Academic literature on the topic 'Hyperbranched polyacetal'

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Journal articles on the topic "Hyperbranched polyacetal"

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Chen, Rui, and Liqun Wang. "Synthesis of an amphiphilic hyperbranched polymer as a novel pH-sensitive drug carrier." RSC Advances 5, no. 26 (2015): 20155–59. http://dx.doi.org/10.1039/c4ra16935b.

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An amphiphilic hyperbranched polymer containing large amounts of pH sensitive bonds was synthesized. The hydrophobic chains are hyperbranched polyacetals and the hydrophilic chains are polyethylene glycols, attached to the hyperbranched polyacetals by hydrazone bonds.
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Chatterjee, Saptarshi, and S. Ramakrishnan. "Hyperbranched Polyacetals with Tunable Degradation Rates." Macromolecules 44, no. 12 (2011): 4658–64. http://dx.doi.org/10.1021/ma2004663.

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Kudo, Hiroto, Shuhei Matsubara, Hiroki Yamamoto, and Takahiro Kozawa. "Synthesis and Resist Properties of Hyperbranched Polyacetals." Journal of Photopolymer Science and Technology 28, no. 1 (2015): 125–29. http://dx.doi.org/10.2494/photopolymer.28.125.

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Yi, Lu, Jin Yu-cun, Cao Mo-yuan, et al. "SYNTHESIS AND CHARACTERIZATION OF CORE-CONTANING HYPERBRANCHED POLYACETALS WITH HYDROLYSABLE BACKBONE." Acta Polymerica Sinica 013, no. 3 (2013): 391–97. http://dx.doi.org/10.3724/sp.j.1105.2013.12302.

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Duan, Xiao, Yalan Wu, Mengsi Ma, et al. "Amphiphilic polymer–drug conjugates based on acid-sensitive 100% hyperbranched polyacetals for cancer therapy." Journal of Materials Science 52, no. 16 (2017): 9430–40. http://dx.doi.org/10.1007/s10853-017-1135-1.

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Liu, Na, Joan Vignolle, Jean-Marc Vincent, et al. "One-Pot Synthesis and PEGylation of Hyperbranched Polyacetals with a Degree of Branching of 100%." Macromolecules 47, no. 5 (2014): 1532–42. http://dx.doi.org/10.1021/ma4026509.

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Matsukizono, Hiroyuki, Kozo Matsumoto, and Takeshi Endo. "Multifunctional Cyclic Carbonates Comprising Hyperbranched Polyacetals: Synthesis and Applications to Polymer Electrolytes and Networked Polymer Materials." Journal of Polymer Science Part A: Polymer Chemistry 57, no. 23 (2019): 2295–303. http://dx.doi.org/10.1002/pola.29526.

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Klein, Rebecca, Christoph Schüll, Elena Berger-Nicoletti, Michael Haubs, Klaus Kurz, and Holger Frey. "ABA Triblock Copolymers Based on Linear Poly(oxymethylene) and Hyperbranched Poly(glycerol): Combining Polyacetals and Polyethers." Macromolecules 46, no. 22 (2013): 8845–52. http://dx.doi.org/10.1021/ma4015565.

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Kudo, Hiroto, Mari Fukunaga, Kohei Shiotsuki, et al. "Synthesis of hyperbranched polyacetals containing C-(4-t-butylbenz)calix[4]resorcinarene: Resist properties for extreme ultraviolet (EUV) lithography." Reactive and Functional Polymers 131 (October 2018): 361–67. http://dx.doi.org/10.1016/j.reactfunctpolym.2018.08.013.

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Kudo, Hiroto, Shuhei Matsubara, Hiroki Yamamoto, and Takahiro Kozawa. "Synthesis of hyperbranched polyacetals via a n + b2 -type polyaddition (n = 3, 8, 18, and 21): Candidate resists for extreme ultraviolet lithography." Journal of Polymer Science Part A: Polymer Chemistry 53, no. 20 (2015): 2343–50. http://dx.doi.org/10.1002/pola.27686.

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Dissertations / Theses on the topic "Hyperbranched polyacetal"

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Liu, Na. "Nouveaux polymères issus de la polymérisation par étapes organocatalysée de monomères aldéhydiques : polyaldols et polybenzoïnes linéaires et polyacétals hyperramifiés." Thesis, Bordeaux 1, 2013. http://www.theses.fr/2013BOR15265/document.

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A partir des mêmes briques élémentaires portant des fonctions aldéhydes et mettant en jeu des catalyseurs différents, trois types de nouveaux polymères ont été synthétisés par la polymérisation par étape dans ce travail. Dans la première partie, bis-cétone et bis-aldéhyde monomères ont directement polymérisé dans des conditions stoechiométriques par ce processus offrant polyaldols. Divers catalyseurs et des effets de la nature du solvant ont ensuite été étudiés. Dans la deuxième partie, nous avons travaillé sur la polymérisation organo-catalysée de monomères bis-aldéhydes par des précurseurs d
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Chatterjee, Saptarshi. "Hyperbranched Polyacetals and Polydithioacetals." Thesis, 2013. http://etd.iisc.ernet.in/2005/3436.

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Dendrimers are a class of perfectly branched symmetric monodisperse macromolecules, which are synthesized using a stepwise procedure. Due to their highly symmetric structure, they possess a definite core, discrete generations and a large number of terminal units. The large number of terminal units and its compact globular conformation endow this class of macromolecules with several unique properties. Over the past two decades, a number of researchers have synthesized a variety of dendrimers and explored their potential applications in various fields ranging from drug delivery, energy harvestin
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