Co-ordination compounds of indium. Part XI. The stepwise one-electron reduction of some neutral indium(III) complexes

D. G. Tuck, M. K. Yang
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引用次数: 8

Abstract

The complex InL3(L = 3-hydroxy-2-methyl-4-pyronato-anion) has been prepared, and its n.m.r., i.r. and Raman spectra compared with those of the parent ligand. Polarographic reduction of this complex, and of In(trop)3(trop = tropolonato-anion) takes place in successive one-electron steps, as in the case of complexes of indium with bidentate sulphur-donor ligands. One-electron polarographic reduction of In (acac)3(acac = acetylacetonato-anion) and In(oxine)3(oxine = quinolin-8-olato-anion) has also been observed, and may be a general property of complexes of indium(III) with bidentate chelating ligands.
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铟配位化合物。一些中性铟(III)配合物的逐步单电子还原
制备了配合物InL3(L = 3-羟基-2-甲基-4-吡啶阴离子),并将其与母体配体的核磁共振、红外和拉曼光谱进行了比较。这种络合物和In(trop)3(trop = tropolonato-阴离子)的极谱还原是在连续的单电子步骤中进行的,就像铟与双齿硫供体配合物的情况一样。还观察到In(acac)3(acac =乙酰丙酮-阴离子)和In(oxine)3(oxine =喹啉-8-丙酮-阴离子)的单电子极谱还原,这可能是铟(III)与双齿螯合配体配合物的一般性质。
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