Search results for "Polymerization"

Surface coatings based on polysilsesquioxanes: Grafting-from approach starting from organic polymers

2009

AbstractPoly(methylsilsesquioxane) (PMSSQ) based hybrid materials are promising candidates to produce substrate-independent stable and adherent surface coatings. Usually these materials are synthesized by controlled radical polymerization from inorganic precursors. The presented synthetic pathway in here demonstrates how to graft PMSSQ networks from an endgroup-functionalized organic polymer and thus enlarges the range of accessible inorganic/organic hybrid coating materials.

Post-Polymerization Modification

2012

The synthesis of functional polymers has been enriched dramatically by post-polymerization modifications. Even though it represents a synthetically very appealing approach, different synthetic concepts of organic reactions are utilized in polymer science for the synthesis of architecturally well-defined multifunctional polymers. The different classes of reactions that provide the synthetic polymer chemist with tools of unprecedented precision, thereby opening the doors for materials synthesis in an interdisciplinary world, will be summarized.

From Polymers to Nanomedicines: New Materials for Future Vaccines

2013

Nanomedicine is the medical application of nanotechnology and therefore covers various kinds of nanoparticles. In this chapter, we would like to provide a brief introduction and overview of nanoparticles for the modulation of the immune system. In general, these nano-sized objects can be inorganic colloids, organic colloids (synthesized by emulsion polymerization or mini-/nanoemulsion techniques), polymeric aggregates (micelles or polymersomes), core cross-linked aggregates (nanohydrogels, crosslinked micelles, or polyplexes), multifunctional polymer coils, dendritic polymers or perfect dendrimers. A special focus is set on polymeric materials, because the chemical composition of the partic…

Amino acid-based cholinium ionic liquids as sustainable catalysts for pet depolymerization

2021

Chemical recycling to monomers is one of the key strategies in tackling the issues deriving from persistent plastic pollution in the environment, and poly(ethylene terephthalate) (PET) is among the most used polymers in modern society. In this context, we herein describe the glycolysis of PET to bis-hydroxyethyl terephthalate (BHET), promoted by basic cholinium salts differing for the anions, also comprising amino acid anions. We investigated the optimal reaction conditions, finding that the best-performing catalyst is [Ch][Gly], in the presence of which a conversion of 85% and a yield of 51% are achieved at 150 °C after 6 h, from PET deriving from a clear water bottle. We used our protocol…

Collapse of Cylindrical Brushes with 2-Isopropyloxazoline Side Chains Close to the Phase Boundary

2013

A high-molar-mass cylindrical brush polymer with a main chain degree of polymerization of Pw = 1047 is synthesized by free-radical polymerization of a poly-2-isopropyloxazoline macromonomer with Pn = 28. The polymerization is conducted above the lower phase transition temperature of the macromonomer, i.e., in the phase-separated regime, which provides a sufficiently concentrated macromonomer phase mandatory to obtain high-molar-mass cylindrical brushes. Upon heating to the phase transition temperature, the hydrodynamic radius is observed to shrink from 34 to 27 nm. Further increase in temperature resulted in aggregated chains which were observed to coexist with single chains until eventuall…

1984

Influence de la structure de chaine sur le type de phase et relation entre la masse moleculaire et les temperatures de transition

1984

Two-Dimensional Assembly Formation of Hydrophobic Helical Peptides at the Air/Water Interface: Fluorescence Microscopic Study

1995

Monolayer formation of hydrophobic α-helical peptides, X-(Ala-Aib) 8 -Y (X=Boc-, HOOCCH 2 CH 2 CO-, biotinyl, biotinyl-(Sar) 3 -; Y=OMe, OBzl, OH), at the air/water interface was studied by the fluorescence microscopic method. Some peptides showed a mound in the π-A isotherm. When the monolayer containing a small amount of FITC-labeled peptide was held at the surface pressure corresponding to the top of the mound, bright and dark domains were observed by fluorescence microscopy. Domain formation was also observed by the addition of a cationic dye (DiIC 1 ) into the subphase underneath the peptide monolayer. The mound in the π-A isotherm is, therefore, ascribed to the phase transition from a…

Photosensitive functionalized surface-modified quantum dots for polymeric structures via two-photon-initiated polymerization technique.

2015

In this paper, the surface modification of CdSe- and CdZnS-based quantum dots (QDs) with a functional silica shell is reported. Functionalized silica shells are prepared by two routes: either by ligand exchange and a modified Stober process or by a miniemulsion process with amphiphilic poly(oxyethylene) nonylphenylether also know as Igepal CO-520 (IG) as oligomeric amphiphile and modified silica precursors. The polymerizable groups on the functionalized silica shell allow covalent bonding to a polymer matrix and prevent demixing during polymerization and crosslinking. This allows the homogeneous incorporation of QDs in a crosslinked polymer matrix. This paper furthermore demonstrates that t…

Reaction kinetics in dense two-dimensional polymer solutions : an excimer probe study

1994

We report measurements of the time dependent reaction rate of excimer formation in two-dimensional solutions of a polymerized amphiphile with partially pyrene-labelled chains in monolayers at the air-water-interface. We find a time dependent reaction rate for excimer formation obeying a power law r(t) ∞ t -β . The exponent β has a value of 0.22±0.12. This value is consistent with β=1/4, as has been predicted for bimolecular diffusion-controlled reactions in two-dimensional polymer melts by de Gennes. The measurements demonstrate the usefulness of the excimer technique to explore polymer dynamics