Search Results - St pie, Marcin

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  1. 1
    Difluorenoheteroles: topological control of π conjugation in diradicaloids and mixed-valence radical ions

    Difluorenoheteroles: topological control of π conjugation in diradicaloids and mixed-valence radical ions by Prajapati, Bibek, Kwenda, Tendai, Lis, Tadeusz, Chmielewski, Piotr J, Gómez-García, Carlos J, Majewski, Marcin A, St pie, Marcin

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  2. 2
    Pentacosacyclenes: cruciform molecular nanocarbons based on cyclooctatetraene

    Pentacosacyclenes: cruciform molecular nanocarbons based on cyclooctatetraene by Kumar, Rakesh, Chmielewski, Piotr J, Lis, Tadeusz, Czarnecki, Miros aw, St pie, Marcin

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  3. 3
    1,3-Dipolar cycloaddition of polycyclic azomethine ylide to norcorroles: towards dibenzoullazine-fused derivatives

    1,3-Dipolar cycloaddition of polycyclic azomethine ylide to norcorroles: towards dibenzoullazine-fused derivatives by Li, Sha, Sun, Yahan, Li, Xiaofang, Smaga, Oskar, Koniarz, Sebastian, St pie, Marcin, Chmielewski, Piotr J

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  4. 4
    Carbocyclization approaches to electron-deficient nanographenes and their analogues

    Carbocyclization approaches to electron-deficient nanographenes and their analogues by Zhylitskaya, Halina, Stępień, Marcin

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  5. 5
    5,10-Dimesityldiindeno[1,2-:2′,1′-]phenanthrene: a stable biradicaloid derived from Chichibabin's hydrocarbon

    5,10-Dimesityldiindeno[1,2-:2′,1′-]phenanthrene: a stable biradicaloid derived from Chichibabin's hydrocarbon by Majewski, Marcin A, Chmielewski, Piotr J, Chien, Alan, Hong, Yongseok, Lis, Tadeusz, Witwicki, Maciej, Kim, Dongho, Zimmerman, Paul M, St pie, Marcin

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  6. 6
    Acenaphthylene-fused ullazines: fluorescent π-extended monopyrroles with tunable electronic gaps

    Acenaphthylene-fused ullazines: fluorescent π-extended monopyrroles with tunable electronic gaps by Hager, Joanna, Kang, Seongsoo, Chmielewski, Piotr J, Lis, Tadeusz, Kim, Dongho, Stępień, Marcin

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  7. 7
    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

    Extension of antiaromatic norcorrole by cycloadditionElectronic supplementary information (ESI) available: Synthetic and separation details, spectroscopic characterization of the c... by Fu, Xinliang, Meng, Yankui, Li, Xiaofang, St pie, Marcin, Chmielewski, Piotr J

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  8. 8
    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

    Chrysaorenes: assembling coronoid hydrocarbons via the fold-in synthesisElectronic supplementary information (ESI) available: Experimental procedures, spectra of new compounds, and... by Majewski, Marcin A, Lis, Tadeusz, Cybi ska, Joanna, St pie, Marcin

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  9. 9
    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

    Synthesis of a peripherally conjugated 5-6-7 nanographeneElectronic supplementary information (ESI) available: Experimental procedures, spectra of new compounds, and details of com... by y a, Marika, Go ka, El bieta, Chmielewski, Piotr J, Cybi ska, Joanna, St pie, Marcin

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  10. 10
    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

    Möbius-Hückel topology switching in an expanded porphyrin cation radical as studied by EPR and ENDOR spectroscopyElectronic supplementary information (ESI) available: Details of th... by Möbius, Klaus, Plato, Martin, Klihm, Gudrun, Laurich, Christoph, Savitsky, Anton, Lubitz, Wolfgang, Szyszko, Bartosz, St pie, Marcin, Latos-Gra y ski, Lechos aw

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  11. 11
    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

    The effect of π-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoidsElectronic supplementary information (ESI) available: Synth... by Sung, Young Mo, Szyszko, Bartosz, My liborski, Radomir, St pie, Marcin, Oh, Juwon, Son, Minjung, Latos-Gra y ski, Lechos aw, Kim, Dongho

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