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Inne
Preparation and structural characterization of cDHAP-cyclic form of dihydroxyacetone phosphate-revealing chair and skew conformations of 1,3,2-dioxaphosphorinane ring.
Autorzy
Rok wydania
2013
Czasopismo
Numer woluminu
368
Strony
96-103
DOI
10.1016/j.carres.2012.12.020
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
A cyclic form of dihydroxyacetone phosphate, cDHAP, was obtained by the acidic hydrolysis of its dimethyl acetal (MeO)(2)cDHAP, and was crystallized in the hydrate, cDHAP-H (gem-diol; 1,3,2-dioxaphosphinane-2,5,5-triol 2-oxide) and the ketone, cDHAP-K (2-hydroxy-1,3,2-dioxaphosphinan-5-one 2-oxide) forms. The synthesis, MS and NMR analyses, crystallization and solid state structures determined by X-ray crystallography are described. The equilibrium state between the hydrate and ketone was established, revealing ∼86% of cDHAP-H in aqueous solution at room temperature. The striking structural feature of the ketone and hydrate forms of the same cyclic phosphate diester in the crystalline state is different conformations of the six-membered P/O/C/C/C/O 1,3,2-dioxaphosphorinane ring, namely chair (C) in cDHAP-H·H2O (9a-H) and skew (S) in cDHAP-K (9a-K). Apart from one previous report on the non-chair-puckered, disordered [(MeO)2cDHAP]- anion in the crystal of its ammonium salt (Ślepokura, K. Carbohydr. Res. 2008, 343, 113-131), this is the unique example of the cyclic phosphate diester in skew conformation. Both 9a-H and 9a-K crystallize with the phosphate group protonated, which has been so far rarely observed in the cyclic phosphates. Deformation of the phosphate group and flattening of the chair-puckered ring in 9a-H is typical of protonated P/O/C/C/C/O rings. However, the skew-puckered 9a-K shows different values of O-P-O angles versus the same lengths of P-O(endo) and P-O(exo) bonds.
Słowa kluczowe
cDEHAP, cyclic dioxaphosphorinane ring, skew conformation, X-ray crystal structure
Adres publiczny
http://dx.doi.org/10.1016/j.carres.2012.12.020