Naslov
The Proton Affinity of the Superbase 1, 8-Bis(tetramethylguanidino)naphthalene and Some Related Compounds - A Theoretical Study

Autori
Kovačević, Borislav ; Maksić, Zvonimir B.

Izvornik
Chemistry - A European Journal (0947-6539) 8 (2002), 7; 1694-1702

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Sažetak
The spatial and electronic structure of the very strong neutral organic bases TMGN, TMGF and some related compounds are explored by ab initio computational methods. Their affinity towards the proton is scrutinized both in the gas phase and in acetonitrile. The protonation at the most basic center (imine nitrogen) yields asymmetric and relatively strong intramolecular hydrogen bonds (IHB). It is found that the angular strain effect and steric repulsion practically vanish in TMGN implying that its high absolute proton affinity (APA) has its origin in the inherent basicity of the guanidine fragment and a relatively strong IHB in [TMGN]H++. The nonbonded repulsions in TMGF are higher than in TMGN, which in conjunction with a slightly stronger IHB in the corresponding conjugate acid makes it more basic: APA(TMGF) > APA(TMGN). An interesting new phenomenon is observed in both TMGN and TMGF: the proton triggers the resonance stabilization not only in the directly bonded guanidine moiety, but also in the other guanidine fragment placed more distantly from proton, albeit in a less pronounced manner. The latter feature is termed as partial protonation. It supports the hydrogen bonding and contributes to the IHB stabilization. Convincing evidence is presented that the solvent effect in acetonitrile is determined by two antagonistic factors: (1) the intrinsic (gas phase) proton affinity and (2) the size effect given by the ratio between the positive charge in molecular cation (conjugate acid) and the magnitude of the molecular surface. The resulting pK_a values are given by an interplay of these factors.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

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