El auto-ensamblaje donde debido a la interacción con el disolvente moléculas de un compuesto anfifílico se asocian espontáneamente es un proceso general que puede servir para la preparación de entidades supramoleculares de gran tamaño con aplicación en la preparación de materiales tanto dispersos en fase liquida como sólidos insolubles. Por otra parte la asociación supramolecular puede ocurrir también entre moléculas diferentes y cuando una de ellas es una cápsula molecular esta puede albergar en su interior una molécula de tamaño inferior al de su abertura. Los CB[n] son oligómeros cíclicos de unidades de glicol uril unidas por puentes metileno que definen una cavidad en forma de calabaza hueca que permite alojar en su interior moléculas de colorantes fluorescentes. En la presente tesis doctoral se ha desarrollado una matriz de sensores para sales de amonio cuaternarias, ?-aminoácidos y ácido ?-hidroxibutírico. De la misma manera los CBs pueden también formar complejos con acetanilidas conteniendo grupos aminopropil. En la presente tesis doctoral se va a sacar ventaja del auto-ensamblaje de líquidos iónicos con estructura de imidazolio simétrico sustituído con dos grupos ?-alquenilo para formar liposomas. Otro tema de interés será establecer como el proceso de auto-ensamblaje influye en la asociación supramolecular entre líquidos iónicos con estructura de imidazolio y cucurbituriles. Por último el ensamblaje entre iones inorgánicos y biopolímeros naturales se empleará para pre-organizar los precursores inorgánicos de manera que cuando estos sufran polimerización el biopolímero actúe como agente plantilla controlando el tamaño de las partículas inorgánicas formadas. El objetivo general de la presente tesis doctoral es estudiar procesos de agregación que ocurren de manera espontánea en el seno de disoluciones acuosas y que dan lugar a la formación de complejos supramoleculares huésped-hospedador o a la formación de entidades supramoleculares de tipo liposomas. / Buaki Sogo, M. (2012). APLICACIÓN DE FENÓMENOS DE AUTO-ENSAMBLAJE Y ASOCIACIÓN SUPRAMOLECULAR CON CUCURBIT[n]URIL PARA EL DESARROLLO DE MATRICES DE SENSORES Y MATERIALES FUNCIONALES [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/17830

Le cucurbitacee possono essere attaccate da più di 200 malattie, una corretta gestione è dunque fondamentale per ridurre il rischio di perdite di produzione, sia in termini di quantità sia in termini di qualità. Tra le malattie più importanti che attaccano le cucurbitacee ci sono l’oidio e la peronospora delle cucurbitacee. Podosphaera xanthii e Golovinomyces cichoracearum sono gli agenti causali dell’oidio. È stato studiato l’effetto della temperature sulla germinazione dei conidi in ambiente controllato a 6 temperature costanti (da 10 a 35°C, ad intervalli di 5C°) da 3 a 72 ore. La temperature ottimale per la germinazone, l’infezione e la sporulazione è risultata essere rispettivamente 24.4, 25.7 e 21.3°C per P. xanthii e 17.9, 17.3 e 16.2°C per G. cichoracearum. Un modello meccanicistico è stato sviluppato per il rischio che i due agenti patogeni causassero un attacco di oidio. Il modello simula la germinazione su foglie infettate sulla base delle condizioni ambientali di temperatura e umidità relativa. Le equazioni che calcolano la germinazione delle dei conidi di entrambi i funghi sono state sviluppate sulla base di dati presenti in bibliografia. Un secondo modello meccanicistico è stato sviluppato per Pseudoperonospora cubensis, agente causale della peronospora delle cucurbitacee. Il modello calcola la data di comparsa dei sintomi e la probabilità del superamento di determinate soglie di gravità della malattia, sulla base di sotto-processi dell’infezione. Il passaggio da uno stato dell’infezione al successivo è dipendente dalle condizioni ambientali. Entrambi i modelli sono stati validati confrontando i dati ottenuti dai modelli con dati indipendenti rilevati in coltivazioni del nord Italia. / Cucurbits are potentially affected by more than 200 diseases of diverse etiologies, so a good disease management is crucial to reduce the risk of high yield losses in terms of quantity and quality. Among the more important diseases there are powdery and downy mildew. Podosphaera xanthii and Golovinomyces cichoracearum are the causal agents of cucurbit powdery mildew. The effect of temperature on conidial germination was studied in controlled condition at 6 constant temperature (from 10 to 35°C, step 5°C) for 3 to 72 hours. Optima temperature for conidial germination, infection and sporulation were 24.4, 25.7 and 21.3°C respectively for P. xanthii and 17.9, 17.3 and 16.2°C for G. cichoracearum. A mechanistic model was developed for the risk posed by P. xanthii and G. cichoracearum to cause cucurbit powdery mildew. The model simulates germination on infected leaves on the base of environmental conditions of temperature and relative humidity. Equation regulating spore germination of both fungi were developed using published data. Another mechanistic model was develop also for Pseudoperonospora cubensis, causal agent of cucurbit downy mildew. The model calculates the symptoms appearance and the probability of overtaking severity threshold based on sub-processes of infection. Changes from one state of the infection to the following one depend on environmental conditions. Both models were validated by comparing model outputs with independent data sets collected in fields located in the north of Italy.

