Abstract: Process for curing a thermoset resin comprising the step of contacting said resin with (i) one or more imines of the structure Formula (I), wherein —y=0 or 1, z=1-4, and y+z?2, —X is independently selected from O, S, P, NH, N—R1, and N—OH, —R1 is selected from linear or branched, cyclic, bi-cyclic, or tri-cyclic alkylene groups with 2-18 carbon atoms, arylene groups with 6-12 carbon atoms, and aralkylene groups with 2-18 carbon atoms, —R2-R5 are individually selected from hydrogen, linear or branched alkyl groups having 1-18 carbon atoms, cycloalkyl groups having 3-12 carbon atoms, aryl groups having 6-12 carbon atoms, aralkyl groups having 6-18 carbon atoms, alkoxy groups having 1-6 carbon atoms, and aryloxy groups; —each of said R-groups may optionally be substituted with O, S, Si, P, or N-containing substituents, —R4 and R5; R3 and R4; R2, R5 and R1 and R3 may optionally form ring, and (ii) a peroxide.

Abstract: An unsaturated polyester resin composition comprising an unsaturated polyester, an acetoacetate functional monomer; a multifunctional di- or tri-acrylate monomer; and an allyl ether-functional monomer/oligomer, wherein the resin composition is substantially free of styrene.

Abstract: The object of a present invention is an alkyd resin as well as the method for preparing such a resin, said alkyd resin comprising: a preferably biosourced, polyacid component or its preferably biosourced acid anhydride; a first polyol component, preferably biosourced, having at least two hydroxyl groups; a second biosourced polyol component having at least one 1,4:3,6-dianhydrohexitol unit; and a component based on biosourced oil or its corresponding biosourced fatty acid.

Abstract: An initiator composition, including: at least two compounds represented by the chemical formula of R—CO—O—O—CO—R and a compound represented by the chemical formula of R1—CO—O—O—R2, where R represents a C2-C12 alkyl or a C6-C10 aryl or substituted aryl, R1 represents a C1-C10 alkyl or a C6-C10 aryl, and R2 represents a C1-C10 alkyl.

Abstract: A process for preparing a high molecular weight heteraromatic polyester or copolyester is disclosed. A process for preparing a high molecular weight heteroaromatic polyester or copolyester includes the steps of: (a) processing comonomers by mixing together to form a homogeneous solution (1) at least one heteroaromatic dicarboxylic acid having 2-12 carbon atoms or a diester or an acid anhydride derived therefrom, or a mixture thereof; (2) at least one alcohol having 2 to 12 carbon atoms and at least two hydroxyl functionalities; and (3) optionally aromatic or aliphatic dicarboxylic acids or diesters or acid anhydrides derived therefrom; (b) converting the paste/solution obtained in step a) into an esterification product containing at least one diester or at least one oligoester formed from the at least one heteroaromatic dicarboxylic acid and the at least one alcohol; and (c) polycondensing/copolycondensing the reaction product obtained from step b) under reduced pressure.

Abstract: Branched polyesters with sulfonate groups can be obtained by reacting components A, B, optionally C, and optionally D to yield branched polyesters, then reacting these branched polyesters with hydrogen sulfite. Component A is at least one ?,?-olefinically unsaturated dicarboxylic acid, component B is at least one di- or higher-functional alcohol, optional component C is at least one di- or higher-functional carboxylic acid or hydroxycarboxylic acid without an ?,?-olefinically unsaturated bond, and optional component D is at least one compound of formula CH3(—O—CH2—CH2)n—OH. In reacting the branched polyesters with hydrogen sulfite, a molar amount of hydrogen sulfite is at most 95 mol %, based on an amount of ?,?-olefinically unsaturated dicarboxylic acid.

Abstract: A fluorooxyalkylene group-containing polymer composition including a liner fluorooxyalkylene group-containing polymer represented by the formula (1) which has a hydrolysable group at a terminal and is hereinafter called “one-terminal modified polymer”, and a liner fluorooxyalkylene group-containing polymer represented by the following formula (2) which has hydrolysable groups at the both terminals and is hereinafter called “both-terminal modified polymer”, wherein an amount of the both-terminal modified polymer is 0.1 mole % or more and less than 10 mole %, relative to a total mole of the one-terminal modified polymer and the both-terminal modified polymer.

Abstract: The invention relates to a hybrid resin, which is suitable in particular for impregnating paper webs. The hybrid resin according to the invention can be advantageously used for improving the mechanical properties of counteracting layers in multilayer boards.

