Abstract: A method for producing a polyamide resin characterized by comprising thermally polycondension of tetramethylene diamine and either an aliphatic dicarboxylic acid having 7 or more carbon atoms or a salt thereof, and then being melt-polymerized at a temperature equal to or higher than the melting point thereof until the relative viscosity of a 0.01 g/ml solution thereof in 98% sulfuric acid solution with a 0.01 g/ml content at 25° C. becomes 2.2-5.0.

Abstract: Provided herein is a non-naturally occurring microbial organism having a methanol metabolic pathway that can enhance the availability of reducing equivalents in the presence of methanol. Such reducing equivalents can be used to increase the product yield of organic compounds produced by the microbial organism, such as 1,4-butanediol (BDO). Also provided herein are methods for using such an organism to produce BDO.

Abstract: A biodegradable polyesteretheramide for manufacturing films and molded products, for example for application in the protection of foodstuff products and films for agriculture, contains a compound with at least 3 groups capable of reacting with one or several types of the active groups present in the reaction mixture, that is, compounds which, while containing ether groups in their structure, have active groups capable of reacting in the reaction mixture to form amide groups, and which simplifies and shortens the preparation process, reducing its economic cost and obtaining products of greater transparency and higher strain at failure, while maintaining other properties such as resistance to tearing and puncture, and allowing greater widths of films to be made with smaller thicknesses.

Abstract: Disclosed is a method of preparing porous polybenzimidazole. The method includes providing polyaminoimide by reacting aromatic amine including at least two ortho-positioned amino groups and acid dianhydride, obtaining polypyrrolone from the polyaminoimide, subjecting the polypyrrolone to alkaline treatment, and subjecting the alkaline-treated polypyrrolone to heat treatment. The polybenzimidazole shows permeability and selectivity for various gases due to a fractional free volume and well-connected picopores.

Abstract: Hydroxypolyamides, hydroxypolyamide products, and post-hydroxypolyamides are disclosed as gel forming agents. Hydroxypolyamides and post-hydroxypolyamides are prepared from known methods. Hydroxypolyamide products are produced from a modified polymerization procedure which utilizes strong base for deprotonation of ammonium salts from the esterification of stoichiometrically equivalent polyacid:polyamine salts. The hydroxypolyamide products are capable of gel formation at lower concentrations than hydroxypolyamides and post-hydroxypolyamides from the known methods of preparation, and are therefore superior gel forming agents.

Abstract: This invention relates to poly(ester amide)s (PEAs) comprising inactivated terminal amino and carboxyl groups, methods of synthesizing the inactivated PEAs and uses for them in the treatment of vascular diseases.

Abstract: The present invention relates to compounds of formula I and II, which are functionalized amino acids, and polymers formed from the same. Polymers formed from the functionalized amino acids are expected to have controllable degradation profiles, enabling them to release an active component over a desired time range. The polymers are also expected to be useful in a variety of medical applications.

Abstract: Polyamic acid including structural units of the following Chemical Formulae 1 and 2 is provided: In Chemical Formulae 1 and 2, each substituent is as defined in the detailed description.

Abstract: The present invention relates to the use of a system composed of a base and of a sulphonamide, as a catalyst for the ring-opening (co)polymerization of lactones. The present invention also relates to novel sulphonamides and to a process for the ring-opening (co)polymerization of lactones comprising the use of sulphonamides in combination with a base as a catalytic system.

Abstract: In one aspect, a water soluble binder composition, a method of producing the same and an electrode for a rechargeable battery employing the same is provided.

Abstract: Described are methods for processing material, material processing systems, and processable materials. Preferred embodiments relate to a method of and apparatus for producing formable products such as polymer products and thermoplastic materials.

