# 5-(Pyridin-3-yl)-3,4-dihydro-2H-furan-1-ium (NNKFI): a computational study of its physico-chemical properties

## TL;DR

This paper computationally studies the structure and reactivity of a potential carcinogenic compound called NNKFI.

## Contribution

The first computational analysis of NNKFI's physico-chemical properties is presented.

## Key findings

- C5 is the preferred site for nucleophilic attack in NNKFI.
- The carbonyl structure at O1 is somewhat weakened in NNKFI.
- Cationic charge is delocalized on the furanium moiety with notable carbocation character at C5.

## Abstract

Recent work on the diazonium ion metabolite of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNKDI) suggests that 5-(pyridin-3-yl)-3,4-dihydro-2H-furan-1-ium (NNKFI) may form from NNKDI via an intramolecular reaction. NNKDI is an important carcinogen whose role as an alkylating agent has received significant attention. While there is some experimental evidence supporting NNKFI’s production in vitro, it has not yet been directly observed. Little is known about NNKFI’s structure and reactivity. We report the first in silico examination of this ion. Our study utilized Kohn–Sham density functional theory (B3LYP/6-311G**) and coupled cluster theory (CCSD/6-31G*) to produce energy-optimized structures, vibrational normal modes and molecular orbitals for NNKFI. To gain insight into the chemical properties of this species, we calculated electrostatic potential surfaces, natural population analysis charges and local Fukui indices. We report data and results for NNKFI’s cis and trans conformers. Our work confirms C5 as the preferred site for nucleophilic attack in NNKFI. Stretching motions and predicted bond lengths near O1 are consistent with a somewhat weakened carbonyl structure in this ion. Partial charges, electrostatic potential surfaces and local Fukui indices reveal delocalization of cationic charge on the furanium moiety and notable carbocation character at C5.