CN100387640C - Thermotropic front cholesteric liquid crystal polymer and its preparing method - Google Patents
Thermotropic front cholesteric liquid crystal polymer and its preparing method Download PDFInfo
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- CN100387640C CN100387640C CNB2005100469104A CN200510046910A CN100387640C CN 100387640 C CN100387640 C CN 100387640C CN B2005100469104 A CNB2005100469104 A CN B2005100469104A CN 200510046910 A CN200510046910 A CN 200510046910A CN 100387640 C CN100387640 C CN 100387640C
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Abstract
The present invention relates to a thermotropic front cholesteric liquid crystal polymer which has structural general formulae (1) and (2). A chiral group is arranged in an X primitive which can be a liquid crystal primitive or a non liquid crystal primitive; a Y primitive is a liquid crystal primitive provided with a cholesteric phase, a nematic phase, or a smectic phase; a Z primitive is an ionic primitive, a dye primitive, or a crosslinking structure primitive. A is CH3-, H-, or C2H5-. Under the action of a catalyst, the product preparation adopts graft polymerization, and grafts a monomer onto hydrogen containing siloxane by using one or two methods of solution or melting method polymerization so as to obtain the liquid crystal polymer whose front cholesteric phase width is from 5 DEG C to 360 DEG C, and a liquid crystal polymer network can be obtained through crosslinking treatment. The liquid crystal polymer of the present invention can be used as optical material or colour material of special effects.
Description
Technical field
The invention belongs to technical field of polymer chemistry, particularly thermotropic front cholesteric liquid crystal polymer and preparation method thereof.
Background technology
The present invention has proposed the notion of thermotropic front cholesteric phase first, it is meant that cholesteryl phase is to the phase that exists between the isotropy attitude, its reason be during the present invention finds between this phase region except that having blue phase I, blue phase II and blue III mutually, also exist except that the uncertain phase of indigo plant mutually; Cholesteryl phase comprises mutually blue and uncertain phase promptly, may occur in the wherein preceding cholesteryl phase blue phase or uncertain phase or Lan Xiangzhong exist wherein a kind of, two kinds or three kinds, the definition of therefore preceding cholesteryl phase is more definite, and there is not preceding cholesteryl phase in most cholesteric liquid crystal polymers.The minority cholesteric liquid crystal polymer exists crystallization phases, cholesteryl phase, preceding cholesteryl phase, isotropic phase in proper order with intensification.The present invention has found to exist the liquid crystalline polymers of the preceding cholesteryl phase of broad.
The liquid crystalline polymers and the preparation method that the purpose of this invention is to provide wide preceding cholesteryl phase, preceding cholesteric liquid crystal polymkeric substance has the reflection of selection and selects through performance light, and reflect and see through light and be complementary relationship, also have outstanding optical properties such as circular dichroism, rotatory dispersion, height opticity, can be used for preparing light shielding material, optical switch at optical field; Make anti-fake material in the printing field; Can utilize temperature to raise in addition, polymkeric substance pitch diminishes, and selects reflected light generation blue shift, plays optics and becomes dual effect with temperature, thereby obtain more applications.
For the small molecules cholesteric liquid crystal, crystallization phases, cholesteryl phase, mutually blue and isotropic phase successively appear during intensification, its medium blue comprises blue phase I, blue phase II and the blue phase of III mutually mutually, all there are these complete phases in not all small molecules cholesteric liquid crystal, and the small molecules that has only exists cholesteryl phase, isotropic phase; The small molecules cholesteric liquid crystal that has removes above-mentioned two kinds of phases, also has blue phase I; The small molecules cholesteric liquid crystal that has exists blue phase I, blue phase II and the blue phase of III mutually.But small molecules indigo plant interval mutually is narrower, usually about 1 ℃, and occurs at comparatively high temps, is difficult to have using value.
Mention among the special Open 2003-327966 of Japanese Patent with the blue phase of polymer stabilizing small molecules, make that small molecules indigo plant is mutually interval widely to reach 66 ℃, but temperature range is still narrower, still belongs to the category of the blue phase of small molecules.The report of relevant blue phase liquid crystal polymkeric substance is few up to now, and DNA is a biomacromolecule, and it has very narrow indigo plant interval mutually under finite concentration; In recent years the interval is the wideest mutually is 5 ℃ for the synthetic thermotropic cholest polymkeric substance indigo plant of disclosed report; Smectic polymkeric substance indigo plant interval mutually reaches 11.8 ℃, and these polymkeric substance are blue also narrow mutually and occur at high temperature, and theoretical researching value is only arranged, and have been difficult to actual application value.
