Justin L. Mynar
Lawrence Berkeley National Laboratory
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Publication
Featured researches published by Justin L. Mynar.
Advanced Materials | 2011
Gianmarco Griffini; Jessica D. Douglas; Claudia Piliego; Thomas W. Holcombe; Stefano Turri; Jean M. J. Fréchet; Justin L. Mynar
Solution-processable polymer-based organic photovoltaics (OPVs) have attracted considerable attention over the past two decades because of the many advantages they can provide: lowcost fabrication, fl exible devices, and light-weight construction. [ 1 ] In the most successful OPV device architectures, the photoactive layer is composed of a blend of a p-type conjugated polymer and an n-type fullerene derivative, forming the socalled donor–acceptor bulk heterojunction (BHJ). [ 2 ]
Bioconjugate Chemistry | 2011
Jessica L. Cohen; Stephanie Schubert; Peter R. Wich; Lina Cui; Joel A. Cohen; Justin L. Mynar; Jean M. J. Fréchet
We report a new acid-sensitive, biocompatible, and biodegradable microparticulate delivery system, spermine modified acetalated-dextran (Spermine-Ac-DEX), which can be used to efficiently encapsulate siRNA. These particles demonstrated efficient gene knockdown in HeLa-luc cells with minimal toxicity. This knockdown was comparable to that obtained using Lipofectamine, a commercially available transfection reagent generally limited to in vitro use due to its high toxicity.
Chemical Communications | 2007
Justin L. Mynar; Andrew P. Goodwin; Joel A. Cohen; Ying-Zhong Ma; Graham R. Fleming; Jean M. J. Fréchet
Micelles of dendritic-linear copolymers have been developed to release a payload after infrared stimulus.
Journal of the American Chemical Society | 2008
Justin L. Mynar; Takuya Yamamoto; Atsuko Kosaka; Takanori Fukushima; Noriyuki Ishii; Takuzo Aida
An amphiphilic Gemini-shaped hexa-peri-hexabenzocoronene (1) with azide functionalities self-assembles to form graphitic nanotubes whose interior and exterior surfaces can be post-functionalized by “click chemistry”. A click reaction of the nanotubes with bulky macromolecules such as a dendronized alkyne (G2-alkyne) takes place site-selectively on the exterior surface of the nanotubes, leaving the azide functionalities on the interior surface mostly intact. A subsequent click reaction of the resulting nanotubes with alkynes having a much smaller steric bulk allows the remaining azide groups to be functionalized, affording radially diblock graphitic nanotubes.
Chemical Communications | 2005
Justin L. Mynar; Tae-Lim Choi; Masaru Yoshida; Victor Kim; Craig J. Hawker; Jean M. J. Fréchet
Doubly-dendronized polymers were synthesized by grafting polybenzyl ether dendrons onto a poly(hydroxy) styrene polymer with polyaliphatic esters.
Journal of the American Chemical Society | 2004
Brett A. Helms; Justin L. Mynar; Craig J. Hawker; Jean M. J. Fréchet
Journal of the American Chemical Society | 2005
Andrew P. Goodwin; Justin L. Mynar; Ying-Zhong Ma; Graham R. Fleming; Jean M. J. Fréchet
Journal of the American Chemical Society | 2006
Raymond J. Thibault; Kenichi Takizawa; Peter Lowenheilm; Brett A. Helms; Justin L. Mynar; Jean M. J. Fréchet; Craig J. Hawker
Journal of the American Chemical Society | 2011
William C. Floyd; Piper J. Klemm; Danil E. Smiles; Ayano C. Kohlgruber; Valérie C. Pierre; Justin L. Mynar; Jean M. J. Fréchet; Kenneth N. Raymond
ACS Applied Materials & Interfaces | 2010
John J. Chen; Teresa L. Chen; Bongsoo Kim; Daniel A. Poulsen; Justin L. Mynar; Jean M. J. Fréchet; Biwu Ma