57 results about "Aromatic moiety" patented technology

An electrochromic device includes: a first insulating substrate; a first conducting layer disposed over the first insulating substrate; an electrochromic layer disposed over the first conducting layer, wherein the electrochromic layer comprises an electrochromic polymer having a polymer backbone comprising one or more meta-conjugated linkers (MCLs) and one or more aromatic moieties (Ars), wherein each of the one or more MCLs is partially conjugated with one of the one or more Ars at a meta position of the one or more MCLs; an electrolyte layer disposed over the electrochromic layer; a second conducting layer disposed over the electrolyte layer; and a second insulating substrate disposed over the second conducting layer. A thickness of the electrochromic layer is from 10 nm to 1500 nm resulting in transmittance of 85%-99.9% at a wavelength of 550 nm at a neutral state of the electrochromic layer.

The invention provides structures and synthesis of a class of piezoelectric monomers and COFs with fluorine-substituted side chains tethered on the peripheral position of an aromatic moiety (thus different functional side chains). The multi-fluoro groups on the mentioned piezoelectric COFs provide abundant piezoelectric active sites, which enable the application as the active layer for PENGs. The exemplary embodiments also provide a process for the fabrication of a piezoelectric COF and a process for the fabrication of the piezoelectric nanogenerator utilizing mentioned piezoelectric COF.

The present inventive concept relates to an electrode material for use in an electrochemical storage device, comprising a modified lignin being a lignin functionalized with at least one aromatic moiety selected from the list of catechol, hydroquinone, and phenols substituted with an alkoxy group, wherein a total content of phenolic hydroxyl groups is at least 4.0 mmol / g, as determined by 31P Nuclear Magnetic Resonance Spectroscopy.

The present disclosure relates to a process for making a polyamide grease thickening agent from an oligomeric intermediate. Particularly, the polyamide grease thickening agent may include at least two para-substituted aromatic moieties, have a molecular weight in a range of from 450 g / mol to 3500 g / mol, and may include at least four amide bonds.

Useful cooking aids for kraft pulping processes are aromatic polycarboxylic acids that: (a) contain an aromatic moiety having an average of at least 2 carboxylic acid groups pendant to the aromatic moiety per molecule; and (b) have an electron affinity of less than -2.80 eV and at least -3.6 eV, or a functional equivalent of the aromatic polycarboxylic acid.

The invention provides a polyamide lubricating grease thickening agent. The polyamide lubricating grease thickening agent has a structure according to a formula I: (MCA-DA-) (PCA-DA) y-PCA-(DA-PCA) y (-DA-MCA) (I). In formula I, at each occurrence, PCA is independently a reacted polycarboxylate, at each occurrence, MCA is independently a reacted monocarboxylate, at each occurrence, DA is independently a reacted n-alkyl diamine, and y is a 0 or a non-zero integer. In addition, in Formula I, the polyamide grease thickener has a weight average molecular weight in the range of from about 450 g / mol to about 2600 g / mol. Further, in Formula I, the structure comprises at least 4 amide bonds and at least two internal aromatic moieties are disubstituted in the para-position.

Provided are an initiator mixture, a composition comprising the same, and a polymer formed from the composition, the initiator mixture comprising: a compound containing a polyaromatic ring; comprising iodine; an ionic compound including boron; comprising a norbornene moiety comprising an oxo group (O =); and a tertiary amine compound including an aromatic moiety, an ester group, and an amine group.

An electrochromic polymer includes a formula ofMCL represents a meta-conjugated linker, and Ac represents an aromatic moiety. The disclosed electrochromic polymer has an absorption onset equal to or smaller than 420 nm in a neutral state and has absorption in visible and / or near-infrared wavelengths in an oxidized state, thus the disclosed electrochromic polymer shows a high transparency and a high optical contrast when used in electrochromic devices.

