Issue 3, 2009

DFT studies on a new class of cage functionalized organic superbases

Abstract

According to DFT calculations, pentacyclo[6.4.0.02,7.03,11.06,10]dodecane (PCD) derivatives have been predicted as organic super bases. The new molecular framework (PCD) is versatile in terms of anchoring different functional groups to achieve high basicities in both gas and solvent phase. Density functional quantum chemical calculations at the B3LYP/6-311+G**//B3LYP/6-31G* level have been performed to calculate the proton affinities of pentacyclo[6.4.0.02,7.03,11.06,10]dodecane (PCD) derivatives and substituted pentacyclo[5.4.0.02,6.03,10.05,9]undecane (PCU) derivatives. The calculated results suggest that these polycyclic cage units can act as organic superbases when anchored with different functional groups. The flexibility in these polycyclic rings allowed the attainment of better hydrogen bonding compared to the prototype 1,8-bis(dimethyl-amino)naphthalene and 1,8-bis(diguanidino)naphthalene. The predicted higher basicities appeared to be due to the interplay of steric repulsions and the strength of hydrogen bonding in these cases. Intramolecular and intermolecular proton transfer barriers have been calculated for these amines and imines.

Graphical abstract: DFT studies on a new class of cage functionalized organic superbases

Supplementary files

Article information

Article type
Paper
Submitted
07 Aug 2008
Accepted
27 Oct 2008
First published
09 Dec 2008

New J. Chem., 2009,33, 583-587

DFT studies on a new class of cage functionalized organic superbases

A. Singh and B. Ganguly, New J. Chem., 2009, 33, 583 DOI: 10.1039/B813745E

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