子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 101 | FLAME RETARDANT CELLULOSE | US13734199 | 2013-01-04 | US20140194617A1 | 2014-07-10 | Dylan J. Boday; Joseph Kuczynski |
| Flame retardant cellulose is prepared comprising cellulose fibers and an organophosphate compound bonded to the cellulose fibers. Accordingly, the bonded phosphate-functional group provides the cellulose fibers with pendant phosphate ester functionality. Numerous phosphate derivatives can be envisaged that will accomplish the intended task. | ||||||
| 102 | Molecule-based magnetic polymers and methods | US13271693 | 2011-10-12 | US08658751B2 | 2014-02-25 | Chang Dae Han; Wenyi Huang |
| Molecule-based magnetic polymers with reasonably high Curie temperature and methods of preparing are provided. In particular, magnetic polymers having repeating units of an organometallic monomer covalently bonded to a monomer having a plurality of unpaired electrons are disclosed. Intrinsically homogeneous magnetic fluids (liquid magnets) and methods of preparing are also provided. | ||||||
| 103 | Fully Backbone Degradable and Functionalizable Polymers Derived from the Ring-Opening Metathesis Polymerization (ROMP) | US13841592 | 2013-03-15 | US20130281644A1 | 2013-10-24 | Laura L. KIESSLING; Joshua Fishman; Lynne Prost |
| Functionalized degradable ROMP (ring-opening metathesis) polymers and methods, starting monomers and synthetic monomeric and polymeric intermediates for preparation of such functionalized polymers. More specifically, monomers having a bicyclic oxazinone structure, a bicyclic urea, or a heteronorbornene core structure, among others, have been found to be substrates for ROMP polymerization. ROMP polymers prepared from these monomers have been found to be both acid and base labile. Additionally, the monomers can be chemically modified at a site distal to the polymerizable moieties and bridgehead carbons. The properties of the resulting polymers and copolymers can be tailored without destabiling the monomer. Polymers and copolymers of the invention are degradable but have a glass temperature of 100° C. or more. | ||||||
| 104 | Thermo-responsive polymer covalently bound with a peptide | US13877910 | 2011-10-06 | US20130281602A1 | 2013-10-24 | Alberto Saiani; Aline Miller; Roland Callens; Laurent Jeannin; Wafa Moussa |
| A thermo-responsive polymer covalently bound with a peptide, wherein the peptide comprises a peptide moiety that is able to self-assemble and a functional peptide moiety comprising a bioactive sequence, and compositions comprising such thermo-responsive polymer covalently bound with a peptide. Methods for the preparation of such thermo-responsive polymers covalently bound with a peptide and the use thereof for the preparation of hydrogels. | ||||||
| 105 | Bioactive amino acid sequence and use therefrom | US13877915 | 2011-10-06 | US20130210147A1 | 2013-08-15 | Laurent Jeannin; Roland Callens; Wafa Moussa |
| Use of the amino acid sequence Har-Gly-Asp (hRGD) as a bioactive sequence in functional peptides to promote cell adhesion, cell growth, and/or cell differentiation, and in the preparation of hydrogels, preferably hydrogels for cell culture. A hydrogel comprising the hRGD sequence, especially a hydrogel wherein the hRGD sequence is part of the hydrogel scaffold. | ||||||
| 106 | Polymerizable higher diamondoid derivatives | US12973513 | 2010-12-20 | US08420768B2 | 2013-04-16 | Jeremy E. Dahl; Robert M. Carlson; Shenggao Liu |
| Higher diamondoid derivatives capable of taking part in polymerization reactions are disclosed as well as intermediates to these derivatives, polymers formed from these derivatives and methods for preparing the polymers. | ||||||
| 107 | SUBSTRATE-INDEPENDENT LAYER-BY-LAYER ASSEMBLY USING CATECHOL-FUNCTIONALIZED POLYMERS | US13622136 | 2012-09-18 | US20130017332A1 | 2013-01-17 | Phillip B. Messersmith; Haeshin Lee; Yuhan Lee; Zhongqiang Liu; Lesley Hamming |
| The present invention provides a simple, non-destructive and versatile method that enables layer-by-layer (LbL) assembly to be performed on virtually any substrate. A novel catechol-functionalized polymer which adsorbs to virtually all surfaces and can serve as a platform for LbL assembly in a surface-independent fashion is also provided. | ||||||
| 108 | Block coordination copolymers | US12478042 | 2009-06-04 | US08309661B2 | 2012-11-13 | Kyoung Moo Koh; Antek G. Wong-Foy; Adam J. Matzger; Annabelle I. Benin; Richard R. Willis |
| The present invention provides compositions of crystalline coordination copolymers wherein multiple organic molecules are assembled to produce porous framework materials with layered or core-shell structures. These materials are synthesized by sequential growth techniques such as the seed growth technique. In addition, the invention provides a simple procedure for controlling functionality. | ||||||
| 109 | Substrate-independent layer-by-layer assembly using catechol-functionalized polymers | US12267822 | 2008-11-10 | US08293867B2 | 2012-10-23 | Phillip B. Messersmith; Haeshin Lee; Yuhan Lee; Zhongqiang Liu; Lesley Hamming |
