9-phenyl-substituted fluorene derivative, and preparation method and application thereof

A technology of phenyl substitution and derivatives, which is applied in the field of organic compound synthesis, can solve the problems of few reports on orange and red phosphorescent materials, and achieve good electroluminescence efficiency, simple synthesis route, and excellent thermal stability

Active Publication Date: 2017-03-22
NANJING UNIV OF POSTS & TELECOMM
View PDF3 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there are few reports on orange and red phosphorescent mate

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
  • 9-phenyl-substituted fluorene derivative, and preparation method and application thereof
  • 9-phenyl-substituted fluorene derivative, and preparation method and application thereof
  • 9-phenyl-substituted fluorene derivative, and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0044] Embodiments of the present invention are further described below in conjunction with the accompanying drawings:

[0045] The present invention designs and synthesizes a class of blue-light host materials with high-efficiency fluorescence emission, the basic structural framework of which is 1,4-bis(9-phenylfluorene)-phenylene, and naphthylaniline as a derivative of functional substituent groups. The molecular structure and configuration of this series of materials were characterized by mass spectrometry (EIMS or TOF), H NMR, C NMR and so on. The photophysical properties of the compounds were studied by UV absorption spectroscopy. The electrochemical properties of the compounds were studied by cyclic voltammetry. The thermodynamic properties of the compounds were studied by differential thermal-differential gravimetric analysis (DTA-TGA).

[0046] 1. The synthetic route is shown in formula 1 below.

[0047] Synthesis of 1,4-bis(9-p-bromophenylfluorene)benzene (DBPFB). ...

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 9-phenyl-substituted fluorene derivative, and a preparation method and an application thereof; the 9-phenyl-substituted fluorene derivative has the following molecular structure defined in the specification. The invention provides a method for simple preparation of a multi-functional organic electroluminescent material; the method is simple in process and low in manufacture cost; through simple solution-method preparation process, high-efficiency green light devices or orange phosphorescent devices can be obtained, and the method is suitable for large-scale industrialized production.

Description

technical field [0001] The invention relates to the field of organic compound synthesis, in particular to a 9-phenyl substituted fluorene derivative, a preparation method and an application thereof. Background technique [0002] Low-energy light sources such as orange and red organic light-emitting diodes (OLEDs) have made great strides in flexible full-color displays, backlighting LCD screens, and next-generation solid-state lighting sources due to their potential applications. (Ying, L.; Ho, C.L.; Wu, H.B.; Cao, Y.; Wong, W.Y. White Polymer Light-Emitting Devices for Solid-State Lighting: Materials, Devices, and Recent Progress. Adv. Mater. 2014, 26, 2459- 2473.) In general, phosphorescent materials are usually dispersed in a suitable host material to avoid triplet annihilation or concentration quenching. (Baldo, M.A.; O'Brien, D.F.; You, Y.; Shoustikov, A.; Sibley, S.; Thompson, M.E.; Forrest, S.R. Highly Efficient Phosphorescent Emission from Organic Electroluminescent ...

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): C07C211/58C07C209/10H01L51/54
Inventor 叶尚辉全梅菡周舟杨敏黄维
Owner NANJING UNIV OF POSTS & TELECOMM
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