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Thematische Bibliographien / Poly(2-Alkyl-2-Oxazoline)s / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Poly(2-Alkyl-2-Oxazoline)s“

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Veröffentlicht am 7. Dezember 2024

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1

Blokhin, Aleksei N., Alla B. Razina und Andrey V. Tenkovtsev. „Novel Amphiphilic Star-Shaped Poly(2-Oxazoline)s with Calix[4]Arene Branching Center“. Key Engineering Materials 899 (08.09.2021): 300–308. http://dx.doi.org/10.4028/www.scientific.net/kem.899.300.

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Novel amphiphlic four-arm star-shaped poly (2-alkyl-2-oxazoline) s with calix [4] arene core were synthesized using the “grafting from” approach. The chlorosulfonated calix [4] arene derivative was synthesized and successfully applied as a multifunctional initiator for the cationic ring-opening polymerization of 2-alkyl-2-oxazolines. Obtained star-shaped poly (2-alkyl-2-oxazoline) s were characterized by means of NMR, UV-Vis spectroscopy and gel-permeation chromatography. It was shown that star-shaped poly (2-isopropyl-2-oxazoline) perform thermosensitivity in aqueous solutions.

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2

Demirel, A. Levent, Pınar Tatar Güner, Bart Verbraeken, Helmut Schlaad, Ulrich S. Schubert und Richard Hoogenboom. „Revisiting the crystallization of poly(2-alkyl-2-oxazoline)s“. Journal of Polymer Science Part B: Polymer Physics 54, Nr. 7 (24.11.2015): 721–29. http://dx.doi.org/10.1002/polb.23967.

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3

de la Rosa, Victor R., Werner M. Nau und Richard Hoogenboom. „Correction: Tuning temperature responsive poly(2-alkyl-2-oxazoline)s by supramolecular host–guest interactions“. Organic & Biomolecular Chemistry 13, Nr. 15 (2015): 4614. http://dx.doi.org/10.1039/c5ob90053k.

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4

Fisher, Adam L., Julia M. H. Schollick, Dirk G. A. L. Aarts und Martin C. Grossel. „Synthesis and gelation properties of poly(2-alkyl-2-oxazoline) based thermo-gels“. RSC Advances 6, Nr. 71 (2016): 66438–43. http://dx.doi.org/10.1039/c6ra06781f.

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Novel thermo-gelling polymers based on poly(2-alkyl-2-oxazoline)s grafted onto a polar carboxymethylcellulose backbone gel are reported which have potential applications in areas such as drug delivery and tissue engineering.

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5

Trachsel, Lucca, Marcy Zenobi-Wong und Edmondo M. Benetti. „The role of poly(2-alkyl-2-oxazoline)s in hydrogels and biofabrication“. Biomaterials Science 9, Nr. 8 (2021): 2874–86. http://dx.doi.org/10.1039/d0bm02217a.

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Poly(2-alkyl-2-oxazoline)s (PAOXAs) have been rapidly emerging as starting materials in the design of tissue engineering supports and for the generation of platforms for cell cultures, especially in the form of hydrogels.

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6

Ates, Sahin, Pinar Tatar-Guner, Yusuf Yagci und A. Levent Demirel. „Synthesis and characterization of polysulfone-g-poly(2-alkyl-2-oxazoline)s“. Designed Monomers and Polymers 16, Nr. 2 (23.08.2012): 137–44. http://dx.doi.org/10.1080/15685551.2012.705500.

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7

Rehfeldt, Florian, Motomu Tanaka, Lorena Pagnoni und Rainer Jordan. „Static and Dynamic Swelling of Grafted Poly(2-alkyl-2-oxazoline)s“. Langmuir 18, Nr. 12 (Juni 2002): 4908–14. http://dx.doi.org/10.1021/la0112559.

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8

Gaertner, Florian C., Robert Luxenhofer, Birgit Blechert, Rainer Jordan und Markus Essler. „Synthesis, biodistribution and excretion of radiolabeled poly(2-alkyl-2-oxazoline)s“. Journal of Controlled Release 119, Nr. 3 (Juni 2007): 291–300. http://dx.doi.org/10.1016/j.jconrel.2007.02.015.

