作者: M. Kaliva , C.P. Raptopoulou , A. Terzis , A. Salifoglou
DOI: 10.1016/S0162-0134(02)00563-9
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摘要: Abstract Vanadium(V) involvement in interactions with physiological ligands biological media prompted us to delve into the systematic pH-dependent synthesis, spectroscopic characterization, and perusal of chemical properties arising aqueous vanadium(V)–citrate species requisite system. To this end, facile reactions led dinuclear complexes (NH 4 ) [V 2 O (C 6 H 5 7 ]·4H ( 1 ]·6H ). Complex were characterized by elemental analysis, FT-IR X-ray crystallography. crystallizes monoclinic space group C 2/ c a =16.998(5) A, b =16.768(5) =9.546(3) β =105.22(1)°, V =2625(1) A 3 , Z =4. triclinic P =9.795(4) =9.942(4) =9.126(3) α =90.32(1)°, =111.69(1)°, γ =108.67(1)°, =774.5(5) =1. The structures consistent presence core, which citrate differing protonation state bound coordination mode past observations. Ultimately, pH dependent transformations series three complexes, ]·2H ), all isolated at values from 7.5, explored revealed an important interconnection among species. Collectively, emerged as determining factor structural attributes adjoining acid–base chemistry unfolding around stable core. results point participation speciation, may relate site-specific protonations–deprotonations on potential processes involving vanadium(V) ligand targets.