Justin E. Poelma
University of California, Santa Barbara
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Publication
Featured researches published by Justin E. Poelma.
Journal of the American Chemical Society | 2014
Sameh Helmy; Frank A. Leibfarth; Saemi Oh; Justin E. Poelma; Craig J. Hawker; Javier Read de Alaniz
A versatile new class of organic photochromic molecules that offers an unprecedented combination of physical properties including tunable photoswitching using visible light, excellent fatigue resistance, and large polarity changes is described. These unique features offer significant opportunities in diverse fields ranging from biosensors to targeted delivery systems while also allowing non-experts ready synthetic access to these materials.
Journal of the American Chemical Society | 2013
Brett P. Fors; Justin E. Poelma; Matthew S. Menyo; Maxwell J. Robb; Daniel M. Spokoyny; John W. Kramer; J. Herbert Waite; Craig J. Hawker
A modular and general method based on a photomediated ATRA reaction for the spatially controlled functionalization of surfaces with visible light is reported. The ability to control reactivity with light intensity combined with the orthogonality of ATRA chemistry allows well-defined chemically differentiated monolayers and complex nonlinear chemical concentration gradients to be easily prepared. Use of light to mediate these reactions permits spatial regulation and the generation of unique, multifunctional chemical gradients.
ACS Nano | 2011
Hyunjung Jung; Dongjune Hwang; Eun Hye Kim; Byung Jae Kim; Won Bo Lee; Justin E. Poelma; Jihyun Kim; Craig J. Hawker; June Huh; Du Yeol Ryu; Joona Bang
Three-dimensional (3D) nanostructures were obtained by the directed formation of multilayer block copolymer (BCP) thin films. The initial step in this strategy involves the assembly and cross-linking of cylinder-forming polystyrene-b-poly(methyl methacrylate) (PS-b-PMMA) BCP, in which 1.5 mol % of reactive azido (-N(3)) groups were randomly incorporated along the styrene backbone. Significantly, assembly of thin films of lamellar-forming BCPs on top of the underlying cross-linked cylindrical layer exhibited perpendicular orientations of microdomains between lamellae and cylinder layers. From the theoretical calculation of free energy in the multilayers, it was found that the nematic interactions between polymer chains at the interface play a critical role in the perpendicular orientation of lamellae on the cross-linked cylinder layers. Removal of the PMMA domains then affords nonsymmetrical nanostructures which illustrate the promise of this strategy for the design of well-defined 3D nanotemplates. It was also demonstrated that this structure can be effectively used to enhance the light extraction efficiency of GaN light-emitting diodes. Furthermore, we anticipate that such 3D nanotemplates can be applied to various areas, including advanced BCP nanolithography and responsive surface coating.
Nature Nanotechnology | 2010
Justin E. Poelma; Craig J. Hawker
Complex nanoscale patterns can be generated by combining the self-assembly of block-copolymer thin films with minimal top-down templating.
Angewandte Chemie | 2013
Justin E. Poelma; Brett P. Fors; Gregory Meyers; John W. Kramer; Craig J. Hawker
ACS Nano | 2012
Justin E. Poelma; Kosuke Ono; Daigo Miyajima; Takuzo Aida; Kotaro Satoh; Craig J. Hawker
Polymer Chemistry | 2012
Kotaro Satoh; Justin E. Poelma; Luis M. Campos; Brian C. Stahl; Craig J. Hawker
Journal of Polymer Science Part A | 2015
Anna Melker; Brett P. Fors; Craig J. Hawker; Justin E. Poelma
Journal of Polymer Science Part A | 2016
Christian W. Pester; Justin E. Poelma; Benjaporn Narupai; Shrayesh N. Patel; Gregory M. Su; Thomas E. Mates; Yingdong Luo; Christopher K. Ober; Craig J. Hawker; Edward J. Kramer
ACS Macro Letters | 2013
Kristian Kempe; Justin E. Poelma; Hyunjung Jung; Joona Bang; Richard Hoogenboom; Helen Tran; Craig J. Hawker; Ulrich S. Schubert; Luis M. Campos