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Intimate relationship between C-I reductive elimination, aryl scrambling and isomerization processes in Au() complexes
Ist Teil von
Chemical communications (Cambridge, England), 2023-02, Vol.59 (14), p.1975-1978
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2023
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
19
F NMR monitoring shows that heating
trans
-[Au
III
Rf
2
I
2
]
−
solutions (Rf = C
6
F
3
Cl
2
-3,5) leads to formation of
cis
-[AuRf
2
I
2
]
−
, [AuRf
3
I]
−
and [AuRfI
3
]
−
via
kinetic competition between isomerization and Rf/I scrambling. The system evolution is driven by the easy Rf-I reductive elimination from [AuRfI
3
]
−
(forming also [AuI
2
]
−
), which is faster than any of the Rf-Rf couplings from the coexisting species, hindering the commonly desired and thermodynamically preferred C-C coupling. A kinetic model where I
−
dissociation triggers both isomerization and transmetalation steps is proposed, which fits well the experimental data. DFT calculations support that the lower bond strength of Au
III
-I compared to other halides produces a pathway switch that makes C-I coupling kinetically preferred. Consequently, it is better avoided in reactions looking for C-C coupling.
The easier C-I reductive elimination, compared to other halides, promotes the Ar
F
/I scrambling from [Au
III
Ar
F
2
I
2
]
−
compounds, hindering the C-C coupling.