Poised on the brink between a bistable complex and a compound.

[reaction: see text] An enmeshed supramolecular complex, based on a semi-dumbbell-shaped component containing an asymmetrically substituted tetrathiafulvalene site and a 1,5-dioxynaphthalene site for encirclement by a cyclobis(paraquat-p-phenylene) ring component and with a "speed bump" in the form of an thiomethyl group situated between the two recognition sites, has been self-assembled. This complex is a mixture in acetone solution of two slowly interconverting [2]pseudorotaxanes, one of which is on the verge of being a [2]rotaxane at room temperature.

[1]  J. F. Stoddart,et al.  A [2]Catenane-Based Solid State Electronically Reconfigurable Switch , 2000 .

[2]  J. Fraser Stoddart,et al.  Slow shuttling in an amphiphilic bistable [2]rotaxane incorporating a tetrathiafulvalene unit , 2001 .

[3]  A. Harada,et al.  Cyclodextrin-based molecular machines. , 2001, Accounts of chemical research.

[4]  T R Kelly,et al.  Progress toward a rationally designed molecular motor. , 2001, Accounts of chemical research.

[5]  I. Harrison The effect of ring size on threading reactions of macrocycles , 1972 .

[6]  Stoddart,et al.  Artificial Molecular Machines. , 2000, Angewandte Chemie.

[7]  J. Fraser Stoddart,et al.  Rotaxane or Pseudorotaxane? That Is the Question!† , 1998 .

[8]  M Venturi,et al.  Artificial molecular-level machines: which energy to make them work? , 2001, Accounts of chemical research.

[9]  Stoddart,et al.  Self-assembly of an amphiphilic , 2000, Organic letters.

[10]  B. Feringa,et al.  In control of motion: from molecular switches to molecular motors. , 2001, Accounts of chemical research.

[11]  Fritz Vögtle,et al.  A New Synthetic Strategy towards Molecules with Mechanical Bonds: Nonionic Template Synthesis of Amide-Linked Catenanes and Rotaxanes , 1997 .

[12]  J F Stoddart,et al.  Molecular-based electronically switchable tunnel junction devices. , 2001, Journal of the American Chemical Society.

[13]  Stoddart,et al.  Electronically configurable molecular-based logic gates , 1999, Science.

[14]  David J. Williams,et al.  IMPROVED TEMPLATE-DIRECTED SYNTHESIS OF CYCLOBIS(PARAQUAT-P-PHENYLENE) , 1996 .

[15]  David J. Williams,et al.  Simple Mechanical Molecular and Supramolecular Machines: Photochemical and Electrochemical Control of Switching Processes , 1997 .

[16]  J. Fraser Stoddart,et al.  Controlled dethreading/rethreading of a scorpion-like pseudorotaxane and a related macrobicyclic self-complexing system , 2001 .

[17]  C. Schalley,et al.  On the way to rotaxane-based molecular motors: studies in molecular mobility and topological chirality. , 2001, Accounts of chemical research.

[18]  J. F. Stoddart,et al.  Binding studies between tetrathiafulvalene derivatives and cyclobis(paraquat-p-phenylene). , 2001, The Journal of organic chemistry.

[19]  J. Fraser Stoddart,et al.  Fabrication and Transport Properties of Single-Molecule-Thick Electrochemical Junctions , 2000 .

[20]  P. Pallavicini,et al.  Molecular machines based on metal ion translocation. , 2001, Accounts of chemical research.

[21]  C. Dietrich-Buchecker,et al.  Shuttles and muscles: linear molecular machines based on transition metals. , 2001, Accounts of chemical research.

[22]  J. F. Stoddart,et al.  Interlocked and Intertwined Structures and Superstructures , 1996 .

[23]  M. Ikeda,et al.  Positive allosteric systems designed on dynamic supramolecular scaffolds: toward switching and amplification of guest affinity and selectivity. , 2001, Accounts of chemical research.

[24]  David J. Williams,et al.  A Molecular Chameleon: Chromophoric Sensing by a Self-Complexing Molecular Assembly. , 1998, Angewandte Chemie.

[25]  Leonid M. Goldenberg,et al.  A Redox-Active Tetrathiafulvalene [2]Pseudorotaxane: Spectroelectrochemical and Cyclic Voltammetric Studies of the Highly-Reversible Complexation/Decomplexation Process , 1997 .

[26]  J F Stoddart,et al.  Switching devices based on interlocked molecules. , 2001, Accounts of chemical research.