Abstract
This study meticulously examines the criteria for assigning electron
rearrangements along the
intrinsic reaction coordinate (IRC) leading to bond formation and breaking processes during the
pyrolytic isomerization of cubane (CUB) to 1,3,5,7 cyclooctatetraene (COT) from both
thermochemical and bonding perspectives. The computed gas phase activation enthalpies obtained
using state-of-the-art DFT functionals strongly align with experimental values. Notably, no cusp-type
function was detected in the initial thermal conversion step of CUB to bicyclo[4.2.0]octa 2,4,7 triene
( as evidenced by examining the modulus of the Hessian determinant at all potentially
degenerate critical points (CPs) and their relative distances. Contrary to previous reports, all relevant
fluxes of the pairing density must be described in terms of fold unfolding. The transannular ring
opening in the second step highlights characteristics indicative of a cusp-type catastrophe, facilitating
a direct comparison with fold features. This fact underscores the critical role of density symmetry
persistence near topographical events in determining the type of bifurcation. A fold cusp unified
model for scaling the polarity of chemical bonds is proposed, integrating ubiquitous reaction classes
such as isomerization, bimolecular nucleophilic substitution, and cycloaddition. The analysis reveals
that bond polarity index (BPI) values within the [0, 10-5] au interval correlate with cusp unfolding,
whereas fold spans over a broader [10-3, ∞) au spectrum. These insights emphasize that the cusp
polynomial is suitable for describing chemical processes involving symmetric electron density
distributions, particularly those involving homolytic bond cleavages; in contrast, fold characterizes
most chemical events The elucidated unified model accurately captures the CUB to COT stepwise
reaction mechanism, as illustrated by the sequence of catastrophes describing ELF topology changes
along the IRC. The rigorous application of BET and identifying unfoldings that describe crucial
electron rearrangements are highlighted as essential for understanding and predicting chemical
reactivity.