Search results for "polymerization"

From Defined Reactive Diblock Copolymers to Functional HPMA-Based Self-Assembled Nanoaggregates

2008

This paper describes the synthesis of functional amphiphilic poly( N-(2-hydroxypropyl) methacrylamide)-block-poly(lauryl methacrylate) copolymers by RAFT polymerization via the intermediate step of activated ester block copolymers (pentafluoro-phenyl methacrylate). Block copolymers with molecular weights from 12000-28000 g/mol and PDIs of about 1.2 have been obtained. The amphiphilic diblock copolymers form stable super structures (nanoaggregates) by self-organization in aqueous solution. The diameters of these particles are between 100 and 200 nm and depend directly on the molecular weight of the block copolymer. Furthermore, we investigated the impact of these nanoaggregates on cell viabi…

Synthesis and Characterization of Stimuli-Responsive Star-Like Polypept(o)ides: Introducing Biodegradable PeptoStars

2017

tar-like polymers are one of the smallest systems in the class of core crosslinked polymeric nanoparticles. This article reports on a versatile, straightforward synthesis of three-arm star-like polypept(o)ide (polysarcosine-block-polylysine) polymers, which are designed to be either stable or degradable at elevated levels of glutathione. Polypept(o)ides are a recently introduced class of polymers combining the stealth-like properties of the polypeptoid polysarcosine with the functionality of polypeptides, thus enabling the synthesis of materials completely based on endogenous amino acids. The star-like homo and block copolymers are synthesized by living nucleophilic ring opening polymerizat…

Novel cationic polyaspartamide with covalently linked carboxypropyl-trimethyl ammonium chloride as a candidate vector for gene delivery

2006

Abstract The non-viral gene vector properties of a protein-like polymer, the α,β-poly(N-2-hydroxyethyl)- d , l -aspartamide (PHEA) were investigated after its derivatization with 3-(carboxypropyl)trimethyl-ammonium chloride (CPTA) as molecule bearing cationic groups, in order to obtain stable polycations able to condense DNA. PHEA was firstly functionalized with hydrazide pendant groups by reaction with hydrazine monohydrate (HYD), obtaining the polyhydrazide α,β-poly(N-2-hydroxyethyl/carbazate)- d , l -aspartamide (PHEA–HYD). In this paper we reported that polymer functionalization degree can be easily modulated by varying reaction conditions, so allowing us to produce two PHEA derivatives…

Hydrogen-bonded dimers of a thiacalixarene substituted by carbamoylmethylphosphineoxide groups at the wide rim.

2006

A thiacalix[4]arene derivative bearing four carbamoylmethylphosphineoxide groups at the wide rim forms hydrogen-bonded, dimeric capsules with S8 symmetry in the crystalline state and in apolar solvents, where the inclusion of cationic guests could be proved by 1H NMR and ESI mass spectra.

Der abbau von polyoxymethylenen. Poloxymethylene. 14. Mitteilung

1960

Quantitative Untersuchungen uber die Zersetzung von Polyoxymethylenen unter verschiedenen Bedingungen zeigen, das im wesentlichen 5 Abbaureaktionen unterschieden werden konnen 1 Depolymerisation vom Kettenende her, 2 Autoxydative Spaltung, 3 Abbau durch Sekundarprodukte der Autoxydation, 4 Thermische Degradation, 5 Hydrolyse und Acidolyse. Die einzelnen Reaktionen lassen sich experimentell getrennt untersuchen. Es werden Moglichkeiten angegeben, den Abbau zu unterdrucken. Eine Methode zur Prufung der thermischen Stabilitat von Polyoxymethylenen wird vorgeschlagen. It is shown by quantitative measurements of the degradation of polyoxymethylenes under different conditions that essentially fiv…

ChemInform Abstract: Transition Metal Derivatives of Low Oxidation State Phosphorus Oxoacids: Synthetic Pathways and Structural Studies

2010

Abstract A general synthetic approach intended to rationalize the solution preparative chemistry of transition metal phosphites and hypophosphites is presented. As previously shown for other derivatives containing also tetrahedral or pseudotetrahedral oxoanions, the hydrolytic processes affecting the cationic moieties play a determinant role on the very nature of the final solid. In fact, despite the limited number of donor atoms in the anions, the crystal chemistry of these compounds is quite intricate because of both the variety of possible cationic aggregates and the many ways to interconnect them through pseudotetrahedral anionic groups.

Über den angriff des carboniumions am monomeren styrol bei der kationischen copolymerisation von trioxane und styrol. 19. Mitt. über polyoxymethylene

1962

Bei der Saure-katalysierten Hydrolyse von kationisch dargestellten Copolymeren aus Trioxan und Styrol entsteht 4-Phenyl-1,3-Dioxan. Das last sich nur so erklaren, das in Analogie zur radikalischen und zur anionischen Polymerisation der Angriff des Carboniumions ebenfalls am β-Kohlenstoffatom des Styrols erfolgt. Formation of 4-phenyl-1,3-dioxan occurs during the acid catalyzed hydrolysis of cationically produced copolymers of trioxane and styrene. The only possible explanation involves an attack of the carboniumion at the β-carbonatom of styrene analogous to the radical and anionic polymerization.

Some new examples of cationic polymerization

1986

Preparation, proprietes et polymerisation cationique de cis et trans-methoxyvinylchlorure. Le polymere trans est surtout threodiisotactique. Copolymerisation du cis avec le trans ou le styrene ou le dioxolanene-1,3. Polymerisation de la phenyl-2 oxazoline et de la conidine

Polymere ester von säuren des Phosphors, 3. Polymerisation des 2-Äthoxy-2-oxo-1,3,2-dioxaphospholans

1975

2-Athoxy-2-oxo-1,3,2-dioxaphospholan (1) wird durch verschiedene Alkoholate sehr schnell und in hoher Ausbeute zu Poly[oxy(athoxyphosphoryl)oxyathylen] (3) polymerisiert. Die Produkte sind hochviskos und farbols. Sie losen sich in Wasser, Alkoholen, Tetrahydrofuran, Dioxan, Methylenchlorid, Chloroform und Dimethylsulfoxid; unloslich sind sie in Ather und in Kohlenwasserstoffen. Polymerisationsgrade bis 83 (M = 12600) wurden gemessen. In wasriger Losung bei Raumtemperatur erfolgte auch nach Tagen kein merklicher hydrolytischer Abbau. Der mutmaslich anionische Polymerisationsmechanismus und mogliche Nebenreaktionen werden kurz diskutiert. 2-Ethoxy-2-oxo-1,3,2-dioxaphospholane (1) is polymeriz…

1984

Alkaline hydrolyses of anionic phenyl esters such as 4-acetoxy-3-nitrobenzoic acid and 4-butyryloxy-3-nitrobenzoic acid were examined in the presence of cationic and polymeric liposomes, liposomes of low molecular weight compounds, and micelles. All the additives accelerate the reaction due to the hydrophobic interaction between substrates and additives and the electrostatic interaction both between substrates and additives and between OH− and additives. In the Arrhenius plots of the reactions catalyzed by the liposomes, discontinuous regions were observed due to the phase transition of liposomes from the gel state to the liquid crystal state. Activation parameters ΔH≠, ΔS≠ and ΔV≠ for thes…