Denat Franck, Diaz-Fernandez Yuri Antonio, Pallavicini Piersandro, Pasotti Luca, Rousselin Yoann, Sok Nicolas
Institut de Chimie Moléculaire de l'Université de Bourgogne, UMR CNRS 5260, Université de Bourgogne, 9 avenue Alain Savary, 21078, Dijon, France.
Dalton Trans. 2009 Sep 14(34):6751-8. doi: 10.1039/b907289f. Epub 2009 Jul 15.
Three 13aneN4 macrocyclic ligands have been prepared bearing a -CH(2)NHR side arm (R = H, n-C(5)H(11), n-C(10)H(21)) on a carbon atom. When Cu(2+) is complexed in the macrocyclic ring, the amino group of the side arm undergoes an acid-base protonation equilibrium but it is not able to coordinate apically the metal cation even when it is deprotonated. The Cu(2+) complex with the ligand bearing the longest appended aliphatic chain is fully confined inside Triton X-100 micelles, and its ability to bind and sequestrate a series of anions inside micelles has been studied at two different pH values, i.e. both with protonated and neutral side-arm amino group. The favourable role played by the protonated amino group in the side arm has been demonstrated.
已制备出三种13aneN4大环配体,其在碳原子上带有-CH(2)NHR侧链(R = H、正戊基、正癸基)。当Cu(2+)在大环环中络合时,侧链的氨基会发生酸碱质子化平衡,但即使去质子化也无法以顶端方式配位金属阳离子。与带有最长附加脂肪链的配体形成的Cu(2+)络合物完全被限制在Triton X-100胶束内部,并且已在两个不同的pH值下研究了其在胶束内部结合和螯合一系列阴离子的能力,即在质子化和中性侧链氨基的情况下。已证明侧链中质子化氨基所起的有利作用。