期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 27, 期 27, 页码 7516-7524出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202100662
关键词
dynamic covalent chemistry; imine and hydrazone ligand formation; synergistic catalysis
资金
- ERC [SUPRADAPT 290585]
- University of Strasbourg Institute for Advanced Study (USIAS)
- China Scholarship Council [201606870040]
Optimizing C=N bond formation and C/N component exchange is crucial in Dynamic Covalent Chemistry (DCC). The synergistic effect achieved by combining metallo- and organo-catalysis leads to a powerful co-catalysis strategy for bond formation in DCC through interconnected chemical transformations, showing true catalytic effects. The presence of metal salts and auxiliary amines accelerates reaction rates and turnover, indicating marked rate accelerations and turnover through true catalysis.
Optimizing C=N bond formation and C/N component exchange has major significance in Dynamic Covalent Chemistry (DCC). Imine and hydrazone generation from their aldehyde, amine and hydrazine components showed large accelerations in presence of AgOTf or Zn(OTf)(2), up to 10(4) for the Zn(II)-(p-anisidine)imine complex. Zn(OTf)(2) and auxiliary p-anisidine together accelerated 630 times the formation of the Zn(II)-hydrazone complex, revealing a strong synergistic effect, traced to very fast initial formation of the reactive Zn(II)-imine complex presenting a C=N bond metallo-activated towards reaction with the hydrazine component. Reactions involving more entities showed kinetically faster and thermodynamically simpler outputs due to dynamic competition within a mixture of higher complexity. Catalytic amounts of metal salts and auxiliary amine gave similar marked rate accelerations and turnover, indicating true catalysis. The synergistic effect achieved by combining metallo- and organo-catalysis points to a powerful co-catalysis strategy of bond-formation in DCC through interconnected chemical transformations.
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