Patent classifications
C09B43/00
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.
Dichroic azo-azomethine dyes for liquid crystal compositions
Azo-azomethine dyes, a dichroic dye mixture including azo-azomethine dyes, a liquid crystal composition with the azo-azomethine dyes, and methods for producing the dyes and dye compositions. The dyes can be used in liquid crystal systems, transmissive displays, and smart windows. ##STR00001##
Dichroic pigment compounds and compositions 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; n, m, and p are each independently an integer of 0 to 2; and Ar.sup.1 represents a nitrogen-containing saturated heterocyclic group which is a 5 to 8-membered ring and in which (i) N is bonded to a phenylene group and (ii) at least one -position is an oxygen atom or a sulfur atom.
Dichroic pigment compounds and compositions 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; n, m, and p are each independently an integer of 0 to 2; and Ar.sup.1 represents a nitrogen-containing saturated heterocyclic group which is a 5 to 8-membered ring and in which (i) N is bonded to a phenylene group and (ii) at least one -position is an oxygen atom or a sulfur atom.
COMPOUND AND COMPOSITION CONTAINING 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.
COMPOUND AND COMPOSITION CONTAINING 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; n, m, and p are each independently an integer of 0 to 2; and Ar.sup.1 represents a nitrogen-containing saturated heterocyclic group which is a 5 to 8-membered ring and in which (i) N is bonded to a phenylene group and (ii) at least one -position is an oxygen atom or a sulfur atom.
COMPOUND AND COMPOSITION CONTAINING 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; n, m, and p are each independently an integer of 0 to 2; and Ar.sup.1 represents a nitrogen-containing saturated heterocyclic group which is a 5 to 8-membered ring and in which (i) N is bonded to a phenylene group and (ii) at least one -position is an oxygen atom or a sulfur atom.
Composition comprising hueing agent
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.
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.