A composition suitable for use in an organic light-emitting layer (103) of an organic light-emitting device having an anode (101) and a cathode (105), the composition comprising a fluorescent light-emitting material, a first triplet-accepting material and a second triplet-accepting material that is different from the first triplet-accepting material. The fluorescent light-emitting material may be a repeat unit of a light-emitting polymer, and the first and second triplet-accepting materials may independently be repeat units of the light-emitting polymer or may be mixed with the fluorescent light-emitting material.

A polymer compound having an excellent crosslinking ability is provided. The polymer compound has at least one terminal constitutional unit represented by the formula (1) and a constitutional unit represented by the formula (2):

##STR00001##

In the constitutional unit represented by formula (1), mT represents an integer of 0 to 5, nT represents an integer of 1 to 4, cT represents an integer of 0 to 1, Q.sup.T represents a crosslinkable group, K.sup.T represents an alkylene group or the like and Ar.sup.T represents an aromatic hydrocarbon group or the like. In the constitutional unit represented by formula (2), mA represents an integer of 0 to 5, n represents an integer of 1 to 4, Ar.sup.1 represents an aromatic hydrocarbon group or the like, K.sup.A represents an alkylene group or the like and Q.sup.1 represents a crosslinkable group.

A composition comprising (1) a first crosslinkable polymer compound having an aromatic conjugated repeating unit and a crosslinkable group and having at least one of a light emitting property and charge transportability, and (2) a second crosslinkable polymer compound having an aromatic conjugated repeating unit and a crosslinkable group at least one of which is different from the aromatic conjugated repeating unit in the first crosslinkable polymer compound and the crosslinkable group in the first crosslinkable polymer compound, and having at least one of a light emitting property and charge transportability, wherein at least one of the first crosslinkable polymer compound and the second crosslinkable polymer compound has a crosslinkable group represented by the following formula (Z-3) or (Z-4): ##STR00001##
in the formulae, R.sup.c represents a hydrogen atom, or a substituent such as an unsubstituted or substituted alkyl group or the like, the plurality of R.sup.c moieties may be the same or different.

The present invention relates to compounds for use in electronic devices, preferably organic electroluminescent devices. The invention furthermore relates to processes for the preparation of these compounds and to electronic devices comprising these compounds, preferably in a function as matrix materials and/or as electron-transport materials.

Water-soluble, conjugated polymers containing one or more dibenzosilole monomer residues, as well as compositions, kits, and methods of making and using such polymers are disclosed. Also disclosed are dibenzosilole derivatives substituted with one or more water-solubilizing groups, and methods of making and using such derivatives to prepare water-soluble dibenzosilole polymers.

A light-emitting electrochemical cell 10 includes an emitting layer 12 and electrodes 13 and 14, one on each side of the emitting layer 12. The emitting layer 12 contains a light-emitting material and an ionic compound. The ionic compound has general formula (1), wherein M is N or P; R.sub.1, R.sub.2, R.sub.3, and R.sub.4 each independently represent a C1-C20 saturated aliphatic group; and X is preferably an anion having a phosphoric ester bond or a sulfuric ester bond. The light-emitting material is preferably an organic light-emitting polymer, a metal complex, an organic low molecular compound, or a quantum dot.

##STR00001##

The present invention relates to copolymers containing indenocarbazole derivatives having electron- and hole-transporting properties, in particular for use in the interlayer, emission layer and/or charge-transport layer of electroluminescent devices. The invention furthermore relates to a process for the preparation of the compounds according to the invention and to electronic devices comprising these compounds.

A dental matrix according to the present invention comprises (a) a metal matrix band comprising an internal surface and an external surface; and (b) an organic light emitting diode (OLED) layer disposed on at least a first portion of the internal surface of the metal matrix band, the OLED layer comprising a first electroluminescent polymer disposed between a first and a second electrode layer. Applying an electrical current across the OLED generates light energy suitable for curing dental restoration material with the light energy being applied from the interproximal space.

A problem to be solved of the invention is to provide a package of a liquid composition for an organic electroluminescent device including a phosphorescent material and a solvent with extended storage lifetime, which may be produced with high working efficiency. A solving means of the problem is a package of a liquid composition for an organic electroluminescent device having a liquid composition for an organic electroluminescent device including a phosphorescent material and a solvent, and a container that contains the liquid composition for an organic electroluminescent device, wherein the package of a liquid composition for an organic electroluminescent device has a transmittance of light, that is a wavelength component of from 500 nm to 780 nm, from outside of the package to inside of the container of 15% or less.

An ink composition containing a P-type semiconductor material, an N-type semiconductor material and two or more solvents including a first solvent and a second solvent, wherein the total amount of the first solvent and the second solvent is 70% by weight or more with respect to 100% by weight of all the solvents contained in the ink composition; the boiling point of the first solvent is lower than the boiling point of the second solvent; the boiling point of the first solvent is 120° C. or more and 400° C. or less; and the hydrogen bond Hansen solubility parameter H1 (MPa.sup.0.5) of the first solvent and the hydrogen bond Hansen solubility parameter H2 (MPa.sup.0.5) of the second solvent are in the relation of 0.5≦(H2−H1)≦5.0.