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9

de la Rosa, Victor R., Werner M. Nau und Richard Hoogenboom. „Tuning temperature responsive poly(2-alkyl-2-oxazoline)s by supramolecular host–guest interactions“. Organic & Biomolecular Chemistry 13, Nr. 10 (2015): 3048–57. http://dx.doi.org/10.1039/c4ob02654c.

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A poly[(2-ethyl-2-oxazoline)-ran-(2-nonyl-2-oxazoline)] random copolymer was synthesized and its thermoresponsive behavior in aqueous solution modulated by the addition of different supramolecular host molecules.

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10

Ong, C. H., S. H. Goh und H. S. O. Chan. „Miscibility of conductive blends of poly(o-anisidine) with poly(2-alkyl-2-oxazoline)s“. Journal of Applied Polymer Science 65, Nr. 2 (11.07.1997): 391–97. http://dx.doi.org/10.1002/(sici)1097-4628(19970711)65:2<391::aid-app20>3.0.co;2-1.

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11

Kobayashi, Shiro, Yasuo Shimano und Takeo Saegusa. „Synthesis of Poly[ethylene-co-(vinyl acetate)-g-(2-alkyl-2-oxazoline)]s“. Polymer Journal 23, Nr. 11 (November 1991): 1307–15. http://dx.doi.org/10.1295/polymj.23.1307.

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12

Gauche, Cony, und Maria Isabel Felisberti. „Colloidal Behavior of Cellulose Nanocrystals Grafted with Poly(2-alkyl-2-oxazoline)s“. ACS Omega 4, Nr. 7 (09.07.2019): 11893–905. http://dx.doi.org/10.1021/acsomega.9b01269.

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13

Shimano, Yasuo, Kumiko Sato und Shiro Kobayashi. „Synthesis of novel macromonomers and telechelics of poly(2-alkyl-2-oxazoline)s“. Journal of Polymer Science Part A: Polymer Chemistry 33, Nr. 16 (30.11.1995): 2715–23. http://dx.doi.org/10.1002/pola.1995.080331605.

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14

Rettler, Erik F. J., Johannes M. Kranenburg, Hanneke M. L. Lambermont-Thijs, Richard Hoogenboom und Ulrich S. Schubert. „Thermal, Mechanical, and Surface Properties of Poly(2-N -alkyl-2-oxazoline)s“. Macromolecular Chemistry and Physics 211, Nr. 22 (13.10.2010): 2443–48. http://dx.doi.org/10.1002/macp.201000338.

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15

Everaerts, Melissa, Ali Tigrine, Victor R. de la Rosa, Richard Hoogenboom, Peter Adriaensens, Christian Clasen und Guy Van den Mooter. „Unravelling the Miscibility of Poly(2-oxazoline)s: A Novel Polymer Class for the Formulation of Amorphous Solid Dispersions“. Molecules 25, Nr. 16 (06.08.2020): 3587. http://dx.doi.org/10.3390/molecules25163587.

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Water-soluble polymers are still the most popular carrier for the preparation of amorphous solid dispersions (ASDs). The advantage of this type of carrier is the fast drug release upon dissolution of the water-soluble polymer and thus the initial high degree of supersaturation of the poorly soluble drug. Nevertheless, the risk for precipitation due to fast drug release is a phenomenon that is frequently observed. In this work, we present an alternative carrier system for ASDs where a water-soluble and water-insoluble carrier are combined to delay the drug release and thus prevent this onset of precipitation. Poly(2-alkyl-2-oxazoline)s were selected as a polymer platform since the solution properties of this polymer class depend on the length of the alkyl sidechain. Poly(2-ethyl-2-oxazoline) (PEtOx) behaves as a water-soluble polymer at body temperature, while poly(2-n-propyl-2-oxazoline) (PPrOx) and poly(2-sec-butyl-2-oxazoline) (PsecBuOx) are insoluble at body temperature. Since little was known about the polymer’s miscibility behaviour and especially on how the presence of a poorly-water soluble drug impacted their miscibility, a preformulation study was performed. Formulations were investigated with X-ray powder diffraction, differential scanning calorimetry (DSC) and solid-state nuclear magnetic resonance spectroscopy. PEtOx/PPrOx appeared to form an immiscible blend based on DSC and this was even more pronounced after heating. The six drugs that were tested in this work did not show any preference for one of the two phases. PEtOx/PsecBuOx on the other hand appeared to be miscible forming a homogeneous blend between the two polymers and the drugs.

