Epoxy resin with high thermal conductivity (λ) are widely used in electronic packaging, bonding, and coating. However, those with high intrinsic λ, typically synthesized using biphenyl or aromatic rings extended by ester linkages as the mesogenic unit, often exhibit high liquid crystal transition temperatures and poor processability. In this study, a series of naphthalene-based liquid crystal epoxy monomers (LCE) were synthesized, using naphthalene as the mesogenic unit and modifying the flexible chain length on both sides. The resulting LCE were cured within their liquid crystal phase to form naphthalene liquid crystal epoxy resin (LCER). The results show that the network order, radius of gyration, and low-frequency vibrational density of states all initially increase and then decrease with increasing flexible chain length. For LCER2, with a three-carbon flexible chain, these parameters reach their maximum values, facilitating phonon diffusion and enhancing λ. The liquid crystal transition temperature, λ, heat resistance index, and storage modulus of LCER2 were 67~78oC, 0.40 W/(m·K), 158.8oC and 2059 MPa, respectively, approximately 2.2 times higher than that of E-51 resin (0.18 W/(m·K)). This work offers insights into designing epoxy resins with low liquid crystal transition temperature, high intrinsic λ, and excellent mechanical properties for thermal management.
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http://dx.doi.org/10.1002/anie.202501459 | DOI Listing |
Angew Chem Int Ed Engl
March 2025
Northwestern Polytechnical University, School of Chemistry and Chemical Engineering, CHINA.
Epoxy resin with high thermal conductivity (λ) are widely used in electronic packaging, bonding, and coating. However, those with high intrinsic λ, typically synthesized using biphenyl or aromatic rings extended by ester linkages as the mesogenic unit, often exhibit high liquid crystal transition temperatures and poor processability. In this study, a series of naphthalene-based liquid crystal epoxy monomers (LCE) were synthesized, using naphthalene as the mesogenic unit and modifying the flexible chain length on both sides.
View Article and Find Full Text PDFSmall
March 2025
Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.
The fabrication of liquid crystalline (LC) organogel via supramolecular interactions between Deoxyribonucleic acid (DNA) and lyotropic cationic surfactant containing cyanobiphenyl moiety is reported. The fabricated organogel endows dominantly viscous behavior in dimethyl sulfoxide (DMSO) and elastic behavior in n-propanol (n-PrOH), respectively. By judiciously controlling the viscosity, DMSO organogels can be drawn to form a fiber with an elongation of up to 4.
View Article and Find Full Text PDFJ Phys Condens Matter
March 2025
Department of Chemistry, University of Basel, Gebäude 1096 / Mattenstrasse 22, Basel, 4058, SWITZERLAND.
Lipidic mesophases (LMPs) are lyotropic liquid crystals formed by the self-assembly of lipid in water, offering diverse phase symmetries with unique physicochemical properties. However, a fundamental understanding of how the dynamics relate to the composition and structure remains limited. In this study, we substitute water with glycerol, which closely resembles the headgroup structure of phytantriol, as the solvent to explore phytantriol-based LMPs in a pure glycerol environment.
View Article and Find Full Text PDFSmall
March 2025
School of Materials Science and Engineering, Peking University, Beijing, 100871, PR China.
The reversible isomerization behavior of molecular switches in liquid crystal elastomers (LCEs) usually only can be monotonically repeated, because the molecular motion environment is the same for each isomerization cycle in a permanently cross-linked polymer network. Therefore, achieving a tunable photostationary state (PSS) in the same LCE material system is a significant challenge. Herein, a spiropyran-based material (SPBM) as the molecular switch is introduced into a LCE system, which constructed a typical photo-responsive material with reversible isomerization behavior.
View Article and Find Full Text PDFACS Sens
March 2025
Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.
The surface-induced ordering of liquid crystals (LC) has been harnessed to detect a wide range of chemical and biological stimuli. In most sensor designs, the information-rich response of the LC is transduced from an analyte-triggered change in the out-of-plane orientation of the LC. Quantifying the out-of-plane LC orientation, however, is often complicated by simultaneous changes in the in-plane orientation of the LC when using polarized light for transduction.
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