Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/5810
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dc.contributor.authorAbbasoglu, Rza-
dc.contributor.authorMagerramov, Abel-
dc.date.accessioned2009-08-07T05:21:54Z-
dc.date.available2009-08-07T05:21:54Z-
dc.date.issued2009-08-
dc.identifier.issn0975-0975 (Online); 0376-4710 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/5810-
dc.description1091-1095en_US
dc.description.abstractFull geometric optimization of 3,4-benzobicyclo[3.2.1]- octadiene (BBOD) has been carried out by DFT/B3LYP method using the 6-311G(d), 6-311G(d,p) and 6-311+G(d,p) basis sets. The double bond is endo-pyramidalized and its two faces are not equivalent. The BBOD-Cl2 system have been investigated by B3LYP/6-311+G(d,p) method and stable configurations determined. The stable configurations of the BBOD-Cl2 system correspond to BBOD…Cl2(exo) and BBOD…Cl2(endo) molecular complexes which are formed by the exo and endo orientation respectively of Cl2 molecule to the double bond of BBOD in axial position. Exo-complex is relatively more stable than the endo-complex. Exo-chloronium cation was found to be more stable than endo-chloronium cation by the DFT method. Exo-facial selectivity is expected in the addition reaction to BBOD of chlorine. The non-classical delocalized chlorocarbonium cation(IV) is the most stable ion among the cationic intermediates, and the ionic addition reaction occurs via this cation. The mechanism of the addition reaction is also discussed.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-A Vol.48A(08) [August 2009]en_US
dc.subjectTheoretical chemistryen_US
dc.subjectElectrophilic additionsen_US
dc.subjectDensity functional calculationsen_US
dc.subjectAddition reactionsen_US
dc.subjectGeometric optimizationen_US
dc.titleDensity functional theory investigation of electrophilic addition reaction of chlorine to 3,4-benzobicyclo[3.2.1]-octadieneen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.48A(08) [August 2009]

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