Unlock instant, AI-driven research and patent intelligence for your innovation.

Compound and composition

A compound and composition technology, applied in the field of compounds and compositions, can solve the problems of low dichroic ratio of polarizing films and the like

Inactive Publication Date: 2017-08-18
SUMITOMO CHEM CO LTD
View PDF9 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the dichroic ratio of the polarizing film containing the disazo dye is low

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
  • Compound and composition
  • Compound and composition
  • Compound and composition

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0307]

[0308] 0.30 g of the compound represented by the formula (2A), 0.48 g of triethylamine, 0.023 g of N,N-dimethylaminopyridine, and 3.0 g of tetrahydrofuran were mixed. After cooling the obtained mixture to 0°C, 0.39 g of the compound represented by the formula (3A) was added dropwise. The resulting mixture was stirred at 25°C for 18 hours. The obtained reaction mixture was concentrated, washed with ethyl acetate and water, and filtered. The obtained solid was washed with acetonitrile and then dried to obtain 0.129 g of a compound represented by formula (1A) (hereinafter referred to as compound (IA)) as an orange solid.

[0309] Mw: 489 (LC-MS)

[0310] Maximum Absorption Wavelength (λ max2 )=441nm (chloroform solution)

Embodiment 2

[0312]

[0313] 0.30 g of the compound represented by the formula (2B), 0.41 g of triethylamine, 0.020 g of N,N-dimethylaminopyridine, and 4.5 g of tetrahydrofuran were mixed. After cooling the obtained mixture to 0° C., 0.21 g of the compound represented by the formula (3A) was added dropwise. The resulting mixture was stirred at 25°C for 18 hours. The obtained reaction mixture was concentrated, washed with ethyl acetate and water, and filtered. The obtained solid was washed with acetonitrile and then dried to obtain 0.189 g of a compound represented by the formula (1B) (hereinafter referred to as compound (IB)) as an orange solid.

[0314] Mw: 544 (LC-MS)

[0315] Maximum Absorption Wavelength (λ max2 )=430nm (chloroform solution)

[0316] [Polymerizable liquid crystal compound]

[0317] The polymerizable liquid crystal compound used is a compound represented by the following formula (4-6) [hereinafter referred to as compound (4-6)], a compound represented by the fol...

Embodiment 3

[0338] [Preparation of composition]

[0339] Composition (1) was obtained by mixing the following components and stirring at 80 degreeC for 1 hour.

[0340] Polymerizable liquid crystal compound: 75 parts of compound (4-6)

[0341] Compound (4-8) 25 parts

[0342] Compound (1): Compound (1A) 2.5 parts

[0343] Polymerization Initiator:

[0344] 6 parts of 2-dimethylamino-2-benzyl-1-(4-morpholinophenyl)butan-1-one (IRGACURE369; manufactured by Ciba Specialty Chemicals)

[0345] Leveling agent:

[0346] Polyacrylate compound (BYK-361N; manufactured by BYK-Chemie)

[0347] 1.5 servings

[0348] Solvent: 250 parts of chloroform

[0349] [Measurement of Phase Transition Temperature]

[0350] In the same manner as compound (4-6), the phase transition temperatures of the components contained in composition (1) were determined. After the temperature is raised to 140°C, the composition transforms into a nematic phase at 115°C, a smectic A phase at 105°C, and a smectic B phase ...

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
wavelengthaaaaaaaaaa
thicknessaaaaaaaaaa
widthaaaaaaaaaa
Login to View More

Abstract

The present invention provides a compound that has a maximum absorption in a wavelength range of 350-550 nm and functions as a dichroic pigment. Provided is a compound represented by formula (1): [In the formula, R1 represents a hydrogen atom or the like, R2 a hydrogen atom or the like, R3 a hydrogen atom or the like, Z -CO- or the like, and Y a group represented by formula (Y1): (In the formula, * represents a site of bonding with N.) or a group represented by formula (Y2): (In the formula, * represents a site of bonding with N, P1 and P2 each independently represent -S- or the like, and Q1 and Q2 each independently represent =N- or the like.)]

Description

technical field [0001] The present invention relates to compounds and compositions. Background technique [0002] Patent Document 1 describes a polarizing film comprising a dichroic light-absorbing compound (dichroic dye) dispersed in an aligned polymerizable liquid crystal compound. However, there is no description of a dichroic dye having an absorption maximum at a wavelength of 350 to 550 nm. [0003] Patent Document 2 describes a disazo dye having a 1,4-naphthyl structure as a dichroic dye having an absorption maximum at a wavelength of 350 to 550 nm. However, the dichroic ratio of the polarizing film containing this disazo dye is low. [0004] prior art literature [0005] patent documents [0006] Patent Document 1: Japanese National Publication No. 2007-510946 [0007] Patent Document 2: Japanese Patent No. 1454637 Contents of the invention [0008] The problem to be solved by the invention [0009] A compound that functions as a dichroic dye and has an absor...

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): C07D513/04C09K19/20C09K19/30C09K19/38C09K19/60G02B5/30G02F1/1335G09F9/00H01L51/50H05B33/02
CPCC07D513/04C09K19/20C09K19/60G09F9/00C09K19/2014C09K19/3068C09K19/3852G02F1/13475G02B5/3033C09K2019/0448G02F2202/043C09B43/32C09K19/601G02B5/3016G02F1/133528H10K59/8791C09K19/02G02B5/30G02F1/1335H05B33/02H10K50/00H10K50/86C09B56/00C09K19/3809G02B5/3083
Inventor 飞田宪之大川春树
Owner SUMITOMO CHEM CO LTD