Summary of the invention
Problem at available liquid crystal polymkeric substance and technology of preparing existence the invention provides a kind of thermotropic front cholesteric liquid crystal polymer and preparation method thereof.
The preparation of front cholesteric liquid crystal polymer of the present invention is two or more monomer, is grafted on the hydrogen-containing siloxane, under the effect of catalyzer, adopts graft polymerization, prepares with one or both methods in solution or the melting method polymerization.
Polymerization single polymerization monomer comprises nematic liquid crystal monomer, smectic liquid crystal monomer, cholesteric liquid crystal monomer, blue phase monomer, non-liquid crystal chiral monomer, ion monomer, thermochromic dye monomer, linking agent monomer.The monomer that adopts is wherein at least a for monomer and one of them the kind monomer with chirality has liquid crystal unit, or at least a monomer has the chiral liquid crystal primitive.
The initial substance that chiral monomer is provided is one or both in menthol, diosgenin, Isosorbide, left-handed amylalcohol, cholesterol, the ergosterol, and structural formula is as follows respectively:
Ion monomer adopts one or both in azochlorosulfonate acid ion monomer, carboxylic acid ion monomer, the ammonium ion monomer, and they can be liquid crystal ion monomer or non-liquid crystal ion monomer.
The thermochromic dye monomer adopts and to have Victoria Green WPB lactone, anthraquinone ester class, the amino Material of Fluoran that replaces and in the triarylmethane compound one or both.
Select monomer for use by following design, adopt method of the present invention all can obtain the liquid crystalline polymers that the differing temps interval has preceding cholesteryl phase.
The liquid crystal monomer that relates to is below represented to contain the courage steroid liquid crystal of cholesterol or ergosterol and derivative thereof with Ch; N
*Expression does not contain the chiral nematic liquid crystal of cholesterol or ergosterol and derivative thereof; C
*Represent non-liquid crystal chiral monomer; S is that smectic class liquid crystal monomer (comprises chiral smectic class S
*); BP represents blue phase; N represents nematic liquid crystal; D represents dye monomer, can be liquid crystal monomer, also can be non-liquid crystal monomer; I represents to have the ionic monomer, can be liquid crystal monomer, also can be non-liquid crystal monomer.
(1) non-liquid crystal chiral monomer (C
*) and nematic liquid crystal monomer (N) copolymerization, its mole proportioning is C
*: N is 0.1～50%: 99.9～50%, and best proportioning is 1～20%: 99～80%.
(2) non-liquid crystal chiral monomer (C
*) and cholesteric liquid crystal monomer (Ch) copolymerization, its mole proportioning C
*: Ch is 0.1～50%: 99.9～50%, and best proportioning is 1～30%: 99～70%.
(3) non-liquid crystal chiral monomer (C
*) and smectic liquid crystal monomer (S) copolymerization, its mole proportioning C
*: S is 0.1～50%: 99.9～50%, and best proportioning is 1～20%: 99～80%.
(4) the chiral liquid crystal monomer (comprises courage steroid Ch, non-courage steroid N
*With blue BP mutually) and nematic liquid crystal monomer (N) copolymerization, its mole proportioning Ch (N
*, BP): N is 99.9～1%: 0.1～99%, and best proportioning is 99～50%: 1～50%.
(5) the chiral liquid crystal monomer (comprises courage steroid Ch, non-courage steroid N
*With blue BP mutually) and cholesteric liquid crystal monomer (Ch) copolymerization, its mole proportioning Ch (N
*, BP): Ch is 99.9～0.1%: 0.1～99.9%, and best proportioning is 99～60%: 1～40%.
(6) the chiral liquid crystal monomer (comprises courage steroid Ch, non-courage steroid N
*With blue BP mutually) (S comprises S with the smectic liquid crystal monomer
*) copolymerization, its mole proportioning Ch (N
*, BP): S is 1～99%: 99～1%, and best proportioning is 5～50%: 95～50%.
(7) different chiral nematic liquid crystal monomer N
*Between copolymerization, its mole proportioning N
* 1: N
* 2Be 1～99%: 99～1%, best proportioning is 40～60%: 60～40%.
(8) (1)～(7) and dye monomer (D) copolymerization, its mole proportioning is 1: 0.01～40%, best proportioning is 1: 0.05～30%.
(9) (1)～(7) and azochlorosulfonate acid ion (I
SO3 -) monomer or carboxylic acid ion (I
COO -) monomer or ammonium ion (I
NH4 +) monomer copolymerization, proportioning is 1: 0.01～20%, best proportioning is 1: 0.05～10%.
