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Beilstein J. Org. Chem. 2022, 18, 459–468, doi:10.3762/bjoc.18.48
Graphical Abstract
Figure 1: Chemical structures of 1 and POZ-DBPHZ.
Scheme 1: Synthesis of compound 1.
Figure 2: Steady-state UV–vis absorption (Abs) and photoluminescence (PL) spectra of dilute solutions (c ≈ 10...
Figure 3: Time-resolved PL decay profiles (intensity vs delay time) and spectra of 1 in a), b) Zeonex® and c,...
Figure 4: The characteristics of the OLED devices: a) electroluminescence spectra; b) current density-bias ch...
Figure 5: Schematics of the TADF mechanisms along with NTOs for the relevant electronic states for a) D–A com...
Beilstein J. Org. Chem. 2018, 14, 1046–1050, doi:10.3762/bjoc.14.92
Scheme 1: Decarboxylative functionalization using PhI(OAc)2/I2 system.
Scheme 2: Substrate scope. Reactions were conducted on a 0.5 mmol scale at a 0.2 or 0.4 M concentration on th...
Scheme 3: Hydrolysis of acetates.
Scheme 4: Mechanistic investigations.
Scheme 5: Proposed reaction pathway.
Beilstein J. Org. Chem. 2015, 11, 9–15, doi:10.3762/bjoc.11.2
Scheme 1: Synthetic routes to 7,8-diaza[5]helicene.
Scheme 2: Oxidant-controlled transformations of BINAMs.
Scheme 3: Substrate scope of the oxidative ring-closure of BINAMs. Reaction conditions: 1 (0.1 mmol), t-BuOCl...
Scheme 4: Oxidative ring-closure of 3.
Scheme 5: A possible reaction pathway of the oxidative ring-closure of 1a.
Figure 1: UV–vis absorption spectra of 2a, 2b, 2d, and 2f.