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Ab initio study on pericyclic reactions involving heteroatoms

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dc.contributor.advisor Bachrach, Steven M., 1959- en_US Bapat, Abhiram en_US 2015-12-18T18:48:48Z 2015-12-18T18:48:48Z 1998
dc.description Includes bibliographical references. en_US
dc.description.abstract This thesis consists of work involving use of computational chemistry for studying the reactions of heteroatomic systems. It is interesting to observe how the reaction mechanism for classical organic reactions are affected by the introduction of sulfur or phosphorous as heteroatoms. The ab initio molecular orbital theory was used to investigate the sigmatropic rearrangement involving sulfur atoms. The energetics of the [1,3]- hydrogen shift in thioacetaldehyde and 1,3-propanedithial are calculated at MP4SDTQ/6-31 **// MP2/6-31G** + ZPE(HF/6-31G**). The results are compared to the [l,3]-hydrogen shift in acetaldehyde and malonaldehyde. The thiocarbonyl form is compared with the thiol form in terms of stability. The activation energy for the [l,5]-hydrogen shift in 1,3-propanedithial is 2.70 kcal/mol at MP4SDTQ/6- 31**+ ZPE(HF/6-31G**), which is 0.4 kcal/mol lower than in malonaldehyde. The activation barrier for the antarafacial TS of 1,3-propanedithial is approximately 15 kcal/mol lower than that of malonaldehyde. The second part of the thesis includes the study of phosphorous Bergmantype cyclization based on computational chemistry. These results will be compared with the Bergman-type cyclization which has been studied extensively, both experimentally and theoretically. The theoretical calculations have been carried at CASSCF level. The activation energy obtained in the electrocyclization of (Z)- hexa-l,5-diphospha-l,5-diyne-3-ene was approximately 27.8 kcal/mol at CASSCF/6-31G* level. en_US
dc.format.extent 41 pages en_US
dc.language.iso eng en_US
dc.publisher Northern Illinois University en_US
dc.rights NIU theses are protected by copyright. They may be viewed from Huskie Commons for any purpose, but reproduction or distribution in any format is prohibited without the written permission of the authors. en_US
dc.subject.lcsh Heterocyclic chemistry en_US
dc.subject.lcsh Organic reaction mechanisms en_US
dc.title Ab initio study on pericyclic reactions involving heteroatoms en_US
dc.title.alternative Ab-initio study on pericyclic reactions involving heteroatoms en_US
dc.type.genre Dissertation/Thesis en_US
dc.type Text en_US
dc.contributor.department Department of Chemistry en_US M.S. (Master of Science) en_US

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