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On the Potential Use of Squaraine Derivatives as Photosensitizers in Photodynamic Therapy: A TDDFT and RICC2 Survey

机译:在光动力疗法中的光敏剂潜在使用Squaraine衍生物:TDDFT和RICC2调查

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A time-dependent density functional theory (TDDFT) and the second-order ap- proximated coupled-cluster model with the resolution of identity approximation (RICC2) studies are reported here for some classes of squaraine derivatives. These compounds have a sharp electronic band, ranging from the visible to near-red part of the spectrum, with an high molar absorption coefficient. These features make them potential photosensitizers in the photodynamic therapy of cancer (PDT), in which a light source, a photosensitizer, and molecular oxygen (302) are combined to give cytotoxic singlet oxygen (102) as a final result in a photochemical process. For the examined structures, the introduction of different substituents (electron donating, electron withdrawing, or fused rings) in the parent molecule, in order to give different squaraine derivatives, changes the maximum absorption wavelength (!?max) from 620 to 730 nm, giving a near-red absorbing photosensitizer that can better penetrate human tissue to damage tumor cells. Theoretical results, obtained from both TDDFT/PBEO and RICC2, are able to reproduce qualitatively the substitution effect on max, resulting in a useful tool for testing different structure modifications and, in general, for the molecular design of PDT photosensitizers. Calculated vertical excitation energies (singlet-singlet transitions) generally agree with experimental data within 0.3 eV. The singlet oxygen generation ability of these compounds requires that their triplet energy, for a type II reaction mechanism, should be greater than 0.98 eV. Theoretical triplet energies from the RICC2 method suggests that this requisite is fulfilled for all compounds, though the results are generally overestimated with respect to experiment by 0.7 eV, whereas TDDFT/ PBE0 triplet energies, which are underestimated within 0.2 eV in few cases, lie close to the above-mentioned limit and can be considered suitable for PDT applications.
机译:在此针对某些类Squaraine衍生物报告具有分辨率近似(RICC2)研究的时间依赖性密度泛函理论(TDDFT)和二阶耦合簇模型。这些化合物具有尖锐的电子频带,从光谱的近红部分的可见光,具有高摩尔吸收系数。这些特征使它们在癌症(PDT)的光动力学治疗中使它们具有潜在的光敏剂,其中聚合物,光敏剂和分子氧(302)组合以使细胞毒性单态氧(102)作为光化学过程的最终结果。对于检查的结构,在母体分子中引入不同的取代基(电子捐赠,电子抽出或融合环),以便给出不同的Squaraine衍生物,从620到730 nm改变最大吸收波长(!最大值),给出近红吸收光敏剂,可以更好地穿透人体组织以损害肿瘤细胞。从TDDFT / PBEO和RICC2获得的理论结果,能够定性地重现对MAX的替代作用,导致用于测试不同的结构修饰的有用工具,并且通常用于PDT光敏剂的分子设计。计算的垂直励磁能量(单线态转变)通常在0.3eV内的实验数据一致。这些化合物的单次氧产生能力要求其三重态能量,用于II型反应机制,应大于0.98eV。来自RICC2方法的理论三重态能表明,对于所有化合物来满足该必要条件,尽管结果在0.7eV中的实验中通常高估结果,而TDDFT / PBE0三重态能量在少数情况下被低估在0.2eV内,但请靠近到上述限度,可考虑适用于PDT应用。

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    Dipartimento di Chimica and Centro di Calcolo ad Alte Prestazioni per Elaborazioni Parallele e Distribuite-Centro d'Eccellenza MURST Universita delta Calabria 1-87030 Arcavacata di Rende Italy;

    Dipartimento di Chimica and Centro di Calcolo ad Alte Prestazioni per Elaborazioni Parallele e Distribuite-Centro d'Eccellenza MURST Universita delta Calabria 1-87030 Arcavacata di Rende Italy;

    Dipartimento di Chimica and Centro di Calcolo ad Alte Prestazioni per Elaborazioni Parallele e Distribuite-Centro d'Eccellenza MURST Universita delta Calabria 1-87030 Arcavacata di Rende Italy;

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  • 中图分类 化学键的量子力学理论;
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