Hückel Molecular Orbital Quantities of {X,Y}-Cyclacene Graphs Under Next-Nearest-Neighbour Approximations in Analytical Forms

• Published in: Zeitschrift für Naturforschung. A, A journal of physical sciences Vol. 74; no. 6; pp. 469 - 488
• Main Authors: Ghosh, Tapanendu, Mondal, Swapnadeep, Mondal, Sukanya, Mandal, Bholanath
• Format: Journal Article
• Language: English
• Published: De Gruyter 26.06.2019
• Subjects: Cyclacene Graphs; Cyclic Dimer and HOMO–LUMO Gap; Electron Density-Bond Order-Free Valence; Next-Nearest-Neighbour Approximations; Total π-Electron Energy
• ISSN: 0932-0784; 1865-7109
• DOI: 10.1515/zna-2018-0488

Hückel molecular orbital (HMO) quantities, viz., electron densities, charge densities, bond orders, free valences, total π-electron energies and highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO–LUMO) or band gaps of {X,Y}-cyclacene graphs under next-nearest-neighbour ( ) approximations are expressed in analytical forms within a certain range of approximation parameter ( ). The critical values of for {X,Y}-cyclacenes with varying X (=C, N, B) and Y (=C, N, B) are calculated. For {X,X}-cyclacenes with a π-electron on each atom, all HMO quantities except total π-electron energies for a given value of are found to be independent of X. The cyclic dimer (CD) is constructed in obtaining the eigenvalues corresponding to the singular points of the density of states (DOS) of such {X,Y}-cyclacene. Although the HOMO–LUMO gap of the CD differs from that of the cyclacene with a large number of repeating units (i.e. n ⟶ ∞) but becomes the same for = 0. The analytical expressions can be used for facile computer programming in obtaining the HMO quantities. Such interaction approximations actually release, to some extent, the strain that results in due to the geometrical structures of such cyclacenes, which is evident from the plots of strain energy per segment vs. contribution of such interactions on the total π-electron energy, where the slopes decrease with an increase in m. The vertical absorption energy difference for singlet-triplet states bears excellent linear correlation with the HOMO–LUMO gaps for a certain m value ( = 0.3) in the case of an even n, but for an odd n, such energy difference remains invariant.