| 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 |
| RE32952 |
Method of preparing N-acryloyl-.alpha.-amino acids |
June 13, 1989 |
| A novel, one-pot procedure for the preparation of N-acryloyl-.alpha.-amino acids involves the steps of:(i) reacting a ketone, an ammonium salt, and a cyanide salt in water, optionally in the presence of ammonium hydroxide and a co-solvent, to form an aminonitrile;(ii) acryloylating the a |
| 7579359 |
1-alkoxy 1H-imidazo ring systems and methods |
August 25, 2009 |
| Imidazo-containing compounds (e.g., imidazonaphthyridines, imidazopyridines, imidazoquinolines, and imidazote-trahydroquinolines) with an alkoxy substituent at the 1-position, pharmaceutical compositions containing the compounds and methods of use of these compounds as immunomodulato |
| 7557177 |
Ring-opened azlactone initiators for atom transfer radical polymerization |
July 7, 2009 |
| Initiators for atom transfer radical polymerizations are described. The initiators have an azlactone or ring-opened azlactone moiety to provide telechelic (co)polymers. |
| 7368487 |
Aqueous ink jet printable compositions |
May 6, 2008 |
| Ink jet printable compositions comprise an aqueous vehicle, particles of a self-crosslinking polymer, and optional colorant. In one embodiment, an ink jet printable ink may comprise an aqueous vehicle, a colorant, and a silyl-terminated sulfopoly(ester-urethane) polymer. In another e |
| 7294742 |
Ring-opened azlactone initiators for atom transfer radical polymerization |
November 13, 2007 |
| Initiators for atom transfer radical polymerizations are described. The initiators have an azlactone or ring-opened azlactone moiety to provide telechelic (co)polymers. |
| 7166696 |
Solid phase synthesis supports and methods |
January 23, 2007 |
| Functionalized supports and methods for solid phase synthesis. Preferably, the functionalized support is azlactone-functionalized. |
| 6992217 |
Ring-opened azlactone initiators for atom transfer radical polymerization |
January 31, 2006 |
| Initiators for atom transfer radical polymerizations are described. The initiators have an azlactone or ring-opened azlactone moiety to provide telechelic (co)polymers. |
| 6991851 |
Dry-peelable temporary protective coatings |
January 31, 2006 |
| A dry-strippable coating composition can be incorporated into a composite article and comprises a dried water-borne polyurethane dispersion including a release additive comprising a releasing co-solvent or other selected release material. When water is removed from the polyurethane d |
| 6969749 |
Azlactone initiators for atom transfer radical polymerization |
November 29, 2005 |
| Initiators for atom transfer radical polymerizations are described. The initiators have an azlactone or ring-opened azlactone moiety to provide telechelic (co)polymers. |
| 6894133 |
Azlactone initiators for atom transfer radical polymerization |
May 17, 2005 |
| Initiators for atom transfer radical polymerizations are described. The initiators have an azlactone or ring-opened azlactone moiety to provide telechelic (co)polymers. |
| 6787635 |
Solid phase synthesis supports and methods |
September 7, 2004 |
| Functionalized supports and methods for solid phase synthesis. Preferably, the functionalized support is azlactone-functionalized. |
| 6692823 |
Microfibrillated articles comprising hydrophillic component |
February 17, 2004 |
| Described are hydrophilic fibrillated articles that include melt-processable polymer and hydrophilic component such as hydrophilic surfactant or hydrophilic polymer, as well as methods of preparing such articles. |
| 6416838 |
Compositions and articles made therefrom |
July 9, 2002 |
| The present invention relates to a composition comprising a first monomer having the formula CH.sub.2.dbd.CHCOOR.sup.1, where R.sup.1 is a linear alkyl group having from 9 to 16 carbon atoms or a branched alkyl group having from 9 to 30 carbon atoms, and whose homopolymer has a Tg less t |
| 6245922 |
Chromophoric photocrosslinking compound |
June 12, 2001 |
| A photoactive compound that is the reaction product of an alkenyl azlactone compound and a nucleophilic aromatic ketone is described. Mer units derived from this compound can be used, for example, to crosslink via a hydrogen abstracting mechanism acrylic polymers in which they are in |
| 6139594 |
Abrasive article with tie coat and method |
October 31, 2000 |
| An abrasive article is provided that includes a tie coat which improves adhesion between an abrasive layer and a backing in the abrasive article. The tie coat is preferably formed from a tie coat precursor comprising a sulfopoly(ester-urethane) component comprising in its backbone at lea |
| 5993935 |
Covalently reactive particles incorporated in a continous porous matrix |
November 30, 1999 |