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16

Hoogenboom, Richard, Martin W. M. Fijten, Hanneke M. L. Thijs, Bart M. van Lankvelt und Ulrich S. Schubert. „Microwave-assisted synthesis and properties of a series of poly(2-alkyl-2-oxazoline)s“. Designed Monomers and Polymers 8, Nr. 6 (01.01.2005): 659–71. http://dx.doi.org/10.1163/156855505774597704.

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17

Trachsel, Lucca, Matteo Romio, Shivaprakash N. Ramakrishna und Edmondo M. Benetti. „Fabrication of Biopassive Surfaces Using Poly(2‐alkyl‐2‐oxazoline)s: Recent Progresses and Applications“. Advanced Materials Interfaces 7, Nr. 19 (06.08.2020): 2000943. http://dx.doi.org/10.1002/admi.202000943.

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18

R. de la Rosa, Victor, Werner Nau und Richard Hoogenboom. „Thermoresponsive Interplay of Water Insoluble Poly(2-alkyl-2-oxazoline)s Composition and Supramolecular Host–Guest Interactions“. International Journal of Molecular Sciences 16, Nr. 12 (02.04.2015): 7428–44. http://dx.doi.org/10.3390/ijms16047428.

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19

Chen, C. H., J. Wilson, W. Chen, R. M. Davis und J. S. Riffle. „A light-scattering study of poly(2-alkyl-2-oxazoline)s: effect of temperature and solvent type“. Polymer 35, Nr. 17 (August 1994): 3587–91. http://dx.doi.org/10.1016/0032-3861(94)90532-0.

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20

Wang, Wen-Li, Kousuke Kawai, Hiroaki Sigemitsu und Ren-Hua Jin. „Crystalline lamellar films with honeycomb structure from comb-like polymers of poly(2-long-alkyl-2-oxazoline)s“. Journal of Colloid and Interface Science 627 (Dezember 2022): 28–39. http://dx.doi.org/10.1016/j.jcis.2022.07.041.

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21

Obeid, Rodolphe, Elena Maltseva, Andreas F. Thünemann, Fumihiko Tanaka und Françoise M. Winnik. „Temperature Response of Self-Assembled Micelles of Telechelic Hydrophobically Modified Poly(2-alkyl-2-oxazoline)s in Water“. Macromolecules 42, Nr. 6 (24.03.2009): 2204–14. http://dx.doi.org/10.1021/ma802592f.

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22

Zschoche, Stefan, Juan Rueda, Volodymyr Boyko, Franziska Krahl, Karl-Friedrich Arndt und Brigitte Voit. „Thermo-Responsive Nanogels Based on Poly[NIPAAm-graft- (2-alkyl-2-oxazoline)]s Crosslinked in the Micellar State“. Macromolecular Chemistry and Physics 211, Nr. 9 (26.02.2010): 1035–42. http://dx.doi.org/10.1002/macp.200900559.

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23

Trachsel, Lucca, Castro Johnbosco, Thamar Lang, Edmondo M. Benetti und Marcy Zenobi-Wong. „Double-Network Hydrogels Including Enzymatically Crosslinked Poly-(2-alkyl-2-oxazoline)s for 3D Bioprinting of Cartilage-Engineering Constructs“. Biomacromolecules 20, Nr. 12 (12.11.2019): 4502–11. http://dx.doi.org/10.1021/acs.biomac.9b01266.