A dried delivery particle comprising a benefit agent core material and a shell encapsulating the core material is described, along with a process for forming such a delivery particle and articles of manufacture. The shell is a polymeric material that is the reaction product of chitosan derived from an aqueous phase, and a cross-linking agent comprising an isocyanate component comprising a mixture of two or more di- and / or poly-isocyanates derived from an oil phase, the di- and / or poly-isocyanates each comprising at least one aromatic moiety. The delivery particle of the invention has improved release characteristics with lower free oil, lower leakage in matrices and carriers, and with enhanced degradation characteristics in OECD test method 301B.

A combination of retarders and regulators for hydration reaction of cementitious binders including clinkers based on Ye'elimite. Set retarders are calcium complexing agents, consisting of sugar acids, sugars, sugar alcohols, hydroxycarboxylic acids, phosphates, phosphonates, borates and amines. Regulator general formula (I) iswhere M is H, NH4 or chosen from monovalent or divalent metal of groups Ia, IIa, IIIa, Ib, IIb, IVb, VIb, VIIb or VIIIb of periodic table of elements, where M is a divalent metal, a second equivalent of R—SO3 is present, and M is chosen from group consisting of H, NH4, Li, Na, K, MgX, CaX, or NiX with X═RSO3, and R is chosen from H, NH2, OH or from hydrocarbon chain with 1-18 C atoms which may be substituted by N and / or O and / or which may be linear or branched and / or which contain one or more unsaturated bonds and / or cycloaliphatic and / or aromatic moieties.

To provide a new type of electrochromic polymer and a device using this polymer. [Solution] Electrochromic polymers are JPEG2026057544000090.jpg21170 (In the formula, MCL represents the meta-conjugated linker, and Ac represents the aromatic moiety) The disclosed electrochromic polymer has absorption initiation below 420 nm in the neutral state and absorption in the visible and / or near-infrared wavelengths in the oxidized state. Therefore, when used in an electrochromic device, the disclosed electrochromic polymer exhibits high transparency and high optical contrast.

Improved delivery particles comprising a beneficial agent core material and a shell encapsulating the core material are described, as well as methods and articles for forming such delivery particles. The shell is a polymeric material that is the reaction product of chitosan from an aqueous phase and a crosslinking agent comprising an isocyanate component comprising a mixture of two or more diisocyanates and / or polyisocyanates from an oil phase, each comprising at least one aromatic moiety. The delivery particles of the invention have improved release characteristics, lower leakage in matrices and vehicles, and enhanced degradation characteristics in OECD Test Method 301 B.

The present disclosure provides a polyamide grease thickener having a structure according to formula I: (MCA-DA-)(PCA-DA) y -PCA-(DA-PCA) y (-DA-MCA)(I). In formula I, in each occurrence, PCA is independently a reacted polycarboxylate, in each occurrence, MCA is independently a reacted monocarboxylate, in each occurrence, DA is independently a reacted n-alkyldiamine, and y is an integer other than 0 or zero. Additionally, in formula I, the weight average molecular weight of the polyamide grease thickener ranges from about 450 g / mol to about 2600 g / mol. Additionally, in formula I, the structure contains at least four amide bonds, and at least two internal aromatic moieties are disubstituted in the para position.

Iodinated compounds, hydrogels formed from the iodinated compounds, and methods of making and using the iodinated compounds and hydrogels are provided. In some aspects, the present disclosure relates to a system for forming a hydrogel comprising (a) a first composition comprising a polyiodized polyamino compound comprising a polyamino moiety linked to a polyiodized aromatic moiety by an amide or ester group, and (b) a second composition comprising a reactive multi-arm polymer comprising a plurality of hydrophilic polymer arms having reactive end groups reactive with the amino groups of the polyiodized polyamino compound. Other aspects of the present disclosure relate to medical hydrogels and methods of making medical hydrogels based on such compositions. Further aspects of the present disclosure relate to methods of making polyiodized polyamino compounds.

