CN110016110A - A kind of brush block polymer and its synthetic method and application - Google Patents

A kind of brush block polymer and its synthetic method and application Download PDF

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Publication number
CN110016110A
CN110016110A CN201810016123.2A CN201810016123A CN110016110A CN 110016110 A CN110016110 A CN 110016110A CN 201810016123 A CN201810016123 A CN 201810016123A CN 110016110 A CN110016110 A CN 110016110A
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nbpm
brush block
block copolymer
ndm
reaction
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CN110016110B (en
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任丽霞
张同周
袁晓燕
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Tianjin University
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Tianjin University
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F293/00Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
    • C08F293/005Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent

Abstract

The invention discloses a kind of brush block polymer and its synthetic method and applications, the synthetic method of the brush block copolymer, the following steps are included: the norbornene monomer NBPM with biphenyl structural is taken to be dissolved into organic solvent, G-3 catalyst is added, it is stirred to react at 20-40 DEG C, so that monomer NBPM homopolymerization, then the norbornene monomer NDM with decane based structures dissolved is added in above-mentioned reaction solution that the reaction was continued, to realize NBPM, the copolymerization of NDM, terminator quenching reaction is added after the reaction was completed, finally obtain target brush block copolymer PNBPM-b-PNDM.The invention enables photon crystal materials can be applied to optical sensor, light valve and pigment and dyestuff etc., has great practical value.

