How much aromatic are naphthalene and graphene?

Publication date: Available online 11 June 2019Source: Computational and Theoretical ChemistryAuthor(s): Vaibhav A. Dixit, Yashita Y. SinghAbstractNaphthalene, polyacenes and graphene are considered aromatic. Existing models for polyacenes predict a linearly increasing aromatic stabilization energy (ASE) and give little insights into their high reactivity and decreasing stability. Graphene’s aromaticity has been studied only qualitatively suggesting alternate Clar’s sextet and two-electrons per ring, and ASE estimates are missing. In this paper, various Enthalpy of Hydrogenation (ΔHhydro) and isodesmic schemes have been proposed and compared for the estimation of naphthalene ASE. Results show that ΔHhydro schemes are simple to design, are equivalent to isodesmic schemes, and unconjugated unsaturated reference systems predict ASE values in agreement with literature reports. Partially aromatic reference systems underestimate ASE. ΔHhydro schemes require calculations for a smaller number of structures, and offer scope for experimental validation, and involve enthalpy differences. Polyacene (X-axis extensions of benzene) ASE estimates (using ΔHhydro scheme) correlate well with experimental instability data and offer new chemical physical insights. ASEs extrapolated from quadratic and logarithmic regression models have been used to estimate the largest polyacene with limiting ASE values. ASE values for Pyrene (Y-axis extension of benzene) and higher analogues (here called ...
Source: Computational and Theoretical Chemistry - Category: Chemistry Source Type: research