An electrochromic device includes a first insulating substrate; a first conducting layer disposed over the first insulating substrate; an electrochromic layer disposed over the first conducting layer, an electrolyte layer disposed over the electrochromic layer; a second conducting layer disposed over the electrolyte layer; and a second insulating substrate disposed over the second conducting layer. The electrochromic layer includes an electrochromic polymer having a polymer backbone comprising one or more meta-conjugated linkers (MCLs) and one or more aromatic moieties (Ars). Each of the one or more MCLs is partially conjugated with one of the one or more Ars at a meta position of the one or more MCLs. The thickness of the electrochromic layer is from 10 nm to 5800 nm resulting in transmittance of 70%-99.9% at a wavelength of 550 nm at a neutral state of the electrochromic layer.

Label-free autofluorescence-detected photothermal mid-IR (AF-PTIR) microscopy is applied to test the distribution of materials within a sample. Two-photon excited UV-fluorescence (TPE-UVF) supports autofluorescence of native aromatic moieties using visible-light optics. Thermal modulation of the fluorescence quantum yield serves to report on infrared absorption, enabling infrared spectroscopy in the fingerprint region with a spatial resolution dictated by fluorescence. AF-PTIR provides high selectivity and sensitivity in image contrast for aromatic fluorescent materials, complementing broadly applicable optical photothermal IR (O-PTIR) microscopy based on photothermal modulation of refractive index / scattering. Mapping the fluorescent material distribution can be used to improve processes such as powdered dosage form manufacturing, with high spatial variance potentially producing variability in both delivered dosage and product efficacy. The ubiquity of aromatic moieties within active pharmaceutical ingredient candidates in particular suggests the viability of AF-PTIR in combination with O-PTIR to improve the confidence of chemical classification in spatially heterogeneous dosage forms.

The present disclosure provides a polyamide grease thickening agent having the structure according to Formula I: (MCA-DA-)(PCA-DA)y-PCA-(DA-PCA)y(-DA-MCA) (I). In Formula I, at each occurrence PCA is independently a reacted polycarboxylate, at each occurrence MCA is independently a reacted monocaboxylate, at each occurrence DA is independently a reacted n-alkyl diamine, and y is 0 or a non-zero integer. Additionally, in Formula I, a weight-average molecular weight of the polyamide grease thickener is in a range of from about 450 g / mol to about 2600 g / mol. Additionally, in Formula I, the structure includes at least 4 amide bonds and at least two internal aromatic moieties are di-substituted in a para position.

In some aspects, the present disclosure provides iodinated polyamino compounds that comprise a polyamino moiety that is coupled to an iodinated aromatic moiety through a linkage that comprises an ether group, and optionally an amide group. Other aspects of the present disclosure pertain to systems for forming hydrogels that comprise (a) an iodinated polyamino compound that comprises a polyamino moiety that is coupled to an iodinated aromatic moiety through a linkage that comprises an ether group, and optionally an amide group, and (b) a reactive polymer that forms crosslinks with the iodinated polyamino compound. Still other aspects of the present disclosure pertain to crosslinked products formed from such systems and methods of treatment using such systems.

Disclosed herein is a 2K coating system consisting of two components (A) and (B) being separate from each other, where (A) includes at least one constituent (a1) containing at least one aromatic moiety and bearing on average at least two primary and / or secondary amino groups, where (B) includes at least one constituent (b1) containing at least one aromatic moiety and bearing on average at least two isocyanate groups, where each of (A) and (B) has a solid content of at least 95 wt.-%, based on the total weight of the respective component, and constituent (b1) present in component (B) bears carbodiimide and / or uretonimine units and at least one structural unit (I). Also disclosed herein are a coating composition obtainable by mixing components (A) and (B), a method of using said coating composition as sealant, a method of applying the coating composition to a substrate, and a sealed substrate.

The present disclosure relates to a process for making a polyamide grease thickening agent from an oligomeric intermediate. Particularly, the polyamide grease thickening agent may include at least two para-substituted aromatic moieties, have a molecular weight in a range of from 450 g / mol to 3500 g / mol, and may include at least four amide bonds.