| The present invention provides a simple, non-destructive and versatile method that enables layer-by-layer (LbL) assembly to be performed on virtually any substrate. A catechol-functionalized polymer which adsorbs to virtually all surfaces and can serve as a platform for LbL assembly in a surface-independent fashion is also provided. | ||||||
| 110 | Method for Preparing Inorganic Resins on the Basis of Hydrogen-Free, Polymeric Isocyanates for Preparing Nitride, Carbide and Carbonitride Networks and Use Thereof as Protective Coatings | US13384662 | 2010-07-21 | US20120207933A1 | 2012-08-16 | Carsten Ludwig Schmidt; Martin Jansen |
| The present invention relates to methods for producing inorganic resins, comprising the polymerisation of at least one hydrogen-free, inorganic isocyanate which may be converted into a pure, hydrogen-free polymer by CO2 abstraction, to resins which are produced by this method, and to the use of such resins for producing coatings. | ||||||
| 111 | PROCESS FOR PREPARATION OF CYCLODEXTRIN OLIGOMERS OR POLYMERS, PRODUCTS OBTAINED AND USES | US12446309 | 2007-10-18 | US20100303754A1 | 2010-12-02 | Frederic Turpin; Carole Brigand; Yves Cenatiempo; EI Mustapha Belgsir |
| A process for the preparation of cyclodextrin oligomers or polymers, whereby the cyclodextrin molecules are coupled to one another covalently via a spacer arm, based on a coupling reaction between an alkyne and an azide producing the formation of an aromatic heterocyclic bridge between the coupled units. Also described are the cyclodextrin oligomers or polymers that are obtained and their uses. | ||||||
| 112 | MOLECULE-BASED MAGNETIC POLYMERS AND METHODS | US12717607 | 2010-03-04 | US20100155649A1 | 2010-06-24 | Chang Dae Han; Wenyi Huang |
| Molecule-based magnetic polymers with high Curie temperature and methods of preparing are provided. In particular, magnetic polymers having repeating units of an electron-donor metallocene-containing monomer covalently bonded to an electron-acceptor monomer having a plurality of unpaired electrons are disclosed. Intrinsically homogeneous magnetic fluids (liquid magnets) and methods of preparing are also provided. | ||||||
| 113 | Materials having crosslinked polyrotaxane and process for producing the same | US11579842 | 2005-05-06 | US07612142B2 | 2009-11-03 | Kohzo Ito; Jun Araki |
| A material having crosslinked polyrotaxane which has further improved swelling properties, especially one having a crosslinked polyrotaxane which changes in swelling property with change in pH; and a material having a crosslinked polyrotaxane which is responsive especially at a high speed to a change of the surrounding electric field. The materials have a crosslinked polyrotaxane comprising at least two polyrotaxane molecules which each comprises cyclic molecules, a linear molecule which includes the cyclic molecules in cavities of cyclic molecules in a skewered manner, and capping groups, each of which locates at each end of the linear molecule in order to prevent the dissociation of the cyclic molecules, the least two polyrotaxane molecules having been bound to each other through a chemical bonding between the cyclic molecules thereof, wherein the cyclic molecules have hydroxy groups (—OHs) and part of the hydroxy groups are substituted with a group having an ionic group. | ||||||
| 114 | Diamondoid-containing low dielectric constant materials | US10784915 | 2004-02-24 | US07306671B2 | 2007-12-11 | Jeremy E. Dahl; Robert M. Carlson; Shenggao Liu |
| Novel uses of diamondoid-containing materials in the field of microelectronics are disclosed. Embodiments include, but are not limited to, thermally conductive films in integrated circuit packaging, low-k dielectric layers in integrated circuit multilevel interconnects, thermally conductive adhesive films, thermally conductive films in thermoelectric cooling devices, passivation films for integrated circuit devices (ICs), and field emission cathodes. The diamondoids employed in the present invention may be selected from lower diamondoids, as well as the newly provided higher diamondoids, including substituted and unsubstituted diamondoids. The higher diamondoids include tetramantane, peritamantane, hexamantane, heptamantane, octamantane, nonamantane, decamantane, and undecamantane. The diamondoid-containing material may be fabricated as a diamondoid-containing polymer, a diamondoid-containing sintered ceramic, a diamondoid ceramic composite, a CVD diamondoid film, a self-assembled diamondoid film, and a diamondoid-fullerene composite. | ||||||
| 115 | Method for the Production of an Isotropic Polymeric Network | US10552472 | 2004-04-14 | US20070269657A1 | 2007-11-22 | Roelof Marissen; Ronald Lange; Betty Coussens; Jozef Put; Joachim Dijk Van; Jacobus Loontjens |
