Abstract
A kinetic model for the integration of self-replication with the formation of a mechanically interlocked molecular architecture, namely a rotaxane, is presented. The logical steps required to convert this model into molecular structures through consideration of the design criteria highlighted by the model are discussed and executed. Ultimately, despite careful design, the rotaxane synthesised did not replicate as expected. The reasons for this failure are traced by experiment and computation to the sub-optimal association constant for the pseudorotaxane complex required to form the replicating rotaxane. Additionally, a deleterious supramolecular steric effect, operating through the proximity of the macrocyclic component of the pseudorotaxane to the transition state for the stoppering reaction is identified computationally. (C) 2008 Elsevier Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 8464-8475 |
Number of pages | 12 |
Journal | Tetrahedron |
Volume | 64 |
DOIs | |
Publication status | Published - 1 Sept 2008 |
Keywords
- molecular recognition
- self-replication
- rotaxanes
- kinetics
- DIELS-ALDER REACTION
- RECOGNITION-INDUCED CONTROL
- AMIDE-BASED ROTAXANES
- TEMPLATE SYNTHESIS
- SELF-REPLICATION
- BUILDING-BLOCKS
- CHEMICAL MODIFICATION
- SEMIEMPIRICAL METHODS
- INFORMATION RATCHET
- BORANE REDUCTION