Abstract: A polycarbonate resin having a high refractive index, a low Abbe number and a high moisture and heat resistance is provided. In an embodiment, a polycarbonate resin including a structural unit represented by general formula (1) below is provided.

Abstract: Techniques regarding star polymers with enhanced antimicrobial functionality are provided. For example, a polymer is provided that can comprise a core that can have a singlet oxygen generator and that can generate a singlet oxygen species upon irradiation with light. The polymer can also comprise a plurality of polycarbonate arms covalently bonded to the core. The plurality of polycarbonate arms can be degradable and can comprise a cation. Further, the plurality of polycarbonate arms can have antimicrobial functionality.

Abstract: A one-component thermosetting epoxy resin adhesive, including a) at least one epoxy resin A of formula (II) wherein substituents R? and R? independently of one another are H or CH3 and index s has value of 0-12, fraction of epoxy resin A being from 20-70 wt.-%, based on total weight of one-component thermosetting epoxy resin adhesive; and b) at least one epoxy novolac EN of formula where R2= or CH2, R1=H or methyl and z=0-7, fraction of epoxy novolac EN being from 1-8 wt.-% based on total weight of one-component thermosetting epoxy resin adhesive; and c) at least one latent hardener B for epoxy resins; and d) at least one accelerator C for epoxy resins; and e) at least at least one toughness improver D, fraction of toughness improver D being from 5-40 wt.-%, based on total weight of one-component thermosetting epoxy resin adhesive.

Abstract: Provided is a compound represented by General Formula (1) in General Formula (1), Ar1 and Ar2 independently represent a group selected from the following Formulae,

Abstract: Disclosed herein are a cannabidiol (CBD)-containing bio-based polyurethane composite material and a preparation thereof. The composite material is prepared from a component A and a component B in a weight ratio of 100:(20-50), where the component A includes 40-60 parts by weight of a vegetable oil-based polyol, 35-50 parts by weight of polyether polyol I, 0-10 parts by weight of polyether polyol II, 0.5-5 parts by weight of CBD, 0-5 parts by weight of a natural pigment, 0.5-3 parts by weight of silicon oil, 0-5 parts by weight of a cross-linking agent, 0.2-1 part by weight of a catalyst and 0.8-4 parts by weight of water, and the component B includes 20-50 parts by weight of modified methylene diphenyl diisocyanate (MDI).

Abstract: Provided herein are polymeric ?-hydroxy aldehyde or ?-hydroxy ketone reagents which can be conjugated to amine-containing compounds to form stable conjugates in a single-step reaction. In selected embodiments, the polymeric reagent itself incorporates an internal proton-abstracting (basic) functional group, to promote more efficient reaction. The substituent is appropriately situated, via a linker if necessary, to position the group for proton abstraction, preferably providing a 4- or 5-bond spacing between the abstracting atom and the hydrogen atom on the ?-carbon. Also provided are methods of using the reagents and stable, solubilized conjugates of the reagents with biologically active compounds. In preferred embodiments, the polymeric component of the reagent or conjugate is a polyethylene glycol.

Abstract: Techniques regarding post polymerization modifications to polycarbonate polymers via a flow reactor are provided. For example, one or more embodiments described herein can comprise a cyclic carbonate monomer that can be employed to facilitate polymerization of one or more polycarbonate platforms susceptible to post polymerization modification. For instance, one or more embodiments can regard a cyclic carbonate molecular backbone covalently bonded to an aryl halide functional group via in accordance with a chemical structure selected from the group consisting of: In the chemical structures, “R1” can be selected from the group consisting of a hydrogen atom and a functional group comprising a first alkyl group; “L” can represent a linkage group, comprising: a second alkyl group and an end group having at least one member selected from the group consisting of an oxygen atom and a nitrogen atom; and “A” can represent the aryl halide functional group.