Abstract: Disclosed are a novel ionic organic compound and a method for producing the ionic organic compound by a simple process. Also disclosed are a hydrogelling agent composed of an ionic organic compound obtained by the method, an alcohol gelling agent, a gel which uses the gelling agent, while using water or methanol as a medium, and a carbon nanotube dispersant composed of the compound. Specifically disclosed is an ionic organic compound represented by general formula (1). The compound is obtained by a condensation reaction of (A) an aromatic diamide compound or cyclohexane diamide compound having a 4-(chloromethyl)benzamide group at both ends, and (B) a compound selected from N,N,N?,N?-tetramethylalkylenediamines which may have a substituent wherein there are 1-6 carbon atoms between nitrogen atoms. The thus-obtained ionic organic compound serves as a gelling agent which is capable of gelling a neutral aqueous solution or an alcohol.

Abstract: Ionic and ionogenic comb copolymers are disclosed along with personal care products that employ them as a modifier that results in increased sensory attributes and increased effectiveness in the deposition of actives and can also act as a thickening agent. The copolymer includes one or more repeating units derived from olefinically unsaturated anionic or anionogenic or zwitterionic comonomers, and one or more repeating units having the formula in which Y is a moiety forming part of a copolymer backbone, Z is a moiety that exhibits association with other Z moieties or with other moieties within the ultimate formulation in which the copolymer will be employed, and b is a bond or moiety that links the Z moiety to the Y moiety. In certain embodiments, the copolymer also includes repeating units derived from acrylamide monomers, olefinically unsaturated hydrophilic monomers or other olefinically unsaturated monomers.

Abstract: Disclosed is a polyamide composition including at least one semi-aromatic copolyamide, said semi-aromatic copolyamide consisting essentially of 40 to 60 mole percent repeat units of the formula —C(O)(CH2)4C(O)NHCH2ArCH2NH—??(I) and 40 to 60 mole percent repeat units of the formula —C(O)(CH2)4C(O)NH(CH2)6NH—??(II) wherein Ar is a meta-substituted benzene ring. Also disclosed are molded articles including the polyamide composition.

Abstract: Disclosed embodiments concern using at least one triazine, typically an amine or polyamine triazine (referred to as amino triazines), in combination with at least one ionomer or ionomer precursor to form compositions useful for making sporting equipment, such as golf ball components. The ionomer or ionomer precursor typically includes plural acid functional groups, such as carboxyl or carboxylate groups, that react or form salts with the amino triazine. Specific examples, without limitation, of suitable amino triazines include guanamine, 6-methyl-1,3,5-triazine-2,4-diamine(acetoguanamine), 6-nonyl-1,3,5-triazine-2,4-diamine(nonylguanamine), 6-phenyl-1,3,5-triazine-2,4-diamine(benzoguanamine) and 2,4,6-triamino-triazine(melamine).

Abstract: A radiation-curable acrylate-modified aminoamide resin which is the Michael addition product of an aminoamide thermoplastic polymer derived from a polymerised unsaturated fatty acid with a polyol ester having at least three (meth)acrylate ester groups, the aminoamide thermoplastic polymer having an amine number of from 40 to 60 mgKOH/g, the ratio of the initial (meth) acrylate groups of the polyol ester to the initial amino functional groups of the aminoamide polymer being at least 4:1, is liquid at 25° C., and is useful as the resin component of various types of energy-curable coating composition, including inks, varnishes and lacquers, especially lithographic inks.

Abstract: The present invention provides a branched, a dendritic, or a hyperbranched poly(amino ester) having a polymer backbone comprising a plurality of branches, wherein the polymer backbone has at least one secondary and at least one tertiary amine linkage. Branched poly(amino ester)s are prepared via a Michael addition reaction of a tris(acrylate ester)monomer with a diamine monomer. In one aspect, the diamine monomer has a primary amino group and a secondary amino group. The poly(amino ester) compounds can be end-capped by reacting with a suitable agent. The present invention also provides applications including, but are not limited to, the delivery of bioactive agents, such as drugs, DNA or RNA; or biocompatible imaging.

Abstract: The invention relates to novel ampholytic copolymers having a controlled architecture. These copolymers can particularly be used in aqueous compositions.

