Alrefai et al., 2021 - Google Patents
Broadly versus Barely Variable Complex Chromophores of Planar Nickel (II) from κ3-N, N′, C and κ3-N, N′, O Donor PlatformsAlrefai et al., 2021
- Document ID
- 9660517247467341729
- Author
- Alrefai R
- Hörner G
- Schubert H
- Berkefeld A
- Publication year
- Publication venue
- Organometallics
External Links
Snippet
This work reports on complex chromophores of planar nickel (II) of the general formula [(κ3- N, N′, C/O) Ni–ER], which combines a κ2-N, N′-coordinate aromatic N-heterocycle with a pendant phenyl/phenol donor and the variable coligands ER (= carboxylato, phenolato …
- 229910052757 nitrogen 0 title abstract description 42
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic 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
- C07D213/02—Heterocyclic 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
- C07D213/04—Heterocyclic 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
- C07D213/06—Heterocyclic 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
-
- 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
- C07F15/0033—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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
- C07F5/02—Boron 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
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C-Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
-
- 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
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
-
- 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
- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic System
-
- 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
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic System
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Gernert et al. | Cyclic (amino)(aryl) carbenes enter the field of chromophore ligands: Expanded π system leads to unusually deep red emitting CuI compounds | |
Brooks et al. | Synthesis and characterization of phosphorescent cyclometalated platinum complexes | |
Li et al. | Synthetic control of excited-state properties in cyclometalated Ir (III) complexes using ancillary ligands | |
Wang et al. | Synthesis, structure, and photophysical properties of two four-coordinate CuI–NHC complexes with efficient delayed fluorescence | |
Zhao et al. | Series of new cationic iridium (III) complexes with tunable emission wavelength and excited state properties: structures, theoretical calculations, and photophysical and electrochemical properties | |
Maubert et al. | Absorption spectra and photophysical properties of a series of polypyridine ligands containing appended pyrenyl and anthryl chromophores and of their ruthenium (II) and osmium (II) complexes | |
Radwan et al. | Manipulating the excited states of cyclometalated iridium complexes with β-ketoiminate and β-diketiminate ligands | |
Baron et al. | Click chemistry on a ruthenium polypyridine complex. An efficient and versatile synthetic route for the synthesis of photoactive modular assemblies | |
Stonelake et al. | Spectroscopic and theoretical investigation of color tuning in deep-red luminescent iridium (III) complexes | |
Donato et al. | Mono-and dinuclear cationic iridium (III) complexes bearing a 2, 5-dipyridylpyrazine (2, 5-dpp) ligand | |
Baik et al. | Enhancing the Photochemical Stability of N, C-Chelate Boryl Compounds: C− C Bond Formation versus C C Bond cis, trans-Isomerization | |
Zaarour et al. | Linear and nonlinear optical properties of tris-cyclometalated phenylpyridine Ir (III) complexes incorporating π-conjugated substituents | |
Jager et al. | Facile synthesis of Bistridentate RuII complexes based on 2, 6-di (quinolin-8-yl) pyridyl ligands: sensitizers with microsecond 3MLCT excited state lifetimes | |
Ng et al. | Synthesis, characterization, and photophysical study of luminescent rhenium (I) diimine complexes with various types of N-heterocyclic carbene ligands | |
Brown et al. | Influence of sulfur oxidation state and substituents on sulfur-bridged luminescent copper (I) complexes showing thermally activated delayed fluorescence | |
Cárdenas et al. | Synthesis, X-ray structure, and electrochemical and excited-state properties of multicomponent complexes made of a [Ru (tpy) 2] 2+ unit covalently linked to a [2]-catenate moiety. Controlling the energy-transfer direction by changing the catenate metal ion | |
Bens et al. | Chromium (0) and Molydenum (0) Complexes with a Pyridyl-Mesoionic Carbene Ligand: Structural,(Spectro) electrochemical, Photochemical, and Theoretical Investigations | |
Chen et al. | Luminescent heterotrinuclear complexes with Pt (diimine)(dithiolate) and metal diphosphine as components | |
Lentijo et al. | Highly fluorescent platinum (II) organometallic complexes of perylene and perylene monoimide, with Pt σ-bonded directly to the perylene core | |
Liao et al. | Iridium (III) complexes bearing tridentate chromophoric chelate: phosphorescence fine-tuned by phosphine and hydride ancillary | |
Kern et al. | Complexes containing 2, 9-bis (p-biphenylyl)-1, 10-phenanthroline units incorporated into a 56-membered ring. Synthesis, electrochemistry, and photophysical properties | |
Zhao et al. | Triarylboron/triarylamine-functionalized 2, 2′-bipyridine ligands and their copper (I) complexes | |
Lozada et al. | Yellow-Emitting, Pseudo-Octahedral Zinc Complexes of Benzannulated N^ N^ O Pincer-Type Ligands | |
Jarosz et al. | Platinum (II) terpyridyl-acetylide dyads and triads with nitrophenyl acceptors via a convenient synthesis of a boronated phenylterpyridine | |
Hu et al. | Bi-1, 10-phenanthrolines and their mononuclear Ru (II) complexes |