(10) the chiral liquid crystal monomer (comprises courage steroid Ch, non-courage steroid N
*With blue BP mutually) and dye monomer (D) copolymerization, its mole proportioning is 1: 0.01～40%, best proportioning is 1: 0.05～30%.
(11) the chiral liquid crystal monomer (comprises courage steroid Ch, non-courage steroid N
*With blue BP mutually) and azochlorosulfonate acid ion (I
SO3 -) monomer or carboxylic acid ion (I
COO -) monomer or ammonium ion (I
NH4 +) monomer copolymerization, proportioning is 1: 0.01～20%, best proportioning is 1: 0.05～10%.
The hydrogen-containing siloxane (its main chain is as shown in target product) that the present invention adopts, the structure m+n+p of straight chain is 5～50, and the best is 7～35, and wherein the value of m is 5～50, and the value of n is 0～45, the value of p is 0～25; Cyclic structure m+n+p is 4～12, and the best is 5～8, and wherein the value of m is 4～12, and the value of n is 0～8, and the value of p is 0～4.
The preparation method of liquid crystalline polymers of the present invention is: monomer and hydrogen-containing siloxane are dissolved in the solvent, solvent adopts toluene, dimethylbenzene or hexanaphthene, press catalyzer with respect to the per-cent adding 0.05～8% of reactant total mass, under 15～130 ℃ of conditions, react and disappear up to si-h bond, or monomer mixed with hydrogen-containing siloxane, press catalyzer with respect to the per-cent adding 0.05～8% of reactant total mass, under molten state, react and disappear up to si-h bond, product is put into methyl alcohol or ethanol, product after filtration, vacuum-drying obtains polymerization produce crystalline substance.
The composition of one or more in catalyzer employing platinum, antimony, lithium, cobalt and acid or the organic salt that uses in the polymerization process.
Prepared thermotropic front cholesteric liquid crystal polymer is expressed as follows with general formula:
M+n+p is 5～0 in the linear chain structure, and the best is 7～35, and wherein the value of m is 5～50, and the value of n is 0～45, and the value of p is 0～25; M+n+p is 4～12 in the ring texture, and the best is 5～8, and wherein the value of m is 4～12, and the value of n is 0～8, and the value of p is 0～4.
Wherein X, Y, Z are three kinds of different primitives, and the X primitive is the chirality primitive, and when n=0, the X primitive is the chiral liquid crystal primitive, and the chirality composition is provided by one or both of following primitive, can be liquid crystal unit, also can be non-liquid crystal unit.
The Y primitive is the liquid crystal unit with cholesteryl phase or nematic phase or smectic phase or blue phase, and the Z primitive is ion primitive or dyestuff primitive or crosslinking structure primitive.
A can be CH
3-or H-or C
2H
5-.
The preceding courage steroid temperature range of thermotropic front cholesteric liquid crystal polymer can be determined with the method for differential scanning calorimeter (DSC) or polarized light microscopy analysis (POM).In addition, can measure second-order transition temperature (Tg), fusing point (Tm), clearing point (Tc) and the heat decomposition temperature of subject polymer with differential scanning calorimeter in conjunction with thermogravimetric analyzer (TG); Characterize liquid crystal texture and phase structure with polarizing microscope and x-ray diffractometer, Electronic Speculum; Elementary composition with in the elemental analyser characterize polymers is with spectrophotometer (as ultraviolet/visible/near infrared spectrometer) and range estimation sign optical property.
Adopt thermotropic front cholesteric liquid crystal polymer can advance～go on foot preparation thermotropic front cholesteric liquid crystal polymer network.Method is as follows:
1, the liquid crystalline polymers of the preceding cholesteryl phase that obtains with (1)～(11) of transparent crosslinkable thermosetting resin and above-mentioned design is carried out photocuring or thermofixation.
2, (1)～(11) that obtain by design but the liquid crystalline polymers and the preceding cholesteric liquid crystal polymer network of linking agent effect preparation of reactive group are arranged.
The linking agent that adopts comprises non-liquid crystal cross linking agent or liquid crystal cross linking agent: two ends, three ends or the following functional group of four end bands: carboxyl, hydroxyl, two key, triple bond.Linking agent can have ion, as sulfonic group, carboxyl, ammonium, phosphate group etc.Linking agent can have chiral radicals, also can not be with chiral radicals.
3, utilize the crosslinked self-assembly between the ion to form polymer network.
A. the front cholesteric liquid crystal polymer that adopts the band ammonium and carboxyl liquid crystal monomer or non-liquid crystal monomer or liquid crystalline polymers (can for the courage steroid, to be listed as, smectic) self-assembly.
