Bis(o-Aminophenolato)germanium(II) and Tin(II) Complexes in Hydroboration Reactions of Aromatic Aldehydes

Stable tin(II) (dippAmP)2Sn (I) and germanium(II) (dippAmP)2Ge (II) complexes based on 4,6-di-tert-butyl-N-(2,6-diisopropylphenyl)-o-aminophenol were synthesized and characterized. The compounds are monomeric and contain, in addition to covalent element(II)–oxygen bonds, additional coordination bonds involving the secondary amino groups of the chelating ligand. The synthesized compounds were tested as homogeneous catalysts for the hydroboration of various substituted aldehydes to the corresponding boronate esters. Optimization of the catalytic reaction conditions made it possible to reduce the catalyst loading to 0.02 mol % while maintaining quantitative conversion under mild conditions. The molecular structure of complex II was established by X-ray diffraction analysis (CCDC no. 2423247, II).

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Publication Details

Journal
Russian Journal of Coordination Chemistry
Published
2025-04-01
DOI
https://doi.org/10.1134/s1070328425600238
Primary Topic
Organoboron and organosilicon chemistry
Type
article
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article

Bis(o-Aminophenolato)germanium(II) and Tin(II) Complexes in Hydroboration Reactions of Aromatic Aldehydes

Anton V. Cherkasov, К. В. Арсеньева, A. V. Klimashevskaya, Alexandr V. Piskunov
Russian Journal of Coordination Chemistry
Organoboron and organosilicon chemistry
article

Bis(o-Aminophenolato)germanium(II) and Tin(II) Complexes in Hydroboration Reactions of Aromatic Aldehydes

Anton V. Cherkasov, К. В. Арсеньева, A. V. Klimashevskaya, Alexandr V. Piskunov
article en

Abstract

Stable tin(II) (dippAmP)2Sn (I) and germanium(II) (dippAmP)2Ge (II) complexes based on 4,6-di-tert-butyl-N-(2,6-diisopropylphenyl)-o-aminophenol were synthesized and characterized. The compounds are monomeric and contain, in addition to covalent element(II)–oxygen bonds, additional coordination bonds involving the secondary amino groups of the chelating ligand. The synthesized compounds were tested as homogeneous catalysts for the hydroboration of various substituted aldehydes to the corresponding boronate esters. Optimization of the catalytic reaction conditions made it possible to reduce the catalyst loading to 0.02 mol % while maintaining quantitative conversion under mild conditions. The molecular structure of complex II was established by X-ray diffraction analysis (CCDC no. 2423247, II).

Russian Journal of Coordination ChemistryVol. 51(4)
G.A. Razuvaev Institute of Organometallic Chemistry (RU)
Clean water and sanitation
Openalex Percentile: Top 87%
Organoboron and organosilicon chemistry
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