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6919312 
Journal Article 
Transmission of Electronic Substituent Effects through a Benzene Framework: A Computational Study of 4-Substituted Biphenyls Based on Structural Variation 
Campanelli, AR; Domenicano, A; Ramondo, F; , 
2012 
1 
Journal of Physical Chemistry A
ISSN: 1089-5639
EISSN: 1520-5215 
AMER CHEMICAL SOC 
WASHINGTON 
116 
31 
8209-8217 
English 
22784397 
WOS:000307264300013 
The transmission of substituent effects through a benzene framework has been studied by a novel approach, based on the structural variation of the Ph group in p-Ph-C6H4-X molecules. The molecular structures of many 4-substituted biphenyls were determined from MO calculations at the HF/6-31G* and B3LYP/6-311++G** levels of theory. The twist angle between the phenyl probe (ring B) and the benzene framework carrying the substituent (ring A) was set at 90 degrees to prevent pi-electron transfer from one ring to the other and at 0 degrees to maximize it. The structural variation of the probe is best represented by a linear combination of the internal ring angles, termed S-F(BIPH(o)) and S-F(BIPH(c)) for the orthogonal and coplanar conformations of the molecules, respectively. Regression analysis of these parameters using appropriate explanatory variables reveals a composite field effect, a substantial proportion of which is originated by resonance-induced pi-charges on the carbon atoms of ring A. Field-induced polarization of the pi-system of ring A also contributes to the structural variation of the probe. Thus, the S-F(BIPH(o)) parameter is very well reproduced by a linear combination of the pi-charges on the ortho, meta, and para carbons of ring A, an uncommon example of a quantitative relationship between molecular geometry and electron density distribution. Comparison of S-F(BIPH(o)) with the gas-phase acidities of para-substituted benzoic acids shows that, while the deprotonating carboxylic probe is more sensitive to pi-electron withdrawal than donation, the phenyl probe is equally sensitive to both. While the ability of the orthogonal biphenyl system to exchange pi-electrons with the para substituent is the same as that of the benzene ring in Ph-X molecules, an increase by about 18% occurs when the conformation is changed from orthogonal to coplanar. The structural variation of the probe becomes more complicated, however. This is due to pi-electron transfer from one ring to the other, which is shown to introduce quadratic terms in the regressions.