Eastern North Dakota has received excessive rainfall events since 1995, and soils are prone to waterlogging. This research evaluated the effects of subsurface tile drainage, raised beds, and iron-chelate (Fe-EDDHA) seed-application on iron-deficiency chlorosis (IDC) incidence in soybean [Glycine max (L.) Merr.], soybean growth, and yield, across six environments during 2013 and 2014. Tile drainage without beds increased soybean yield and reduced IDC by 11%. Beds resulted in more vigorous plants with 9% more biomass and increased soybean yield by 6%. There was no yield advantage to using both tile and raised beds within the same field. The Fe-EDDHA reduced plant population and IDC expression, increased plant biomass, but did not result in a yield increase. Farmers are encouraged to consider utilizing raised beds as a means to mitigate excess water. Additional research is needed to determine the cause of lower established plant density after seed application with Fe-EDDHA. / Minnesota Soybean Research and Promotion Council / North Dakota Soybean Council / DuPont Pioneer

Certain ligand substitution reactions proceed to a complete displacement of the chelate ligand. Certain reactions proceed through a mechanism involving an initial fission of the tungsten-sulfur bond to afford a coordinatively-unsaturated intermediate which is rapidly attacked by chlorobenzene. The resulting solvated intermediate establishes an equilibrium which involves desolvation-solvation. Although main group organometallic chemistry has received a great deal of attention, this discussion will be centered in organotransition metal chemistry, in particular, metal carbonyls.

A series of studies were initiated to investigate growth responses of Kentucky bluegrass (Poa praetensis L.) and creeping bentgrass (Agrostis palustris Huds.) to foliar applications of two plant growth regulators (PGR) and/or chelated Fe (Na Fe diethylene triamine pentaacetate). Environmental variables considered were N levels, soil moisture regimes, and saline irrigations. The two materials investigated for PGR properties were a commercial product called Roots (a cold-water extract of seaweed and peat humus fortified with "intermediate metabolites" and thiamine) and the systemic fungicide propiconazole, trade name: (Banner) and chemical name: [1- {(2-(2,4-dichlorophenyl)-4-propyl-l,3-dioxolan-2yl}methyl-l H-1,2,4-triazole]. Fortified seaweed extract (FSE) was applied at 9.3 L/ha, and propiconazole (PPC) was applied at 0.93 L a.i/ha. Each was applied alone or in conjunction with chelated Fe at 0.11 kg a.i/ha. Kentucky bluegrass foliage height, root and shoot dry weight, and several foliar nutrients increased following PGR treatments when grown under either limited soil moisture or saline irrigation. Foliar applications of PGR and/or chelated Fe to creeping bentgrass reduced wilting and evapotranspiration, and increased leaf water status, root strength, and shoot dry matter at two levels of N during and after drought stress. / Ph. D.

Los dos baños de cobre más utilizados comercialmente son el baño ácido a base de sulfato y el baño alcalino a base de cianuro. Los baños alcalinos son utilizados principalmente para producir recubrimientos en piezas con geometría compleja y para evitar la deposición galvánica cuando se deposita un metal en un sustrato menos noble. Debido a la toxicidad de los compuestos de cianuro, se han desarrollado baños alternativos usando diferentes agentes complejantes. El punto de partida de la presente investigación es un baño primario sin cianuros para deposición de cobre en sustratos de Zamak desarrollado en el Instituto de Investigaciones Tecnológicas del Estado de Sao Paulo / Brasil. La sustitución de materias primas como el cianuro debe ser económicamente ventajosa y técnicamente viable. De esta manera, la investigación presentada pretendió proponer una alternativa para el tratamiento de residuos líquidos del baño ya mencionado con la finalidad de recuperar de manera simultánea el agua y las materias primas en un sistema cerrado. Se ha estudiado el proceso de separación por membranas de intercambio iónico, la electrodiálisis, usando un sistema en escala de laboratorio y una disolución sintética que simulaba las aguas residuales del baño a base de HEDP. Se ha evaluado la viabilidad del sistema por medio del análisis de los parámetros de operación, como la extracción de iones, la tasa de desmineralización, el porcentaje de concentración, la eficiencia de la intensidad calculada para cada especie y el consumo medio de energía. Debido a que el ácido HEDP es un agente quelante, se ha evaluado el transporte de los quelatos Cu(II) HEDP a través de membranas de intercambio de aniones por medio de métodos