C07F9/6568

Chromium complex and catalyst therefrom

The invention relates to oligomerization of olefins, such as ethylene, to higher olefins, such as a mixture of 1-hexene and 1-octene, using a catalyst system that comprises a) a source of chromium b) one or more activators and c) a phosphacycle-containing ligating compound. Additionally, the invention relates to a phosphacycle-containing ligating compound and a process for making said compound.

COMPOUND, ORGANIC ELECTROLUMINESCENT DEVICE AND DISPLAY DEVICE
20210098709 · 2021-04-01 ·

The present disclosure relates to a compound, an organic electroluminescent device, and a display device. The compound has a structure of formula (I)

##STR00001## X is selected from a C atom, a Si atom, a B atom, or a P atom; Y.sub.1 to Y.sub.4 are each independently selected from a C atom or an N atom; A and B are each independently selected from any one or more of a substituted or unsubstituted C6-C40 aryl group and a substituted or unsubstituted C4-C40 heteroaryl group; R.sub.1 is selected from carbonyl, C1-C9 alkyl, a substituted or unsubstituted C6-C18 aryl group, and a substituted or unsubstituted C4-C30 heteroaryl group; and R.sub.2 and R.sub.3 are each independently selected from any one of a C1-C9 alkyl group, a substituted or unsubstituted C6-C18 aryl group, and a substituted or unsubstituted C4-C30 heteroaryl group, and n is selected from 0 or 1.

PHOSPHONIUM ION CHANNEL BLOCKERS AND METHODS FOR USE
20210128589 · 2021-05-06 ·

The invention provides compounds of Formula (I), or pharmaceutically acceptable salts thereof:

##STR00001##

The compounds, compositions, methods and kits of the invention are useful for the treatment of pain, itch, and neurogenic inflammation.

HETEROATOMIC-BASED HOLE-TRANSPORT MATERIALS
20210122773 · 2021-04-29 ·

Heteroatomic hole transport materials are provided. The hole transport materials include a non-carbon core: two, four, or eight aromatic groups covalently bound to the non-carbon core; a. terminal substituted diphenylamine end unit on each aromatic group: and optionally aromatic linker groups linking the aromatic groups and the substituted diphenylamine end units. In some embodiments the non-carbon core is non-carbon central atom such as Si, Ge, B.sup., P.sup.+Sn or Pb. In other embodiments, the non-carbon core is a cubic silsesquioxane. Also provided are methods for making these materials. The materials are particularly useful as hole transport materials in perovskite solar cells.

Process for oligomerization

The invention relates to oligomerization of olefins, such as ethylene, to higher olefins, such as a mixture of 1-hexene and 1-octene, using a catalyst system that comprises a) a source of chromium b) one or more activators and c) a phosphacycle-containing ligating compound. Additionally, the invention relates to a phosphacycle-containing ligating compound and a process for making said compound.

Process for oligomerization

The invention relates to oligomerization of olefins, such as ethylene, to higher olefins, such as a mixture of 1-hexene and 1-octene, using a catalyst system that comprises a) a source of chromium b) one or more activators and c) a phosphacycle-containing ligating compound. Additionally, the invention relates to a phosphacycle-containing ligating compound and a process for making said compound.

Phosphepine matrix compound for a semiconducting material
10941168 · 2021-03-09 · ·

The present invention relates to a compound comprising at least one phosphepine ring and having the phosphorus atom of the phosphepine ring substituted with at least one monovalent substituent R, a semiconducting material comprising the compound, and electronic device comprising the semiconducting material.

PHOSPHAVIOLOGEN DERIVATIVES, METHODS OF MAKING THE SAME, AND USES THEREOF
20210002310 · 2021-01-07 ·

The present invention relates to new phosphaviologen derivatives, methods of making phosphaviologen derivatives, and uses thereof, including uses in electrochromic devices and organic battery materials. The phosphaviologen derivatives described herein have strong electron-accepting properties and can be used to provide phosphaviologen derivative-containing electronic materials. In certain embodiments, the phosphaviologen derivatives include dimeric phosphaviologens.

##STR00001##

COMPOUND, ORGANIC ELECTROLUMINESCENCE DEVICE AND DISPLAY DEVICE

The present disclosure relates to the field of organic electroluminescence, in particular to a compound, an organic electroluminescence device and a display device. The compound has a structure shown in a formula (I):

##STR00001##

and X is selected from O atom or S atom; X.sub.1-X.sub.8 are each independently selected from C atoms or N atoms, and at least one of X.sub.1-X.sub.8 is N atoms; A and B are each independently selected from any one or more of the substituted or unsubstituted C6-C40 aryl, and substituted or unsubstituted C4-C40 heteroaryl; R.sub.1 is selected from C1-C9 alkyl, substituted or unsubstituted C6-C18 aryl, substituted or unsubstituted C4-C30 heteroaryl.

Organic electroluminescent device, thin luminous film, display apparatus, and lighting apparatus

An organic electroluminescent device contains an anode, a cathode, and an organic layer containing at least one luminous layer. The organic layer is disposed between the anode and the cathode. At least one luminous layer contains a -conjugated compound exhibiting no overlap between the electron density distributions of the HOMO and the LUMO in the molecule, such that electron transition between the HOMO and the LUMO occurs by a through-space interaction in the molecule. The -conjugated compound has a -conjugated aromatic ring at a moiety on which at least one of the HOMO and the LUMO is localized.