Abstract: Branched polyesters with sulfonate groups obtainable by the reaction of the components A, B, optionally C and optionally D to give branched polyesters, where the component A is selected from the group of ?,?-olefinically unsaturated dicarboxylic acids, and the component B is selected from the group of tri- or higher-functional alcohols, the optional component C is selected from the group of difunctional alcohols or of difunctional carboxylic acids without ?,?-olefinically unsaturated bonds, the optional component D is selected from fatty acids or fatty alcohols, and the subsequent reaction of the resulting branched polyesters with hydrogen sulfite, where the molar amount of hydrogen sulfite is at most 95 mol %, based on the amount of ?,?-olefinically unsaturated dicarboxylic acid.

Abstract: Binder compositions and methods for making and using same are provided. In at least one specific embodiment, the binder composition can include at least one unsaturated compound having two or more unsaturated carbon-carbon bonds and at least one free radical precursor. At least one of the unsaturated carbon-carbon bonds can be a pi-bond that is not conjugated with an aromatic moiety and can be capable of free radical addition. The free radical precursor can be present in an amount of about 7 wt % to about 99 wt %, based on the weight of the one or more unsaturated compounds.

Abstract: The invention relates to a heat curable composition for fire-resistant or intumescent composite parts, which is free of any halogen additive or halogen structure in the components thereof, and which comprises: a) 100 parts by weight of a dry resin, including a1) an unsaturated polyester having an acid index lower than 10 and/or a2) a vinyl ester; b) 40 to 200 parts by weight of a reactive thinner among ethylenically unsaturated monomers; c) 20 to 110 parts by weight of a thermal expansion agent selected from melamine and derivatives thereof, guanidine, glycine, urea, triisiocynurates, and azodicarbinamide; d) 0 to 250 parts by weight of aluminium trihydrate; e) 10 to 80 parts by weight of a carbonisation precursor agent selected from multifunctional polyols; f) 50 to 200 parts by weight of a compound selected from a phosphorus derivative and/or a boric acid derivative; g) optionally at least one metal oxide; h) optionally other additives and fillers; i) optionally reinforcements containing natural or syntheti

Abstract: Solution suitable for accelerating the cure of a curable resin using a peroxide, said accelerator solution comprising (i) at least one organic solvent, (ii) a manganese salt, a copper salt, or a combination thereof, and (iii) an iron complex of a tetradentate, pentadentate or hexadentate nitrogen donor ligand.

Abstract: A shape-memory polymers comprising at least one monomer subunit represented by the following structural formula (1).

Abstract: An air drying auto-oxidisable resin composition comprising components: a) a drier comprising a manganese carboxylate complex, and b) a polymer comprising unsaturated fatty acid residues, wherein the manganese carboxylate complex a) has the following structure I: wherein R1?H, C1-C20 alkyl optionally substituted with heteroatoms, or C6-C20 aryl optionally substituted with heteroatoms; X and Y are independently selected from O and OC(R3)O, in which a=4 when X?O, and a=3 when X?OC(R3)O, and in which b=4 when Y?O, and b=3 when Y?OC(R3)O; R2=C1-C20 alkyl optionally substituted with heteroatoms, C6-C20 aryl optionally substituted with heteroatoms, or a polymeric residue; and R3?C1-C20 alkyl optionally substituted with heteroatoms, C6-C20 aryl optionally substituted with heteroatoms, or a polymeric residue.

Abstract: Described are polyesters comprising (a) a dicarboxylic acid component comprising 2,5-furandicarboxylic acid residues; optionally, aromatic dicarboxylic acid residues and/or modifying aliphatic dicarboxylic acid residues and ethylene glycol residues. The polyesters may be manufactured into articles such as fibers, films, bottles, coatings, or sheets.

Abstract: Described are polyesters comprising (a) a dicarboxylic acid component comprising 2,5-furandicarboxylic acid residues; optionally, aromatic dicarboxylic acid residues and/or modifying aliphatic dicarboxylic acid residues, 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues and ethylene glycol. The polyesters may be manufactured into articles such as fibers, films, bottles, coatings, or sheets.

