An organic electroluminescence device includes an anode, an emitting layer, and a cathode in this order. The emitting layer comprises a delayed fluorescent compound M2 and a compound M3 having at least one deuterium atom, and the compound M3 is not a compound having a partial structure represented by a formula (1C) or (2C). S.sub.1(M2) of the compound M2 and S.sub.1(M3) of the compound M3 satisfy a relationship of S.sub.1(M3)>S.sub.1(M2). In the formulae (1C) and (2C), Y.sub.41 to Y.sub.48 are each independently a N atom, CR, or a C atom bonded to another atom or the like in the compound M3, where each R is independently a H atom or a substituent, at least one of Y.sub.41 to Y.sub.48 is a N atom, and at least one of Y.sub.41 to Y.sub.48 is a C atom bonded to another atom or the like in the compound M3.

##STR00001##

An organic electroluminescence device includes an anode, an emitting layer, and a cathode in this order. The emitting layer comprises a delayed fluorescent compound M2 and a compound M3 having at least one deuterium atom, and the compound M3 is not a compound having a partial structure represented by a formula (1C) or (2C). S.sub.1(M2) of the compound M2 and S.sub.1(M3) of the compound M3 satisfy a relationship of S.sub.1(M3)>S.sub.1(M2). In the formulae (1C) and (2C), Y.sub.41 to Y.sub.48 are each independently a N atom, CR, or a C atom bonded to another atom or the like in the compound M3, where each R is independently a H atom or a substituent, at least one of Y.sub.41 to Y.sub.48 is a N atom, and at least one of Y.sub.41 to Y.sub.48 is a C atom bonded to another atom or the like in the compound M3.

##STR00001##

An organic light emitting device comprising a first electrode, a second electrode provided to face the first electrode, and a light emitting layer provided between the first electrode and the second electrode and including a first compound represented by Chemical Formula 1 and a second compound represented by Chemical Formula 2, the organic light emitting device which exhibits low driving voltage, high emission efficiency, and long lifespan characteristics.

##STR00001##

An organic light emitting device comprising a first electrode, a second electrode provided to face the first electrode, and a light emitting layer provided between the first electrode and the second electrode and including a first compound represented by Chemical Formula 1 and a second compound represented by Chemical Formula 2, the organic light emitting device which exhibits low driving voltage, high emission efficiency, and long lifespan characteristics.

##STR00001##

An organic electroluminescence device includes: an anode; a cathode; and an emitting layer provided between the anode and the cathode, in which the emitting layer contains a delayed fluorescent compound M2 and a compound M3 represented by a formula (3) and a singlet energy S.sub.1(M2) of the compound M2 and a singlet energy S.sub.1(M3) of the compound M3 satisfy a relationship of a numerical formula (Numerical Formula 1) below, S.sub.1(M3)>S.sub.1(M2) . . . (Numerical Formula 1). In the formula (3), A3 is a group represented by a formula (3a) or the like.

##STR00001##

A compound represented by the following general formula has excellent light-emitting characteristics and emits light at a short wavelength. Y.sup.1 is N—R.sup.A; Y.sup.2 is O, S, C═O or N—R.sup.A; R.sup.A is an aryl group, etc.; R.sup.1 to R.sup.11 each are a hydrogen atom or a substituent; at least one of R.sup.1 to R.sup.3 is a carbazolyl group substituted with an aryl group, etc.

##STR00001##

A compound represented by the following general formula has excellent light-emitting characteristics and emits light at a short wavelength. Y.sup.1 is N—R.sup.A; Y.sup.2 is O, S, C═O or N—R.sup.A; R.sup.A is an aryl group, etc.; R.sup.1 to R.sup.11 each are a hydrogen atom or a substituent; at least one of R.sup.1 to R.sup.3 is a carbazolyl group substituted with an aryl group, etc.

##STR00001##

The present invention relates to a phenyl-derivative compound substituted with at least two electron acceptors and at least two electron donors. Formula (I) R.sup.AaR.sup.DbR.sup.ScC.sub.6 wherein a is 2, 3 or 4; b is 2, 3 or 4; c is 0, 1 or 2; a+b−c=6; R.sup.A is at each occurrence independently a group with −M-effect; R.sup.B is at each occurrence independently a group with +−M-effect; R.sup.S is as defined in claim 1. Said compound is suited for use in organic electronic devices, particularly in organic electroluminescent devices.

The present invention relates to a phenyl-derivative compound substituted with at least two electron acceptors and at least two electron donors. Formula (I) R.sup.AaR.sup.DbR.sup.ScC.sub.6 wherein a is 2, 3 or 4; b is 2, 3 or 4; c is 0, 1 or 2; a+b−c=6; R.sup.A is at each occurrence independently a group with −M-effect; R.sup.B is at each occurrence independently a group with +−M-effect; R.sup.S is as defined in claim 1. Said compound is suited for use in organic electronic devices, particularly in organic electroluminescent devices.

The present disclosure provides an organic compound represented by general formula [1] below. ##STR00001## In formula [1], Ar.sub.1 and Ar.sub.2 each represent an alkyl group having 1 to 8 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a heteroaromatic group having 3 to 17 carbon atoms. Ar.sub.1 and Ar.sub.2 may be the same or different. Ar.sub.3 and Ar.sub.4 are each a substituent having a carbazolyl group. Ar.sub.3 and Ar.sub.4 may be the same or different. Ar.sub.1 to Ar.sub.4 may be substituted. At least one of Ar.sub.1 to Ar.sub.4 has a tert-butyl group. The total number of tert-butyl groups in one molecule of the organic compound is 2 or more.