Cyclisation of alkoxy radicals. A semiempirical MNDO-PM3 study
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1994
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Royal Society of Chemistry
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The reactivity of the butoxy and 3-methylcyclohexyl radicals, as representatives of alkoxy radicals, was studied by MNDO-PM3 semiempirical MO method. In both cases it was found that the oxy radical underwent easily 1,5-H migration giving a δ-hydroxyalkyl radical. The hydrogen abstraction reaction goes through two transition states. The first transition state (TS) with short O-H distance has an energy very similar to, or lower than, the TS for 1,5-H migration. The second TS is of higher energy and is much product-like. The overall cyclisation reaction has a high activation energy (over 40 kcal mol-1), and is therefore unlikely to occur spontaneously. Most likely, the cyclisation step needs assistance of some other surrounding molecules to speed up the reaction.
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Journal of the Chemical Society, Perkin Transactions 2, 1994, 4, 877-881Publisher:
- Royal Society of Chemistry
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IHTMTY - JOUR AU - Juranić, Ivan AU - Mihailović, Milhailo Lj. AU - Dabović, Milan PY - 1994 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/2710 AB - The reactivity of the butoxy and 3-methylcyclohexyl radicals, as representatives of alkoxy radicals, was studied by MNDO-PM3 semiempirical MO method. In both cases it was found that the oxy radical underwent easily 1,5-H migration giving a δ-hydroxyalkyl radical. The hydrogen abstraction reaction goes through two transition states. The first transition state (TS) with short O-H distance has an energy very similar to, or lower than, the TS for 1,5-H migration. The second TS is of higher energy and is much product-like. The overall cyclisation reaction has a high activation energy (over 40 kcal mol-1), and is therefore unlikely to occur spontaneously. Most likely, the cyclisation step needs assistance of some other surrounding molecules to speed up the reaction. PB - Royal Society of Chemistry T2 - Journal of the Chemical Society, Perkin Transactions 2 T1 - Cyclisation of alkoxy radicals. A semiempirical MNDO-PM3 study IS - 4 SP - 877 EP - 881 UR - https://hdl.handle.net/21.15107/rcub_cer_2710 ER -
@article{ author = "Juranić, Ivan and Mihailović, Milhailo Lj. and Dabović, Milan", year = "1994", abstract = "The reactivity of the butoxy and 3-methylcyclohexyl radicals, as representatives of alkoxy radicals, was studied by MNDO-PM3 semiempirical MO method. In both cases it was found that the oxy radical underwent easily 1,5-H migration giving a δ-hydroxyalkyl radical. The hydrogen abstraction reaction goes through two transition states. The first transition state (TS) with short O-H distance has an energy very similar to, or lower than, the TS for 1,5-H migration. The second TS is of higher energy and is much product-like. The overall cyclisation reaction has a high activation energy (over 40 kcal mol-1), and is therefore unlikely to occur spontaneously. Most likely, the cyclisation step needs assistance of some other surrounding molecules to speed up the reaction.", publisher = "Royal Society of Chemistry", journal = "Journal of the Chemical Society, Perkin Transactions 2", title = "Cyclisation of alkoxy radicals. A semiempirical MNDO-PM3 study", number = "4", pages = "877-881", url = "https://hdl.handle.net/21.15107/rcub_cer_2710" }
Juranić, I., Mihailović, M. Lj.,& Dabović, M.. (1994). Cyclisation of alkoxy radicals. A semiempirical MNDO-PM3 study. in Journal of the Chemical Society, Perkin Transactions 2 Royal Society of Chemistry.(4), 877-881. https://hdl.handle.net/21.15107/rcub_cer_2710
Juranić I, Mihailović ML, Dabović M. Cyclisation of alkoxy radicals. A semiempirical MNDO-PM3 study. in Journal of the Chemical Society, Perkin Transactions 2. 1994;(4):877-881. https://hdl.handle.net/21.15107/rcub_cer_2710 .
Juranić, Ivan, Mihailović, Milhailo Lj., Dabović, Milan, "Cyclisation of alkoxy radicals. A semiempirical MNDO-PM3 study" in Journal of the Chemical Society, Perkin Transactions 2, no. 4 (1994):877-881, https://hdl.handle.net/21.15107/rcub_cer_2710 .