Abstract: Polyesteramides prepared from decreased perfection diamide diester monomers. The polymers exhibit improved physical properties.

Abstract: A biodegradable cross-linked cationic multi-block copolymer of linear polyethylenimine (LPEI) wherein the LPEI blocks are linked together by hydrophilic linkers with a biodegradable disulfide bond and methods of making thereof. The biodegradable cross-linked cationic multi-block copolymer may also contain pendant functional moieties which are preferably receptor ligands, membrane permeating agents, endosomolytic agents, nuclear localization sequences, pH sensitive endosomolytic peptides, chromogenic or fluorescent dyes.

Abstract: The present invention provides hydmoxyapatite-targeting, multiarm polymer reagents suitable for reaction with biologically active agents to form conjugates, the polymeric reagents comprising one or more polymer chains and a plurality of hydroxyapatile-targeting moieties located at the terminus of one or more of the polymer chains. The multiarm polymers are optionally divided or separated by one or more degradable linkages into polymer segments having a molecular weight suitable for renal clearance. The polymeric reagents of the invention can have a substantially linear structure, although branched or multiarm structures are contemplated as well. The invention is suited for applications in which use of a high molecular weight polymer is desired, such as a total polymer number average molecular weight of at least about 30,000 Da for linear polymers and 20,000 Da for multiarm polymers. Each structure includes one or more linkages capable of degradation in vivo.

Abstract: A forensic marker is disclosed including a marker that is added to the host material and is detectable for at least the expected life of the host material. The marker is inert with respect to the host material in that it does not significantly affect the desired qualities of the host material (e.g. weight, adhesive properties, structural integrity, etc). The marker is detectable, for example, by instruments, during the life of the host material.

Abstract: A polyamide resin composition for reflectors, which gives a molding having high mechanical strength and excellent heat resistance and which stably exhibits a high reflectance and can provide a reflector that resists a decrease in reflectance caused by heating, particularly in a LED production process and a reflow soldering process. A reflector obtained by molding the resin composition is also provided. The polyamide resin composition is composed of defined amounts of a polyamide resin (A), an inorganic filler (B) and a white pigment (C) (with the proviso that the total of the components (A), (B) and (C) does not exceed 100% by weight). The components of the polyamide resin (A) are defined and the polyamide resin (A) has a terminal amino group concentration of 70 to 230 mmol/kg.

Abstract: A thermally curable solder resist composition for a flexible printed circuit board is provided. The solder resist composition includes (a) 50-100 parts by weight of an epoxy resin, wherein the epoxy resin includes at least an aliphatic polyester modified epoxy resin having formula (I) or (II), in which, each of R1 and R2, independently, is a C6-38 saturated or an unsaturated carbon chain, R3 is ether, phenyl, a C6-38 heterocyclic or C6-38 saturated carbon chain, n is an integer of 1-10 and the aliphatic polyester modified epoxy resin had a molecular weight of 1000-5000; (b) 1-10 parts by weight of a curing agent; and (c) 1-10 parts by weight of a catalyst.

Abstract: The invention is directed to composition, preparation and use of composite materials based on an adhesive with solids levels above 45% by weight that contain stable polyamidoamine-epihalohydrin resins (PAE resins) of solids greater than 40% where the relative high solids of the PAE enables the high solids content of the adhesive. Furthermore, at least 45% of the solids portion of the adhesive is made up of a combination of the solids of the PAE resin and the solids of the protein source. The invention is also directed an adhesive comprised of the PAE in combination with a soy protein source. The invention is also directed toward use of the adhesive in composite materials and in particular wood containing composite materials, and more specifically wood fiber or particle based composites.