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24

Samaro, Aseel, Maarten Vergaelen, Martin Purino, Ali Tigrine, Victor R. de la Rosa, Niloofar Moazami Goudarzi, Matthieu N. Boone, Valérie Vanhoorne, Richard Hoogenboom und Chris Vervaet. „Poly(2-alkyl-2-oxazoline)s: A polymer platform to sustain the release from tablets with a high drug loading“. Materials Today Bio 16 (Dezember 2022): 100414. http://dx.doi.org/10.1016/j.mtbio.2022.100414.

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25

Park, Joon-Sik, und Kazunori Kataoka. „Comprehensive and Accurate Control of Thermosensitivity of Poly(2-alkyl-2-oxazoline)s via Well-Defined Gradient or Random Copolymerization“. Macromolecules 40, Nr. 10 (Mai 2007): 3599–609. http://dx.doi.org/10.1021/ma0701181.

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26

Rettler, Erik F. J., Hanneke M. L. Lambermont-Thijs, Johannes M. Kranenburg, Richard Hoogenboom, Miriam V. Unger, Heinz W. Siesler und Ulrich S. Schubert. „Water uptake of poly(2-N-alkyl-2-oxazoline)s: influence of crystallinity and hydrogen-bonding on the mechanical properties“. Journal of Materials Chemistry 21, Nr. 43 (2011): 17331. http://dx.doi.org/10.1039/c1jm12541a.

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27

Villano, Luca Del, Roald Kommedal, Martin W. M. Fijten, Ulrich S. Schubert, Richard Hoogenboom und Malcolm A. Kelland. „A Study of the Kinetic Hydrate Inhibitor Performance and Seawater Biodegradability of a Series of Poly(2-alkyl-2-oxazoline)s“. Energy & Fuels 23, Nr. 7 (16.07.2009): 3665–73. http://dx.doi.org/10.1021/ef900172f.

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28

Diehl, Christina, Ina Dambowsky, Richard Hoogenboom und Helmut Schlaad. „Self-Assembly of Poly(2-alkyl-2-oxazoline)s by Crystallization in Ethanol-Water Mixtures Below the Upper Critical Solution Temperature“. Macromolecular Rapid Communications 32, Nr. 21 (29.08.2011): 1753–58. http://dx.doi.org/10.1002/marc.201100421.

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29

Bloksma, Meta M., Sarah Rogers, Ulrich S. Schubert und Richard Hoogenboom. „Main-chain chiral poly(2-oxazoline)s: Influence of alkyl side-chain on secondary structure formation in solution“. Journal of Polymer Science Part A: Polymer Chemistry 49, Nr. 13 (28.04.2011): 2790–801. http://dx.doi.org/10.1002/pola.24712.

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30

Morgese, Giulia, Yvonne Gombert, Shivaprakash N. Ramakrishna und Edmondo M. Benetti. „Mixing Poly(ethylene glycol) and Poly(2-alkyl-2-oxazoline)s Enhances Hydration and Viscoelasticity of Polymer Brushes and Determines Their Nanotribological and Antifouling Properties“. ACS Applied Materials & Interfaces 10, Nr. 48 (05.11.2018): 41839–48. http://dx.doi.org/10.1021/acsami.8b17193.

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31

Bloksma, Meta M., Marco M. R. M. Hendrix, Silke Rathgeber, Ulrich S. Schubert und Richard Hoogenboom. „Main-Chain Chiral Poly(2-oxazoline)s: Influence of Alkyl Side-Chain on Secondary Structure Formation in the Solid State“. Macromolecular Symposia 350, Nr. 1 (April 2015): 43–54. http://dx.doi.org/10.1002/masy.201400023.

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32

Brunzel, Michaela, Michael Dirauf, Martin Sahn, Justyna A. Czaplewska, Nicole Fritz, Christine Weber, Ivo Nischang und Ulrich S. Schubert. „On the identification and quantification of proton-initiated species in the synthesis of poly(2-alkyl-2-oxazoline)s by high resolution liquid chromatography“. Journal of Chromatography A 1653 (September 2021): 462364. http://dx.doi.org/10.1016/j.chroma.2021.462364.

