The dynamic-coupling basis of the conformational optical activity of chelated metal complexes

P. L. Fereday, S. Mason
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引用次数: 4

Abstract

The absolute configuration of (–)-stilbene diamine is shown to be (R,R), and the c.d. spectra of the cobalt(III) complexes with this ligand are found to support the dynamic-coupling or polarisability mechanism for the conformational optical activity due to chirally-puckered chelate rings in metal complexes, but not the static field mechanism in which that optical activity arises from the charges of the ligand atoms.
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螯合金属配合物构象光学活性的动态耦合基础
(-)-二苯二胺的绝对构型显示为(R,R),与该配体的钴(III)配合物的cd光谱支持金属配合物中手性皱化螯合环引起构象光学活性的动态耦合或极化机制,但不支持由配体原子的电荷引起光学活性的静态场机制。
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