Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 156 entries
Sorted by: Best Match Show Resources per page
Synthesis of Polymerizable Cyclodextrin Derivatives for Use in Adhesion-Promoting Monomer Formulations.

Journal of research of the National Institute of Standards and Technology

Bowen RL, Carey CM, Flynn KM, Guttman CM.
PMID: 27504209
J Res Natl Inst Stand Technol. 2009 Feb 01;114(1):1-9. doi: 10.6028/jres.114.001. Print 2009.

The synthesis of the cyclodextrin derivatives reported herein was assisted by extensive literature research together with structure-property relationships derived from three-dimensional molecular modeling. These studies led to the hypothesis that many of the 21 hydroxyl groups on beta-cyclodextrin molecules...

Cite
Bowen RL, Carey CM, Flynn KM, et al. Synthesis of Polymerizable Cyclodextrin Derivatives for Use in Adhesion-Promoting Monomer Formulations. J Res Natl Inst Stand Technol. 2009;114(1):1-9doi: 10.6028/jres.114.001.
Bowen, R. L., Carey, C. M., Flynn, K. M., & Guttman, C. M. (2009). Synthesis of Polymerizable Cyclodextrin Derivatives for Use in Adhesion-Promoting Monomer Formulations. Journal of research of the National Institute of Standards and Technology, 114(1), 1-9. https://doi.org/10.6028/jres.114.001
Bowen, Rafael L, et al. "Synthesis of Polymerizable Cyclodextrin Derivatives for Use in Adhesion-Promoting Monomer Formulations." Journal of research of the National Institute of Standards and Technology vol. 114,1 (2009): 1-9. doi: https://doi.org/10.6028/jres.114.001
Bowen RL, Carey CM, Flynn KM, Guttman CM. Synthesis of Polymerizable Cyclodextrin Derivatives for Use in Adhesion-Promoting Monomer Formulations. J Res Natl Inst Stand Technol. 2009 Feb 01;114(1):1-9. doi: 10.6028/jres.114.001. Print 2009. PMID: 27504209; PMCID: PMC4651609.
Copy Download .nbib Format: NLM
Fabrication of Robust and Antifouling Superhydrophobic Surfaces via Surface-Initiated Atom Transfer Radical Polymerization.

ACS applied materials & interfaces

Xue CH, Guo XJ, Ma JZ, Jia ST.
PMID: 25832484
ACS Appl Mater Interfaces. 2015 Apr 22;7(15):8251-9. doi: 10.1021/acsami.5b01426. Epub 2015 Apr 10.

Superhydrophobic surfaces were fabricated via surface-initiated atom transfer radical polymerization of fluorinated methacrylates on poly(ethylene terephthalate) (PET) fabrics. The hydrophobicity of the PET fabric was systematically tunable by controlling the polymerization time. The obtained superhydrophobic fabrics showed excellent chemical...

Cite
Xue CH, Guo XJ, Ma JZ, et al. Fabrication of Robust and Antifouling Superhydrophobic Surfaces via Surface-Initiated Atom Transfer Radical Polymerization. ACS Appl Mater Interfaces. 2015;7(15):8251-9doi: 10.1021/acsami.5b01426.
Xue, C. H., Guo, X. J., Ma, J. Z., & Jia, S. T. (2015). Fabrication of Robust and Antifouling Superhydrophobic Surfaces via Surface-Initiated Atom Transfer Radical Polymerization. ACS applied materials & interfaces, 7(15), 8251-9. https://doi.org/10.1021/acsami.5b01426
Xue, Chao-Hua, et al. "Fabrication of Robust and Antifouling Superhydrophobic Surfaces via Surface-Initiated Atom Transfer Radical Polymerization." ACS applied materials & interfaces vol. 7,15 (2015): 8251-9. doi: https://doi.org/10.1021/acsami.5b01426
Xue CH, Guo XJ, Ma JZ, Jia ST. Fabrication of Robust and Antifouling Superhydrophobic Surfaces via Surface-Initiated Atom Transfer Radical Polymerization. ACS Appl Mater Interfaces. 2015 Apr 22;7(15):8251-9. doi: 10.1021/acsami.5b01426. Epub 2015 Apr 10. PMID: 25832484.
Copy Download .nbib Format: NLM
Semi-micro reversed-phase liquid chromatography for the separation of alkyl benzenes and proteins exploiting methacrylate- and polystyrene-based monolithic columns.

