Novel red methine dyes, methods for the preparation thereof, and use thereof for dyeing plastics, especially vinyl polymers, provide red colourings with improved colour strengths and improved colour brilliance.

The present application discloses stilbene derivative compounds and phenylbenzofuran compositions, useful in the manufacture of dye-sensitized solar cells and other similar technology.

The present disclosure provides a method for preparing a near-infrared region II fluorescent small molecule. The method utilizes organic full synthesis to construct a novel structured fluorescent probe small molecule, belonging to the fields of chemical sensing technology and fluorescence imaging. Compared with the currently studied fluorescent probe with a benzobisthiadiazole structure, the near-infrared region II fluorescent small molecule has the advantages of simple synthesis method, easy modification, stable structure, high fluorescence quantum yield and the like.

An organic dye corresponding to one of the following structures (I) or (II): eD-pi-conjugated chromophore-L-A (I), or A-L-pi-conjugated chromophore-eD (II), where eD represents an electron donor segment, L represents a covalent bond or a spacer segment and in particular a pi-conjugated spacer segment, A represents an electron acceptor segment capable of forming a covalent bond with a semiconductor, in which the pi-conjugated chromophore comprises at least one unit of formula (III):

##STR00001##

in which the radicals R1 and R2, which are identical or different, represent an optionally substituted aryl group; the radicals R3 to R8, which are identical or different, represent a hydrogen, an optionally substituted alkyl group or an optionally substituted aryl group; and X1 and X2, which are identical or different, are chosen from S, Se and O.

Fluorescent chromophores nicknamed BOPHY are provided. The chromophores may be readily synthesized in two steps from readily available reagents via the coupling of a pyrrole aldehyde or ketone with hydrazine, followed by reaction with BF.sub.3. The resultant symmetric and dimeric tetracycle is comprised of two BF.sub.2 units in six-member chelate rings, appended by pyrrole units on the periphery. The quantum yield of fluorescence for the unmodified compound and the tetramethyl variant are near unity, with values 95 and 92% respectively in CH.sub.2Cl.sub.2.

The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow colorings with improved light fastness and improved thermostability.

The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability.

The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability.

The present disclosure provides a compound of Formula (I), (II), or (III):

##STR00001##

an ionic derivative thereof, an isomer thereof, or a salt thereof. The present disclosure also provides conjugates of the compounds, and methods of using the compounds and the conjugates. The disclosure also provides the use of the compounds and conjugates in methods of sequencing nucleic acids.

A photoelectric conversion element, including a first electrode, a second electrode, and at least one organic layer being present between the first electrode and the second electrode, in which the organic layer contains at least two kinds of compounds having the same skeletons and different substituents in combination.