Albela B, Chottard G, Girerd J J
Laboratoire de Chimie Inorganique et Matériaux Moléculaires, ESA CNRS 7071, Université Pierre et Marie Curie, 75252 Paris cedex 05, France.
J Biol Inorg Chem. 2001 Apr;6(4):430-4. doi: 10.1007/s007750100220.
A biologically relevant dinuclear manganese mono-mu-oxo complex with a bound phenolate ligand in three oxidation states, (III,III), (III,IV) and (IV,IV), was studied using resonance Raman spectroscopy. Depending upon the excitation frequency, phenolate vibrations or mu-oxo vibrations were enhanced, which allowed us to assign the UV-visible absorption spectra. In the case of the mixed valence species (III,IV), the mu-oxo vibration at 854 cm-1 has been assigned by isotopic substitution (H2(18)O) to nu as(Mn-O-Mn). This preferential enhancement of the asymmetric vibration stresses the asymmetric character of the bridge.
利用共振拉曼光谱研究了一种具有生物学相关性的双核锰单-μ-氧配合物,该配合物带有一个结合的酚盐配体,处于三种氧化态,即(III,III)、(III,IV)和(IV,IV)。根据激发频率的不同,酚盐振动或μ-氧振动会增强,这使我们能够对紫外可见吸收光谱进行归属。对于混合价态物种(III,IV),通过同位素取代(H2(18)O)将854 cm-1处的μ-氧振动归属为νas(Mn-O-Mn)。这种不对称振动的优先增强突出了桥的不对称特性。