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33

Rettler, Erik F. J., Miriam V. Unger, Richard Hoogenboom, Heinz W. Siesler und Ulrich S. Schubert. „Water Uptake of Poly(2-N-Alkyl-2-Oxazoline)s: Temperature-Dependent Fourier Transform Infrared (FT-IR) Spectroscopy and Two-Dimensional Correlation Analysis (2DCOS)“. Applied Spectroscopy 66, Nr. 10 (Oktober 2012): 1145–55. http://dx.doi.org/10.1366/12-06650.

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34

Bouten, P. J. M., Dietmar Hertsen, Maarten Vergaelen, Bryn D. Monnery, Saron Catak, Jan C. M. van Hest, Veronique Van Speybroeck und Richard Hoogenboom. „Synthesis of poly(2-oxazoline)s with side chain methyl ester functionalities: Detailed understanding of living copolymerization behavior of methyl ester containing monomers with 2-alkyl-2-oxazolines“. Journal of Polymer Science Part A: Polymer Chemistry 53, Nr. 22 (29.06.2015): 2649–61. http://dx.doi.org/10.1002/pola.27733.

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35

Mint, Kelly, Joshua P. Morrow, Nicole M. Warne, Xie He, David Pizzi, Shaffiq Zainal Osman Shah, Gregory K. Pierens et al. „Comparison of the hydrophilicity of water-soluble poly(2-alkyl-2-oxazoline)s, poly(2-alkyl-2-oxazine)s and poly(2,4-dialkyl-2-oxazoline)s“. Polymer Chemistry, 2024. http://dx.doi.org/10.1039/d4py00332b.

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Poly(cyclic imino ether)s (PCIEs) including poly(2-alkyl-2-oxazoline) (POx), poly(2-alkyl-2-oxazine) (POz) and poly(2,4-dialkyl-2-oxazoline) (PdOx) are a rapidly emerging polymer class for use in biomedical and therapeutic applications due to the biocompatibility and...

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36

Wiesner (née Diehl), Fiona, Christian Petri, Simone Hageneder, Cleiton Kunzler, Sven Klees, Petra Frank, Matthias Pertiller, Jakub Dostalek, Wolfgang Knoll und Ulrich Jonas. „Thermoresponsive and Photocrosslinkable Poly(2‐alkyl‐2‐oxazoline) Toolbox – Customizable Ultralow‐Fouling Hydrogel Coatings for Blood Plasma Environments“. Macromolecular Rapid Communications, 20.11.2023. http://dx.doi.org/10.1002/marc.202300549.

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AbstractThis study focuses on developing surface coatings with excellent antifouling properties, crucial for applications in the medical, biological, and technical fields, for materials and devices in direct contact with living tissues and bodily fluids such as blood. Our approach combines thermoresponsive poly(2‐alkyl‐2‐oxazoline)s, known for their inherent protein‐repellent characteristics, with established antifouling motifs based on betaines. The polymer framework was constructed from various monomer types, including a novel benzophenone‐modified 2‐oxazoline for photocrosslinking and an azide‐functionalized 2‐oxazoline, allowing subsequent modification with alkyne‐substituted antifouling motifs through copper(I)‐catalyzed azide‐alkyne cycloaddition. From these polymers surface‐attached networks were created on benzophenone‐modified gold substrates via photocrosslinking, resulting in hydrogel coatings with several micrometers thickness when swollen with aqueous media. Given that poly(2‐alkyl‐2‐oxazoline)s can exhibit a lower critical solution temperature in water, we compared their temperature‐dependent solubility to the swelling behavior of the surface‐attached hydrogels upon thermal stimulation. The antifouling performance of these hydrogel coatings in contact with human blood plasma was further evaluated by surface plasmon resonance and optical waveguide spectroscopy. All surfaces demonstrated extremely low retention of blood plasma components, even with undiluted plasma. Notably, hydrogel layers with sulfobetaine moieties allowed efficient penetration by plasma components, which could then be easily removed by rinsing with buffer.This article is protected by copyright. All rights reserved

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37

Pribus, Marek, Luboš Jankovič, Valériá Bizovská Kureková, Martin Barlog und Jana Madejová. „Intercalation Characteristics of Montmorillonite Modified with Poly(2-n-alkyl-2-oxazoline)s“. Macromolecules, 26.08.2024. http://dx.doi.org/10.1021/acs.macromol.4c00291.