B. the front cholesteric liquid crystal polymer that adopts the band ammonium and sulfonic group liquid crystal monomer or non-liquid crystal monomer or liquid crystalline polymers (can for the courage steroid, to be listed as, smectic) self-assembly.
C. the front cholesteric liquid crystal polymer that adopts the band ammonium with contain halogen family element (fluorine, chlorine, bromine, iodine) liquid crystal monomer or non-liquid crystal monomer or liquid crystalline polymers (can for the courage steroid, to row, smectic) self-assembly.
D. adopt the front cholesteric liquid crystal polymer that has carboxyl and the liquid crystal monomer or non-liquid crystal monomer or the liquid crystalline polymers self-assembly that have ammonium.
E. adopt and have sulfonic front cholesteric liquid crystal polymer and the liquid crystal monomer or non-liquid crystal monomer or the liquid crystalline polymers self-assembly that have ammonium.
F. adopt and have the front cholesteric liquid crystal polymer and the liquid crystal monomer or non-liquid crystal monomer or the liquid crystalline polymers self-assembly that have ammonium that halogen family comprises fluorine, chlorine, bromine, iodine.
4, generate polymer network by liquid crystal monomer and linking agent direct reaction, described in monomer such as design (1)～(7) and (10)～(11).
The thermotropic front cholesteric liquid crystal polymer of the present invention's preparation, preceding cholesteryl phase is wide to reach 5～360 ℃, can utilize its optical property and thermochromic properties to reach application purpose.For example as optical material, comprise, also can be used for preparing pigment, comprise being used to prepare multicolor printing, drawing, false proof, advertisement, clothes pigment as light shielding material, optical switch, polaroid.The thermotropic front cholesteric liquid crystal polymer of the present invention's preparation can obtain the front cholesteric liquid crystal polymer network through crosslinking Treatment, can be used as optical material, comprise as light shielding material, optical switch, can also be used to prepare pigment, comprise being used to prepare multicolor printing, drawing, false proof, advertisement pigment.In addition, thermochromic dye monomer and liquid crystal monomer copolymerization, can prepare the front cholesteric liquid crystal polymer that existing thermochromism has photochromic dual-use function again.
Description of drawings
Fig. 1 is the selection reflection wavelength of thermotropic front cholesteric liquid crystal polymer under different angles.
Fig. 2 is for showing the polarisation photo of thermotropic front cholesteric liquid crystal polymer texture.
Embodiment
Below be the structural formula explanation of all kinds of representatives that relate among the present invention:
(1)C
* 1
R
1Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2-(n=0～8).
(2)C
* 2
R
2Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(3)C
* 3
R
3, R
4Be CH
2=CH (CH
2)
nCO-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2-(n=0～8), CH
3(CH
2)
n-(n=0～10)
(4)C
* 4
R
5Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～-8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8), CH
3(CH
2)
n-(n=0～10)
R
6Be CH
2=CH (CH
2)
nCO-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2-(n=0～8), CH
3(CH
2)
n-(n=0～10)
(5)C
* 5
R
7Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8), CH
3(CH
2)
n-(n=0～10)
(6)N
* 1
R
8Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(7)N
* 2
R
13Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(8) N
* 3Or BP
1
R
9Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
R
10For-(CH
2)
nCOO-(n=0～8) ,-COO (CH
2)
nCH
2O-(n=0～8) ,-(CH
2)
nCH
2O-(n=0～8) ,-O (CH
2)
nCH
2O-(n=0～8) ,-OOC (CH
2)
nCOO-(n=1～8).
(9) N
* 4Or BP
2
R
11Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
R
12For-(CH
2)
nCOO-(n=0～8) ,-COO (CH
2)
nCH
2O-(n=0～8) ,-(CH
2)
nCH
2O-(n=0～8) ,-O (CH
2)
nCH
2O-(n=0～8) ,-OOC (CH
2)
nCOO-(n=1～8).
(10)Ch
1
(11)Ch
2
R
14Be CH
2=CH (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8).
(12)Ch
3
R
15Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(13)Ch
4
R
16Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(14)Ch
5
R
17Be CH
2=CH (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8).
(15)Ch
6
R
18Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(16)N
1
R
19Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
R
20Be CH
3(CH
2)
n-(n=0～10), CH
3(CH
2)
nO-(n=0～10).
(17)N
2
R
21Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
R
22Be CH
3(CH
2)
n-(n=0～1O), CH
3(CH
2)
nO-(n=0～10), or CH
3(CH
2)
nCOO-(n=0～10).
