Vickers Matthew S, Beer Paul D
Inorganic Chemistry Laboratory, South Parks Road, Oxford, OX1 3QR.
Chem Soc Rev. 2007 Feb;36(2):211-25. doi: 10.1039/b518077p. Epub 2006 Dec 5.
This tutorial review describes the evolution of the field of chemical templation, in particular, emphasising the impact its application has made to the synthesis of mechanically interlocked structures. Recent advances in the use of negatively charged template species for the synthesis of interlocked structures are detailed, with the main focus of this review describing the development of a general anion templation strategy that combines anion recognition with ion-pairing. The versatility of this methodology is demonstrated by the chloride anion templated synthesis of a series of interpenetrated pseudorotaxane, rotaxane and catenane structures. Upon template removal, the mechanically interlocked rotaxanes and catenanes are shown to bind anions within their topologically unique anion binding clefts by virtue of electrostatic and hydrogen bonding interactions, exhibiting a strong selectivity for the chloride halide anion template. The incorporation of the photo-active rhenium(I) bipyridyl signalling group into the rotaxane structural framework highlights the potential of these interlocked systems in future chemical sensor design.
本教程综述描述了化学模板领域的发展历程,尤其强调了其应用对机械互锁结构合成所产生的影响。详细介绍了使用带负电荷的模板物种合成互锁结构的最新进展,本综述的主要重点是描述一种将阴离子识别与离子对相结合的通用阴离子模板策略的发展。通过氯离子模板合成一系列互穿假轮烷、轮烷和索烃结构,证明了该方法的通用性。去除模板后,机械互锁的轮烷和索烃通过静电和氢键相互作用在其拓扑独特的阴离子结合裂缝内结合阴离子,对氯化物阴离子模板表现出很强的选择性。将光活性铼(I)联吡啶信号基团引入轮烷结构框架,突出了这些互锁体系在未来化学传感器设计中的潜力。