The present application, which pertains to the technical field of organic materials, provides a nitrogen-containing compound, an electronic component, and an electronic device. The structure of the nitrogen-containing compound is shown in Formula 1, in which A is the group represented by Formula 2. The nitrogen-containing compound can improve the performance of electronic component. ##STR00001##

Provided are a novel compound and an organic electronic device using the same. The novel compound is represented by the following Formula (I):

##STR00001## wherein X.sup.1 and X.sup.2 are each independently C(R.sup.a), and the two (R.sup.a)s are the same or different; X.sup.3 and X.sup.4 are each independently C(R.sup.b), and the two (R.sup.b)s are the same or different; the two (R.sup.a)s are joined together to form an aryl ring and the two (R.sup.b)s are joined together to form an oxygen-containing heteroaryl ring, a sulfur-containing heteroaryl ring, or a polycyclic aromatic ring; wherein Y.sup.1 and Y.sup.2 are the same or different; Y.sup.1 and Y.sup.2 are each represented by NR′R″; R′ and R″ are the same or different; at least one of R′ and R″ is an aryl group.

The present disclosure relates to compositions and methods related to bicyclo[2.2.1] heptanamine-containing compounds and salts.

The present disclosure relates to compositions and methods related to bicyclo[2.2.1] heptanamine-containing compounds and salts.

Provided are a novel compound and an organic electronic device using the same. The novel compound is represented by the following Formula (I): ##STR00001##

A salt represented by formula (I):

##STR00001##

wherein Q.sup.1 and Q.sup.2 independently each represent a fluorine atom or a C1-C6 perfluoroalkyl group,
R.sup.1 and R.sup.2 independently each represent a hydrogen atom, a fluorine atom or a C1-C6 perfluoroalkyl group,
z represents an integer of 0 to 6,
X.sup.1 represents *C(O)O, *OC(O), *OC(O)O or O, where * represents a binding site to C(R.sup.1)(R.sup.2) or C(Q.sup.1)(Q.sup.2)-,
A.sup.1 represents a C2-C36 divalent hydrocarbon group in which a methylene group can be replaced by an oxygen atom, a sulfur atom, a carbonyl group or a sulfonyl group and in which a hydrogen atom can be replaced by a substituent,
R.sup.3 represents a hydrogen atom or a methyl group, and
Z.sup.+ represents an organic cation.

Disclosed is a continuous process for the preparation of ingenol-3-mebutate by reaction, in solution, of ingenol or ingenol anion and angelic anhydride or an equivalent angelylating agent. The continuous flow process is preferably performed in the presence of a base such as lithium hexamethyl disilazane (LiHMDS) and/or an activating agent such as dicyclohexylcarbodiimide (DCC). Also disclosed is a process for recycling the other reaction products obtained in the continuous process for preparation of ingenol-3-mebutate for formation of ingenol, which can then be recycled to form ingenol-3-mebutate. ##STR00001##

A novel compound is disclosed, which is represented by the following Formula (I):

##STR00001##

wherein Ar.sub.1, Ar.sub.2, Ar.sub.3, Ar.sub.4, L, Q, G, n1, n2, m1, m2 and q represent the same as defined in the specification. In addition, an organic electronic device is also disclosed, and an organic layer therein comprises the novel compound of the present invention.

A novel compound is disclosed, which is represented by the following Formula (I):

##STR00001##

wherein Ar.sub.1, Ar.sub.2, Ar.sub.3, Ar.sub.4, L, Q, G, n1, n2, m1, m2 and q represent the same as defined in the specification. In addition, an organic electronic device is also disclosed, and an organic layer therein comprises the novel compound of the present invention.

A novel compound is disclosed, which is represented by the following Formula (I):

##STR00001##

wherein Ar.sub.1, Ar.sub.2, Ar.sub.3, Ar.sub.4, L, Q, n1, n2, m1, and m2 represent the same as defined in the specification. In addition, an organic electronic device is also disclosed, and an organic layer therein comprises the novel compound of the present invention.