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Polarons, Bipolarons, and Side-By-Side Polarons in Reduction of Oligofluorenes

机译:减少低聚芴中的极化子,双极化子和侧面极化子

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摘要

The nature of charge carriers in conjugated polymers was elucidated through optical spectroscopy following single- and multielectron reduction of 2,7-(9,9-dihexylfluorene) oligomers, F_n', n = 1—10, yielding spectra with the two bands typical of polarons upon single reduction. For short oligomers addition of a second electron gave a single band demonstrating the classic polaron-bipolaron transition. However, for long oligomers double reductions yielded spectra with two bands, better described as two polarons, possibly residing side-by-side in the F_n chains. The singly reduced anions do not appear to delocalize over the entire length of the longer conjugated systems; instead they are polarons occupying approximately four fluorene repeat units. The polarons of F_3 and F_4 display sharp absorption bands, but for longer oligomers the bands broaden, possibly due to fluctuations of the lengths of these unconfined polarons. DFT calculations with long-range-corrected functionals were fully consistent with the experiments describing polarons in anions, bipolarons in dianions of short oligomers, and side-by-side polarons in dianions of long oligomers, while results from standard functionals were not compatible with the experimental results. The computations found F_(10)~(2-) , for example, to be an open-shell singlet ((S~2) ≈ l), with electrons in two side-by-side orbitals, while dianions of shorter oligomers experienced a gradual transition to bipolarons with states of intermediate character at intermediate lengths. The energies and extinction coefficients of each anionic species were measured by ultraviolet—visible—near-infrared absorption spectroscopy with chemical reduction and pulse radiolysis. Reduction potentials determined from equilibria mirrored oxidation potentials reported by Chi and Wegner. Anions of oligomers four or more units in length contained vestigial neutral (VN) absorption bands that arise from neutral parts of the chain. Energies of the VN bands correspond to those of oligomers shorter by four units.
机译:通过2,7-(9,9-二己基芴)低聚物F_n',n = 1-10的单电子和多电子还原后,通过光谱法阐明了共轭聚合物中电荷载流子的性质,得出了两个典型的能带:单还原时的极化子。对于短的低聚物,第二个电子的添加给出了一个单带,证明了经典的极化子-双极化子跃迁。然而,对于长的低聚物,双重还原产生具有两个谱带的光谱,更好地描述为两个极化子,可能并排存在于F_n链中。单一还原的阴离子在较长的共轭体系的整个长度上似乎不会离域;相反,它们是占据约四个芴重复单元的极化子。 F_3和F_4的极化子显示出陡峭的吸收带,但是对于较长的低聚物,该频带变宽,可能是由于这些无限制极化子的长度波动所致。使用远程校正功能的DFT计算与描述阴离子中的极化子,短低聚物的阴离子中的双极化子以及长寡聚物的阴离子中的并排极化子的实验完全一致,而标准官能团的结果与实验结果。计算发现F_(10)〜(2-)例如是一个开壳单重态((S〜2)≈l),电子在两个并排的轨道上,而较短的低聚物的二价阴离子经历了逐渐过渡到双极化子,在中间长度处具有中间特征的状态。通过具有化学还原和脉冲辐射分解作用的紫外-可见-近红外吸收光谱法测量每种阴离子物质的能量和消光系数。由Chi和Wegner报告的平衡电位确定的还原电位反映了氧化电位。长度为四个或更多单位的低聚物的阴离子包含残留中性(VN)吸收带,该吸收带是由链的中性部分引起的。 VN带的能量对应于短4个单元的低聚物的能量。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第26期|p.10852-10863|共12页
  • 作者单位

    Chemistry and Physics Department, Dowling College, Oakdale, NY,Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry and Physics Department, Dowling College, Oakdale, NY,Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry and Physics Department, Dowling College, Oakdale, NY,Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry Department ,Department of Biomolecular Engineering, Kyoto Institute ofTechnology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan;

    Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, NY;

    Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry Department Brookhaven National Laboratory, Upton, NY;

    Chemistry DepartmentBrookhaven National Laboratory, Upton, NY;

  • 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);
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  • 入库时间 2022-08-18 03:13:36

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