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Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds (CROSBI ID 215039)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Barić, Danijela ; Kovačević, Borislav Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds // Croatica chemica acta, 87 (2014), 4; 459-464. doi: 10.5562/cca2490

Podaci o odgovornosti

Barić, Danijela ; Kovačević, Borislav

engleski

Towards the Strongest Neutral Organic Superbases Based on Intramolecular H-bonds

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.

organic superbases; intramolecular hydrogen bonds; DFT calculations

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Podaci o izdanju

87 (4)

2014.

459-464

objavljeno

0011-1643

10.5562/cca2490

Povezanost rada

Kemija

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