Abstract: Disclosed is an oligoaniline compound represented by the formula (1), (2), (3) or (4) below, which exhibits high solubility in a low-polarity solvent. This oligoaniline compound is suitable as a charge-transporting material which enables to realize excellent device characteristics such as low driving voltage when applied to an OLED device. (In the formulae, R1-R20 independently represent a hydrogen atom, a halogen atom, a hydroxy group, an amino group, a silanol group, a thiol group, a carboxyl group, a sulfonic acid group, a phosphate group, a phosphoric acid ester group, an ester group, a thioester group, an amide group, a nitro group, a monovalent hydrocarbon group, an organoxy group, an organoamino group, an organosilyl group, an organothio group, an acyl group or a sulfonic group; m, n, l and k independently represent an integer respectively satisfying 1?m?20, 1?n?20, 1?l?20 and 1?k?20; and X represents a fluorinated aryl group).

Abstract: A cement dispersant that includes a copolymer resulting from a reaction of components (A) to (C), where: (A) is an ester compound obtained by adding 0 to 10 moles of C2-4 alkylene oxide to 1 mole of at least one compound of Formula (1) RO-(AO)n-H (where R is a C1-12 alkyl group, A is a C2-4 alkylene group, and n is an integer of 0 to 7) and subjecting the resulting adduct to a reaction with an ?,?-unsaturated carboxylic acid, in which the compound of Formula (1) contains not more than 5% by mass of the constituent compounds having n of 3 or less relative to the total mass of the compound of Formula (1); (B) is an ?,?-unsaturated carboxylic acid or a salt thereof; and (C) is another copolymerizable monomer, where appropriate, or a salt thereof.

Abstract: A polyamic acid composition including a polyamic acid, the polyamic acid having an imidization ratio of from about 5.0% to about 25.0%, and being obtained by reacting a diamine compound, a tetracarboxylic dianhydride and an acid monoanhydride at an amount ratio that satisfies the following formula (1): 0.970<Y/X<0.998 and Formula (2): 0.00<Z/2(X?Y)<0.50. In Formula (1) and Formula (2), X represents a content (mol) of the diamine compound, Y represents a content (mol) of the tetracarboxylic dianhydride, and Z represents a content of the acid monoanhydride (mol).

Abstract: A polymer dye has repeating units of formula (I): Each of R1, R2, and R3 is independently a monocyclic carbocyclic group, a condensed polycyclic carbocyclic group, a monocyclic heterocyclic group, or a condensed polycyclic heterocyclic group. In any case, each of R1, R2, and R3 independently may have a substituent. R1 is a divalent group, and R2 and R3 are monovalent groups. D is an organic dye group and n is an integer of from 0 to 10. The polymer dye has a number-average molecular weight of from 500 to 500,000. The dye can be a component in a film. The dye can also be included in various industrial materials in automobiles; communication instruments, such as mobile phones, PDA, remote controllers, mobile information terminals, electronic dictionaries, and electronic organizers; home electric appliances; construction parts; and the like.

Abstract: Polyamide having a melting point between 330° C. and 370° C., said polyamide comprising: a diamine component (a) comprising between 0 and 55 mole %, based on the total number of moles of the diamine component (a), of at least one aliphatic diamine having more than 6 carbon atoms, and between 45 and 100 mole %, based on the total number of moles of the diamine component (a), of at least one aliphatic diamine having at most 6 carbon atoms, and a dicarboxylic acid component (b) comprising more than 50 mole %, based on the total number of moles of the dicarboxylic acid component (b), of terephthalic acid, with the exception of a certain specific polyamide (P*).

Abstract: The present invention provides a liquid-crystal display device that can efficiently provide both effects of improvement in a response time and suppression of image sticking in a display screen. The liquid-crystal display device according to the present invention is a liquid-crystal display device including a pair of substrates each including an electrode and an alignment film and a liquid crystal layer interposed between the pair of substrates, wherein the alignment film comprises a copolymer comprising a first monomer unit including a first side chain including a photoreactive functional group and a second monomer unit including a second side chain including a repeated structure.