Abstract: Branched polyesters with sulfonate groups obtainable by the reaction of the components A, B, optionally C and optionally D to give branched polyesters, where the component A is selected from the group of ?,?-olefinically unsaturated dicarboxylic acids, and the component B is selected from the group of tri- or higher-functional alcohols, the optional component C is selected from the group of difunctional alcohols or of difunctional carboxylic acids without ?,?-olefinically unsaturated bonds, the optional component D is selected from fatty acids or fatty alcohols, and the subsequent reaction of the resulting branched polyesters with hydrogen sulfite, where the molar amount of hydrogen sulfite is at most 95 mol %, based on the amount of ?,?-olefinically unsaturated dicarboxylic acid.

Abstract: Branched polyesters with sulfonate groups can be obtained by reacting components A, B, optionally C, and optionally D to yield branched polyesters, then reacting these branched polyesters with hydrogen sulfite. Component A is at least one ?,?-olefinically unsaturated dicarboxylic acid, component B is at least one di- or higher-functional alcohol, optional component C is at least one di- or higher-functional carboxylic acid or hydroxycarboxylic acid without an ?,?-olefinically unsaturated bond, and optional component D is at least one compound of formula CH3(—O—CH2—CH2)n—OH. In reacting the branched polyesters with hydrogen sulfite, a molar amount of hydrogen sulfite is at most 95 mol %, based on an amount of ?,?-olefinically unsaturated dicarboxylic acid.

Abstract: The present disclosure provides processes for the preparation of unsaturated polyesters. In embodiments, a process of the present disclosure includes reacting an organic diol with a cyclic alkylene carbonate in the presence of a first catalyst to thereby form a polyalkoxy diol, optionally adding thereto a further amount of cyclic alkylene carbonate in the presence of a second catalyst, and subsequently polycondensing the resulting mixture with a dicarboxylic acid in combination with an anhydride.

Abstract: A coating composition including an unsaturated resin selected from polyesters, alkyds or combinations thereof; an alkoxy (meth)acrylic functional monomer, and a thermoplastic compound containing active hydrogen groups; a curing agent; and a curing promoter such as at least one metal drier.

Abstract: The present invention relates to a process for preparing an unsaturated polyester resin comprising itaconate ester units as reactive unsaturations by reacting at least itaconic acid and/or itaconic anhydride and at least one diol, wherein the process is effected in the presence of an inhibitor having a gelation activity factor less than or equal to (0.5) and having an efficiency factor of from (0.55) up to 1.

Abstract: The present invention relates to an unsaturated polyester resin comprising itaconate ester units as reactive unsaturation, wherein the resin comprises itaconate, citraconate and mesaconate ester units. Preferably, the resin comprises itaconate, citraconate and mesaconate ester units in an amount of from 40 to 90 mol % itaconate, from 2 to 30 mol % citraconate and from 5 to 40 mol % mesaconate in which 100 mol % is the total amount of itaconate, citraconate and mesaconate esters units.

Abstract: This disclosure relates to catalysts for the auto-oxidative drying of polymers, in particular for polymers used in paints or inks, based on unsaturated fatty acids, mostly from vegetal origin A compound is divulged for use as a polymerisation agent in coatings, characterized in that it comprises a cobalt-bearing alkyd polymer, said polymer having a cobalt content of 0.5 to 6% by weight, a mean molecular weight of more than 3000, and comprising cobalt carboxylate sequences Several processes are presented to illustrate the synthesis of the cobalt-bearing polymer These polymers retain the catalytic effect of cobalt towards the drying of polymers, while they greatly suppress the toxicity of cobalt by being essentially insoluble in water.

Abstract: Methods of making unsaturated polyester compositions are provided and include reacting: (i) plant and animal oil triglycerides, an alkyl ester of a saturated or unsaturated fatty acid or mixtures thereof; (ii) a difunctional, or polyfunctional glycol or mixtures thereof; (iii) a difunctional or polyfunctional acid, their anhydrides or alkyl esters and mixtures thereof; (iv) a strained cycloolefin; (v) a component(s) that function as a compound capable of initiating polymerization at high temperature and which is stable at room temperature; and (vi) low profile additives, fillers and reinforcements.

Abstract: A method of making an aliphatic polyester prepolymer, comprising: reacting, alone or in combination with other reactants, a diol with at least a first diacid (or a diester of said first diacid) to produce an aliphatic polyester prepolymer. The first diacid is preferably a trans-beta-hydromuconic acid (HMA). In some embodiments, the diol contains at least one ether linkage. In some embodiments the diol is further reacted with at a second diacid, or a diester of said second diacid, wherein said second diacid is different from said first diacid. Prepolymers produced from such processes and articles formed therefrom are also described.

