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Nickel carbonyl complexes, reactive intermediates

Thus, as is the case for the st pincer derivatives with nickel, Moulton and Shaw also reported the first PCP pincer rhodium and iridium derivatives and studied their reactivity toward carbon monoxide [4]. Hence, the (PCP) rhodium derivative (38) affords complex (40), as a product of the decomposition of the unstable hydrido chloro carbonyl intermediate (39) via a hydrodechlorination process, although this compound is obtained impure. To favor the hydrodechlorination process, an alternative route was attempted employing EtONa as base. This approach afforded exclusively compound (40) (Scheme 2.21). It is noteworthy that analogous reactions with the iridium analogous to complex (38) only afford impure samples of the carbonyl species analogous to complex (40). [Pg.38]


See other pages where Nickel carbonyl complexes, reactive intermediates is mentioned: [Pg.154]    [Pg.368]    [Pg.615]    [Pg.154]    [Pg.566]    [Pg.566]    [Pg.169]    [Pg.196]    [Pg.327]    [Pg.117]    [Pg.66]    [Pg.707]    [Pg.1274]    [Pg.282]   
See also in sourсe #XX -- [ Pg.134 ]

See also in sourсe #XX -- [ Pg.134 ]




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Complex Reactive

Complex intermediate

Intermediate reactivity

Intermediates nickel

Intermediates, reactive

Nickel carbonyl

Nickel carbonyl complexes

Nickel carbonylation

Nickel complexes carbonylation

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