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Difluorenoheteroles: topological control of π conjugation in diradicaloids and mixed-valence radical ions
Chemical science (Cambridge), 2024-07, Vol.15 (26), p.111-119
2024
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1,3-Dipolar cycloaddition of polycyclic azomethine ylide to norcorroles: towards dibenzoullazine-fused derivatives
Chemical communications (Cambridge, England), 2022-06, Vol.58 (45), p.651-6513
2022
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Carbocyclization approaches to electron-deficient nanographenes and their analogues
Organic chemistry frontiers an international journal of organic chemistry, 2018-08, Vol.5 (15), p.2395-2414
2018
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5,10-Dimesityldiindeno[1,2-:2′,1′-]phenanthrene: a stable biradicaloid derived from Chichibabin's hydrocarbon
Chemical science (Cambridge), 2019-03, Vol.1 (11), p.3413-342
2019
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Acenaphthylene-fused ullazines: fluorescent π-extended monopyrroles with tunable electronic gaps
Organic chemistry frontiers an international journal of organic chemistry, 2022-06, Vol.9 (12), p.3179-3185
2022
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Extension of antiaromatic norcorrole by cycloadditionElectronic supplementary information (ESI) available: Synthetic and separation details, spectroscopic characterization of the compounds, electrochemistry, calculation details, calculated structures (PDB format). CCDC 1817605. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8cc00447a
2018-03
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Chrysaorenes: assembling coronoid hydrocarbons via the fold-in synthesisElectronic supplementary information (ESI) available: Experimental procedures, spectra of new compounds, and details of computational studies. CCDC 1407282 and 1407283. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5cc06046j
2015-10
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Synthesis of a peripherally conjugated 5-6-7 nanographeneElectronic supplementary information (ESI) available: Experimental procedures, spectra of new compounds, and details of computational studies. See DOI: 10.1039/c5sc03280f
2015-12
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Möbius-Hückel topology switching in an expanded porphyrin cation radical as studied by EPR and ENDOR spectroscopyElectronic supplementary information (ESI) available: Details of the DFT calculations of 14N- and 1H hyperfine couplings of the cation radicals of the Möbius and Hückel conformers. See DOI: 10.1039/c4cp05745g
2015-02
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The effect of π-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoidsElectronic supplementary information (ESI) available: Synthetic procedures, and additional spectroscopic and crystallographic data together with computational details. CCDC 1002418 and 1002419. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c4cc03855j
2014-07
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