No description available.

Negative impacts from intensifying agriculture have generated concerns that pollinator-dependent crop species, such as courgette Cucurbita pepo L., may be experiencing a pollination deficit. This thesis explores the extent to which pollination influences fruit set; how pollination could be improved; and how in doing so growers’ profits and agricultural resilience could increase, using UK field-grown courgettes as a model system. Inspired by evidence of parthenocarpy (fruit set in the absence of fertilisation) in courgette, a systematic review showed extensive use of parthenocarpy to circumvent the need for pollination in other ‘pollinator-dependent’ crop species across the globe. Nonetheless, pollination significantly increased yield and pollinators were abundant enough to fulfil the pollination requirements of courgette, which if extrapolated to the rest of the UK, equates to pollinators contributing approximately £2.7 million to annual UK courgette production. Furthermore, wild flowers within fields were shown to be effective at increasing the abundance of bumblebees and solitary bees. Further exploration of the mutualistic relationship between courgettes and pollinators showed that courgette can improve populations of Bombus terrestris (using the Bumble-BEEHAVE model), an important pollinator of courgette. This thesis concludes that pollination is a vital mechanism for ensuring optimal courgette yields and that whilst pollination levels were maximal at study sites, simple management, such as encouraging wild flowers within courgette fields could help to attract pollinators to courgette flowers and support bees’ nutritional requirements beyond the extensive, yet transient, resource provided by courgette. Understanding a crop’s requirement for pollinators can also aid growers in their decision making about what varieties and sites should be used which could increase their agricultural resilience and further their economic advantage. Further work is needed to understand how other environmental factors interact with pollination to influence fruit set so that growers can prioritise key regulating services in their management for optimal crop yields.

Supramolecular systems comprised of non-covalent interactions are reversible in nature. This intrinsic reversibility of these systems is essential in achieving several functions, making it crucial to understand the dynamics of supramolecular systems. However, studies on the dynamics of supramolecular systems have always lagged behind structural and thermodynamic characterization of innumerable supramolecular systems developed. The first objective of this work was to understand the dynamics leading to a shift in the acidity constant (pKa) for 2-aminoanthracenium cation (AH+) upon binding with cucurbit[7]uril (CB[7]) host molecule. The adiabatic deprotonation of free AH+ in water was found to be inhibited in the complex with CB[7]. Different spectral characteristics for the protonated and deprotonated form of the guest molecule were used to understand the mechanism of this pKa shift associated with the binding to CB[7]. The results suggested that the pKa shift upon binding with CB[7] is a result of the slowing down of the deprotonation step in the complex, whereas the association rate constant did not change very much. The second objective of this work was to understand the role of cations on the binding dynamics of the N-phenyl-2-naphthyl amine (Ph-A-Np) binding to CB[7]. Ph-A-Np has two binding sites, which can lead to 1:1 and 2:1 host-guest complexes. The results indicate a switch in the binding mechanism for Ph-A-Np at low and high concentration regimes of sodium ions. Sodium ion was found to reduce the binding affinity of the naphthyl group to CB[7] whereas the complex formed by the phenyl group with CB[7] bound to one sodium ion was found to be stabilized. The final objective of this work was to study how structural changes to a guest molecule can affect the binding dynamics for the formation of a 2:1 “capsule” like complex with octa acid (OA). The dissociation for the OA capsule with pyrene (Py) as the encapsulated guest was shown to happen in 2.7 s previously. Two pyrene derivatives, 1-methylpyrene (MePy) and 1-pyrenemethanol (PyMeOH) were chosen as guest molecules to study the effect of these substituents on pyrene on the capsule dissociation dynamics. The results show that the residence time for the guests in the OA capsule depends on the substituents. For PyMeOH and MePy a shorter and longer residence time respectively in the capsule was observed when compared to Py. / Graduate / 2019-09-30