Abstract: A colloidal suspension includes an organic phase and a complex of Formula I as precursor for Ziegler-Natta catalyst synthesis: XTiClp(OR1)4-p.YMg(OR2)q(OR3)t??(I). In Formula I, a molar ratio of X to Y (X/Y) is from 0.2 to 5.0, p is 0 or 1, 0<q<2, 0<t<2, the sum of q and t is 2, R1, R2, and R3 are each independently a linear or branched alkyl, a linear or branched heteroalkyl, a cycloalkyl, a substituted cycloalkyl, a substituted heterocycloalkyl, a substituted aryl, or a (heteroaryl)alkyl; and R2 is not the same as R3.

Abstract: The poly(pro-drug) material includes one or more alternating therapeutic compounds and biodegradable hydrocarbyl groups. The therapeutic compounds and biodegradable hydrocarbyl groups are separated by cleavable linker compounds. The therapeutic compounds, such as estrogen, curcumin, and fingolimod, include a plurality of substitutable functional groups that provide reaction sites for complexing with the cleavable linkers and in turn one or more polymers, such that the poly(pro-drug) material ends up composed of the therapeutic compound itself. In aqueous media and at physiological temperature and pH, the poly(pro-drug) materials degrade to release the therapeutic compounds from the material with a zero-order release profile. Advantageously, the poly(pro-drug) materials release the therapeutic compounds on time scales of years. The poly(pro-drug) materials also exhibit reduced to allow for prolonged implantation within a patient.

Abstract: Four conjugated copolymers with a donor/acceptor architecture including 4,4-dihexadecyl-4H-cyclopenta[1,2-b:5,4-b?]dithiophene as the donor structural unit and benzo[2,1,3]thiodiazole fragments with varying degrees of fluorination have been synthesized and characterized. It has been shown that the HOMO levels were decreased after the fluorine substitution. The field-effect charge carrier mobility was similar for all polymers with less than an order of magnitude difference between different acceptor units.

Abstract: A polycarbonate resin composition of the present invention comprises: a polycarbonate resin; and a polycarbonate polyol comprising a terminal hydroxyl group and a repeat unit represented by Formula 1. The polycarbonate resin composition exhibits good properties in terms of color, impact resistance, stiffness and the like even after irradiation with ionizing radiation.

Abstract: The present invention provides silicon-based polycarbonates, processes for their preparation and their use in the synthesis of copolymers, in particular segmented copolymers such as polyurethanes for biomedical applications.

Abstract: Provided is a method capable of producing a retardation film having an elongated shape and having a slow axis in an oblique direction with high production efficiency while precisely controlling the direction of the slow axis and the variation of the direction. The method of producing a retardation film of the present invention includes: holding the left and right end portions of a film with left and right variable pitch-type clips configured to have clip pitches changing in a longitudinal direction, respectively; preheating the film; obliquely stretching the film; and releasing the clips holding the film.

Abstract: Polymers, co-polymers, and monomers using CO2 as a reagent and methods of production thereof are described. Polymerization methods include converting CO2 into a polymerizable monomer by exciting the CO2 with a light source.

Abstract: Provided is a method capable of producing a retardation film suppressed in biaxiality, having a small Nz coefficient, and having a slow axis in an oblique direction with high production efficiency. The production method for a retardation film of the present invention includes: holding left and right side edge portions of a film to be stretched with left and right variable pitch-type clips configured to have clip pitches changing in a longitudinal direction, respectively; preheating the film; reducing, under a state in which a position at which the clip pitch of the clips on one side out of the left and right clips starts to reduce and a position at which the clip pitch of the clips on another side starts to reduce are set to different positions in the longitudinal direction, the clip pitch of each of the clips to a predetermined pitch to subject the film to oblique stretching; and releasing the clips holding the film.

Abstract: The present invention relates to an alkoxysilane-terminated prepolymer, characterized in that it is obtainable by reaction of at least A) a polyol, B) a compound having two or more isocyanate groups, and C) an alkoxysilane having at least an isocyanate group and/or an isocyanate-reactive group, wherein the polyol A) comprises at least a polyethercarbonatepolyol obtainable by addition of carbon dioxide and alkylene oxides onto H-functional starter molecules. The present invention further relates to a process for preparing the alkoxysilane-terminated prepolymer of the present invention and also to a composition and a multicomponent system comprising an alkoxysilane-terminated prepolymer of the present invention. The present invention further relates to a shaped article obtainable by polymerizing the alkoxysilane-terminated prepolymer of the present invention, by polymerizing a composition of the present invention or by polymerizing a multicomponent system of the present invention.

