Year |
Citation |
Score |
2014 |
Kurt P, Chakravorty A, Zeng X, Wynne KJ. Strongly amphiphilic wetting behavior for polyurethanes with polyoxetane soft blocks having -CF2H terminated side chains Polymer (United Kingdom). 55: 2170-2178. DOI: 10.1016/J.Polymer.2014.03.011 |
0.527 |
|
2014 |
Wynne KJ, Kurt P, Makal U, Fujiwara T, Brunson K, Chakravorty A, Wood L, Ohman DE. Functional Fluorous Copolyoxetane Polymer Surface Modifiers Handbook of Fluoropolymer Science and Technology. 201-234. DOI: 10.1002/9781118850220.ch10 |
0.626 |
|
2013 |
Wynne KJ, Kurt P, Brunson K, Chakravorty A, Gupta M, Zhang W, Wood L, Ohman DE. Health and safety via surface modification of polyurethanes Acs Symposium Series. 1135: 303-318. DOI: 10.1021/bk-2013-1135.ch018 |
0.517 |
|
2011 |
Chakrabarty S, King A, Kurt P, Zhang W, Ohman DE, Wood LF, Lovelace C, Rao R, Wynne KJ. Highly effective, water-soluble, hemocompatible 1,3-propylene oxide-based antimicrobials: poly[(3,3-quaternary/PEG)-copolyoxetanes]. Biomacromolecules. 12: 757-69. PMID 21280645 DOI: 10.1021/Bm101381Y |
0.665 |
|
2010 |
Gupta ML, Brunson K, Chakravorty A, Kurt P, Alvarez JC, Luna-Vera F, Wynne KJ. Quantifying surface-accessible quaternary charge for surface modified coatings via streaming potential measurements. Langmuir : the Acs Journal of Surfaces and Colloids. 26: 9032-9. PMID 20334402 DOI: 10.1021/La904849U |
0.737 |
|
2008 |
Kurt P, Gamble LJ, Wynne KJ. Surface characterization of biocidal polyurethane modifiers having poly(3,3-substituted)oxetane soft blocks with alkylammonium side chains. Langmuir : the Acs Journal of Surfaces and Colloids. 24: 5816-24. PMID 18444667 DOI: 10.1021/La800203Y |
0.674 |
|
2007 |
Wynne KJ, Makal U, Kurt P, Gamble L. Model fluorous polyurethane surface modifiers having co-polyoxetane soft blocks with trifluoroethoxymethyl and bromomethyl side chains. Langmuir : the Acs Journal of Surfaces and Colloids. 23: 10573-80. PMID 17824629 DOI: 10.1021/La701684A |
0.701 |
|
2007 |
Kurt P, Wood L, Ohman DE, Wynne KJ. Highly effective contact antimicrobial surfaces via polymer surface modifiers. Langmuir : the Acs Journal of Surfaces and Colloids. 23: 4719-23. PMID 17388618 DOI: 10.1021/La063718M |
0.678 |
|
2007 |
Kurt P, Wynne KJ. Co-polyoxetanes with alkylammonium and fluorous or PEG-like side chains: Soft blocks for surface modifying polyurethanes Macromolecules. 40: 9537-9543. DOI: 10.1021/Ma071763A |
0.674 |
|
2007 |
Grunzinger SJ, Kurt P, Brunson KM, Wood L, Ohman DE, Wynne KJ. Biocidal activity of hydantoin-containing polyurethane polymeric surface modifiers Polymer. 48: 4653-4662. DOI: 10.1016/J.Polymer.2007.06.010 |
0.745 |
|
2005 |
Makal U, Uilk J, Kurt P, Cooke RS, Wynne KJ. Ring opening polymerization of 3-semifluoro- and 3-bromomethyloxetanes to poly(2,2-substituted-1,3-propylene oxide) telechelics for soft blocks in polyurethanes Polymer. 46: 2522-2530. DOI: 10.1016/J.Polymer.2005.01.069 |
0.544 |
|
2003 |
Yilgor E, Atilla GE, Ekin A, Kurt P, Yilgor I. Isopropyl alcohol: An unusual, powerful, 'green' solvent for the preparation of silicone-urea copolymers with high urea contents Polymer. 44: 7787-7793. DOI: 10.1016/j.polymer.2003.10.048 |
0.332 |
|
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