3m Innovative Properties Company

University of Kentucky Research Foundation

Outrider Technologies, Inc.

Battelle Savannah River Alliance, LLC

John E Anthony

Marcia M Payne

Robert Steven Clough

Sean Parkin

Richard M Flynn

George G I Moore

Dennis Edward Vogel

David H Redinger

James Craig Novack

Susan Anne Odom

Aaron L Washington, Ii

Gregg Alexander Caldwell

John T Bobbitt, Iii

Brent Peters

David L Eaton

James C Nicholson

James C Novack

George GI Moore

Derivatized malachite green leuco dyes for use in radio-chromic systems are described. The dyes have the following structure: in which Ar is a substituted phenyl or thiophene ring in which at least one substitution of the Ar ring is not ortho to the bond between the ring and the linking carbon, and in which R, R, R, and Rare independently selected from methyl, alkyl, or alkyl halide. The systems include the dyes in conjunction with an activator, e.g., a halogenated activator, and a carrier, e.g., a fluid carrier or an encapsulating polymeric matrix.

Malachite green based radio-chromic compounds and radiation sensing systems incorporating the compounds

Silylethynyl pentacenes and compositions containing silylethynyl pentacenes are disclosed. Exemplary pentacene compounds have 6,13-silylethynyl substitution with one or more groups (e.g., R, R' and R&#x2033;) covalently bonded to each Si atom of the silylethynyl groups. Methods of making and using silylethynyl pentacenes and compositions containing silylethynyl pentacenes are also disclosed. Substrates and devices comprising the silylethynyl pentacenes and compositions are also disclosed.

Silylethynyl pentacene compounds and compositions and methods of making and using the same

Fluorinated silylethynyl pentacenes and compositions containing fluorinated silylethynyl pentacenes are disclosed. Methods of making and using fluorinated silylethynyl pentacenes and compositions containing fluorinated silylethynyl pentacenes are also disclosed.

Fluorinated silylethynyl pentacene compounds and compositions and methods of making and using the same

The present disclosure provides a method of preparing silylethynyl compounds in which two of the hydrocarbyl groups bonded to the silicon exclusive of the ethynyl group, are the same and one is different, that may be used in preparing novel silylethynyl functionalized acene semiconductor chromophores.

Synthesis of silylacetylenes

Synthesis of silyl acetylenes

Novel silylethynylated heteroacenes and electronic devices made with those compounds are disclosed.

Silylethynylated heteroacenes and electronic devices made therewith

Novel substituted pentacenes and electronic devices made with those substituted pentacenes are disclosed.

Substituted pentacenes and electronic devices made with substituted pentacenes

Growing community of inventors

Lexington, KY, United States of America

John E Anthony