A water-based ink for ink-jet recording includes dyes and water. The dyes include a blue dye having a hue angle of 220° to 280°; a yellow dye having a hue angle of 70° to 120°; and a copper phthalocyanine dye. A mass ratio (C/B) of a content (C) of the copper phthalocyanine dye to a content (B) of the blue dye in an entire amount of the water-based ink is equal to or more than 0.5, and a total content of the dyes in the entire amount of the water-based ink is equal to or more than 6% by mass.

The present disclosure provides a nano dye molecule, a color filter, and a display panel. The nano dye molecule comprises a gold nanocluster and a plurality of dye groups which are connected to the gold nanocluster by gold-sulfur bonds and cover an outer periphery of the gold nanocluster.

The present application relates to exocyclic amine-substituted coumarin derivatives and their uses as fluorescent labels. These compounds may be used as fluorescent labels for nucleotides in nucleic acid sequencing applications.

The present disclosure provides a nano dye molecule, a color filter, and a display panel. The nano dye molecule comprises a gold nanocluster and a plurality of dye groups which are connected to the gold nanocluster by gold-sulfur bonds and cover an outer periphery of the gold nanocluster.

The present invention provides a plastic article containing suspended photochromic dye molecules, and the said suspended photochromic dye molecules suspended in liquid micro-droplets of a suspension medium, and the said micro-droplets of the said suspension medium containing the said suspended photochromic dye molecules are embedded inside a solid polymer matrix, and the said solid polymer matrix is formed by polymerization of liquid polymer precursors. The invented structure of a plastic article containing suspended photochromic dye molecules exhibits fast response time and enhances photochromic performance.

The azomethine compound provided by this case is a compound showing high chroma and having excellent light resistance.

The present invention relates to dissymmetric azomethine direct dyes of formula (I) and the leuco forms thereof of formula (II), and also to the use thereof for dyeing keratin fibres, in particular human keratin fibres such as the hair: ##STR00001##
in which formula (I) or (II) R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, n and n are as defined in the description. The compounds of formula (I) or (II) according to the invention can give powerful, chromatic and sparingly selective colourings with good colour build-up, which are resistant to the various attacking factors to which keratin fibres may be subjected, such as inclement weather, light, washing and perspiration.

Provided are any one of the following fluorescent compounds and a fluorescent labeled biological substance having this fluorescent compound.

##STR00001##

X represents CR.sup.5 or N, and R.sup.1 to R.sup.7, Q.sup.1, Q.sup.2, L.sup.1, and L.sup.2 each represent a specific group.

a ring .sub.1 and a ring .sub.2 are a 5- to 8-membered ring,

At least one of R.sup.1 to R.sup.7, L.sup.1, L.sup.2, Q.sup.1, or Q.sup.2 has a specific hydrophilic group.

However, in a case where the ring .sub.1 and the ring .sub.2 are a 6-membered ring, and L.sup.1 and L.sup.2 are an arylene group, R.sup.5 is not an aryl group substituted with a linear alkyl group having 18 or more carbon atoms. In addition to the regulation of the ring .sub.1, the ring .sub.2, L.sup.1, and L.sup.2, in a case where R.sup.5 has a substituent having a dipyrromethene boron complex structure, the dipyrromethene boron complex structure has a structure in which a dipyrromethene skeleton is coordinately bonded to a boron atom in the tridentate or tetradentate coordination.

The present invention pertains to the field of optical functional materials, in particular relates to a fluorescent dye having a structure as shown in Formula (I). The fluorescent dye having the structure is covalently bonded to the biological macromolecule, and is stable. The fluorescent dye has high sensitivity, and can be used for different applications, such as cell imaging, fluorescent probes, laser dyes, and fluorescence sensors, and exhibits excellent utility. The preparation method provided by the present invention has low raw material costs, high yields, and employs a simple process that does not produce pollution, simple process. The prepared fluorescent dye has a novel structure and excellent properties, and is suitable for wide range of applications in the fields of biology and environmental science.

The present invention pertains to the field of optical functional materials, in particular relates to a fluorescent dye having a structure as shown in Formula (I). The fluorescent dye having the structure is covalently bonded to the biological macromolecule, and is stable. The fluorescent dye has high sensitivity, and can be used for different applications, such as cell imaging, fluorescent probes, laser dyes, and fluorescence sensors, and exhibits excellent utility. The preparation method provided by the present invention has low raw material costs, high yields, and employs a simple process that does not produce pollution, simple process. The prepared fluorescent dye has a novel structure and excellent properties, and is suitable for wide range of applications in the fields of biology and environmental science.