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Law School:
The University of Texas School of Law
Education:
The University of Texas School of Law, JD Georgetown University, BS
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Synthesis Of Methylene Malonates Substantially Free Of Impurities
Adam G. Malofsky - Loveland OH, US Tanmoy Dey - Stamford CT, US Jeffrey M. Sullivan - Goshen OH, US Yangbin Chen - Lima NY, US Stanley C. Wojciak - New Britain CT, US Bernard M. Malofsky - Bloomfield CT, US
Assignee:
Bioformix Inc. - Loveland OH
International Classification:
C07C 69/34
US Classification:
560190
Abstract:
The present invention provides improved methods for the chemical synthesis of methylene malonates using the Knovenagel synthesis reaction. The method of the invention provides for improved methylene malonates by significantly reducing or eliminating the formation of alternative and/or deleterious side products, significantly reducing or eliminating unwanted consumption of methylene malonates, and significantly reducing or eliminating the degradation of methylene malonates. These advantages result in methylene malonates, which upon recovery, are of higher quality, greater purity, improved yield and possess overall improved performance characteristics (e. g. , improved cure speed, retention of cure speed, improved shelf-life and/or stability).
A method including forming a formulation by contacting one or more photoinitiators with a composition including one or more 1, 1-disubstituted alkene compounds having a purity of about 85 mole percent or more based on total weight of the 1, 1-disubsituted alkene compounds; and exposing the formulation to ultraviolet radiation for initiating free radical polymerization, anionic polymerization, or both, to cure the formulation to form a non-tacky surface. The teachings also contemplate a polymer prepared according to the methods as disclosed.
A class of alkanol amine ligands reacted with bismuth carboxylates lends unique curability properties to isocyanate and polyols for production of polyurethane for CASE applications, including growing demand for polyurethane spray-foam. The amino-alcohol ligand, when associated with bismuth neodecanoate, offers improved moisture and solvent resistance during B-side (polyol) storage, cure rates analogous to tin-based curatives, and overall good final physical properties of the cured polyurethane.
Polymers Including A Methylene Beta-Ketoester And Products Formed Therefrom
The present teachings are directed at 1,1-di substituted alkene monomers (e.g., methylene beta-ketoester monomers), methods for producing the same, polymerizable compositions including a methylene beta-ketoester monomer, and polymers, compositions and products formed therefrom. The monomer preferably is a high purity monomer. In the method for producing the methylene beta-ketoesters of the invention, a beta-ketoester may be reacted with a source of formaldehyde. The methylene beta-ketoester monomers may be used in monomer-based products (e.g., inks, adhesives, coatings, sealants or reactive molding) and polymer-based products (e.g., fibers, films, sheets, medical polymers, composite polymers and surfactants).
Polymers Containing A 1,1-Disubstituted Alkene Compound
Disclosed is a block copolymer having a first polymer block including a first primary monomer that is a 1,1-disubstituted alkene compound, wherein the first primary monomer is present at a concentration of about 50 weight percent or more, based on the total weight of the first polymer block, the first polymer block covalently bonded to a second polymer block including a second primary monomer different from the first primary monomer, wherein the second primary monomer is present at a concentration of about 50 weight percent or more, based on the total weight of the second polymer block. Also disclosed is a polymer comprising at least one monomer of a 1,1-disubstituted alkene compound having a weight average molecular weight of about 3000 daltons or more, wherein the polymer is substantially free of a melting temperature and is substantially free of a glass transition temperature of about 15 C. or more.
Polymers Including A Methylene Beta-Ketoester And Products Formed Therefrom
The present teachings are directed at 1,1-disubstituted alkene monomers (e.g., methylene beta-ketoester monomers), methods for producing the same, polymerizable compositions including a methylene beta-ketoester monomer, and polymers, compositions and products formed therefrom. The monomer preferably is a high purity monomer. In the method for producing the methylene beta-ketoesters of the invention, a beta-ketoester may be reacted with a source of formaldehyde. The methylene beta-ketoester monomers may be used in monomer-based products (e.g., inks, adhesives, coatings, sealants or reactive molding) and polymer-based products (e.g., fibers, films, sheets, medical polymers, composite polymers and surfactants).
Polymer And Other Compounds Functionalized With Terminal 1,1-Disubstituted Alkene Monomer(S) And Methods Thereof
- Loveland OH, US Jeffrey M. Sullivan - Goshen OH, US Kshitij K. Parab - Loveland OH, US Ami Doshi - Loveland OH, US Alexander R. Holzer - Loveland OH, US Matthew Reilman - Cincinnati OH, US
International Classification:
C08G 63/16 B32B 27/36 C08G 63/87 C12P 7/62
Abstract:
Functionalized compounds including residues of one or more 1,1-disubstituted alkene compounds. Preferably the functionalized compound includes the residue of two or more 1,1-disubstituted alkene compounds, which are spaced apart. The functionalized compound may be produced by a transesterification reaction. The functionalized compounds may be employed in a polymerizable composition and may be used to prepare new polymers, (for example by reacting the alkene group).
- Loveland OH, US Jeffrey M. Sullivan - Goshen OH, US Kshitij K. Parab - Loveland OH, US Elliott King - Milford OH, US William Barrett - Bethel OH, US
International Classification:
C08G 63/60 C07C 69/593 C08G 64/42 C12P 7/62
Abstract:
Disclosed are compositions comprising polyester macromers containing in one or more chains the residue of one or more diols and one or more diesters wherein the residue of the one or more diols and the one or more diesters alternate along the chain and a portion of the diesters are 1,1-diester-1-alkenes, and optionally one or more dihydrocarbyl dicarboxylates, and at least one terminal end comprises the residue of one of the 1,1-diester-1 alkenes and wherein one or more terminal ends may comprise the residue of one or more diols. The chains may contain the residue of the one or more diols and one or more diesters comprising one or more diesters 1,1-diester-1 alkenes and optionally one or more dihydrocarbyl dicarboxylates randomly disposed along the chains. Disclosed are methods of preparing the polyester macromers and incorporating them in a variety of polyester containing compositions such as coatings and films.
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Florida State University Jan 1, 2005 - 2009
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Applied Materials Oct 2005 - Nov 2010
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Applied Materials Apr 2004 - Oct 2005
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University of Wisconsin - Madison Jul 1997 - Feb 1999
University of Wisconsin - Madison Aug 1994 - Jul 1997
Grinnell College 1990 - 1994
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