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Beilstein J. Org. Chem. 2023, 19, 1766–1775, doi:10.3762/bjoc.19.129
Graphical Abstract
Figure 1: Chemical structures of the molecular components used in this work: Co(II) complex 1 as the novel ca...
Figure 2: ORTEP drawing of crystal polymorph 1a (left) and 1b (right), shown at the 50% probability level. Hy...
Figure 3: UV–vis absorbance of complex 1 in DMA. Inset: zoom-in of the 500–800 nm range to visualize the low-...
Figure 4: Cyclic voltammetry of complex 1 in 0.1 M TBAPF6 solution of (a) DMA and (b) DMA/TEOA 5:1 (v/v). Bla...
Figure 5: Time evolution of CO (blue squares) and H2 (red triangles) with the power functional fitting (blue ...
Scheme 1: Proposed mechanism for the photoinduced reduction of carbon dioxide with the system presented in th...
Beilstein J. Org. Chem. 2022, 18, 1088–1099, doi:10.3762/bjoc.18.111
Scheme 1: Reactions of tetrazoloquinoxalines 1 to 1,2,3-triazoloquinoxalines 3 via CuAAC and denitrogenative ...
Scheme 2: Synthesis of tetrazolo[1,5-a]quinoxalines. Reaction conditions: (a) 9, THF or 4 M HCl, 70–110 °C, 2...
Scheme 3: Synthesis of 1,2,3-triazole-substituted quinoxalines via CuAAC from tetrazolo[1,5-a]quinoxaline (11a...
Scheme 4: Mechanism of CuAAC vs denitrogenative annulation.
Scheme 5: Synthesis of bis(tetrazolo)[1,5-a:5',1'-c]quinoxaline (24) and conversion to triazoloimidazoquinoxa...
Scheme 6: Synthesis of rhenium tricarbonyl complexes 27a–d and ORTEP diagrams of the resulting molecular stru...
Scheme 7: Synthesis of rhenium tricarbonyl complex 29 and ORTEP diagram of the resulting molecular structure ...
Scheme 8: Synthesis of a TIQ rhenium complex and ORTEP diagram of the obtained product 30 with the thermal el...
Figure 1: UV–vis absorption spectra of the obtained metal complexes (18 µM solutions) in acetonitrile at 20 °...
Figure 2: Cyclic voltammetry traces for rhenium complexes 27a–d, 29 and 30: 0.5 mM in MeCN solution with 0.1 ...
Beilstein J. Org. Chem. 2019, 15, 1172–1180, doi:10.3762/bjoc.15.114
Scheme 1: Summary of the most recent methods to obtain different BCPs from 1.
Scheme 2: Screening reaction performed with different types of irradiation (see Figure 1).
Figure 1: Optimization of the reaction conditions. The relative conversion was determined by GC–MS. The use o...
Figure 2: Molecular structure of 6a (displacement parameters are drawn at 50% probability level), distance C1...
Scheme 3: Proposed mechanism of the propellane insertion into disulfide bonds.
Scheme 4: The insertion of 1 into dibenzyl disulfide (12) led to the formation of BCP 13 and traces of [2]sta...
Scheme 5: Reaction of propellane (1) with the two disulfides 10a and 10d. When two different disulfides were ...
Figure 3: NMR spectra of pure 6a (green) and 6d (red) and the obtained mixture with the new compound 15 (blue...
Scheme 6: The reaction of 1 with the two disulfides 10a and 10e led to the known products 6a, 6e and to the u...