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首页> 外文期刊>Journal of the American Chemical Society >Octasubstituted Metal-Free Phthalocyanine as Core of Phosphorus Dendrimers:A Probe for the Properties of the Internal Structure
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Octasubstituted Metal-Free Phthalocyanine as Core of Phosphorus Dendrimers:A Probe for the Properties of the Internal Structure

机译:八取代的无金属酞菁为磷树枝状聚合物的核心:内部结构性质的探针

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摘要

The synthesis of a new family of phosphorus dendrimers built from an octasubstituted metal-free phthalocyanine core is described up to generation 5.This core is used as a sensor and a probe for analyzing the properties of the internal structure and the influence of each structural part (core,branches,surface) upon the whole structure.UV-visible spectra show both a hyperchromic and bathochromic effect on the Q-bands with increasing generation,indicating that the chromophore is more isolated,and that the dendritic shell mimics a highly polar solvent.There is no evidence for aggregation,except for generation 0,showing again the isolation of the core.However,the dendritic shell is permeable to aqueous acids and bases,as demonstrated by the reversible splitting of the Q-band in an acidic medium (neutral form of the phthalocyanine) and the single Q-band in a basic medium (dianionic form),even for generation 4.The fluorescence quantum yield for the neutral form increases with increasing generation.The dianionic form of generation 0 is poorly fluorescent,whereas generations 3 and 4 (G_3 and G_4) exhibit better fluorescence.The cores of G_3 and G_4 are highly sensitive optical sensors for H_3O~+ and OH~-.These experiments are carried out in THF/water mixtures,and the influence of water on the structure has been checked.The hydrodynamic radius of generation 4 is measured by NMR diffusion (pulse gradient spin-echo) experiments.R_H varies from 35.4 A at 4 mol % of water to 32.5 A at 64 mol % of water in THF,indicating the hydrophobic nature of these dendrimers.
机译:直到第5代为止,都描述了由八取代的无金属酞菁核构建的新的磷树枝状聚合物家族的合成。该核用作传感器和探针,用于分析内部结构的性质以及每个结构部分的影响(核心,分支,表面)。UV可见光谱显示Q波段的增色和红变效应随着世代的增加而增加,表明发色团更孤立,并且树突壳模仿高极性溶剂除了第0代外,没有任何聚集的证据再次表明了核的分离。但是,如在酸性介质中Q带的可逆分裂所示,树突状壳可渗透酸和碱的水溶液(酞菁的中性形式)和基本介质中的单个Q带(二价阴离子形式),甚至对于第四代也是如此。中性形式的荧光量子产率随着生成的增加而增加第0代的双阴离子形式的荧光较差,而第3代和第4代(G_3和G_4)表现出更好的荧光.G_3和G_4的核心是对H_3O〜+和OH〜-的高度敏感的光学传感器。在THF /水混合物中分离出水,并检查了水对结构的影响。通过NMR扩散(脉冲梯度自旋回波)实验测量了第4代的流体力学半径。在4 mol%的水下,R_H从35.4 A变化在THF中的64mol%的水下,其分子量为32.5A,表明这些树枝状聚合物的疏水性。

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  • 来源
    《Journal of the American Chemical Society》 |2005年第45期|p.15762-15770|共9页
  • 作者单位

    Contribution from the Laboratoire de Chimie de Coordination du CNRS,205 route de Narbonne,31077 Toulouse Cedex 4,France and the Laboratoire IMRCP CNRS UMR 5623,Universite Paul Sabatier,118 route de Narbonne,31062 Toulouse Cedex 4,France;

    Contribution from the Laboratoire de Chimie de Coordination du CNRS,205 route de Narbonne,31077 Toulouse Cedex 4,France and the Laboratoire IMRCP CNRS UMR 5623,Universite Paul Sabatier,118 route de Narbonne,31062 Toulouse Cedex 4,France;

    Contribution from the Laboratoire de Chimie de Coordination du CNRS,205 route de Narbonne,31077 Toulouse Cedex 4,France and the Laboratoire IMRCP CNRS UMR 5623,Universite Paul Sabatier,118 route de Narbonne,31062 Toulouse Cedex 4,France;

    Contribution from the Laboratoire de Chimie de Coordination du CNRS,205 route de Narbonne,31077 Toulouse Cedex 4,France and the Laboratoire IMRCP CNRS UMR 5623,Universite Paul Sabatier,118 route de Narbonne,31062 Toulouse Cedex 4,France;

    Contribution from the Laboratoire de Chimie de Coordination du CNRS,205 route de Narbonne,31077 Toulouse Cedex 4,France and the Laboratoire IMRCP CNRS UMR 5623,Universite Paul Sabatier,118 route de Narbonne,31062 Toulouse Cedex 4,France;

    Contribution from the Laboratoire de Chimie de Coordination du CNRS,205 route de Narbonne,31077 Toulouse Cedex 4,France and the Laboratoire IMRCP CNRS UMR 5623,Universite Paul Sabatier,118 route de Narbonne,31062 Toulouse Cedex 4,France;

    Contribution from the Laboratoire de Chimie de Coordination du CNRS,205 route de Narbonne,31077 Toulouse Cedex 4,France and the Laboratoire IMRCP CNRS UMR 5623,Universite Paul Sabatier,118 route de Narbonne,31062 Toulouse Cedex 4,France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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