| People | Locations | Statistics |
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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Mata, F. Javier De La
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (10/10 displayed)
- 2023Removing lead from water with carboxylate dendrimers and magnetic nanoparticles modified with carboxylate dendrimerscitations
- 2023Ruthenium metallodendrimer against triple-negative breast cancer in micecitations
- 2023Combination of Copper Metallodendrimers with Conventional Antitumor Drugs to Combat Cancer in In Vitro Modelscitations
- 2023Lipid-coated ruthenium dendrimer conjugated with doxorubicin in anti-cancer drug delivery: Introducing protocolscitations
- 2023Carbosilane ruthenium metallodendrimer as alternative anti-cancer drug carrier in triple negative breast cancer mouse model: A preliminary studycitations
- 2021Organometallic dendrimers based on Ruthenium(II) N-heterocyclic carbenes and their implication as delivery systems of anticancer small interfering RNAcitations
- 2020Fine-Tuning the Interaction and Therapeutic Effect of Cu(II) Carbosilane Metallodendrimers in Cancer Cells: An In Vitro Electron Paramagnetic Resonance Studycitations
- 2014Synthesis of new amphiphilic water‐stable hyperbranched polycarbosilane polymerscitations
- 2013Characterization of Dendrimers and Their Interactions with Biomolecules for Medical use by Means of Electron Magnetic Resonancecitations
- 2004Tris(pyrazolyl)borate carbosilane dendrimers and metallodendrimerscitations
Places of action
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article
Synthesis of new amphiphilic water‐stable hyperbranched polycarbosilane polymers
Abstract
<jats:title>Abstract</jats:title><jats:p><jats:bold>New amphiphilic hyperbranched polymers possessing hydrophobic skeletons and hydrophilic terminal groups have been prepared and characterized. The synthetic strategy involved the formation of a new stable matrix with aromatic units within a carbosilane backbone, as well as the use of a classical polycarbosilane matrix. Both of them with allyl groups on the surface have narrow polydispersity values. Molecular weight and polydispersity of the hyperbranched polymers were obtained using gel permeation chromatography with multi‐angle light scattering, and determination of the average number of functional groups present on the surface was achieved using <jats:styled-content style="fixed-case"><jats:sup>1</jats:sup>H NMR</jats:styled-content> spectroscopy. The introduction of ionic groups was carried out via thiol–ene reactions with various thiol derivatives. The thermal properties of the polymers were also analysed using differential scanning calorimetry and zeta potential measurements. © 2013 Society of Chemical Industry</jats:bold></jats:p>