Organic three-order nonlinear optical material 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate and synthesizing method thereof

A technology of methylpyridine trifluorosulfonate and dimethylaminostyrene, which is applied in nonlinear optics, organic chemistry, sulfonate preparation, etc., can solve the complicated preparation process, long response time, limited research progress and other problems. Practical application, etc.

Active Publication Date: 2012-07-11
FUJIAN INST OF RES ON THE STRUCTURE OF MATTER CHINESE ACAD OF SCI
View PDF4 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the nonlinear effect of inorganic materials mainly originates from the lattice distortion and resonance absorption of the material, and the response time is often relatively long, which is far from meeting the development requirements of modern optical communication technology.
In addition, inorganic materials have disadvantages such as cumbersome preparation process, few types to choose from, and easy deliquescence, which greatly limit their research progress and practical application.

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
  • Organic three-order nonlinear optical material 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate and synthesizing method thereof
  • Organic three-order nonlinear optical material 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate and synthesizing method thereof
  • Organic three-order nonlinear optical material 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate and synthesizing method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment example 1

[0021] Implementation Case 1 Synthesis of 4-(4-dimethylaminostyryl)picoline iodide

[0022] Dissolve 0.01 mol of 4-methylpyridine, 0.01 mol of methyl iodide and 0.01 mol of 4-dimethylaminobenzaldehyde in 100-150 mL of methanol, stir and slowly raise the temperature to 65-70°C, add 3-5 mL of piperidine as The catalyst was refluxed for 10-12 hours, and the color of the solution gradually changed from light yellow to dark red. After the solution was cooled and crystallized, filtered and dried, 4-(4-dimethylaminostyryl)picoline iodide was obtained , and the yield was 84.2%.

[0023]

[0024] According to Example 1: 0.02 mol of 4-picoline, 0.02 mol of methyl iodide and 0.02 mol of 4-dimethylaminobenzaldehyde were dissolved in 100-150 mL of methanol, stirred and slowly heated to 65-70°C and refluxed for 48 h, the color of the solution gradually changed from light yellow to dark red. After the solution was crystallized by cooling, filtered and dried, 4-(4-dimethylaminostyryl)pic...

Embodiment example 2

[0026] Implementation Case 2 Synthesis of 4-(4-Dimethylaminostyryl)methylpyridine trifluorosulfonate

[0027] Under the condition of 50°C, react 0.01 mol 4-(4-dimethylaminostyryl)picoline iodide with 0.01-0.012 mol silver trifluorosulfonate in 50-75 mL methanol for about 2 h, filter After the precipitate was removed, the solution was allowed to stand and cooled to crystallize to obtain red needle-like or massive 4-(4-dimethylaminostyryl)picoline trifluorosulfonate crystals with a yield of 90.4%.

[0028] At room temperature, react 0.01 mol 4-(4-dimethylaminostyryl)picoline iodide with 0.01-0.012 mol silver trifluorosulfonate in 50-75 mL methanol for about 2 h, remove the precipitate by filtration, After the solution was allowed to stand and the solvent was slowly evaporated, red blocky 4-(4-dimethylaminostyryl)picoline trifluorosulfonate crystals were obtained with a yield of 84.7%.

[0029] At 50°C, 0.01 mol of 4-(4-dimethylaminostyryl)picoline iodide was dissolved in 75 m...

Embodiment example 3

[0030] Implementation Case 3 The third-order nonlinear optical properties of 4-(4-dimethylaminostyryl)picoline trifluorosulfonate

[0031](1) Absorption spectrum of 4-(4-dimethylaminostyryl)picoline trifluorosulfonate

[0032] The 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate prepared in the above examples was formulated into 2×10 -5 mol / L acetone solution, measure its absorption spectrum in the range of 350-800 nm.

[0033] The 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate prepared in the above examples was formulated into 2×10 -5 mol / L methanol solution, and measure its absorption spectrum in the range of 350-800 nm.

[0034] The 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate prepared in the above examples was formulated into 2×10 -5 mol / L ethanol solution, and measure its absorption spectrum in the range of 350-800 nm.

[0035] The 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate prepared in the above examples was...

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 relates to an organic three-order nonlinear optical material 4-(4-dimethylaminostyryl) methylpyridine trifluorosulfonate and a synthesizing method thereof, and belongs to the field of functional materials. The chemical formula of the material is C17H19N2O3F3S, the material belongs to a monoclinic system at room temperature, the space group of the material is P21 / C, and the cell parameters comprise that a is 17.508 (5), b is 7.607 (2), c is 13.533 (4) A, alpha is 90.0 degrees, beta is 93.712 (6) degrees, gamma is 90.0 degrees Z is 4, V is 1,798.4 (10) A <3>. The three-order nonlinear optical material has good thermal stability, high nonlinear absorption effect and self-defocusing property; and raw materials adopted in the preparation process are easily obtained, the chemical synthesis route is simple, the reaction conditions are mild, and the method has potential implementation value.

Description

[0001] technical field [0002] The invention belongs to the field of functional materials, and in particular relates to a synthesis method of 4-(4-dimethylaminostyryl)picoline trifluorosulfonate and an application as an organic third-order nonlinear optical material. Background technique [0003] Optical fiber communication technology is an important way to meet the requirements of ultra-large capacity information collection, processing, transmission, storage and display. However, there are a large number of electronic devices used for signal switching and processing in existing optical fiber communication systems. Due to the disadvantages of clock skew, serious crosstalk, high loss, and slow response, these devices have become the "limitation point" that limits the improvement of information carrying capacity. bottleneck". Using third-order nonlinear optical materials to prepare optical components such as all-optical switches, optical computing, optical cross-connectors, ...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C07D213/38C07C309/06C07C303/32G02F1/361
Inventor 罗军华孙志华陈天亮洪茂椿
Owner FUJIAN INST OF RES ON THE STRUCTURE OF MATTER CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products