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dc.contributor.advisorPhilp, Douglas
dc.contributor.authorKosikova, Tamara
dc.coverage.spatialxvii, 403 p.en_US
dc.date.accessioned2017-05-24T10:28:11Z
dc.date.available2017-05-24T10:28:11Z
dc.date.issued2017-06-21
dc.identifier.urihttps://hdl.handle.net/10023/10835
dc.description.abstractMolecular recognition plays an essential role in the self-assembly and self-organisation of biological and chemical systems alike—allowing individual components to form complex interconnected networks. Within these systems, the nature of the recognition and reactive processes determines their functional and structural properties, and even small changes in their identity or orientation can exert a dramatic effect on the observed properties. The rapidly developing field of systems chemistry aims to move away from the established paradigm in which molecules are studied in isolation, towards the study of networks of molecules that interact and react with each other. Taking inspiration from complex natural systems, where recognition processes never operate in isolation, systems chemistry aims to study chemical networks with the view to examining the system-level properties that arise from the interactions and reactions between the components within these systems. The work presented in this thesis aims to advance the nascent field of systems chemistry by bringing together small organic molecules that can react and interact together to form interconnected networks, exhibiting complex behaviour, such as self-replication, as a result. Three simple building blocks are used to construct a network of two structurally similar replicators and their kinetic behaviour is probed through a comprehensive kinetic analysis. The selectivity for one of the recognition-mediated reactive processes over another is examined within the network in isolation as well as in a scenario where the network is embedded within a pool of exchanging components. The interconnected, two-replicator network is examined under far-from-equilibrium reaction-diffusion conditions, showing that chemical replicating networks can exhibit signs of selective replication—a complex phenomenon normally associated with biological systems. Finally, a design of a well-characterised replicator is exploited for the construction of a network integrating self-replication with a another recognition-directed process, leading to the formation of a mechanically-interlocked architecture—a [2]rotaxane.en
dc.description.sponsorshipEPSRC grant EP/K503162/1 (DTG012)en
dc.description.sponsorshipFunded by EPSRC grant EP/K503162/1 (DTG012)en
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.subjectSelf-replicationen
dc.subjectComplexityen
dc.subjectReaction networksen
dc.subjectAutocatalysisen
dc.subjectCrosscatalysisen
dc.subjectReaction-diffusion environmenten
dc.subjectDynamic covalent libraryen
dc.subjectRotaxaneen
dc.subjectMechanically-interlocked architecturesen
dc.subjectOrigin-of-life questionen
dc.subjectSystem-level behaviouren
dc.subject.lccQD262.K78
dc.subject.lcshMolecular recognitionen
dc.titleDeveloping complexity using networks of synthetic replicatorsen_US
dc.typeThesisen_US
dc.contributor.sponsorEngineering and Physical Sciences Research Council (EPSRC)en_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US


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