Luo et al., 2017 - Google Patents
Hyperbranched conjugated polymers containing 1, 3-butadiene units: Metal-free catalyzed synthesis and selective chemosensors for Fe 3+ ionsLuo et al., 2017
View HTML- Document ID
- 2065180327465249915
- Author
- Luo C
- Liu Y
- Zhang Q
- Cai X
- Publication year
- Publication venue
- RSC Advances
External Links
Snippet
Hyperbranched conjugated polymers (P1 and P2) containing 1, 3-butadiene repeating units appended with carboxylic ester groups were synthesized in good yield by metal-free catalyzed polymerization of diethyl 4, 4′-(5-formyl-1, 3-phenylene)(2E, 2′ E)-bis (but-2 …
- 150000002500 ions 0 title abstract description 44
Classifications
-
- 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
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/124—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one nitrogen atom in the ring
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/026—Wholly aromatic polyamines
- C08G73/0266—Polyanilines or derivatives thereof
-
- 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
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
-
- 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
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/10—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aromatic carbon atoms, e.g. polyphenylenes
-
- 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
- C09K2211/10—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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Luo et al. | Hyperbranched conjugated polymers containing 1, 3-butadiene units: Metal-free catalyzed synthesis and selective chemosensors for Fe 3+ ions | |
Wu et al. | A conjugated hyperbranched polymer constructed from carbazole and tetraphenylethylene moieties: convenient synthesis through one-pot “A 2+ B 4” Suzuki polymerization, aggregation-induced enhanced emission, and application as explosive chemosensors and PLEDs | |
Liu et al. | Design and synthesis of bipyridyl-containing conjugated polymers: effects of polymer rigidity on metal ion sensing | |
Hu et al. | Hyperbranched conjugated poly (tetraphenylethene): synthesis, aggregation-induced emission, fluorescent photopatterning, optical limiting and explosive detection | |
Shu et al. | Conjugated poly (aryleneethynylenesiloles) and their application in detecting explosives | |
Wu et al. | New tetraphenylethylene-containing conjugated polymers: Facile synthesis, aggregation-induced emission enhanced characteristics and application as explosive chemsensors and PLEDs | |
Bao et al. | A fluorescent conjugated polymer for trace detection of diamines and biogenic polyamines | |
Ding et al. | Reaction-based conjugated polymer fluorescent probe for mercury (II): good sensing performance with “turn-on” signal output | |
Srinivas et al. | Water-soluble anionic poly (p-phenylene vinylenes) with high luminescence | |
Kaya et al. | Synthesis and characterization of fluorescent graft fluorene-co-polyphenol derivatives: the effect of substituent on solubility, thermal stability, conductivity, optical and electrochemical properties | |
Yeldir et al. | Synthesis and characterization of a pyrene-based Schiff base and its oligomer: Investigation of fluorescent Cr3+ probe | |
CN102899032B (en) | Electropolymerizable fluorescent sensing material and application on fluorescent or electropolymerizable detection of metal ions | |
Kaya et al. | Reaction conditions, photophysical, electrochemical, conductivity, and thermal properties of polyazomethines | |
Yang et al. | Triphenylamine-based linear conjugated polyfluorenes with various pendant groups: Synthesis, characterization, and ion responsive properties | |
Bilici et al. | A comparative study of 9, 9-bis (4-aminophenyl) fluorene polymers prepared by catalytic and non-catalytic oxidative polymerisation methods | |
Cao et al. | Polytriazole bridged with 2, 5-diphenyl-1, 3, 4-oxadiazole moieties: A highly sensitive and selective fluorescence chemosensor for Ag+ | |
Liu et al. | 2, 6-Substituted pyridine derivative-containing conjugated polymers: synthesis, photoluminescence and ion-sensing properties | |
Liu et al. | Polyannulation of internal alkynes and O-acyloxime derivatives to synthesize functional poly (isoquinoline) s | |
US6833432B2 (en) | Conjugated poly(2,7-carbazole) derivatives and process for the preparation thereof | |
Feng et al. | Hyperbranched copolymer containing triphenylamine and divinyl bipyridyl units for fluorescent chemosensors | |
Ran et al. | Synthesis and fluorescence study of conjugated polymers based on 2, 4, 6-triphenylpyridine moieties | |
Yu et al. | Synthesis, characterization and aggregation-induced emission of alternating copolymers containing cyclophanes and tetraphenylethenes | |
KR100692623B1 (en) | Aromatic Amine Polymer Compounds for Chemical Sensors and Reaction Intermediates and Resin Compositions Comprising the Same | |
Ma et al. | Syntheses, characterization, and energy transfer properties of benzothiadiazole-based hyperbranched polyfluorenes | |
Kim et al. | Synthesis of chromo‐and fluorogenic poly (ortho‐diaminophenylene) chemosensors for fluoride anion |