C07D209/88

Spirobifluorene compounds for organic electroluminescent devices

Spirobifluroene compounds of the formula (1) which are suitable for use in electronic devices, ##STR00001##
and in particular organic electroluminescent devices, and to electronic devices that include the spirobifluorene compounds.

Spirobifluorene compounds for organic electroluminescent devices

Spirobifluroene compounds of the formula (1) which are suitable for use in electronic devices, ##STR00001##
and in particular organic electroluminescent devices, and to electronic devices that include the spirobifluorene compounds.

HETEROCYCLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING SAME

Provided are a heterocyclic compound represented by Formula 1 and an organic light-emitting device including the heterocyclic compound. The organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; an organic layer between the first electrode and the second electrode and including an emission layer; and at least one of the heterocyclic compound.

##STR00001##

HETEROCYCLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING SAME

Provided are a heterocyclic compound represented by Formula 1 and an organic light-emitting device including the heterocyclic compound. The organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; an organic layer between the first electrode and the second electrode and including an emission layer; and at least one of the heterocyclic compound.

##STR00001##

Oxime ester photoinitiators

Oxime ester compounds of the formula I, II, III, IV or V ##STR00001##
wherein
Z is for example ##STR00002##
Z.sub.1 for is NO.sub.2, unsubstituted or substituted C.sub.7-C.sub.20 aroyl or unsubstituted or substituted C.sub.4-C.sub.20heteroaroyl; provided that at least one Z.sub.1 is other than NO.sub.2; Z.sub.2 is for example unsubstituted or substituted C.sub.7-C.sub.20aroyl; R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 for example are hydrogen, halogen, or unsubstituted or substituted C.sub.1-C.sub.20alkyl, unsubstituted or substituted C.sub.6-C.sub.20aryl, or unsubstituted or substituted C.sub.4-C.sub.20heteroaryl; R.sub.9, R.sub.10, R.sub.11, R.sub.12 and R.sub.13 for example are hydrogen, halogen, OR.sub.16, unsubstituted or substituted C.sub.1-C.sub.20alkyl; provided that R.sub.9 and R.sub.13 are neither hydrogen nor fluorine; R.sub.14 is for example unsubstituted or substituted C.sub.6-C.sub.20aryl or C.sub.3-C.sub.20heteroaryl Q is for example C.sub.6-C.sub.20arylene or C.sub.3-C.sub.20heteroarylene; Q.sub.1 is —C.sub.1-C.sub.20alkylene-CO—; Q.sub.2 is naphthoylene; Q.sub.3 is for example phenylene; L is for example O-alkylene-O—; R.sub.15 is for example hydrogen or C.sub.1-C.sub.20alkyl; R.sub.20 is for example hydrogen, or unsubstituted or substituted C.sub.1-C.sub.20alkyl; are effective photoinitiators.

Oxime ester photoinitiators

Oxime ester compounds of the formula I, II, III, IV or V ##STR00001##
wherein
Z is for example ##STR00002##
Z.sub.1 for is NO.sub.2, unsubstituted or substituted C.sub.7-C.sub.20 aroyl or unsubstituted or substituted C.sub.4-C.sub.20heteroaroyl; provided that at least one Z.sub.1 is other than NO.sub.2; Z.sub.2 is for example unsubstituted or substituted C.sub.7-C.sub.20aroyl; R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 for example are hydrogen, halogen, or unsubstituted or substituted C.sub.1-C.sub.20alkyl, unsubstituted or substituted C.sub.6-C.sub.20aryl, or unsubstituted or substituted C.sub.4-C.sub.20heteroaryl; R.sub.9, R.sub.10, R.sub.11, R.sub.12 and R.sub.13 for example are hydrogen, halogen, OR.sub.16, unsubstituted or substituted C.sub.1-C.sub.20alkyl; provided that R.sub.9 and R.sub.13 are neither hydrogen nor fluorine; R.sub.14 is for example unsubstituted or substituted C.sub.6-C.sub.20aryl or C.sub.3-C.sub.20heteroaryl Q is for example C.sub.6-C.sub.20arylene or C.sub.3-C.sub.20heteroarylene; Q.sub.1 is —C.sub.1-C.sub.20alkylene-CO—; Q.sub.2 is naphthoylene; Q.sub.3 is for example phenylene; L is for example O-alkylene-O—; R.sub.15 is for example hydrogen or C.sub.1-C.sub.20alkyl; R.sub.20 is for example hydrogen, or unsubstituted or substituted C.sub.1-C.sub.20alkyl; are effective photoinitiators.

Rechargeable lithium-ion cell

A rechargeable lithium-ion cell has a cell capacity and includes a positive electrode having a recharged potential and a negative electrode. The rechargeable lithium-ion cell also includes a charge-carrying electrolyte. The charge-carrying electrolyte includes a charge-carrying medium and a lithium salt. The rechargeable lithium-ion cell also includes a redox shuttle having the following structure. ##STR00001##

Rechargeable lithium-ion cell

A rechargeable lithium-ion cell has a cell capacity and includes a positive electrode having a recharged potential and a negative electrode. The rechargeable lithium-ion cell also includes a charge-carrying electrolyte. The charge-carrying electrolyte includes a charge-carrying medium and a lithium salt. The rechargeable lithium-ion cell also includes a redox shuttle having the following structure. ##STR00001##

Nitrogen-containing compound, electronic element and electronic device

The present disclosure provides a nitrogen-containing compound, an electronic element and an electronic device, which belongs to the technical field of organic materials. The nitrogen-containing compound has a structure of Chemical Formula 1, wherein R.sub.1 and R.sub.2 are each independently selected from hydrogen or a group represented by Chemical Formula 1-1, and one and only one of R.sub.1 and R.sub.2 has the group of Chemical Formula 1-1; when R.sub.1 or R.sub.2 is selected from hydrogen, said R.sub.1 and R.sub.2 may be replaced by R.sub.4. The nitrogen-containing compound can improve the performance of electronic elements.

Nitrogen-containing compound, electronic element and electronic device

The present disclosure provides a nitrogen-containing compound, an electronic element and an electronic device, which belongs to the technical field of organic materials. The nitrogen-containing compound has a structure of Chemical Formula 1, wherein R.sub.1 and R.sub.2 are each independently selected from hydrogen or a group represented by Chemical Formula 1-1, and one and only one of R.sub.1 and R.sub.2 has the group of Chemical Formula 1-1; when R.sub.1 or R.sub.2 is selected from hydrogen, said R.sub.1 and R.sub.2 may be replaced by R.sub.4. The nitrogen-containing compound can improve the performance of electronic elements.