electroquímicos. Se han construido curvas cronopotenciométricas y curvas intensidad-potencial para diferentes disoluciones sintéticas que contenían los mismos compuestos que el baño original. Se ha establecido la relación entre la presencia de los quelatos en las disoluciones y los grupos fijos de intercambio de aniones. Por fin, se han realizado las pruebas de deposición usando electrólitos conteniendo los compuestos reciclados y se han evaluado las características de los depósitos obtenidos. Los resultados indicaron que el sistema de electrodiálisis usando membranas de intercambio de aniones con grupos de intercambio de base fuerte ha podido producir disoluciones tratadas y un concentrado conteniendo los iones del baño. Se ha podido añadir el concentrado al baño original para compensar eventuales perdidas del arrastre sin afectar la calidad de los depósitos. Por lo tanto, la aplicación de la electrodiálisis demostró ser una alternativa viable para la recuperación del agua y de las materias primas de la disolución evaluada, reduciendo la generación de residuos líquidos y ahorrando los recursos naturales. / The two most common commercial copper baths are the acid sulfate copper bath and the alkaline cyanide copper bath. Alkaline copper baths are mostly used to coat parts with complex geometry and to avoid galvanic deposition when depositing a metal on a less noble substrate. Because of the toxicity of cyanide compounds, alternative baths have been developed using different complexing agents. The starting point of the present study is a cyanide free strike bath developed for copper plating on Zamak substrates developed by the Institute for Technological Research of the State of São Paulo/ Brazil. The replacement of a raw material such as cyanide must be economically advantageous and technically feasible. Therefore, this study intended to propose an alternative to the treatment of liquid wastes from the mentioned bath, aiming at simultaneous water reclamation and chemicals recovery in a closed system. The electrodialysis membrane separation process was studied, using a laboratory-scale system operating with a synthetic solution simulating the rinsing waters from the HEDP-based bath. The feasibility of the technique was evaluated by analyzing operational parameters such as ion extraction, demineralization rate, concentration rate, current efficiency for each anionic specie and average energy consumption. Because HEDP is a chelating agent, the transport of Cu(II) HEDP chelates through anion exchange membranes was also evaluated by means of electrochemical methods. Chronopotentiometric and current-voltage curves were constructed for different model solutions containing the same compounds as the original bath. A relation between the presence of chelates in the solutions and the fixed ion exchange group could be established. Lastly, deposition tests were performed using electrolytes containing the recycled inputs and the characteristics of the coatings were analyzed. The results showed that an electrodialysis stack using strongly basic anion exchange membranes was suitable to produce treated solutions and a concentrate containing the ions from the bath. The concentrate could be added to the copper bath to compensate eventual drag-out losses without affecting the quality of the coatings. Thus, the application of electrodialysis was shown to be a feasible alternative for recovering water and inputs from the evaluated solution, reducing the wastewater generation and saving natural resources. / Els dos banys de coure més utilitzats comercialment són el bany àcid a base de sulfat i el bany alcalí a base de cianur. Els banys alcalins són utilitzats principalment per a produir recobriments en peces amb geometria complexa i per a evitar la deposició galvànica quan es deposita un metall en un substrat menys noble. A causa de la toxicitat dels compostos de cianur, s'han desenrotllat banys alternatius usant diferents agents complexants. El punt de partida de la present investigació és un bany primari sense cianurs per a deposició de coure en substrats de Zamak desenrotllat en l'Institut d'Investigacions Tecnològiques de l'Estat de Sao Paulo / Brasil. La substitució de matèries primeres com el cianur ha de ser econòmicament avantatjosa i tècnicament viable. D'aquesta manera, la investigació presentada va pretendre proposar una alternativa per al tractament de residus líquids del bany ja mencionat amb la finalitat de recuperar de manera simultània l'aigua i les matèries primeres en un sistema tancat. S'ha estudiat el procés de separació per membranes d'intercanvi iònic, electrodiàlisi, usant un sistema en escala de laboratori i una dissolució sintètica que simulava les aigües