Academic literature on the topic 'Interactions supramoléculaires'
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Journal articles on the topic "Interactions supramoléculaires"
Sakho, Adama Moussa, Aboubacar Diallo, Kaba Conde, Damany Keita, Mamady Kourouma, Dong Sheng Zhu, and Bangaly Dioumessy. "Synthèse, caractérisation et l’activité anti-tumorale d’un complexe organo-étain carboxylique." International Journal of Biological and Chemical Sciences 14, no. 3 (June 19, 2020): 1133–43. http://dx.doi.org/10.4314/ijbcs.v14i3.38.
Full textFAVERDIN, P., and C. LEROUX. "Avant-propos." INRAE Productions Animales 26, no. 2 (April 16, 2013): 71–76. http://dx.doi.org/10.20870/productions-animales.2013.26.2.3137.
Full textDissertations / Theses on the topic "Interactions supramoléculaires"
Trabolsi, Ali. "Etudes des interactions dans des édifices supramoléculaires." Université Louis Pasteur (Strasbourg) (1971-2008), 2006. http://www.theses.fr/2006STR13210.
Full textThe research data presented in this PhD dissertation contribute to a better understanding of the ionic and molecular recognition mechanisms, which are involved in the self-assembly of novel photochemical supramolecules. We first have focused our attention on strapped Zn(II) porphyrinic receptors which possess a fine-tuned and appropriate architecture for the strong and selective recognition of imidazole substrates. The flexibility of these receptors associated to a set of strong (Zn-N coordination bond) and weak (hydrogen bond, - and CH- interactions) intramolecular interactions are responsible of the specificity and efficiency of the binding processes. The efficiency of the recognition processes is adjusted and controlled by the nature and bulkiness of the substituents. Our physico-chemical approach thus helped to guide the synthesis toward new imidazole-porphyrin substrates and was an essential stage toward the development of stable photochemical devices for which the photoinduced energy migration processes are very efficient. We also explored the possibility to pair C60 and polyphenylnevinylene oligomers or metalloporphyrins using a supramolecular approach. Axial coordination of nitrogen bases on Zn(II) porphyrins and ionic recognition of ammoniums by 18C6 crown-ethers were chosen as primary interactions. To strengthen these edifices, assembly strategies with polytopic receptors were processed and successfully led to the formation of stable edifices. The photoinduced processes within these new supramolecules were studied. The first strategy relies on positively cooperative association of two substrates, which mainly results from secondary - interactions between two C60 units positioned in a syn conformation. The second strategy uses multivalent supramolecular chemistry and is based on the macrocyclization process of bivalent substrates with ditopic receptors
Marmin, Thomas. "Premiers nanovecteurs supramoléculaires ciblant le cerveau par transport actif." Mémoire, Université de Sherbrooke, 2017. http://hdl.handle.net/11143/10492.
Full textAbstract : Delivering drug into the body to target specific organs, while minimizing side effects, is an enormous scientific challenge. Current research reveals that there are many pitfalls for delivering therapeutic compounds to the central nervous system. Many diseases (autism, schizophrenia, Alzheimer's, etc.) linked to the central nervous system affect the quality of life and entail significant costs for society. This thesis is based on the improvement in the accessibility of therapeutic compounds to the brain by passing the blood-brain barrier, a biological barrier difficult to cross. To introduce drugs into the central nervous system, this barrier must be overcome. This is very difficult because it is remarkably effective in protecting the brain. This is why we will develop a new strategy based on a new type of transporter. We propose to use macrolactams having the property of stacking in the form of supramolecular tubes of adequate stability. It will then be possible to graft medicines and also agents capable of opening the blood-brain barrier. This manuscript describes the development of these new chiral macrocycles, the results of various structural analyses proving the presence of robust tubes and systems, and finally the functionalization of the macrocycles by a medicinal agent (doxorubicin).
Moussawi, Mhamad aly. "Assemblages à base de polyoxométallates : des interactions fondamentales aux matériaux hybrides supramoléculaires." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLV078/document.
