Beyler Maryline, Heitz Valérie, Sauvage Jean-Pierre, Ventura Barbara, Flamigni Lucia, Rissanen Kari
Laboratoire de Chimie Organo-Minérale, Institut de Chimie, Université de Strasbourg-CNRS/UMR 7177, 4, rue Blaise Pascal, 67070 Strasbourg-Cedex, France.
Inorg Chem. 2009 Sep 7;48(17):8263-70. doi: 10.1021/ic900887q.
A pentaporphyrinic assembly was formed in one step, quantitatively, from a gable like zinc(II) bis-porphyrin and a free-base meso-tetrakis(4-pyridyl)porphyrin, because of the formation of four zinc-nitrogen coordination bonds. The X-ray crystal structure obtained shows a symmetrical structure, the free-base porphyrin being located at the center of a square formed by the four zinc atoms of the two zinc(II) bis-porphyrins. The two phenanthrolines connecting the zinc porphyrins are respectively above and below the plane of the central free-base porphyrin because of favorable CH-pi interactions between several porphyrinic assemblies within the crystal. Spectrophotometric and spectrofluorimetric titrations and studies reveal a high association constant for the porphyrinic assembly in the order of 10(14) M(-2). As expected, energy transfer from the zinc porphyrin component to the central free-base porphyrin quenches the fluorescence of the zinc porphyrin components whereas no sensitization of the emission of the free-base porphyrin was observed. Hypotheses on this unusual behavior are discussed.
由于形成了四个锌 - 氮配位键,一种山墙状双锌(II)卟啉和一种游离碱中位 - 四(4 - 吡啶基)卟啉一步定量地形成了一种五卟啉组装体。所获得的X射线晶体结构显示出对称结构,游离碱卟啉位于由两个双锌(II)卟啉的四个锌原子形成的正方形中心。由于晶体中几个卟啉组装体之间有利的C - H - π相互作用,连接锌卟啉的两个菲咯啉分别位于中心游离碱卟啉平面的上方和下方。分光光度法和荧光分光光度滴定及研究表明,卟啉组装体的缔合常数很高,约为10(14) M(-2)。正如预期的那样,从锌卟啉组分到中心游离碱卟啉的能量转移淬灭了锌卟啉组分的荧光,而未观察到游离碱卟啉发射的敏化现象。讨论了关于这种异常行为的假设。