residuals del bany a base d'HEDP. S'ha avaluat la viabilitat del sistema per mitjà de l'anàlisi dels paràmetres d'operació, com l'extracció d'ions, la taxa de desmineralització, el percentatge de concentració, l'eficiència de la intensitat calculada per a cada espècie i el consum mitjà d'energia. Pel fet que l'àcid HEDP és un agent quelant, s'ha avaluat el transport dels quelats Cu (II)-HEDP a través de membranes d'intercanvi d'anions per mitjà de mètodes electroquímics. S'han construït corbes cronopotenciomètriques i corbes intensitat-potencial per a diferents dissolucions sintètiques que contenien els mateixos compostos que el bany original. S'ha establit la relació entre la presència dels quelats en les dissolucions i els grups fixos d'intercanvi d'anions. Finalment, s'han realitzat les proves de deposició usant electròlits contenint els compostos reciclats i s'han avaluat les característiques dels depòsits obtinguts. Els resultats van indicar que el sistema d'electrodiàlisi usant membranes d'intercanvi d'anions amb grups d'intercanvi de base forta ha pogut produir dissolucions tractades i un concentrat que conté els ions del bany. S'ha pogut afegir el concentrat al bany original per a compensar eventuals perdudes de l'arrossegament sense afectar la qualitat dels depòsits. Per tant, l'aplicació de l'electrodiàlisi va demostrar ser una alternativa viable per a la recuperació de l'aigua i de les matèries primeres de la dissolució avaluada, reduint la generació de residus líquids i estalviant els recursos naturals. / Scarazzato, T. (2017). Treatment of a cyanide-free copper electroplating solution by electrodialysis: study of ion transport and evaluation of water and inputs recovery [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/98502

Thesis (MSc (Chemistry and Polymer Science))--Stellenbosch University, 2008. / N,N-dialkyl-N-acyl(aroyl)thiourea ligands form stable chelated complexes in a cis configuration with the platinum group metals. Such chelated complexes are generally considered substitutionally “inert” in solution, however, it was found that cis-bis(N,Ndialkyl- N-acyl(aroyl)thioureato)M(II) complexes (M = Ni(II), Pd(II) or Pt(II)) readily undergo facile chelate metathesis reactions in solution at room temperature. Upon mixing two different parent complexes, a mixed-ligand product formed in solution, with an equilibrium, or steady state, between the two parent complexes and the mixed-ligand product being attained after a period of time: M(LA)2 + M(LB)2 M(LA)(LB). All three complexes remained in solution even with a ten-fold excess of one parent complex. The presence of the mixed-ligand products in solution was confirmed by liquid chromatography-mass spectrometry (LC-MS), nuclear magnetic resonance (NMR) spectra and a crystal structure of the mixed-ligand complex cis-Pd(L3-S,O)(L4-S,O). Though a number of attempts were made, it was not possible to either isolate or synthesise the mixed-ligand complexes exclusively. The equilibrium distribution and the rate of the metathesis reaction were influenced by a number of factors, including the central metal ion, the substituents on the complexed ligands and the reaction medium. In addition to these, a number of other factors, some unexpected, also played a role in the rate of the reaction. Initial concentration of the parent complexes, the age of the solutions upon mixing and the presence of impurities or additives all contributed to the overall rate of reaction. The results from these rate studies highlighted the necessity for extensively purified compounds. In addition to chelate metathesis reactions, the exchange between a cis-Pd(L-S,O)2 complex and an unbound HL ligand in solution was also investigated. Again, even with an excess of unbound ligand, all three possible complexes were present in solution. It has been shown previously that these complexes undergo a photoinduced cis-trans isomerisation under intense light, and it has been proposed that the reverse trans-cis process, which occurs in the dark, may be a metathesis reaction. In light of this, the relationship between these chelate metathesis reactions and the reverse trans-cis reaction was briefly investigated. Though the metathesis reactions were a general phenomenon in the Ni(II), Pd(II) and Pt(II) complexes of the aforementioned ligands, the experiments focused mainly on the cis-Pd(L-S,O)2 complexes due to the favourable timescales of their metathesis reactions. The primary technique to observe these reactions was reversed-phase high-performance liquid chromatography (rp-HPLC). The timescales involved in the cis-Pd(L-S,O)2 metathesis reactions as well as the stability of the Pd(II) complexes under the HPLC conditions made this technique ideal.

