The present invention relates to an organic light emitting diode comprising: a first electrode; a second electrode facing the first electrode; a hole injecting layer or a hole transport layer, which is interposed between the first electrode and the second electrode; and a light emitting layer, wherein the hole injecting layer or the hole transport layer comprises at least one type of amine compound represented by chemical formula A or chemical formula B, and the chemical formula A and the chemical formula B are the same as those included in the description of the invention.

The present invention relates to an organic light emitting diode comprising: a first electrode; a second electrode facing the first electrode; a hole injecting layer or a hole transport layer, which is interposed between the first electrode and the second electrode; and a light emitting layer, wherein the hole injecting layer or the hole transport layer comprises at least one type of amine compound represented by chemical formula A or chemical formula B, and the chemical formula A and the chemical formula B are the same as those included in the description of the invention.

A tetracarboxylic dianhydride represented by the following general formula (1): ##STR00001##
[in the formula (1), R.sup.1, R.sup.2, and R.sup.3 each independently represent a hydrogen atom and the like, and n represents an integer of 0 to 12], wherein a ratio of a summed amount of a specific stereoisomer (A) and a specific stereoisomer (B) is 50% by mole or more relative to a total amount of stereoisomers based on three-dimensional configurations of two norbornane rings in the general formula (1), and a content ratio of the stereoisomer (A) is 30% by mole or more relative to the total amount of the stereoisomers.

A tetracarboxylic dianhydride represented by the following general formula (1): ##STR00001##
[in the formula (1), R.sup.1, R.sup.2, and R.sup.3 each independently represent a hydrogen atom and the like, and n represents an integer of 0 to 12], wherein a ratio of a summed amount of a specific stereoisomer (A) and a specific stereoisomer (B) is 50% by mole or more relative to a total amount of stereoisomers based on three-dimensional configurations of two norbornane rings in the general formula (1), and a content ratio of the stereoisomer (A) is 30% by mole or more relative to the total amount of the stereoisomers.

Disclosed herein is an organic light-emitting diode, comprising: a first electrode; a second electrode facing the first electrode; and an electron-blocking layer and a light-emitting layer sequentially interposed between the first electrode and the second electrode, wherein the light-emitting layer comprises at least one of the amine compounds represented by the following Chemical Formula A or B, and the electron-blocking layer comprises the compound represented by the following Chemical Formula C. Chemical Formulas A, B and C are as described in the Specification.

Disclosed herein is an organic light-emitting diode, comprising: a first electrode; a second electrode facing the first electrode; and an electron-blocking layer and a light-emitting layer sequentially interposed between the first electrode and the second electrode, wherein the light-emitting layer comprises at least one of the amine compounds represented by the following Chemical Formula A or B, and the electron-blocking layer comprises the compound represented by the following Chemical Formula C. Chemical Formulas A, B and C are as described in the Specification.

Provided are novel rhodol-based compounds, the preparation method thereof, and use thereof in Tl.sup.+ flux assays. The fluorescent thallium ion sensor compounds have a rhodol fluorophore attached to an amino dicarboxylic acid metal binding moiety. The compounds are prepared in the “pro-dye” form, with the rhodol oxygen and the carboxylic acids of the metal binding unit masked by protecting groups. The disclosed compounds may be used as more red-shifted and less pH-sensitive variants of Thallos.

Provided are novel rhodol-based compounds, the preparation method thereof, and use thereof in Tl.sup.+ flux assays. The fluorescent thallium ion sensor compounds have a rhodol fluorophore attached to an amino dicarboxylic acid metal binding moiety. The compounds are prepared in the “pro-dye” form, with the rhodol oxygen and the carboxylic acids of the metal binding unit masked by protecting groups. The disclosed compounds may be used as more red-shifted and less pH-sensitive variants of Thallos.

The present disclosure relates to novel sesquiterpenoid compounds as SHP2 and/or POLE3 inhibitors for potential treatment for cancers, and to methods of making and using the sesquiterpenoid compounds. The present invention therefore provides a method of using the disclosed compounds as chemosensitizations agent to a DNA damaging drugs for cancers.

The present disclosure relates to novel sesquiterpenoid compounds as SHP2 and/or POLE3 inhibitors for potential treatment for cancers, and to methods of making and using the sesquiterpenoid compounds. The present invention therefore provides a method of using the disclosed compounds as chemosensitizations agent to a DNA damaging drugs for cancers.