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首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Effect of aza substitution on the photophysical and electrochemical properties of porphycenes: Characterization of the near-IR-absorbing photosensitizers 2,7,12,17-tetrakis(p-substituted phenyl)-3,6,13,16-tetraazaporphycenes
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Effect of aza substitution on the photophysical and electrochemical properties of porphycenes: Characterization of the near-IR-absorbing photosensitizers 2,7,12,17-tetrakis(p-substituted phenyl)-3,6,13,16-tetraazaporphycenes

机译:氮杂取代对卟啉的光物理和电化学性质的影响:吸收近红外光的光敏剂2,7,12,17-四(对取代苯基)-3,6,13,16-四氮杂卟啉的表征

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摘要

The need for new photodynamic-therapy photosensitizers has stimulated the search of new families of compounds absorbing strongly in the 700-900 nm range, the region where tissue is most transparent to radiation capable to induce the photodynamic effect. Using computational chemistry techniques, 3,6,13,16-tetraazaporphycenes were previously identified as interesting target candidates. This work reports on the photophysical and electrochemical properties of selected members of this new family of macrocycles. Compared to porphycenes, the tetra-aza counterparts show stronger absorption in the near-infrared, lower-lying singlet and triplet excited states, and substantially larger internal conversion quantum yield (Phi(IC) = 0.93). Energy transfer to oxygen is observed, which results in the formation of the cytotoxic species singlet oxygen. The process is found to be reversible, consistent with a triplet-energy value close to that of singlet oxygen.
机译:对新型光动力疗法光敏剂的需求刺激了对在700-900 nm范围内强烈吸收的新化合物家族的研究,该区域是组织对能够诱发光动力效应的辐射最透明的区域。使用计算化学技术,以前已将3,6,13,16-四氮杂卟啉确定为有趣的目标候选物。这项工作报告了这个新的大环族成员的选定成员的光物理和电化学性质。与卟啉相比,四氮杂对映体在近红外,位于较低的单线态和三线态激发态下显示出更强的吸收,并且内部转换量子产率大大提高(Phi(IC)= 0.93)。观察到能量转移到氧气,这导致细胞毒性物质单线态氧的形成。发现该过程是可逆的,与接近单重态氧的三重态能量值一致。

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