K. Dodi et al., COMPLEXES OF ZN2-(ALPHA-HYDROXYBENZYL)THIAMINE MONOPHOSPHATE CHLORIDE(, CD2+, AND HG2+ WITH 2), Inorganic chemistry, 35(22), 1996, pp. 6513-6519
The binding sites of Zn2+, Cd2+, and Hg2+ in complexes with 2-(alpha-h
ydroxybenzyl)thiamine monophosphate chloride, (LH)Cl-+(-), have been i
nvestigated in the solid state [2-(alpha-hydroxybenzyl)thiamin monopho
sphate chloride monoprotonated at the phosphate group and protonated a
t N-1' is denoted as (LH)Cl-+(-); therefore, the ligand monoprotonated
at the phosphate group and deprotonated at N-1' is L]. Complexes of f
ormulae MLCl(2), M(LH)Cl-3, and (MCl(4))(2-)(LH)(2)(+) (M = Zn2+, Cd2, and Hg2+) were isolated in aqueous and methanolic solutions, dependi
ng on pH. The crystal structure of the complex of formula HgL(2)Cl(2)
was solved, together with that of the free ligand (LH)Cl-+(-), by X-ra
y crystallography. HgL(2)Cl(2) crystallizes in C2/c, with a = 32.968(6
) Angstrom, b = 7.477(2) Angstrom, c = 21.471(4) Angstrom, beta = 118.
19(1)degrees, V = 4665(2) Angstrom(3), and Z = 4. (LH)Cl-+(-) crystall
izes in Cc, with a = 10.951(3) Angstrom, b = 17.579(4) Angstrom, c = 1
3.373(3) Angstrom, beta = 105.36(2)degrees, V = 2482.4(10) Angstrom(3)
, and Z = 4. Mercury(II) binds to the N(1') of the pyrimidine ring. Bo
th ligands are in the S conformation [Phi(T) = -98.1(9)degrees and Phi
(P) = 176.1(10)degrees for HgL(2)Cl(2) and Phi(T) = 104.1(5)degrees an
d Phi(P) = 171.9(6)degrees for (LH)Cl-+(-)]. P-31 and C-13 NMR spectra
, together with vibrational spectra (IR/Raman), are used to deduce the
binding sites of the metal and the protonation states of the ligand a
t various pH values. It is found that solid-state P-31 NMR spectroscop
y is particularly useful in characterizing these complexes as the P-31
shielding tensors are sensitive to the state of the phosphate group.
On the other hand, the P-31 NMR spectra indicate that direct bonding b
etween Zn2+ and Cd2+ to the phosphate can occur under certain preparat
ion conditions. Solid-state C-13 NMR and vibrational (IR/Raman) spectr
oscopic results are also in agreement with the other techniques.