| Patent Number |
Title Of Patent |
Date Issued |
| RE34652 |
Fluorinated, acrylamide-functional monomers |
June 28, 1994 |
| Novel fluorinated, acrylamide monomers are prepared from 2-alkenyl azlactones reacted with fluorinated alcohols. The novel monomers have the formula ##STR1## wherein R.sup.1 and R.sup.6 are independently hydrogen or methyl;R.sup.2 and R.sup.3 independently can be an alkyl, cycloalkyl |
| RE34348 |
Fluorinated polymers derived from acrylamide-functional monomers |
August 17, 1993 |
| Novel fluorinated, acrylamide monomers are prepared from 2-alkenyl azlactones reacted with fluorinated alcohols. The novel monomers have the formula ##STR1## wherein R.sup.1 and R.sup.6 are independently hydrogen or methyl; R.sup.2 and R.sup.3 independently can be an alkyl, cyclo |
| 6762256 |
Initiator/amidine complexes, systems comprising the complexes, and polymerized compositions made |
July 13, 2004 |
| Initiator systems of the invention comprise a complexed initiator comprising a complex of an amidine complexing agent and an initiator; and a decomplexer. The initiator systems are useful for initiating polymerization of at least one monomer to form polymerized compositions. Kits of |
| 6740717 |
Initiator/amidine complexes, systems comprising the complexes, and polymerized compositions made |
May 25, 2004 |
| Initiator systems of the invention comprise a complexed initiator comprising a complex of an amidine complexing agent and an initiator; and a decomplexer. The initiator systems are useful for initiating polymerization of at least one monomer to form polymerized compositions. Kits of |
| 6573398 |
Secondary aspartic acid amide esters |
June 3, 2003 |
| New secondary amines are described which are prepared from inexpensive, commercially available raw materials, are stable at room temperature, and are reactive toward electrophiles. The secondary amines are prepared by the addition of one or more primary amines with one or more male ( |
| 6486090 |
Initiator/hydroxide and initiator/alkoxide complexes, systems comprising the complexes, and poly |
November 26, 2002 |
| Initiator systems of the invention comprise: a complexed initiator comprising at least one of a complex of a complexing agent comprising at least one hydroxide and an initiator or a complex of a complexing agent comprising at least one alkoxide and an initiator; and a decomplexer. The |
| 6479602 |
Polymerization initiator systems and bonding compositions comprising vinyl aromatic compounds |
November 12, 2002 |
| Polymerization initiator systems comprising an organoborane and a vinyl aromatic compound are described. The polymerization initiator systems are particularly useful in formulating two-part curable bonding compositions, particularly those that cure to acrylic adhesives, more particularly |
| 6469199 |
Secondary aspartic acid amide esters |
October 22, 2002 |
| New secondary amines are described which are prepared from inexpensive, commercially available raw materials, are stable at room temperature, and are reactive toward electrophiles. The secondary amines are prepared by the addition of one or more primary amines with one or more male ( |
| 6440573 |
Secondary amine-functional silanes, silane-functional polymers therefrom, and resulting cured po |
August 27, 2002 |
| Secondary amine-functional silanes comprising at least one ester group and at least one amide group are disclosed. The secondary amine-functional silanes are preparable from relatively inexpensive, commercially available raw ingredients, are stable at room temperature and are reactive to |
| 6410667 |
Initiator/amidine complexes, systems comprising the complexes, and polymerized compositions made |
June 25, 2002 |
| Initiator systems of the invention comprise a complexed initiator comprising a complex of an amidine complexing agent and an initiator; and a decomplexer. The initiator systems are useful for initiating polymerization of at least one monomer to form polymerized compositions. Kits of |
| 6384165 |
Organoborane amine complex initiator systems and polymerizable compositions made therewith |
May 7, 2002 |
| A composition comprises organoborane amine complex and 1,4-dioxo-2-butene-functional material. The composition can form a part of a polymerization initiator system that also includes a compound that is reactive with the amine portion of the complex. The system can be used to initiate |
| 6383655 |
Low odor polymerizable compositions useful for bonding low surface energy substrates |
May 7, 2002 |
| Low odor polymerizable compositions comprise monomer blends having a average monomer fluorophilicity of at least 3.25, an average boiling point of at least about 160.degree. C., and wherein the monomer blend is polymerizable to a polymer having a glass transition temperature of at le |
| 6252023 |
Organoborane amine complex inatator systems and polymerizable compositions made therewith |
June 26, 2001 |
| A composition comprises organoborane amine complex and 1,4-dioxo-2-butene-functional material. The composition can form a part of a polymerization initiator system that also includes a compound that is reactive with the amine portion of the complex. The system can be used to initiate |
| 6204343 |
Room temperature curable resin |
March 20, 2001 |
| A curable composition for electrical applications, the curable composition comprising (i) a compound having at least two .alpha.,.beta.-unsaturated groups and an equivalent weight of less than 250 g/mol, (ii) a catalyst capable of initiating a Michael reaction and (iii) a Michael donor h |
| 6162938 |
Secondary amine-functional silanes, silane-functional polymers therefrom, and resulting cured po |
December 19, 2000 |
| Secondary amine-functional silanes comprising at least one ester group and at least one amide group are disclosed. The secondary amine-functional silanes are preparable from relatively inexpensive, commercially available raw ingredients, are stable at room temperature and are reactive to |
| 6018009 |
Crosslinked isocyanate functional polymer supports |
January 25, 2000 |
