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

Zhao et al., 2011 - Google Patents

Substituent effects on the intramolecular charge transfer and fluorescence of bimetallic platinum complexes

Zhao et al., 2011

Document ID
15238593642041711237
Author
Zhao G
Yu F
Zhang M
Northrop B
Yang H
Han K
Stang P
Publication year
Publication venue
The Journal of Physical Chemistry A

External Links

Snippet

An investigation of a series of platinum-containing organometallic complexes for the study of fluorescence phenomena in organometallic chromophores controlled by the intramolecular charge transfer (ICT) is presented in this work. We report steady-state and time-resolved …
Continue reading at pubs.acs.org (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
    • C07F15/0033Iridium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
    • C07F15/0073Rhodium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1003Carbocyclic compounds
    • C09K2211/1007Non-condensed systems

Similar Documents

Publication Publication Date Title
Zhao et al. Substituent effects on the intramolecular charge transfer and fluorescence of bimetallic platinum complexes
Pomestchenko et al. Room temperature phosphorescence from a platinum (II) diimine bis (pyrenylacetylide) complex
Frath et al. Facile synthesis of highly fluorescent boranil complexes
DiLuzio et al. High-throughput screening and automated data-driven analysis of the triplet photophysical properties of structurally diverse, heteroleptic iridium (III) complexes
Tyson et al. Excited state processes in ruthenium (II)/pyrenyl complexes displaying extended lifetimes
McGarrah et al. Toward a molecular photochemical device: a triad for photoinduced charge separation based on a platinum diimine bis (acetylide) chromophore
Lai et al. Luminescent Mononuclear and Binuclear Cyclometalated Palladium (II) Complexes of 6-Phenyl-2, 2 ‘-bipyridines: Spectroscopic and Structural Comparisons with Platinum (II) Analogues1, 2
Dias et al. Bright phosphorescence of a trinuclear copper (I) complex: luminescence thermochromism, solvatochromism, and “concentration luminochromism”
Glazer et al. Ruthenium complexes that break the rules: structural features controlling dual emission
Hupp et al. Synthesis, Structures, and Photophysical Properties of a Series of Rare Near-IR Emitting Copper (I) Complexes
Ishimatsu et al. Solvent effect on thermally activated delayed fluorescence by 1, 2, 3, 5-tetrakis (carbazol-9-yl)-4, 6-dicyanobenzene
Abrahamsson et al. A 3.0 μs room temperature excited state lifetime of a bistridentate RuII− polypyridine complex for rod-like molecular arrays
Lee et al. Iridium cyclometalates with tethered o-carboranes: impact of restricted rotation of o-carborane on phosphorescence efficiency
Benito et al. Polymorphic copper iodide clusters: insights into the mechanochromic luminescence properties
Brooks et al. Synthesis and characterization of phosphorescent cyclometalated platinum complexes
Perruchas et al. Mechanochromic and thermochromic luminescence of a copper iodide cluster
Farley et al. Controlling emission energy, self-quenching, and excimer formation in highly luminescent N∧ C∧ N-coordinated platinum (II) complexes
DePriest et al. Structure, physical, and photophysical properties of platinum (II) complexes containing bidentate aromatic and bis (diphenylphosphino) methane as ligands
Miller et al. Long-lived and efficient emission from mononuclear amidophosphine complexes of copper
Rachford et al. Boron Dipyrromethene (Bodipy) Phosphorescence Revealed in [Ir (ppy) 2 (bpy-C C-Bodipy)]+
Massue et al. Synthesis of luminescent 2-(2′-hydroxyphenyl) benzoxazole (HBO) borate complexes
Abrahamsson et al. A new strategy for the improvement of photophysical properties in ruthenium (II) polypyridyl complexes. Synthesis and photophysical and electrochemical characterization of six mononuclear ruthenium (II) bisterpyridine-type complexes
Wu et al. Long-lived room temperature deep-red/near-IR emissive intraligand triplet excited state (3IL) of naphthalimide in cyclometalated platinum (II) complexes and its application in upconversion
Lee et al. A photochromic platinum (II) bis (alkynyl) complex containing a versatile 5, 6-dithienyl-1, 10-phenanthroline
Nagai et al. Highly intense fluorescent diarylboron diketonate