Aromatic stability benzene

The pattern of orbital energies is different for benzene than it would be if the six tt electrons were confined to three noninteracting double bonds The delocalization provided by cyclic conjugation in benzene causes its tt electrons to be held more strongly than they would be in the absence of cyclic conjugation Stronger binding of its tt electrons is the factor most responsible for the special stability—the aromaticity—of benzene... 

Cyclic compounds that contain at least one atom other than carbon within their ring are called heterocyclic compounds, and those that possess aromatic stability are called het erocyclic aromatic compounds Some representative heterocyclic aromatic compounds are pyridine pyrrole furan and thiophene The structures and the lUPAC numbering system used m naming their derivatives are shown In their stability and chemical behav lor all these compounds resemble benzene more than they resemble alkenes... 

We will return to the aromatic stabilization of benzene in more detail in Chapter 9, but substituted benzenes provide excellent examples of how proper use of the resonance concept can be valuable in predicting reactivity. Many substituents can be readily classified... 

Whereas the initial hydrogenation both breaks a % bond and destroys any aromatic stabilization , the second hydrogenation only breaks a % bond. The difference between the two then corresponds to any aromatic stabilization. Is this difference large as in benzene (see discussion at left) or is it neglible Is cyclooctatetraene aromatic ... 

The kinetic stabilities and the donor-acceptor properties of cyclic conjugated molecules [68] have been described (Scheme 12) in the theoretical subsection (Sect. 2.2.2) to be controlled by the phase property. There is a parallelism between the thermodynamic and kinetic stabilities. An aromatic molecule, benzene, is kinetically stable, and an antiaromatic molecule, cyclobutadiene, is kinetically unstable (Scheme 13). 

Arynes present structural features of some interest. They clearly cannot be acetylenic in the usual sense as this would require enormous deformation of the benzene ring in order to accommodate the 180° bond angle required by the sp1 hybridised carbons in an alkyne (p. 9). It seems more likely that the delocalised 7i orbitals of the aromatic system are left largely untouched (aromatic stability thereby being conserved), and that the two available electrons are accommodated in the original sp2 hybrid orbitals (101) ... 

This mesomerism (or resonance )59 between equivalent Kekule structures was recognized as the quintessential feature underlying the aromaticity of benzene, conferring highly distinctive symmetry, stability, and reactivity patterns. 

Despite its unsaturated nature, benzene with its sweet aroma, isolated by Michael Faraday in 1825 [1], demonstrates low chemical reactivity. This feature gave rise to the entire class of unsaturated organic substances called aromatic compounds. Thus, the aromaticity and low reactivity were connected from the very beginning. The aromaticity and reactivity in organic chemistry is thoroughly reviewed in the book by Matito et al. [2]. The concepts of aromaticity and antiaromaticity have been recendy extended into main group and transition metal clusters [3-10], The current chapter will discuss relationship among aromaticity, stability, and reactivity in clusters. 

The gas-phase chemistry of borazine B3N3H6 (147) and the conjugate N-protonated acid B3N3H7+ indicates analogies with benzene,189 although the aromatic stabilization energy of neutral borazine is only 30% that of benzene, and the reactivities of benzene and borazine are not similar (Scheme 62). Comparable conclusions were reached when HOMA and Iq aromaticity indices were used.190a... 

Let us consider the origins of benzene s aromatic stabilization. Another cyclic hydrocarbon, cyclooctatetraene (pronounced cyclo-octa-tetra-ene), certainly looks conjugated according to our criteria, but chemical evidence shows that it is very much more reactive than benzene, and does not undergo the same types of reaction. It does not possess the enhanced aromatic stability characteristic of benzene. 

We can draw Frost circles (see Section 2.9.3) to show the relative energies of the molecular orbitals for pyridine and pyrrole. The picture for pyridine is essentially the same as for benzene, six jt electrons forming an energetically favourable closed shell (Figure 11.1). For pyrrole, we also get a closed shell, and there is considerable aromatic stabilization over electrons in the six atomic orbitals. 

The determination of the energy of aromatic stabilization of borepin by calculating the energies of isodesmic reactions (62) and (63) with a correction for the strain leads to the value 12.7 kcal/mol (89MI6). The same energy calculated with the same basis set (6-31G ) is for benzene... 

An estimate of the aromatic stabilization energy of silabenzene, based on the calculation of the ISE (STO-3G basis set) (78JA6499), concludes that its value is 2/3 of the benzene stabilization energy. Possible ap-... 

The lowering of the aromatic stabilization energy of silabenzene, compared to benzene, leads one to expect that the energy of the antiaromatic stabilization of silacyclobutadiene (253) would be lower than in the case of cyclobutadiene. 

According to ab initio calculations of the energies of the homodesmotic (86) and the hyperhomodesmotic (87) reactions (85CC1121), the aromatic stabilization energy of (286) amounts to, respectively, 51 and 48% of that of benzene ... 

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