Description

A kind of brush block polymer and its synthetic method and application
Technical field
The present invention relates to the preparation technical field of brush block copolymer, more particularly to a kind of brush block polymer and Its synthetic method and application.
Background technique
Photonic crystal is because the presence of internal photon forbidden band structure can regulate and control the propagation of light wave, to make it have very big Application value, such as do special pigment, waveguide and reflectance coating.Responsive photonic crystals are that a kind of reflection wavelength can be with Extraneous physics or the material of electrochemical conditions variation and change.This material is in addition to the period necessary to conventional photonic crystals Except property structure, it is necessary to which there are responsiveness groups.It common are two methods and introduce responsiveness group: (1) utilizing responsiveness Material carrys out direct construction photon crystal structure as matrix, such as prepares 1-D photon crystal using block polymer self assembly, Segment swelling is to show the change of reflection wavelength under solvent atmosphere.(2) photon crystal structure is prepared first, then will Responsiveness is material doped into matrix, forms stable photonic crystal composite material.As needed, pass through both the above method It can design and prepare the different Responsive photonic crystals material such as Ph, temperature, chemical solvent, electric field and magnetic field.
Thermo-sensitive photonic crystal is a kind of to study relatively broad Responsive photonic crystals material.From Asher (A.Asher, Et al. Science 1996,274,959.) start sex work since, the similar Thermo-sensitive photonic crystal material of numerous structures Material is reported.Wherein it is more be colloidal crystal is embedded in it is temperature sensitive made from poly(N-isopropylacrylamide) (PNIPAM) Property hydrogel photonic crystal.Because PNIPAM is a kind of thermally sensitive polymeric, with lower critical solution temperature (LCST, about 32 DEG C), when the temperature increases, polymer becomes hydrophobic from hydrophilic, discharge moisture and volume contraction, so that the grain in colloidal crystal Sub- spacing reduces, and leads to reflection wavelength blue shift.When the temperature decreases, and can restore to original state.Although utilizing such method The photon crystal material of preparation has more apparent temperature-responsive sexual behaviour, but process is more complex, and is difficult to prepare big model The photon crystal material enclosed.Because of a kind of simple possible of the invention, inexpensive technology carrys out the one-dimensional photon of preparation temperature responsiveness Crystalline material is particularly important.
A kind of novel brush block copolymer (PNBPM-b-PNDM) of invention, it is molten by simple low boiling point Agent film self assembly has obtained a series of 1-D photon crystal materials, and has apparent temperature-responsive in a heated condition Behavior.Be expected in terms of obtain practical application.
Summary of the invention
In view of the technical drawbacks of the prior art, it is an object of the present invention to provide a kind of brush block polymer and Its synthetic method, the Thermo-sensitive 1-D photon crystal being prepared by simple self assembly mode, is expected in light sensing Practical application is obtained in terms of device, light valve and pigment and dyestuff.
The technical solution adopted to achieve the purpose of the present invention is:
A kind of brush block copolymer of the invention, is denoted as PNBPM-b-PNDM, structural formula are as follows:
Wherein m is the degree of polymerization of NBPM, m=100-1500;N is the degree of polymerization of NDM, n=100-1500;Backbone polymerization Degree is 200-3000;
Wherein: the structural formula of NBPM are as follows:
The structural formula of NDM are as follows:
Preferably, m=n.
Another aspect of the present invention further includes the synthetic method of the brush block copolymer, comprising the following steps:
It takes the norbornene monomer NBPM with biphenyl structural to be dissolved into organic solvent, G-3 catalyst is added, in 20- It is stirred to react at 40 DEG C, so that monomer NBPM homopolymerization, the norbornene monomer with decane based structures that then will have been dissolved NDM's is added in above-mentioned reaction solution that the reaction was continued, to realize the copolymerization of NBPM, NDM, terminator is added after the reaction was completed and quenches It goes out reaction, finally obtains target brush block copolymer PNBPM-b-PNDM.
Preferably, the molar ratio of described G-3, NBPM and NDM are as follows: 1:(100-1500): (100-1500).
Preferably, the molar ratio of described G-3, NBPM and NDM are as follows: 1:(300-800): (300-800).
Another aspect of the present invention further includes that the brush block copolymer is preparing Thermo-sensitive 1-D photon crystal material Application on material.
Preferably, the brush block copolymer passes through self assembly 1-D photon crystal material.
The self assembly object of the brush block copolymer, i.e., the described 1-D photon crystal material have the property that
The degree of polymerization m of the NBPM is the polymerization degree n of 180-220, NDM when being 180-220, the self assembly object heating Preceding is in mulberry, blue after heating, preferably m=200, n=200.