| The present invention relates to a method for the production of an isotropic polymeric network comprising multifunctional molecules with a functionality of at least 5 by reacting in a solvent the multifunctional molecules with a coupling agent, wherein the coupling agent is present in an amount which is sufficient to couple the multifunctional molecules to at least 5 other multifunctional molecules and wherein the sum, ρ, of the amounts of the multifunctional molecules and coupling agent per unit of volume, in kg/m3, is at least equal to the value as given by expression (I) in which a=0.2 d=the diameter of the multifunctional molecule, including the length of the bonds to the middle of atoms of the coupling agent to which it is attached. L=the length of the coupling agent, measured between the middle of the atoms that are connected to the multifunctional molecule. m1=the molecular mass of the multifunctional molecule as present in the isotropic 20 polymeric network m2=the molecular mass of the coupling agent as present in the isotropic polymeric network n=the functionality of the multifunctional molecule (n≧5). The invention furthermore relates to an isotropic polymeric network with a density lower than 1000 kg/m3 and a specific Young's modulus of at least 0.01 GPa.m3/kg, shaped articles hereof and the use of the isotropic polymeric network as construction material. | ||||||
| 116 | Diamondoid-containing thermally conductive materials | US10892037 | 2004-07-14 | US07276222B2 | 2007-10-02 | Jeremy E. Dahl; Robert M. Carlson; Shenggao Liu |
| Novel uses of diamondoid-containing materials in the field of microelectronics are disclosed. Embodiments include, but are not limited to, thermally conductive films in integrated circuit packaging, thermally conductive adhesive films, and thermally conductive films in thermoelectric cooling devices. The diamondoids employed in the present invention may be selected from lower diamondoids, as well as the newly provided higher diamondoids, including substituted and unsubstituted diamondoids. The higher diamondoids include tetramantane, pentamantane, hexamantane, heptamantane, octamantane, nonamantane, decamantane, and undecamantane. The diamondoid-containing material may be fabricated as a diamondoid-containing polymer, a diamondoid-containing sintered ceramic, a diamondoid ceramic composite, a CVD diamondoid film, a self-assembled diamondoid film, and a diamondoid-fullerene composite. | ||||||
| 117 | Diamondoid-containing field emission devices | US10784885 | 2004-02-24 | US07160529B2 | 2007-01-09 | Jeremy E. Dahl; Robert M. Carlson; Shenggao Liu |
| Novel uses of diamondoid-containing materials in the field of microelectronics are disclosed. Embodiments include, but are not limited to, thermally conductive films in integrated circuit packaging, low-k dielectric layers in integrated circuit multilevel interconnects, thermally conductive adhesive films, thermally conductive films in thermoelectric cooling devices, passivation films for integrated circuit devices (ICs), and field emission cathodes. The diamondoids employed in the present invention may be selected from lower diamondoids, as well as the newly provided higher diamondoids, including substituted and unsubstituted diamondoids. The higher diamondoids include tetramantane, pentamantane, hexamantane, heptamantane, octamantane, nonamantane, decamantane, and undecamantane. The diamondoid-containing material may be fabricated as a diamondoid-containing polymer, a diamondoid-containing sintered ceramic, a diamondoid ceramic composite, a CVD diamondoid film, a self-assembled diamondoid film, and a diamondoid-fullerene composite. | ||||||
| 118 | Compositions comprising cyclohexamantane | US10012335 | 2001-12-12 | US07094937B2 | 2006-08-22 | Jeremy E. Dahl; Robert M. Carlson |
| Disclosed are compositions comprising C26H30 hexamantane, referred to herein as peri-condensed hexamantane, fully condensed hexamantane, and cyclohexamantane. These enriched cyclohexamantane compositions comprise at least 5 percent by weight cyclohexamantane based upon the total weight of the composition. | ||||||
| 119 | Nucleation of diamond films using higher diamondoids | US10864768 | 2004-06-10 | US20050019576A1 | 2005-01-27 | Jeremy Dahl; Robert Carlson; Shenggao Liu |
| Novel uses of higher diamondoids are disclosed. Specifically, higher diamondoids may be used to nucleate diamond films and diamond-like carbon films. Such higher diamondoids include iso-tetramantane [1(2)3], anti-tetramantane [121], the two enantiomers of skew-tetramantane [123], the ten possible pentamantane, the thirty nine possible hexamantanes, the one hundred sixty heptamantanes, as well as the various octamantanes, nonamantanes, decamantanes, and undecamantanes. | ||||||
| 120 | Processes for the purification of higher diamondoids and compositions comprising such diamondoids | US10017821 | 2001-12-12 | US06844477B2 | 2005-01-18 | Jeremy E. Dahl; Robert M. Carlson |
| Disclosed are processes for the recovery and purification of higher diamondoids from a hydrocarbonaceous feedstock. Specifically disclosed is a multi-step recovery process for obtaining diamondoid compositions enhanced in tetramantane components and higher diamondoid components. Also disclosed are compositions comprising at least about 10 weight percent of non-ionized tetramantane components and higher diamondoid components and at least about 0.5 weight percent of non-ionized pentamantane components and higher diamondoid components based on the total weight of diamondoid components present. | ||||||
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