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pro vyhledávání: '"Jesse L. Davis"'
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
Chain exchange behaviors in self-assembled block copolymer (BCP) nanoparticles (NPs) at room temperature are investigated through observations of structural differences between parent and binary systems of BCP NPs with and without crosslinked domains
Externí odkaz:
https://doaj.org/article/4d8bfaf6f50e40c3a80c8ef3cf217a06
Publikováno v:
Macromolecules. 51:3691-3701
Relations between molecular design, chemical functionality, and stimulus-triggered response are important for a variety of applications of polymeric systems. Here, reactive amphiphilic block copolymers (BCPs) of poly(2-vinylpyridine)-block-poly(2-vin
Autor:
Kamlesh Bornani, Xu Wang, Juan Pablo Hinestrosa, S. Michael Kilbey, Jimmy W. Mays, Jesse L. Davis
Publikováno v:
Macromolecules. 49:2288-2297
In comparison to the behavior of linear block copolymers, much less is known about the structure and properties of highly branched polymeric materials. Motivated by this, the solution properties of a series of 26- and 40-arm polystyrene–poly(2-viny
Publikováno v:
Macromolecules. 47:7138-7150
The self-assembly of binary mixtures of architecturally and compositionally diverse surfactant-like polystyrene–poly(2-vinylpyridine) (PS–PVP) block copolymers (BCPs) in solution and in thin films has been systematically studied. PS–PVP BCPs of
Autor:
Tzvetelin D. Iordanov, Olga V. Przhonska, Jesse L. Davis, Artëm E. Masunov, Alexei D. Kachkovski, Andrew Levenson
Publikováno v:
International Journal of Quantum Chemistry. 109:3592-3601
Charge localization and dynamics in conjugated organic molecules, as well as their spectral signatures are of great importance for photonic and photovoltaic applications. Intramolecular charge delocalization in polymethine dyes occurs through π-conj
Autor:
Kamlesh Bornani, S. Michael Kilbey, Xu Wang, Jesse L. Davis, Weiyu Wang, Xiaojun Wang, Jimmy W. Mays, Juan Pablo Hinestrosa
Publikováno v:
Soft matter. 11(32)
Self-assembly of semi-flexible/flexible block copolymers in a selective solvent is examined using a set of diblock copolymers where the chain microstructure of the semi-flexible block is manipulated in order to tune chain stiffness. Conceptually, the