Index Name
Gal, Yeong-SoonAlternative Writings
Gal, Y.S.; Gal, YeongsoonSimilar Names
Gal, Y.-S.Co-authors
Cho, Hyun-Nam; Choi, Byung-Chun; Choi, Sam-Kwon; Chun, Jong-Han; Gui, Tai-Long; Hwang, Chan-Koo; Hwang, Jin-Taek; Jang, Mi-Sun; Jang, Sang-Hee; Jeong, Hwan-Hee; Jeong, Yeon Tae; Jin, Sung-Ho; Jung, Hwan-Hee; Jung, Min-Ho; Jung, Seung-Jin; Jwa, Seung-Taek; Kim, Bong-Shik; Kim, Dong-Won; Kim, Hyun Gyu; Kim, Mi-Kyoung; Kim, Mi-Ra; Kim, Sang-Youl; Kim, Sang-Yul; Kim, Sung-Chul; Kim, Sung-Hoon; Kim, Sung-Hyun; Ko, Jang-Myoun; Koh, Kwang-Nak; Koo, Bon-Kweon; Kwak, Young-Woo; Lee, Chang-Jun; Lee, Eun-Jae; Lee, Hyung-Jong; Lee, Jae-Wook; Lee, Ji-Hoon; Lee, Jin-Kook; Lee, Min Young; Lee, Sang-Gu; Lee, Sang-Seob; Lee, Seok-Joo; Lee, Won-Chul; Lee, Won-Chull; Lim, Kwon-Taek; Lyoo, Won Seok; Moon, Seong-Bae; Naidu, B. Vijaya Kumar; Naidu, B.V.K.; Park, Jong-Wook; Park, Seong-Ha; Park, Sung-Min; Park, Young-Il; Shim, Jong-Min; Shim, Sang-Yeon; Shim, Yoon-Bo; Shin, Won Suk; Suh, Han-Na; Suh, Hong-Suk; Wang, Dong-Xing; Wang, Jian-Min; Wang, Yue; Yin, Jing-HuaPublication Titles
1997: Thermal properties and morphology of liquid crystalline copolyester and polyester elastomer blends1999: Double ring-forming cyclopolymerization of tripropargylammonium salts by transition metal catalysts
1999: Polymerization of 4-hydroxy-n-propargylpiperidine by transition metal catalysts
1999: Synthesis and electro-optical properties of poly(2-ethynylpyridiniumtosylate) having propagyl side chain
2000: Polymerization of 1-butyl-2-trimethylsilylacetylene by transition metal catalysts
2002: Cyclopolymerization of dipropargyl derivatives by Cp2MoCl2-EtAlCl2 catalyst system
2002: Synthesis and Characterization of Highly Luminescent Asymmetric Poly(p-phenylene vinylene) Derivatives for Light-Emitting Diodes
2003: Polymerization of 4-Dimethylamino-N-propargylpyridinium Bromide by Transition Metal Catalysts
2006: Synthesis and Characterization of Regiosymmetric Poly(3,4-propylenedioxythiophene) Derivative
2006: Synthesis and EL Properties of Light-Emitting Polymers by Gilch Polymerization
2006: Synthesis and Electro-Optical Properties of Poly(4-ethynylaniline)
2006: Synthesis and Optical Properties of Poly(2-substituted-9,9-dipropargylfluorene)s
2007: Electrochemical Properties of Ionic Conjugated Polymer with Azobenzene Moieties
2007: Introduction of Interlayer via Oxetane Based Crosslinking Method for Blue Polymer Light-Emitting Diode Applications
2007: Photovoltaic Properties of N-Pyrrolidinyl Substituted Perylenebis(dicarboximide) Derivatives
2007: Polymeric Photovoltaic Devices Based on Tricomponent System Composed of a Blend of Donor and PCBM Acceptor Material
2007: Synthesis and Characterization of a Light-Emitting Poly(p-phenylenevinylene)-Based Copolymer Containing 1,3,4-Oxadiazole Functionality
2007: Synthesis and Electro-Optical Propertiesof a Polyacetylene Derivative: Poly(Ethynylestradiol3-Methyl Ether)
2007: Synthesis and Electrochemical Properties of Poly[N-(6-azidohexyl)-2-ethynylpyridinium tetraphenylborate]
2007: Synthesis and Properties of Conjugated Polymer with Carboxylic Acids
2008: Electro-Optical and Electrochemical Properties of Poly(2-ethynylpyridine)
2008: Electrochemical Properties of a Self-Dopable Ionic Conjugated Polymer: Poly[2-ethynyl-N-(4-sulfobutyl)pyridinium betaine]
2008: Synthesis and Properties of a Polyacetylene Derivative: Poly(17α-Ethynylestradiol)
2009: Electro-Optical and Electrochemical Properties of Poly(2-ethynyl-N-glycidylpyridinium bromide)
2009: Electro-Optical and Electrochemical Properties of Poly(phenylacetylene)
2009: Multiple Morphologies of Self-Assembled Amphiphilic Poly(FOMA-b-EO) Diblock Copolymers
2009: Preparation, Structural and Spectral Properties of Poly(2-ethynylbenzyl alcohol)
Sources
Chem. Mater., 14, 643J. Macromol. Sci., Pure Appl. Chem., A34, 1645
J. Macromol. Sci., Pure Appl. Chem., A36, 1503
J. Macromol. Sci., Pure Appl. Chem., A36, 429
J. Macromol. Sci., Pure Appl. Chem., A36, 531
J. Macromol. Sci., Pure Appl. Chem., A37, 133
J. Macromol. Sci., Pure Appl. Chem., A39, 237
J. Macromol. Sci., Pure Appl. Chem., A40, 401
Mol. Cryst. Liq. Cryst., 444, 1
Mol. Cryst. Liq. Cryst., 444, 129
Mol. Cryst. Liq. Cryst., 458, 237
Mol. Cryst. Liq. Cryst., 459, 19
Mol. Cryst. Liq. Cryst., 462, 103
Mol. Cryst. Liq. Cryst., 462, 189
Mol. Cryst. Liq. Cryst., 462, 59
Mol. Cryst. Liq. Cryst., 463, 63
Mol. Cryst. Liq. Cryst., 471, 137
Mol. Cryst. Liq. Cryst., 471, 335
Mol. Cryst. Liq. Cryst., 472, 239
Mol. Cryst. Liq. Cryst., 472, 271
Mol. Cryst. Liq. Cryst., 491, 270
Mol. Cryst. Liq. Cryst., 491, 348
Mol. Cryst. Liq. Cryst., 492, 229
Mol. Cryst. Liq. Cryst., 508, 173
Mol. Cryst. Liq. Cryst., 513, 196
Mol. Cryst. Liq. Cryst., 513, 293
Mol. Cryst. Liq. Cryst., 513, 320
