Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Priscilla G. Taylor"'
Autor:
Barbara Baird, Kari M. Midthun, Christopher K. Ober, Sotiris E. Kakabakos, Jin-Kyun Lee, Panagiota S. Petrou, Priscilla G. Taylor, Carol Newby, Margarita Chatzichristidi
Publikováno v:
Biomacromolecules. 14:993-1002
The ability to spatially deposit multiple biomolecules onto a single surface with high-resolution while retaining biomolecule stability and integrity is critical to the development of micro- and nanoscale bio-devices. While conventional lithographic
Autor:
Brian N. Kim, Jin-Kyun Lee, Sang Yoon Yang, Manfred Lindau, Alex Zakhidov, George G. Malliaras, Priscilla G. Taylor, Christopher K. Ober
Publikováno v:
Advanced Materials
Advanced Materials, Wiley-VCH Verlag, 2011, 23, pp.H184
Advanced Materials, Wiley-VCH Verlag, 2011, 23, pp.H184
The advent of organic electronics has made available a host of materials and devices with unique properties for interfacing with biology.1–2 One example is the use of conducting polymer coatings on metal electrodes that are implanted in the central
Autor:
Jin-Kyun Lee, Héctor D. Abruña, Priscilla G. Taylor, Mitk’El B. Santiago-Berríos, Andrew B. Holmes, Hon Hang Fong, Christopher K. Ober, Georgia E. McCluskey, Alex Zakhidov, George G. Malliaras
Publikováno v:
Macromolecules. 43:1195-1198
The challenging synthesis of semiperfluoroalkyl polyfluorenes and characterization of their electro-optical properties has been reported. Solutions of conjugated polymers can be dispensed onto the desired area by inkjet printing or screen printing, o
Autor:
George G. Malliaras, Christopher K. Ober, Alex Zakhidov, Priscilla G. Taylor, John A. DeFranco, Margarita Chatzichristidi, Hon Hang Fong, Jin-Kyun Lee
Publikováno v:
Advanced Materials. 21:2314-2317
2009 WILEY-VCH Verlag Gmb Organic electronics is an emerging technology opening new opportunities in the field of large-area electronics. It has received enormous attention as a technology platform that enables flexible, large-scale devices by exploi
Hydrofluoroethers as Orthogonal Solvents for the Chemical Processing of Organic Electronic Materials
Autor:
John A. DeFranco, George G. Malliaras, Margarita Chatzichristidi, Hon Hang Fong, Christopher K. Ober, Jin-Kyun Lee, Alex Zakhidov, Priscilla G. Taylor
Publikováno v:
Advanced Materials. 20:3481-3484
A study was conducted to demonstrate a new approach for chemicalprocessing of organic electronic materials. It was demonstrated that the approach is based on the use of fluorous solvents, segregated hydrofluoroethers (HFE). The study also demonstrate
Publikováno v:
Chemistry of Materials. 18:4513-4518
Diazonium salt-functionalized oligoanilines have been synthesized and assembled on hydride passivated silicon surfaces for subsequent incorporation into hybrid molecule−silicon device architectures. The targeted oligoanilines were synthesized using
Publikováno v:
Physics and Chemistry of Liquids. 41:73-80
Experimental solubilities are reported at 25.0°C for 9-fluorenone dissolved in 40 different organic nonelectrolyte solvents containing ether-, chloro-, hydroxy-, cyano and t -butyl-functional groups. Results of these measurements are used to test th
Publikováno v:
Journal of Chemical & Engineering Data. 48:1341-1343
Experimental solubilities are reported for anthracene dissolved in seven binary alcohol + 2-methyl-1-butanol solvent mixtures at 25 °C. The alcohol cosolvents studied were 1-propanol, 2-propanol, 1-butanol, 2-butanol, 2-methyl-1-propanol, 3-methyl-1
Publikováno v:
Journal of Chemical & Engineering Data. 48:736-738
Experimental solubilities are reported for pyrene dissolved in seven binary alcohol + acetonitrile solvent mixtures at 26 °C. The alcohol cosolvents studied were 1-propanol, 2-propanol, 1-butanol, 2-butanol, 2-methyl-1-propanol, 3-methyl-1-butanol,
Publikováno v:
Journal of Chemical & Engineering Data. 48:720-722
Experimental solubilities are reported for anthracene dissolved in six binary alcohol + acetonitrile solvent mixtures at 25 °C. The alcohol cosolvents studied were methanol, ethanol, 1-pentanol, 2-pentanol, 2-methyl-1-pentanol, and 4-methyl-2-pentan