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使用三脚架结构单元构建巨型树枝状大分子。

Construction of giant dendrimers using a tripodal building block.

作者信息

Ruiz Jaime, Lafuente Gustavo, Marcen Sylvia, Ornelas Catia, Lazare Sylvain, Cloutet Eric, Blais Jean-Claude, Astruc Didier

机构信息

Laboratoire de Chimie Organique et Organométallique, UMR CNRS No. 5802, Université Bordeaux I, 33405 Talence Cedex, France.

出版信息

J Am Chem Soc. 2003 Jun 18;125(24):7250-7. doi: 10.1021/ja021147o.

DOI:10.1021/ja021147o
PMID:12797798
Abstract

Giant pentane-soluble organo-silicon dendrimers have been synthesized using a triallylphenol brick according to a new divergent construction that uses a hydrosilylation-nucleophilic substitution sequence up to the ninth generation (G(9)). All the reactions were monitored by (1)H, (13)C, and (29)Si NMR until G(9), indicating that they were clean at the NMR accuracy until this last generation. MALDI TOF mass spectra were recorded for G(1) to G(4) and show the nature and amounts of defects that are intrinsic to the divergent construction. This technique and SEC (recorded up to G(5)) confirm the monodispersity (1.00 to 1.02) from G(1) to G(5). HRTEM and AFM images recorded for the high generations disclose the expected smooth dendrimer size progression and the globular shape. At G(9), the theoretical number of termini (TNT) is 177 407 branches (abbreviation: G(9)-177 047). It is estimated that more than 10(5) terminal branches are actually present in the G(9) dendrimer, far beyond the De Gennes "dense-packing" limit (6000 branches), and it is believed that the branch termini turn inside the dendrimer toward the core. This is corroborated by lower reaction rates and yields for the highest generation numbers presumably due to intradendritic reactions. It is probable that the dendritic construction is limited by the density of branches inside the dendrimer, i.e., far beyond the dense-packing limit.

摘要

使用三烯丙基苯酚构建模块,通过一种新的发散式合成方法合成了巨型戊烷可溶有机硅树枝状大分子,该方法采用硅氢化-亲核取代序列,最高合成至第九代(G(9))。所有反应通过¹H、¹³C和²⁹Si NMR监测至G(9),表明直至最后一代,在NMR精度范围内反应均很纯净。记录了G(1)至G(4)的基质辅助激光解吸电离飞行时间质谱(MALDI TOF),显示出发散式合成固有的缺陷性质和数量。该技术和尺寸排阻色谱法(SEC,记录至G(5))证实了从G(1)到G(5)的单分散性(1.00至1.02)。对高代数树枝状大分子记录的高分辨透射电子显微镜(HRTEM)和原子力显微镜(AFM)图像揭示了预期的树枝状大分子尺寸平滑增长和球状形状。在G(9)时,理论末端数(TNT)为177407个分支(缩写:G(9)-177047)。据估计,G(9)树枝状大分子中实际存在超过10⁵个末端分支,远远超过了德热纳“密集堆积”极限(6000个分支),并且据信分支末端在树枝状大分子内部转向核心。这可能是由于树状大分子内部反应导致最高代数的反应速率和产率较低而得到证实。树枝状结构很可能受到树枝状大分子内部分支密度的限制,即远远超过密集堆积极限。

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