Full textIn this work, we report in the first part the substitution of molybdenum by tungsten within Keplerate-type anions [{Mo6}12Mo30O312E60(AcO)30]42- (E = O or S). Introducing tungsten to the synthesis medium resulted in the isolation of a series of compounds, [{WxMo6- x}12Mo30O312E60(AcO)30]42, with variable metal content within their pentagonal units {M6}. An outstanding observation revealed the selective occupation of the central position in the pentagonal unit by the W atoms. This revelation was stretched to reach other historical structures as Mo-blue wheel [Mo154O462H14(H2O)70]14- and Krebs [Mo36O112(H2O)16]8- anions that also showed the same preferential occupation of W atoms for the heptacoordinated site. In the second part, we focus on the fabrication of a three-component hybrid material based on polyoxometalates (POMs), metallic clusters and -cyclodextrin ( -CD). Investigation of such material has been conducted using bottom-up approach by investigating the specific interactions between CD and both types ofinorganic units. Finally, the three componentsassociate together to give a well orderedpolymer-like hybrid chain that is derived ashydrogel and single crystals. In the last part, we extend the CD-POMinvestigation to reach giant POM structures asthe Mo-blue ring. A non-conventional complexation results from this interaction explained by the encapsulation of the organic macrocycle within the inorganic torus. Increasing the complexity of the system by introducing a third species provoked the formation of a hierarchical hybrid assembly
Vebr, Aurélien. "Interaction synergique entre le pH, la température et les interactions supramoléculaires pour la conception de matériaux polymères intelligents." Electronic Thesis or Diss., Université de Lille (2022-....), 2022. https://pepite-depot.univ-lille.fr/ToutIDP/EDSMRE/2022/2022ULILR084.pdf.
Full textThis PhD thesis focuses on the development and the characterization of smart stimuli-responsive polymeric materials based on combining polymers with supramolecular host-guest interactions. Due to their capacity to respond to an external trigger, such as temperature, pH, light, or electrical signal, in a predetermined fashion, interest in stimuli-responsive polymers has steadily grown over the past decades. However, developing a macromolecular system able to respond in a synergistic fashion to multiple signals to mimic nature is still a very challenging research field. In this thesis, we focused on the creation of dual thermo- and pH-responsive polymeric materials with supramolecular properties for host-guest interaction aiming to utilize the host entities that can be released and/or induce a change in properties.Chapter 2 will focus on a copolymer system, based on N-isopropylacrylamide (NIPAm) and Acrylic acid (AA), for which the Cloud Point temperature (Tcp) will be studied regarding the pH and the presence of organic salts. In Chapter 3, we will use a derivative from the previously studied polymer, but containing a supramolecular recognition unit: naphthalenes (Napht). The presence of the Napht moieties will allow the host-guest association with the supramolecular host BBox, leading to a modification of the polymer's properties depending on the concentration of the host, the pH, and the temperature. In the next step, in chapter 4, we evolved this 2D polymeric system into a 3D hydrogel, containing NIPAm, AA, and Napht moieties. The swelling, the volume phase transition, and the ability of the material to maintain or break the host-guest interaction were studied at various pH, and temperatures. Finally, the last chapter deals with a new supramolecular host: the Red Box. This analog from the previously studied BBox was associated with thermoresponsive polymers to promote, for the first time reported in the literature, the dissociation of host-guest complexes based on Red Box
Bertrand, Arthur. "Élaboration d'agents de transfert fonctionnalisés, précurseurs de copolymères supramoléculaires par liaisons hydrogène et interactions hôte/invité." Phd thesis, INSA de Lyon, 2011. http://tel.archives-ouvertes.fr/tel-00735755.
Full textGoubran-Botros, Hany. "Etude des interactions de biomolécules et de structures supramoléculaires (ex : cellules) avec les ions métalliques immobilisés." Compiègne, 1990. http://www.theses.fr/1990COMPD334.
Full textThis study deals with the interactions between biomolecules and chelated metal ions attached to insoluble or soluble polymers. We have demonstrated the conservation of recognition mechanism between biomolecules, from the peptide to the supramolecular structure (e. G. Cell), and chelated transition metals in different microenvironments of the metal. This recognition seems to be mediated through coordination between the chelated metal and specific amino acid residues, mainly histidine residues, located on the surface of proteins. Extension of the Immobilized Metal ion Affinity (IMA) principle to new techniques is presented. Immobilized Metal ion Affinity Electrophoresis (IMAE) is used for the analytical quantification of the recognition between metal chelates and proteins. The faisability of Immobilized Metal ion Affinity Partition (IMAP) both for analytical and preparative purposes mediated by the histidine residues is developed. The concept of Immobilized Metal ion Affinity Chromatography (IMAC) as well as IMAP had also been extended to study eukaryotic cell properties. Thus, IMAC, IMAE and IMAP all seem to operate on the same physico-chemical basis with proteins and whole cells
Bertrand, Arthur. "Élaboration d’agents de transfert fonctionnalisés, précurseurs de copolymères supramoléculaires par liaisons hydrogène et interactions hôte/invité." Thesis, Lyon, INSA, 2011. http://www.theses.fr/2011ISAL0157/document.