Abstract: The present invention provides a method capable of producing a retardation film having an elongated shape, having high uniaxiality and a high in-plane alignment property, and having a slow axis in an oblique direction with high production efficiency.

Abstract: A conjugated polymer-based optoelectronic material includes: an optoelectronic conjugated polymer having a main chain and side chains; and an organic diluent which is at least partially miscible with the conjugated polymer. Molecules of the organic diluent physically react with the side chains of the conjugated polymer to form hydrogen bonds therebetween, thereby generating molecular constraints in the conjugated polymer to suppress molecular deformation of the conjugated polymer that occurs soon after the conjugated polymer is excited.

Abstract: Described is a high solids coating composition having exceptional rheological properties and appearances comprising (a) a thermosetting binder, (b) from about 0.1 to about 10 wt. % based on binder solids of solid polyurea particles prepared by the reaction of a mixture of a polyisocyanate and an amino reactant comprising a primary or secondary monoamine that optionally has a hydroxyl or ether group or both, and (c) from about 2 to about 25 wt. % on resin solids of an acrylic polymer having a number average molecular weight of from about 2000 to about 8000 and a glass transition temperature of from about 50 to about 120° C.

Abstract: Embodiments of the invention provide for methods of producing a polycarbonate polyol. The method includes charging a vessel with butanediol, charging the vessel with a polymerization catalyst, and adding to the vessel dimethyl carbonate at a rate of at least 2.0 g of DMC per minute per kg of BDO to produce polycarbonate polyol at a polycarbonate polyol yield of at least 80% of a theoretical yield.

Abstract: The invention provides polycarbonate resins which are excellent in terms of light resistance, transparency, hue, heat resistance, thermal stability, and mechanical strength. The invention relates to a polycarbonate resin composition containing: a polycarbonate resin at least containing structural units derived from a dihydroxy compound having the portion represented by the following formula (1) as part of the structure thereof; and a bluing agent. The invention further relates to a polycarbonate resin composition including: a polycarbonate resin (A) containing structural units derived from a dihydroxy compound represented by the following formula (2) as part of the structure thereof; and a bluing agent. CH2—O??(1) The case where the portion represented by the general formula (1) constitutes —CH2—O—H is excluded.

Abstract: The present invention relates to a process for preparing branched polyethers and/or polyether-like structures, to these branched polyethers themselves, and to their use.

Abstract: A photoconductor that includes, for example, a supporting substrate, an optional anticurl layer, an optional ground plane layer, an optional hole blocking layer, an optional adhesive layer, a photogenerating layer, a charge transport layer, and an optional protective coating, and where the photogenerating layer contains a polyarylatecarbonate.

Abstract: The present invention discloses new catalyst systems based on complexes of divalent metals supported by chelating phenoxy ligands for immortal ring-opening polymerisation of cyclic esters and cyclic carbonates.

Abstract: A process for manufacturing a polycarbonate, having a glass transition temperature greater than or equal to 50° C., includes: a step (1) of introducing into a reactor a monomer of formula (I) and R1 and R2 being identical or different alkyl groups; a step (2) of introducing into the reactor at least one cyclic diol or a mixture of diols (B) including at least 20 mol % of cyclic diols; a subsequent step (3) of polycondensation via transesterification of the mixture of monomers including the monomers (A) and (B); a step (4) of recovering the polycarbonate formed during step (3).

Abstract: A polymer production apparatus, including: supplying unit containing first supplying unit to supply raw materials containing monomer, and second supplying unit to supply compressive fluid; contacting unit to bring the monomer and the compressive fluid into contact together; and outlet configured to discharge reaction product of the monomer, wherein reaction unit is provided between the contacting unit and the outlet, where the reaction unit is to pass the monomer from the contacting unit side to the outlet side, while allowing the monomer to carry out a polymerization reaction in the presence of the compressive fluid, and wherein the reaction unit contains circulation unit containing first pipe and second pipe, where a fluid is passed through the first pipe from the contacting unit side to the outlet side, and the second pipe is to return the fluid from return port provided upstream extrusion unit to inlet provided upstream the return port.

