Yang et al., 2023 - Google Patents
DAD type cyclohexyl and cycloheptyl-modified benzo [d] imidazole derivatives with different aggregation-induced emission enhancement (AIEE) and …Yang et al., 2023
- Document ID
- 9672455796724961852
- Author
- Yang Y
- Liu S
- Deng D
- Chen Z
- Pu S
- Publication year
- Publication venue
- Journal of Molecular Structure
External Links
Snippet
Four tetraphenylethylene or triphenylamine-functionalized donor-acceptor-donor type benzo [d] imidazole derivatives 1–4 with different cycloalkyl substituents were successfully developed and characterized. All of these fluorogenic compounds showed remarkable …
- 238000004220 aggregation 0 title abstract description 29
Classifications
-
- 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
-
- 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
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
-
- 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
- C09K9/00—Tenebrescent materials, i.e. materials for which the range of wavelength for energy absorption is changed as result of excitation by some form of energy
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Mukherjee et al. | Stimuli and shape responsive ‘boron-containing’luminescent organic materials | |
Shen et al. | Effects of substitution with donor–acceptor groups on the properties of tetraphenylethene trimer: aggregation-induced emission, solvatochromism, and mechanochromism | |
Wang et al. | Aqueous nanoaggregation-enhanced one-and two-photon fluorescence, crystalline J-aggregation-induced red shift, and amplified spontaneous emission of 9, 10-bis (p-dimethylaminostyryl) anthracene | |
Zhang et al. | Aggregation-induced emission enhancement and mechanofluorochromic properties of α-cyanostilbene functionalized tetraphenyl imidazole derivatives | |
Gao et al. | Aggregation-induced emission and mechanofluorochromism of tetraphenylbutadiene modified β-ketoiminate boron complexes | |
Wang et al. | Polymorphism and Multicolor Mechanofluorochromism of a D-π-A Asymmetric 4 H-Pyran Derivative with Aggregation-Induced Emission Property | |
Zhu et al. | Branched triphenylamine luminophores: aggregation-induced fluorescence emission, and tunable near-infrared solid-state fluorescence characteristics via external mechanical stimuli | |
Wu et al. | Highly efficient solid-state emission of diphenylfumaronitriles with full-color AIE, and application in explosive sensing, data storage and WLEDs | |
Zhang et al. | Aggregation-induced emission-active tetraphenylethylene derivatives containing arylimidazole unit for reversible mechanofluorochromism and selective detection of picric acid | |
Zhao et al. | Mechanofluorochromism of difluoroboron β-ketoiminate boron complexes functionalized with benzoxazole and benzothiazole | |
Gao et al. | Tetraphenylethene modified β-ketoiminate boron complexes bearing aggregation-induced emission and mechanofluorochromism | |
Lei et al. | Piezochromism, acidochromism, solvent-induced emission changes and cell imaging of D-π-A 1, 4-dihydropyridine derivatives with aggregation-induced emission properties | |
Wang et al. | Mechanochromic luminescence of AIEE-active tetraphenylethene-containing cruciform luminophores | |
Zhan et al. | Modulation of the emission behavior and mechanofluorochromism by electron-donating moiety of D-π-A type quinoxaline derivatives | |
Yan et al. | A novel coumarin-based red fluorogen with AIE, self-assembly, and TADF properties | |
Zhan et al. | Phenothiazine substituted phenanthroimidazole derivatives: Synthesis, photophysical properties and efficient piezochromic luminescence | |
Zhou et al. | Phenothiazine and diphenylsulfone-based donor–acceptor π-systems exhibiting remarkable mechanofluorochromism | |
Sun et al. | Self-assembling and piezofluorochromic properties of tert-butylcarbazole-based Schiff bases and the difluoroboron complex | |
Lu et al. | New frog-type Dibenzo [a, c][1, 2, 5] thiadiazolo [3, 4-i] phenazine heterocyclic derivatives with aggregation-enhanced one-and two-photon excitation NIR fluorescence | |
Xu et al. | The evident aggregation-induced emission and the reversible mechano-responsive behavior of carbazole-containing cruciform luminophore | |
Zhang et al. | Enabling DPP derivatives to show multistate emission and developing the multifunctional materials by rational branching effect | |
Li et al. | Tetrahydro [5] helicene-based dye with remarkable and reversible acid/base stimulated fluorescence switching properties in solution and solid state | |
Yang et al. | D-π-A type carbazole and triphenylamine derivatives with different π-conjugated units: Tunable aggregation-induced emission (AIE) and mechanofluorochromic properties | |
Cheng et al. | High contrast mechanochromic luminescence of aggregation-induced emission (AIE)-based 9, 9-dimethyl-9, 10-dihydroacridine-containing cruciform luminophores | |
Deng et al. | Benzothiadiazole-based dibenzobenzimidazole derivatives with aggregation-induced deep-red fluorescence and different mechanically responsive fluorescence features |