Enantiomerization of pendant-arm triaza macrocyclic lithium(I) and sodium(I) complex ions.
The first reported enantiomerization of six-coordinate alkali metal complex ions, represented by 1,4,7-tris(2-hydroxyethyl)-1,4,7-triazacyclononanelithium(I) and its sodium(I) analogue in methanol, has been characterized by variable-temperature 13C{1H} n.m.r. spectroscopy. The respective kinetic parameters are: k = (1·11 ± 0·05) × 106 and (2·27 ± 0·09) × 105 s-1 at 298·2 K, ΔH = 27·2 ± 0·3 and 21·7±0·2 kJ mol-1, and ΔS = –36·3 ± 1·3 and –69·6±1·2 J K-1 mol-1. Molecular orbital calculations show that these enantiomers have distorted trigonal prismatic structures consistent with the interpretation of the n.m.r. spectra. For the Li+, Na+, K+, Rb+ and Cs+ complex ions log(K/dm3 mol−1) = 3·13±0·09, 3·52±0·05, 3·23±0·05, 2·78±0·10 and 2·47±0·08, respectively, at 298·2 K and I = 0·05 mol dm-3 (NEt4 ClO4) in methanol, where K is the complex ion stability constant.
Diastereomeric Δ-1,4,7,10-Tetrakis((R)-2-hydroxy-2-phenylethyl)-1,4,7,10-tetraazacyclododecane and Its Alkali Metal Complex Ions. A Potentiometric Titration, Nuclear Magnetic Resonance, and Molecular Orbital StudyJ. Am. Chem. Soc.1998,120, 2862−2869