| A composite article is provided having covalently reactive particles incorporated in a continuous, porous matrix. The reactive particles have surfaces of covalently reactive functional groups capable of directly forming covalent chemical bonds with ligands without need for an interme |
| 5951749 |
Water-based pigmented inks |
September 14, 1999 |
| Water-based pigmented inks are disclosed. Such inks are formed from water-based dispersions of pigment particles having novel dispersants therein. The dispersions are formed from the reaction product of an amino acid compound with a nitrogen reactive compound with subsequent hydrolysis |
| 5929160 |
Method for reducing water uptake in silyl terminated sulfopoly(ester-urethanes) |
July 27, 1999 |
| A method of decreasing the water uptake in a sulfopoly(ester-urethane) by preparing said sulfopoly(ester-urethane) from a chain extended sulfopolyester polyol which itself has been prepared in a two-step method, said sulfopoly(ester-urethane) comprising in its backbone at least one n |
| 5840106 |
Water-based pigmented inks |
November 24, 1998 |
| Water-based pigmented inks are disclosed. Such inks are formed from water-based dispersions of pigment particles having novel dispersants therein. The dispersions are formed from the reaction product of an alkenyl azlactone with an N-substituted amino acid compound. Subsequent to the |
| 5747626 |
Silyl terminated sulfopoly(ester-urethane pavement marking compositions |
May 5, 1998 |
| A pavement marking composition comprises a sulfopoly(ester-urethane) polymer which comprises in its backbone at least one non-terminal arylene or alkylene group comprising a pendant sulfonic acid group or salt thereof, the polymer of said pavement marking composition being terminated |
| 5714632 |
Azlactone-based surfactants |
February 3, 1998 |
| A compound of the formula ##STR1## wherein Q is an organic group of at least two carbon atoms having at least m substituents,m is 1, 2, 3, 4, 5 or 6, andn is 0 or 1.R.sup.3 is H or methyl,R.sup.8 and R.sup.9 are independently hydrogen, alkyl group or aryl,R.sup.12 and R.sup.13 are indepe |
| 5705676 |
Chromogenic leuco redox-dye-releasing compounds for photothermographic elements |
January 6, 1998 |
| A photothermographic element comprising a support bearing at least one heat-developable, photosensitive, image-forming photothermographic emulsion layer comprising:(a) a photosensitive silver halide;(b) a non-photosensitive, reducible source of silver;(c) a chromogenic leuco dye reducing age |
| 5696289 |
Blocked leuco dyes for photothermographic elements |
December 9, 1997 |
| A photothermographic element containing a support bearing at least one heat-developable, photosensitive, image-forming photothermographic emulsion layer is provided. The emulsion layer comprises:(a) a photosensitive silver halide;(b) a non-photosensitive, reducible source of silver;(c) a leu |
| 5492805 |
Blocked leuco dyes for photothermographic elements |
February 20, 1996 |
| A photothermographic element containing a support bearing at least one heat-developable, photosensitive, image-forming photothermographic emulsion layer is provided. The emulsion layer comprises:(a) a photosensitive silver halide;(b) a non-photosensitive, reducible source of silver;(c) a leu |
| 5492804 |
Chromogenic leuco redox-dye-releasing compounds for photothermographic elements |
February 20, 1996 |
| A photothermographic element comprising a support bearing at least one heat-developable, photosensitive, image-forming photothermographic emulsion layer comprising:(a) a photosensitive silver halide;(b) a non-photosensitive, reducible source of silver;(c) a chromogenic leuco dye reducing age |
| 5403902 |
Polymeric supports |
April 4, 1995 |
| Azlactone-functional polymer supports are useful reactive supports for the attachment of functional materials to provide novel adduct beads. The adduct beads are useful as complexing agents, catalysts, polymeric reagents, chromatographic supports, and as enzyme- or other biologically |
| 5336742 |
Polymeric supports |
August 9, 1994 |
| Azlactone-functional polymer supports are useful reactive supports for the attachment of functional materials to provide novel adduct beads. The adduct beads are useful as complexing agents, catalysts, polymeric reagents, chromatographic supports, and as enzyme- or other biologically |
| 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 |
| 5300420 |
Stabilizers for photothermography with nitrile blocking groups |
April 5, 1994 |
| Photothermographic compositions comprising a photographic silver halide, an organic silver salt, and a reducing agent for the organic silver salt, display improved stabilty in the presence of a compound having a nucleus of the formula: ##STR1## wherein: A represents any monovalen |
| 5292840 |
Polymeric supports |
March 8, 1994 |
