Zhou et al., 2019 - Google Patents
AIEgens-lightened functional polymers: synthesis, properties and applicationsZhou et al., 2019
- Document ID
- 4039977049525467775
- Author
- Zhou S
- Wan H
- Zhou F
- Gu P
- Xu Q
- Lu J
- Publication year
- Publication venue
- Chinese Journal of Polymer Science
External Links
Snippet
Recently, polymers with aggregation-induced emission (AIE) effects have attracted significant attention due to their broad applications in luminescence sensors, stimuli responsive materials, electroluminescence devices, etc. In this review, we summarize recent …
- 230000015572 biosynthetic process 0 title description 17
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
- 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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/14—Macromolecular compounds
- C09K2211/1408—Carbocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
- C08G83/003—Dendrimers
-
- 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
- H01L51/0034—Organic polymers or oligomers
- H01L51/0043—Copolymers
-
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Zhou et al. | AIEgens-lightened functional polymers: synthesis, properties and applications | |
Hu et al. | Recent progress in AIE-active polymers | |
Sun et al. | Achieving purely organic room temperature phosphorescence in aqueous solution | |
Barman et al. | Review on recent trends and prospects in π‐conjugated luminescent aggregates for biomedical applications | |
Kaeser et al. | Fluorescent nanoparticles based on self‐assembled π‐conjugated systems | |
Hu et al. | AIE macromolecules: syntheses, structures and functionalities | |
Wang et al. | Rigidity and polymerization amplified red thermally activated delayed fluorescence polymers for constructing red and single‐emissive‐layer white OLEDs | |
Mei et al. | Aggregation-induced emission: together we shine, united we soar! | |
Tuncel | π-Conjugated nanostructured materials: preparation, properties and photonic applications | |
Wang et al. | Hyperbranched polytriazoles with high molecular compressibility: aggregation-induced emission and superamplified explosive detection | |
Dong et al. | Reversible photoisomerization of azobenzene-containing polymeric systems driven by visible light | |
Liu et al. | Bright far-red/near-infrared fluorescent conjugated polymer nanoparticles for targeted imaging of HER2-positive cancer cells | |
Lu et al. | Polyfluorene-based light-emitting rod− coil block copolymers | |
Wang et al. | Recent advances of polymer‐based pure organic room temperature phosphorescent materials | |
Chen et al. | Unveiling the different emission behavior of polytriazoles constructed from pyrazine-based AIE monomers by click polymerization | |
Zou et al. | Recent advances in synthesis and application of organic near-infrared fluorescence polymers | |
Huang et al. | Aggregation-induced emission-active hyperbranched poly (tetrahydropyrimidine) s synthesized from multicomponent tandem polymerization | |
Fang et al. | Hyperbranching-enhanced-emission effect discovered in hyperbranched poly (4-(cyanomethyl) phenyl methacrylate) | |
Gao et al. | Di (naphthalen-2-yl)-1, 2-diphenylethene-based conjugated polymers: aggregation-enhanced emission and explosive detection | |
Song et al. | A Universal strategy for producing fluorescent polymers based on designer hyperbranched polyethylene ternary copolymers | |
Wu et al. | Stimuli-responsive conjugated rod-coil block copolymers: Synthesis, morphology, and applications | |
Sonawane et al. | Blue, green, and orange-red emission from polystyrene microbeads for solid-state white-light and multicolor emission | |
Yu et al. | Alternating thermally activated delayed fluorescence copolymers featuring through-space charge transfer for efficient electroluminescence | |
Terayama et al. | Structural design of conjugated polymers for fluorescence bioimaging in the second near‐infrared window | |
Jia et al. | Controlling AIE and ACQ properties of conjugated carbazole-tetraphenylethene copolymers by ethynylene spacer |