The formation of cyclophosphazenes containing several ligands or substituent groups gives rise to an attractive derivative set, for development of novel applications, with variable properties. Here, it is possible to unravel the role of different functional groups attached to the N 3P 3 backbone, to reach a better understanding of the bonding character in the cyclic [─P─N─] skeleton. We employed the extended transition state-natural orbital for the chemical valence scheme to unravel the σ and π orbital kernels that are involved in the assembling of such structures, by varying the acceptor-donor characteristics of the ─CF 3, ─NO 2, ─COOH, ─CN, ─NH 2, ─OH, and ─OCH 3 groups, where ─NO 2 behaves as a stronger electron-withdrawing substituent rather than ─CF 3, ─COOH, and ─CN, denoting that the nature of the ligand-phosphazene interaction contributes to some degree to the bond strength of the cyclic [─P─N─] backbone. Our results reveal that the electron-withdrawing ─NO 2 group leads to higher σ and π [─P─N─] orbital-energy contributions, which is reflected in a shortening of the [─P─N─] distance, contrasting with the case of electron-donating groups such as ─NH 2, ─OH, and ─OCH 3 within the phosphazene set. These insights allow further variation and modulation of the bonding in the [─P─N─] ring.
Áreas temáticas de ASJC Scopus
- Óptica y física atómica y molecular
- Física de la materia condensada
- Química física y teórica