Abstract: A resinous compound of the formulas or a salt thereof, wherein G1 is —X1C(O)OR1, —X2OC(O)R2, or —X2OH; G2 is R4, R12, —C(O)R2, —C(O)X1C(O)OR1, or —C(O)X2OC(O)R2; R1 is an alkyl having from 10 to 80 carbon atoms; R2 is an alkyl having from 2 to 40 carbon atoms; each R3 and R4 is independently hydrogen, alkyl, arylalkyl or alkylaryl; each R5 and each R6 is independently hydrogen or alkyl; X1 and X2 are both a straight or branched alkylene group; t1 is 1 to 20; t2 and t3 is independently 0 to 20; u1 is 1 to 30; u2 and u3 is independently 0 to 30; each R7 and each R8 is independently hydrogen, alkyl, or alkoxyl; each R9 and each R10 is independently hydrogen, alkyl, or alkoxyl; Ar is a substituted or unsubstituted aromatic moiety; p is 1 to 5; q is 1 to 12; A? is selected from the group consisting of Cl?, Br?, I?, HSO4?, HSO3?, CH3SO3?, NO3?, HCOO?, CH3COO?, H2PO4?, SCN?, BF4?, ClO4?, SSO3?, PF6?, and SbCl6?; and J is alkyl, arylalkyl, or alkylaryl.

Abstract: Polymer, comprising at least one heterocyclic 3-membered-ring compound and one iodine-containing compound.

Abstract: A phosphazene-based polymer hydrogel with a chemical cross-linkings formed by radiating ultraviolet (UV) and/or mixing with cross-linking agent and/or enzyme, and a method of preparing the same are provided. The hydrogel shows a sol-gel behavior and has an excellent solidity by containing the phosphazene-based polymer that is capable of cross-linking at a certain concentration.

Abstract: The present application, at least in part, is directed to a method of providing a substantially constant rheological profile of an oil-based drilling fluid over a temperature range of about 120° F. to about 40° F. In some embodiments, the method comprises adding a drilling fluid additive to the drilling fluid, wherein the drilling fluid additive consists essentially of a polyamide and a set of at least one or more mono-carboxyl units. The polyamide has (a) repeat units of (i) a poly-carboxyl unit with at least two carboxylic moieties; and (ii) a polyamine unit having an amine functionality of two or more and the one or more mono-carboxyl units being positioned on the polyamide at a position selected from the group consisting of: an end position, a pendant position and combinations thereof.

Abstract: A protective polymeric coating is applied to the surface of various objects which are to be exposed to a harsh environment. The protective polymeric coating covers the exposed surface, where the polymeric coating includes a polyimide polymer. The polyimide polymer in the polymeric coating has a backbone with at least one non-terminal phenyl group. A linkage is connected to the non-terminal phenyl group, where the linkage can be an amide linkage or an ester linkage. An oligomeric silsesquioxane compound is connected to the linkage through an organic substituent, where the oligomeric silsesquioxane is not incorporated into the polymer backbone. The polymeric coating provides protection to the underlying object.

Abstract: Disclosed is a method of manufacturing a conductive coating film having superior chemical resistance or solvent resistance and durability by chemically bonding a resin having an amine group (—NH2) with carbon nanotubes having a carboxyl group (—COOH). The conductive material having high bondability with carbon nanotubes and superior electrical properties includes carbon nanotubes uniformly contained therein, and thus has appropriate surface resistivity, and thereby can be used for antistatic, electrostatic dissipation and electromagnetic shielding purposes and in transparent or opaque electrodes depending on the resistivity value.

Abstract: A process for the preparation of a composition comprising hyperbranched polymeric compounds, which comprises a step of reacting a mixture comprising one or more compounds of the following formula (I): AR(B)n wherein A and B are functional groups, R is an (n+1)-valent organic group containing one or more thioether groups and n is an integer of at least 2 characterized in that A is an amino group or a hydroxyl group, and B is a carboxylic acid group or an ester or anhydride thereof, under reaction conditions wherein A reacts with B and forms a linking amide group, while A does not react with A and B does not react with B.

