Department of Organic and Nuclear Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 12840 Praha 2, Czech Republic.
Inorg Chem. 2010 Oct 4;49(19):8897-903. doi: 10.1021/ic101061p.
The complexation abilities of 2,2'-bipyridine (bipy) and 2,2'-bipyridyl-N,N'-dioxide (bipydiox) toward zinc(II) and the influence of these ligands on the properties and reactivities of the investigated complexes are compared by means of mass spectrometry, IR multiphoton dissociation spectroscopy, and theoretical calculations. The binding energy of bipydiox to zinc is slightly smaller than that of bipy, namely, by 0.1 eV in the mixed complex (bipy)(bipydiox)ZnCl. Accordingly, the differences in the properties and reactivities of the complexes of zinc(II)/bipydiox and zinc(II)/bipy are only minor. The mechanism of decarboxylation of (L)Zn(CH(3)COO) (L = bipy or bipydiox) is investigated in detail. The substantial difference between the ligands stems only from the possibility of oxygen transfer from bipydiox, which is here, however, observed only as a high-energy channel in the fragmentation of complexes (bipydiox)Zn(CH(3)COO).
通过质谱、红外多光子解离光谱和理论计算,比较了 2,2'-联吡啶(bipy)和 2,2'-联吡啶-N,N'-二氧化物(bipydiox)与锌(II)的络合能力,以及这些配体对所研究配合物性质和反应性的影响。bipydiox 与锌的结合能略小于 bipy,即在混合配合物(bipy)(bipydiox)ZnCl中,小 0.1eV。因此,锌(II)/bipydiox 和锌(II)/bipy 配合物的性质和反应性差异仅微乎其微。详细研究了(L)Zn(CH(3)COO)(L = bipy 或 bipydiox)的脱羧反应机理。配体之间的实质性差异仅源于 bipydiox 从氧转移的可能性,然而,在这里,仅在复合物(bipydiox)Zn(CH(3)COO)的碎裂中观察到作为高能通道。