Journal of separation science

Masini JC.
PMID: 26960001
J Sep Sci. 2016 May;39(9):1648-55. doi: 10.1002/jssc.201600049. Epub 2016 Apr 14.

Monolithic columns were synthesized inside 1.02 mm internal diameter fused-silica lined stainless-steel tubing. Styrene and butyl, hexyl, lauryl, and glycidyl methacrylates were the functional monomers. Ethylene glycol dimethacrylate and divinylbenzene were the crosslinkers. The glycidyl methacrylate polymer was modified...

Cite
Masini JC. Semi-micro reversed-phase liquid chromatography for the separation of alkyl benzenes and proteins exploiting methacrylate- and polystyrene-based monolithic columns. J Sep Sci. 2016;39(9):1648-55doi: 10.1002/jssc.201600049.
Masini, J. C. (2016). Semi-micro reversed-phase liquid chromatography for the separation of alkyl benzenes and proteins exploiting methacrylate- and polystyrene-based monolithic columns. Journal of separation science, 39(9), 1648-55. https://doi.org/10.1002/jssc.201600049
Masini, Jorge Cesar. "Semi-micro reversed-phase liquid chromatography for the separation of alkyl benzenes and proteins exploiting methacrylate- and polystyrene-based monolithic columns." Journal of separation science vol. 39,9 (2016): 1648-55. doi: https://doi.org/10.1002/jssc.201600049
Masini JC. Semi-micro reversed-phase liquid chromatography for the separation of alkyl benzenes and proteins exploiting methacrylate- and polystyrene-based monolithic columns. J Sep Sci. 2016 May;39(9):1648-55. doi: 10.1002/jssc.201600049. Epub 2016 Apr 14. PMID: 26960001.
Copy Download .nbib Format: NLM
ansa-Zirconocene ester enolates: synthesis, structure, reaction with organo-lewis acids, and application to polymerization of methacrylates.

Journal of the American Chemical Society

Bolig AD, Chen EY.
PMID: 15080695
J Am Chem Soc. 2004 Apr 21;126(15):4897-906. doi: 10.1021/ja031558k.

The synthesis, structural characterization, and abstraction chemistry of ansa-zirconocene ester enolate complexes relevant to the isospecific polymerization of methacrylates are reported. Reactions of rac-(EBI)ZrMe(OTf) and rac-(EBI)Zr(OTf)(2) [EBI = C(2)H(4)(Ind)(2)] with 1 and 2 equiv of lithium isopropylisobutyrate in toluene...

Cite
Bolig AD, Chen EY. ansa-Zirconocene ester enolates: synthesis, structure, reaction with organo-lewis acids, and application to polymerization of methacrylates. J Am Chem Soc. 2004;126(15):4897-906doi: 10.1021/ja031558k.
Bolig, A. D., & Chen, E. Y. (2004). ansa-Zirconocene ester enolates: synthesis, structure, reaction with organo-lewis acids, and application to polymerization of methacrylates. Journal of the American Chemical Society, 126(15), 4897-906. https://doi.org/10.1021/ja031558k
Bolig, Andrew D, and Chen, Eugene Y-X. "ansa-Zirconocene ester enolates: synthesis, structure, reaction with organo-lewis acids, and application to polymerization of methacrylates." Journal of the American Chemical Society vol. 126,15 (2004): 4897-906. doi: https://doi.org/10.1021/ja031558k
Bolig AD, Chen EY. ansa-Zirconocene ester enolates: synthesis, structure, reaction with organo-lewis acids, and application to polymerization of methacrylates. J Am Chem Soc. 2004 Apr 21;126(15):4897-906. doi: 10.1021/ja031558k. PMID: 15080695.
Copy Download .nbib Format: NLM
Supported ATRP of fluorinated methacrylates in supercritical carbon dioxide: preparation of scCO2 soluble polymers with low catalytic residues.

Chemical communications (Cambridge, England)

Grignard B, Calberg C, Jérôme C, Wang W, Howdle S, Detrembleur C.
PMID: 19009087
Chem Commun (Camb). 2008 Nov 30;(44):5803-5. doi: 10.1039/b812297k. Epub 2008 Oct 01.