The degree of polymerization m of the NBPM is the polymerization degree n of 280-320, NDM when being 280-320, the self assembly object heating It is preceding blue, it is in bright green, preferably m=300, n=300 after heating.
The degree of polymerization m of the NBPM is the polymerization degree n of 380-420, NDM when being 380-420, and the self assembly object is in green Color takes on a red color, preferably m=400 after heating, n=400.
The degree of polymerization m of the NBPM is the polymerization degree n of 480-520, NDM when being 480-520, the self assembly object heating Before take on a red color, after heating be in taupe, preferably m=500, n=500.
The self-assembling method of the brush block copolymer, comprising the following steps: by the brush block copolymer of synthesis (PNBPM-b-PNDM) it is dispersed in tetrahydrofuran (THF), on the glass sheet by mixed liquor coating, solvent is waved at room temperature Thin polymer film is obtained after hair.
Preferably, the self-assembling method further includes thermal quenching step, specially takes the thin polymer film to be placed in and puts It is placed in flat heater platform, keeps 1-24h under the conditions of 50-300 DEG C.
The self-assembling method of the brush block copolymer can regulate and control the color of polymerizate.
The degree of polymerization m of the NBPM is the polymerization degree n of 180-220, NDM when being 180-220, the self assembly object heating Preceding is in mulberry, blue after heating, preferably m=200, n=200;The degree of polymerization m of the NBPM is the poly- of 280-320, NDM It is blue before the self assembly object heating when right n is 280-320, it is in bright green, preferably m=300, n=300 after heating; The degree of polymerization m of the NBPM is the polymerization degree n of 380-420, NDM when being 380-420, and the self assembly object is in green, after heating It takes on a red color, preferably m=400, n=400;The degree of polymerization m of the NBPM is the polymerization degree n of 480-520, NDM when being 480-520, It takes on a red color before the self assembly object heating, is in taupe, preferably m=500, n=500 after heating.
Compared with prior art, the beneficial effects of the present invention are:
Brush block copolymer of the invention is synthesized by a series of controllable ring-opening metathesis polymerization (ROMP) of activity What method obtained, one-dimensional photonic crystal film is prepared by low boiling point solvent self assembly first, then by heating, Have studied its Thermo-sensitive feature.Reflectance spectrum test shows that being heat-treated back reflection wavelength has more apparent red shift, and reflectivity Decrease to some degree shows it with obvious temperature-responsive.Furthermore we have also obtained backbone polymerization degree and master Linear relationship chart between reflection wavelength preferably combines the relationship between material structure and performance.The invention enables Photon crystal material can be applied to optical sensor, light valve and pigment and dyestuff etc., have great practical value.
Detailed description of the invention
The synthetic line of 1 brush block copolymer (PNBPM-b-PNDM) of Fig. 1 embodiment.
The nuclear magnetic spectrum of 1 brush block copolymer (PNBPM-b-PNDM) of Fig. 2 embodiment.
2 brush block copolymer (PNBPM-b-PNDM) self assembly of Fig. 3 embodiment heat treatment front and back compares picture.
The reflectance spectrum figure of 2 photon crystal film of Fig. 4 embodiment.A1-A6 and B1-B6 respectively represents hot group of BCP1-BCP6 Fill the reflectance spectrum of front and back.
Specific embodiment
The present invention is described in further detail below in conjunction with the drawings and specific embodiments.It should be appreciated that described herein Specific embodiment be only used to explain the present invention, be not intended to limit the present invention.
Embodiment 1
The preparation method of brush block copolymer B CP1-6: its preparation route as shown in Figure 1,
The general structure of BCP1-6 are as follows:
The synthesis step of BCP1 (m=200, n=200) is as follows:
NBPM (57.6mg, 91.2 μm of ol) are added in 10mL polymerization bottle, G-3 is added in 1mL dry methylene chloride (0.41mg, 0.46×10-3Mmol dichloromethane solution 0.1mL) is stirred to react 30 minutes, at normal temperature then by 1.1mL The solution of methylene chloride containing NDM (72.2mg, 91.2 μm of ol) is added in above-mentioned reaction solution that the reaction was continued 1 hour, entirely Charging and reaction process carry out in glove box.1mL vinyl ethyl ether quenching reaction is added after the reaction was completed.Remove gloves Case precipitates in anhydrous methanol, and centrifugation, vacuum drying obtains the brush block copolymer B CP1 that backbone polymerization degree is 400, The degree of polymerization that the degree of polymerization of middle NBPM is 200, NDM is 200.
The synthesis step of BCP2 (m=300, n=300) is as follows:
NBPM (57.6mg, 91.2 μm of ol) are added in 10mL polymerization bottle, G-3 is added in 1mL dry methylene chloride (0.27mg, 0.31×10-3Mmol dichloromethane solution 0.1mL) is stirred to react 30 minutes, at normal temperature then by 1.1mL The solution of methylene chloride containing NDM (72.2mg, 91.2 μm of ol) is added in above-mentioned reaction solution that the reaction was continued 1 hour, entirely Charging and reaction process carry out in glove box.1mL vinyl ethyl ether quenching reaction is added after the reaction was completed.Remove gloves Case precipitates in anhydrous methanol, and centrifugation, vacuum drying obtains the brush block copolymer B CP2 that backbone polymerization degree is 600, The degree of polymerization that the degree of polymerization of middle NBPM is 300, NDM is 300.