(18)N
3
R
23With R
24Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8), CH
3(CH
2)
n-(n=0～10), CH
3(CH
2)
nO-(n=0～10), or CH
3(CH
2)
nCOO-(n=0～10).
(19)N
4
R
25Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
R
26Be CH
3(CH
2)
n-(n=0～10), CH
3(CH
2)
nO-(n=0～10), or CH
3(CH
2)
nCOO-(n=0～10).
(20)S
1
R
27Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(21)S
2
R
28Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(22)S
3
R
29Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(23)S
4
(24)C
C1
CH
2＝CH(CH
2)
8COO(CH
2)
nOOC(CH
2)
8CH＝CH
2(n＝0～8)
(25)C
C2
CH
2＝CHCOO(CH
2)n?OOCCH＝CH
2(n＝0～8)
(26)C
C3
(27)C
LC1
R
30Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(28)C
LC2
R
31Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(29)C
LC3
R
32Be CH
2=CH (CH
2)
nCOO-(n=0～8), CH
2=CH (CH
2)
nCH
2O-(n=0～8), CH
2=CH (CH
2)
nCH
2-(n=0～8), CH
2=CH CH
2O (CH
2)
nCOO-(n=0～8), or CH
2=CH CH
2O (CH
2)
nCH
2O-(n=0～8).
(30)C
LC4
n＝2，4，6
(31)D
JZ
(32)D
WZ
(33)D
W1
(34)D
W2
(35)D
W3
(36)
I
10 CH
2＝CHCH
2N
+(CH
2CH
3)
3Br
-
Following examples 1～embodiment 15 all can be different monomers graft copolymerization to hydrogen-containing siloxane, and hydrogen-containing siloxane can be a straight chain, also can be ring-type.Because the monomer difference, mol ratio difference, following examples all can obtain the front cholesteric liquid crystal polymer in differing temps interval.In following examples, C
* 1Can be by C
* 2～C
* 5Replace N
1Can be by N
2～N
4Replace Ch
1Can be by Ch
2～Ch
5Replace S
1Can be by S
2～S
3Replace N
* 1Can be by N
* 2～N
* 4Replace BP
1Can be by BP
2Replace D
JZCan be by D
WZ～D
W3Replace C
C1Can be by C
C2～C
C3Replace C
LC1Can be by C
LC2～C
LC4Replace.Following proportioning is mol ratio.
Embodiment 1
Chiral monomer vinylformic acid menthol ester (C
* 1Class) with nematic liquid crystal monomer 4-undecylenic acid-4 '-ethoxybenzoic acid biphenyl ester (N
3Class), mole proportioning C
* 1: N
5The two kinds of monomers and the hydrogen-containing siloxane that are 1: 1 are dissolved in the toluene, and 1 mole of monomer adds 5.0 mmole platinic acid, disappears up to si-h bond 65 ℃ of reactions, and product is put into methyl alcohol, product after filtration, vacuum-drying obtains polymeric articles.Its preceding cholesteryl phase temperature range is 35.3 ℃ to 175.4 ℃.
Embodiment 2
Chiral monomer vinylformic acid menthol ester (C
* 1Class) with cholesteric liquid crystal monomer 2-(hendecene acyloxy)-5-(4-(4-phenetole methanoyl)-4 '-biphenyl oxygen carbonyl methanoyl) Isosorbide (Ch
1Class), mole proportioning C
* 1: Ch
1The two kinds of monomers and the hydrogen-containing siloxane that are 1: 1 are dissolved in the dimethylbenzene, and 1 mole of monomer adds 3.0 mmole platinic acid, disappears up to si-h bond 89 ℃ of reactions, and product is put into methyl alcohol, product after filtration, vacuum-drying obtains polymeric articles.Its preceding cholesteryl phase temperature range is 20.1 ℃ to 138.7 ℃.
Embodiment 3
Chiral monomer vinylformic acid menthol ester (C
* 1Class) with smectic monomer 4-allyloxy benzoyloxy-4 '-different hot acyloxy-biphenyl (S
1Class), mole proportioning C
* 1: S
1The two kinds of monomers and the hydrogen-containing siloxane that are 1: 1 are dissolved in the hexanaphthene, and 1 mole of monomer adds 8.0 mmole platinic acid, disappears up to si-h bond 53 ℃ of reactions, and product is put into methyl alcohol, product after filtration, vacuum-drying obtains polymeric articles.Its preceding cholesteryl phase temperature range is-20.1 ℃ to 148.1 ℃.