Synthesis of poly(2,2,2-trifluoroethyl methacrylate) by supported ATRP was investigated in supercritical carbon dioxide using a copper salt ligated to a polymeric ligand immobilised onto silica; after polymerisation, fluorinated polymers with well defined molecular weight and low polydispersity were obtained.

Cite
Grignard B, Calberg C, Jérôme C, et al. Supported ATRP of fluorinated methacrylates in supercritical carbon dioxide: preparation of scCO2 soluble polymers with low catalytic residues. Chem Commun (Camb). 2008;(44):5803-5doi: 10.1039/b812297k.
Grignard, B., Calberg, C., Jérôme, C., Wang, W., Howdle, S., & Detrembleur, C. (2008). Supported ATRP of fluorinated methacrylates in supercritical carbon dioxide: preparation of scCO2 soluble polymers with low catalytic residues. Chemical communications (Cambridge, England), (44), 5803-5. https://doi.org/10.1039/b812297k
Grignard, Bruno, et al. "Supported ATRP of fluorinated methacrylates in supercritical carbon dioxide: preparation of scCO2 soluble polymers with low catalytic residues." Chemical communications (Cambridge, England) vol. ,44 (2008): 5803-5. doi: https://doi.org/10.1039/b812297k
Grignard B, Calberg C, Jérôme C, Wang W, Howdle S, Detrembleur C. Supported ATRP of fluorinated methacrylates in supercritical carbon dioxide: preparation of scCO2 soluble polymers with low catalytic residues. Chem Commun (Camb). 2008 Nov 30;(44):5803-5. doi: 10.1039/b812297k. Epub 2008 Oct 01. PMID: 19009087.
Copy Download .nbib Format: NLM
Free radical generation upon plasma treatment of cotton fibers and their initiation efficiency in surface-graft polymerization.

Journal of colloid and interface science

Andreozzi L, Castelvetro V, Ciardelli G, Corsi L, Faetti M, Fatarella E, Zulli F.
PMID: 16112228
J Colloid Interface Sci. 2005 Sep 15;289(2):455-65. doi: 10.1016/j.jcis.2005.03.058.

Low-temperature plasma was used to activate mercerized cotton fabrics, to be followed by grafting with various methacrylates. Careful analysis of the experimental electron spin resonance (ESR) lineshapes of cotton samples treated at different RF powers made it possible to...

Cite
Andreozzi L, Castelvetro V, Ciardelli G, et al. Free radical generation upon plasma treatment of cotton fibers and their initiation efficiency in surface-graft polymerization. J Colloid Interface Sci. 2005;289(2):455-65doi: 10.1016/j.jcis.2005.03.058.
Andreozzi, L., Castelvetro, V., Ciardelli, G., Corsi, L., Faetti, M., Fatarella, E., & Zulli, F. (2005). Free radical generation upon plasma treatment of cotton fibers and their initiation efficiency in surface-graft polymerization. Journal of colloid and interface science, 289(2), 455-65. https://doi.org/10.1016/j.jcis.2005.03.058
Andreozzi, Laura, et al. "Free radical generation upon plasma treatment of cotton fibers and their initiation efficiency in surface-graft polymerization." Journal of colloid and interface science vol. 289,2 (2005): 455-65. doi: https://doi.org/10.1016/j.jcis.2005.03.058
Andreozzi L, Castelvetro V, Ciardelli G, Corsi L, Faetti M, Fatarella E, Zulli F. Free radical generation upon plasma treatment of cotton fibers and their initiation efficiency in surface-graft polymerization. J Colloid Interface Sci. 2005 Sep 15;289(2):455-65. doi: 10.1016/j.jcis.2005.03.058. PMID: 16112228.
Copy Download .nbib Format: NLM
Heterocyclic methacrylates for clinical applications-further studies of water sorption.

Journal of materials science. Materials in medicine

Sawtell RM, Downes S, Patel MP, Clarke RL, Braden M.
PMID: 15348817
J Mater Sci Mater Med. 1997 Nov;8(11):667-74. doi: 10.1023/a:1018531722265.

