APA 6th Edition Barić, D. i Kovačević, B. (2014). Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds. Croatica Chemica Acta, 87 (4), 459-464. https://doi.org/10.5562/cca2490
MLA 8th Edition Barić, Danijela i Borislav Kovačević. "Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds." Croatica Chemica Acta, vol. 87, br. 4, 2014, str. 459-464. https://doi.org/10.5562/cca2490. Citirano 15.01.2021.
Chicago 17th Edition Barić, Danijela i Borislav Kovačević. "Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds." Croatica Chemica Acta 87, br. 4 (2014): 459-464. https://doi.org/10.5562/cca2490
Harvard Barić, D., i Kovačević, B. (2014). 'Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds', Croatica Chemica Acta, 87(4), str. 459-464. https://doi.org/10.5562/cca2490
Vancouver Barić D, Kovačević B. Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds. Croatica Chemica Acta [Internet]. 2014 [pristupljeno 15.01.2021.];87(4):459-464. https://doi.org/10.5562/cca2490
IEEE D. Barić i B. Kovačević, "Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds", Croatica Chemica Acta, vol.87, br. 4, str. 459-464, 2014. [Online]. https://doi.org/10.5562/cca2490
Sažetak Utilizing several different trialkylarsine oxides and substituted pyridine N-oxides as a hydrogen bond acceptors in tri-substituted guanidines we designed several very basic superbases possessing intramo-lecular hydrogen bonds (IHB-superbases), with proton affinity in the gas phase that comes very close to that of paradigmatic P4-tBu Schwesinger superbase and with pKa in acetonitrile up to 36
units.