Abstract: Polymer bound multidentate complexes are prepared by reacting pendant benzyl chloride and benzyl iodide groups on a variety of polymer supports, including crosslinked polystyrene, with 3,3'-iminodiproprionitrile and reducing the nitrile groups by treatment with, for example, a boron hydride-tetrahydrofuran complex to form the amine. The amine is a precursor for other ligand systems; for example, the primary amine groups formed condense with an aldehyde or ketone to yield five coordinate Schiff base ligands. The polydentate amine ligand systems are useful for synthesis of chelating agents for sequestering metal ions from solution for purification or concentration purposes. Metal complexes of these ligands with manganese, iron, cobalt, nickel, copper, and zinc can be prepared which are useful as heterogeneous oxidation catalysts.

Abstract: Novel telechelic olefin and hydroxy polymers particularly those of polyisobutylene are prepared according to the process set forth herein. Preparation of a telechelic diolefin polyisobutylene includes the steps of refluxing a solution of telechelic dihalogen polyisobutylene, adding a solution of a strong base such as potassium t-butoxide and stirring to form the telechelic diolefin polyisobutylene. This telechelic diolefin can be converted to the telechelic dihydroxy by refluxing a solution of the former, hydroborating the diolefin to a polymeric borane and oxidizing the polymeric borane to form the telechelic dihydroxy polyisobutylene. The processes are also applicable to the conversion of trihalogenated polyisobutylenes to telechelic triolefin and trihydroxy polyisobutylene tristars.

Abstract: This invention relates to novel metal catalysts of a solid nonionic crosslinked resin having amine or phosphine borane adducts on or in which a reduced metal is precipitated, the method of producing said catalysts and their use in catalysis.

Abstract: This invention relates to novel metal catalysts of a solid nonionic crosslinked resin having amine or phosphine borane adducts on or in which a reduced metal is precipitated, the method of producing said catalysts and their use in catalysis.

Abstract: Polymers containing recurring 2,5-oxolanylene units wherein at least 60 percent of the units are joined directly to one another so as to provide segments consisting of at least 6 of said units.

Abstract: Substances (I) capable of being converted into higher-molecular weight materials under the influence of a cationic catalyst, such as 1,2-epoxides, aminoplasts, vinyl monomers or prepolymers, or phenoplasts, are so converted by exposure to actinic irradiation or by heating in the presence of an aryloxysulfoxonium salt of formula ##STR1## where either R.sup.6 and R.sup.7 separately denote lower alkyl (optionally substituted by halogen and interrupted in the chain by --O-- or --SO.sub.2 --), or an aryl or aryloxy group, or R.sup.6 and R.sup.7 together denote a divalent group forming with the S atom a heterocyclic radical; R.sup.8 denotes an aryl group; M denotes an atom of a metal or metalloid; X denotes a halogen atom; and n is 4, 5, or 6, for instance,p-chlorophenoxy-p-tolyl-p-phenoxysulfoxonium hexafluorophosphate and 1-phenoxy-1-oxidotetrahydrothiophenium tetrafluorborate.

Abstract: A family of negative resins, capable of undergoing crosslinking under the effect of more or less energetic photons (gamma radiation, X-rays, ultraviolet or visible light), applicable to the protection of objects against atmospheric agents and to the production of masks of the type used in the production of integrated circuits. The typical compound according to the invention contains at least one substance of which the chemical formula comprises a thiirane ring: ##STR1## such as 2,3-epithiopropyl methacrylate copolymerized with a vinyl monomer, such as methyl methacrylate. Crosslinking is facilitated by photoinitiators, such as aryl diazonium and aryl iodonium salts liberating Lewis acids. By selecting the photoinitiator, it is possible to act on the spectral region where irradiation is effective.

Abstract: Polymer bound multidentate complexes are prepared by reacting pendant benzyl chloride and benzyl iodide groups on a variety of polymer supports, including crosslinked polystyrene, with 3,3'-iminodiproprionitrile and reducing the nitrile groups by treatment with, for example, a boron hydride-tetrahydrofuran complex to form the amine. The amine is a precursor for other ligand systems; for example, the primary amine groups formed condense with an aldehyde or ketone to yield five coordinate Schiff base ligands. The polydentate amine ligand systems are useful for synthesis of chelating agents for sequestering metal ions from solution for purification or concentration purposes. Metal complexes of these ligands with manganese, iron, cobalt, nickel, copper, and zinc can be prepared which are useful as heterogeneous oxidation catalysts.

Abstract: A process for the preparation of modified poly-N-vinylpyrrolid-2-one containing two identical reactive groups, wherein polyvinylpyrrolidone is treated with complex hydrides, with or without further reaction of the modified polyvinylpyrrolidone with a reactive bifunctional compound, to give a polymer which has a molecular weight at least 2.5 times as great as that of the starting polymer.

Abstract: An aqueous agent for treating wood and wooden materials, optionally containing customary additives, such as water-soluble wood protecting agents effective as insecticides and/or fungicides, comprises an organic binder drying by oxidation, said organic binder consisting essentially of the reaction product of an acid and a 1,3-butadiene substrate polymer modified to carry amino groups, wherein(1) the amino group carrying 1,3-butadiene polymer has a double bond content corresponding to an iodine number of at least 200 g iodine/100 g, of which a double bond content of at least 100, measured as iodine number, is derived from cis-1,4-structural elements of the 1,3-butadiene substrate polymer per se;(2) the amino group content of the amino group carrying 1,3-butadiene polymer is at least 50 mg-atoms of nitrogen/100 g of polymer; and(3) the 1,3-butadiene substrate polymer per se has at least 70 molar percent butadiene units and a molecular weight (Mn) of 500-6,000.

