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Porphyrins Sheathed in Quadrupolar Solvation Spheres of Hexafluorobenzene: Solvation-Induced Fluorescence Enhancement and Conformational Confinement DOI: 10.1021/acs.jpcc.7b04083

Porphyrins Sheathed in Quadrupolar Solvation Spheres of Hexafluorobenzene: Solvation-Induced Fluorescence Enhancement and Conformational Confinement DOI: 10.1021/acs.jpcc.7b04083

Bodipy–Anthracene Dyads as Triplet Photosensitizers: Effect of Chromophore Orientation on Triplet-State Formation Efficiency and Application in Triplet–Triplet Annihilation Upconversion DOI: 10.1021/acs.orglett.7b02047

Bodipy–Anthracene Dyads as Triplet Photosensitizers: Effect of Chromophore Orientation on Triplet-State Formation Efficiency and Application in Triplet–Triplet Annihilation Upconversion DOI: 10.1021/acs.orglett.7b02047

Expanding the Scope of Ligand Substitution from [M(S2C2Ph2] (M = Ni2+, Pd2+, Pt2+) To Afford New Heteroleptic Dithiolene Complexes DOI: 10.1021/acs.inorgchem.7b00971

Expanding the Scope of Ligand Substitution from [M(S2C2Ph2] (M = Ni2+, Pd2+, Pt2+) To Afford New Heteroleptic Dithiolene Complexes DOI: 10.1021/acs.inorgchem.7b00971

A versatile synthetic approach to design tailor-made push-pull chromophores with intriguing and tunable photophysical signatures https://doi.org/10.1016/j.dyepig.2017.08.014

A versatile synthetic approach to design tailor-made push-pull chromophores with intriguing and tunable photophysical signatures https://doi.org/10.1016/j.dyepig.2017.08.014

Triple-BODIPY organic nanoparticles with particular fluorescence emission https://doi.org/10.1016/j.dyepig.2017.08.026

Triple-BODIPY organic nanoparticles with particular fluorescence emission https://doi.org/10.1016/j.dyepig.2017.08.026

Construction of new fluorophores by Diels-Alder reaction of diacenaphthothiophenes https://doi.org/10.1016/j.tet.2017.08.016

Construction of new fluorophores by Diels-Alder reaction of diacenaphthothiophenes https://doi.org/10.1016/j.tet.2017.08.016

Iptycene-Containing Azaacenes with Tunable Luminescence DOI: 10.1055/s-0036-1589503

Iptycene-Containing Azaacenes with Tunable Luminescence DOI: 10.1055/s-0036-1589503

Synthesis and Structures of Zigzag Shaped [12]Cyclo-p-phenylene Composed of Dinaphthofuran Units and Biphenyl Units DOI: 10.1021/acs.joc.7b01053

Synthesis and Structures of Zigzag Shaped [12]Cyclo-p-phenylene Composed of Dinaphthofuran Units and Biphenyl Units DOI: 10.1021/acs.joc.7b01053

New Molecular Design Concurrently Providing Superior Pure Blue, Thermally Activated Delayed Fluorescence and Optical Out-Coupling Efficiencies  DOI: 10.1021/jacs.7b03848

New Molecular Design Concurrently Providing Superior Pure Blue, Thermally Activated Delayed Fluorescence and Optical Out-Coupling Efficiencies DOI: 10.1021/jacs.7b03848

Controlling Vilsmeier-Haack processes in meso-methylBODIPYs: A new way to modulate finely photophysical properties in boron dipyrromethenes https://doi.org/10.1016/j.dyepig.2017.02.030

Controlling Vilsmeier-Haack processes in meso-methylBODIPYs: A new way to modulate finely photophysical properties in boron dipyrromethenes https://doi.org/10.1016/j.dyepig.2017.02.030