Abstract: A golf ball having a polymer layer that has been subjected to impregnation treatment with an isocyanate and/or isothiocyanate-containing olefin compound exhibits at least one improved golf ball attribute, such as scuff resistance or spin performance, compared with an original golf ball that has not been treated by impregnation.

Abstract: A polyester resin for a toner, obtained by polycondensing a carboxylic acid component and an alcohol component, wherein the carboxylic acid component and/or the alcohol component contains an aromatic compound represented by the formula (Ia): wherein R1a is a hydrogen atom, a hydroxyl group, or a methoxy group; and Xa is a hydrogen atom, an aldehyde group, an allyl group, a vinyl group, a methoxy group, or a hydroxyl group or carboxyl group which may have a linking group. The toner for electrophotography containing a polyester resin for a toner of the present invention is suitably used for a resin binder of a toner used in developing and the like of latent images formed in electrophotography, electrostatic recording method, electrostatic printing method or the like.

Abstract: The present invention relates to a two-component composition comprising a first component and a second component, wherein the first component being a non-aqueous resin composition comprising an unsaturated polyester resin or vinyl ester resin, a transition metal compound selected from a copper, iron, manganese or titanium compound, a potassium compound, and the resin composition contains less than 0.01 mmol cobalt per kg primary resin system and less than 0.01 mmol vanadium per kg primary resin system; and the second component comprises a peroxide compound.

Abstract: Among other aspects, provided herein are multi-armed polymer conjugates comprising an alkanoate-linker, compositions comprising such conjugates, and related methods of making and administering the same. Methods of treatment employing such conjugates and related uses are also provided. The conjugates are prepared with high drug loading efficiencies.

Abstract: Unsaturated polyester compositions are disclosed that are obtainable by reacting: (i) plant and animal oil triglycerides, an alkyl ester of a saturated or unsaturated fatty acid or mixtures thereof; (ii) a difunctional, or polyfunctional glycol or mixtures thereof; (iii) a difunctional or polyfunctional acid, their anhydrides or alkyl esters and mixtures thereof; (iv) a strained cycloolefin; (v) a component(s) that function as a compound capable of initiating polymerization at high temperature and which is stable at room temperature; and (vi) low profile additives, fillers, and reinforcements. Also disclosed are methods for the preparation of the polyesters and the use of the polyesters in closed and open mold compositions such as sheet molding compound (SMC), bulk molding compounding (BMC), resin transfer molding (RTM), pultrusion, infusion, filament winding, and spray up.

Abstract: There are disclosed a silicone rubber based pressure sensitive adhesive sheet comprising a transparent substrate film and a silicone rubber layer which is formed by coating the surface of the transparent substrate film with silicone rubber in an amount of 5 to 100 g/m2 (after drying) containing addition type organopolysiloxane composed of organopolysiloxane having a siloxane bond as a principal skeleton and bearing an alkenyl group and of organohydrogenpolysiloxane, the silicone rubber further containing 0.01 to 3.0 parts by mass of a platinum catalyst based on 100 parts by mass of the addition type organopolysiloxane, and then by curing the resultant coating, and which has adhesion for float glass in accordance with JIS Z 0237 being in the range of 10 to 1000 mN/25 mm, holding power (load of one kg) of at least 24 hours and a 100% modulus in the range of 0.3 to 1.5 MPa.

Abstract: A coating composition including an unsaturated resin selected from polyesters, alkyds or combinations thereof; an alkoxy(meth)acrylic functional monomer, and a thermoplastic compound containing active hydrogen groups; a curing agent; and a curing promoter such as at least one metal drier.

Abstract: The invention relates to a new modified polyacrylate comprising fluorinated oxetane (FOX) polymer units functionalized with an unsaturated dicarboxylic acid and siloxane units and to its use as slip- and leveling agent and anti-cratering agent for a variety of applications. Thus, the invention relates to a slip- and leveling agent characterized in that it comprises a copolymer which is obtained by copolymerizing A at least one unit of a fluorinated oxetane polymer functionalized with an unsaturated dicarboxylic acid; B at least one terminal reactive polysiloxane unit; C at least one alkyl(meth)acrylate unit or cycloalkyl(meth)acrylate unit and/or (meth)acrylic acid and/or other units originating from vinylic compounds that can form radicals.

