Tian et al., 2014 - Google Patents
Design and synthesis of new stable fluorenyl-based radicalsTian et al., 2014
- Document ID
- 3517099002723888972
- Author
- Tian Y
- Uchida K
- Kurata H
- Hirao Y
- Nishiuchi T
- Kubo T
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
Organic neutral radicals have long fascinated chemists with a fundamental understanding of structure–reactivity relationships in organic reactions and with applications as new functional materials. However, the elusive nature of these radicals makes the synthesis …
- 230000015572 biosynthetic process 0 title abstract description 45
Classifications
-
- 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
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
- H01L51/0071—Polycyclic condensed heteroaromatic hydrocarbons
- H01L51/0072—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
-
- 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
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
- H01L51/0071—Polycyclic condensed heteroaromatic hydrocarbons
- H01L51/0073—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ringsystem, e.g. cumarine dyes
-
- 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
-
- 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
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Tian et al. | Design and synthesis of new stable fluorenyl-based radicals | |
Zhu et al. | Extraordinary redox activities in ladder-type conjugated molecules enabled by B← N coordination-promoted delocalization and hyperconjugation | |
Cao et al. | The impact of antiaromatic subunits in [4 n+ 2] π-systems: Bispentalenes with [4 n+ 2] π-electron perimeters and antiaromatic character | |
Shu et al. | High-spin diradical dication of chiral π-conjugated double helical molecule | |
Kubota et al. | Synthesis and fluorescence properties of thiazole–boron complexes bearing a β-ketoiminate ligand | |
Abe | Diradicals | |
Sun et al. | Zethrenes, extended p-quinodimethanes, and periacenes with a singlet biradical ground state | |
Xin et al. | Azulene-based BN-heteroaromatics | |
Kasemthaveechok et al. | Axially and helically chiral cationic radical bicarbazoles: SOMO–HOMO level inversion and chirality impact on the stability of mono-and diradical cations | |
Ohashi et al. | 4, 8, 12, 16-Tetra-Tert-Butyl-s-Indaceno [1, 2, 3-Cd: 5, 6, 7-c ‘d ‘] Diphenalene: a four-stage amphoteric redox system | |
Saito et al. | Polycyclic π-electron system with boron at its center | |
Li et al. | Magnetic bistability in a discrete organic radical | |
Sakurai et al. | Electron-or hole-transporting nature selected by side-chain-directed π-stacking geometry: liquid crystalline fused metalloporphyrin dimers | |
Omer et al. | Electrochemical behavior and electrogenerated chemiluminescence of star-shaped D− A compounds with a 1, 3, 5-triazine core and substituted fluorene arms | |
Shimizu et al. | HOMO–LUMO energy-gap tuning of π-conjugated zwitterions composed of electron-donating anion and electron-accepting cation | |
Echeverri et al. | Untangling the mechanochromic properties of benzothiadiazole-based luminescent polymorphs through supramolecular organic framework topology | |
Li et al. | [6] Cyclo-para-phenylmethine: an analog of benzene showing global aromaticity and open-shell diradical character | |
Huong et al. | Π-conjugated molecules containing naphtho [2, 3-b] thiophene and their derivatives: theoretical design for organic semiconductors | |
Miyoshi et al. | Fluoreno [2, 3-b] fluorene vs Indeno [2, 1-b] fluorene: Unusual Relationship between the Number of π Electrons and Excitation Energy in m-Quinodimethane-Type Singlet Diradicaloids | |
Oki et al. | Synthesis and isolation of antiaromatic expanded azacoronene via intramolecular vilsmeier-type reaction | |
Putta et al. | Rational design of lamellar π–π stacked organic crystalline materials with short interplanar distance | |
Chen et al. | Dicyanomethylenated acridone based crystals: torsional vibration confinement induced emission with supramolecular structure dependent and stimuli responsive characteristics | |
Anamimoghadam et al. | Electronically stabilized nonplanar phenalenyl radical and its planar isomer | |
Gao et al. | Stabilizing radical cation and dication of a tetrathiafulvalene derivative by a weakly coordinating anion | |
Guo et al. | Large aromatic hydrocarbon radical cation with global aromaticity and state-associated magnetic activity |