期刊
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
卷 2021, 期 29, 页码 2958-2975出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.202100400
关键词
Pincer complexes; Nickel; Palladium; Hydroxide complexes; Reaction mechanisms
资金
- Spanish Research Agency (AEI) [PGC2018-095768-B-100, PY20_0104]
- European Union (Feder Funds) [PGC2018-095768-B-100, PY20_0104]
- Junta de Andalucia [PGC2018-095768-B-100, PY20_0104]
The study investigated the reactions of pincer hydroxide complexes with dimethyl carbonate and organic electrophiles, shedding light on the irreversible cleavage of DMC by Ni and Pd hydroxides. The computational DFT models satisfactorily reproduced the kinetic and thermodynamic features of these reactions, explaining the primary cause preventing methanol carboxylation catalysis by Ni or Pd pincers.
The reactions of the pincer hydroxide complexes [((PCP)-P-iPr)M(OH)] (M=Ni, Pd) with dimethyl carbonate (DMC), and a set of organic electrophiles including benzaldehyde have been investigated in the context of our ongoing investigation on the synthesis of alkyl carbonates from CO2 and alcohols. The final outcome of such reactions is diverse, but for PhCHO and DMC the first step is a mechanistically similar addition of the [M]-OH linkage across the carbonyl functionality, that leads to unstable adducts. DMC is cleaved irreversibly by both Ni and Pd hydroxides, affording the corresponding methylcarbonates [((PCP)-P-iPr)MOCO2Me] and methanol, whereas PhCHO affords benzoate complexes [[((PCP)-P-iPr)MOCO2Ph]. The main kinetic and thermodynamic features of these reactions were reproduced satisfactorily by computational DFT models. The calculations throw light on the true causes of irreversibility of DMC cleavage by nucleophilic hydroxide complexes, which is the primary cause that prevents methanol carboxylation from being catalysed by the Ni or Pd pincers.
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