The synthesis step of BCP3 (m=400, n=400) is as follows:
NBPM (57.6mg, 91.2 μm of ol) are added in 10mL polymerization bottle, G-3 is added in 1mL dry methylene chloride (0.21mg, 0.23×10-3Mmol dichloromethane solution 0.1mL) is stirred to react 30 minutes, at normal temperature then by 1.1mL The solution of methylene chloride containing NDM (72.2mg, 91.2 μm of ol) is added in above-mentioned reaction solution that the reaction was continued 1 hour, entirely Charging and reaction process carry out in glove box.1mL vinyl ethyl ether quenching reaction is added after the reaction was completed.Remove gloves Case precipitates in anhydrous methanol, and centrifugation, vacuum drying obtains the brush block copolymer B CP3 that backbone polymerization degree is 800, The degree of polymerization that the degree of polymerization of middle NBPM is 400, NDM is 400.
The synthesis step of BCP4 (m=500, n=500) is as follows:
NBPM (57.6mg, 91.2 μm of ol) are added in 10mL polymerization bottle, G-3 is added in 1mL dry methylene chloride (0.16mg, 0.18×10-3Mmol dichloromethane solution 0.1mL) is stirred to react 30 minutes, at normal temperature then by 1.1mL The solution of methylene chloride containing NDM (72.2mg, 91.2 μm of ol) is added in above-mentioned reaction solution that the reaction was continued 1 hour, entirely Charging and reaction process carry out in glove box.1mL vinyl ethyl ether quenching reaction is added after the reaction was completed.Remove gloves Case precipitates in anhydrous methanol, and centrifugation, vacuum drying obtains the brush block copolymer B CP4 that backbone polymerization degree is 1000, The degree of polymerization that the degree of polymerization of middle NBPM is 500, NDM is 500.
The synthesis step of BCP5 (m=700, n=700) is as follows:
NBPM (57.6mg, 91.2 μm of ol) are added in 10mL polymerization bottle, G-3 is added in 1mL dry methylene chloride (0.12mg, 0.13×10-3Mmol dichloromethane solution 0.1mL) is stirred to react 30 minutes, at normal temperature then by 1.1mL The solution of methylene chloride containing NDM (72.2mg, 91.2 μm of ol) is added in above-mentioned reaction solution that the reaction was continued 1 hour, entirely Charging and reaction process carry out in glove box.1mL vinyl ethyl ether quenching reaction is added after the reaction was completed.Remove gloves Case precipitates in anhydrous methanol, and centrifugation, vacuum drying obtains the brush block copolymer B CP5 that backbone polymerization degree is 1400, The degree of polymerization that the degree of polymerization of middle NBPM is 700, NDM is 700.
The synthesis step of BCP6 (m=1000, n=1000) is as follows:
NBPM (57.6mg, 91.2 μm of ol) are added in 10mL polymerization bottle, G-3 (0.082 is added in 1mL dry methylene chloride mg,0.092×10-3Mmol dichloromethane solution 0.1mL) is stirred to react 30 minutes at normal temperature, then contains 1.1mL The solution of the methylene chloride of NDM (72.2mg, 91.2 μm of ol) is added in above-mentioned reaction solution that the reaction was continued 1 hour, entire to feed It is carried out in glove box with reaction process.1mL vinyl ethyl ether quenching reaction is added after the reaction was completed.Glove box is removed, It precipitating, is centrifuged in anhydrous methanol, vacuum drying obtains the brush block copolymer B CP6 that backbone polymerization degree is 2000, wherein The degree of polymerization that the degree of polymerization of NBPM is 1000, NDM is 1000.
It is illustrated in figure 2 the nucleus magnetic hydrogen spectrum figure of block polymer BCP4, it is known that all monomers convert completely, and each Peak can be belonged to well.
Embodiment 2
Synthesized serial brush block copolymer (BCP1-BCP6) solvent volatilization self assembly and heat treatment condition:
The tetrahydrofuran solution that the brush block copolymer (BCP1-BCP6) of synthesis is prepared to 10mg/mL respectively, will mix Drop coating obtains 6 kinds of different thin polymer films after solvent volatilization completely, as in clean horizontal glass on piece to liquid dropwise Manufactured 1-D photon crystal material.Then one-dimensional photonic crystal film obtained is heated under the conditions of 130 DEG C 30min studies its Thermo-sensitive feature.It is illustrated in figure 2 BCP1-BCP6 heat treatment front and back self assembly picture, is shown obvious Light reflex and temperature sensitive sexual behaviour it is obvious.It is in mulberry before the self assembly object heating of BCP1, it is blue after heating;BCP2 Self assembly object heating before it is blue, after heating be in bright green;The self assembly object of BCP3 takes on a red color after heating in green, BCP4 Self assembly object heating before take on a red color, after heating be in taupe.
Fig. 3 is the reflectance spectrum figure of BCP1-BCP6 heat treatment front and back, and heating back reflection wavelength has apparent red shift, reflects Rate decrease to some degree shows that Thermo-sensitive 1-D photon crystal material is succeeded preparation.
The above is only a preferred embodiment of the present invention, it is noted that for the common skill of the art For art personnel, various improvements and modifications may be made without departing from the principle of the present invention, these are improved and profit Decorations also should be regarded as protection scope of the present invention.

