Proton Affinities of Dicyanogen Isomers: Is There a Preferred Site of Protonation for CNCN?

Citations Over Time

Abstract

A variety of high-level ab initio techniques [including G2(QCI) and CBS-APNO] have been employed to characterize the various isomers of neutral and protonated C2N2. Notable findings of this study are the following: first, that the calculated proton affinity of NCCN (655 kJ mol-1) is approximately 20 kJ mol-1 below the accepted experimental value, and second that the respective proton affinities of the two terminal atoms of cyanogen cyanide, CNCN, are virtually identical (∼692 kJ mol-1). The barrier to unimolecular isomerization between HCNCN+ and CNCNH+ is large; thus, protonation of CNCN at room temperature should generate these two species, as distinct isomers, in comparable amounts. In consequence, we anticipate that the investigation of CNCN protonation presents a considerable experimental challenge.

Related Papers

• → Evaluated Gas Phase Basicities and Proton Affinities of Molecules; Heats of Formation of Protonated Molecules(1984)1,324 cited
• → Calculation of Proton Affinities Using Density Functional Procedures: A Critical Study(1996)68 cited
• → Proton affinities of 2-iminoimidazolines with bulky N-alkyl-substituents(2012)14 cited
• → Alkylammonium Cation Affinities of Nitrogenated Organobases: The Roles of Hydrogen Bonding and Proton Transfer(2021)1 cited
• → Theoretical proton affinities of α1 adrenoceptor ligands(2005)11 cited