Výsledky vyhledávání - "Marc J. Junge"

Study of a carbazole–bromobenzothiadiazole derived fluorescent molecular rotor: crystal structure, redox activity, and solvatofluorochromic effects

Autor: Zahra A. Tabasi, Yuming Zhao, Marc J. Junge, Maryam F. Abdollahi, Erin T. Chernick

Publikováno v: New Journal of Chemistry. 46:572-581

This work investigated the properties of a four-component molecular ensemble, in which a carbazole (CBz) donor and a benzothiadiazole (BTD) acceptor are connected through a phenylthiophene (PT) bridge. The multiple rotational freedoms at the C--C sin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3d3ae95943552d0cfb60ec9582abc7ba
https://doi.org/10.1039/d1nj04274b

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Synthesis of Chiral Donor–Acceptor Dyes to Study Electron Transfer Across a Chiral Bridge

Autor: Mike A Kordan, Marc J. Junge, Erin T. Chernick

Publikováno v: The Journal of Organic Chemistry. 85:13793-13807

Chiral organic dyes comprising a donor (D), spacer (S), primary acceptor (A1), chiral bridge (B(S)), and final acceptor/radical (A2)/(R) have been synthesized and fully characterized. The goal behind this synthetic pursuit is to study whether the chi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::266453bb203586c0c5e930fefab5bc48
https://doi.org/10.1021/acs.joc.0c01914

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Metalated Porphyrin Stable Free Radicals: Exploration of Electron Spin Communication and Dynamics

Autor: Ryan M. Young, Norbert Grzegorzek, Matthew D. Krzyaniak, Marc J. Junge, Michael R. Wasielewski, Haochuan Mao, Patrick Michel, Erin T. Chernick, Emmaline R. Lorenzo

Publikováno v: The Journal of Physical Chemistry A. 124:6168-6176

Switchable coupling between two qubits is important for quantum information science (QIS). As a proof of concept, a series of mesosubstituted porphyrins have been synthesized with a (2,2,6,6-tetramethylpiperidin-1-yl)oxyl stable free radical (SFR) ap

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eadc541756d4ab9119e3cfce1543c159
https://doi.org/10.1021/acs.jpca.0c03176

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6,6′,11,11′-Tetra((triisopropylsilyl)ethynyl)-anti-[2.2](1,4)tetracenophane: a covalently coupled tetracene dimer and its structural, electrochemical, and photophysical characterization

Autor: Holger F. Bettinger, Bernd Speiser, Claudio Schrenk, Andreas Schnepf, Andreas Göttler, Ralf Einholz, Marc J. Junge, Simon Schundelmeier, Marie-Sophie Sättele

Publikováno v: Organic Chemistry Frontiers. 4:853-860

[2.2]-Acenophanes are a class of compounds with two acene units interconnected by two ethano bridges. Due to the short bridges, the two acene subunits are in close proximity and can result in a modification of properties compared to the monomeric ace

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2e6971178565a99729fd356d7d351178
https://doi.org/10.1039/c7qo00117g

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