Instituto de Ciências Exatas e Naturais, Programa de Pos-Graduação em Fisica, Universidade Federal do Pará, Belém, PA, Brazil.
Department of Chemistry, The University of North Carolina at Chapel Hill, Murray Hall, Chapel Hill, NC, United States.
Spectrochim Acta A Mol Biomol Spectrosc. 2019 May 15;215:327-333. doi: 10.1016/j.saa.2019.02.024. Epub 2019 Feb 11.
The changing of the electronic and vibronic states due to the insertion of Zn(II), Cu(II), Ni(II) or Co(II) ions in the meso-tetrakis(4-pyridyl)porphyrin ring center is investigated. The combination of absorption, photoluminescence, Raman and infrared spectroscopies with second-derivative-based spectral deconvolution analysis reveals that the structuration of both B- and Q-bands is very sensitive to the decorating ion. Similar to free base porphyrins, metal(II) meso-tetra(4-pyridyl)porphyrins also present their Q-band constituted of multiple electronic transitions, where the central ion plays an important role in the selection of vibration modes that mediate the vibronic transitions. Our novel results will expand and reinterpret current assignments for metal(II) meso-tetra(4-pyridyl)porphyrins vibrational modes available in the literature.
研究了 Zn(II)、Cu(II)、Ni(II) 或 Co(II) 离子插入卟啉环中心对电子和振子态的变化。吸收、光致发光、拉曼和红外光谱与基于二阶导数的光谱去卷积分析相结合,表明 B-和 Q-带的结构对修饰离子非常敏感。与自由碱基卟啉类似,金属(II)meso-四(4-吡啶基)卟啉也呈现出由多个电子跃迁组成的 Q 带,其中中心离子在选择介导振子跃迁的振动模式方面起着重要作用。我们的新结果将扩展和重新解释文献中现有金属(II)meso-四(4-吡啶基)卟啉振动模式的当前分配。