Claims (10)

1. a kind of brush block copolymer, which is characterized in that its structural formula are as follows:
Wherein m is the degree of polymerization of NBPM, m=100-1500;N is the degree of polymerization of NDM, n=100-1500;Backbone polymerization degree is 200-3000;
Wherein: the structural formula of NBPM are as follows:
The structural formula of NDM are as follows:
2. a kind of brush block copolymer as described in claim 1, which is characterized in that m=n.
3. a kind of brush block copolymer as described in claim 1, which is characterized in that prepare in accordance with the following methods: taking and have The norbornene monomer NBPM of biphenyl structural is dissolved into organic solvent, and G-3 catalyst is added, is stirred to react at 20-40 DEG C, So that monomer NBPM homopolymerization, then above-mentioned anti-by being added to for the norbornene monomer NDM with decane based structures dissolved It answers in liquid that the reaction was continued, to realize the copolymerization of NBPM, NDM, terminator quenching reaction is added after the reaction was completed, finally obtains target Brush block copolymer (PNBPM-b-PNDM).
4. a kind of brush block copolymer as described in claim 1, which is characterized in that mole of described G-3, NBPM and NDM Than are as follows: 1:(100-1500): (100-1500).
5. a kind of brush block copolymer as claimed in claim 4, which is characterized in that mole of described G-3, NBPM and NDM Than are as follows: 1:(300-800): (300-800).
6. the synthetic method of brush block copolymer as described in claim 1, which comprises the following steps:
It takes the norbornene monomer NBPM with biphenyl structural to be dissolved into organic solvent, G-3 catalyst is added, at 20-40 DEG C Under be stirred to react so that monomer NBPM homopolymerization, then by the norbornene monomer NDM's with decane based structures dissolved plus Enter into above-mentioned reaction solution that the reaction was continued, to realize the copolymerization of NBPM, NDM, terminator quenching reaction is added after the reaction was completed, most Target brush block copolymer (PNBPM-b-PNDM) is obtained eventually.
7. the synthetic method of brush block copolymer as claimed in claim 6, which is characterized in that described G-3, NBPM and NDM Molar ratio are as follows: 1:(100-1500): (100-1500).
8. the synthetic method of brush block copolymer as claimed in claim 7, which is characterized in that described G-3, NBPM and NDM Molar ratio are as follows: 1:(300-800): (300-800).
9. brush block copolymer as described in claim 1 is preparing the application on Thermo-sensitive 1-D photon crystal material.
10. brush block copolymer as claimed in claim 5 is preparing the application on Thermo-sensitive 1-D photon crystal material, Be characterized in that: the brush block copolymer passes through self assembly 1-D photon crystal material.
CN201810016123.2A 2018-01-08 2018-01-08 Brush-shaped block polymer and synthesis method and application thereof Expired - Fee Related CN110016110B (en)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006323319A (en) * 2005-05-20 2006-11-30 Sumitomo Bakelite Co Ltd Optical waveguide structure
JP2009275213A (en) * 2008-04-17 2009-11-26 Riken Technos Corp Thermoplastic elastomer composition
CN104693423A (en) * 2015-02-02 2015-06-10 华东师范大学 Cross-linkable high dielectric norbornene copolymer and norbornene cross-linked polymer and preparation methods thereof
CN107043445A (en) * 2017-05-09 2017-08-15 长春理工大学 A kind of rigid brush block copolymer and synthetic method

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006323319A (en) * 2005-05-20 2006-11-30 Sumitomo Bakelite Co Ltd Optical waveguide structure
JP2009275213A (en) * 2008-04-17 2009-11-26 Riken Technos Corp Thermoplastic elastomer composition
CN104693423A (en) * 2015-02-02 2015-06-10 华东师范大学 Cross-linkable high dielectric norbornene copolymer and norbornene cross-linked polymer and preparation methods thereof
CN107043445A (en) * 2017-05-09 2017-08-15 长春理工大学 A kind of rigid brush block copolymer and synthetic method

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
KIM, DAE-YOON等: "Hierarchical superstructures of norbornene-based polymers depending on dendronized side-chains", 《POLYMER CHEMISTRY》 *
LI, YUKUN等: "Well-Defined Amphiphilic Double-Brush Copolymers and Their Performance as Emulsion Surfactants", 《MACROMOLECULES》 *
王倩等: "以降冰片烯为主链的二联苯甲壳型液晶高分子的设计与合成1", 《2016年两岸三地高分子液晶态与超分子有序结构学术研讨会(暨第十四届全国高分子液晶态与超分子有序结构学术论文报告会)论文集——主题A:液晶高分子的合成与分子设计》 *

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