The invention concerns a phosphoric acid ester of Formula (I) or (II), wherein: A, B and R represents an aliphatic, cycloaliphatic and / or aromatic moiety; Q represents —CH2—, —O— or —COO—; n+m is inferior to 3; and X+Y is less than 7, and wherein the phosphoric acid ester has an average molecular weight Mn of 70 to 10,000 g / mol. The invention also concern the process for making the phosphoric acid ester of Formula (I) or (II), and there us as dispersants of particles in a liquid medium, such as water, solvent, plasticizer or resin. Advantageously, the process allows the preparation of new high performing polymeric phosphate esters with less acidic character that are majorly a phosphate diester. Also, a 100% active liquid solvent free polyester phosphate ester can be effectively prepared.

The present invention relates to an adhesive composition, its use in the production of MicroLED display panels, a receiving layer comprising the adhesive composition, and a transfer tape. The adhesive composition comprises: a) at least one elastomeric component in an amount from 42% to 85% by weight, based on the total weight of the adhesive composition, where the elastomeric component comprises at least 80% by weight of a polyvinyl aromatic-polydiene block copolymer composition C, where composition C is as defined in the specification; b) at least one hydrocarbon modifier having aromatic moieties in an amount of at least 15% by weight, based on the total weight of the adhesive composition, having an MMAP cloud point of-30 to + 30 DEG C, a softening temperature below 80 DEG C; and c) optionally additional additives wherein the adhesive composition has a total aromatic content consisting of components a), b) and c), the total aromatic content being at least 20% (by weight) of the total weight of the adhesive composition as determined according to the test VII of the specification.

The present disclosure is generally directed to antimicrobial polymers, and methods of preparation thereof. In embodiments, an antimicrobial polymer may comprise a polymeric moiety, an aromatic moiety comprising a naphthoic acid derivative bonded to the polymeric moiety, a pendant group comprising a cation and a linking group bonded to the pendant group and aromatic moiety. Methods of preparation include reacting naphthoic acid or a derivative thereof with a polymer to form a primary intermediate, reacting an alcohol group on the primary intermediate with an acyl halide to form a secondary intermediate, reacting a terminal halide on the acyl halide to form a cationic group on the secondary intermediate.

A crosslinked microporous membrane (crosslinked polymer) composition useful in gas separation, the membrane comprising: (i) an aromatic polymer containing a multiplicity of benzene rings; and (ii) a multiplicity of fluorinated aromatic moieties, each fluorinated aromatic moiety containing at least two separate methylene (—CH2—) linkages connected to benzene rings on the aromatic polymer; wherein the cross-linked microporous membrane possesses micropores having a pore size of up to 2 nm. Also described are methods for producing the crosslinked polymer and a microporous carbon material produced by pyrolysis of the crosslinked polymer membrane. Also described are methods for using the crosslinked polymer and microporous carbon material for gas or liquid separation, filtration, or purification.

Process for the preparation of acetal-protected sugars comprising the step of reacting a diol group of a sugar selected from the group consisting of valeralose and hexaldehyde with one or both compounds of formula (Ia) and / or formula (Ib) in the presence of a homogeneous or heterogeneous catalyst, to form an acetal protected sugar selected from the group consisting of compounds of formula (II), formula (III) and formula (IV); wherein R1 and / or R2 are each independently-Z-X, and wherein Z is a linear, branched or cyclic hydrocarbon moiety having 1 to 10 carbon atoms, optionally substituted by 1 to 4 C1-C4 alkyl groups or 1 to 4 halogen atoms, or Z is-B-D, where B is a linear hydrocarbon moiety having 1 to 3 carbon atoms and may be present or absent, D is an aromatic moiety having 6 carbon atoms, wherein Z may be present or absent, and X is-COOH,-CH (COOH) 2,-COOR3, CHO,-C2H3,-C2H,-CHOR4OR5,-N3,-NHR6,-NR7R8,-F,-Cl,-Br,-I, or, if Z is present, X is-OH, NH2, or-SH, optionally substituted by 1 to 4 C1-C4 alkyl groups, 1 to 2-OH groups, 1 to 2-OCH3 groups, or 1 to 4 halogen atoms, and wherein Z may be present or absent,-COOR3, CHO,-C2H3,-C2H,-CHOR4OR5,-N3,-NHR6,-NR7R8,-F,-Cl,-Br,-I; r3, R4 and R5 are independently selected from the group consisting of linear, branched or cyclic hydrocarbon moieties having 1 to 20 carbon atoms and optionally substituted by 1 to 4 C1 to C4 alkyl groups and / or 1 to 4 halogen atoms selected from the group consisting of fluorine, chlorine, bromine and iodine; r6 is a C1-C4 alkyl group; r7, R8 and R9 are each independently a C1-C4 alkyl group; r30 and R31 are each independently selected from the group consisting of hydrogen and a linear or branched hydrocarbon moiety having 1 to 4 carbon atoms, with the proviso that R30 and R31 cannot be hydrogen at the same time; r < 10 > is selected from the group consisting of-H,-OH,-CH2OH,-OR13 or-CH2OR14; r < 11 > and R < 12 > are independently selected from the group consisting of-OH or-OR13; r13 and R14 are independently selected from hydrocarbon moieties having from 1 to 10 carbon atoms; and n and p are each independently 0 or 1.

