3 article(s) from Minakata, Satoshi
Chemical structures of 1 and POZ-DBPHZ.
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Synthesis of compound 1.
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Steady-state UV–vis absorption (Abs) and photoluminescence (PL) spectra of dilute solutions (c ≈ 10...
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Time-resolved PL decay profiles (intensity vs delay time) and spectra of 1 in a), b) Zeonex® and c,...
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The characteristics of the OLED devices: a) electroluminescence spectra; b) current density-bias ch...
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Schematics of the TADF mechanisms along with NTOs for the relevant electronic states for a) D–A com...
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Beilstein J. Org. Chem. 2022, 18, 459–468, doi:10.3762/bjoc.18.48
Decarboxylative functionalization using PhI(OAc)2/I2 system.
Substrate scope. Reactions were conducted on a 0.5 mmol scale at a 0.2 or 0.4 M concentration on th...
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Hydrolysis of acetates.
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Proposed reaction pathway.
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Beilstein J. Org. Chem. 2018, 14, 1046–1050, doi:10.3762/bjoc.14.92
Synthetic routes to 7,8-diazahelicene.
Oxidant-controlled transformations of BINAMs.
Substrate scope of the oxidative ring-closure of BINAMs. Reaction conditions: 1 (0.1 mmol), t-BuOCl...
Oxidative ring-closure of 3.
A possible reaction pathway of the oxidative ring-closure of 1a.
UV–vis absorption spectra of 2a, 2b, 2d, and 2f.
Beilstein J. Org. Chem. 2015, 11, 9–15, doi:10.3762/bjoc.11.2
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