Relevant bibliographies by topics / Thermoresponsivity

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  1. Journal articles

Academic literature on the topic 'Thermoresponsivity'

Author: Grafiati
Published: 1 April 2023

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Journal articles on the topic "Thermoresponsivity"

1

Pineda-Contreras, Beatriz A., Holger Schmalz, and Seema Agarwal. "pH dependent thermoresponsive behavior of acrylamide–acrylonitrile UCST-type copolymers in aqueous media." Polymer Chemistry 7, no. 10 (2016): 1979–86. http://dx.doi.org/10.1039/c6py00162a.

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2

Li, Yinwen, Huilong Guo, Yunfei Zhang, et al. "Pseudo-graft polymer based on adamantyl-terminated poly(oligo(ethylene glycol) methacrylate) and homopolymer with cyclodextrin as pendant: its thermoresponsivity through polymeric self-assembly and host–guest inclusion complexation." RSC Adv. 4, no. 34 (2014): 17768–79. http://dx.doi.org/10.1039/c3ra47861k.

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3

Amemori, Shogo, Kazuya Iseda, Shizuka Anan, Toshikazu Ono, Kenta Kokado, and Kazuki Sada. "Thermoresponsivity of polymer solution derived from a self-attractive urea unit and a self-repulsive lipophilic ion unit." Polymer Chemistry 8, no. 26 (2017): 3921–25. http://dx.doi.org/10.1039/c7py00591a.

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4

Zhang, Hongcan, Jian Zhang, Wenxue Dai, and Youliang Zhao. "Facile synthesis of thermo-, pH-, CO2- and oxidation-responsive poly(amido thioether)s with tunable LCST and UCST behaviors." Polymer Chemistry 8, no. 37 (2017): 5749–60. http://dx.doi.org/10.1039/c7py01351e.

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Multi-responsive N-substituted poly(amido thioether) copolymers synthesized by one-pot amine–thiol–acrylate polyaddition could exhibit composition-dependent and stimuli-triggered single or double thermoresponsivity.
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5

Fischer, Thorsten, Dan E. Demco, Radu Fechete, Martin Möller, and Smriti Singh. "Poly(vinylamine-co-N-isopropylacrylamide) linear polymer and hydrogels with tuned thermoresponsivity." Soft Matter 16, no. 28 (2020): 6549–62. http://dx.doi.org/10.1039/d0sm00408a.

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Poly(vinylamine-co-N-isopropylacrylamide) linear polymers and hydrogels with tuned thermoresponsivity have been synthetized. They morphology and chain dynamics where investigated by rheology and <sup>1</sup>H NMR spectroscopy, relaxometry and diffusometry.
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6

Cazares-Cortes, Esther, Benjamin C. Baker, Kana Nishimori, Makoto Ouchi, and François Tournilhac. "Polymethacrylic Acid Shows Thermoresponsivity in an Organic Solvent." Macromolecules 52, no. 15 (2019): 5995–6004. http://dx.doi.org/10.1021/acs.macromol.9b00412.

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7

Liu, Fangyao, and Seema Agarwal. "Thermoresponsive Gold Nanoparticles with Positive UCST-Type Thermoresponsivity." Macromolecular Chemistry and Physics 216, no. 4 (2014): 460–65. http://dx.doi.org/10.1002/macp.201400497.

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8

Marsili, Lorenzo, Michele Dal Bo, Federico Berti, and Giuseppe Toffoli. "Chitosan-Based Biocompatible Copolymers for Thermoresponsive Drug Delivery Systems: On the Development of a Standardization System." Pharmaceutics 13, no. 11 (2021): 1876. http://dx.doi.org/10.3390/pharmaceutics13111876.

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Chitosan is a natural polysaccharide that is considered to be biocompatible, biodegradable and non-toxic. The polymer has been used in drug delivery applications for its positive charge, which allows for adhesion with and recognition of biological tissues via non-covalent interactions. In recent times, chitosan has been used for the preparation of graft copolymers with thermoresponsive polymers such as poly-N-vinylcaprolactam (PNVCL) and poly-N-isopropylamide (PNIPAM), allowing the combination of the biodegradability of the natural polymer with the ability to respond to changes in temperature.
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9

Burova, Tatiana V., Valerij Y. Grinberg, Natalia V. Grinberg, et al. "Salt-Induced Thermoresponsivity of a Cationic Phosphazene Polymer in Aqueous Solutions." Macromolecules 51, no. 20 (2018): 7964–73. http://dx.doi.org/10.1021/acs.macromol.8b01621.

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10

Ghosh, Partha S., and Andrew D. Hamilton. "Supramolecular Dendrimers: Convenient Synthesis by Programmed Self-Assembly and Tunable Thermoresponsivity." Chemistry - A European Journal 18, no. 8 (2012): 2361–65. http://dx.doi.org/10.1002/chem.201103051.

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