The room temperature polymerizing system comprising poly(ethyl methacrylate)-tetra hydrofurfuryl methacrylate (PEM/THFMA) has potential in orthopaedic and dental applications, and earlier work has shown it to have unusual water absorption characteristics. This aspect has been studied in further detail, by...

Cite
Sawtell RM, Downes S, Patel MP, et al. Heterocyclic methacrylates for clinical applications-further studies of water sorption. J Mater Sci Mater Med. 1997;8(11):667-74doi: 10.1023/a:1018531722265.
Sawtell, R. M., Downes, S., Patel, M. P., Clarke, R. L., & Braden, M. (1997). Heterocyclic methacrylates for clinical applications-further studies of water sorption. Journal of materials science. Materials in medicine, 8(11), 667-74. https://doi.org/10.1023/a:1018531722265
Sawtell, R M, et al. "Heterocyclic methacrylates for clinical applications-further studies of water sorption." Journal of materials science. Materials in medicine vol. 8,11 (1997): 667-74. doi: https://doi.org/10.1023/a:1018531722265
Sawtell RM, Downes S, Patel MP, Clarke RL, Braden M. Heterocyclic methacrylates for clinical applications-further studies of water sorption. J Mater Sci Mater Med. 1997 Nov;8(11):667-74. doi: 10.1023/a:1018531722265. PMID: 15348817.
Copy Download .nbib Format: NLM
Reactivity of methacrylates in insertion polymerization.

Journal of the American Chemical Society

Rünzi T, Guironnet D, Göttker-Schnetmann I, Mecking S.
PMID: 21043463
J Am Chem Soc. 2010 Nov 24;132(46):16623-30. doi: 10.1021/ja107538r. Epub 2010 Nov 02.

Polymerization of ethylene by complexes [{(P^O)PdMe(L)}] (P^O = κ(2)-(P,O)-2-(2-MeOC(6)H(4))(2)PC(6)H(4)SO(3))) affords homopolyethylene free of any methyl methacrylate (MMA)-derived units, even in the presence of substantial concentrations of MMA. In stoichiometric studies, reactive {(P^O)Pd(Me)L} fragments generated by halide abstraction from [({(P^O)Pd(Me)Cl}μ-Na)(2)]...

Cite
Rünzi T, Guironnet D, Göttker-Schnetmann I, et al. Reactivity of methacrylates in insertion polymerization. J Am Chem Soc. 2010;132(46):16623-30doi: 10.1021/ja107538r.
Rünzi, T., Guironnet, D., Göttker-Schnetmann, I., & Mecking, S. (2010). Reactivity of methacrylates in insertion polymerization. Journal of the American Chemical Society, 132(46), 16623-30. https://doi.org/10.1021/ja107538r
Rünzi, Thomas, et al. "Reactivity of methacrylates in insertion polymerization." Journal of the American Chemical Society vol. 132,46 (2010): 16623-30. doi: https://doi.org/10.1021/ja107538r
Rünzi T, Guironnet D, Göttker-Schnetmann I, Mecking S. Reactivity of methacrylates in insertion polymerization. J Am Chem Soc. 2010 Nov 24;132(46):16623-30. doi: 10.1021/ja107538r. Epub 2010 Nov 02. PMID: 21043463.
Copy Download .nbib Format: NLM
Comparison of annular diffusion denuder and high volume air samplers for measuring per- and polyfluoroalkyl substances in the atmosphere.

Analytical chemistry

Ahrens L, Shoeib M, Harner T, Lane DA, Guo R, Reiner EJ.
PMID: 22066738
Anal Chem. 2011 Dec 15;83(24):9622-8. doi: 10.1021/ac202414w. Epub 2011 Nov 28.

Overestimation of the particle phase concentration collected on glass-fiber filters (GFFs) has been reported for perfluoroalkyl carboxylic acids (PFCAs) using conventional high volume air samplers. In this study, per- and polyfluoroalkyl substances (PFASs) were determined in the gas and...

