C09B57/00

INK JET RECORDING INK AND INK JET RECORDING METHOD

Provided is an ink jet recording ink containing a near-infrared absorbing colorant represented by Formula 1, a polymerizable monomer, a polymerization initiator, and a dispersant, in which a content of the polymerizable monomer is 50% by mass or more with respect to a total amount of the ink jet recording ink, and a difference between an SP value of the polymerizable monomer and an SP value of the dispersant is 3.8 MPa.sup.1/2 to 16.0 MPa.sup.1/2. Also provided is an ink jet recording method.

##STR00001##

The description of a ring A, a ring B, X.sup.A, X.sup.B, G.sup.A, G.sup.B, kA, and kB in Formula 1 will not be repeated.

Efficient organic light-emitting diodes and fabrication of the same
09853220 · 2017-12-26 · ·

Light-emitting devices comprising light-emitting diodes are described herein. These devices may include a substrate, a reflective anode, a hole-injection layer, a hole-transport layer, an emissive component, an electron-transport layer, a cathode, an enhancement layer, and a light-scattering layer. The emissive component may include first and second fluorescent light-emitting layers with an intervening phosphorescent light-emitting layer or first and second phosphorescent light-emitting layers with an intervening fluorescent light-emitting layer.

Efficient organic light-emitting diodes and fabrication of the same
09853220 · 2017-12-26 · ·

Light-emitting devices comprising light-emitting diodes are described herein. These devices may include a substrate, a reflective anode, a hole-injection layer, a hole-transport layer, an emissive component, an electron-transport layer, a cathode, an enhancement layer, and a light-scattering layer. The emissive component may include first and second fluorescent light-emitting layers with an intervening phosphorescent light-emitting layer or first and second phosphorescent light-emitting layers with an intervening fluorescent light-emitting layer.

Chalcogen-containing organic compound and a use thereof

A compound is represented by Formula (1): ##STR00001## wherein, each X is independently oxygen, sulfur, or selenium; m is 0 or 1; each n is independently 0 or 1; R.sup.1-R.sup.3 are each independently, for example, hydrogen or alkyl having 1 to 20 carbons; wherein (i) in the case of m=0, it is excluded that all of R.sup.1-R.sup.3 are hydrogen at the same time; (ii) in the case of m=0, n=0 and in the case that m is 0, one of n is 0 and the other is 1, it is excluded that “both of X are sulfur and all R.sup.3s are the same atoms or groups at the same time”; (iii) in the case of m=0, n=1, it is excluded that all R.sup.3s are the same atoms or groups at the same time, and at least one of R.sup.3s is hydrogen.

Condensed-cyclic compound and organic light-emitting diode comprising the same

A condensed-cyclic compound is represented by Formula 1, and an organic light-emitting diode includes the condensed-cyclic compound. The organic light-emitting diode includes a first electrode, a second electrode facing the first electrode, and an organic layer. The organic layer includes an emission layer and the condensed-cyclic compound. The condensed-cyclic compound can be included in the emission layer as a host, and the emission layer may further include a dopant. ##STR00001##

Condensed-cyclic compound and organic light-emitting diode comprising the same

A condensed-cyclic compound is represented by Formula 1, and an organic light-emitting diode includes the condensed-cyclic compound. The organic light-emitting diode includes a first electrode, a second electrode facing the first electrode, and an organic layer. The organic layer includes an emission layer and the condensed-cyclic compound. The condensed-cyclic compound can be included in the emission layer as a host, and the emission layer may further include a dopant. ##STR00001##

DYE FOR MATERIAL WITH AMIDE FUNCTIONAL GROUPS AND DYEING METHOD OF USING THE SAME

A dye for a material with amide functional groups and a dyeing method of using the same are provided. The dye includes a compound represented by Formula (I) and a solvent. Based on the total weight of the dye of 100 wt %, a content of the compound represented by Formula (I) is 40 wt % to 95 wt %.

##STR00001##

In Chemical Formula (I), R.sub.1, R.sub.2 and R.sub.3 are each independently H, —OH or —COOH, wherein at least one of R.sub.1, R.sub.2 and R.sub.3 is —OH or —COOH.

Organic electroluminescent materials and devices

A compound having the structure of Formula I ##STR00001##
is disclosed. In the structure of Formula I, each of R.sub.1, R.sub.2, and R.sub.3 is independently a hydrogen, a non-fused aryl group having one meta-substituent, or a non-fused heteroaryl six-membered ring having one or more meta-substituents; each meta-substituent is a non-fused aryl or non-fused heteroaryl six-membered ring optionally substituted with further substituents selected from the group consisting of non-fused aryl groups, non-fused heteroaryl groups, and alkyl groups; and at least one of R.sub.1, R.sub.2, and R.sub.3 is a non-fused aryl having one meta-substituent or a heteroaryl six-membered ring having at least one meta-substituent, wherein each meta-substituent is a non-fused aryl or non-fused heteroaryl group further substituted with a chain of at least two non-fused aryl or non-fused heteroaryl groups. The compounds may be useful in phosphorescent organic light emitting devices.

Organic electroluminescent materials and devices

A compound having the structure of Formula I ##STR00001##
is disclosed. In the structure of Formula I, each of R.sub.1, R.sub.2, and R.sub.3 is independently a hydrogen, a non-fused aryl group having one meta-substituent, or a non-fused heteroaryl six-membered ring having one or more meta-substituents; each meta-substituent is a non-fused aryl or non-fused heteroaryl six-membered ring optionally substituted with further substituents selected from the group consisting of non-fused aryl groups, non-fused heteroaryl groups, and alkyl groups; and at least one of R.sub.1, R.sub.2, and R.sub.3 is a non-fused aryl having one meta-substituent or a heteroaryl six-membered ring having at least one meta-substituent, wherein each meta-substituent is a non-fused aryl or non-fused heteroaryl group further substituted with a chain of at least two non-fused aryl or non-fused heteroaryl groups. The compounds may be useful in phosphorescent organic light emitting devices.

Aromatic heterocyclic derivative, material for organic electroluminescent element, and organic electroluminescent element

An aromatic heterocyclic derivative is represented by a formula (1) below. ##STR00001##
In the formula (1), X.sub.1 to X.sub.3 each are a nitrogen atom or CR.sub.1, with a proviso that at least one of X.sub.1 to X.sub.3 is a nitrogen atom. A is represented by a formula (2) and B is represented by a formula (4) below. ##STR00002##