CN101113200A - Method for preparing backbone chain type liquid crystal elastomer - Google Patents
Method for preparing backbone chain type liquid crystal elastomer Download PDFInfo
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- CN101113200A CN101113200A CNA2007100277936A CN200710027793A CN101113200A CN 101113200 A CN101113200 A CN 101113200A CN A2007100277936 A CNA2007100277936 A CN A2007100277936A CN 200710027793 A CN200710027793 A CN 200710027793A CN 101113200 A CN101113200 A CN 101113200A
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Abstract
The invention provides a preparation method of a backbone liquid crystal elastomer. A prepolymer is made from the silicon hydrogen addition reaction with the materials of diene monomer containing mesogenic units, polysiloxane containing hydrogen and silane coupling agent under the function of catalyst, then the prepolymer is fabricated into a low crosslinked density network structure containing mesogenic units connects through the hydrolysis of siloxane, finally the liquid crystal elastomer is acquired through suitable stretching. The method is characterized by simple operation, being difficult to be gel, and easy control for elastomer crosslinked density, etc.
Description
Technical field
The present invention relates to the elastomeric technology of preparing of backbone chain type liquid crystal, specifically be meant method for preparing backbone chain type liquid crystal elastomer.
Background technology
The world today, Materials science with rapid changepl. never-ending changes and improvements is towards multi-functional and high differently-oriented directivity development, and typical case's representative of this supramolecular system is exactly liquid crystal elastic body (LCE).LCE grows up on the basis of liquid crystalline polymers, and its cross-linking density is low, has the double properties of elastomerics and liquid crystal concurrently.Because of its property such as orientation, ferroelectricity, piezoelectricity and optical nonlinearity under the mechanical force field action, not only can be used to prepare piezoelectric transducer, and can also be applied to fields such as atresia filtering membrane and nonlinear optical material, so, to the molecular designing of liquid crystal elastic body, the research of structure and structure and properties has caused the extensive concern of academia.
According to the position difference of mesomorphic unit in polymer chain, liquid crystal elastic body can be divided into backbone chain type, side chain type and mixed type.Side chain liquid crystalline polymer can synthesize by macromolecular reaction or the vinyl monomer polymerization that contains liquid crystal unit; And the main chain liquid crystal polymer can be synthesized by condensation and polyaddition by the monomer that contains bifunctional; The hybrid type liquid crystal elastomerics all contains crosslinked the obtaining of polymer of liquid crystal unit by main chain and side chain, and its preparation method is the same with the backbone chain type liquid crystal elastomerics.
In general, main chain liquid crystal elastomerics solubleness is low, second-order transition temperature is high, make its synthetic accordingly relative difficulty with the property testing experiment, thereby the report of relevant synthetic aspect is fewer.Mainly contain following two kinds about the elastomeric synthetic method report of backbone chain type liquid crystal at present: (1) is liquid crystal monomer and the aliphatic diacid prepared in reaction that contains diepoxy group with the end chain; (2) will hang down molecule diene class liquid crystal unit and end hydrogen polysiloxanes and 2,4,6, the mixture of 8-tetramethyl cyclotetrasiloxane hydrogen siloxane is by step addition reaction of silicon with hydrogen preparation.Because epoxy group(ing) self becomes ether or become two reactions of ester to vie each other with carboxylic acid, the network structure that makes them form is very complicated.And polysiloxane-based liquid crystal elastic body mainly utilizes addition reaction of silicon with hydrogen to prepare.Adopt 2,4,6 in solution, when 8-tetramethyl cyclotetrasiloxane hydrogen siloxane was made linking agent, content of crosslinking agent higher position slightly easily produced gel.
Summary of the invention
The objective of the invention is to overcome the shortcoming and defect of above-mentioned prior art, provide a kind of simple to operate, be difficult for the backbone chain type liquid crystal elastomer production method that gel, elastomer crosslinked density are easy to control.
