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.

An organic EL device is provided, including at least an anode, a hole transport layer, a light-emitting layer, an electron transport layer, and a cathode in this order, wherein the hole transport layer contains an arylamine compound represented by the following formula (1), wherein Ar.sub.1 to Ar.sub.8 and n1 are defined in the specification, and the electron transport layer contains a compound having a benzoazole ring structure represented by the following formula (2), wherein Ar.sub.9, Ar.sub.10, X, Y.sub.1, Z.sub.1 and Z.sub.2 are defined in the specification. ##STR00001## ##STR00002##

An organic electroluminescence device (OLED) of an embodiment includes a first electrode, a second electrode, and an emission layer disposed between the first electrode and the second electrode The emission layer may include a condensed polycyclic compound represented by Formula 1, which is connected to two or three substituents represented by Formula 2, and the OLED may exhibit excellent luminous efficiency: ##STR00001##

An organic electroluminescence device of an embodiment includes a first electrode, a second electrode, and an emission layer disposed between the first electrode and the second electrode, and the emission layer includes a polycyclic compound represented by Formula 1. The organic electroluminescence device may exhibit high luminous efficiency and/or service life characteristics: ##STR00001##

A hole transport material, a manufacturing method thereof, and an electroluminescent device are provided. A main chain of a molecular structure of the hole transport material includes spiro aromatic amine, and a branch chain of the molecular structure of the hole transport material includes an aryl group or a heteroaryl group. The hole transport material can effectively improve performance of hole injection and hole transport, thereby balancing electrons and holes in electroluminescent devices and realizing relatively low voltage and relatively high efficiency.

Provided is a compound that can improve the luminous efficiency, stability and life span of the element, an organic electronic element using the same, and an electronic device thereof.

A compound of Formula I,

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is disclosed. In Formula I, M is Pd or Pt; each of X.sup.1 to X.sup.12 is C or N; each of X.sup.13 and X.sup.14 is CH, CD or N; each of Z.sup.1, Z.sup.2, and Z.sup.3 is C or N; L.sup.1 is selected from a variety of bivalent linkers; X is selected from O, S, Se, NR′, and CR″R′″; each R, R′, R.sup.1, R.sup.2, R.sup.3, R.sup.A, R.sup.B, R.sup.C, R.sup.D, and R.sup.E is hydrogen or a General Substituent; at least one of Z.sup.1, Z.sup.2, and Z.sup.3 is a carbon atom substituted with a substituent with a molecular weight of at least 16. Formulations, OLEDs, and consumer products that include Formula I are also disclosed.

A photoelectric conversion device includes a first electrode and a second electrode facing each other, a photoelectric conversion layer between the first electrode and the second electrode and configured to absorb light in at least one part of a wavelength spectrum of light and to convert it into an electric signal, and an organic auxiliary layer between the first electrode and the photoelectric conversion layer and having a higher charge mobility than a charge mobility of the photoelectric conversion layer. An organic sensor may include the photoelectric conversion device. An electronic device may include the organic sensor.

A compound is represented by a formula (1). n is 2 to 4, m is 1 to 4, q is 0 to 3, and m+n+q=6; CN is a cyano group; D.sub.1 is a group represented by a formula (2), (3) or (3X), the plurality of D.sub.1 are the same; and Rx is a hydrogen atom or substituent. R.sub.1 to R.sub.8 are each independently a hydrogen atom or substituent. R.sub.31 to R.sub.38 and R.sub.41 to R.sub.48 are each independently a hydrogen atom or substituent; p, px and py are each independently 1 to 4; A to C are each independently a cyclic structure represented by a formula (131) or (132). R.sub.19 and R.sub.20 are each independently a hydrogen atom or substituent. X.sub.1 is a sulfur atom or the like, and * represents a bonding position with a carbon atom of a benzene ring in the formula (1).

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There is provided a polycyclic aromatic compound having a single boron-nitrogen bond and including a core structure of Core A, Core B, or Core C

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In the formulas: Q.sup.1 and Q.sup.2 are the same or different and are a single bond, O, S, NR.sup.12, BR.sup.12, CR.sup.13R.sup.14, or SiR.sup.13R.sup.14; and R.sup.12-R.sup.14 are the same or different and are alkyl, carbocyclic aryl, heteroaryl, or substituted derivatives thereof.