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Reactions of bicyclo(2,2. 1)hepta-2,5-diene in the presence of zeolites (in Russian)

Journal Article · · Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00956579· OSTI ID:6226916
In the interaction of bicyclo(2.2.1)hepta-2,5-diene with decationized and rare-earth zeolites (H-TsVM, H-Ultrasil, H-mordenite, NaNdY), including the dealuminized NdNaY', wide-pore aluminosilicates and filled zeolite (AShNTs), activated under conditions such that sorbed water remains in (or is added to) the catalyst, alcohols are formed - 3-hydroxynortricyclane and 3-dehydronorborneol - together with ethers 3-(tricyclo(2.2.1.0/sup 2,6/)-3'-heptyloxy)-bicyclo(2.2.1)hept-5-ene and 3,3'-oxydinortricyclane. With aromatic compounds in the presence of wide-pore REE-Y zeolites and also AShNTs, activated at 500/sup 0/C, norbornadiene forms alkylated products such as endo-5-phenyl-2-norbornene from benzene.
Research Organization:
Institute of Chemical Physics, Moscow, USSR
OSTI ID:
6226916
Journal Information:
Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States), Journal Name: Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States) Vol. 35:6; ISSN BACCA
Country of Publication:
United States
Language:
Russian