Purpose of the present invention is achieved through the following technical solutions: this method for preparing backbone chain type liquid crystal elastomer, and it may further comprise the steps and processing condition:
The first step: the diene class monomer that contains mesomorphic unit of 0.001mol~0.1mol, the hydrogen containing siloxane of 0.0006mol~0.14mol, the silane coupling agent of 0.0004mol~0.08mol and the catalyzer of reactant total mass 0.005%~0.1% are joined in the reaction flask, guarantee that two keys equate with the active hydrogen mole number;
Second step: add 5ml~50ml solvent in reaction flask, solvent can react 5~72 hours under 50~100 ℃ of stirrings for toluene, dioxane or tetrahydrofuran (THF) etc., obtained prepolymer reaction liquid;
The 3rd step: directly pour above-mentioned prepolymer reaction liquid into mould, solvent volatilizees naturally, utilizes airborne moisture to make the siloxanes hydrolytic crosslinking, forms the liquid crystal elastic body crude product of cross-linked network structure, in baking oven, placed 8~30 hours under 60~90 ℃ then, make the siloxanes hydrolytic crosslinking complete;
The 4th step: the liquid crystal elastic body crude product of above-mentioned cross-linked network structure stretched obtains the liquid crystal elastic body finished product.
The diene class monomer that contains mesomorphic unit of the present invention, its mesomorphic unit is in the centre of molecule, and the two ends of molecule are the end capped vinyl monomer of carbon-carbon double bond;
The hydrogen of described hydrogen containing siloxane that is to say that at the two ends of molecule a hydrogeneous polysilane molecule only contains two active hydrogens, and the molecular-weight average of hydrogeneous polysilane is 200~10000.
Described silane coupling agent only contains an active hydrogen or a carbon-carbon double bond, is specially Trimethoxy silane, triethoxyl silane, vinyltrimethoxy silane or vinyltriethoxysilane.
Described catalyzer is a catalyst made from platonic, is specially H
2PtCl
6
In described the 3rd step, also add promotor such as the water of 0.01ml~0.5ml in the reaction solution in the past, make the siloxanes hydrolytic crosslinking, form the liquid crystal elastic body crude product of cross-linked network structure;
In perhaps described the 3rd step, also other silane coupling agents that in the past add 0.1ml~5ml in the reaction solution carry out coupling, form the liquid crystal elastic body crude product of cross-linked network structure, described other silane coupling agents are made up of methyl, alkoxyl group and siloxane groups, do not have other functional groups.
In described the 4th step, described tensile tensile strength is 10
2~10
6Pa, stretching time are 20~100 hours.
In the elastomeric two kinds of synthetic methods of backbone chain type liquid crystal, the network structure that adopts Resins, epoxy to form is very complicated at present.And the polysiloxane-based liquid crystal elastic body of backbone chain type mainly adopts 2,4,6, and when 8-tetramethyl cyclotetrasiloxane hydrogen siloxane was made linking agent, content of crosslinking agent higher position slightly easily produced gel.The present invention compared with prior art has following advantage and beneficial effect: operate fairly simple; Structure is clear and definite, is difficult for gel; Degree of crosslinking is controlled easily.
Embodiment
Below in conjunction with embodiment, the present invention is described in further detail, but embodiments of the present invention are not limited thereto.
Embodiment one
(1) with the hydrogen containing siloxane of two of 10mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 7mmol, the H of the triethoxyl silane of 6mmol and reactant total mass 0.01%
2PtCl
6, join in the 50ml round-bottomed flask;
(2) add 15ml exsiccant toluene in reaction flask, reaction is 10 hours under 100 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) directly pour above-mentioned prepolymer reaction liquid into mould, solvent volatilizees naturally, utilizes airborne moisture to make the siloxanes hydrolytic crosslinking, forms the liquid crystal elastic body crude product of cross-linked network structure, and 80 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 1000Pa, and the time is to obtain the liquid crystal elastic body finished product in 50 hours.
Embodiment two
(1) with the hydrogen containing siloxane of two of 1mmol-(4-allyloxy phenylformic acid) '-biphenyl diphenol ester, 1.2mmol, the H of the vinyltriethoxysilane of 0.4mmol and reactant total mass 0.05%
2PtCl
6Join in the reaction flask;
(2) add 5ml exsiccant dioxane in reaction flask, reaction is 40 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) directly pour above-mentioned prepolymer reaction liquid into mould, solvent volatilizees naturally, utilizes airborne moisture to make the siloxanes hydrolytic crosslinking, forms the liquid crystal elastic body crude product of cross-linked network structure, and 60 ℃ of bakings of a conventional oven 30 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 100Pa, and the time is to obtain the liquid crystal elastic body finished product in 100 hours.
