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How does methylation suppress the electron-induced decomposition of 1-methyl-nitroimidazoles?

机译:甲基化如何抑制1-甲基 - 硝基咪唑的电子诱导的分解?

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The efficient decomposition of nitroimidazoles (NIs) by low energy electrons is believed to underlie their radiosensitizing properties. Recent dissociative electron attachment (DEA) measurements showed that methylation at the N1 site unexpectedly suppresses the electron-induced reactions in 4(5)-NI. We report theoretical results that provide a clear interpretation of that astounding finding. Around 1.5 eV, DEA reactions into several fragments are initiated by a pi* resonance, not considered in previous studies. The autoionization lifetime of this anion state, which limits the predissociation dynamics, is considerably shorter in the methylated species, thereby suppressing the DEA signals. On the other hand, the lifetime of the pi* resonance located around 3 eV is less affected by methylation, which explains why DEA is still observed at these energies. Our results demonstrate how even a simple methylation can significantly modify the probabilities for DEA reactions, which may be significant for NI-based cancer therapy. Published by AIP Publishing.
机译:据信,通过低能量电子的硝基咪唑(NIS)的有效分解使其放射敏化性能下降。最近的解离电子附着(DEA)测量表明,N1位点的甲基化意外地抑制了4(5)-NI中的电子诱导的反应。我们报告了理论结果,提供了对这种令人震惊的发现的明确解释。大约1.5 eV,DEA反应成几个片段由PI *共振开始,在以前的研究中不考虑。这种阴离子状态的自动化寿命限制了预处理动态,在甲基化物质中相当短,从而抑制了DEA信号。另一方面,位于3eV的PI *谐振的寿命不太受甲基化的影响,这解释了为什么DEA在这些能量中仍然观察到。我们的结果表明,即使是简单的甲基化也可以显着改变DEA反应的概率,这对于基于Ni的癌症治疗可能是显着的。通过AIP发布发布。

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