Abstract: A method of sealing at least one gas leak in an engine including the steps of locating at least one gas leak, pre-mixing an alkyl polyether composition and a crosslinking composition to form a dental impression material, or applying the alkyl polyether and crosslinking components to an engine in the vicinity of at least one located gas leak, and repeating the aforementioned steps as many times as neccessary to seal a substantial number of gas leaks in an engine.

Abstract: Systems and methods of producing chemical compounds are disclosed. An example chemical production system includes a combustion chamber having intake ports for entry of a gas mixture. An igniter ignites the gas mixture in the intake chamber to facilitate a reaction at a high temperature and high pressure. A nozzle restricts exit of the ignited gas mixture from the combustion chamber. An expansion chamber cools the ignited gas. The expansion chamber has an exhaust where the cooled gas exits the expansion chamber. A chemical compound product is formed in the expansion chamber.

Abstract: Compositions of and processes for preparing a polyamine-polyamidoamine-epihalohydrin resin generally include reacting a first polyamine, a polyamidoamine, and an epihalohydrin to form the polyamine-polyamidoamine-epihalohydrin (PPAE) resin, wherein the polyamidoamine is prepared by reacting a polycarboxylic acid or a polycarboxylic acid derivative with a second polyamine to form the polyamidoamine, wherein a molar ratio of the polyamine to the polycarboxylic acid is 1.05 to 2.0. The PPAE resin can be used in an adhesive formulation for use in creping applications for forming paper products such as tissue products.

Abstract: The present disclosure provides polyamides and amidoamine curing agents including the reaction product of (1) a modified amine component comprising at least one multifunctional amine of structure 1: wherein R1 is selected from C1-C16 linear, cyclic, and branched alkyl, alkenyl, and alkaryl groups; R2 and R4 are hydrogen, R3 is R1 or hydrogen, X, Y, and Z are independently selected from C2-C10 alkylene, hexylene and cycloalkylene groups, n=0, 1, 2, 3, 4, 5, 6, or 7; and (2) a fatty acid component. Exemplary fatty acid components include at least one of monomer fatty acids, dimer fatty acids, trimer fatty acids, polymer fatty acids, esters of monomer, dimer, trimer, and polymer fatty acids and combinations thereof. The method for making the curing agents and articles formed therefrom are also disclosed.

Abstract: This invention refers to a novel process for the synthesis of polyethylene imine (PEI)-based pigment dispersants characterized by a “grafting from” approach, allowing the manufacture of solvent based dispersant systems. The polyethylene imine (PEI)-based pigment dispersant can be presented by the formula (I) X-(T)m-P-(T)n-H wherein P is a polyethyleneimine (PEI) back-bone; T is a residue —CO-A-O— wherein A is C2-C12 alkylene optionally substituted with C1-C6 alkyl with the proviso that each linkage between P and T is an amide bond and each linkage between X and T is an ester bond, X is a modifier or terminator residue R—CO— wherein R is a linear or branched, saturated or unsaturated alkanecarboxylic acids having from 1 to 22 carbon atoms or an unsaturated fatty acid residue or a hydroxycarboxylic residue or a polyester residue obtained from polycondensation of hydroxycarboxylic acids, or an acid terminated polyether; n, m independently are a number from 1 to 100.

Abstract: One aspect of the present invention relates to the use of a polyamide as a binder for printing inks, wherein the polyamide is a reaction product (P) of (1) one or more compounds which are chosen from the group of primary and/or secondary monoamines and polyamines with (2) a dimer fatty acid and (3) a carboxylic monoacid, with the proviso that the dimer fatty acid (2) building block of (P) contains at least 30% by weight of monomer fatty acid.

