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Hyonseok Hwang, Ph.D. - Publications

Affiliations: 
2003 University of Texas at Austin, Austin, Texas, U.S.A. 
Area:
Condensed Phase Chemical Dynamics
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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 So H, Mun MS, Kim M, Kim JH, Lee JH, Hwang H, An DK, Lee KM. Deboronation-Induced Ratiometric Emission Variations of Terphenyl-Based --Carboranyl Compounds: Applications to Fluoride-Sensing. Molecules (Basel, Switzerland). 25. PMID 32455846 DOI: 10.3390/Molecules25102413  0.34
2020 Kim S, Lee JH, So H, Kim M, Mun MS, Hwang H, Park MH, Lee KM. Insights into the effects of substitution position on the photophysics of mono-o-carborane-substituted pyrenes Inorganic Chemistry Frontiers. 7: 2949-2959. DOI: 10.1039/D0Qi00563K  0.306
2020 Hong JH, Kim S, So H, Lee JH, Hwang H, Lee KM. Intriguing ‘Turn-on’ phosphorescent response in the near infrared region upon fluoride binding: Dipyrromethene chelating-based Triarylboryl‒Iridium(III) conjugates Dyes and Pigments. 183: 108706. DOI: 10.1016/J.Dyepig.2020.108706  0.318
2019 So H, Kim JH, Lee JH, Hwang H, An DK, Lee KM. Planarity of terphenyl rings possessing o-carborane cages: turning on intramolecular-charge-transfer-based emission. Chemical Communications (Cambridge, England). PMID 31737876 DOI: 10.1039/C9Cc07729D  0.32
2019 Kim S, So H, Lee JH, Hwang H, Kwon H, Park MH, Lee KM. Photophysical Properties of Spirobifluorene-Based -Carboranyl Compounds Altered by Structurally Rotating the Carborane Cages. Molecules (Basel, Switzerland). 24. PMID 31731632 DOI: 10.3390/Molecules24224135  0.356
2019 Kim S, Lee JH, So H, Ryu J, Lee J, Hwang H, Kim Y, Lee KM, Park MH. Spirobifluorene-based o-Carboranyl Compounds: Insights into the Rotational Effect of Carborane Cages on Photoluminescence. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31657858 DOI: 10.1002/Chem.201904491  0.338
2019 Ryu CH, Kwak SW, Lee HW, Lee JH, Hwang H, Kim M, Chung Y, Kim Y, Park MH, Lee KM. Carbazole-Appended Salen-Indium Conjugate Systems: Synthesis and Enhanced Luminescence Efficiency. Inorganic Chemistry. PMID 31483629 DOI: 10.1021/Acs.Inorgchem.9B01948  0.338
2019 Kwak SW, Jin H, Lee JH, Hwang H, Kim M, Kim Y, Chung Y, Lee KM, Park MH. Systematic Control of the Overlapping Energy Region for an Efficient Intramolecular Energy Transfer: Functionalized Salen-Al/Triphenylamine Guest-Host Assemblies. Inorganic Chemistry. PMID 30694658 DOI: 10.1021/Acs.Inorgchem.8B03005  0.303
2019 Jin H, Bae HJ, Kim S, Lee JH, Hwang H, Park MH, Lee KM. 2-Phenylpyridine- and 2-(benzo[b]thiophen-2-yl)pyridine-based o-carboranyl compounds: impact of the structural formation of aromatic rings on photophysical properties. Dalton Transactions (Cambridge, England : 2003). PMID 30631864 DOI: 10.1039/C8Dt04367A  0.356
2019 Jin H, Kim S, Bae HJ, Lee JH, Hwang H, Park MH, Lee KM. Effect of Planarity of Aromatic Rings Appended to o-Carborane on Photophysical Properties: A Series of o-Carboranyl Compounds Based on 2-Phenylpyridine- and 2-(Benzo[b]thiophen-2-yl)pyridine. Molecules (Basel, Switzerland). 24. PMID 30621119 DOI: 10.3390/Molecules24010201  0.344
2018 Kwak SW, Jin H, Shin H, Lee JH, Hwang H, Lee J, Kim M, Chung Y, Kim Y, Lee KM, Park MH. A salen-Al/carbazole dyad-based guest-host assembly: enhancement of luminescence efficiency via intramolecular energy transfer. Chemical Communications (Cambridge, England). PMID 29682672 DOI: 10.1039/C8Cc01528G  0.307
2018 Kwak SW, Kwon H, Lee JH, Hwang H, Kim M, Chung Y, Kim Y, Lee KM, Park MH. Salen-indium/triarylborane triads: synthesis and ratiometric emission-colour changes by fluoride ion binding. Dalton Transactions (Cambridge, England : 2003). PMID 29582029 DOI: 10.1039/C8Dt00153G  0.335
2018 Hyun K, Jin H, Woo WH, Shin H, Lee JH, Hwang H, Kim M, Lee KM, Park MH, Kim Y. Systematic design of indium-based luminophores with color-tunable emission via combined manipulation of HOMO and LUMO levels Dyes and Pigments. 158: 285-294. DOI: 10.1016/J.Dyepig.2018.05.055  0.347
