사진

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Park, Young S. (박영석)

Department
School of Natural Science(자연과학부)
Research Interests
Bottom-up synthesis of graphene nanoribbons, Organic solar cells
Lab
Advanced Organic Materials Lab
Website
https://sites.google.com/site/youngsparkunist
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Issue DateTitleAuthor(s)TypeViewAltmetrics
2020-05Unveiling 79-year-old ixene and its BN-doped derivativePati, Palas Baran; Jin, Eunji; Kim, Yohan, et alARTICLE5
2018-07Contorted polycyclic aromatic hydrocarbon: promising Li insertion organic anodePark, Jaehyun; Lee, Cheol Woo; Joo, Se Hun, et alARTICLE508 Contorted polycyclic aromatic hydrocarbon: promising Li insertion organic anode
2018-06ipso-Arylative polymerization as a route to π-conjugated polymers: synthesis of poly(3-hexylthiophene)Shih, Feng-Yang; Tian, Sisi; Gallagher, Nicholas, et alARTICLE238 ipso-Arylative polymerization as a route to π-conjugated polymers: synthesis of poly(3-hexylthiophene)
2016-03Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene DerivativesPark, Young S.; Dibble, David J.; Kim, Juhwan, et alARTICLE608 Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives
2016-01An Aza-Diels-Alder Approach to Crowded BenzoquinolinesMazaheripour, Amir; Dibble, David J.; Umerani, Mehran J., et alARTICLE577 An Aza-Diels-Alder Approach to Crowded Benzoquinolines
2015-05Synthesis of Polybenzoquinolines as Precursors for Nitrogen-Doped Graphene NanoribbonsDibble, David J.; Park, Young S.; Mazaheripour, Amir, et alARTICLE463 Synthesis of Polybenzoquinolines as Precursors for Nitrogen-Doped Graphene Nanoribbons
2015-02An Aza-Diels-Alder Route to PolyquinolinesDibble, David J.; Umerani, Mehran J.; Mazaheripour, Amir, et alARTICLE459 An Aza-Diels-Alder Route to Polyquinolines
2014-09Polymerization of Tellurophene Derivatives by Microwave-Assisted Palladium-Catalyzed ipso-Arylative PolymerizationPark, Young S.; Wu, Qin; Nam, Chang-Yong, et alARTICLE467 Polymerization of Tellurophene Derivatives by Microwave-Assisted Palladium-Catalyzed ipso-Arylative Polymerization
2014-07Effects of heteroatom substitution in conjugated heterocyclic compounds on photovoltaic performance: from sulfur to telluriumPark, Y. S.; Kale, T. S.; Nam, C. -Y., et alARTICLE401 Effects of heteroatom substitution in conjugated heterocyclic compounds on photovoltaic performance: from sulfur to tellurium
2012-03Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar CellsNam, Chang-Yong; Qin, Yang; Park, Young S., et alARTICLE432 Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar Cells
2011-06Conductance of Single Cobalt Chalcogenide Cluster JunctionsBoardman, Brycelyn M.; Widawsky, Jonathan R.; Park, Young S., et alARTICLE368 Conductance of Single Cobalt Chalcogenide Cluster Junctions
2010-07Reliable Formation of Single Molecule Junctions with Air-Stable Diphenylphosphine LinkersParameswaran, R.; Widawsky, J. R.; Vazquez, H., et alARTICLE449 Reliable Formation of Single Molecule Junctions with Air-Stable Diphenylphosphine Linkers
2009-08Frustrated Rotations in Single-Molecule JunctionsPark, Young S.; Widawsky, Jonathan R.; Kamenetska, Maria, et alARTICLE457 Frustrated Rotations in Single-Molecule Junctions
2009-03Formation and Evolution of Single-Molecule JunctionsKamenetska, M.; koentopp, M.; Whalley, A. C., et alARTICLE414 Formation and Evolution of Single-Molecule Junctions
2007-12Contact chemistry and single-molecule conductance: A comparison of phosphines, methyl sulfides, and aminesPark, Young S.; Whalley, Adam C.; Kamenetska, Maria, et alARTICLE448 Contact chemistry and single-molecule conductance: A comparison of phosphines, methyl sulfides, and amines
2007-02Electronics and chemistry: Varying single-molecule junction conductance using chemical substituentsVenkataraman, Latha; Park, Young S.; Whalley, Adam C., et alARTICLE477 Electronics and chemistry: Varying single-molecule junction conductance using chemical substituents
2003-06Comparison of the liquid crystalline properties of dimesogenic compounds bearing alkoxy and perfluoroalkoxy tailsLee, Jun-Woo; Park, Yongseok; Jin, Jung-Il, et alARTICLE507 Comparison of the liquid crystalline properties of dimesogenic compounds bearing alkoxy and perfluoroalkoxy tails
2003-02Dimeric liquid crystalline compounds having a central malonic acid moiety: effect of the length of the spacers and terminal chainsPark, Young Suk; Lee, Kyung-Hoon; Lee, Jun-Woo, et alARTICLE496 Dimeric liquid crystalline compounds having a central malonic acid moiety: effect of the length of the spacers and terminal chains
2002-09Dimeric compounds containing malonic acid as the central linking unit: synthesis and mesomorphic propertiesPrasad, Veena; Lee, Kyung-Hoon; Park, Young Suk, et alARTICLE556 Dimeric compounds containing malonic acid as the central linking unit: synthesis and mesomorphic properties
2002-09Synthesis and liquid crystalline properties of hyperbranched aromatic polyesters consisting of azoxybenzene mesogens and polymethylene spacersPark, Young Suk; Lee, Jun-Woo; Jin, Jung-IlARTICLE523

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