Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Silane coupling agent with double stimulation response and preparation method and application thereof

A technology of dual stimulus response and silane coupling agent, applied in the field of preparation of silane coupling agent, can solve the problems of cumbersome conditions, complex synthesis, single control method, etc., and achieve the effect of simple modification method and improved hydrophobicity

Inactive Publication Date: 2019-09-06
SOUTH CHINA UNIV OF TECH
View PDF2 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, this method is complicated to synthesize, the conditions are cumbersome, polymerization reaction is required, and the control method is single, which can only be realized by changing the relevant anions.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Silane coupling agent with double stimulation response and preparation method and application thereof
  • Silane coupling agent with double stimulation response and preparation method and application thereof
  • Silane coupling agent with double stimulation response and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044] Under nitrogen protection, add 1g (2.8mmol) 3-hydroxyl, 5-ferrocenehexyloxymethylbenzoate, 1.52g (4.2mmol) hexabromohexyloxyazobenzene, 1.37g to a 150mL three-necked flask (4.2mmol) cesium carbonate, 50mL N, N-dimethylformamide (DMF), warming up to 85 ℃ for reaction, during the reaction, use thin-layer chromatography to determine the reaction process, after 12 hours, the reaction is complete, stop heating, and cool After reaching room temperature, the cesium carbonate was removed by suction filtration, the cesium salt was rinsed with dichloromethane until it was colorless, and the solvent was removed by rotary evaporation under reduced pressure to obtain an orange-yellow crude product. The crude product was dissolved in methyl ethyl ketone, put into the refrigerator to cool and crystallize, and repeated 3 times to obtain 3-ferrocenehexyloxy, 5-azophenylhexyloxymethyl benzoate.

[0045]Under nitrogen protection, add 10mL of anhydrous tetrahydrofuran to a 150mL three-neck...

Embodiment 2

[0055] Under nitrogen protection, add 1g (2.6mmol) 3-hydroxyl, 5-ferrocene octyloxymethyl benzoate, 0.8g (2.6mmol) hexabromooctyloxyazobenzene, 0.54g to a 150mL three-necked flask (3.9mmol) Potassium Carbonate, 50mL N, N-dimethylformamide (DMF), warming up to 85 ° C for reaction, during the reaction, use thin layer chromatography to determine the reaction process, after 12 hours, the reaction is complete, stop heating, and cool After reaching room temperature, potassium carbonate was removed by suction filtration, the potassium salt was rinsed with dichloromethane until it was colorless, and the solvent was removed by rotary evaporation under reduced pressure to obtain an orange-yellow crude product. The crude product was dissolved in methyl ethyl ketone, put into the refrigerator to cool and crystallize, and repeated 3 times to obtain 3-ferrocenyl octyloxy, 5-azobenzyloxybenzoic acid methyl ester.

[0056] Under nitrogen protection, 10 mL of anhydrous tetrahydrofuran was adde...

Embodiment 3

[0062] Under nitrogen protection, add 1g (2.5mmol) 3-hydroxy, 5-ferrocenedecyloxymethylbenzoate, 1.54g (3.75mmol) hexabromodecyloxyazobenzene, 1.22g to a 150mL three-necked flask (3.75mmol) cesium carbonate, 50mL N, N-dimethylformamide (DMF), warming up to 85 ℃ for reaction, during the reaction, use thin layer chromatography to determine the reaction process, after 12 hours, the reaction is complete, stop heating, and cool After reaching room temperature, the cesium carbonate was removed by suction filtration, the cesium salt was rinsed with dichloromethane until it was colorless, and the solvent was removed by rotary evaporation under reduced pressure to obtain an orange-yellow crude product. Dissolve the crude product in butanone, put it in the refrigerator to cool and crystallize, and repeat 3 times to obtain 3-ferrocenyldecyloxy, 5-azophenyldecyloxybenzoic acid methyl ester.

[0063] Under nitrogen protection, 10 mL of anhydrous tetrahydrofuran was added to a 150 mL three-...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a silane coupling agent with double stimulation response and a preparation method and application thereof. The preparation method comprises the following steps that 3-hydroxyl,5-dicyclopentadienyl alkoxy methyl benzoate and bromoalkoxy azobenzene generate 3-dicyclopentadienyl alkoxy,5-azobenzene alkoxy methyl benzoate under base catalysis, and then the 3-dicyclopentadienylalkoxy,5-azobenzene alkoxy methyl benzoate is reduced to a 3-dicyclopentadienyl alkoxy,5-azobenzene alkoxy benzyl alcohol end capping agent; under the protection of nitrogen, the 3-dicyclopentadienylalkoxy,5-azobenzene alkoxy benzyl alcohol, propyl isocyanate triethoxysilane and a catalyst organic tin are added into methylbenzene, the temperature is increased to 80-110 DEG C, and a reaction is carried out to obtain the dicyclopentadienyl azobenzene silane coupling agent. The silane coupling agent can be used for modifying the surface of glass, and the modified glass has the characteristic ofbeing able to be oxidized by ultraviolet light for double stimulation response to change the hydrophilicity of the surface.

Description

technical field [0001] The present invention relates to a preparation method of a silane coupling agent with double stimulus response, in particular to a preparation method of a silane coupling agent modified with ferroceneazobenzene; the silane coupling agent can be used for glass surface modification properties, to prepare glass with controllable surface wettability. Background technique [0002] Silane coupling agent is a kind of organosilicon compound with special structure, which has both reactive groups that can be combined with inorganic materials (such as glass, cement, metal, etc.) and reactive groups that can be combined with organic materials, so it can The surface properties of inorganic substances are changed by silane coupling agents. [0003] The wettability of the solid surface is one of the very important surface properties. Controlling the wettability of the surface is very important in many practical applications. The hydrophobic / hydrophilic reversible ma...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C07F7/18C03C17/30
CPCC03C17/30C07F7/1892
Inventor 任碧野严小龙杜柱康
Owner SOUTH CHINA UNIV OF TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products