2018 Lee JH, Ryu CH, Yu S, Hwang H, Lee KM. Quinolinol-based Al/Triarylborane Dyad Assembly: Alteration of Electronic Transition States Mediated by Fluoride Anion Binding Bulletin of the Korean Chemical Society. 39: 1294-1301. DOI: 10.1002/Bkcs.11595  0.313
2017 Kwak SW, Choi BH, Lee JH, Hwang H, Lee J, Kwon H, Chung Y, Lee KM, Park MH. Synthesis and Dual-Emission Feature of Salen-Al/Triarylborane Dyads. Inorganic Chemistry. PMID 28537404 DOI: 10.1021/Acs.Inorgchem.7B00768  0.302
2017 Shin N, Yu S, Lee JH, Hwang H, Lee KM. Biphenyl- and Fluorene-Based o-Carboranyl Compounds: Alteration of Photophysical Properties by Distortion of Biphenyl Rings Organometallics. 36: 1522-1529. DOI: 10.1021/Acs.Organomet.7B00093  0.305
2017 You DK, Lee JH, Hwang H, Kwon H, Park MH, Lee KM. Deboronation-induced ratiometric emission sensing of fluoride by 1,3,5-tris-(o-carboranyl-methyl)benzene Tetrahedron Letters. 58: 3246-3250. DOI: 10.1016/J.Tetlet.2017.07.017  0.328
2017 You DK, Lee JH, Choi BH, Hwang H, Lee MH, Lee KM, Park MH. Effects of Multi-Carborane Substitution on the Photophysical and Electron-Accepting Properties of o -Carboranylbenzene Compounds European Journal of Inorganic Chemistry. 2017: 2496-2503. DOI: 10.1002/Ejic.201700192  0.374
2016 Sohn C, Jeong J, Lee JH, Choi BH, Hwang H, Bae GT, Lee KM, Park MH. Novel aluminum-BODIPY dyads: intriguing dual-emission via photoinduced energy transfer. Dalton Transactions (Cambridge, England : 2003). PMID 26937761 DOI: 10.1039/C5Dt05067G  0.312
2016 Choi BH, Lee JH, Hwang H, Lee KM, Park MH. Novel Dimeric o-Carboranyl Triarylborane: Intriguing Ratiometric Color-Tunable Sensor via Aggregation-Induced Emission by Fluoride Anions Organometallics. 35: 1771-1777. DOI: 10.1021/Acs.Organomet.6B00172  0.344
2016 Lee JH, Hwang H, Lee KM. p-Terphenyl-based di-o-carboranyl compounds: Alteration of electronic transition state by terminal phenyl groups Journal of Organometallic Chemistry. 825: 69-74. DOI: 10.1016/J.Jorganchem.2016.10.028  0.355
2014 Kim JH, Lee JH, Hwang H, Kim HL, Kwon CH. Determination of precise pyrimidine cationic structure by vacuum ultraviolet mass-analyzed threshold ionization spectroscopy. Physical Chemistry Chemical Physics : Pccp. 16: 1590-6. PMID 24317499 DOI: 10.1039/C3Cp53521E  0.34
2012 Shin MS, Lee JH, Hwang H, Kwon CH, Kim HL. Photodissocaition dynamics of propiolic Acid at 212 nm: The OH production channel Bulletin of the Korean Chemical Society. 33: 3618-3624. DOI: 10.5012/Bkcs.2012.33.11.3618  0.362
2010 Lee JH, Hwang H, Kwon CH, Kim HL. Photodissociation dynamics of propargyl alcohol at 212 nm: the OH production channel. The Journal of Physical Chemistry. A. 114: 2053-8. PMID 20050711 DOI: 10.1021/Jp9091865  0.349
2010 Jung H, Hwang H, Park K, Kim J, Kim D, Kang Y. Palladium-Catalyzed Cross-Coupling Reactions of Dithienosilole with Indium Reagents: Synthesis and Characterization of Dithienosilole Derivatives and Their Application to Organic Light-Emitting Diodes Organometallics. 29: 2715-2723. DOI: 10.1021/Om100222B  0.306
2006 Kim H, Hwang H, Rossky PJ. Quantum simulation of solution phase intramolecular electron transfer rates in betaine-30. The Journal of Physical Chemistry. A. 110: 11223-9. PMID 17004730 DOI: 10.1021/Jp063222D  0.544
2004 Hwang H, Rossky PJ. An analysis of electronic dephasing in the spin-boson model. The Journal of Chemical Physics. 120: 11380-5. PMID 15268171 DOI: 10.1063/1.1742979  0.525
2004 Hwang H, Rossky PJ. Harmonic Model Description of the Franck-Condon Density for a Betaine Dye Molecule Journal of Physical Chemistry A. 108: 2607-2616. DOI: 10.1021/Jp0370324  0.5
2004 Hwang H, Rossky PJ. Electronic decoherence induced by intramolecular vibrational motions in a betaine dye molecule Journal of Physical Chemistry B. 108: 6723-6732. DOI: 10.1021/Jp037031B  0.521
2001 Lockwood DM, Hwang H, Rossky PJ. Electronic decoherence in condensed phases Chemical Physics. 268: 285-293. DOI: 10.1016/S0301-0104(01)00302-0  0.637
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