| Insoluble supports are prepared which possess high surface areas and efficiently dispersed isocyanate groups. These reactive supports are useful for covalently binding proteins which preferably are enzymes and provide catalysts for conducting organic reactions. |
| 6005062 |
Secondary aspartic acid amide esters |
December 21, 1999 |
| New secondary amines are described which are prepared from inexpensive, commercially available raw materials, are stable at room temperature, and are reactive toward electrophiles. The secondary amines are prepared by the addition of one or more primary amines with one or more male ( |
| 5866651 |
Hydroxycarbamoylalkoxysilane-based poly(ether-urethane) sealants having improved paint adhesion |
February 2, 1999 |
| The present invention pertains to moisture curable sealant compositions based on alkoxysilane functional poly(ether-urethane)s prepared from hydroxycarbamoylalkoxysilanes which provide improved paint adhesion even in the absence of polar solvents or polar plasticizers. The present in |
| 5760152 |
Crosslinked isocyanate functional polymer supports |
June 2, 1998 |
| Insoluble supports are prepared which possess high surface areas and efficiently dispersed isocyanate groups. These reactive supports are useful for covalently binding proteins which preferably are enzymes and provide catalysts for conducting organic reactions. |
| 5723516 |
Inorganic particles coated with organic polymeric binders composite sheets including same and me |
March 3, 1998 |
| A granular material is presented comprising inorganic particles coated with an organometallic polymeric binder, the organometallic polymeric binder comprising the reaction product of water with at least one component of a binder precursor composition. The binder precursor composition is |
| 5679779 |
Crosslinked isocyanate-functional polymer supports |
October 21, 1997 |
| Insoluble supports are prepared which possess high surface areas and efficiently dispersed isocyanate groups. These reactive supports are useful for covalently binding proteins which preferably are enzymes and provide catalysts for conducting organic reactions. |
| 5587502 |
Hydroxy functional alkoxysilane and alkoxysilane functional polyurethane made therefrom |
December 24, 1996 |
| The present invention provides a moisture-curable alkoxysilane functional polyurethane prepared from a hydroxy functional alkoxysilane. The hydroxy functional alkoxysilane is a hydroxyalkylenecarbamoylalkylene-alkoxysilanes referred to as a "hydroxycarbamoylsilane". The alkoxysilane |
| 5437932 |
High speed aqueous solvent developable photopolymer compositions |
August 1, 1995 |
| Novel photosensitive compositions based on azlactone derived polymers are described. The polymers have a hydroearbyl backbone and pendant peptide groups with free-radically polymerizable functionality attached thereto, said polymer further comprising at least one oxyacid group or salt |
| 5364693 |
Orthopedic support materials |
November 15, 1994 |
| The present invention provides a water-curable resin composition for use in an orthopedic cast composed of a water-reactive liquid organometallic compound having at least one hydrolyzable group per molecule and a viscosity of no greater than about 100,000 centipoise under ambient con |
| 5346939 |
Water curable resin compositions |
September 13, 1994 |
| The present invention provides a water-curable resin composition for use in the preparation of composite materials. The resin composition is composed of a water-reactive liquid organometallic compound having a viscosity of no greater than about 500,000 centipoise under ambient conditions |
| 5314975 |
Fluorinated acrylamide silane monomers and polymers |
May 24, 1994 |
| The present invention provides novel fluorinated acrylamide silane monomers which are useful as adhesion promoting agents in optical fiber cladding compositions. Polymerization of the novel monomers, optionally in the presence compatible ethylenically-unsaturated monomers, provides h |
| 5268473 |
Azlactone Michael adducts |
December 7, 1993 |
| Azlactone-functional Michael adducts are disclosed which are the Michael reaction products of 2-alkenyl azlactones and Michael donors selected from carbon and nitrogen nucleophiles. Reaction products which contain a plurality of azlactone groups are useful as step growth monomers in |
| 5235015 |
High speed aqueous solvent developable photopolymer compositions |
August 10, 1993 |
| Novel photosensitive compositions based on azlactone derived polymers are described. The polymers have a hydrocarbyl backbone and pendant peptide groups with free-radically polymerizable functionality attached thereto, said polymer further comprising at least one oxyacid group or salt |
| 5210248 |
Fluorinated acrylamide silane monomers and polymers |
May 11, 1993 |
| The present invention provides novel fluorinated acrylamide silane monomers which are useful as adhesion promoting agents in optical fiber cladding compositions. Polymerization of the novel monomers, optionally in the presence compatible ethylenically-unsaturated monomers, provides h |
| 5149806 |
Azlactone Michael adducts |
September 22, 1992 |
| Azlactone-functional Michael adducts are disclosed which are the Michael reaction products of 2-alkenyl azlactones and Michael donors selected from carbon and nitrogen nucleophiles. Reaction products which contain a plurality of azlactone groups are useful as step growth monomers in |
| 5081197 |
Oligo(2-alkenyl azlactones) |
January 14, 1992 |
| This invention provides novel azlactone-functional oligomers of 2-alkenyl azlactones in which oligomerization has occurred predominantly via the 2-alkenyl group. Oligomerization of the 2-alkenyl group provides oligomers having 2 to 15 mer units with predominantly carbon-carbon backbone |
| 5045615 |
Fluorinated polymers derived from acrylamide-functional monomers |
September 3, 1991 |
| Novel fluorinated, acrylamide monomers are prepared from 2-alkenyl azlactones reacted with fluorinated alcohols. The novel monomers have the formula ##STR1## wherein R.sup.1 and R.sup.6 are independently hydrogen or methyl; R.sup.2 and R.sup.3 independently can be an alkyl, cyclo |