Les traceurs sont des espèces permettant de déterminer la position ou la distribution d'un produit et ceux-ci sont aujourd'hui présents dans de très nombreux domaines. Bien que chacune des applications possède un cahier des charges bien spécifique, il est possible de les retrouver dans des domaines aussi divers que la médecine (agents de contraste), l'anticontrefaçon ou encore l'exploration géologique. Nous avons ainsi développé des traceurs d'eau d'injection pétrolière composés de complexes de lanthanides. Ces traceurs, dérivés du DOTA, ont pu être détectés à des concentrations inférieures au ppb, grâce à un appareillage simple et compact. Cette détection fut rendue possible par l'utilisation de la fluorescence en temps résolu, qui permet de contourner le bruit de fond créé par la fluorescence intrinsèque des résidus pétroliers présents dans les eaux de production. Nous avons également montré comment il était possible, grâce à une synthèse en microémulsion, d'encapsuler différents luminophores au sein d'une nanoparticule composée d'un coeur d'or et d'une coquille de silice. Ainsi, ces nanoparticules ont pu être utilisées comme traceurs intelligents afin de recueillir des informations sur les propriétés physicochimiques au sein des puits comme la température, le pH, la proportion entre différents solvants, etc. Enfin nous avons pu montrer comment une utilisation judicieuse des lanthanides et des propriétés complexantes des inhibiteurs de dépôts minéraux pouvait permettre leur dosage grâce à une méthode à la fois simple et rapide. Ce dosage permettra alors d'ajuster leur concentration dans les différents puits de production de pétrole / Tracers are objects allowing the determination of the position or the distribution of a product; tracers are currently used in a great variety of domains. Despite the fact that each field has it's own specifications, it is possible to find tracers in medicine (contrast agents), anti-counterfeiting or geological exploration. We have developed lanthanide complex tracers for oil field injection waters. Those tracers, derived from the DOTA, have been detected at concentration lower than 1 ppb, thanks to a simple and compact apparatus. This detection has been made possible by the use of time-resolved fluorescence spectroscopy, this technique allows us to get rid of the background noise created by the intrinsic fluorescence of oil residues that are present in production waters. We also demonstrated how we can, through a reverse microemulsion synthesis, encapsulate several different dyes inside a single nanoparticle composed of a gold core and a silica shell. We showed as well, how those particles can be used as smart tracers to gather data, such as temperature, pH, solvents, etc. inside the well. Finally the use of lanthanides and scale inhibitors properties allowed us to create a simple and fast dosing protocol of such scale inhibitors in injection waters. This dosage will then allow the quick adjustment of their concentration inside each well

Foram conduzidos dois experimentos com o objetivo de avaliar a eficiência do uso de quelatos de ferro no cultivo hidropônico de rúcula em ambiente protegido. O delineamento experimental utilizado foi o inteiramente casualizado com 4 repetições e 6 tratamentos: Fe-IDHA (ácido D,L aspártico, N-(1,2 dicarboxietil) tetra sódico), Fe-EDTA (ácido etilenodiamino tetra acetic), Fe-ORGÂNICO (a base de aminoácidos), Fe-EDDHA (ácido etilenodiamino - di (o - hidroxifenil-acético o-o 4,8%) e Fe-HBED (ácido N, n`-Bis (2-Hidroxibenzil) N- etilenodiamina n`dipropiônico) e testemunha (sem adição de ferro). O primeiro experimento foi conduzido no período de 8 de maio a 7 de junho de 2012 e o segundo entre 13 de junho e 13 de julho de 2012. As mudas de rúcula, da cultivar \"Folha Larga\", foram transplantadas aos 10 DAS. As avaliações biométricas foram realizadas aos 10, 15, 20, 25 e 30 dias após o transplante (DAT) para: altura das plantas, número de folhas, área foliar, massa fresca e seca das folhas e massa seca das raízes. Aos 15, 20, 25 e 30 dias após o transplante (DAT) foram determinados o índice relativo de clorofila (IRC) e os teores de nitrogênio e ferro das folhas. Todos os quelatos possibilitaram fornecimento suficiente de ferro para o adequado crescimento e produtividade de rúcula em NFT. Plantas submetidas aos tratamentos Fe-HBED e Fe-EDDHA foram estatisticamente semelhantes ao quelato Fe-EDTA e Fe-ORGÂNICO, mas superiores ao Fe-IDHA e testemunha em relação ao crescimento. / Two experiments were carried out to evaluate the efficiency of using iron chelates in hydroponic rocket salad in a greenhouse. The experimental design was completely randomized with 4 replications and six treatments: Fe-IDHA, Fe-EDTA, Fe-ORGÂNIC, Fe-EDDHA and Fe-HBED) and control. The first experiment was conducted from May 8 to June 7, 2012 and the second between 13 June and 13 July 2012. The seedlings of rocket salad variety Folha Larga were transplanted at 10 DAS. The biometric evaluations were performed at 10, 15, 20, 25 and 30 DAT, and analyzed to: plant height, number of leaves, leaf area, fresh and dry weight of leaves and dry weight of roots. At 15, 20, 25 and 30 days after transplanting (DAT) were determined relative chlorophyll index (RCI) and nitrogen and iron contents of the leaves. All chelates made it possible sufficient supply of iron for the adequate growth and productivity of rocket in NFT. Plants subjected to treatments Fe-HBED and Fe- EDDHA were statistically similar to chelate Fe-EDTA and Fe-ORGANIC, but higher than the Fe-IDHA and control in relation to growth.

