Preferential cyclotrimerization of 5-(aminomethyl)-2-furancarboxylic acid (AMFC): Electrostatic and orbital interactions studies

Monika Sharma, Praveen Kumar, Harjinder Singh, Tushar K. Chakraborty

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4 Scopus citations

Abstract

An attempt is made to develop a theoretical understanding beyond a phenomenological observation of the preferential cyclotrimerization of 5-(aminomethyl)-2-furancarboxylic acid (AMFC). Such cyclopeptides are of great interest due to their considerable bioactivity. A detailed analysis of the molecular properties such as electrostatic potentials, and electron densities is carried out. The electrostatic potentials (ESP) in the region around molecular skeletons are investigated to provide justification for the preferential formation of the cyclic tripeptide over the cyclic dipeptide from the building block, AMFC. The ESP are calculated and computed on the molecular surfaces of the oligopeptides. The surfaces are provided by the 0.002-electrons/bohr3 contour of the total electronic density function. There are repulsions observed in the dimer due to the proximity of the ethereal oxygen atoms of the furan rings. The possibility of counter-balancing the strain observed in rings by the presence of O⋯H-N hydrogen bonds in the oligopetides is also investigated. Natural bond orbital (NBO) analysis is done to find the second-order interactions, and atoms in molecules (AIM) calculations are performed to explore the interactions between the donor and acceptor moieties in the molecule.

Original languageEnglish
Pages (from-to)109-115
Number of pages7
JournalJournal of Molecular Structure: THEOCHEM
Volume764
Issue number1-3
DOIs
StatePublished - May 30 2006

Keywords

  • AIM
  • Ab initio
  • Aminomethyl furancarboxylic acid (AMFC)
  • ESP
  • NBO

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