Core and periphery functionalized dendrimers for transition metal catalysis; a covalent and a non-covalent approach

Joost N.H Reek, Debby de Groot, G.Eric Oosterom, Paul C.J Kamer, Piet W.N.M van Leeuwen
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引用次数: 29

Abstract

Dendrimers are well-defined hyperbranched macromolecules with characteristic globular structures for the larger systems. The recent impressive strides in synthetic procedures increased the accessibility of functionalized dendrimers at a practicable scale, resulting in a rapid development of dendrimer chemistry. Dendrimers have inspired many chemists to develop new materials and several applications have been explored, catalysis being one of them. The position of the catalytic site(s) as well as the spatial separation of the catalysts within the dendritic framework is of crucial importance. Dendrimers that are functionalized with transition metals in the core can potentially mimic properties of enzymes, their efficient natural counterparts, whereas the surface-functionalized systems have been proposed to fill the gap between homogeneous and heterogeneous catalysis. We prepared both core- and periphery-functionalized dendritic catalysts that are sufficiently large to enable separation by modern nanofiltration techniques. Here we review our recent findings using these promising novel transition metal-functionalized dendrimers as catalysts in several reactions. We will discuss some of the consequences of the architecturally different systems that have been studied and will elaborate on a novel non-covalent strategy of dendrimer functionalization.

核心和外围功能化枝状大分子的过渡金属催化;共价和非共价方法
树状大分子是定义明确的超支化大分子,具有较大体系的球状结构特征。最近在合成过程中令人印象深刻的进步增加了功能化树状大分子在实际规模上的可及性,导致了树状大分子化学的快速发展。树状大分子激发了许多化学家开发新材料,并探索了几种应用,催化就是其中之一。催化位点的位置以及催化剂在树突框架内的空间分离是至关重要的。用过渡金属功能化的树状大分子可以潜在地模拟酶的性质,而表面功能化的系统已经被提出填补均相和多相催化之间的空白。我们制备了核心功能化和外围功能化的树突催化剂,它们足够大,可以通过现代纳滤技术进行分离。在这里,我们回顾了我们最近在几种反应中使用这些有前途的新型过渡金属功能化树状大分子作为催化剂的发现。我们将讨论已经研究过的结构不同系统的一些后果,并将详细阐述一种新的非共价枝状大分子功能化策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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