Cite
Ahrens L, Shoeib M, Harner T, et al. Comparison of annular diffusion denuder and high volume air samplers for measuring per- and polyfluoroalkyl substances in the atmosphere. Anal Chem. 2011;83(24):9622-8doi: 10.1021/ac202414w.
Ahrens, L., Shoeib, M., Harner, T., Lane, D. A., Guo, R., & Reiner, E. J. (2011). Comparison of annular diffusion denuder and high volume air samplers for measuring per- and polyfluoroalkyl substances in the atmosphere. Analytical chemistry, 83(24), 9622-8. https://doi.org/10.1021/ac202414w
Ahrens, Lutz, et al. "Comparison of annular diffusion denuder and high volume air samplers for measuring per- and polyfluoroalkyl substances in the atmosphere." Analytical chemistry vol. 83,24 (2011): 9622-8. doi: https://doi.org/10.1021/ac202414w
Ahrens L, Shoeib M, Harner T, Lane DA, Guo R, Reiner EJ. Comparison of annular diffusion denuder and high volume air samplers for measuring per- and polyfluoroalkyl substances in the atmosphere. Anal Chem. 2011 Dec 15;83(24):9622-8. doi: 10.1021/ac202414w. Epub 2011 Nov 28. PMID: 22066738.
Copy Download .nbib Format: NLM
Modeling spin-forbidden monomer self-initiation reactions in spontaneous free-radical polymerization of acrylates and methacrylates.

The journal of physical chemistry. A

Liu S, Srinivasan S, Tao J, Grady MC, Soroush M, Rappe AM.
PMID: 25188223
J Phys Chem A. 2014 Oct 09;118(40):9310-8. doi: 10.1021/jp503794j. Epub 2014 Sep 24.

A spin-forbidden reaction is a reaction in which the total electronic spin-state changes. The standard transition-state theory that assumes a reaction occurs on a single potential energy surface with spin-conservation cannot be applied to a spin-forbidden reaction directly. In...

Cite
Liu S, Srinivasan S, Tao J, et al. Modeling spin-forbidden monomer self-initiation reactions in spontaneous free-radical polymerization of acrylates and methacrylates. J Phys Chem A. 2014;118(40):9310-8doi: 10.1021/jp503794j.
Liu, S., Srinivasan, S., Tao, J., Grady, M. C., Soroush, M., & Rappe, A. M. (2014). Modeling spin-forbidden monomer self-initiation reactions in spontaneous free-radical polymerization of acrylates and methacrylates. The journal of physical chemistry. A, 118(40), 9310-8. https://doi.org/10.1021/jp503794j
Liu, Shi, et al. "Modeling spin-forbidden monomer self-initiation reactions in spontaneous free-radical polymerization of acrylates and methacrylates." The journal of physical chemistry. A vol. 118,40 (2014): 9310-8. doi: https://doi.org/10.1021/jp503794j
Liu S, Srinivasan S, Tao J, Grady MC, Soroush M, Rappe AM. Modeling spin-forbidden monomer self-initiation reactions in spontaneous free-radical polymerization of acrylates and methacrylates. J Phys Chem A. 2014 Oct 09;118(40):9310-8. doi: 10.1021/jp503794j. Epub 2014 Sep 24. PMID: 25188223.
Copy Download .nbib Format: NLM
Concentration effects in the base-catalyzed hydrolysis of oligo(ethylene glycol)- and amine-containing methacrylic monomers.

Designed monomers and polymers

Kazantsev OA, Orekhov DV, Sivokhin AP, Kamorin DM, Savinova MV.
PMID: 29491787
Des Monomers Polym. 2016 Sep 14;20(1):136-143. doi: 10.1080/15685551.2016.1231034. eCollection 2017.

Concentration effects in the base-catalyzed hydrolysis of water-soluble methacrylates (3-(N,N-dimethylaminoethyl) methacrylate (DMAEMA), 2-hydroxyethyl methacrylate (HEMA) and oligo(ethylene glycol) methacrylates (OEGMAs)) have been studied. These monomers are rapidly hydrolyzed in the presence of bases at the room temperature in dilute...