Embodiment three
(1) with 2 of 10mmol, the hydrogen containing siloxane of 5-two-[(4-allyloxy) benzoyloxy] just own ester of phenylformic acid, 6.5mmol, the H of the Trimethoxy silane of 7mmol and reactant total mass 0.005%
2PtCl
6Join in the reaction flask;
(2) add 15ml exsiccant tetrahydrofuran (THF) in reaction flask, reaction is 72 hours under 60 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) directly pour above-mentioned prepolymer reaction liquid into mould, solvent volatilizees naturally, utilizes airborne moisture to make the siloxanes hydrolytic crosslinking, forms the liquid crystal elastic body crude product of cross-linked network structure, and 70 ℃ of bakings of a conventional oven 20 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
4Pa, the time is to obtain the liquid crystal elastic body finished product in 60 hours.
Embodiment four
(1) with the hydrogen containing siloxane of two of 10mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 12.5mmol, the H of the vinyltrimethoxy silane of 5mmol and reactant total mass 0.05%
2PtCl
6, join in the 50ml round-bottomed flask;
(2) add 15ml exsiccant dioxane in reaction flask, reaction is 30 hours under 90 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) directly pour above-mentioned prepolymer reaction liquid into mould, solvent volatilizees naturally, utilizes airborne moisture to make siloxanes hydrolytic crosslinking shape, becomes the liquid crystal elastic body crude product of cross-linked network structure, and 80 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
4Pa, the time is to obtain the liquid crystal elastic body finished product in 60 hours.
Embodiment five
(1) with the hydrogen containing siloxane of two of 100mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 140mmol, the H of the triethoxyl silane of 80mmol and reactant total mass 0.01%
2PtCl
6, join in the 250ml round-bottomed flask;
(2) add 50ml exsiccant toluene in reaction flask, reaction is 50 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) directly pour above-mentioned prepolymer reaction liquid into mould, solvent volatilizees naturally, utilizes airborne moisture to make the siloxanes hydrolytic crosslinking, forms the liquid crystal elastic body crude product of cross-linked network structure, and 90 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
6Pa, the time is to obtain the liquid crystal elastic body finished product in 20 hours.
Embodiment six
(1) with the hydrogen containing siloxane of two of 100mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 70mmol, the H of the triethoxyl silane of 60mmol and reactant total mass 0.01%
2PtCl
6, join in the 250ml round-bottomed flask;
(2) add 50ml exsiccant toluene in reaction flask, reaction is 30 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) directly pour above-mentioned prepolymer reaction liquid into mould, solvent volatilizees naturally, utilizes airborne moisture to make the siloxanes hydrolytic crosslinking, forms the liquid crystal elastic body crude product of cross-linked network structure, and 90 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
5Pa, the time is to obtain the liquid crystal elastic body finished product in 40 hours.
Embodiment seven
(1) with the hydrogen containing siloxane of two of 100mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 70mmol, the H of the triethoxyl silane of 60mmol and reactant total mass 0.01%
2PtCl
6, join in the 250ml round-bottomed flask;
(2) add 50ml exsiccant dioxane in reaction flask, reaction is 30 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) add 0.2mL water in prepolymer reaction liquid, directly pour mould behind the mixing into, solvent volatilizees naturally, the siloxanes hydrolytic crosslinking, and the liquid crystal elastic body crude product of formation cross-linked network structure, 90 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
5Pa, the time is to obtain the liquid crystal elastic body finished product in 40 hours.
Embodiment eight
(1) with the hydrogen containing siloxane of two of 10mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 7mmol, the H of the triethoxyl silane of 60mmol and reactant total mass 0.01%
2PtCl
6, join in the 250ml round-bottomed flask;
(2) add 50ml exsiccant dioxane in reaction flask, reaction is 30 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) in prepolymer reaction liquid, add 0.5mL n-hexyl Trimethoxy silane, directly pour mould behind the mixing into, solvent volatilizees naturally, utilize airborne moisture to make the siloxanes hydrolytic crosslinking, form the liquid crystal elastic body crude product of cross-linked network structure, 90 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
5Pa, the time is to obtain the liquid crystal elastic body finished product in 40 hours.
