D
Daisuke Sakamaki
Researcher at Kyoto University
Publications - 72
Citations - 1475
Daisuke Sakamaki is an academic researcher from Kyoto University. The author has contributed to research in topics: Nanowire & Radical. The author has an hindex of 21, co-authored 67 publications receiving 1183 citations. Previous affiliations of Daisuke Sakamaki include Osaka Prefecture University & Osaka University.
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Nitrogen-embedded buckybowl and its assembly with C 60
TL;DR: The synthesis of a π-extended azacorannulene with nitrogen in its centre is reported, which may be of interest in the fields of curved π systems as fullerene hosts, anisotropic π donors and precursors to nitrogen-containing nanocarbon materials.
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Charge carrier mobility in organic molecular materials probed by electromagnetic waves
TL;DR: The present perspective highlights the evaluation methodologies of charge carrier mobility in organic materials, as well as the merits and demerits of techniques examining the feasibility of organic molecules, crystals, and supramolecular assemblies in semiconductor applications.
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Fusion of Phosphole and 1,1′‐Biacenaphthene: Phosphorus(V)‐Containing Extended π‐Systems with High Electron Affinity and Electron Mobility
Yoshihiro Matano,Arihiro Saito,Tatsuya Fukushima,Yasuaki Tokudome,Furitsu Suzuki,Daisuke Sakamaki,Hironori Kaji,Akihiro Ito,Kazuyoshi Tanaka,Hiroshi Imahori +9 more
TL;DR: A profusion of phospholes: Diacenaphtho[1,2-b:1',2'-d]phospholes, a new class of arene-fused phosphole π-systems, were synthesized and their structural and electrochemical properties studied.
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A Facile and Versatile Approach to Double N‐Heterohelicenes: Tandem Oxidative C ? N Couplings of N‐Heteroacenes via Cruciform Dimers
TL;DR: The developed method is very facile and enables the synthesis of a double helicene in only two steps from commercially available naphthalene derivatives, and their stability towards racemization was remarkably higher than those of typical [5]helicenes.
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N‐Substituted Dicyanomethylphenyl Radicals: Dynamic Covalent Properties and Formation of Stimuli‐Responsive Cyclophanes by Self‐Assembly
TL;DR: It is demonstrated that triphenylamine and carbazole, substituted with a dicyanomethyl radical, are useful motifs for dynamic covalent chemistry as they have the appropriate bond strength between monomer units as well as high stability and synthetic simplicity.