Cite
Kazantsev OA, Orekhov DV, Sivokhin AP, et al. Concentration effects in the base-catalyzed hydrolysis of oligo(ethylene glycol)- and amine-containing methacrylic monomers. Des Monomers Polym. 2016;20(1):136-143doi: 10.1080/15685551.2016.1231034.
Kazantsev, O. A., Orekhov, D. V., Sivokhin, A. P., Kamorin, D. M., & Savinova, M. V. (2017). Concentration effects in the base-catalyzed hydrolysis of oligo(ethylene glycol)- and amine-containing methacrylic monomers. Designed monomers and polymers, 20(1), 136-143. https://doi.org/10.1080/15685551.2016.1231034
Kazantsev, Oleg A, et al. "Concentration effects in the base-catalyzed hydrolysis of oligo(ethylene glycol)- and amine-containing methacrylic monomers." Designed monomers and polymers vol. 20,1 (2017): 136-143. doi: https://doi.org/10.1080/15685551.2016.1231034
Kazantsev OA, Orekhov DV, Sivokhin AP, Kamorin DM, Savinova MV. Concentration effects in the base-catalyzed hydrolysis of oligo(ethylene glycol)- and amine-containing methacrylic monomers. Des Monomers Polym. 2016 Sep 14;20(1):136-143. doi: 10.1080/15685551.2016.1231034. eCollection 2017. PMID: 29491787; PMCID: PMC5812183.
Copy Download .nbib Format: NLM
Silicon Oxycarbide/Carbon Nanohybrids with Tiny Silicon Oxycarbide Particles Embedded in Free Carbon Matrix Based on Photoactive Dental Methacrylates.

ACS applied materials & interfaces

Wang M, Xia Y, Wang X, Xiao Y, Liu R, Wu Q, Qiu B, Metwalli E, Xia S, Yao Y, Chen G, Liu Y, Liu Z, Meng JQ, Yang Z, Sun LD, Yan CH, Müller-Buschbaum P, Pan J, Cheng YJ.
PMID: 27186647
ACS Appl Mater Interfaces. 2016 Jun 08;8(22):13982-92. doi: 10.1021/acsami.6b05032. Epub 2016 May 26.

A new facile scalable method has been developed to synthesize silicon oxycarbide (SiOC)/carbon nanohybrids using difunctional dental methacrylate monomers as solvent and carbon source and the silane coupling agent as the precursor for SiOC. The content (from 100% to...

Cite
Wang M, Xia Y, Wang X, et al. Silicon Oxycarbide/Carbon Nanohybrids with Tiny Silicon Oxycarbide Particles Embedded in Free Carbon Matrix Based on Photoactive Dental Methacrylates. ACS Appl Mater Interfaces. 2016;8(22):13982-92doi: 10.1021/acsami.6b05032.
Wang, M., Xia, Y., Wang, X., Xiao, Y., Liu, R., Wu, Q., Qiu, B., Metwalli, E., Xia, S., Yao, Y., Chen, G., Liu, Y., Liu, Z., Meng, J. Q., Yang, Z., Sun, L. D., Yan, C. H., Müller-Buschbaum, P., Pan, J., & Cheng, Y. J. (2016). Silicon Oxycarbide/Carbon Nanohybrids with Tiny Silicon Oxycarbide Particles Embedded in Free Carbon Matrix Based on Photoactive Dental Methacrylates. ACS applied materials & interfaces, 8(22), 13982-92. https://doi.org/10.1021/acsami.6b05032
Wang, Meimei, et al. "Silicon Oxycarbide/Carbon Nanohybrids with Tiny Silicon Oxycarbide Particles Embedded in Free Carbon Matrix Based on Photoactive Dental Methacrylates." ACS applied materials & interfaces vol. 8,22 (2016): 13982-92. doi: https://doi.org/10.1021/acsami.6b05032
Wang M, Xia Y, Wang X, Xiao Y, Liu R, Wu Q, Qiu B, Metwalli E, Xia S, Yao Y, Chen G, Liu Y, Liu Z, Meng JQ, Yang Z, Sun LD, Yan CH, Müller-Buschbaum P, Pan J, Cheng YJ. Silicon Oxycarbide/Carbon Nanohybrids with Tiny Silicon Oxycarbide Particles Embedded in Free Carbon Matrix Based on Photoactive Dental Methacrylates. ACS Appl Mater Interfaces. 2016 Jun 08;8(22):13982-92. doi: 10.1021/acsami.6b05032. Epub 2016 May 26. PMID: 27186647.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 156 entries