Abstract: The invention relates to a slip- and leveling agent characterized in that it comprises a copolymer which is obtained by copolymerizing A. at least one unit of a mono- or di perfluoroester of an unsaturated dicarboxylic-acid; B. at least one terminal reactive polysiloxane unit; C. at least one alkyl(meth)acrylate unit or cycloalkyl(meth)acrylate unit and/or (meth)acrylic acid and/or other units originating from vinylic compounds that can form radicals.

Abstract: Biodegradable poly(ester-amides) are synthesized from amino acids, diols and dicarboxylic acids where one or both of the diols and dicarboxylic acids contain unsaturation; e.g., from di-p-nitrophenyl dicarboxylates and p-toluenesulfonic acid salts of bis(alpha-amino acid) disesters of diols where one or both of the dicarboxylate and diol moieties contain unsaturation or from di-p-nitrophenyl dicarboxylates, and p-toluene-sulfonic acid salts of bis(alpha-amino acid) diesters of diols and p-toluenesulfonic acid salt of lysine ester where one or both of the dicarboxylate and diol moieties contain unsaturation. The polymers are useful as biodegradable carriers for drugs of other bioactive agents.

Abstract: A bioderived plasticizer for biopolymers includes a compatibilizing unit and a polyester plasticizing unit. The plasticizer improves the flexibility of biopolymers while not adversely affecting their modulus. The compatibilizing unit renders the plasticizer more miscible with the desired base biopolymer and includes a lower alkyl (C3 to C7) organic acid. The polyester plasticizing unit is formed from monomers comprising a multifunctional alcohol and an aliphatic anhydride or its equivalent dicarboxylic acid and ester derivatives. The polyester plasticizing unit may optionally include one or more difunctional alcohols in combination with the multifunctional alcohol. The resulting the bioderived plasticizer has a low glass transition temperature (Tg), preferably between ?20° C. to 30° C. The plasticizer is preferably amorphous.

Abstract: Copolyetherester compositions comprising a melt-mixed blend of one or more copolyetherester(s) comprising a multiplicity of recurring long chain ester units and short chain ester units joined head-to-tail through ester linkages, and (b) about 0.25 to about 15 weight percent of one or more polyhydric alcohols having more than two hydroxyl groups; wherein all weight percentages are based on the total weight of the copolyetherester composition. Molded or extruded thermoplastic articles formed from the copolyetherester compositions, wherein 2 mm test bars prepared from said copolyetherester composition, and exposed at a test temperature of 150° C. for a test period of about 120 hours, in an atmosphere of air, and tested according to according to ISO 527-2/5A method have, on average, a retention of tensile strain at break of at least 50 percent as compared with an unexposed control having identical composition and shape.

Abstract: We report Michael addition products between primary amines and activated ?,?-unsaturated compounds exemplified by diethyl methylenemalonate (DEMM). In various embodiments, the reaction proceeds with high yields in the absence of strong base or Lewis acid catalyst under mild reaction conditions. Depending on the state of steric hindrance in the amine, the reaction products are a double Michael addition product or a so-called vicarious Michael addition reaction product.

Abstract: Dendrimeric compounds and polymers are also provided wherein the dendrimer core is derived from the Michael reaction products. The branching pattern of the core and the multiplicity of the Michael addition lead to flexibility in designing and synthesizing dendrimeric materials. The Michael addition products are from a reaction between primary amines and activated ?,?-unsaturated compounds exemplified by diethyl methylenemalonate (DEMM). In various embodiments, the reaction proceeds with high yields in the absence of strong base or Lewis acid catalyst under mild reaction conditions. Depending on the state of steric hindrance in the amine, the reaction products are a double Michael addition product or a so-called vicarious Michael addition reaction product.

Abstract: Provided are a porous organosilicate polymer composite prepared by heating an organic/inorganic hybrid polymer in which an organosilicate polymer is chemically bonded to a radial pore-forming polymer ended with a hydrolyzable alkoxysilyl group and used as a core molecule, and a semiconductor device using an organosilicate polymer composite film including the porous organosilicate polymer composite. The organosilicate polymer composite film has a very low dielectric constant, and thus, is useful as a dielectric film of the semiconductor device.

Abstract: Compounds exhibiting angiogenic properties incorporating the structure of Formula I: R3—NH—NH—C(?O)—R2—P—R1 ??(I) wherein P is a water-soluble, biodegradable polymer, R1 is hydrogen, lower alkyl, lower alkoxy or —R2—C(?O)—NH—NH—R3; each R2 is independently —CH2—, —NH— or O; and each R3 is independently hydrogen or a residue of a naturally occurring alpha-L-amino acid or dipeptide thereof. Polymer networks crosslinked with hydrazide compounds are also disclosed, together with implantable medical devices incorporating the compounds and crosslinked polymers, and angiogenesis-promoting treatment methods, including wound-treatment methods.