Chromatographic media for the chromatographic purification of a biomolecule of interest comprising a substrate and a copolymer grafted onto the substrate. The copolymer comprises: an aliphatic moiety of an aliphatic hydrophobic monomer; an aromatic moiety of an aromatic hydrophobic monomer; a hydrophilic portion of the neutral hydrophilic monomer; and at least one of an electropositive portion of a positively charged monomer and an electronegative portion of a negatively charged monomer. The copolymer exhibits: a hydrophobic-to-hydrophilic ratio of the aliphatic moiety and the aromatic moiety to the hydrophilic moiety, the hydrophobic-to-hydrophilic ratio being selected based on the relative surface hydrophilicity of the target biomolecule and the relative surface hydrophobicity of the target biomolecule; and an aliphatic-aromatic ratio of the aliphatic moiety to the aromatic moiety, the aliphatic-aromatic ratio being selected based on relative surface aliphatic characteristics of the target biomolecule and relative surface aromatic characteristics of the target biomolecule.

A laundry treatment composition includes a delivery particle. The delivery particle includes a core and shell surrounding the core, and the core includes a perfume and the shell includes a polymeric material that is the reaction product of chitosan. The reaction product of chitosan is derived from an aqueous phase and a cross-linking agent. The cross-linking agent includes an isocyanate component, the isocyanate component including a mixture of two or more di- and / or poly-isocyanates, derived from an oil phase, the di- and / or poly-isocyanates each including an aromatic moiety; and the mixture of di- and / or poly-isocyanates including an aromatic moiety includes at least one alpha-aromatic isocyanate and at least one beta-aromatic isocyanate.

An electrochromic polymer includes a formula ofMCL represents a meta-conjugated linker, and Ac represents an aromatic moiety. The disclosed electrochromic polymer has an absorption onset equal to or smaller than 420 nm in a neutral state and has absorption in visible and / or near-infrared wavelengths in an oxidized state, thus the disclosed electrochromic polymer shows a high transparency and a high optical contrast when used in electrochromic devices.

Embodiments of a process for producing a high pressure ethylene-based polymer include polymerizing an ethylene monomer feed and optionally an additional comonomer feed via free radical polymerization at a pressure of at least 1000 atmospheres (atm) in the presence of a free radical scavenger to produce a high pressure ethylene-based polymer, wherein the radical scavenger comprises Structure 1: wherein: n may be 0 to 100; r1, R2 and R3 are each independently H, a (C1-C40) hydrocarbyl group, a (C1-C40) heterohydrocarbyl group, or an aromatic-containing moiety; and R4 to R8 are each independently H, OH, a (C1-C40) hydrocarbyl group, a (C1-C40) heterohydrocarbyl group, or an aromatic-containing moiety, provided that at least one of R4 to R8 must be OH. # imgabs0 #

The present disclosure relates to a process for making a polyamide grease thickening agent from an oligomeric intermediate. Particularly, the polyamide grease thickening agent may include at least two para-substituted aromatic moieties, have a molecular weight in a range of from 450 g / mol to 3500 g / mol, and may include at least four amide bonds.