Supramolecular systems, which are formed by the noncovalent intermolecular interactions between molecules, are highly dynamic. The high reversibility of supramolecular systems leads to some functional features that cannot be achieved by the single chemical component. The kinetic information for the supramolecular systems can not be inferred from thermodynamic studies or structural studies. Furthermore, the information provided by the dynamic study can be employed to infer or explain the results from the thermodynamic study and the structural study. The first objective of this work was to study the dynamics and the binding mechanism of cucurbit[7]uril with a charged guest molecule (2-naphthyl-1-ethylammonium cation, NpAmH+). In general, the binding affinity of cucurbit[7]uril to the positively charged guests are very high compared with other host systems such as cyclodextrins and bile salt aggregates. In this work, the complexation of cucurbit[7]uril and NpAmH+ was studied from a kinetic point of view. Results showed that the high binding affinity of cucurbit[7]uril to NpAmH+ was due to the high association rate constant and the low dissociation rate constant for the complexation of cucurbit[7]uril and NpAmH+. Moreover, the competition between co-cations and NpAmH+ for the binding sites of cucurbituril molecules retarded the complexation process for cucurbit[7]uril binding to NpAmH+ and decreased the overall equilibrium constant for the formation of cucurbit[7]uril-NpAmH+ complex. The second objective of this work was to study the chiral recognition observed for the formation of 2:2 complexes between β-cyclodextrin and 2-naphthyl-1-ethanol (NpOH). The binding of β-cyclodextrin and NpOH leads to the formation of two 1:1 complexes and three 2:2 complexes. The binding dynamics of NpOH with β-cyclodextrin in the 1:1 complex is fast and occurs within microseconds. A much slower dynamics was observed for the formation of the 2:2 complex. Results showed that more 2:2 complex were formed for (R)-NpOH than for (S)-NpOH, which is due to the difference of the dissociation rate constant of the 2:2 complex for both NpOH enantiomers. The dissociation rate constant of the 2:2 complex for (R)-NpOH is 46.8% lower than that for (S)-NpOH while the association rate constant of the 2:2 complex are similar for both NpOH enantiomers. The third objective of this work was to study the dynamics and the binding mechanism of octa acid with pyrene. As known from the work of other researchers, the accessibility of small molecules (e.g. I- or O2) to pyrene bound to octa acid is largely limited by the octa acid capsule. In this study, a two-step successive process was observed for the complexation of octa acid and pyrene. The first step, which was related to the formation of octa acid-pyrene 1:1 complex, was sufficiently fast to be viewed as a pre-equilibrium process. The second step, which was related to the formation of octa acid-pyrene 2:1 complex, was slow on the millisecond – second time scale. The high binding affinity of octa acid to pyrene was observed, which is due to the low dissociation rate constant for the octa acid-pyrene 2:1 complex. / Graduate

This thesis describes the host-guest chemistry between Cucurbit[7]uril (CB[7]) and CB[8] and a series of guests including bispyridinium cations, phenols and  napthalenes. These guests are bound to ruthenium polypyridine complexes or ruthenium based water oxidation catalysts (WOCs). The investigations are based upon utilizing the covalently linked photosensitizer and the electronic effects and chemical processes are investigated. / QC 20100927

Supramolecular interactions are of great importance in the fabrication of new functional materials. In particular, colloidal assembly via supramolecular pathway has contributed to numerous innovations in material chemistry, on account of its specific, directional and dynamic non-covalent interactions. By taking advantage of the non-covalent supramolecular interactions, tailored complementary colloidal building blocks which are normally incompatible with each other could be integrated interdependently, forming novel hybrid materials with emerging properties. This thesis mainly focuses on the design, preparation and characterization of novel colloidal assemblies based on cucurbit[n]urils host-guest interactions, including hybrid ‘raspberry-like’ colloids, catalytic polymeric nanocomposites, advanced structured colloids, and supramolecular polymer colloidal hydrogel.

