Aromaticity in transition structures. Schleyer, P. v. R., Wu, J. I, Cossío, F. P, & Fernández, I. Chemical Society Reviews, 43(14):4909–4921, 2014. Publisher: The Royal Society of Chemistry ISBN: 0306-0012
Aromaticity in transition structures [link]Paper  doi  abstract   bibtex   
Aromaticity is an essential concept in chemistry, employed to account for the unusual stability, reactivity, molecular structures, and other properties of many unsaturated organic compounds. This concept was later extended to inorganic molecules and to saturated systems with mobile electrons, as well as to transition structures, the focus of the present review. Although transition structures are inherently delocalized, not all exhibit aromaticity. We contrast here examples of pericyclic reaction transition structures (where aromaticity is significant) with those for illustrative pseudo-pericyclic reactions (where aromaticity is less or not important). Non-pericyclic reactions may also have aromatic transition structures. State-of-the-art computational methods to evaluate the aromaticity of transition structures are described briefly.
@article{schleyer_aromaticity_2014,
	title = {Aromaticity in transition structures},
	volume = {43},
	url = {http://dx.doi.org/10.1039/C4CS00012A},
	doi = {10.1039/C4CS00012A},
	abstract = {Aromaticity is an essential concept in chemistry, employed to account for the unusual stability, reactivity, molecular structures, and other properties of many unsaturated organic compounds. This concept was later extended to inorganic molecules and to saturated systems with mobile electrons, as well as to transition structures, the focus of the present review. Although transition structures are inherently delocalized, not all exhibit aromaticity. We contrast here examples of pericyclic reaction transition structures (where aromaticity is significant) with those for illustrative pseudo-pericyclic reactions (where aromaticity is less or not important). Non-pericyclic reactions may also have aromatic transition structures. State-of-the-art computational methods to evaluate the aromaticity of transition structures are described briefly.},
	number = {14},
	journal = {Chemical Society Reviews},
	author = {Schleyer, Paul von Ragué and Wu, Judy I and Cossío, Fernando P and Fernández, Israel},
	year = {2014},
	note = {Publisher: The Royal Society of Chemistry
ISBN: 0306-0012},
	pages = {4909--4921},
}

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