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富电子铁/钌芳基炔基配合物的三阶非线性光学:三种状态之间的氧化还原切换。

Electron-rich iron/ruthenium arylalkynyl complexes for third-order nonlinear optics: redox-switching between three states.

机构信息

Sciences Chimiques de Rennes, CNRS (UMR 6226), Université de Rennes 1, Campus de Beaulieu, 35042 Rennes Cedex, France.

出版信息

Chemistry. 2011 May 9;17(20):5561-77. doi: 10.1002/chem.201003427. Epub 2011 Apr 14.

Abstract

The new [(η(2)-dppe)(η(5)-C(5)Me(5))Fe(C≡C-1,4-C(6)H(4)C≡C)Ru(η(2) -dppe)(2) C≡C(C(6)H(5))] complex (3-H) and its hexanuclear relative [{(η(2)-dppe)(η(5)-C(5) Me(5))Fe(C≡C-1,4-C(6)H(4)-C≡C)Ru(η(2)-dppe)(2)(C≡C-1,4-C(6)H(4)C≡C)(3)(1,3,5-C(6)H(3))] (4) have been synthesized and characterized. The linear and cubic nonlinear optical properties of these compounds in their various redox states have been studied along with those of the analogous complexes [(η(2)-dppe)(η(5)-C(5)Me(5))Fe(C≡C-1,4-C(6)H(4)C≡C)Ru(η(2)-dppe)(2)R]PF(6) (n=0-2; R=Cl, 2-Cl; R=C≡C(4-C(6)H(4)NO(2)),3-NO(2)). We show that molecules exhibiting large third-order nonlinearities can be obtained by assembling such dinuclear Fe/Ru units around a central 1,3,5-substituted C(6)H(3) core. These data are discussed with a particular emphasis on the large changes in their nonlinear (third-order) optical properties brought about by oxidation. Experimental and computational (DFT) evidence for the electronic structures of these compounds in their various redox states is presented using 3-H(n+) as a prototypical model. Single crystals of this complex in its mono-oxidized state (3-H[PF(6)]) provide the first structural data for such carbon-rich Fe(III) /Ru(II) heteronuclear mixed-valent (MV) systems. Although experimental evidence for the structure of the dioxidized states was more difficult to obtain, the theoretical study reveals that 3-H(2+) can be considered to have a biradical structure with two independent spins. The low-lying absorptions that appear in the near-infrared (NIR) range for all these compounds following oxidation correspond to intervalence charge-transfer (IVCT) bands for the mono-oxidized states and to ligand-to-metal charge-transfer (LMCT) transitions for the dioxidized states. These play a crucial role in the strong optical modulation achieved. The possibility of accessing additional states with distinct linear or nonlinear optical properties is also briefly discussed.

摘要

[(η(2)-dppe)(η(5)-C(5)Me(5))Fe(C≡C-1,4-C(6)H(4)C≡C)Ru(η(2)-dppe)(2) C≡C(C(6)H(5))] 配合物(3-H)及其六核相关物 [{(η(2)-dppe)(η(5)-C(5) Me(5))Fe(C≡C-1,4-C(6)H(4)-C≡C)Ru(η(2)-dppe)(2)(C≡C-1,4-C(6)H(4)C≡C)(3)(1,3,5-C(6)H(3))] (4) 已被合成和表征。研究了这些化合物在不同氧化还原态下的线性和立方非线性光学性质,以及类似配合物 [(η(2)-dppe)(η(5)-C(5)Me(5))Fe(C≡C-1,4-C(6)H(4)C≡C)Ru(η(2)-dppe)(2)R]PF(6) (n=0-2; R=Cl, 2-Cl; R=C≡C(4-C(6)H(4)NO(2)),3-NO(2)) 的线性和立方非线性光学性质。我们表明,通过在中心 1,3,5-取代的 C(6)H(3)核周围组装这种双核 Fe/Ru 单元,可以获得具有大三阶非线性的分子。这些数据与氧化引起的非线性(三阶)光学性质的巨大变化进行了讨论。使用 3-H(n+) 作为原型模型,提出了这些化合物在各种氧化还原态下的电子结构的实验和计算(DFT)证据。该配合物在其单氧化态(3-H[PF(6)])中的单晶提供了此类富含碳的 Fe(III) /Ru(II) 杂核混合价(MV)系统的第一个结构数据。尽管获得二氧化态结构的实验证据更加困难,但理论研究表明,3-H(2+) 可以被认为具有两个独立自旋的双自由基结构。所有这些化合物在氧化后出现在近红外(NIR)范围内的低能吸收对应于单氧化态的间价电荷转移(IVCT)带和二氧化态的配体到金属电荷转移(LMCT)跃迁。这些在实现强光学调制中起着至关重要的作用。还简要讨论了获得具有独特线性或非线性光学性质的附加状态的可能性。

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