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Ground and excited state properties of polyamine chains bearing two terminal naphthalene units

机译:带有两个末端萘单元的多胺链的基态和激发态性质

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摘要

A series of compounds bearing two naphthalene units linked through methylene groups to both ends of differentnopen-chain polyamines has been investigated. The fluorescence emission studies show the presence of an excimernspecies whose formation depends on the protonation state and length of the polyamine chains and implies thenexistence of a bending movement in the excited state allowing the two naphthalene units to approach and interact.nThis interpretation was clearly proven by time-resolved fluorescence with the appearance of double exponentialndecays with a rise time observed at the excimer emission wavelength. For comparison purposes one bis-chromophoricncompound containing a rigid chain, and two mono-chromophoric analogs bearing a single terminal naphthalene unitnwere studied. Their emission spectra show a unique band and the fluorescence decays, are single exponential at pHnvalues where just one species is present in the ground state, showing that in these cases no excimer or exciplex speciesnis formed. The kinetics of excimer formation was used to evaluate the influence of the length and the pH in thenflexibility of the polyamine chain.
机译:已经研究了一系列带有两个通过亚甲基连接到二齿戊烷开链多胺两端的萘单元的化合物。荧光发射研究表明,存在一种准分子物种,其形成取决于质子化状态和多胺链的长度,并暗示着在激发态下存在弯曲运动,使两个萘单元能够接近并相互作用。在准分子发射波长观察到的时间分辨荧光,出现双指数衰减,上升时间。为了进行比较,研究了一种含刚性链的双发色化合物和两个带有单个萘单元的单发色类似物。它们的发射光谱显示出一个独特的谱带,并且荧光衰减在pHn值下呈单指数,其中基态仅存在一种,这表明在这些情况下没有形成准分子或激基复合物。准分子形成的动力学用于评估长度和pH对多胺链柔性的影响。

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  • 来源
    《J.Chem.Soc., Perkin Transaction 2》 |2002年第5期|p.991-998|共8页
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    aDepartamento de Química (CQC), Faculdade de Ciências e Tecnologia,Universidade de Coimbra, 3004-535 Coimbra, Portugal. E-mail: sseixas@ci.uc.ptbDepartament de Química Inorgànica, Facultat de Química, Universitat de València,Spain C/Dr. Moliner 50, 46100 Burjassot (València), Spain. E-mail: enrique.garcia-es@uv.escDepartamento de Química, Centro de Química Fina e Biotecnologia, Universidade Nova deLisboa, Quinta da Torre 2825 Monte de Caparica, Portugal. E-mail: fjp@dq.fct.unl.ptdDepartamento de Química Orgánica, Facultat de Farmacia, Universitat de València, Spain.Avda. Vicent Andrés Estellés s. 46100 Burjassot (València), Spain;

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