Abstract: A coating composition is produced by forming an aqueous dispersion of a crosslinking agent and a resin that comprises the reaction product of an alkyd polymer, an optional surfalkyd, diacetone acrylamide, another acrylate monomer and optionally aromatic monomers wherein the reaction product is neutralized with either ammonia or an amine. A coating of the aqueous dispersion on wood exhibits at least some of the following desired properties: rapid dry time, good tannin blocking, good resistance to picking up dirt, good hot box stability and good exterior durability. Additionally, the inventive coatings appear to provide improved crosslinking compared to coatings comprising resins not neutralized with an amine or ammonia and/or not containing a surfalkyd.

Abstract: An antistatic composition containing various types of polymers such as a polyamide, an aliphatic polyester, an elastomer thereof and a polyurethane elastomer, and a metal salt in specific amounts, and preferably, an antistatic composition in which an additive component such as an organic compound which has an —{O(AO)n}— group (A represents an alkylene group having 2 to 4 carbon atoms, and n represents an integer of 1 to 7) and all molecular chain terminals of which are CH3 and/or CH2 groups is compounded as needed.

Abstract: Absorbable heterochain polymers carrying acid or basic groups, capable of ionic conjugation with basic or acidic bioactive agents, respectively, are produced by free-radical addition of unsaturated functional monomers onto absorbable liquid polymers and subsequent generation of reactive functionality or by direct copolymerization of a carboxylic initiator with cyclic monomers to produce liquid carboxyl-bearing copolyesters or polyester carbonates.

Abstract: The invention relates to a mixture of biodegradable polyesters which includes an aromatic-aliphatic polyester (A), an aliphatic polyester (B) and a polylactic acid polymer (C) in which the concentration of A varies, with respect to (A+B) in the range between 40 and 70% by weight, and the concentration of C with respect of (A+B+C) is of between 6 and 30% by weight.

Abstract: A blend activatable with actinic radiation and solid at room temperature, comprising (A) at least one crystalline compound containing on average per molecule at least one reactive functional group having at least one bond which can be activated with actinic radiation, and (B) at least one amorphous compound containing on average per molecule at least one reactive functional group having at least one bond which can be activated with actinic radiation; process for its preparation, and its use.

Abstract: A composite cured product body is provided, which includes a first cured product part formed from a condensation reaction curable silicone rubber, and a second cured product part adhering to a surface of said first cured part formed from an addition reaction curable organopolysiloxane composition. The addition reaction curable organopolysiloxane composition includes: (A) an organopolysiloxane with at least 2 alkenyl groups bonded to silicon atoms, (B) an organohydrogenpolysiloxane with at least 2 hydrogen atoms bonded to silicon atoms, (C) a hydrosilylation reaction catalyst, and (D) at least one organopolysiloxane with at least one monovalent group bonded to a silicon atom and represented by the formula (1): —O—SiR2(OH)??(1) or the formula (2): —R1—Si(OR2)aR33-a??(2).

Abstract: It is an object of the present invention to provide a compound having a (meth)acryloyl group that is suitably used in various applications, a process for producing such compound simply and under mild conditions, and an useful photo-curable composition and aqueous photo-curable composition comprising such compound.

Abstract: The present invention is directed to medical devices or pharmaceutical composition, each containing a synthetic, biodegradable, biocompatible polymer that is the reaction product of a polybasic acid or derivative thereof, a monoglyceride, and a cationic polyol.

Abstract: The present invention includes a co-polymer film which can be applied over a surface of an article to form a continuous surface that is more biocompatible and has a smoother surface morphology than an untreated article. In general the co-polymer film of the invention can be formed by providing a hydrophobic polymer block, such as polydimethylsiloxane (PDMS) with functional —OH end groups and reacting the —OH ends with a conventional monomer or prepolymer of a film-forming polymer capable of reacting with —OH groups. Such reactions are exemplified, using as reactive PDMS a triblock copolymer of the polylactone-polysiloxane-polylactone (PL-PDMS-PL) type, or silicone polyesters. The —OH groups of the polylactone blocks can react with any of a variety of isocyanates in a suitable solvent to form a polymer having PDMS incorporated with its structure.