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Ni-catalyzed mild hydrogenolysis and oxidations of C-O bonds via carbonate redox tags.

ABSTRACT: Oxygenated molecules are omnipresent in natural as well as artificial settings making the redox transformation of the present C-O bonds a central tool for their processing. However, the required (super)stoichiometric redox agents which traditionally include highly reactive and hazardous reagents pose multiple practical challenges including process safety hazards or special waste management requirements. Here, we report a mild Ni-catalyzed fragmentation strategy based on carbonate redox tags for redox transformations of oxygenated hydrocarbons in the absence of any external redox equivalents or other additives. The purely catalytic process enables the hydrogenolysis of strong C(sp²)-O bonds including that of enol carbonates as well as the catalytic oxidation of C-O bonds under mild conditions down to room temperature. Additionally, we investigated the underlying mechanism and showcased the benefits of carbonate redox tags in multiple applications. More broadly, the work herein demonstrates the potential of redox tags for organic synthesis.

SUBMITTER: Toupalas G

PROVIDER: S-EPMC10163265 | biostudies-literature | 2023 May

REPOSITORIES: biostudies-literature

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Ni-catalyzed mild hydrogenolysis and oxidations of C-O bonds via carbonate redox tags.

Toupalas Georgios G Ribadeau-Dumas Loélie L Morandi Bill B

Nature communications 20230505 1

Oxygenated molecules are omnipresent in natural as well as artificial settings making the redox transformation of the present C-O bonds a central tool for their processing. However, the required (super)stoichiometric redox agents which traditionally include highly reactive and hazardous reagents pose multiple practical challenges including process safety hazards or special waste management requirements. Here, we report a mild Ni-catalyzed fragmentation strategy based on carbonate redox tags for ...[more]

PMID: 37147279

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Project description:A recent report established that the tetrabutylammonium (TBA) salt of hexavanadopolymolybdate TBA4H5[PMo6V6O40] (PV6Mo6) serves as the redox buffer with Cu(II) as a co-catalyst for aerobic deodorization of thiols in acetonitrile. Here, we document the profound impact of vanadium atom number (x = 0-4 and 6) in TBA salts of PVxMo12-xO40(3+x)- (PVMo) on this multicomponent catalytic system. The PVMo cyclic voltammetric peaks from 0 to -2000 mV vs Fc/Fc+ under catalytic conditions (acetonitrile, ambient T) are assigned and clarify that the redox buffering capability of the PVMo/Cu catalytic system derives from the number of steps, the number of electrons transferred each step, and the potential ranges of each step. All PVMo are reduced by varying numbers of electrons, from 1 to 6, in different reaction conditions. Significantly, PVMo with x ≤ 3 not only has much lower activity than when x > 3 (for example, the turnover frequencies (TOF) of PV3Mo9 and PV4Mo8 are 8.9 and 48 s-1, respectively) but also, unlike the latter, cannot maintain steady reduction states when the Mo atoms in these polyoxometalate (POMs) are also reduced. Stopped-flow kinetics measurements reveal that Mo atoms in Keggin PVMo exhibit much slower electron transfer rates than V atoms. There are two kinetic arguments: (a) In acetonitrile, the first formal potential of PMo12 is more positive than that of PVMo11 (-236 and -405 mV vs Fc/Fc+); however, the initial reduction rates are 1.06 × 10-4 s-1 and 0.036 s-1 for PMo12 and PVMo11, respectively. (b) In aqueous sulfate buffer (pH = 2), a two-step kinetics is observed for PVMo11 and PV2Mo10, where the first and second steps are assigned to reduction of the V and Mo centers, respectively. Since fast and reversible electron transfers are key for the redox buffering behavior, the slower electron transfer kinetics of Mo preclude these centers functioning in redox buffering that maintains the solution potential. We conclude that PVMo with more vanadium atoms allows the POM to undergo more and faster redox changes, which enables the POM to function as a redox buffer dictating far higher catalytic activity.

Dataset Information

Ni-catalyzed mild hydrogenolysis and oxidations of C-O bonds via carbonate redox tags.

Publications

Ni-catalyzed mild hydrogenolysis and oxidations of C-O bonds via carbonate redox tags.

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