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Synthesis and phase behavior of chiral liquid crystalline polymeric networks derived from menthol.
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- High Performance Polymers, 2012, v. 24, n. 8, p. 673, doi. 10.1177/0954008312449843
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- Article
Side-chain Cholesteric Liquid Crystalline Elastomers Derived from Nematic Bis-olefinic Crosslinking Units.
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- Macromolecular Chemistry & Physics, 2003, v. 204, n. 17, p. 2123, doi. 10.1002/macp.200350072
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- Article
New thermochromic liquid–crystalline polymer: Synthesis and phase behavior.
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- Journal of Applied Polymer Science, 2005, v. 98, n. 1, p. 329
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- Article
New side‐chain liquid‐crystalline ionomers. I. Synthesis and characterization of a homopolymer derived from ionic mesogenic groups.
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- Journal of Applied Polymer Science, 2004, v. 93, n. 6, p. 2511
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- Article
Synthesis, structures, and properties of side-chain cholesteric liquid-crystalline polysiloxanes.
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- Journal of Applied Polymer Science, 2003, v. 89, n. 14, p. 3944
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- Article
Synthesis and properties of side chain cholesteric liquid-crystalline polyacrylates containing two mesogenic groups.
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- Journal of Applied Polymer Science, 2003, v. 88, n. 8, p. 1936
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- Article
Synthesis and phase behavior of chiral side-chain liquid-crystalline polysiloxanes containing two mesogenic groups.
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- Journal of Applied Polymer Science, 2002, v. 86, n. 11, p. 2670, doi. 10.1002/app.11213
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- Article
Liquid crystalline properties of cholesteric elastomers based on a mesogenic monomer containing menthyl groups.
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- Polymer International, 2012, v. 61, n. 7, p. 1186, doi. 10.1002/pi.4198
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- Article
Cholesteric monomer and elastomers containing menthyl groups: Synthesis and phase behavior.
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- Journal of Applied Polymer Science, 2012, v. 125, n. 5, p. 3849, doi. 10.1002/app.36701
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- Article
Synthesis, structure, and phase behavior of new chiral liquid-crystalline polysiloxanes based on mesogenic menthyl monomers.
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- Journal of Applied Polymer Science, 2009, v. 111, n. 6, p. 3016, doi. 10.1002/app.29318
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- Article
Synthesis and phase behavior of new cholesteric liquid-crystalline copolymers containing chiral mesogenic groups derived from menthol derivatives.
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- Journal of Applied Polymer Science, 2008, v. 109, n. 4, p. 2187, doi. 10.1002/app.28045
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- Article
Side-chain copolymers containing smectic monomer and chiral reagent-Synthesis and characterization.
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- Journal of Applied Polymer Science, 2008, v. 108, n. 2, p. 1265, doi. 10.1002/app.27670
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- Article
Synthesis and mesomorphic properties of cholesteric elastomers based on chiral mesogenic crosslinking agent.
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- Journal of Applied Polymer Science, 2008, v. 107, n. 2, p. 1343, doi. 10.1002/app.26785
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- Article
Synthesis and mesomorphic properties of side‐chain cholesteric liquid‐crystalline polymers containing menthyl groups.
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- Journal of Applied Polymer Science, 2006, v. 102, n. 6, p. 5559
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- Article
Synthesis and mesomorphic properties of a new side‐chain, chiral smectic, liquid‐crystalline elastomer.
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- Journal of Applied Polymer Science, 2006, v. 100, n. 5, p. 4234
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- Article
Synthesis and characterization of side‐chain cholesteric liquid‐crystalline polymers derived from steroid substituents.
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- Journal of Applied Polymer Science, 2006, v. 99, n. 5, p. 2330
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- Article
Study on the structure, melting, and nonisothermal crystallization behaviors of isotactic polypropylene with nematic liquid crystalline polymer as a new β-nucleating agent.
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- Polymer Science -- Series A, 2015, v. 57, n. 1, p. 67, doi. 10.1134/S0965545X15010058
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- Article
New chiral liquid crystalline monomers, polymers, and elastomers derived from menthol derivatives: synthesis and mesomorphism.
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- Journal of Materials Science, 2014, v. 49, n. 3, p. 1229, doi. 10.1007/s10853-013-7806-7
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- Article
A nematic liquid crystalline polymer as highly active novel β-nucleating agent for isotactic polypropylene.
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- Journal of Materials Science, 2013, v. 48, n. 11, p. 4032, doi. 10.1007/s10853-013-7215-y
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- Article
Synthesis and Self-Assembled Behavior of pH-Responsive Chiral Liquid Crystal Amphiphilic Copolymers Based on Diosgenyl-Functionalized Aliphatic Polycarbonate.
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- Nanomaterials (2079-4991), 2017, v. 7, n. 7, p. 169, doi. 10.3390/nano7070169
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- Article