Embodiment nine
(1) with the hydrogen containing siloxane of two of 100mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 70mmol, the H of the triethoxyl silane of 60mmol and reactant total mass 0.01%
2PtCl
6, join in the 250ml round-bottomed flask;
(2) add 50ml exsiccant dioxane in reaction flask, reaction is 30 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) add 0.01mL water in prepolymer reaction liquid, directly pour mould behind the mixing into, solvent volatilizees naturally, siloxanes hydrolytic crosslinking shape, and the liquid crystal elastic body crude product of one-tenth cross-linked network structure, 90 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
5Pa, the time is to obtain the liquid crystal elastic body finished product in 40 hours.
Embodiment ten
(1) with the hydrogen containing siloxane of two of 100mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 70mmol, the H of the triethoxyl silane of 60mmol and reactant total mass 0.01%
2PtCl
6, join in the 250ml round-bottomed flask;
(2) add 50ml exsiccant dioxane in reaction flask, reaction is 30 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) add 0.5mL water in prepolymer reaction liquid, directly pour mould behind the mixing into, solvent volatilizees naturally, the siloxanes hydrolytic crosslinking, and the liquid crystal elastic body crude product of formation cross-linked network structure, 90 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
5Pa, the time is to obtain the liquid crystal elastic body finished product in 40 hours.
Embodiment 11
(1) with the hydrogen containing siloxane of two of 10mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 7mmol, the H of the triethoxyl silane of 60mmol and reactant total mass 0.01%
2PtCl
6, join in the 250ml round-bottomed flask;
(2) add 50ml exsiccant dioxane in reaction flask, reaction is 30 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) in prepolymer reaction liquid, add 0.1mL n-hexyl Trimethoxy silane, directly pour mould behind the mixing into, solvent volatilizees naturally, utilize airborne moisture to make the siloxanes hydrolytic crosslinking, form the liquid crystal elastic body crude product of cross-linked network structure, 90 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
5Pa, the time is to obtain the liquid crystal elastic body finished product in 40 hours.
Embodiment 12
(1) with the hydrogen containing siloxane of two of 10mmol-(4-allyloxy phenylformic acid) Resorcinol ester, 7mmol, the H of the triethoxyl silane of 60mmol and reactant total mass 0.01%
2PtCl
6, join in the 250ml round-bottomed flask;
(2) add 50ml exsiccant dioxane in reaction flask, reaction is 30 hours under 80 ℃ of induction stirring, obtains prepolymer reaction liquid;
(3) in prepolymer reaction liquid, add 5mL n-hexyl Trimethoxy silane, directly pour mould behind the mixing into, solvent volatilizees naturally, utilize airborne moisture to make the siloxanes hydrolytic crosslinking, form the liquid crystal elastic body crude product of cross-linked network structure, 90 ℃ of bakings of a conventional oven 8 hours make the siloxanes hydrolytic crosslinking complete;
(4) the liquid crystal elastic body crude product is stretched, tensile strength is 10
5Pa, the time is to obtain the liquid crystal elastic body finished product in 40 hours.
As mentioned above, just can realize the present invention preferably.
Claims (9)
1. method for preparing backbone chain type liquid crystal elastomer is characterized in that may further comprise the steps and processing condition:
The first step: the diene class monomer that contains mesomorphic unit of 0.001mol~0.1mol, the hydrogen containing siloxane of 0.0006mol~0.14mol, the silane coupling agent of 0.0004mol~0.08mol and the catalyzer of reactant total mass 0.005%~0.1% are joined in the reaction flask, guarantee that two keys equate with the active hydrogen mole number;
Second step: add 5ml~50ml solvent in reaction flask, solvent is toluene, dioxane or tetrahydrofuran (THF), reacts 5~72 hours under 50~100 ℃ of stirrings, obtains prepolymer reaction liquid;
The 3rd step: directly pour above-mentioned prepolymer reaction liquid into mould, solvent volatilizees naturally, utilizes airborne moisture to make the siloxanes hydrolytic crosslinking, forms the liquid crystal elastic body crude product of cross-linked network structure, in baking oven, placed 8~30 hours under 60~90 ℃ then, make the siloxanes hydrolytic crosslinking complete;
The 4th step: the liquid crystal elastic body crude product of above-mentioned cross-linked network structure stretched obtains the liquid crystal elastic body finished product.