Abstract: A family of negative resins, capable of undergoing crosslinking under the effect of more or less energetic photons (gamma radiation, X-rays, ultraviolet or visible light), applicable to the protection of objects against atmospheric agents and to the production of masks of the type used in the production of integrated circuits. The typical compound according to the invention contains at least one substance of which the chemical formula comprises a thiirane ring: ##STR1## such as 2,3-epithiopropyl methacrylate copolymerized with a vinyl monomer, such as methyl methacrylate. Crosslinking is facilitated by photoinitiators, such as aryl diazonium and aryl iodonium salts liberating Lewis acids. By selecting the photoinitiator, it is possible to act on the spectral region where irradiation is effective.

Abstract: A four-component composition is disclosed comprising 100 parts of a non-aminoplast hydroxyl-bearing polymer; about 5-100 parts of a (poly)glycol monoether having an atmospheric boiling point of about 300.degree. C. or greater; an aminoplast or phenolic resin capable of curing the hydroxyl-bearing polymer and a strong acid catalyst for the reaction between the first and third components. Optionally, a pigment may be added to the composition.

Abstract: This invention relates to cross-linkable film-forming compositions which contain a polymer with pendant isocyano groups and a trialkylborane cross-linking agent and to the use of the compositions in ambient temperature-cure finishes.

Abstract: A glass composition for effecting crosslinking of a polycarboxylic acid cement and cement compositions formed therefrom. The glass is of the aluminoborate type and comprises 40 to 75 mole % boric oxide, not more than 60 mole % zinc oxide, not more than 50 mole % calcium oxide and not more than 20 mole % alumina. Cements formed from the glasses have a wide range of applications including structural cements, dental filler and orthopaedic cements.

Abstract: Polymers of p-methyl styrene can be cross-linked with chemical cross-linking agents, such as peroxides, to produce insoluble products. The methyl styrene used has a high content of the para-isomer. An important end use is for rigid food or beverage containers subjected to thermal conditions.

Abstract: Polymer bound multidentate complexes are prepared by reacting pendant benzyl chloride and benzyl iodide groups on a variety of polymer supports, including crosslinked polystyrene, with 3,3'-iminodiproprionitrile and reducing the nitrile groups by treatment with, for example, a boron hydride-tetrahydrofuran complex to form the amine. The amine is a precursor for other ligand systems; for example, the primary amine groups formed condense with an aldehyde or ketone to yield five coordinate Schiff base ligands. The polydentate amine ligand systems are useful for synthesis of chelating agents for sequestering metal ions from solution for purification or concentration purposes. Metal complexes of these ligands with manganese, iron, cobalt, nickel, copper, and zinc can be prepared which are useful as heterogeneous oxidation catalysts.

Abstract: A process for the preparation of modified poly-N-vinylpyrrolid-2-one containing two identical reactive groups, wherein polyvinylpyrrolidone is treated with complex hydrides, with or without further reaction of the modified polyvinylpyrrolidone with a reactive bifunctional compound, to give a polymer which has a molecular weight at least 2.5 times as great as that of the starting polymer.

Abstract: The graft copolymer is the reaction of a backbone polymer having allylic chloride groups therein and monomers forming a pendant graft polymer in the presence of a coinitiator. The monomers have the formula ##STR1## wherein R is an alkyl group having from 1 to 15 carbon atoms, a cycloalkyl group having from 4 to 15 carbon atoms, an aryl group having from 6 to 15 carbon atoms, combinations thereof, or hydrogen. The amount of the pendant graft polymer portion by weight ranges from about 0.5 percent to about 90 percent based upon the total weight of the total graft copolymer with the pendant graft polymer being substituted on the polymer backbone in lieu of the chlorine atom of the allylic chloride group.

Abstract: The discoloration of polyvinyl chloride that usually occurs when a slurry containing this polymer is heated at a temperature above 70.degree. C. to reduce its monomer content to less than 10 ppm is minimized or prevented by carrying out the heating step in the presence of an oxidizing agent.

Abstract: In the hydrogenation of polymers or copolymers synthesized from dienes, or containing diene hydrocarbons, which is as a rule carried out in an organic solvent using hydrogen in the presence of conventional complex hydrogenation catalysts based on metals of sub-group 8 of the periodic table of the elements and aluminum trialkyls it is important to have from 0.5 to 50 moles of water present in the hydrogenation zone per mole of the heavy metal component of the catalyst. The hydrogenation time can be substantially reduced by this measure.

Abstract: Amine containing polymeric microspheres such as polyvinyl pyridine are complexed with metal salts or acids containing metals such as gold, platinum or iron. After reduction with sodium borohydride, the salt is reduced to finely divided free metal or metal oxides, useful as catalysts. Microspheres containing covalent bonding sites can be used for labeling or separating proteins.

Abstract: Sulfone-crosslinked polystyrene cation and anion exchange resins having high solids content when saturated with water are disclosed together with a method of forming increased amounts of sulfone crosslinks using a sulfonating agent or mixture thereof preferably in combination with a boron compound.