High temperature bromination Part XXIII: Bromination of octahydro-1H-indene and octahydro-1H-4,7-methanoindene
dc.contributor.author | Özer, Melek Şermin | |
dc.contributor.author | Kılbaş, Benan | |
dc.contributor.author | Balcı, Metin | |
dc.date.accessioned | 2020-05-01T12:10:22Z | |
dc.date.available | 2020-05-01T12:10:22Z | |
dc.date.issued | 2013 | |
dc.department | DÜ, Fen-Edebiyat Fakültesi, Kimya Bölümü | en_US |
dc.description | WOS: 000330029300030 | en_US |
dc.description.abstract | Thermal and photobromination of octahydro-1H-indene and octahydro-1H-4,7-methanoindene were investigated. Three isomeric tetrabromides (1,3,4,7-tetrabromo-2,3,4,5,6,7-hexahydro-1-H-indene) were formed along with a smaller amount of tribromoindane and a pentabromide by thermal bromination of octahydro-1H-indene. The thermodynamically most stable isomers were formed. Morover, thermal and photochemical bromination of octahydro-1H-4,7-methanoindene furnished bromides resulting regiospecifically from the allylic bromination of the five-membered ring. Furthermore, the double bond formed as the intermediate functional group was also brominated due to its pyramidalization. The mechanism proposed for the formation of product distribution was discussed. | en_US |
dc.description.sponsorship | TUBITAK (Scientific and Technological Research Council of Turkey)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [108-M168]; Department of Chemistry at Middle East Technical University; TUBA (Turkish Academy of Sciences)Turkish Academy of Sciences | en_US |
dc.description.sponsorship | The authors are indebted to TUBITAK (Scientific and Technological Research Council of Turkey), (Grant 108-M168), the Department of Chemistry at Middle East Technical University and TUBA (Turkish Academy of Sciences) for financial support of this work. | en_US |
dc.identifier.doi | 10.3998/ark.5550190.p008.195 | en_US |
dc.identifier.endpage | 404 | en_US |
dc.identifier.issn | 1551-7004 | |
dc.identifier.issn | 1551-7012 | |
dc.identifier.scopusquality | Q4 | en_US |
dc.identifier.startpage | 388 | en_US |
dc.identifier.uri | https://doi.org/10.3998/ark.5550190.p008.195 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/6163 | |
dc.identifier.wos | WOS:000330029300030 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Arkat Usa Inc | en_US |
dc.relation.ispartof | Arkivoc | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Bromination | en_US |
dc.subject | high temperature bromination | en_US |
dc.subject | hydrocarbons | en_US |
dc.subject | substitution | en_US |
dc.title | High temperature bromination Part XXIII: Bromination of octahydro-1H-indene and octahydro-1H-4,7-methanoindene | en_US |
dc.type | Article | en_US |
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