The two most common commercial copper baths are the acid sulfate copper bath and the alkaline cyanide copper bath. Alkaline copper baths are mostly used to coat parts with complex geometry and to avoid galvanic deposition when depositing a metal on a less noble substrate. Because of the toxicity of cyanide compounds, alternative baths have been developed using different complexing agents. The starting point of the present study is a cyanide-free strike bath developed for copper plating on Zamak substrates developed by the Institute for Technological Research of the State of São Paulo/ Brazil. The replacement of a raw material such as cyanide must be economically advantageous and technically feasible. Therefore, this study intended to propose an alternative to the treatment of liquid wastes from the mentioned bath, aiming at simultaneous water reclamation and chemicals recovery in a closed system. The electrodialysis membrane separation process was studied, using a laboratoryscale system operating with a synthetic solution simulating the rinsing waters from the HEDP-based bath. The feasibility of the technique was evaluated by analyzing operational parameters such as ion extraction, demineralization rate, concentration rate, current efficiency for each anionic specie and average energy consumption. Because HEDP is a chelating agent, the transport of Cu(II)-HEDP chelates through anion-exchange membranes was also evaluated by means of electrochemical methods. Chronopotentiometric and current-voltage curves were constructed for different model solutions containing the same compounds as the original bath. A relation between the presence of chelates in the solutions and the fixed ion exchange group could be established. Lastly, deposition tests were performed using electrolytes containing the recycled inputs and the characteristics of the coatings were analyzed. The results showed that an electrodialysis stack using strongly basic anion-exchange membranes was suitable to produce treated solutions and a concentrate containing the ions from the bath. The concentrate could be added to the copper bath to compensate eventual drag-out losses without affecting the quality of the coatings. Thus, the application of electrodialysis was shown to be a feasible alternative for recovering water and inputs from the evaluated solution, reducing the wastewater generation and saving natural resources. / Os dois banhos de cobre comerciais mais comuns são o banho ácido à base de sulfato e o banho alcalino à base de cianeto. Os banhos alcalinos são usados principalmente para recobrir peças com geometria complexa e para evitar a deposição por deslocamento galvânico quando se deposita um metal em um substrato menos nobre. Por causa da toxicidade dos compostos cianídricos, banhos alternativos vêm sendo desenvolvidos usando diferentes agentes complexantes. O ponto de partida do presente estudo é um banho toque isento de cianeto para deposição de cobre em substratos de Zamak, desenvolvido pelo Instituto de Pesquisas Tecnológicas / Brasil. A substituição de matérias-primas como o cianeto deve ser economicamente vantajosa e tecnicamente viável. Desta forma, este estudo pretendeu propor uma alternativa para o tratamento de resíduos líquidos do banho mencionado, visando à recuperação simultânea da água e das matérias-primas em um sistema fechado. Foi estudado o processo de separação por membranas de eletrodiálise, usando um sistema em escala laboratorial operando com uma solução sintética que simulava as águas de lavagem do banho à base de HEDP. A viabilidade da técnica foi avaliada por meio da análise de parâmetros operacionais, como a extração dos íons, a taxa de dessalinização, o percentual de concentração, a eficiência de corrente calculada para cada espécie iônica e o consumo médio de energia. Devido ao HEDP ser um agente quelante, o transporte de quelatos Cu(II)-HEDP através de membranas aniônicas foi avaliado por meio de métodos eletroquímicos. Curvas cronopotenciométricas e curvas corrente-potencial foram construídas para diferentes soluções sintéticas que continham os mesmos compostos que o banho original. A relação entre a presença de quelatos nas soluções e os grupos fixos de troca iônica pôde ser estabelecida. Por fim, testes de deposição foram realizados usando eletrólitos contendo os compostos reciclados e as características dos depósitos foram analisadas. Os resultados mostraram que o sistema de eletrodiálise usando membranas aniônicas contendo grupos de troca fortemente básicos pôde produzir soluções tratadas e um concentrado contendo os íons do banho. O concentrado pôde ser adicionado ao banho original para compensar eventuais perdas por arraste sem afetar a qualidade dos depósitos. Assim, a aplicação da eletrodiálise se mostrou uma alternativa viável para a recuperação de água e de insumos da solução avaliada, reduzindo a geração de efluentes e economizando recursos naturais.

