Provided is a composition, comprising a compound of Chemical Formula 1 and a compound of Chemical Formula 2, wherein at least one of the compound of Chemical Formula 1 and the compound of Chemical Formula 2 includes at least one deuterium:

##STR00001## wherein at least one of R1 to R10 bonds to a * site of Chemical Formula 1-1, and Ar is a substituted or unsubstituted aryl group;

##STR00002## wherein at least one of Y1 to Y10 bonds to a * site of Chemical Formula 2-1, and A and B are each independently a substituted or unsubstituted aromatic hydrocarbon ring or a substituted or unsubstituted aromatic heteroring; a deposition source, an organic electroluminescent device including the same, and a method for manufacturing the same.

A D-A type organic light-emitting material includes a donor moiety and an acceptor moiety. The donor moiety is represented as follows:

##STR00001##

L is selected from any of aryl, heteroaryl, fused aryl and fused heteroaryl. When L is selected from any of aryl and heteroaryl, aryl and heteroaryl each have one or more substituents each selected from any of deuterium, tert-butyl, phenyl, cyano and methylimino, and at least one substituent is selected from cyano and methylimino. When L is selected from any of fused aryl and fused heteroaryl, fused aryl and fused to heteroaryl each have or do not have a substituent. When fused aryl and fused heteroaryl each have a substituent, the substituent is selected from any of deuterium, tert-butyl, phenyl, cyano and methylimino. The acceptor moiety is selected from any of a substituted or unsubstituted fused aromatic rings and a substituted or unsubstituted fused heterocyclic ring.

A compound of Formula I ##STR00001## wherein at least one of R.sup.1 or R.sup.2 includes a polycyclic group selected from the group consisting of Formula A, Formula B, and Formula C: ##STR00002##
wherein X.sup.1, X.sup.2, X.sup.3, and X.sup.4 are independently CR.sup.A or N; X.sup.5, X.sup.6, X.sup.7, and X.sup.8 are independently CR.sup.B or N; X.sup.9, X.sup.10, X.sup.11, and X.sup.12 are independently CR.sup.C or N; X.sup.13, X.sup.14, X.sup.15, and X.sup.16 are independently CR.sup.D or N; X.sup.17, X.sup.18, X.sup.19, and X.sup.20 are independently CR.sup.E or N; X.sup.21, X.sup.22, X.sup.23, and X.sup.24 are independently CR.sup.F or N; X.sup.25, X.sup.26, X.sup.27, and X.sup.28 are independently CR.sup.G or N; X.sup.29, X.sup.30, X.sup.31, and X.sup.32 are independently CR.sup.H or N; Y is selected from the group consisting of O, S, NR, and CRR′; the maximum number of N atoms that can connect to each other within each ring is two; with the proviso that R.sup.1 does not connect to ring B, and R.sup.2 does not connect to ring A, and wherein at least one of R.sup.C and R.sup.D of Formula A is a direct bond or an organic linker, one of R.sup.E and R.sup.F of Formula B is a direct bond or an organic linker, or one of R.sup.G, R.sup.H, and R.sup.N of Formula C is a direct bond or an organic linker.

The present disclosure relates to compounds capable of emitting delayed fluorescence, and uses of these compounds in organic light-emitting diodes.

Provided is a new composition of matter for boron containing organic molecules which can be used as hosts or emitters in OLED devices. The compound can have a structure of Formula I

##STR00001##

The present invention provides a luminescent film containing at least a phosphorescent compound and a fluorescent compound, wherein the convolution integral value J of the emission spectrum of the phosphorescent compound and the absorption spectrum of the fluorescent compound satisfies equation (1), the light emission from the fluorescent compound accounts for at least 90% of the emission spectrum of the luminescent film, and the absolute photoluminescence quantum efficiency (PLQE) of the luminescent film is represented by equation (2). Equation (1): J≥1.5×10.sup.14, Equation (2): PLQE (a film composed of a phosphorescent compound and a host compound)×0.9≤PLQE (a film containing a phosphorescent compound and a fluorescent compound) [The lowest triplet excited state of the host compound is higher than the lowest triplet excited state of the phosphorescent compound, and does not suppress the luminescent property of the phosphorescent compound.]

The near-infrared window of fluorescent heptamethine cyanine dyes greatly facilitates biological imaging because there is deep penetration of the light and negligible background fluorescence. But dye instability, aggregation, and poor pharmacokinetics are current drawbacks that limit performance and the scope of possible applications. All these limitations are simultaneously overcome with a new molecular design strategy that produces a charge balanced and sterically shielded fluorochrome. The key design feature is a meso-Aryl group that simultaneously projects two shielding arms directly over each face of a linear heptamethine polyene. Cell and mouse imaging experiments compared a shielded heptamethine cyanine dye (and several peptide and antibody bioconjugates) to benchmark heptamethine dyes and found that the shielded systems possess an unsurpassed combination of photophysical, physiochemical and biodistribution properties that greatly enhance bioimaging performance.

The present disclosure relates to an organic electroluminescent compound and an organic electroluminescent device comprising the same. The organic electroluminescent device with improved driving voltage and/or power efficiency can be provided by using the organic electroluminescent compound according to the present disclosure.

The present invention relates to a compound of formula (I) and an organic electronic device comprising a semiconductor layer which comprises a compound of formula (I).

Structures of a particle containing a core and at least one shell, a metal oxide material of which is necessarily doped to ensure protection of a material of the core from photodegradation. The core can include any of a thermochromic material, a phase-change material, and a judiciously defined auxiliary material that in turn contains organic and/or polymeric material. Derivative products utilizing a plurality of such particles. Methodologies for producing such particles and derivative products.