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38

Benaoudia, Dihia, Van-Quynh Nguyen, Véronique Bennevault, Pascal Martin, Fabien Montel, Philippe Guégan und Jean-Christophe Lacroix. „Direct Electrografting of Poly(2-alkyl-2-oxazoline)s on Gold, ITO, and Gold Nanoparticles for Biopassivation“. ACS Applied Nano Materials, 01.09.2023. http://dx.doi.org/10.1021/acsanm.3c02379.

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39

Wylie, Ross Andrew Lennox, Robert Miller, Luke Andrew Connal und Greg Guanghua Qiao. „Oligomeric Poly(Oxazoline) as Potential Lithium Battery Electrolytes“. Journal of The Electrochemical Society, 07.06.2022. http://dx.doi.org/10.1149/1945-7111/ac766d.

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Abstract Polymer electrolytes are a promising and inherently suitable material for next generation lithium batteries. Advancement in this field requires the use of new synthetic and fabrication techniques, as well as the investigation of new polymers. Here we report on the development of oligomeric Poly(2-ethyl-2-oxazoline) as a candidate for lithium batteries. By reducing the degree of polymerisation, the glass transition temperature was reduced from 54°C for commercially available 50,000 Da PEtOx to 9.45°C for lab synthesized 890 Da PEtOx. Doping with high concentrations of the lithium salt lithium nitrate, Lithium bis(trifluoromethanesulfonyl)imide, and lithium perchlorate, we demonstrate a glass transition temperature maximum as the polymer electrolyte moves into the polymer-in-salt regime. In this regime we recorded a maximum conductivity of was 3.3 x 10-3 S/cm at 100°C and 67 mol % LiClO4. This study demonstrates the potential for further use of alkyl oxazolines at high lithium salt concentrations and elevated temperatures.

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40

Schubert, Ulrich Sigmar, Philipp Borchers, Michael Dirauf, Maria Strumpf, Helmar Görls, Christine Weber und Martin D. Hager. „Ferrocene Containing Redox-Responsive Poly(2-Oxazoline)s“. Chemical Communications, 2021. http://dx.doi.org/10.1039/d0cc07830a.

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A new monomer, the 2-ferrocene-ethyl-2-oxazoline, was copoly-merized with 2-alkyl-2-oxazolines. The cationic ring opening polymerization (CROP) of 2-oxazolines allows the synthesis of well-defined copolymers with adjustable molar masses as well as...

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41

Tsarenko, Ekaterina, Natalie Göppert, Philipp Dahlke, Mira Behnke, Gauri Gangapurwala, Baerbel Beringer-siemers, Lisa Jaepel et al. „Unveiling the power of liquid chromatography in examining a library of degradable poly(2-oxazoline)s in nanomedicine applications“. Journal of Materials Chemistry B, 2024. http://dx.doi.org/10.1039/d4tb01812e.

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A library of degradable poly(2-alkyl-2-oxazoline) analogues (dPOx) with different length of the alkyl substituents was characterized in detail by gradient elution liquid chromatography. The hydrophobicity increased with elevated side chain...

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42

Finnegan, John R., Emily H. Pilkington, Karen Alt, Md Arifur Rahim, Stephen J. Kent, Thomas P. Davis und Kristian Kempe. „Stealth nanorods via the aqueous living crystallisation-driven self-assembly of poly(2-oxazoline)s“. Chemical Science, 2021. http://dx.doi.org/10.1039/d1sc00938a.

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Triggered by heating, a poly(2-alkyl-2-oxazoline) block copolymer undergoes seeded growth in water forming length tuneable nanorods. Morphology and composition combine to impart low immune cell association and promising blood circulation lifetimes.

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