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Tạp chí khoa học ĐHCT
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Kỷ yếu HN trong nước
Kỷ yếu HN quốc tế
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Bài báo - Tạp chí
21 (2015) Trang: 4428-4439
Tạp chí: Chemistry - A European Journal

A detailed reaction mechanism is proposed for the hydrolysis of the phosphoester bonds in the DNA model substrate bis(4-nitrophenyl) phosphate (BNPP) in the presence of the ZrIV-substituted Keggin type polyoxometalate (Et2NH2)8[{a-PW11O39Zr(m-OH) (H2O)}2]·7H2O (ZrK 2:2) at pD 6.4. Low-temperature 31P DOSY spectra at pD 6.4 gave the first experimental evidence for the presence of ZrK1:1 in fast equilibrium with ZrK 2:2 in purely aqueous solution. Moreover, theoretical calculations identified the ZrK 1:1 form as the potentially active species in solution. The reaction intermediates involved in the hydrolysis were identified by means of 1H/31P NMR studies, including EXSY and DOSY NMR spectroscopy, which were supported by DFT calculations. This experimental/theoretical approach enabled the determination of the structures of four intermediate species in which the starting compound BNPP, nitrophenyl phosphate (NPP), or the end product phosphate (P) is coordinated to ZrK 1:1. In the proposed reaction mechanism, BNPP initially coordinates to ZrK 1:1 in a monodentate fashion, which results in hydrolysis of the first phosphoester bond in BNPP and formation of NPP. EXSY NMR studies showed that the bidentate complex between NPP and ZrK 1:1 is in equilibrium with monobound and free NPP. Subsequently, hydrolysis of NPP results in P, which is in equilibrium with its monobound form.

Các bài báo khác
(2013) Trang: 49
Tạp chí: 16th International Conference on BioInorganic Chemistry (ICBIC), Grenoble, FRANCE, 22-26 July 2013.
(2013) Trang: 61
Tạp chí: 12th Young Belgian Magnetic Resonance Scientist (YBMRS), Blankenberge, Belgium, 02-03 December 2013
 

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