Suh, DH Jung, SH Park, SJ Kim, DY Cho, HN 2024-01-21T06:04:39Z 2024-01-21T06:04:39Z 2021-09-02 2004-12 1542-1406 https://pubs.kist.re.kr/handle/201004/137027 Highly phenyl-substituted fluorene copolymers with hole and electron transporting moieties in the main chain were synthesized by using Diels-Alder polymerization. These polymers show good solubility in common organic solvents, high thermal stability, and strong blue photoluminescence in solid films. Cyclic voltammetry studies revealed that these polymers possess low-lying HOMO energy towels ranging from - 5.99 to - 6.00 eV. English TAYLOR & FRANCIS LTD Synthesis and properties of highly phenyl-substituted fluorene copolymers containing hole and electron transporting moieties via Diels-Alder polymerization Article 10.1080/15421400490506108 1 MOLECULAR CRYSTALS AND LIQUID CRYSTALS, v.424, pp.159 - 165 MOLECULAR CRYSTALS AND LIQUID CRYSTALS 424 159 165 N scie scopus 000226415900021 2-s2.0-24644468156 Chemistry, Multidisciplinary Crystallography Materials Science, Multidisciplinary Chemistry Crystallography Materials Science Article; Proceedings Paper LIGHT-EMITTING DIODES POLYFLUORENE POLYMERS Diels-Alder reaction highly phenyl-substituted fluorene copolymer photoluminescence