Abstract: Cleaning compositions and laundry detergents comprising amphoteric polymers are disclosed. The amphoteric polymers may be comb polymers having polycarboxylate backbones and polyalkoxylate tentacles. In particular, the amphoteric polymer includes: a cationic group structure unit derived from a cationic group-containing monomer; and a carboxyl structure unit derived from a carboxyl group-containing monomer. The cationic group structure unit may be present at a level of 1% to 99% by mass based on 100% by mass of all structure units derived from all monomers in the amphoteric polymer. The carboxyl structure unit may be present at a level of 1% to 99% by mass based on 100% by mass of all the structure units derived from all the monomers in the amphoteric polymer. The cleaning compositions have high anti-soil redeposition ability and solubility with surfactants.

Abstract: The present invention relates generally to substituted polyaniline polymer/copolymer compositions, suitable slats thereof and uses therefore. In one embodiment, the present invention relates to conductive substituted polyaniline polymer/copolymer compositions, suitable slats thereof and uses therefore. In still another embodiment, the present invention relates to self-protonated substituted polyaniline polymer/copolymer compositions, suitable slats thereof and uses therefore. In yet another embodiment, the present invention relates to self-protonated sulfonic acid- or boric acid-substituted polyaniline polymer/copolymer compositions, suitable slats thereof and uses therefore. In still another embodiment, the one or more various polyaniline polymer/copolymer compositions of the present invention are both biodegradable and conducting polymer compositions.

Abstract: Disclosed herein is a method for producing a purified 2-aryl-3,3-bis(4-hydroxyaryl) phthalimidine of formula (I) wherein R1 is hydrogen or a C1-25 hydrocarbyl group and R2 is a hydrogen, a C1-25 hydrocarbyl group, or a halogen, and wherein the method comprises dissolving a crude phthalimidine compound in an aqueous base solution; precipitating the dissolved, crude phthalimidine compound from the aqueous base solution by adding an acid in an amount effective to lower the pH of the solution to 9.0 to 12.0, to provide a semicrude phthalimidine compound; and isolating the semicrude phthalimidine compound from the aqueous base solution, to provide the purified 2-aryl-3,3-bis(4-hydroxyaryl)phthalimidine of formula (I), and having a phenolphthalein compound content of less than 2,500 ppm, based on the weight of the purified 2-aryl-3,3-bis(4-hydroxyaryl)phthalimidine.

Abstract: An electrically conductive polymer obtained by oxidative polymerization of a heterocycle-containing aromatic compound as a monomer, wherein the heterocycle-containing aromatic compound is represented by the formula: A-B. In the above formula, A represents a substituted or unsubstituted thiophene ring group, or a substituted or unsubstituted pyrrole ring group; B represents a substituted or unsubstituted hydrocarbon aromatic ring group, a substituted or unsubstituted thiophene ring group, or a substituted or unsubstituted pyrrole ring group; the ring represented by A and the ring represented by B are directly linked; however, A and B represent structures that are different from each other. The compound can be produced by a coupling reaction using a hypervalent iodine reactant.

Abstract: The present invention provides an amphiphilic molecule having a plurality of zwitterionic functional groups in its hydrophilic moiety and a molecular assembly comprising the amphiphilic molecule as a constituent lipid. The molecular assembly of the present invention forms a stable vesicular structure under a physiological pH environment to carry a substance of interest in the vesicular structure, and can release the substance of interest to the outside of the vesicular structure when it is deformed under an acidic pH environment. The molecular assembly of the present invention can be used as a carrier for a drug, a probe, a nucleic acid, a protein or the like.

Abstract: Disclosed embodiments concern using at least one triazine, typically an amine or polyamine triazine (referred to as amino triazines), in combination with at least one ionomer or ionomer precursor to form compositions useful for making sporting equipment, such as golf ball components. The ionomer or ionomer precursor typically includes plural acid functional groups, such as carboxyl or carboxylate groups, that react or form salts with the amino triazine. Specific examples, without limitation, of suitable amino triazines include guanamine, 6-methyl-1,3,5-triazine-2,4-diamine (acetoguanamine), 6-nonyl-1,3,5-triazine-2,4-diamine (nonylguanamine), 6-phenyl-1,3,5-triazine-2,4-diamine (benzoguanamine) and 2,4,6-triamino-triazine (melamine).