Novel branched oligoarylsilanes of general formula (I) ##STR00001##
A method of preparation of branched oligoarylsilanes is that a compound of general formula (III)
Y-Q.sub.k-SiAr.sub.n—R).sub.3  (III),
where Y stands for a residue of boronic acid or its ester or Br or I, reacts under Suzuki conditions with a reagent of general formula (IV)
A-X.sub.m-A  (IV),
where A stands for: Br or I, provided that Y stands for a residue of boronic acid or its ester; or a residue of boronic acid or its ester, provided that Y stands for Br or I. A technical result is preparation of novel compounds, featured by a high luminescence efficiency, efficient intramolecular energy transfer from some molecular fragments to others, and an increased thermal stability.

A light-emitting device including a condensed cyclic compound represented by Formula 1, wherein the condensed cyclic compound of Formula 1 may be used in the emission layer of the light-emitting device:

##STR00001##

where the detailed description of Formula 1 is the same as described in the present specification.

The invention described in the present specification relates to a color conversion film including a resin matrix; and an organic fluorescent substance dispersed in the resin matrix, wherein the organic fluorescent substance includes a green fluorescent substance having a maximum light emission wavelength in a 510 nm to 560 nm range when irradiating light including a 450 nm wavelength, and a red fluorescent substance having a maximum light emission wavelength in a 600 nm to 660 nm range when irradiating light including a 450 nm wavelength, the green fluorescent substance and the red fluorescent substance have a molar ratio of 5:1 to 50:1, and the color conversion film has a light emission peak with a full width at half maximum (FWHM) of 50 nm or less in a 510 nm to 560 nm range and a light emission peak with a FWHM of 90 nm or less in a 600 nm to 660 nm range when irradiating light, a method for preparing the same, and a backlight unit including the color conversion film.

Thermally activated delayed fluorescent compounds and uses thereof are described. The thermally activated delayed fluorescent compounds are an analogues of 9,10-dihydro-9,9-dimethylacridine compounds.

Provided is an organic electronic element comprising a hole transport layer containing a compound of Formula (1) and an emitting auxiliary layer containing a compound of Formula (2), capable of improving the light emitting efficiency, stability, and life span of an electronic device using the same.

Described herein are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moiety D, each moiety D is covalently attached to either the moiety B or the moiety A, and each moiety B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D, and B are defined herein.

An aromatic amine derivative represented by the following formula (1) wherein at least one of Ar.sub.1 to Ar.sub.4 is a heterocyclic group represented by the following formula (2) wherein X.sub.1 is an oxygen atom or a sulfur atom. ##STR00001##

Disclosed herein are articles and devices, such as photo-selective films, which may be used to influence the growth of photosynthetic organisms. These article and devices may comprise one or more compounds of Formula (I) and/or Formula (II), along with one or more optional auxiliary dyes. Methods of controlling the growth of plants and for the manufacture of said articles and devices are also disclosed herein.

An organometallic compound represented by Formula 1:

##STR00001##

wherein in Formula 1, groups and variables are the same as described in the specification.

This invention relates to the development of heterocyclic materials for use as blue phosphorescent materials in OLED devices. The materials are based on a pair of 5-membered aromatic or psuedoaromatic rings bonded to one another and complexed to a transition metal. The materials were determined computationally to have appropriate triplet energies for use as blue emitters and to possess sufficient chemical stability for use in devices.