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Issue 27, 2005
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Extremal acidity of Rees polycyanated hydrocarbons in the gas phase and DMSO – a density functional study

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Abstract

It is shown by using the density functional theory (DFT) calculations that Rees tricyclic[10]annulene 1 and its benzo-annelated derivative 2, substituted by CN groups at all peripheral sp2 carbon positions, represent hyperstrong neutral superacids in the gas-phase and DMSO.

Graphical abstract: Extremal acidity of Rees polycyanated hydrocarbons in the gas phase and DMSO – a density functional study

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Publication details

The article was received on 10 Feb 2005, accepted on 25 Apr 2005 and first published on 31 May 2005


Article type: Communication
DOI: 10.1039/B502006A
Citation: Chem. Commun., 2005, 3412-3414
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    Extremal acidity of Rees polycyanated hydrocarbons in the gas phase and DMSO – a density functional study

    R. Vianello and Z. B. Maksić, Chem. Commun., 2005, 3412
    DOI: 10.1039/B502006A

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