M
Michael Kuepfert
Researcher at New York University
Publications - 15
Citations - 607
Michael Kuepfert is an academic researcher from New York University. The author has contributed to research in topics: Nanoreactor & Electrochromism. The author has an hindex of 7, co-authored 15 publications receiving 415 citations. Previous affiliations of Michael Kuepfert include Ciba Specialty Chemicals & Novartis.
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Journal ArticleDOI
Four Shades of Brown: Tuning of Electrochromic Polymer Blends Toward High-Contrast Eyewear
Anna M. Österholm,D. Eric Shen,Justin A. Kerszulis,Rayford H. Bulloch,Michael Kuepfert,Aubrey L. Dyer,John R. Reynolds +6 more
TL;DR: A set of brown ECP blends that can be incorporated as the active material in user-controlled, high-contrast, fast-switching, and fully solution-processable electrochromic lenses with colorless transmissive states and colored states that correspond to commercially available sunglasses are created.
Journal ArticleDOI
Tuning the painter's palette: subtle steric effects on spectra and colour in conjugated electrochromic polymers
Justin A. Kerszulis,K. E. Johnson,Michael Kuepfert,D. Khoshabo,Aubrey L. Dyer,Aubrey L. Dyer,John R. Reynolds +6 more
TL;DR: A series of vibrantly coloured π-conjugated electrochromic polymers (ECPs) were designed and synthesized with the goal of extracting structure-property relationships from subtle changes in steric strain or relaxation as discussed by the authors.
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Conjugated Polymer Blends for High Contrast Black-to-Transmissive Electrochromism
Lisa R. Savagian,Anna M. Österholm,Dwanleen Eric Shen,Dylan T. Christiansen,Michael Kuepfert,John R. Reynolds +5 more
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Compartmentalized Nanoreactors for One-Pot Redox-Driven Transformations
TL;DR: In this article, a poly(2-oxazoline)-based shell cross-linked micelles (SCMs) are used as nanoreactors to realize one-pot redox-driven deracemizations of secondary alcohols in aqueous media.
Journal ArticleDOI
Synthetic studies on N-alkoxyamines: a mild and broadly applicable route starting from nitroxide radicals and aldehydes.
TL;DR: A broad variety of 2,2,6,6-tetramethylpiperidine-based N-alkoxyamines were prepared in a newly found reaction by means of a copper-catalyzed fragmentation reaction of aldehyde peroxides in the presence of TEM PO or TEMPO derivatives.