A sensory material with high sensitivity, selectivity, and photostability has been developed for vapor probing of organic amines. The sensory material is a perylene-3,4,9,10-tetracarboxyl compound having amine binding groups and the following formula ##STR00001## where A and A′ are independently chosen from N—R1, N—R2, and O such that both A and A′ are not O, and R1 through R10 are amine binding moieties, solubility enhancing groups, or hydrogen such that at least one of R1 through R10 is an amine binding moiety. This perylene compound can be formed into well-defined nanofibers. Upon deposition onto a substrate, the entangled nanofibers form a meshlike, highly porous film, which enables expedient diffusion of gaseous analyte molecules within the film matrix, leading to a milliseconds response for vapor sensing.

An organic electroluminescent element using a compound represented by the following general formula (I) emits dark blue light and has small changes in the chromaticity and in the driving voltage even after driving for a long period of time: ##STR00001##
wherein R.sup.1 to R.sup.6; Q.sup.1 and Q.sup.2; X.sup.1, X.sup.2, X.sup.3 and X.sup.4 are as defined herein.

An organic electroluminescent element using a compound represented by the following general formula (I) emits dark blue light and has small changes in the chromaticity and in the driving voltage even after driving for a long period of time: ##STR00001##
wherein R.sup.1 to R.sup.6; Q.sup.1 and Q.sup.2; X.sup.1, X.sup.2, X.sup.3 and X.sup.4 are as defined herein.

The present disclosure relates to an organic electroluminescent compound represented by formula 1 and an organic electroluminescent device comprising the same. By comprising the organic electroluminescent compound of the present disclosure, an organic electroluminescent device having improved driving voltage and/or luminous efficiency characteristics can be provided.

The present invention relates to a cyanoaryl substituted compound of formula (I), (I) wherein m is 0-4; R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are selected from hydrogen, chlorine, bromine and C.sub.6-C.sub.24-aryl, which carries one to three cyano; each R.sup.1 independently from each other is selected from bromine, chlorine, cyano, —NRaRb, C.sub.1-C.sub.24-alkyl, C.sub.1-C.sub.24-haloalkyl, C1-C24-alkoxy, C.sub.1-C.sub.24-haloalkoxy, C.sub.3-C.sub.24-cycloalkyl, heterocycloalkyl, heteroaryl, C.sub.6-C.sub.24-aryl, C.sub.6-C.sub.24-aryloxy, C.sub.6-C.sub.24-aryl-C.sub.1-C.sub.10-alkylene, etc., with the proviso that at least one of the radicals R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 is C.sub.6-C.sub.24-aryl, which carries one to three cyano; X is O, S, SO or SO.sub.2; A is a diradical of the formulae (A.1), (A.2), (A.3), or (A.4) wherein *, R.sup.6, (R.sup.7)n, (R.sup.8)o and (R.sup.9)p are as defined in the claims and in the description. The invention also relates to the use of said compound(s) in color converters, to said color converters and their use, to lighting devices, to a backlight unit for liquid crystal displays; a liquid crystal display device and a self-emissive display device comprising at least one compound (I). ##STR00001##

The present invention relates to a cyanoaryl substituted compound of formula (I), (I) wherein m is 0-4; R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are selected from hydrogen, chlorine, bromine and C.sub.6-C.sub.24-aryl, which carries one to three cyano; each R.sup.1 independently from each other is selected from bromine, chlorine, cyano, —NRaRb, C.sub.1-C.sub.24-alkyl, C.sub.1-C.sub.24-haloalkyl, C1-C24-alkoxy, C.sub.1-C.sub.24-haloalkoxy, C.sub.3-C.sub.24-cycloalkyl, heterocycloalkyl, heteroaryl, C.sub.6-C.sub.24-aryl, C.sub.6-C.sub.24-aryloxy, C.sub.6-C.sub.24-aryl-C.sub.1-C.sub.10-alkylene, etc., with the proviso that at least one of the radicals R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 is C.sub.6-C.sub.24-aryl, which carries one to three cyano; X is O, S, SO or SO.sub.2; A is a diradical of the formulae (A.1), (A.2), (A.3), or (A.4) wherein *, R.sup.6, (R.sup.7)n, (R.sup.8)o and (R.sup.9)p are as defined in the claims and in the description. The invention also relates to the use of said compound(s) in color converters, to said color converters and their use, to lighting devices, to a backlight unit for liquid crystal displays; a liquid crystal display device and a self-emissive display device comprising at least one compound (I). ##STR00001##

The present invention provides compounds of Formula (I) which can be used as SGK inhibitors; pharmaceutical compositions comprising the compounds of the invention; as well as uses and methods for treating a disease mediated by SGK by administering the compounds of the invention. ##STR00001##

The present invention provides compounds of Formula (I) which can be used as SGK inhibitors; pharmaceutical compositions comprising the compounds of the invention; as well as uses and methods for treating a disease mediated by SGK by administering the compounds of the invention. ##STR00001##

A compound is represented by one selected from Formulae 1 and 2:

##STR00001##

Wherein the components of Formulae 1 and 2 are each independently defined as set forth in the present disclosure. An organic light-emitting device includes at least one of the compound represented by one selected from Formulae 1 and 2.

A compound is represented by one selected from Formulae 1 and 2:

##STR00001##

Wherein the components of Formulae 1 and 2 are each independently defined as set forth in the present disclosure. An organic light-emitting device includes at least one of the compound represented by one selected from Formulae 1 and 2.