Mechanically interlocked molecules catenanes

Mechanically interlocked molecules, such as bistable catenanes [13] and [2]rotax-anes [14], constitute some of the most appropriate candidates to serve as nanoscale switches and machines in the rapidly developing fields of nanoelectronics [15] and nanoelectromechanical systems (NEMS) [16]. The advantages of using mechanically interlocked molecules in the fields of molecular electronics and... 

Fig. 2 Graphical representations of the structures of mechanically interlocked molecules (MIMs) a catenane (left) and a rotaxane (right)...

A special issue devoted to molecular machines appeared in Accounts of Chemical Research in 2001. It reflects the current interest for this field in which ruthenium complexes act as important tools. Molecular machines are characterized by a mobile part and a stationary part. Photochemical and electrochemical inputs can make a machine work, offering the advantage of being switched on and off easily and rapidly. Mechanically interlocked molecules, such as rotaxanes and catenanes, are suitable candidates. Crown ethers, cyclophanes, and calixarenes are representative families of the cyclic... 

Fig. 1 Different topologies cf mechanically interlocked molecules (a) catenane, (b) rotaxane. (c) pseudorotaxane,(d) oligocatenane, (e) [3]rotaxane, and (t) pretzelane.

During the past 20 years, mechanically interlocked molecules, known as catenanes and rotaxanes, many of them redox-active, have become readily accessible using template-directed protocols that rely upon the precepts of molecular recognition and self-assembly and the tenets of supramolecular assistance to covalent synthesis. By incorporating different recognition units with dissimilar redox properties into appropriate components, these compounds can often be induced to switch hysteretically between ground and metastable co-con-... 

Mechanically interlocked molecules (MIMs), such as catenanes and rotaxanes, are molecules with at least two components that are not covalently bound, but interlocked in such a manner that they cannot be separated without the breaking of a covalent bond. Since this physical linkage is known as a mechanical bond [24], we refer to the stereochemistry of MIMs as mechanostereochemistry [25]. MIMs have been appreciated for their synthetic challenge and aesthetic value [26] as well as their potential applications. In particular, MIMs have garnered much interest as artificial molecular switches and machines [27-31] because their internal noncovalent bonding interactions can be modulated by external stimuli to control the relative translational and/or circumrotational motions of their interlocked... 

Like rotaxanes, catenanes are mechanically interlocked molecules. However, instead of interlocking one ring shaped macrocycle and a dumbbell shape, catenanes consist of interlocked macrocycles. The number of macrocycles contained in a catenane is indicated by the numeral that precedes it. Catenanes have bistable and multistable forms and a switchable, bistable [2]catenane is commonly exploited in nanotechnology and molecular electronics because its behavior can be controlled by electrochemical processes [89]. Collier et al. was the first to demonstrate the electroactivity of interlocked catenanes [90]. The authors affixed phospholipid counterions to a monolayer of [2]catenanes and then sandwiched this system between two electrodes. This work resulted in a molecular switching device that opened at a positive potential of 2 V and closed at a negative potential of 2 V. 

Mechanically interlocked molecular compounds, including catenanes, rotax-anes, and carceplex, are constituted of molecules composed of two or more components that cannot be separated from each other [95-98]. The development of strategy for achieving controlled self-assembling systems by non-covalent interaction enables one to prepare such attractive compounds for applications in nanoscale molecular devices. The dithiafulvene derivatives are effective electron donors, which are good candidates to form those supramolecular systems with appropriate acceptors by virtue of intermolec-ular CT interactions. In this chapter, dithiafulvene polymers forming rotax-ane structures are especially described. 

Interlocked molecules are those assemblies of two or more molecules which are linked by a so-called mechanical bond [2]. The individual molecules are not connected covalently in any way but are linked via their spatial relationship to one another. The nature of this phenomenon is such that it necessarily involves a macrocyclic component as one or more of the molecules which compose the assembly. The simplest forms of these assemblies are represented by a [2]rotaxane and a [2]catenane (Figure 10.1), where the bracketed numeral preceding the name indicates the number of individual molecules comprising the interlocked product. The synthesis of a rotaxane may be executed by a number of different routes, only one of which involves the formation of a macrocyclic component in the final... 

Before going on to discuss molecular electronic machines, it will be useful to describe their structural foundation at a molecular level, namely those based on interlocked molecules. Interlocked molecules can take on a variety of forms, the most common being catenanes, rotaxanes, knots [16], and carceplexes [17]. For the purpose of this review, only catenanes, rotaxanes and their geometrically related complexes - pseudorotaxanes [18] - will be discussed. When conferred with the ability to undergo some mechanical motion as a result of an applied stimulus - be it chemical, electrochemical, or photochemical - these interlocked molecular and interpenetrated supramo-lecular systems often take on the characteristics of molecular machines [19]. 

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