Abstract: A compound of formula (I), formula (II), or a combination thereof, and salts thereof is described. Each A may be independently an optionally substituted conjugated species or an optionally substituted aromatic species. Each R may be independently an optionally substituted C1-C40 linear alkyl chain, an optionally substituted branched alkyl chain, an optionally substituted alkyl chain containing heteroatoms, substituted alkyl chains, or H. Each R2 may be independently an optionally substituted C1-C40 linear alkyl chain, an optionally substituted branched alkyl chain, an optionally substituted alkyl chain containing heteroatoms, substituted alkyl chains, H, or part of a cyclic boronate ester with an other R2. Each n may be independently less than or equal to 3 and greater than or equal to 1. Each x may be independently less than or equal to 3.

Abstract: A formulation including: an organic semiconducting polymer selected from the diketopyrrolopyrrole (DPP) and fused thiophene co-polymer structures of the formulas (I), (II), or combinations thereof, or salts thereof, in an amount of from 0.1 to 5 wt % based on the total weight of the formulation: formulas (I) and (II), respectively, where m is an integer from 1 to 2, n is an integer from 4 to 80, X and Y are independently selected from a divalent heteroaryl, such as a thiophene, R1, R2, R3, and R4 is each a hydrocarbylene substituent as defined herein, a first solvent is selected from a cyclic aliphatic in an amount of from 2 to 98 wt %; and a second solvent selected from an aromatic in an amount of from 98 to 2 wt %. Also disclosed are method of making and using the disclosed formulations, for example, for use in electronic devices.

Abstract: A compound of formula (I), formula (II), or a combination thereof, and salts thereof is described. Each A may be independently an optionally substituted conjugated species or an optionally substituted aromatic species. Each R may be independently an optionally substituted C1-C40 linear alkyl chain, an optionally substituted branched alkyl chain, an optionally substituted alkyl chain containing heteroatoms, substituted alkyl chains, or H. Each R2 may be independently an optionally substituted C1-C40 linear alkyl chain, an optionally substituted branched alkyl chain, an optionally substituted alkyl chain containing heteroatoms, substituted alkyl chains, H, or part of a cyclic boronate ester with an other R2. Each n may be independently less than or equal to 3 and greater than or equal to 1. Each x may be independently less than or equal to 3.

Abstract: The disclosure relates to thiophene-based ditin compounds and methods of making and using such compounds. The disclosed compounds are novel structures having organotin groups on a conjugated aryl group spaced from and adjacent to a fused thiophene moiety. The formation of trialkyl tin groups spaced away from the fused thiophene moieties is advantageous in that it allows for novel polymerization via Stille coupling.

Abstract: A compound of formula (I), formula (II), or a combination thereof, and salts thereof is described. Each A may be independently an optionally substituted conjugated species or an optionally substituted aromatic species. Each R may be independently an optionally substituted C1-C40 linear alkyl chain, an optionally substituted branched alkyl chain, an optionally substituted alkyl chain containing heteroatoms, substituted alkyl chains, or H. Each R2 may be independently an optionally substituted C1-C40 linear alkyl chain, an optionally substituted branched alkyl chain, an optionally substituted alkyl chain containing heteroatoms, substituted alkyl chains, H, or part of a cyclic boronate ester with an other R2. Each n may be independently less than or equal to 3 and greater than or equal to 1. Each x may be independently less than or equal to 3.

Abstract: Described herein are heterocyclic organic compounds of following formulae: More specifically, described herein are fused heterocyclic naphthalene compounds, polymers based on fused heterocyclic naphthalene compounds, methods for making these compounds, and uses thereof. The compounds described have improved polymerization and stability properties that allow for improved material processibility for use as organic semiconductors (OSCs).

Abstract: A formulation including: an organic semiconducting material; and a carrier liquid including at least one of: a first liquid of the formulas (III) or (II): or mixtures of formulas (III) and (II); and a second liquid of a saturated or unsaturated cyclic hydrocarbylene compound of the formula (I): where the respective R1-8, x, and n are as defined herein, and optionally a tertiary liquid carrier, as defined herein. Also disclosed are semiconducting articles prepared with the formulations as defined herein.

Abstract: Articles utilizing strengthened glass substrates, for example, ion-exchanged glass substrates, in combination with organic molecules or polymers are described along with methods for making the articles. The articles are useful in electronics-based devices that utilize organic thin film transistors.

Abstract: Methods and apparatus provide for a transistor, including: a semiconductor layer including molecules, protons, and/or ions, etc. diffused therein from a photoactive material; a channel disposed on or in the semiconductor layer; a source disposed on or in the semiconductor layer; a drain disposed on or in the semiconductor layer; and a gate electrically coupled to the semiconductor layer.

Abstract: Described herein are compositions including heterocyclic organic compounds based on fused thiophene compounds, polymers based on fused thiophene compounds, and methods for making the monomers and polymer along with uses in thin film-based and other devices.

Abstract: The present invention relates generally to mercaptofunctional high ?? EO chromophores and EO polymers, and particularly to mercaptofunctional high ?? EO chromophores and EO polymers useful for making electro-optical devices and systems. Mercaptofunctional high ?? EO chromophores are covalently bonded to poly(imido sulfide) polymers producing high Tg, low optical loss, covalently bonded, high ?? EO chromophore containing polymers. Methods of synthesizing these EO materials using mild polymerization conditions are also described.

