Provided is a compound of Chemical Formula 1:

##STR00001## wherein X is O or S; L1 and L2 each independently is a direct bond or a substituted or unsubstituted arylene group; X1 is N or CR1, X2 is N or CR2, X3 is N or CR3, and at least two of X1 to X3 are N; R1 to R3 each independently is hydrogen, deuterium, or a substituted or unsubstituted alkyl, aryl or heteroaryl group; Ar1 and Ar2 each independently is hydrogen, deuterium, or a substituted or unsubstituted alkyl, aryl or heteroaryl group; positions at which

##STR00002##

is substituted with

##STR00003##

are asymmetric; m1, m2, n1 and n2 each independently is 0 or 1; and m1+m2 is 1, and n1+n2 is 1, and an organic light emitting device comprising the same.

This invention relates to a photocleavable mass tag and the use thereof, and particularly to a thiochromene-type compound useful for MALDI-TOF (Matrix-Assisted Laser Desorption/Ionization Time-Of-Flight) mass spectrometry or matrix-less LDI-TOF (Laser Desorption/Ionization Time-Of-Flight) mass spectrometry and the use thereof.

A compound includes two or more structures shown by the following general formula (1-1) in the molecule, ##STR00001##
Ar represents an aromatic ring or one that contains at least one nitrogen atom and/or sulfur atom optionally having a substituent, and two Ars are optionally bonded with each other to form a ring structure; the broken line represents a bond with Y; Y represents a divalent or trivalent organic group having 6 to 30 carbon atoms that contains an aromatic ring or a heteroaromatic ring optionally having a substituent, the bonds of which are located in a structure of the aromatic ring or the heteroaromatic ring; R represents a hydrogen atom or a monovalent group having 1 to 68 carbon atoms. This compound can be cured even in an inert gas not only in air atmosphere without forming byproducts, and can form an organic under layer film.

An organic compound represented by formula (1). In formula (1), each of R.sub.1 to R.sub.22 is independently selected from the group consisting of a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted aryloxy group, a silyl group, and a cyano group.

##STR00001##

Provided is a compound of Chemical Formula 1: ##STR00001## wherein X is O or S; L1 and L2 each independently is a direct bond or a substituted or unsubstituted arylene group; X1 is N or CR1, X2 is N or CR2, X3 is N or CR3, and at least two of X1 to X3 are N; R1 to R3 each independently is hydrogen, deuterium, or a substituted or unsubstituted alkyl, aryl or heteroaryl group; Ar1 and Ar2 each independently is hydrogen, deuterium, or a substituted or unsubstituted alkyl, aryl or heteroaryl group; positions at which ##STR00002## is substituted with ##STR00003## are asymmetric; m1, m2, n1 and n2 each independently is 0 or 1; and m1+m2 is 1, and n1+n2 is 1, and an organic light emitting device comprising the same.

Provided is a compound of Chemical Formula 1: ##STR00001## wherein X is O or S; L1 and L2 each independently is a direct bond or a substituted or unsubstituted arylene group; X1 is N or CR1, X2 is N or CR2, X3 is N or CR3, and at least two of X1 to X3 are N; R1 to R3 each independently is hydrogen, deuterium, or a substituted or unsubstituted alkyl, aryl or heteroaryl group; Ar1 and Ar2 each independently is hydrogen, deuterium, or a substituted or unsubstituted alkyl, aryl or heteroaryl group; positions at which ##STR00002## is substituted with ##STR00003## are asymmetric; m1, m2, n1 and n2 each independently is 0 or 1; and m1+m2 is 1, and n1+n2 is 1, and an organic light emitting device comprising the same.

The invention relates to compounds with benzindenofluorene base bodies having a structure of formula (I): ##STR00001##
and to the use thereof in electronic devices, in particular in organic electroluminescent devices.

A compound includes two or more structures shown by the following general formula (1-1) in the molecule,

##STR00001##

Ar represents an aromatic ring or one that contains at least one nitrogen atom and/or sulfur atom optionally having a substituent, and two Ars are optionally bonded with each other to form a ring structure; the broken line represents a bond with Y; Y represents a divalent or trivalent organic group having 6 to 30 carbon atoms that contains an aromatic ring or a heteroaromatic ring optionally having a substituent, the bonds of which are located in a structure of the aromatic ring or the heteroaromatic ring; R represents a hydrogen atom or a monovalent group having 1 to 68 carbon atoms. This compound can be cured even in an inert gas not only in air atmosphere without forming byproducts, and can form an organic under layer film.

A compound shown by the following general formula (1-1),

##STR00001##

AR1 and AR2 each independently represent an aromatic ring or an aromatic ring containing at least one nitrogen and/or sulfur atom, two AR1s, AR1 and AR2, or two AR2s are optionally bonded; AR3 represents a benzene, naphthalene, thiophene, pyridine, or diazine ring; A represents an organic group; B represents an anionic leaving group; Y represents a divalent organic group; p is 1 or 2; q is 1 or 2; r is 0 or 1; s is 2 to 4; when s=2, Z represents a single bond, divalent atom, or divalent organic group; and when s=3 or 4, Z represents a trivalent or quadrivalent atom or organic group. This compound cures to form an organic film, and also forms an organic under layer film.

This invention relates to a photocleavable mass tag and the use thereof, and particularly to a thiochromene-type compound useful for MALDI-TOF (Matrix-Assisted Laser Desorption/Ionization Time-Of-Flight) mass spectrometry or matrix-less LDI-TOF (Laser Desorption/Ionization Time-Of-Flight) mass spectrometry and the use thereof.