A method for chlorinating blue anthrone, violanthrone or isoviolanthrone is provided. Reaction is carried out with a chlorinating agent (any one of sulfonyl chloride, thionyl chloride and triphosgene) in a reaction solvent (a Lewis acid ionic liquid with anions being of a transition metal halide) for 2 h to 40 h at a chlorination temperature not lower than room temperature and not higher than 120° C.; and then the reaction product is subjected to post-treatment to obtain a target product. The present disclosure cuts off a generation route of harmful substances such as dioxins and their derivatives from the source. There are no dioxins or similar substances generated in the product, and the reaction has high atomic utilization rate and low energy consumption, which fills the gap in the field of chemical technologies at home and abroad.

A compound is represented by a formula (20) below. In the formula (20), a least one pair of a pair of X.sub.21 and X.sub.22, a pair of X.sub.22 and X.sub.23 and a pair of X.sub.23 and X.sub.24 are carbon atoms to be bonded to the structure represented by the formula (20a), ##STR00001##

Provided is a compound of Chemical Formula 1: ##STR00001##
and an organic light emitting device comprising the same.

There is disclosed a compound Formula I ##STR00001##
In Formula I: Z is CR.sup.4R.sup.5, C═CR.sup.4R.sup.5, SiR.sup.4R.sup.5, GeR.sup.4R.sup.5, NR.sup.4a, PR.sup.4a, P(O)R.sup.4a, O, S, SO, SO.sub.2, Se; SeO, SeO.sub.2, Te, TeO, or TeO.sub.2; R.sup.1-R.sup.3 are the same or different at each occurrence and are D, aryl, heteroaryl, alkyl, amino, silyl, germyl, deuterated aryl, deuterated heteroaryl, deuterated alkyl, deuterated amino, deuterated silyl, or deuterated germyl, where two groups selected from R.sup.1, R.sup.2, and R.sup.3 can be joined together to form a fused ring; R.sup.4-R.sup.5 are the same or different at each occurrence and are H, D, aryl, heteroaryl, alkyl, amino, silyl, germyl, deuterated aryl, deuterated heteroaryl, deuterated alkyl, deuterated amino, deuterated silyl, or deuterated germyl; R.sup.4ais alkyl, silyl, germyl, aryl, or a deuterated analog thereof; a is an integer from 0-4; b and c are the same or different and are an integer from 0-3.

The present disclosure relates to an organic compound having a fused aromatic or hetero aromatic ring including a carbazole or fluorene moiety and a group having excellent charge mobility property, and a light emitting diode and a light emitting device having the organic compound. The organic compound can be applied into the light emitting diode by using solution process and has very deep HOMO energy level. When the organic compound is applied into a chare transfer layer, a HOMO energy level bandgap between the charge transfer layer and an emitting material layer is reduced so that holes and electrons can be injected into the emitting material layer in a balanced manner.

The present invention relates to novel light-emitting materials. These materials comprise a non-aromatic spiro polycyclic group. This new side chain could reduce the stacking of the light-emitting materials and result in high PLQY.

The invention relates to specific phenanthrenes, the use of the compound in an electronic device, and an electronic device containing at least one of said compounds. The invention further relates to a method for producing the compound and a formulation and composition containing one or more of the compounds.

Methods, systems, and apparatus for monitoring and controlling electronic devices through the use of wired and wireless protocols. The systems and apparatuses may monitor their environment for signals from electronic devices. They may then take and disambiguate the signals that are received from the devices in their environment in order to identify said devices and associate control signals with them. The systems and apparatuses may then use communication means to send control signals to the identified electronic devices. Input and output transmission means for the systems and apparatuses may include, but are not limited to, powerline communication, Wi-Fi, Bluetooth, ZigBee, and 6LoWPAN. Signal processing and device identification may be done onboard the device, or may be done at a remote location. Multiple apparatuses or systems may be connected together into networks, including mesh networks, in order to make for a more robust architecture.

The present invention generally discloses an organic optoelectronic material and organic electroluminescent (herein referred to as organic EL) device, organic photovoltaics (herein referred to as OPV) device and organic thin-film transistor (herein referred to as OTFT) device using the organic optoelectronic material. More specifically, the present invention relates to the organic optoelectronic material formula (1), and an organic EL device, OPV device and OTFT device employing the organic optoelectronic material can improve performance.

A compound is represented by a formula (1) below. In the formula (1), n is 1 or 2. Ar.sup.1 is represented by a formula (2) below. Ar.sup.2 represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, or a substituted or unsubstituted heterocyclic group having 1 to 20 ring atoms. Ar.sup.3 is represented by a formula (3) below. ##STR00001##