Abstract: The present invention provides polycarbonate polyol compositions with improved characteristics. Such polycarbonate polyol compositions are useful in thermosetting applications for the production of coatings for consumer products.

Abstract: A process for the preparation of polyesters or polycarbonates including (i) the provision of cyclic esters or cyclic carbonates, (ii) polymerizing by ring-opening in the presence of a betaine based metal-free catalyst showing formula ?X—R1—Y+(R2)3 wherein X is S, O or Se, Y is N or P, R1 is linear or cyclic alkyl or aryl, and R2 is linear or cyclic alkyl. and under polymerizing conditions in the presence of an alcohol or amine based initiator.

Abstract: A polymer of sulfonated poly(arylene ether)s (PAEs) and a manufacturing method thereof are provided. A main structure of the PAEs has a first side formed by multi-phenyl glycol monomer and a second side formed by multi-phenyl dihalo monomer with an electron-withdrawing group. The glycol monomer and the dihalo monomer are reacted with each other by a nucleophilic displacement reaction, so as to form the main structure of the PAEs. A film made of the PAEs has a better size stability under a high water uptake.

Abstract: Embodiments of the invention are directed to Ge comprising heterocyclic compounds which can be used for the preparation of homopolymers and copolymers. The copolymers can be donor-acceptor (DA) alternating copolymers where the donor unit is a Ge comprising heterocyclic unit. The polymers can be used as materials in solar cells and other photovoltaic devices, transistors, diodes, light emitting devices (LEDs), conductors, supercapacitors, batteries, and electrochromic devices.

Abstract: A process to produce polycarbamate comprising providing urea in liquid form; and adding the urea in liquid form to a polyol in a reduced gradient profile to form polycarbamate product is provided. Also provided are: (a) a reaction product of the process and (b) an apparatus for operating the process.

Abstract: A n-type ladder copolymer including, a n-type ladder copolymer formed with alternating perylene and pyridine units having chemical structure A having two end groups, where perylene units having at least one solubilizing group attaching at position(s) 1, 6, 7, and/or 12, where R1, R2, R3, and R4 solubilizing group(s) are each independently selected from the group consisting of aryl, alkyl aryl, alkoxy aryl, and aryloxy aryl, and where n repeat units ranging from about 4 to about 400

Abstract: A copolycarbonate having a low water absorption coefficient and excellent heat resistance, low temperature characteristics and surface hardness. The copolycarbonate (Z) of the present invention contains a unit (A) represented by the following formula and a unit (B) represented by the following formula (B) as main recurring units, the (A/Bn=1) molar ratio of the unit (A) and the unit (Bn=1) being 40/60 to 99/1. The unit (Bn=1) is a single unit constituting a block. (R1) is an alkylene group or cycloalkylene group, all of which may be substituted by an aromatic group having 6 to 12 carbon atoms. R2 is an alkylene group, cycloalkylene group or arylene group, all of which may be substituted by an aromatic group having 6 to 12 carbon atoms. “r” and “s” are each independently an integer of 0 to 4 “l” is 0 or 1. “m” is 0 or 1. “n” is an integer of 1 to 100.

Abstract: A fuel cell catalyst layer having sulfonated poly(arylene ether)s and a manufacturing method therefor are provided. The manufacturing method includes steps of: providing at least one type of sulfonated poly(arylene ether)s; mixing the sulfonated poly(arylene ether)s with a catalyst composition to prepare a catalyst slurry; and coating the catalyst slurry to form a film which is dried to be an electrode catalyst layer, in which the weight ratio of the sulfonated poly(arylene ether)s is 5-50 wt %. The sulfonated poly(arylene ether)s in the electrode catalyst layer can provide good thermal stability, glass transition temperature, chemical resistance, mechanical properties, water impermeability, low proton transmission loss, and a relatively simple process to shorten the manufacturing time and lower the cost thereof.

Abstract: An organic semiconductor compound may be represented by the above Chemical Formula 1 or Chemical Formula 2, and an organic thin film may include the organic semiconductor compound according to Chemical Formula 1 or 2.

