Download Hypercarbon Chemistry by George A. Olah PDF

By George A. Olah

The basic re-creation of the e-book that positioned hypercarbon chemistry at the mapA finished and modern remedy of the chemistry of hydrocarbons (alkanes, alkenes, alkynes, and aromatics) in the direction of electrophiles, Hypercarbon Chemistry, moment variation bargains with all significant features of such chemistry serious about hydrocarbon differences, and of the structural and response chemistry of carboranes, combined hydrides during which either carbon and boron atoms perform the polyhedral molecular frameworks.Despite the firmly verified tetravalency, carbon can bond at the same time to 5 or extra different atoms. "Hypercarbon" bonding permeates a lot natural, inorganic and organometallic chemistry, and the booklet serves because the compendium for this phenomenon.Copious diagrams illustrate the wealthy number of hypercarbon buildings referred to now, and styles therein. person chapters take care of particular different types of compound (e.g. organometallics, carboranes, carbocations) or differences that continue via brief hypercarbon species, detailing primary chemistry, together with reactivity, selectivity, stereochemistry, mechanistic elements and extra.

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Bottom: allowing for resonance between the four (C5H5+) or five (C6Me62+) ways of allocating such bond networks to these pyramidal species generates the following two-center bond orders (numbers of electron pairs per C–C link). 18. MO diagrams showing how neutral C4H4 and cationic C5H5+ and C6Me62+ would be antiaromatic if polygonal. MO treatments are preferred in such cases. The manner in which these same cations, (C5H5)+ and (C6Me6) 2+, can be treated in MO terms is worth illustrating here for the purpose of comparison with the localized bond schemes just discussed, and also to underline the relationship between these pyramidal systems and normal aromatic ring systems.

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