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Photoinduced Hole Injection into a Self-Assembled π-Extended G-Quadruplex

机译:将光致空穴注入自组装的π扩展G四链体中

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摘要

We have prepared a G-quadruplex (GQ-1) that incorporates an 8-(4′- aminophenylethynyl)guanine (GEAn) electron donor covalently attached to a 4- aminonaphthalene-1,8-imide (ANl) chromophore and a naphthalene-1,8:4,5-bis- (dicarboximide) (NDI) electron acceptor (GEAn-ANI-NDI, 1). In the presence of KPF_6 in tetrahydrofuran (THF), 1 self-assembles into a monodisperse, C_4-symmetric GQ-1 with small spatial intraquadruplex overlap between the ANI-NDI units. Photoexcitation of monomeric 1 induces the two-step charge transfer GEAn-~(1*)ANI- NDI → GEAn~(+•)-ANI~(-•)-NDI → GEAn~(+•)-ANI-NDI~(-•) that occurs in τ_(CS1) = 5 ps and τ_(CS2) = 330 ps, respectively, while charge recombination in ca. 300 ns. Sharpening of the GEAn~(+•) transient absorption and a shift of the ethynyl vibrational frequency in 1 were observed, concomitant with the stepwise electron transfer from ANI~(-•) to NDI. Formation of GQ-1 from 1 in THF increases the secondary charge-shifting rate (τ_(CS2) =110 ps) and results in no change in ethynyl vibrational frequency. Charge recombination in GQ-1 is slowed by enhanced radical-pair intersystem crossing driven by the greater number of hyperfine couplings in the assembly. Moreover, time-resolved EPR spectroscopy shows that the spin-spin-exchange interaction (J) between the radicals of GEAn~(+•)-ANI-NDI~(-•) within GQ-1 is smaller than that of 1, suggesting that the spin (charge) density in GEAn~(+•) is more dispersed in GQ-1. The spectroscopic results are consistent with hole sharing among the guanines within the G-quadruplex that is kinetically competitive with the formation of GEAn~(+•). This suggests that G-quadruplexes can serve as effective hole conduits in ordered donor-acceptor assemblies.
机译:我们准备了一个G四联体(GQ-1),其中包含一个8-(4'-氨基苯基乙炔基)鸟嘌呤(GEAn)电子供体,该电子供体共价连接到4-氨基萘-1,8-酰亚胺(ANl)发色团和萘- 1,8:4,5-双-(二甲叉酰亚胺)(NDI)电子受体(GEAn-ANI-NDI,1)。在四氢呋喃(THF)中存在KPF_6的情况下,1会自组装为单分散的C_4对称GQ-1,在ANI-NDI单元之​​间存在小的空间四链体重叠。单体1的光激发引起两步电荷转移GEAn-〜(1 *)ANI-NDI→GEAn〜(+•)-ANI〜(-•)-NDI→GEAn〜(+•)-ANI-NDI〜( -•)分别在τ_(CS1)= 5 ps和τ_(CS2)= 330 ps时发生,而电荷重组大约在。 300 ns。观察到GEAn〜(+•)瞬态吸收的锐化和乙炔基振动频率的位移为1,同时伴随着电子从ANI〜(-•向NDI的逐步转移。在THF中从1形成GQ-1会增加次级电荷转移速率(τ_(CS2)= 110 ps),并且不会导致乙炔基振动频率的变化。 GQ-1中的电荷重组由于组件中更多数量的超精细偶联驱动的增强的自由基对系统间交叉而减慢了速度。此外,时间分辨EPR光谱显示GQ-1中GEAn〜(+•)-ANI-NDI〜(-•)的自由基之间的自旋-自旋-交换相互作用(J)小于1。 GEAn〜(+•)中的自旋(电荷)密度更分散在GQ-1中。光谱结果与G-四链体中鸟嘌呤之间的空穴共享一致,这与GEAn〜(+•)的形成具有动力学竞争性。这表明G-四链体可以用作有序供体-受体组件中的有效孔导管。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2015年第11期|3981-3990|共10页
  • 作者单位

    Department of Chemistry and Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University, Evanston, Illinois 60208-3113, United States;

    Department of Chemistry and Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University, Evanston, Illinois 60208-3113, United States;

    Department of Chemistry and Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University, Evanston, Illinois 60208-3113, United States;

    Department of Chemistry and Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University, Evanston, Illinois 60208-3113, United States;

    Department of Chemistry and Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University, Evanston, Illinois 60208-3113, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:09:33

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