Zentel et al., 1989 - Google Patents
Liquid‐crystalline elastomers with cholesteric and chiral smectic C* phasesZentel et al., 1989
- Document ID
- 12675392519717425785
- Author
- Zentel R
- Reckert G
- Bualek S
- Kapitza H
- Publication year
- Publication venue
- Die Makromolekulare Chemie: Macromolecular Chemistry and Physics
External Links
Snippet
A series of 9 new chiral and crosslinkable liquid‐crystalline copolymers were synthesized and transformed into liquid‐crystalline elastomers by crosslinking using a hydrosilylation reaction. Both the soluble copolymers and the elastomers show cholesteric, smectic A and …
- 239000004990 Smectic liquid crystal 0 title abstract description 78
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
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/20—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters or ethers
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/38—Polymers
- C09K19/3833—Polymers with mesogenic groups in the side chain
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/38—Polymers
- C09K19/3804—Polymers with mesogenic groups in the main chain
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
- C09K19/3441—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
- C09K19/3444—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom the heterocyclic ring being a six-membered aromatic ring containing one nitrogen atom, e.g. pyridine
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/40—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen or sulfur, e.g. silicon, metals
- C09K19/406—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen or sulfur, e.g. silicon, metals containing silicon
- C09K19/408—Polysiloxanes
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K2019/0477—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by the positioning of substituents on phenylene
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/60—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
- C08G63/605—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds the hydroxy and carboxylic groups being bound to aromatic rings
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/54—Additives having no specific mesophase characterised by their chemical composition
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/02—Liquid crystal materials characterised by optical, electrical or physical properties of the components, in general
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Zentel et al. | Liquid‐crystalline elastomers with cholesteric and chiral smectic C* phases | |
Ballauff et al. | Rigid Rod Polymers Having Flexible Side Chains. 3. Structural Investigations on a Novel Layered Mesophase Formed by Thermotropic Poly (1, 4-phenylene-2, 5-dialkoxy terephthalate) s | |
Zentel et al. | New liquid-crystalline polymers with chiral phases | |
Krigbaum et al. | Thermotropic homopolyesters: 5. Investigation of the smectic phase of polyesters based on p, p′-bibenzoic acid | |
Kapitza et al. | Combined liquid‐crystalline polymers with chiral phases, 2. Lateral substituents | |
JP2001505879A (en) | Polymerizable oligomesogen | |
Piao et al. | Combined type liquid crystalline polymers composed of poly (p-phenylene terephthalate) main chain and azobenzene mesogenic side groups attached through polymethylene spacers | |
Jo et al. | Liquid crystal polymers—VI.: Synthesis and properties of main chain thermotropic polyesters with disiloxane spacers | |
Bualek et al. | Crosslinkable liquid‐crystalline combined main‐chain/side‐group polymers with low glass transition temperatures | |
Chiellini et al. | Chiral liquid crystal polymers: 3. Structurally ordered thermotropic polyesters of optically active propyleneglycol ethers | |
Gresham et al. | Phase behavior of cyclic siloxane‐based liquid crystalline compounds | |
Krigbaum et al. | Thermotropic homopolyesters. III. Preparation and properties of polymers based on 4′‐hydroxyphenyl‐4‐hydroxycinnamate | |
Varshney | Liquid crystalline polymers: A novel state of material | |
Reck et al. | Combined liquid‐crystalline polymers: Rigid‐rod type main‐chain polyester with lateral mesogenic groups | |
Mariani et al. | Polymerization of bisacrylic monomers within a liquid-crystalline smectic B solvent | |
JP4054064B2 (en) | Temperature matching retardation layer | |
Keller | Ferroelectric liquid crystalline side-chain polysiloxanes | |
Navarro | Thermotropic functionalized polyesters with main-chain aromatic ortho-linked units | |
Boileau et al. | Synthesis and properties of liquid crystalline polysiloxanes | |
Kaeding et al. | Investigations of a homologous series of chiral siloxane based dimesogenic compounds | |
Yun et al. | Synthesis and characterization of new chiral side chain liquid crystalline polyoxetanes | |
Zheng et al. | Synthesis and mesomorphic properties of side‐chain cholesteric liquid‐crystalline polysiloxanes | |
Khan et al. | Synthesis and mesophase characterization of liquid crystalline polyesters with bulky, rigid, lateral substituents | |
Bracon et al. | New fluorinated monomers containing an ester function in the spacer, precursors of side chain liquid crystalline polysiloxanes | |
Lee et al. | Ferroelectric liquid crystalline polyoxetanes bearing chiral dimesogenic pendants |