Full textOver the past decade, some (rare) examples of block copolymers with supramolecular links between the building blocks have been described. Because the association between macromolecular blocks is a reversible process, such polymers are of great interest in the field of nanostructured materials, self-healing materials, or processing aid. The main goal of this work is to develop new supramolecular architectures, by a combination of RAFT polymerization and H-bonding. In a first step, several chain transfer agents and a radical initiator possessing complementary thymine or diaminopyridine H-bonding moeties were synthesized. These precursors were used to generate a panel of polymers α- or α,ω-functionalized with these H-bonding stickers in a quantitative manner. The self-assembly of the resulting polymer blocks was highlighted by 1H NMR, AFM and rheological measurements. This approach was subsequently adapted to the development of hydrophilic supramolecular comb-shaped polymers, based on the β-cyclodextrin/adamantane host/guest complexation
Bonnefous, Monique. "Contribution à la caractérisation des biovecteurs supramoléculaires, les BVSM : études de leurs interactions cellulaires et biodistributions animales." Paris 11, 1997. http://www.theses.fr/1997PA114858.
Full textFlorent, Tiphaine. "Caractérisation d’inhibiteurs d’anhydrase carbonique IX, études de complexes supramoléculaires et interactions moléculaires par résonance plasmonique de surface." Thesis, Lille 2, 2014. http://www.theses.fr/2014LIL2S057/document.
Full textCarbonic anhydrase (CA) IX expression is increased upon hypoxia and has been proposed as a therapeutic target since it has been associated with poor prognosis, tumor progression and pH regulation. A new class of human carbonic anhydrase IX (hCA IX) inhibitors, diarylpyrazole sulfonamide derivatives, has been synthesized in our team. These compounds have a very limited water solubility which limits their pharmaceutical development. The complexation with cyclodextrins (CDs) offers the possibility to improve their solubility without affecting their original structure and has proved to be one of the most effective. The studies of the complexes formed between our compounds and various CDs have been performed, in order to choose the most appropriate CD. We investigate by NMR and capillary electrophoresis the complexes formed between six original diarylpyrazole sulfonamide derivatives and six CDs (native -, - and - CDs, hydroxypropylated HP--CD, methylated Me--CD or amino NH2--CD) at physiological pH. Futhermore, as these compounds have a chiral center, it was essential to separate their enantiomers and verify their optical purities before envisaging the study of their pharmacological activity. The enantiomeric purification was performed by three separative methods, the high performance liquid chromatography, the supercritical fluid chromatography and the capillary electrophoresis. This study permit to obtain optically pure compound in order to determine affinity of carbonic anhydrase. To determine the affinities of derivatives with isoforms, we performed first a comparison of three label-free methods for quantitative assessment of binding strength between carbonic anhydrase II and sulfonamides derivatives. The formation constants have been determined by surface plasmon resonance, isothermal titration calorimetry and thermal shift assay, which characterize the interaction between two partners. This study was useful to select and to validate the surface plasmon resonance (SPR) for the molecular interaction between carbonic anhydrases and all our derivatives. Affinities of sixteen compounds for three carbonic anhydrase isoforms (CA II, IX and XII) were then determined by SPR. These compounds have nanomolar affinities for three isoforms. Two compounds have affinities with great interest for the isoform CA IX, and a good selectivity CA IX versus CA II and should be considered as lead compounds. Additionally, some of optically pure compounds have shown an enantioselectivity for the AC isoforms
Shahgaldian, Patrick. "Assemblages supramoléculaires : étude de l'effet des interactions de faible énergie : utilisation de systèmes amphiphiles basés sur les calix-arènes." Lyon 1, 2002. http://www.theses.fr/2002LYO10155.
Full textBooks on the topic "Interactions supramoléculaires"
Aseyev, Georgii Georgievich. Electrolytes: Supramolecular Interactions and Non-Equilibrium Phenomena in Concentrated Solutions. Taylor & Francis Group, 2014.
Find full textAseyev, Georgii Georgievich. Electrolytes: Supramolecular Interactions and Non-Equilibrium Phenomena in Concentrated Solutions. Taylor & Francis Group, 2014.
Find full textElectrolytes: Supramolecular Interactions and Non-Equilibrium Phenomena in Concentrated Solutions. Taylor & Francis Group, 2014.
Find full textBook chapters on the topic "Interactions supramoléculaires"
"18. Y a-t-il une interaction de reconnaissance entre les oligosaccharides et l’ADN ?" In Chimie moléculaire et supramoléculaire des sucres, 280–92. EDP Sciences, 1995. http://dx.doi.org/10.1051/978-2-7598-0267-8.c019.
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