APA 6th Edition Molčanov, K., Androš Dubraja, L. i Jurić, M. (2019). Supramolecular Architecture of Chloranilate Salts with Organic Cations: π-stacking vs. Hydrogen Bonding. Croatica Chemica Acta, 92 (2), 297-305. https://doi.org/10.5562/cca3537
MLA 8th Edition Molčanov, Krešimir, et al. "Supramolecular Architecture of Chloranilate Salts with Organic Cations: π-stacking vs. Hydrogen Bonding." Croatica Chemica Acta, vol. 92, br. 2, 2019, str. 297-305. https://doi.org/10.5562/cca3537. Citirano 08.03.2021.
Chicago 17th Edition Molčanov, Krešimir, Lidija Androš Dubraja i Marijana Jurić. "Supramolecular Architecture of Chloranilate Salts with Organic Cations: π-stacking vs. Hydrogen Bonding." Croatica Chemica Acta 92, br. 2 (2019): 297-305. https://doi.org/10.5562/cca3537
Harvard Molčanov, K., Androš Dubraja, L., i Jurić, M. (2019). 'Supramolecular Architecture of Chloranilate Salts with Organic Cations: π-stacking vs. Hydrogen Bonding', Croatica Chemica Acta, 92(2), str. 297-305. https://doi.org/10.5562/cca3537
Vancouver Molčanov K, Androš Dubraja L, Jurić M. Supramolecular Architecture of Chloranilate Salts with Organic Cations: π-stacking vs. Hydrogen Bonding. Croatica Chemica Acta [Internet]. 2019 [pristupljeno 08.03.2021.];92(2):297-305. https://doi.org/10.5562/cca3537
IEEE K. Molčanov, L. Androš Dubraja i M. Jurić, "Supramolecular Architecture of Chloranilate Salts with Organic Cations: π-stacking vs. Hydrogen Bonding", Croatica Chemica Acta, vol.92, br. 2, str. 297-305, 2019. [Online]. https://doi.org/10.5562/cca3537
Sažetak Four novel salts of chloranilic acid (H2CA; 3,6-dichloro-2,5-dihydroxy-1,4-quinone) with organic cations pyridinium (Hpy+), piperazinediium (H2ppz2+), 4,4'-bipyridinediium (H2bpy2+) and 1,10-phenanthrolinium (Hphen+) were prepared and structurally characterised: (Hpy)2CA (1), (H2ppz)CA (2), (H2bpy)CA·4H2O (3) and (Hphen)HCA·MeOH (4). Supramolecular architecture is based on extensive hydrogen bonding and π-stacking. The central motive is chloranilate dianion which acts as an acceptor of two bifurcated hydrogen bonds. Topology and dimensionality of hydrogen bonded networks can be tuned by use of different cations: thus discrete motives, 1D chains and 2D layers were observed. Three different types of π-stacks are present: aromatic stacks, quinoid stacks and stacks of alternating quinoid and aromatic rings.