2. according to the described method for preparing backbone chain type liquid crystal elastomer of claim 1, it is characterized in that, the described diene class monomer that contains mesomorphic unit, its mesomorphic unit is in the centre of molecule, and the two ends of molecule are the end capped vinyl monomer of carbon-carbon double bond.
3. according to the described method for preparing backbone chain type liquid crystal elastomer of claim 1, it is characterized in that, the hydrogen of described hydrogen containing siloxane is at the two ends of molecule, and promptly a hydrogeneous polysilane molecule only contains two active hydrogens, and the molecular-weight average of hydrogeneous polysilane is 200~10000.
4. according to the described method for preparing backbone chain type liquid crystal elastomer of claim 1, it is characterized in that, described silane coupling agent only contains an active hydrogen or a carbon-carbon double bond, comprises Trimethoxy silane, triethoxyl silane, vinyltrimethoxy silane or vinyltriethoxysilane.
5. according to the described method for preparing backbone chain type liquid crystal elastomer of claim 1, it is characterized in that described catalyzer is catalyst made from platonic H
2PtCl
6
6. according to the described method for preparing backbone chain type liquid crystal elastomer of claim 1, it is characterized in that in described the 3rd step, described reaction solution adds promotor such as water, makes the siloxanes hydrolytic crosslinking, forms the liquid crystal elastic body crude product of cross-linked network structure.
7. according to the described method for preparing backbone chain type liquid crystal elastomer of claim 1, it is characterized in that in described the 3rd step, described reaction solution adds other silane coupling agents and carries out coupling, forms the liquid crystal elastic body crude product of cross-linked network structure.
8. according to the described method for preparing backbone chain type liquid crystal elastomer of claim 7, it is characterized in that described other silane coupling agents are made up of methyl, alkoxyl group and siloxane groups, do not have other functional groups.
9. according to the described method for preparing backbone chain type liquid crystal elastomer of claim 1, it is characterized in that described tensile tensile strength is 10
2~10
6Pa, stretching time are 20~100 hours.
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CN101939360B (en) * | 2008-02-07 | 2014-06-25 | 新日铁住金化学株式会社 | Silicone resin, process for producing the same, and curable resin composition comprising the same |
CN107365401A (en) * | 2017-06-15 | 2017-11-21 | 东南大学 | A kind of near-infrared response backbone chain type liquid crystal elastomer and preparation method thereof |
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DE3110048A1 (en) * | 1981-03-16 | 1982-09-30 | Consortium für elektrochemische Industrie GmbH, 8000 München | "COMPOSITIONS CONTAINING LIQUID CRYSTALLINE PHASES BASED ON CYCLIC ORGANOPOLYSILOXANS, THEIR PRODUCTION AND THEIR USE" |
JPH0832786B2 (en) * | 1987-05-15 | 1996-03-29 | 東レ・ダウコーニング・シリコーン株式会社 | Method for producing liquid crystalline organopolysiloxane |
JPH0618882B2 (en) * | 1988-10-24 | 1994-03-16 | 信越化学工業株式会社 | Organopolysiloxane compound having liquid crystal phase |
DE19541820A1 (en) * | 1995-11-09 | 1997-05-15 | Consortium Elektrochem Ind | Liquid crystalline organosiloxanes containing chiral dianhydrohexite derivatives |
DE19750628A1 (en) * | 1997-11-14 | 1999-05-20 | Heino Prof Dr Finkelmann | Preparation of a liquid crystal hydrogel |
TW588084B (en) * | 2000-12-27 | 2004-05-21 | Kanegafuchi Chemical Ind | Curing agents, curable compositions, compositions for optical materials, optical materials, optical materials, their production, and liquid crystal displays and LEDs made by using the materials |
JP2007045759A (en) * | 2005-08-10 | 2007-02-22 | Riyuukoku Univ | Liquid crystal polymer and liquid crystal elastomer and mesogen used for production thereof |
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