Embodiment 4
Cholesteric liquid crystal monomer 2-(hendecene acyloxy)-5-(4-(4-phenetole methanoyl)-4 '-biphenyl oxygen carbonyl methanoyl) Isosorbide (Ch
1Class), with nematic liquid crystal monomer (4-allyloxy) phenylformic acid-4-methoxyl group phenyl ester (N
1Class), proportioning Ch
1: N
1Be 1: 1, the remaining reaction condition is with embodiment 2.Its preceding cholesteryl phase temperature range is 15.1 ℃ to 196.3 ℃.
Embodiment 5
Cholesteric liquid crystal monomer 4-(hendecene acyloxy) cholesterol benzoate (Ch
3Class) with chiral liquid crystal monomer 4-oxygen in Meng acyloxy propionyloxy phenylformic acid-4-hydroxyl-4 '-allyloxy benzoyloxy phenyl ester (BP
2Class), proportioning Ch
1: BP
2Be 1: 1, the remaining reaction condition is with embodiment 1.Its preceding cholesteryl phase temperature range is-40.1 ℃ to 197.8 ℃.
Embodiment 6
Smectic monomer 4-[4-(allyloxy) benzoyloxy-4 '-butyl phenyl ether (S
4Class) with chiral liquid crystal monomer 4-[4-(allyloxy) benzoyloxy]-phenylformic acid-(4-isoamyl alkoxyl group)-phenyl ester (N
* 1Class), proportioning S
4: N
* 1Be 1: 1, the remaining reaction condition is with embodiment 3.Its preceding cholesteryl phase temperature range is 80.1 ℃ to 248.1 ℃.
Embodiment 7
Chiral liquid crystal monomer 4-[4-(allyloxy) benzoyloxy]-phenylformic acid-(4-isoamyl alkoxyl group)-phenyl ester (N
* 1Class) with chiral liquid crystal monomer 4-(4-allyloxy benzoyloxy) benzoyloxy-phenylformic acid isoamyl alcohol ester (N
* 4Class), proportioning N
* 1: N
* 4Be 1: 1, the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 65.7 ℃, and 235.8 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 35.3 ℃ to 175.4 ℃.
Embodiment 8～13, are at embodiment 1～7 described two kinds of monomers and the third monomer copolymerization, are that example specifies proportioning situation, Ch with embodiment 5
1With N
* 1Proportioning is the proportioning among the embodiment 5, with Ch
1+ N
* 1Be 1.Reaction conditions is with embodiment 1.
Embodiment 8
Two kinds of monomers that embodiment 5 adopts and dye monomer D
JZCopolymerization, proportioning are 1: 0.1, and the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 50.1 ℃, and 188.1 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 138.0 ℃.
Embodiment 9:
Two kinds of monomers and non-liquid crystal azochlorosulfonate acid ion monomer I that embodiment 5 adopts
1Copolymerization, proportioning are 1: 0.1, and the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 67.3 ℃, and 195.9 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 128.6 ℃.
Two kinds of monomers that embodiment 5 adopts and liquid crystal azochlorosulfonate acid ion monomer S
7Copolymerization, proportioning are 1: 0.2, and the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 60.1 ℃, and 245.6 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 185.5 ℃.
Embodiment 11
Two kinds of monomers that embodiment 5 adopts and band carboxylic acid liquid crystal monomer I
11Copolymerization, proportioning are 1: 0.2, and the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 64.1 ℃, and 278.5 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 214.3 ℃.
Embodiment 12
The two kinds of monomers that embodiment 5 adopts and the liquid crystal monomer I of ammonium
12Copolymerization, proportioning are 1: 0.2, and the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 35.3 ℃, and 219.4 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 184.1 ℃.
Embodiment 13
The two kinds of monomers that embodiment 5 adopts and the non-liquid crystal monomer I of ammonium
10Copolymerization, proportioning are 1: 0.2, and the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 56.3 ℃, and 186.7 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 130.4 ℃.
Embodiment 14
Chiral liquid crystal monomer 2-(hendecene acyloxy)-5-(4-(4-phenetole methanoyl)-4 '-biphenyl oxygen carbonyl methanoyl) Isosorbide (Ch
1Class) with dye monomer D
JZCopolymerization, proportioning are 1: 0.1, and the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 45.2 ℃, and 161.1 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 115.9 ℃.
Chiral liquid crystal monomer 2-(hendecene acyloxy)-5-(4-(4-phenetole methanoyl)-4 '-biphenyl oxygen carbonyl methanoyl) Isosorbide (Ch
1Class) with liquid crystal azochlorosulfonate acid ion monomer S
7Copolymerization, proportioning are 1: 0.1, and the remaining reaction condition is with embodiment 1.Products therefrom enters preceding cholesteryl phase at 63.1 ℃, and 186.2 ℃ enter the isotropy attitude, and its preceding cholesteryl phase temperature range is 123.1 ℃.
