Journal of Organometallic Chemistry

dc.creatorAballay, A
dc.creatorGodoy, F
dc.creatorBuono-Core, G.E
dc.creatorKlahn, H A
dc.creatorOelckers, B.
dc.creatorGarland, M T
dc.creatorMuñoz, J C
dc.date2020-03-11T20:34:56Z
dc.date2022-07-08T17:07:37Z
dc.date2020-03-11T20:34:56Z
dc.date2022-07-08T17:07:37Z
dc.date2003
dc.date.accessioned2023-08-22T01:45:36Z
dc.date.available2023-08-22T01:45:36Z
dc.identifier11980002
dc.identifier11980002
dc.identifierhttps://hdl.handle.net/10533/240433
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8307477
dc.descriptionPhotochemical reaction of (eta(5)-C5Me5)Re(CO)(3), with 2,4,5-trichloroanisole and 3,4,5-trichlorotrifluoromethylbenzene yields (eta(5)- C5Me5)Re(CO)(2)(C6H2Cl2(MeO))Cl (1) and (eta(5)-C5Me5)Re(CO)(2)(C6H2Cl2(CF3))Cl, (2) formed by insertion of the fragment (eta(5)- C5Me5)Re(CO)(2) into the C-Cl bond of the chloroarenes. The C-Cl bond activation of trichloroanisole occurs at the chlorine ortho respect to the methoxy group as revealed by the X-ray structure of 1. In the case of the reaction with C6H2Cl3(CF3), H-1-NMR spectroscopy indicates that only the C-Cl bond meta respect to CF3 group is cleaved. Complex 1 was isolated as the trans isomer while 2 was obtained as an isomeric mixture (trans-2 and cis-2). The stereochemistry of these complexes has been assigned by IR and C-13-NMR spectroscopies and supported by X-ray crystallography for 1.
dc.descriptionFONDAP
dc.descriptionFONDAP
dc.languageeng
dc.relationhttp://repositorio.uchile.cl/handle/2250/124634
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titlePhotochemical C-C1 bond activation of trichloroarenes by the rhenium complex (n5-C5ME5)Re(CO)3. X-ray structure of trans-(n5-C5Me5)Re(CO)2(2-methoxy-4,5-dichlorophenyl)cloride.
dc.titleJournal of Organometallic Chemistry
dc.typeArticulo
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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