CAU Scholar's Space: Park, Kwangyong

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Park, Kwangyong (박광용)

공과대학 (화학공학과)

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Tel 02-820-5330
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crosscoupling:5||Single crystal:3||mPW1PW91:3||Parallel synthesis:2||HOMO and LUMO:2||HornerWadsworthEmmons reaction:2||nickel catalyst:2||arenesulfonates:2||Diabetes:2||cytotoxicity:2||Organic light emitting diodes:2||dental composite:2||AMPK:2||spiro orthocarbonate:2||chalcone derivatives:2||Combinatorial synthesis:2||ClaisenSchmidt condensation:1||Complexation:1||Conformer:1||Crosscoupling:1||DFT B3LYP:1||DNA nanodevices:1||Device structure:1||Diaminecored tetrastilbene:1||DielsAlder adduct:1||Distyrylarylene derivatives:1||Electron transport layer:1||Fatty acid oxidation:1||Freeradical scavenging activity:1||Fullerene bisadducts:1||Gas adsorption:1||Gibbs free energies:1||Graphene:1||Grignard reagents:1||Halide Anion:1||Heteroditopic:1||Hole transport layer:1||HornerWadsworthEmmons:1||IR:1||Insulin resistance:1||Interfacial layer:1||Liquidphase synthesis:1||Luminescent materials:1||Methylene bridgemonosubstituted tetramethoxycalix[4]arene:1||NHeterocyclic carbene:1||NOESY spectra:1||Oligopphenylene:1||Open circuit voltage:1||Organic fluorescent materials:1||Organic solar cell:1||Organogermanium compound:1||Phloroglucinol:1||Polymer solar cells:1||Polymerbound arenesulfonate preparation:1||Polymerbound arenesulfonates with Aryl Grignard reagents:1||Polymerbound biphenylsulfonate preparation:1||Polymerbound sulfonate preparation:1||Quaterphenyl:1||Reducing power:1||Regioselective substitution:1||S(N)2 reaction:1||SOC:1||Secondharmonic generating efficiency:1||Singlecrystal structure:1||Solidphase synthesis:1||Soluble support:1||Solution process:1||Stability:1||Stilbene:1||Substituted dieckol:1||Sulfonate linker:1||SuzukiMiyaura reaction:1||Terphenyl:1||Tetraaryldiamine:1||Tetrahedral:1||Total synthesis:1||Traceless:1||Traceless cleavage:1||Trihydroxychalcone:1||Triphenylethene:1||UV:1||UV Spectrum:1||Unfunctionalized arenes:1||Work function:1||Xray structure:1||Xray structure analysis:1||active layer:1||alkyl biphenylsulfonates:1||anionic pathway:1||antibacterial:1||antidiabetic compounds:1||aromatic ring cleavage:1||aromatic substituents:1||arylboronic acid:1||asymmetric SOC:1||betafluoropyrrole:1||biaryls:1||biphenylsulfonates:1||bisGMA derivatives:1||bromobenzenesulfonates:1||bromophenols:1||brown algae:1||carboncarbon crosscoupling:1||carbonate:1||chlorine resistance:1||combinatorial synthesis:1||composite membrane:1||crosslinked polybutadiene:1||curing shrinkage:1||cyclic thionocarbonate:1||dental:1||diametral tensile strength:1||dieckol:1||dimethyl cardamonin:1||effect size:1||effectiveness of education:1||electronic activation:1||engineering ethics education:1||engineers' responsibility:1||expandable:1||glycidyl methacrylate derivatives:1||graphene oxides:1||homogeneous nickel catalyst:1||hydrogenolysis:1||layerbylayer:1||manganese peroxidase:1||mechanical strength:1||metaanalysis:1||monomer mixture:1||multifunctional cleavage:1||multilayer nanofilms:1||ndoping:1||nickelcatalyst:1||nonsmalllung cancer cell:1||organic light emitting diode:1||osteogenic differentiation:1||pentaerythritol:1||phlorofucofuroeckolA:1||phlorotannin:1||photopolymerization:1||pipi stacking:1||primary alkyl grignard reagents:1||pyrrole derivatives:1||radical coupling:1||regioselective substitution:1||regiospecific modification:1||resin matrix:1||restoratives:1||reverse osmosis:1||secondary alkyl Grignard reagents:1||selective index:1||solid phase organic synthesis:1||solidphase synthesis:1||spiro orthocarbonates:1||spiroortho:1||stilbenesulfonates:1||substituted hydroquinones:1||substituted phenols:1||sulfonate:1||thermally degradable:1||tincored:1||total synthesis:1||traceless linker:1||traceless multifunctional cleavage:1||transStilbene:1||unsymmetrical terphenyls:1||unsymmetrical transstilbenes:1||vanillylacetone:1||(Z)4 '(1Phenyl2ptolylvinyl)biphenyl4carbaldehyde:1||volumetric shrinkage:1||2(Biphenyl4yl)1(4bromophenyl)1phenylethene:1||2′,4′,6′trimethoxy3′,5′dimethylchalcone:1||2′,4′,6′trimethoxy3′,5′dimethylchalcones:1||4 ',6 'dimethoxy2 'hydroxy3 ',5 'dimethylchalcone:1||Alkali metal cation:1||Aminebased compounds:1||Anticancer activity:1||Arenesulfonate:1||Arenesulfonate, crosscoupling reaction:1||Atherosclerosis:1||Benzaldehyde:1||Benzyne:1||Biaryls:1||BisGMA alternatives:1||Calix[4]diquinone:1||

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