M. Farahbakhsh et al., A DECAVANADATE SANDWICHED BY DIPROTONATED CRYPTANDS-222 - MODEL FOR THE VANADATE-IONOPHORE INTERACTION, Chemische Berichte, 130(8), 1997, pp. 1123-1127
Treatment of a C222-vanadyl-AMP complex (C222 = cryptand-222, AMP = ad
enosine monosphosphate) with. Me2NH in the presence of air yielded cen
trosymmetric dihydrogen-decavanadate H2V10O284-, sandwiched by two dip
rotonated C222 molecules. An X-ray crystal-structure analysis was perf
ormed of this compound with the overall composition [C222(H+)(2)](2)[H
2V10O28]. 2 1/2 H2O. Protonation sites in the anion are mu(2)-oxygen a
toms linking two different vanadium centres. Protonation sites at the
cryptand are the nitrogen and/or oxygen atoms of one of the -[CH2](2)O
[-CH2](2)O[CH2](2)- bridges. The relevance of the compound for the sta
bilisation and transport of the kinase and phosphatase inhibitor decav
anadate by biogenic ionophores is addressed.