[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Soellner et al., 2018 - Google Patents

Diaryl‐1, 2, 3‐triazolylidene platinum (II) complexes

Soellner et al., 2018

Document ID
11773524087278882715
Author
Soellner J
Strassner T
Publication year
Publication venue
Chemistry–A European Journal

External Links

Snippet

Control of the excited state geometry by rational ligand design leads to a new class of phosphorescent emitters with extraordinary photophysical properties. Extension of the π‐ system in the triplet state leading to a significant bathochromic shift of the emission was …
Continue reading at chemistry-europe.onlinelibrary.wiley.com (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
    • C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
    • C07F15/0033—Iridium compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
    • C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
    • C07F15/0073—Rhodium compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
    • C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
    • C07F15/0086—Platinum compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • H—ELECTRICITY
    • H01—BASIC ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077—Coordination compounds, e.g. porphyrin
    • H01L51/0084—Transition metal complexes, e.g. Ru(II)polypyridine complexes
    • H01L51/0087—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising platinum
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1007—Non-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/18—Metal complexes

Similar Documents

Publication Publication Date Title
Soellner et al. Diaryl‐1, 2, 3‐triazolylidene platinum (II) complexes
Soellner et al. Phosphorescent Platinum (II) Complexes with Mesoionic 1H‐1, 2, 3‐Triazolylidene Ligands
Crestani et al. Synthesis and characterization of neutral luminescent diphosphine pyrrole-and indole-aldimine copper (I) complexes
Ladouceur et al. Role of substitution on the photophysical properties of 5, 5′-Diaryl-2, 2′-bipyridine (bpy*) in [Ir (ppy) 2 (bpy*)] PF6 complexes: A combined experimental and theoretical study
Tronnier et al. Enlarging the π system of phosphorescent (C^ C*) cyclometalated platinum (II) NHC complexes
Zhao et al. Highly selective phosphorescent chemosensor for fluoride based on an iridium (III) complex containing arylborane units
Kim et al. Phosphorescence color tuning of cyclometalated iridium complexes by o-carborane substitution
Yu et al. Deep Red to Near‐Infrared Emitting Rhenium (I) Complexes: Synthesis, Characterization, Electrochemistry, Photophysics, and Electroluminescence Studies
Sivchik et al. Improvement of the Photophysical Performance of Platinum‐Cyclometalated Complexes in Halogen‐Bonded Adducts
Elie et al. Role of the Bridging Group in Bis‐Pyridyl Ligands: Enhancing Both the Photo‐and Electroluminescent Features of Cationic (IPr) CuI Complexes
Werrett et al. Proton-induced reversible modulation of the luminescent output of rhenium (I), iridium (III), and ruthenium (II) tetrazolate complexes
Szentkuti et al. Monocyclometalated gold (III) monoaryl complexes—A new class of triplet phosphors with highly tunable and efficient emission properties
Ragni et al. Iridium (III) complexes with sulfonyl and fluorine substituents: synthesis, stereochemistry and effect of functionalisation on their photophysical properties
Giménez et al. Facile Approaches to Phosphorescent Bis (cyclometalated) Pentafluorophenyl PtIV Complexes: Photophysics and Computational Studies
Wang et al. Syntheses and electrochemical, photophysical, and photochemical properties of ruthenium (II) 4, 5-diazafluorenone complexes and their ketal derivatives
Hsu et al. Bis‐tridentate IrIII Phosphors Bearing Two Fused Five‐Six‐Membered Metallacycles: A Strategy to Improved Photostability of Blue Emitters
Tronnier et al. Phosphorescent C∧ C* Cyclometalated PtII Dibenzofuranyl‐NHC Complexes–An Auxiliary Ligand Study
Leopold et al. Changing the Emission Properties of Phosphorescent C^ C*‐Cyclometalated Thiazol‐2‐ylidene Platinum (II) Complexes by Variation of the β‐Diketonate Ligands
Soellner et al. Phosphorescent cyclometalated platinum (II) aNHC complexes
Wu et al. Efficient deep blue platinum acetylide phosphors with acyclic diaminocarbene ligands
Titov et al. Dinuclear CuI and AgI Pyrazolates Supported with Tertiary Phosphines: Synthesis, Structures, and Photophysical Properties
Galán et al. Analyzing the Relation between Structure and Aggregation Induced Emission (AIE) Properties of Iridium (III) Complexes through Modification of Non‐Chromophoric Ancillary Ligands
Hruzd et al. Luminescent cyclometalated alkynylplatinum (II) complexes with 1, 3-di (pyrimidin-2-yl) benzene ligands: Synthesis, electrochemistry, photophysics and computational studies
Stipurin et al. Phosphorescent cyclometalated platinum (II) imidazolinylidene complexes
Moussa et al. Synthesis and Luminescence Properties of Cycloplatinated Complexes with a Chelating N∧ C Pyridine‐Derived N‐Heterocyclic Carbene–Influence of 2, 4, 6‐Triphenylphosphinine versus Triphenylphosphine