Foram conduzidos dois experimentos com o objetivo de avaliar a eficiência do uso de quelatos de ferro no cultivo hidropônico de rúcula em ambiente protegido. O delineamento experimental utilizado foi o inteiramente casualizado com 4 repetições e 6 tratamentos: Fe-IDHA (ácido D,L aspártico, N-(1,2 dicarboxietil) tetra sódico), Fe-EDTA (ácido etilenodiamino tetra acetic), Fe-ORGÂNICO (a base de aminoácidos), Fe-EDDHA (ácido etilenodiamino - di (o - hidroxifenil-acético o-o 4,8%) e Fe-HBED (ácido N, n`-Bis (2-Hidroxibenzil) N- etilenodiamina n`dipropiônico) e testemunha (sem adição de ferro). O primeiro experimento foi conduzido no período de 8 de maio a 7 de junho de 2012 e o segundo entre 13 de junho e 13 de julho de 2012. As mudas de rúcula, da cultivar \"Folha Larga\", foram transplantadas aos 10 DAS. As avaliações biométricas foram realizadas aos 10, 15, 20, 25 e 30 dias após o transplante (DAT) para: altura das plantas, número de folhas, área foliar, massa fresca e seca das folhas e massa seca das raízes. Aos 15, 20, 25 e 30 dias após o transplante (DAT) foram determinados o índice relativo de clorofila (IRC) e os teores de nitrogênio e ferro das folhas. Todos os quelatos possibilitaram fornecimento suficiente de ferro para o adequado crescimento e produtividade de rúcula em NFT. Plantas submetidas aos tratamentos Fe-HBED e Fe-EDDHA foram estatisticamente semelhantes ao quelato Fe-EDTA e Fe-ORGÂNICO, mas superiores ao Fe-IDHA e testemunha em relação ao crescimento. / Two experiments were carried out to evaluate the efficiency of using iron chelates in hydroponic rocket salad in a greenhouse. The experimental design was completely randomized with 4 replications and six treatments: Fe-IDHA, Fe-EDTA, Fe-ORGÂNIC, Fe-EDDHA and Fe-HBED) and control. The first experiment was conducted from May 8 to June 7, 2012 and the second between 13 June and 13 July 2012. The seedlings of rocket salad variety Folha Larga were transplanted at 10 DAS. The biometric evaluations were performed at 10, 15, 20, 25 and 30 DAT, and analyzed to: plant height, number of leaves, leaf area, fresh and dry weight of leaves and dry weight of roots. At 15, 20, 25 and 30 days after transplanting (DAT) were determined relative chlorophyll index (RCI) and nitrogen and iron contents of the leaves. All chelates made it possible sufficient supply of iron for the adequate growth and productivity of rocket in NFT. Plants subjected to treatments Fe-HBED and Fe- EDDHA were statistically similar to chelate Fe-EDTA and Fe-ORGANIC, but higher than the Fe-IDHA and control in relation to growth.

The present work is dealing with the first synthesis and characterisation of amphiphilic diblock copolymers bearing b-dicarbonyl (acetoacetoxy) chelating residues. Polymers were obtained by Group Transfer Polymerisation (GTP)/acetoacetylation and controlled radical polymerisation techniques (RAFT).<br><br>Different micellar morphologies of poly(n-butyl methacrylate)-block-poly[2-(acetoacetoxy)ethyl methacrylate] (pBuMA-b-pAEMA) were observed in cyclohexane as a selective solvent. Depending on the block length ratio, either spherical, elliptical, or cylindrical micelles were formed. The density of the polymer chains at the core/corona interface is considerably higher as compared to any other strongly segregating system reported in the literature. It is demonstrated that there are H-bond interactions existing between acetoacetoxy groups, which increase the incompatibility between block segments. In addition, such interactions lead to the formation of secondary structures (such as b-sheets or globular structures) and larger superstructures in the micrometer length scale.<br><br>Block copolymers were also used to solubilise metal ion salts of different geometries and oxidation states in organic media, in which are otherwise insoluble. Sterically stabilised colloidal hybrid materials are formed, i.e. monodisperse micelles having the metal ion salt incorporated in their core upon complexation with the ligating pAEMA block, whereas pBuMA forms the solvating corona responsible for stabilisation in solution. Systematic studies show that the aggregation behaviour is dependent on different factors, such as the tautomeric form of the beta-dicarbonyl ligand (keto/enol) as well as the nature and amount of added metal ion salt.