Embodiment 16, are that the method with melt polymerization prepares thermotropic front cholesteric liquid crystal polymer.
Embodiment 16
Chiral monomer allyloxy phenylformic acid Isosorbide dibasic acid esters (C
* 4Class) with nematic liquid crystal monomer 4 '-(4-ethylamino benzonitrile acyl-oxygen base)-4-allyloxy phenol benzoate (N
2Class), mole proportioning C
* 1: Ch
1Two kinds of monomers that are 0.55: 0.45 mix with hydrogen-containing siloxane, and 1 mole of monomer adds 7.0 mmole cobalt naphthenates, disappear up to si-h bond 155 ℃ of reactions, the cooling, product is put into ethanol, product after filtration, vacuum-drying obtains polymeric articles.Its preceding cholesteryl phase temperature range is 70.1 ℃ to 258.7 ℃.
Below (embodiment 17～embodiment 29) be the embodiment of preparation front cholesteric liquid crystal polymer network.
Embodiment 17
Front cholesteric liquid crystal polymer that is obtained by embodiment 1 and Resins, epoxy and acid anhydrides or amine curing agent mix, and are heating and curing between liquid crystal area and promptly obtain the corresponding polymer network, and Resins, epoxy and liquid crystalline polymers weight ratio are 0.1: 1.Its preceding cholesteryl phase temperature range is-70.1 ℃ to 198.1 ℃.
Embodiment 18
The front cholesteric liquid crystal polymer that is obtained by embodiment 2 mixes with methyl methacrylate, and photocuring obtains the corresponding polymer network between liquid crystal area, and methyl methacrylate and liquid crystalline polymers weight ratio are 0.15: 1.Its preceding cholesteryl phase temperature range is-90.3 ℃ to 161.4 ℃.
Embodiment 19
Two kinds of monomers that embodiment 4 adopts and the copolymerization of 4-allyloxy phenylformic acid Resorcinol monoesters, proportioning is 1: 0.2, the remaining reaction condition is with embodiment 2, front cholesteric liquid crystal polymer that obtains and linking agent 2,4-dicyano toluene is dissolved in the toluene with proportioning at 1: 0.5,80 ℃ were reacted product vacuum-drying 24 hours.Its preceding cholesteryl phase temperature range is 3.5 ℃ to 147.8 ℃.
Embodiment 20
Have sulfonic front cholesteric liquid crystal polymer and 4,4 '-formic acid biphenyl ester pyridinium bromide (I by what embodiment 9 obtained
13) carry out self-assembly and obtain polymer network, be that two kinds of materials of 1: 0.5 are dissolved in the dimethylbenzene with mol ratio, 96 ℃ of reactions 24 hours, product vacuum-drying.Its preceding cholesteryl phase temperature range is 10.1 ℃ to 192.1 ℃.
Embodiment 21～24, are embodiment 1,3,5,7 and 14 monomer that is adopted and linking agent copolymerization, and direct reaction generates the front cholesteric liquid crystal polymer network.
Embodiment 21
Two kinds of monomers that embodiment 1 adopts and linking agent pair-vinylformic acid butanediol ester (C
C2Class) copolymerization, the proportioning of monomer and linking agent are 1: 0.1, and the remaining reaction condition is with embodiment 1.Its preceding cholesteryl phase temperature range is-30.1 ℃ to 168.7 ℃.
Embodiment 22
Two kinds of monomers that embodiment 3 adopts and linking agent pair-undecylenic acid butanediol ester (C
C1Class) copolymerization, the proportioning of monomer and linking agent are 1: 0.1, and the remaining reaction condition is with embodiment 1.Its preceding cholesteryl phase temperature range is-90.1 ℃ to 128.7 ℃.
Embodiment 23
Two kinds of monomers that embodiment 5 adopts and nematic liquid crystal linking agent pair-4-(4-hendecene acyloxy) phenylformic acid Resorcinol dibasic acid esters (C
LC2Class) copolymerization, the proportioning of monomer and linking agent are 1: 0.1, and the remaining reaction condition is with embodiment 1.Its preceding cholesteryl phase temperature range is-25.6 ℃ to 217.7 ℃.
Embodiment 24
Two kinds of monomers that embodiment 14 adopts and cholesteric liquid crystal linking agent pair-4-(6-acryloxy hexyloxy) the different sorbic alcohol dibasic acid esters of phenylformic acid (C
LC3) copolymerization, the proportioning of monomer and linking agent is 1: 0.1, the remaining reaction condition is with embodiment 1.Its preceding cholesteryl phase temperature range is-16.1 ℃ to 216.6 ℃.
