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Probing the Catalytically Active Species in POM‐Catalysed DNA‐Model Hydrolysis **
Author(s) -
Martins Frederico F.,
SánchezGonzález Ángel,
Lanuza Jose,
Miras Haralampos N.,
Lopez Xabier,
Bandeira Nuno A.,
Gil Adrià
Publication year - 2021
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202004989
Subject(s) - catalysis , chemistry , phosphodiester bond , hydrolysis , electrospray ionization , decomposition , mass spectrometry , organic chemistry , chromatography , rna , biochemistry , gene
Phosphoester hydrolysis is an important chemical step in DNA repair. One archetypal molecular model of phosphoesters is para‐nitrophenylphosphate (pNPP). It has been shown previously that the presence of molecular metal oxide [Mo 7 O 24 ] 6− may catalyse the hydrolysis of pNPP through the partial decomposition of polyoxomolybdate framework resulting in a [(PO 4 ) 2 Mo 5 O 15 ] 6− product. Real‐time monitoring of the catalytic system using electrospray ionisation mass spectrometry (ESI‐MS) provided a glance into the species present in the reaction mixture and identification of potential catalytic candidates. Following up on the obtained spectrometric data, Density Functional Theory (DFT) calculations were carried out to characterise the hypothetical intermediate [Mo 5 O 15 (pNPP) 2 (H 2 O) 6 ] 6− that would be required to form under the hypothesised transformation. Surprisingly, our results point to the dimeric [Mo 2 O 8 ] 4− anion resulting from the decomposition of [Mo 7 O 24 ] 6− as the active catalytic species involved in the hydrolysis of pNPP rather than the originally assumed {Mo 5 O 15 } species. A similar study was carried out involving the same species but substituting Mo by W. The mechanism involving W species showed a higher barrier and less stable products in agreement with the non‐catalytic effect found in experimental results.