Abstract: The present invention relates generally to mercaptofunctional high ?? EO chromophores and EO polymers, and particularly to mercaptofunctional high ?? EO chromophores and EO polymers useful for making electro-optical devices and systems. Mercaptofunctional high ?? EO chromophores are covalently bonded to poly(imido sulfide) polymers producing high Tg, low optical loss, covalently bonded, high ?? EO chromophore containing polymers. Methods of synthesizing these EO materials using mild polymerization conditions are also described.

Abstract: Compounds having a core comprised of an aromatic ring and at least two annulated beta-substituted fused thiophene ring systems of the general formula: -(?-R2—FT2ArFT2-?-R2)—, and polymers or copolymers thereof, of the general formulas: -{-(?-R2—FT2ArFT2-?-R2)-G1-}n-, or -{-G1-(?-R2—FT2ArFT2-?-R2)-G1-G2-}n-, where ?-R2—FT2ArFT2-?-R2, -G1-, -G2-, and n are as defined herein. Also disclosed are compositions, articles, or devices comprising the polymers, and methods for making and using the polymers. The compositions, articles, or devices can be used, for example, for electronic applications, such as light emitting devices and semiconductor devices.

Abstract: A method of making a polymer, including: heating, for a sufficient time and temperature, to polymerize a homogenous mixture including of at least one polymerizable monomer, and a solvent mixture comprised of at least a first liquid and a second liquid, the first liquid being a stronger solvent for the product polymer than the weaker second liquid, and the polymer product precipitates from the homogenous mixture during the heating, as defined herein. Also disclosed are semiconducting articles and printable inks prepared with the resulting narrow polydispersity polymers, as defined herein.

Abstract: Disclosed are compounds having one of the following formulae: wherein X is an aromatic nucleophilic substitution leaving group; R1 is hydrogen, an alkyl group, or an aryl group; and Q1 is a carboxyl protecting group or an aldehyde protecting group. Also disclosed are fused thiophenes that can be prepared using these compounds, as well as stannylthio-containing thiophene, thienothiophene, and dithienothiophene compounds that can be used to prepare fused thiophenes. Methods for making and using the aforementioned compounds, fused thiophenes, and stannylthio-containing thiophene, thienothiophene, and dithienothiophene compounds are also disclosed.

Abstract: Disclosed are compounds having one of the following formulae: wherein X is an aromatic nucleophilic substitution leaving group; R1 is hydrogen, an alkyl group, or an aryl group; and Q1 is a carboxyl protecting group or an aldehyde protecting group. Also disclosed are fused thiophenes that can be prepared using these compounds, as well as stannylthio-containing thiophene, thienothiophene, and dithienothiophene compounds that can be used to prepare fused thiophenes. Methods for making and using the aforementioned compounds, fused thiophenes, and stannylthio-containing thiophene, thienothiophene, and dithienothiophene compounds are also disclosed.

Abstract: The present invention relates generally to mercaptofunctional high ?? EO chromophores and EO polymers, and particularly to mercaptofunctional high ?? EO chromophores and EO polymers useful for making electro-optical devices and systems. Mercaptofunctional high ?? EO chromophores are covalently bonded to poly(imido sulfide) polymers producing high Tg, low optical loss, covalently bonded, high ?? EO chromophore containing polymers. Methods of synthesizing these EO materials using mild polymerization conditions are also described.

Abstract: Disclosed are compounds having one of the following formulae (11), (12), wherein X is an aromatic nucleophilic substitution leaving group; R1 is hydrogen, an alkyl group, or an aryl group; and Q1 is a carboxyl protecting group or an aldehyde protecting group. Also disclosed are fused thiophenes that can be prepared using these compounds, as well as stannylthio-containing thiophene, thienothiophene, and dithienothiophene compounds that can be used to prepare fused thiophenes. Methods for making and using the aforementioned compounds, fused thiophenes, and stannylthio-containing thiophene, thienothiophene, and dithienothiophene compounds are also disclosed.

Abstract: Compounds having a core comprised of an aromatic ring and at least two annulated beta-substituted fused thiophene ring systems of the general formula: -(?-R2—FT2ArFT2-?-R2)—, and polymers or copolymers thereof, of the general formulas: -{-(?-R2—FT2ArFT2-?-R2)-G1-}n-, or -{-G1-(?-R2—FT2ArFT2-?-R2)-G1-G2-}n-, where ?-R2—FT2ArFT2-?-R2, -G1-, -G2-, and n are as defined herein. Also disclosed are compositions, articles, or devices comprising the polymers, and methods for making and using the polymers. The compositions, articles, or devices can be used, for example, for electronic applications, such as light emitting devices and semiconductor devices.

Abstract: The present invention relates generally to mercaptofunctional high ?? EO chromophores and EO polymers, and particularly to mercaptofunctional high ?? EO chromophores and EO polymers useful for making electro-optical devices and systems. Mercaptofunctional high ?? EO chromophores are covalently bonded to poly(imido sulfide) polymers producing high Tg, low optical loss, covalently bonded, high ?? EO chromophore containing polymers. Methods of synthesizing these EO materials using mild polymerization conditions are also described.