| Azlactone-functional polymer supports are useful reactive supports for the attachment of functional materials to provide novel adduct beads. The adduct beads are useful as complexing agents, catalysts, polymeric reagents, chromatographic supports, and as enzyme- or other biologically |
| 5292514 |
Azlactone-functional substrates, corneal prostheses, and manufacture and use thereof |
March 8, 1994 |
| Azlactone-functional substrates, (especially hydrogels), mammalian body implants, and methods of making and using them are disclosed. The azlactone-functional substrates are the reaction product of substrates having azlactone-reactive nucleophilic surfaces and a multi-functional azla |
| 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 |
| 5239013 |
Nonlinear optically active polymers |
August 24, 1993 |
| Organic groups covalently bound to a polymer backbone provide second or third order nonlinear susceptibilities to the polymer. In another aspect, a method is disclosed for providing the novel polymers of the invention. Polymers of the invention can be directionally oriented to provide us |
| 5216084 |
Nonlinear optically active polymers |
June 1, 1993 |
| Organic groups covalently bound to a polymer backbone provide second or third order nonlinear susceptibilities to the polymer. In another aspect, a method is disclosed for providing the novel polymers of the invention. Polymers of the invention can be directionally oriented to provide us |
| 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 |
| 5194623 |
Azlactone based photographic reagents |
March 16, 1993 |
| Novel compounds derived from azlactones act as precursors for photographically active groups. The active groups are released at an appropriate time in the use of photographic and photothermographic systems. |
| 5175081 |
Post-processsing stabilization of photothermographic emulsions |
December 29, 1992 |
| The post-processing stability of silver halide photothermographic emulsions is enhanced by the presence of stabilizing amounts of certain azlactones. |
| 5158866 |
Post-processing stabilization of photothermographic emulsions with amido compounds |
October 27, 1992 |
| The post-processing stability of silver halide photothermographic emulsions is enhanced by the presence of stabilizing amounts of certain structurally defined amido compounds. |
| 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 |
| 4971424 |
Radiation curable cladding compositions |
November 20, 1990 |
| Novel optical fiber cladding compositions containing fluorinated acrylamide monomers are described. The claddings are liquids at room temperature which possess excellent coating viscosities in the pre-polymerized state and are polymerized by actinic radiation. |
| 4946962 |
Bis(thiazolinethiones) |
August 7, 1990 |
| Two classes of certain compounds known as bis(thiazolinethiones), more particularly bis[(3,4-disubstituted)-thiazole-2-thiones], have thiazolinethione heterocycle units linked by alkylene, arylene, or arene groups or by a carbon to carbon single bond. These compounds are useful in th |
| 4898923 |
Polypyridinium copolymer |
February 6, 1990 |
| A novel class of polymers comprises one or more dipyridinium units, having the formula ##STR1## contained within the main polymer backbone where Ar.sup.1, Ar.sup.2, and Ar.sup.3 are aromatic or heteroaromatic nuclei each of which can consist of one ring or two fused or catenated |
| 4871824 |
Variably crosslinked polymeric supports |
October 3, 1989 |
| Azlactone-functional polymer beads are useful reactive supports for the attachment of functional materials to provide novel adduct beads. The adduct beads are useful as complexing agents, catalysts, polymeric reagents, chromatographic supports, and as enzyme- or other biomacromolecul |
| 4852969 |
Silyl 2-amidoacetate and silyl 3-amidopropionate compositions and optical fiber made therefrom |
August 1, 1989 |
| The present invention provides novel silyl 2-amidoacetates and silyl 3-amidopropionates which are the reaction products of azlactone and silanol reactants. The novel products result from nucleophilic addition of a soluble or insoluble, low or high molecular weight reactant containing |
| 4841021 |
Polypyridinium |
June 20, 1989 |
| A novel class of polymers comprises one or more dipyridinium units, having the formula ##STR1## contained within the main polymer backbone where Ar.sup.1, Ar.sup.2, and Ar.sup.3 are aromatic or heteroaromatic nuclei each of which can consist of one ring or two fused or catenated |
| 4816554 |
Poly(amido methyl-benzazole) |
March 28, 1989 |
| A class of polymers comprises one or more 2-amidomethylbenzazole units, ##STR1## contained within the main polymer backbone, wherein Ar is Ar.sup.1 or Ar.sup.2, wherein Ar.sup.1 is a tetravalent aromatic nucleus having two pairs of valences, the members of each pair being situated on |
