voltage | Organic solar cell | Solution processing | Small-molecule donor | Thermal stability | POWER CONVERSION EFFICIENCY | PHYSICS, APPLIED | OPEN-CIRCUIT VOLTAGE | ENERGY & FUELS | PERFORMANCE | MATERIALS SCIENCE, MULTIDISCIPLINARY | BLENDS | CONJUGATED POLYMERS | PHOTOVOLTAIC APPLICATIONS | ARYLENEVINYLENE | EXCHANGE | PHENOTHIAZINE | MORPHOLOGY | Solar cells | Acrylonitrile | Solar batteries | Saturated fatty acids | Nitriles | Annealing | Fysik | Physical Sciences | Naturvetenskap | Atom- och molekylfysik och optik | Atom and Molecular Physics and Optics | Natural Sciences | High open-circuit ltage
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 01/2019, Volume 57, Issue 1, pp. 60 - 69
ABSTRACT The synthesis of two new conjugated polymers based on the relatively under‐exploited monomer,...
dithienobenzimidazole | donor–acceptor | semiconducting polymer | synthesis | ionomers | conducting polymers | conjugated | addition polymerization | DESIGN | POLYMER SCIENCE | ALKYL | PERFORMANCE | donor-acceptor | TRANSISTORS | BENZIMIDAZOLE | UNITS | Thin films | Analysis | Spectrum analysis | Polymerization | Dielectric films | Polymer industry | Polymers | Mass spectrometry | Gravimetric analysis | Nuclear magnetic resonance--NMR | Ultraviolet spectroscopy | Photoluminescence | Ions | Differential thermal analysis | Trimers | Polymeric films | Ionization | Imidazole | Protonation | Chemical synthesis
dithienobenzimidazole | donor–acceptor | semiconducting polymer | synthesis | ionomers | conducting polymers | conjugated | addition polymerization | DESIGN | POLYMER SCIENCE | ALKYL | PERFORMANCE | donor-acceptor | TRANSISTORS | BENZIMIDAZOLE | UNITS | Thin films | Analysis | Spectrum analysis | Polymerization | Dielectric films | Polymer industry | Polymers | Mass spectrometry | Gravimetric analysis | Nuclear magnetic resonance--NMR | Ultraviolet spectroscopy | Photoluminescence | Ions | Differential thermal analysis | Trimers | Polymeric films | Ionization | Imidazole | Protonation | Chemical synthesis
Journal Article
Polymer, ISSN 0032-3861, 03/2015, Volume 60, pp. 215 - 220
Donor–acceptor (D–A) copolymers – containing 1,6-naphthodipyrrolidone as acceptor unit are synthesized and characterized. Copolymers and are prepared upon...
Conjugated polymer | Naphthodipyrrolidone | Low band gap polymer | POLYMER SCIENCE | CONJUGATED POLYMERS | UNITS | ORGANIC PHOTOVOLTAICS | Thermal properties | Density functionals | Polymer industry | Specific gravity | Backbone | Copolymers | Stability | Weight loss | Glass | Joining | Polymers
Conjugated polymer | Naphthodipyrrolidone | Low band gap polymer | POLYMER SCIENCE | CONJUGATED POLYMERS | UNITS | ORGANIC PHOTOVOLTAICS | Thermal properties | Density functionals | Polymer industry | Specific gravity | Backbone | Copolymers | Stability | Weight loss | Glass | Joining | Polymers
Journal Article
Tetrahedron, ISSN 0040-4020, 01/2015, Volume 71, Issue 4, pp. 654 - 662
A series of -shaped donor–acceptor (D–A) dipyrido[3,2- :2′,3′- ]phenazine (dppz) and benzothiadiazole based molecules, extended by different electron-donating...
Ruthenium(II) complex | Benzothiadiazole | Dipyrido[3,2-a:2′,3′-c]phenazine | Thermal stability | Donor–acceptor chromophore | Dipyrido[3 2-a:2′3′-c]phenazine | Donor-acceptor chromophore | CU2 | ELECTROCHEMICAL PROPERTIES | RU(II) COMPLEXES | CHEMISTRY, ORGANIC | CRYSTAL-STRUCTURES | LOW-BAND-GAP | PHOTOPHYSICAL PROPERTIES | LIGHT-SWITCH | DNA | Dipyrido[3,2-a:2 ',3 '-c]phenazine | OFF-ON FLUORESCENT | DERIVATIVES | Chromophores | Ruthenium | Thiophene | Analysis | Luminescence | Displays | Spectra | Derivatives | Isomers | Energy gaps (solid state)
Ruthenium(II) complex | Benzothiadiazole | Dipyrido[3,2-a:2′,3′-c]phenazine | Thermal stability | Donor–acceptor chromophore | Dipyrido[3 2-a:2′3′-c]phenazine | Donor-acceptor chromophore | CU2 | ELECTROCHEMICAL PROPERTIES | RU(II) COMPLEXES | CHEMISTRY, ORGANIC | CRYSTAL-STRUCTURES | LOW-BAND-GAP | PHOTOPHYSICAL PROPERTIES | LIGHT-SWITCH | DNA | Dipyrido[3,2-a:2 ',3 '-c]phenazine | OFF-ON FLUORESCENT | DERIVATIVES | Chromophores | Ruthenium | Thiophene | Analysis | Luminescence | Displays | Spectra | Derivatives | Isomers | Energy gaps (solid state)
Journal Article
Advanced Materials, ISSN 0935-9648, 04/2012, Volume 24, Issue 15, pp. 1956 - 1960
Two squaraine (SQ) donor molecules with different absorption bands are blended together for better coverage of the solar spectrum. The blend SQ device shows a...
squaraine dyes | solar cells | small molecules | blends | organic photovoltaics | THIN-FILMS | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | ORGANIC SOLAR-CELLS | OPEN-CIRCUIT VOLTAGE | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | EFFICIENT | Sunlight | Electric Power Supplies | Phenols - chemistry | Electric Conductivity | Cyclobutanes - chemistry | Electrical engineering | Solar energy industry | Solar cells | Solvents | Annealing | Blends | Polymer blends | Illumination | Devices | Sun
squaraine dyes | solar cells | small molecules | blends | organic photovoltaics | THIN-FILMS | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | ORGANIC SOLAR-CELLS | OPEN-CIRCUIT VOLTAGE | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | EFFICIENT | Sunlight | Electric Power Supplies | Phenols - chemistry | Electric Conductivity | Cyclobutanes - chemistry | Electrical engineering | Solar energy industry | Solar cells | Solvents | Annealing | Blends | Polymer blends | Illumination | Devices | Sun
Journal Article
Solar Energy Materials and Solar Cells, ISSN 0927-0248, 08/2019, Volume 197, pp. 32 - 75
Conjugated polymers have been extensively used for optoelectronic applications such as photovoltaics, light-emitting diodes, thin-film transistors and...
Donor-acceptor | Conjugated polymer | Electrochromic device | El
Donor-acceptor | Conjugated polymer | Electrochromic device | El