Search results for "End-group"

showing 3 items of 93 documents

Darstellung von Oligo[(hydroxy-1,3-phenylen)methylen]en mit Hydroxynitrophenylen- und Alkylhydroxyphenyleneinheiten

1981

Possibilities to synthesize substituted oligo[(hydroxy-1,3-phenylene)methylene]s containing hydroxynitrophenylene and alkylhydroxyphenylene units are discussed. The only successful way to introduce the hydroxynitrophenylene unit consists in the condensation of chloromethylated nitrophenols with an excess of alkylphenols. The resulting compounds can be prolonged stepwise at the alkylhydroxyphenylene end group by alternating hydroxymethylation and further condensation with alkylphenols. Thus, including the hydroxymethylated compounds, 11 dinuclear, 17 trinuclear, and 5 tetranuclear compounds were obtained for the first time. Some of them were characterized by their acetyl derivatives.

chemistry.chemical_compoundEnd-groupchemistryPolymer chemistryCondensationMethyleneDie Makromolekulare Chemie
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1987

Diffusion coefficients D of singly and doubly end-labeled polystyrenes (PS) with molecular weights in the range 6500 ≤ M ≤ 75400 were measured in a PS matrix of molecular weight M′ = 111000, and in matrices with M′ = M. At 212°C, we find no influence of the label. In a power-law description D = D0 · M−α · M′−β we find α = 2,0 for M′ = 111000 and α + β = 2,4 for M = M′. The crossover to Rouse-like behavior for short-M chains is at Me ≈ 18000 for the former (high M′), and at Mc ≈ 33000 in the latter (M′ = M) case. At 185°C, we find a more complex scaling behavior and different D values for singly and doubly labeled PS.

chemistry.chemical_compoundMatrix (mathematics)Range (particle radiation)End-groupchemistryChain (algebraic topology)Molecular massDiffusionPolymer chemistryPolystyreneScalingDie Makromolekulare Chemie
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Polysarcosine-Based Lipids: From Lipopolypeptoid Micelles to Stealth-Like Lipids in Langmuir Blodgett Monolayers.

2016

Amphiphiles and, in particular, PEGylated lipids or alkyl ethers represent an important class of non-ionic surfactants and have become key ingredients for long-circulating (“stealth”) liposomes. While poly-(ethylene glycol) (PEG) can be considered the gold standard for stealth-like materials, it is known to be neither a bio-based nor biodegradable material. In contrast to PEG, polysarcosine (PSar) is based on the endogenous amino acid sarcosine (N-methylated glycine), but has also demonstrated stealth-like properties in vitro, as well as in vivo. In this respect, we report on the synthesis and characterization of polysarcosine based lipids with C14 and C18 hydrocarbon chains and their end g…

polysarcosine; polypeptoids; surfactants; lipids; NCA polymerization; PSarcosinylated lipidsPolymers and PlasticsDispersity02 engineering and technologypolysarcosineDegree of polymerization010402 general chemistry01 natural sciencesMicelleRing-opening polymerizationLangmuir–Blodgett filmArticlesurfactantslipidslcsh:QD241-441PSarcosinylated lipidslcsh:Organic chemistryMonolayerPolymer chemistryOrganic chemistrypolypeptoidsNCA polymerizationChemistryGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesEnd-groupCritical micelle concentrationlipids (amino acids peptides and proteins)0210 nano-technologyPolymers
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