Making use of the non-covalent bond to make materials is of great interest in many fields of research. This PhD thesis describes a variety of highly interdisciplinary research undertaken at the interface between chemistry, materials science, physics and engineering. Chapter 1 is an introductory chapter into the core concepts underlying this thesis. Supramolecular chemistry as a broad research field is briefly reviewed, followed by a focus on host-guest chemistry. The macrocyclic cucurbit[n]urils (CB[n]s) in particular are highlighted with a discussion on their recent applications since their discovery. Emulsions and their controlled generation with microfluidic techniques are then reviewed, as they have been used as templates for self-assembly processes throughout this thesis. A study into the synthesis of extended polymer networks composed entirely from small molecules held together by non-covalent interactions is described in Chapter 2. These highly dynamic and responsive supramolecular polymer networks have not yet been constructed with CB[n] host-guest chemistry. The ability of the larger CB[8] macrocycle to encapsulate multiple guest molecules in a stepwise fashion was taken advantage on in designing the synthesis of branching monomers. The monomers had two (A$_2$) or three (B$_3$) terminal guest moieties for CB[8], which upon combination formed branching supramolecular polymers that were multi-stimuli responsive. However, the polymers precipitated from solution at high concentrations rather than form a cross-linked network, due to competing intra-chain cyclisation and the limited water solubility of CB[8]. By confining these polymers to microfluidic droplets, directed assembly to the liquid-liquid interface could drive polymerisation to form an interfacial cross-linked gel that was both elastic and self-healing. Chapter 3 follows on from these results, describing attempts into constructing hyperbranched supramolecular polymers from an AB$_2$ guest molecule and CB[8] that would form globular polymers. Intramolecular complexation dominated with the guest molecules synthesised (A and B complexing within the molecule), evidenced by a variety of characterisation. Compared to previous works that relied on linear molecules to form a folded conformation for intramolecular complexes, these molecules were pre-organised with a unique cooperative complexation pathway. The stimuli-responsiveness of the complexes was probed, and the formation of self-sorting mixtures was demonstrated with multiple CB[n] and additional guest molecules. Controlling the self-assembly of semi-conducting nanocrystals with CB[7] is detailed in Chapter 4, a process that typically requires harsh conditions or extensive time-scales. Semi-conducting nanocrystals could be assembled instantaneously from water into extended networks that were highly porous with excess CB[7], retaining their nanoscale properties. Limiting quantities of CB[7] could then form nanoscale aggregates that remained in solution. Confinement of these assemblies within microfluidic droplets allowed the synthesis of dense microparticles, that retained their shape after re-dispersal in water. By simply including metallic nanocrystals as a minor component, mixed aggregates could be synthesised analogously. Finally, Chapter 5 draws overall conclusions from the results of this thesis, looking broadly at the potential for future prospects in these areas of research.

This dissertation focuses on the investigation of gas-phase characteristics of cucurbituril host-guest systems using ion mobility spectrometry (IMS) and related techniques. Collision cross-sections (CCS) of alkylammonium complexes of cucurbit[n]uril (CB[n]) are measured to understand the allosteric interactions that induce conformational changes in the complex in the presence of metal cations on one of the portals of the cucurbit[6]uril (CB[6]) host. Cationic species on one CB[6] rim sterically force longer linear alkylammonium guests out of the cucurbituril cavity during complex formation. Similarly, rigid cucurbituril-metal complexes were studied using IMS to demonstrate the effect of long-range ion-neutral interactions on the gas phase mobility of ions. The contributions of charge state and charge distribution to the ion mobility CCS measured using a drift tube ion mobility spectrometer (DTIMS) were studied. This IMS method characterization will help in the study of biomolecules and may answer some of the questions regarding CCS measurements in protein structures, that are still being debated. While most of the studies were done using an IMS system, this dissertation also includes gas phase characterization studies done using Fourier transform ion cyclotron resonance (FTICR) mass spectrometry. A novel gas-phase CCS measurement technique - cross sectional areas using Fourier transform ion cyclotron resonance mass spectrometry (CRAFTI) was attempted on bigger systems like the [cucurbit[6]uril-n-alkylammonium]+ complexes. Infrared multi-photon dissociation (IRMPD), collision induced dissociation (CID), and sustained off-resonance irradiation (SORI) studies were done on many CB[n] systems, which helped to extract useful structural information about the complexes.