Dow Global Technolgoies LLC

Rohm and Haas Company

Rohm and Haas Electronic Materials Korea Ltd.

Blue Cube IP LLC

Robert J Wright

David D Devore

Shaoguang Feng

Clark H Cummins

Brian A Jazdzewski

Gyongyi Gulyas

William L Winniford

Warren E Smith

Zahid Asif

Jeremy Chris Reyes

Liam P Spencer

Zhengming Tang

Hong-Yeop Na

Minrong Zhu

Chong Xing

Michael J Mullins

Bruce Bell

Kaitlyn C Gray

Sukrit Mukhopadhyay

David M Pearson

Matthias Stefan Ober

Kevin A Frazier

Dean M Welsh

Kyoung Moo Koh

Hua Ren

Jing Yan

Timothy De Vries

Stephanie L Potisek

Marty J Null

Jichang Feng

Eric B Ripplinger

Martha P Hernandez

Ashwin R Bharadwaj

Yuchen Liu

Eric P Ripplinger

A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel; said method comprising adding to said petroleum hydrocarbon or liquid biologically derived fuel at least one compound that is a R, R, R, R, R, R, R, R, Rand R-substituted diaryl ether, wherein R, R, R, R, R, R, R, R, Rand Rindependently are hydrogen, hydrocarbyl or hydrocarbyloxy; wherein each compound having formula (I) is present at a level from 0.01 ppm to 20 ppm.

Diaryl ethers as fuel markers

A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel; said method comprising adding to said petroleum hydrocarbon or liquid biologically derived fuel at least one compound that is a R, R, R, R, R, R, Rand R&#x2014;substituted dibenzofuran, wherein R, R, R, R, R, R, Rand Rindependently are hydrogen, hydrocarbyl, hydrocarbyloxy, aryl or aryloxy; provided that R, R, R, R, R, R, Rand Rcollectively have at least two carbon atoms; wherein each compound having formula (I) is present at a level from 0.01 ppm to 20 ppm.

Substituted dibenzofurans as fuel markers

A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel; said method comprising adding to said petroleum hydrocarbon or liquid biologically derived fuel at least one compound that is a R, R, R, R, R, R, R, R, Rand R-substituted xanthene, wherein R, R, R, R, R, R, R, R, Rand Rindependently are hydrogen, hydrocarbyl, hydrocarbyloxy, aryl or aryloxy; wherein each compound of formula (I) is present at a level from 0.01 ppm to 20 ppm.

Xanthenes as fuel markers

An organic compound suitable for organic layers of electronic devices that show improved luminescent properties.

Organic compound and electronic device comprising an organic layer comprising the organic compound

The present disclosure provides a composition. In an embodiment, a composition is provided and comprises a Compound 1 shown below: For Compound 1, Rthrough Rare the same or different. Rthrough Reach is independently selected from the group consisting of hydrogen, unsubstituted hydrocarbyl, substituted hydrocarbyl, cyano, alkoxy, aryloxy, and NR'. R&#x2032; is hydrogen or hydrocarbyl; wherein two or more of adjacent Rto Rmay optionally form one or more ring structures. The Component Z is selected from the group consisting Group Z-1, Group Z-2, Group Z-3, Group Z-4, Group Z-5, Group Z-6 and Group Z-7 shown below: For Compound 1, one or more hydrogen atoms may optionally be substituted with deuterium. 

Compositions with triarylamine derivatives and OLED device containing the same

Organic compounds suitable for organic layers of electronic devices that show improved luminescent properties.

Organic compounds and electronic device comprising an organic layer comprising the organic compounds

Provided is a composition comprising a compound selected from Structure 1, as described herein: 

Compositions with 2,3-disubstituted indoles as charge transport materials, and display devices fabricated therefrom

A novel low viscosity epoxide having the following general Structure (I): Structure (I) wherein R1 and R2 can be, but is not limited to, hydrogen or a hydrocarbon group having from C1 to about C20 carbon atoms; with the proviso that R1 and R2 are not both hydrogen. 

Epoxide compound

A process for preparing a divinylarene dioxide including reacting (a) at least one divinylarene, (b) hydrogen peroxide, (c) at least one iron-containing catalyst, and (d) an excess of amine hydrogen halide, under conditions to form a divinylarene dioxide.

Process for preparing a divinylarene dioxide

A process for preparing a divinylarene dioxide including reacting (a) at least one divinylarene with (b) at least one oxidant in the presence of (c) at least one transition metal complex catalyst, and (d) optionally, in the presence of a solvent, and (e) optionally in the presence of a catalyst modifier under conditions to form a divinylarene dioxide product.

Process for preparing divinylarene dioxides

A process for preparing a divinylarene dioxide including reacting (a) at least one divinylarene; and (b) at least one peracid oxidant compound, under conditions to form a divinylarene dioxide product; wherein the peracid oxidant compound is capable of providing an increased yield of a divinylarene dioxide product.

Growing community of inventors

Sugar Land, TX, United States of America

Robert J Wright