Gambino Dinorah, Otero Lucía, Vieites Marisol, Boiani Mariana, González Mercedes, Baran Enrique J, Cerecetto Hugo
Cátedra de Química Inorgánica, Departamento Estrella Campos, Facultad de Química, Universidad de la República, Montevideo, Uruguay.
Spectrochim Acta A Mol Biomol Spectrosc. 2007 Oct;68(2):341-8. doi: 10.1016/j.saa.2006.11.043. Epub 2006 Dec 8.
The vibrational spectroscopic behavior of a series of 16 palladium(II) complexes with 8 bioactive nitrofuran containing thiosemicarbazones as ligands has been studied in the solid state. The IR and Raman spectra of these complexes and the free nitrofuran thiosemicarbazone ligands were recorded and analyzed. Experimental spectra were satisfactorily described by density functional theory (DFT) calculations. The combination of experimental and theoretical methods allowed us to perform the characterization of the main vibrations that show the mode of coordination of the thiosemicarbazone moiety to palladium even though these vibration bands are located in spectral regions showing a complicated pattern due to the presence of vibrations of the nitrofuran moiety and combination modes involving furan vibrations. A characteristic vibrational spectroscopic pattern has been defined for Pd(II) 5-nitrofuryl thiosemicarbazone complexes. This systematic knowledge may be useful for the analysis of the spectroscopic behavior of other coordination compounds holding the 5-nitrofuran thiosemicarbazone moiety.
对一系列16种以8种含生物活性硝基呋喃的硫代半卡巴腙为配体的钯(II)配合物在固态下的振动光谱行为进行了研究。记录并分析了这些配合物以及游离硝基呋喃硫代半卡巴腙配体的红外光谱和拉曼光谱。通过密度泛函理论(DFT)计算对实验光谱进行了令人满意的描述。实验和理论方法的结合使我们能够对主要振动进行表征,这些振动显示了硫代半卡巴腙部分与钯的配位模式,尽管这些振动带位于由于硝基呋喃部分的振动和涉及呋喃振动的组合模式而呈现复杂图谱的光谱区域。已为Pd(II)5-硝基呋喃基硫代半卡巴腙配合物定义了特征性的振动光谱模式。这种系统的知识可能有助于分析其他含有5-硝基呋喃硫代半卡巴腙部分的配位化合物的光谱行为。