2021
DOI: 10.1016/j.apcata.2020.117943
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AlCl3-catalyzed C-H p hosphination of benzene: A mechanistic study

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Cited by 6 publications
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“…The alkylbenzene is created due to the σ complex is unstable and easily dehydrogenated to generate aromatic products, it is easier to alkylate than benzene and can also obtain polyalkyl-substituted aromatic hydrocarbons. As an example, the benzene ring's reaction mechanism catalyzed by AlCl3 is shown in Scheme 3 [52][53][54]. Notes: "d 002 ", the interlayer spacing; "L c ", aromatic layer thickness; "f 002 ", aromaticity.…”
Section: Catalytic Mechanismmentioning
confidence: 99%
“…The alkylbenzene is created due to the σ complex is unstable and easily dehydrogenated to generate aromatic products, it is easier to alkylate than benzene and can also obtain polyalkyl-substituted aromatic hydrocarbons. As an example, the benzene ring's reaction mechanism catalyzed by AlCl3 is shown in Scheme 3 [52][53][54]. Notes: "d 002 ", the interlayer spacing; "L c ", aromatic layer thickness; "f 002 ", aromaticity.…”
Section: Catalytic Mechanismmentioning
confidence: 99%