The HOMA (Harmonic Oscillator Model of Aromaticity) index, reformulated in 1993, has been very often applied to describe π-electron delocalization for monoand polycyclic π-electron systems. However, different measures of π-electron delocalization were employed for the CC, CX, and XY bonds, and this index seems to be inappropriate for compounds containing heteroatoms. In order to describe proper...

In this contribution, we have evaluated the (anti)aromatic character of thirty-four different borole compounds in their neutral and reduced states based on two aromaticity indices, namely nucleus-independent chemical shift (NICS) and multicenter indices (MCI), calculated at the PBE0/6-31+G(d,p) level of theory. Both indices corroborate the notion that neutral borole compounds are antiaromatic a...

Structures and stabilities of a new family of multi-decker tricarbonyl-bridged sandwich complexes of transition metals (Cr, Mn, Fe) have been studied using DFT B3LYP/6-311+G(df,p) calculations. Stable structures satisfy the (12n + 6) electron-counting rule, where n is the number of metal atoms. Lengthening of the molecular chains is accompanied by growth of aromaticity of the inner basal cycles...

We consider a set of nine polycyclic conjugated hydrocarbons, which includes at one extreme benzene, the prototype of aromatic compounds, and at the other extreme cyclooctatetraene, a well-known nonaromatic compound, while the remaining seven compounds illustrate molecules of decreasing degree of aromaticity. Using the model of conjugated circuits for calculations of ring currents, we report on...

The Baird-aromaticity of BN/CC cyclooctatetraene isosteres (azaboracyclooctatetraenes) in their lowest triplet states (T1) has been explored through computations various aromaticity indices that describe the different aspects (magnetic, electronic, energetic and geometric). While (COT) is aromatic its T1 state following Baird's 4n rule, we now reveal degrees vary with aspect considered. thermod...

Aromatic compounds are characterised by the presence of a ring current when in a magnetic field. As a consequence, current density maps are used to assess (the degree of) aromaticity of a compound. However, often a more discrete set of so-called Nucleus Independent Chemical Shift (NICS) values is used that is derived from the current density. It is shown here that there is no simple one-to-one ...

In this contribution, we have evaluated the (anti)aromatic character of thirty-four different borole compounds in their neutral and reduced states based on two aromaticity indices, namely nucleus-independent chemical shift (NICS) and multicenter indices (MCI), calculated at the PBE0/6-31+G(d,p) level of theory. Both indices corroborate the notion that neutral borole compounds are antiaromatic a...

Most dicyclopenta-fused polyacenes are predicted to be moderately aromatic and diatropic, although they have no (4n + 2)-site conjugated circuits. We applied our graph theory of aromaticity and magnetotropicity to these molecules and found that these anomalous properties arise from a set of non-conjugated circuits, which contribute collectively to aromaticity and diatropicity. This result indic...