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光谱、热和磺胺吡啶药物与堿土金属离子就地配合的抗肿瘤研究。

Spectroscopic, thermal and antitumor investigations of sulfasalazine drug in situ complexation with alkaline earth metal ions.

机构信息

Department of Chemistry, Faculty of Science, Port Said, Port Said University, Egypt.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2011 Nov;82(1):108-17. doi: 10.1016/j.saa.2011.07.010. Epub 2011 Jul 22.

Abstract

The complexes of sulfasalazine (H(3)Suz) with some of alkaline metals Mg(II), Ca(II), Sr(II) and Ba(II) have been investigated. Sulfasalazine complexes were synthesized and characterized by spectroscopic tools; infrared spectra, electronic and mass spectra. The IR spectra of the prepared complexes were suggested that the H(3)Suz behaves as a bi-dentate ligand through the carboxylic and phenolic groups. The molar conductance measurements gave an idea about the non-electrolytic behavior of the H(3)Suz complexes. The thermal decomposition processes for metal(II) complexes of H(3)Suz viz: [M(HSuz)(H(2)O)(4)] (where M = Mg(II), Ca(II), Sr(II) or Ba(II)) have been accomplished on the basis of TG/DTG and DTA studies, and the formula conforms to the stoichiometry of the complexes based on elemental analysis. The kinetic analyses of the thermal decomposition were studied using the Coats-Redfern and Horowitz-Metzger equations. The antitumor and antimicrobial activities of the H(3)Suz and their alkaline metal(II) complexes were evaluated.

摘要

已研究了柳氮磺胺吡啶(H(3)Suz)与一些碱性金属(Mg(II),Ca(II),Sr(II)和 Ba(II))的配合物。通过光谱工具;红外光谱,电子和质谱法合成并表征了柳氮磺胺吡啶配合物。所制备配合物的红外光谱表明,H(3)Suz 通过羧酸和酚基表现为双齿配体。摩尔电导率测量给出了 H(3)Suz 配合物的非电解质行为的想法。基于 TG / DTG 和 DTA 研究,完成了 H(3)Suz 对金属(II)配合物[M(HSuz)(H(2)O)(4)](其中 M = Mg(II),Ca(II),Sr(II)或 Ba(II))的热分解过程,并且基于元素分析,该公式符合配合物的化学计量。通过 Coats-Redfern 和 Horowitz-Metzger 方程研究了热分解的动力学分析。评估了 H(3)Suz 及其碱性金属(II)配合物的抗肿瘤和抗菌活性。

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