Abstract: A method of producing a molded article by melting a granule at a temperature of 280 to 380° C. and molding it, wherein the granule satisfies the following conditions (I) and (II): (I) when 100 parts by weight of the granule is cleaned with 100 parts by weight of a 1N nitric acid aqueous solution, the amount of an Fe compound eluted into the 1N nitric acid aqueous solution cleaning fluid is 1 to 100 ppb in terms of the Fe atom based on the granule; and (II) the granule comprises (A) 100 parts by weight of a polycarbonate resin (component a) and (B) 0.00010 to 0.5 parts by weight of a specific phosphorous-based compound (component b).

Abstract: The invention is a thermosetting coating composition comprised of an aliphatic polycarbonate resin and a cross linker. The aliphatic polycarbonate resins are derived from hydroxyl containing compounds including 2,2,4,4-tetramethyl-1,3-cyclobutanediol (TMCD) and 1,4-cyclohexane dimethanol (CHDM). The coatings made of these polycarbonates exhibit exceptional toughness; they possess a high degree of hardness while maintaining a high level of flexibility/impact resistance. These polycarbonate resins also exhibited better hydrolytic stability as compared to their polyester counterparts.

Abstract: Disclosed herein is a primer composition comprising an inorganic UV absorbing agent and a polymer selected from (i) a copolycarbonate, and (ii) a polyurethane obtained by reaction of a polyisocyanate and a copolycarbonate diol. Also disclosed is a coated article comprising a polymeric substrate, a primer layer disposed on at least one surface of said substrate, and an abrasion-resistant layer disposed on said primer layer, where the primer layer is made from the primer composition of the invention.

Abstract: Disclosed is a curable coating agent composition which exhibits excellent wear resistance and weather resistance when applied as a coating agent to plastic or other substrates to be used outdoors. The curable coating agent composition comprises 95 to 65 parts by mass of a component (A) comprising an urethane adduct compound having weather resistance, 5 to 35 parts by mass of a component (B) comprising a specific organosilicon compound, 0.1 to 10 parts by mass of a component (C) which is a radical polymerization initiator, 1 to 12 parts by mass of a component (D) which is an ultraviolet ray absorber, and 10 to 1,000 parts by mass of a component (E) which is an organic solvent, with respect to 100 parts by mass of the components (A) and (B) in total.

Abstract: Embodiments of the invention provide for methods of producing a polycarbonate polyol. The method includes charging a vessel with butanediol, charging the vessel with a polymerization catalyst, and adding to the vessel dimethyl carbonate at a rate of at least 2.0 g of DMC per minute per kg of BDO to produce polycarbonate polyol at a polycarbonate polyol yield of at least 80% of a theoretical yield.

Abstract: The present invention relates to biodegradable polymer mixtures comprising i) 40% to 95% by weight, based on the total weight of components i to ii, of at least one polyester based on aliphatic or aliphatic and aromatic dicarboxylic acids and aliphatic dihydroxy compounds; ii) 5% to 60% by weight, based on the total weight of said components i to ii, of polyalkylene carbonate, particularly polypropylene carbonate; iii) 0% to 60% by weight, based on the total weight of said components i to iii, of at least one biodegradable homo- or copolyester selected from the group consisting of polylactic acid, polycaprolactone and polyhydroxyalkanoate, and/or of an inorganic or organic filler; iv) 0% to 10% by weight, based on the total weight of said components i to ii, of an epoxy-containing copolymer based on styrene, acrylic ester and/or methacrylic ester, and v) 0% to 15% by weight of an additive selected from the group consisting of lubricant, antiblocking agent, antistat, UV absorber, UV stabilizer, thermal stabil

Abstract: Disclosed is a polymerization fluid for electropolymerization which exhibits a reduced environmental burden and excellent economic efficiency and which can yield a conductive polymer film that has high conductivity and that is dense and highly transparent. The polymerization fluid includes at least one monomer selected from the group consisting of 3,4-disubstituted thiophenes which is dispersed as oil drops in surfactant-free water, and the polymerization fluid is transparent.

Abstract: An intermediate transfer member that includes a terpene polycarbonate, an optional polysiloxane, and an optional conductive filler component.