Claims (5)
1. thermotropic front cholesteric liquid crystal polymer, its main chain comprises linear chain structure and ring texture, general structure is respectively
M+n+p is 5～50 in the linear chain structure, and wherein the value of m is 5～50, and the value of n is 0～45, and the value of p is 0～25, and m+n+p is 4～12 in the ring texture, and wherein the value of m is 4～12, and the value of n is 0～8, and the value of p is 0～4;
Wherein the X primitive is the chirality primitive, and when n=0, the X primitive is the chiral liquid crystal primitive, and the chirality composition is provided by one or both of following primitive,
The Y primitive is the liquid crystal unit with cholesteryl phase or nematic phase or smectic phase or blue phase, and the Z primitive is ion primitive or dyestuff primitive or crosslinking structure primitive, and A is CH
3-or H-or C
2H
5-.
2. the preparation method of the described thermotropic front cholesteric liquid crystal polymer of claim 1, it is characterized in that: monomer and hydrogen-containing siloxane are dissolved in the solvent, add catalyzer, under 15～130 ℃ of conditions, react and disappear up to si-h bond, or monomer mixed with hydrogen-containing siloxane, add catalyzer, under molten state, react and disappear up to si-h bond, product is put into methyl alcohol or ethanol, product after filtration, vacuum-drying, obtain polymeric articles, described monomer comprises the nematic liquid crystal monomer, the smectic liquid crystal monomer, the cholesteric liquid crystal monomer, blue phase monomer, non-liquid crystal chiral monomer, ion monomer, the thermochromic dye monomer, the linking agent monomer, the monomer of employing is wherein at least a for monomer and one of them the kind monomer with chirality has liquid crystal unit, or at least a monomer has the chiral liquid crystal primitive; The initial substance that chiral monomer is provided is one or both in menthol, diosgenin, Isosorbide, left-handed amylalcohol, cholesterol, the ergosterol, and structural formula is as follows respectively:
The menthol diosgenin
The left-handed amylalcohol of Isosorbide
The cholesterol ergosterol
Ion monomer adopts one or both in azochlorosulfonate acid ion monomer, carboxylic acid ion monomer, the ammonium ion monomer, the thermochromic dye monomer adopts and to have Victoria Green WPB lactone, anthraquinone ester class, the amino Material of Fluoran that replaces and in the triarylmethane compound one or both, the linking agent monomer adopts non-liquid crystal cross linking agent or liquid crystal cross linking agent, its two ends, three ends or four end band carboxyls, hydroxyl, two key or triple bond functional group.
3. according to the preparation method of the described thermotropic front cholesteric liquid crystal polymer of claim 2, it is characterized in that solvent adopts toluene, dimethylbenzene or hexanaphthene, the composition of one or more in catalyzer employing platinum, antimony, lithium, cobalt and acid or the organic salt, the catalyzer add-on is 0.05～8% of a reactant total mass.
4. the application of the described thermotropic front cholesteric liquid crystal polymer of claim 1 is characterized in that as optical material.
5. the application of the described thermotropic front cholesteric liquid crystal polymer of claim 1 is characterized in that being used to prepare pigment.
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| CN102453037B (en) * | 2010-10-25 | 2014-06-25 | 财团法人工业技术研究院 | Isosorbitol derivative and liquid crystal display containing same |
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| CN103224626B (en) * | 2013-04-08 | 2015-05-20 | 东北大学 | Metal complex liquid crystal polymer and preparation method thereof |
| CN103409144B (en) * | 2013-08-16 | 2014-11-26 | 东北大学 | Steroid-element-containing cyclic carbonate active liquid crystal monomer and preparation method thereof |
| JPWO2019039092A1 (en) * | 2017-08-22 | 2020-09-17 | Jnc株式会社 | Liquid crystal compositions, liquid crystal display elements, and use of liquid crystal compositions in liquid crystal display elements |
| CN110358549B (en) * | 2018-03-26 | 2020-10-30 | 中国科学院理化技术研究所 | Blue phase liquid crystal composite material |
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| CN111087623B (en) * | 2019-12-30 | 2021-12-03 | 西安工业大学 | Polysiloxane side chain liquid crystal polymer with smectic phase and application thereof |
| CN112142770B (en) * | 2020-09-03 | 2021-03-19 | 徐州工程学院 | Janus oligomer with full-spectrum selective reflection and photoluminescence and preparation method thereof |
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