Synthesis of aggregation-induced luminescence material and its synthesis method

A technology for synthesis and luminescence, which is applied in the direction of luminescent materials, compounds of Group 5/15 elements of the periodic table, analytical materials, etc., which can solve the problems of inability to accurately determine, limit effects, and difficulty in detecting low-abundance molecular species in biological systems, etc. question

Active Publication Date: 2018-12-07
THE HONG KONG UNIV OF SCI & TECH
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

When luminophore molecules are dispersed in aqueous media or combined with biomolecules, they tend to aggregate, which usually quenches their fluorescence, thus greatly limiting their usefulness as bioprobes
The ACQ effect can also make it difficult to detect low-abundance molecular species in biological systems, since the fluorescent signal from the smallest number of luminophores matched to the level of the bioanalyte may be too weak to be accurately determined

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
  • Synthesis of aggregation-induced luminescence material and its synthesis method
  • Synthesis of aggregation-induced luminescence material and its synthesis method
  • Synthesis of aggregation-induced luminescence material and its synthesis method

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0207] In addition, the subject matter of the present application also discloses a method for synthesizing TPE derivatives with activated luminophores showing aggregation-induced luminescence, comprising the steps of: (a) adding benzoyl chloride to DBT or DBF; (b) refluxing the reaction mixture to obtain an intermediate compound; (c) subjecting the intermediate compound to a McMurry coupling reaction to obtain a TPE derivative. In some embodiments, the intermediate compound is dibenzo[b,d]thiophen-2-yl(phenyl)methanone or dibenzo[b,d]furan-2-yl(phenyl)methanone. In another embodiment, aluminum chloride or dichloromethane is added to step (a) of the synthesis process of the TPE derivative.

[0208] In one embodiment, when DBT is used in step (a), the E-isomer of STPE is formed in DCM and methanol solution, wherein in step (a) DBT is dissolved in DCM solution, methanol is gradually Dropwise into the solution. In another embodiment, when DBT is used in step (a), the Z-isomer is...

Embodiment

[0300] Preparation of TPE and its derivatives

[0301] Benzophenone, palladium activated carbon (Pd / C), zinc powder, dibenzosubrone and all benzophenone derivatives were purchased from Aldrich and used without further purification. Tetrahydrofuran (THF) was freshly distilled from sodium benzophenone ketyl under nitrogen atmosphere and used immediately.

[0302] Determined on a Bruker AV 300 spectrometer using tetramethylsilane (TMS; δ=0) as internal standard in deuterated chloroform 1 H and 13 C NMR spectrum. Absorption spectra were measured on a Milton Roy Spectronic 3000 array spectrophotometer. Photoluminescence was recorded on a Perkin-Elmer LS 55 spectrofluorometer. High resolution mass spectra (HRMS) were recorded on a GCT premier CAB048 mass spectrometer operated in MALDI-TOF mode. Single crystal X-ray diffraction intensity data were collected at 100K on a Bruker-Nonices SmartApex CCD diffractometer with graphite monochromatized Mo Kα radiation. Intensity data p...

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

PropertyMeasurementUnit
luminanceaaaaaaaaaa
Login to view more

Abstract

This topic concerns the composition and synthesis of fluorescent materials prepared from tetraphenylethylene (TPE) derivatives that exhibit aggregation-induced emission (AIE) properties. Since TPE derivatives have high efficiency, low turn-on voltage, and excellent brightness, the application of TPE derivatives, such as electroluminescent devices, is further considered here. Furthermore, the applications of TPE derivatives showing AIE properties in various fields such as OLEDs, fingerprint and forensic assay techniques, and various other biological and industrial sectors are explored.

Description

[0001] related application [0002] This patent application claims priority to Provisional Patent Application No. 61 / 958,743, filed August 5, 2013 by the inventors of this application, which is hereby incorporated by reference in its entirety. technical field [0003] The subject matter of this application relates to the composition and synthesis of fluorescent materials prepared from tetraphenylethylene (TPE) derivatives exhibiting aggregation-induced emission (AIE) properties. Further considered here are applications of TPE derivatives, such as electroluminescent devices, due to their high efficiency, low turn-on voltage, and excellent brightness. Furthermore, the applications of TPE derivatives showing AIE properties in various fields such as OLEDs, forensics, latent fingerprint detection, and various other biological and industrial sectors are discussed. Background technique [0004] Electroluminescence refers to the energy absorbed by molecules subjected to an electric...

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 Patents(China)
IPC IPC(8): G01N21/64C09B62/343C07D207/448
CPCC07D407/06C07D409/06C09B23/105C09B23/148C09B57/00C09B57/008C07F9/58C07D307/91C07D333/76C09K11/06C09K11/07G01N33/4833H10K85/371H10K85/60H10K85/626H10K85/636H10K85/6574H10K85/6576H10K50/11C07C13/54C07C15/18C09K2211/1007C09K2211/1011C09K2211/1014C09K2211/1029C09K2211/1088C09K2211/1092C09K2211/188
Inventor 唐本忠谢你林荣业
Owner THE HONG KONG UNIV OF SCI & TECH
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap