Electronic structure calculations (B3LYP/6-311+G**) predict that nucleophilic attack of the aromatic cycloCu4(μ)4 ring yields ligand-stabilized tetranuclear Cu4 clusters formulated as cyclo-Cu4(μ)4Nucn (n = 1-4; Nuc = N2, CO, H2O, NH3 and PH3). Depending on the number of added nucleophiles, the tetranuclear Cu4 clusters adopt planar, bent or 3D tetrahedral geometries. These molecules exhibit ar...

Aromaticity is a property usually linked to the ground state of stable molecules. Although it is well-known that certain excited states are unquestionably aromatic, the aromaticity of excited states remains rather unexplored. To move one step forward in the comprehension of aromaticity in excited states, in this work we analyze the electron delocalization and aromaticity of a series of low-lyin...

In this work, we have analyzed the local aromaticity of the six-membered rings (6-MRs) of planar and pyramidalized pyracylene species through the structurally based harmonic oscillator model of aromaticity (HOMA), the electronically based para-delocalization index (PDI), and the magnetic-based nucleus independent chemical shift (NICS) measurements, as well as with maps of ring current density. ...

Using suitable Density functional theory (DFT) methods and models of various sizes and symmetries, we have obtained the aromaticity pattern of infinite Graphene, which is an intrinsically collective effect, by a process of “spatial” evolution. Using a similar process backwards we obtain the distinct aromaticity pattern(s) of finite nanographenes, graphene dots, antidots, and graphene nanoribbon...

Based on the local Shannon entropy concept in information theory, a new measure of aromaticity is introduced. This index, which describes the probability of electronic charge distribution between atoms in a given ring, is called Shannon aromaticity (SA). Using B3LYP method and different basis sets (6-31G**, 6-31+G** and 6-311++G**), the SA values of some five-membered heterocycles, C(4)H(4)X, a...

As compared to classical organic aromatic compounds, the evaluation of aromaticity in all-metal and semimetal clusters is much more complex. For a series of these clusters, it is frequently found that different methods used to discuss aromaticity lead to divergent conclusions. For this reason, there is a need to evaluate the reliability of the different descriptors of aromaticity to provide cor...

The influence of the substituent nature, as well as the number and position of the substituents, on the aromaticity/antiaromaticity of a comprehensive set of derivatives of cyclopentadienyl anion, cyclopentadiene and cyclopentadienyl cation has been analyzed. The aromaticity/antiaromaticity of substituted cyclopentadienyl derivatives has been measured using energetic, magnetic and structural cr...

The degree of aromaticity of six-membered monoheterocycles with IV-VI group heteroatoms (C(6)H(5)X, where X = SiH, GeH, N, P, As, O(+), S(+), Se(+)) was analyzed using the results of ab initio calculations at the MP2/cc-pvtz level. Values of common aromaticity indices including those based on electronic delocalization properties, structural-dynamic features and magnetic properties all indicate ...

We have studied the topological and local aromaticity of BN-substituted benzene, pyrene, chrysene, triphenylene and tetracene molecules. The nucleus-independent chemical shielding (NICS), harmonic oscillator model of aromaticity (HOMA), para-delocalization index (PDI) and aromatic fluctuation index (FLU) have been calculated to quantify aromaticity in terms of magnetic and structural criteria. ...

In this work, the aromatic fluctuation index (FLU) that describes the fluctuation of electronic charge between adjacent atoms in a given ring is introduced as a new aromaticity measure. This new electronic criterion of aromaticity is based on the fact that aromaticity is related to the cyclic delocalized circulation of pi electrons. It is defined not only considering the amount of electron shar...