Abstract
Reaction of the tetradentate pendant-arm macrocycle 1,4,7-triazacyclononane- N-acetate (L) with Zn(O 3SCF 3) 2 or Mg(O 3SCF 3) 2 in alcohol produces the six-coordinate complexes [ZnL(H 2O)]O 3SCF 3·C 2H 5OH ( 1) and [MgL(H 2O) 2]O 3SCF 3 ( 2). Compounds 1 and 2 were characterized by single-crystal X-ray crystallography. The complex cation of 1 forms a polymeric chain with zinc centers bridged in a syn, anti fashion by acetate pendant arms. The complex cation of 2 is mononuclear, with two adjacent coordination sites on magnesium occupied by water molecules. These labile coordination sites may provide a binding site for activation of substrates in functional modeling of magnesium enzymes such as RuBisCo. 1H and 13C NMR spectroscopy demonstrates that L remains bound to magnesium in methanol solution. Crystal data: 1, orthorhombic, space group P2 12 12 1, a=9.0536(7), b=14.3750(11), c=14.4741(11) Å, V=1883.7(2) Å 3, Z=4, R=0.041; 2, orthorhombic, space group P2 12 12 1, a=8.5949(3), b=13.9694(4), c=14.0076(5) Å, V=1681.83(10) Å 3, Z=4, R=0.0248.
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