C09B43/00

DICHROIC DYE COMPOUND, POLARIZING FILM, AND USES THEREOF
20170226071 · 2017-08-10 ·

A compound having a maximum absorption in a wavelength range of 350 nm to 550 nm that functions as a dichroic dye is provided. In particular, a compound represented by formula (1) is provided. In the compound of formula (1), R.sup.1 represents an alkyl group having 1 to 20 carbon atoms or the like; R.sup.2 represents an acyl group having 1 to 20 carbon atoms or the like; R.sup.3 represents a hydrogen atom or the like; and Y represents a group of formula (Y1). In the formula (Y1), * represents a bonding site with N, or a group of formula (Y2). In the formula (Y2), * represents a bonding site with N; P.sup.1 and P.sup.2 each independently represent —S— or the like; and Q.sup.1 and Q.sup.2 each independently represent ═N— or the like.

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DICHROIC AZO-AZOMETHINE DYES FOR LIQUID CRYSTAL COMPOSITIONS

Dichroic azo-azomethine dyes of formula (A) or (B), wherein Ar.sup.1 to Ar.sup.10 are specific (hetero)aromatic moieties and L is a linking group, as defined in the present claims, a dichroic dye mixture comprising said azo-azomethine dyes and a process for preparing the dyes are provided. The dyes are well suited for combination with liquid crystal material for use, inter alia, in a light absorption anisotropic element, for example, in a switchable optical device or an optically anisotropic film.

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Composition Comprising Hueing Agent
20210269747 · 2021-09-02 ·

This invention relates to a laundry care composition comprising a laundry care ingredient and a polymeric thiophene hueing agent.

Composition Comprising Hueing Agent
20210277335 · 2021-09-09 ·

This invention relates to a laundry care composition comprising a laundry care ingredient and a polymeric thiophene hueing agent.

Composition Comprising Hueing Agent
20230407207 · 2023-12-21 ·

This invention relates to a laundry care composition comprising a laundry care ingredient and a polymeric thiophene hueing agent.

Dichroic azo compound and composition containing the same

A compound serving as a dichroic pigment which has a maximum absorption wavelength in a range of 350 nm to 510 nm is represented by the following Formula (1): ##STR00001##
In Formula (1), R.sup.1 represents a hydrogen atom or a C1-C20 alkyl group; R.sup.2 through R.sup.4 are substituents which are not hydrogen atoms and each independently represent a C1-C4 alkyl group; m, p, and q are each independently an integer of 0 to 2; and R.sup.5 is (i) a C1-C10 alkyl group in which a hydrogen atom is substituted by at least one hydroxy group or (ii) a C1-C10 alkyl group which has carbon atoms and in which at least one O is inserted between the carbon atoms.

Dichroic azo compound and composition containing the same

A compound serving as a dichroic pigment which has a maximum absorption wavelength in a range of 350 nm to 510 nm is represented by the following Formula (1): ##STR00001##
In Formula (1), R.sup.1 represents a hydrogen atom or a C1-C20 alkyl group; R.sup.2 through R.sup.4 are substituents which are not hydrogen atoms and each independently represent a C1-C4 alkyl group; m, p, and q are each independently an integer of 0 to 2; and R.sup.5 is (i) a C1-C10 alkyl group in which a hydrogen atom is substituted by at least one hydroxy group or (ii) a C1-C10 alkyl group which has carbon atoms and in which at least one O is inserted between the carbon atoms.

Composition comprising hueing agent

This invention relates to a laundry care composition comprising a laundry care ingredient and a polymeric thiophene hueing agent.

Composition Comprising Hueing Agent
20240301330 · 2024-09-12 ·

This invention relates to a laundry care composition comprising a laundry care ingredient and a polymeric thiophene hueing agent.

Water-soluble triazabutadienes

Water-soluble triazabutadiene molecules and methods for producing and using such compounds. The triazabutadiene molecules may be more labile at pH levels below physiological pH, such as pH 7, pH 6, pH 5, etc. The triazabutadiene molecules and compounds may be used for depositing diazonium salt and/or cargo in a pH-sensitive manner. The triazabutadiene molecules may alternatively be cleaved in reducing conditions or as a light-catalyzed reaction. The compounds herein may be used for delivery of drugs, as part of detection systems, or for other applications such as underwater adhesive applications.