Abstract: The present invention pertains to copolymers having one or more polyisobutylene segments and one or more biodegradable polymer segments, to methods of making such copolymers, to medical articles that contain such copolymers, and to methods of making such medical articles. According to certain aspects of the invention, copolymers are provided, which comprise a plurality of polyisobutylene segments and a plurality of biodegradable polymer segments. According to certain aspects of the invention, copolymers are provided, which comprise urethane linkages, urea linkages, amide linkages, ester linkages, anhydride linkages, carbonate linkages, linkages commonly described as “click” chemistry linkages, and combinations of two or more types of such linkages.

Abstract: The present invention is a production method of a polycarbonate resin, including a step of performing melt polycondensation by continuously feeding a dihydroxy compound (A) having a predetermined moiety in a part of the structure and a carbonic acid diester each in a liquid state to a reactor, wherein the residence time from liquefaction of the dihydroxy compound to its feeding to a reactor is from 0.1 to 10 hours.

Abstract: Hyperbranched polycarbonates having stabilizing groups, prepared by reaction of (a) at least one compound having at least three alcoholic hydroxyl groups per molecule with (b) at least one reagent of the general formula I (c) and at least one reagent of the general formula X3-(A1)m-X4, where the variables are defined as follows: X1, X2 are identical or different and are selected from among halogen, C1-C10-alkoxy, C6-C10-aryloxy and O—C(?O)-halogen, X3 is a functional group selected from among OH, SH, NH2, NH—C1-C4-alkyl, isocyanate, epoxy, COOH, COOR12, C(?O)—O—C(?O), C(?O)—Cl, R12 is C1-C4-alkyl or C6-C10-aryl, A1 is a spacer or a single bond, m is zero or one. X4 is a group selected from among phenol groups, benzophenones, aromatic amines and nitrogen-comprising heterocycles, in each case substituted or unsubstituted.

Abstract: An object of the present invention is to provide a polycarbonate resin composition comprising a polycarbonate resin containing, as a raw material, isosorbide that is easy to produce and excellent in such as mechanical properties, etc., and a molded body, particularly a foam-molded body, composed of the resin composition. The present invention provides a foam-molded body of a resin composition containing a polycarbonate resin having at least a structural unit derived from a dihydroxy compound represented by the following formula (1): wherein the strain-hardening factor of uniaxial extensional viscosity of said resin composition is from 0.1 to 5.

Abstract: A polycarbonate resin which is excellent in heat resistance, boiling water resistance and surface hardness and has a low water absorption coefficient. The polycarbonate resin comprises a unit (A) represented by the following formula and a unit (B) represented by the following formula as main recurring units, wherein the molar ratio (A/B) of the unit (A) to the unit (B) is 30/70 to 99/1. (In the above formula, X is an alkylene group having 3 to 20 carbon atoms or cycloalkylene group having 3 to 20 carbon atoms, R is an alkyl group having 1 to 20 carbon atoms or cycloalkyl group having 3 to 20 carbon atoms, and “m” is an integer of 1 to 10.

Abstract: The present invention relates to a polycarbonate resin composition, comprising: a polycarbonate resin containing a structural unit derived from a dihydroxy compound having a moiety represented by the following formula (1) [provided that a case where the moiety represented by formula (1) is a moiety constituting —CH2—O—H is excluded]; and an elastomer composed of a core•shell structure, wherein a core layer of the elastomer is at least one member selected from the group consisting of an alkyl (meth)acrylate and a (meth)acrylic acid, and a polycarbonate resin molded article obtained by molding the polycarbonate resin composition: CH2—O??(1).

Abstract: The present invention relates to a polycarbonate resin composition, comprising: a polycarbonate resin containing a structural unit derived from a dihydroxy compound having a moiety represented by the following formula (1) [provided that a case where the moiety represented by formula (1) is a moiety constituting —CH2—O—H is excluded]; and an elastomer composed of a core?shell structure, wherein a core layer of the elastomer is composed of a butadiene-styrene copolymer, and a polycarbonate resin molded article obtained by molding the polycarbonate resin composition: CH2—O??(1).