Myung Ho Hyun

ORCID: 0000-0002-4832-4616
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About
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Research Areas
  • Analytical Chemistry and Chromatography
  • Mass Spectrometry Techniques and Applications
  • Conducting polymers and applications
  • Organic Electronics and Photovoltaics
  • Molecular spectroscopy and chirality
  • Organic Light-Emitting Diodes Research
  • Chromatography in Natural Products
  • Microfluidic and Capillary Electrophoresis Applications
  • Chemical Synthesis and Analysis
  • Analytical Methods in Pharmaceuticals
  • Molecular Sensors and Ion Detection
  • Crystallization and Solubility Studies
  • Semiconductor materials and interfaces
  • Metabolomics and Mass Spectrometry Studies
  • Chemical Reaction Mechanisms
  • Perovskite Materials and Applications
  • Luminescence and Fluorescent Materials
  • Antibiotics Pharmacokinetics and Efficacy
  • Advanced Photocatalysis Techniques
  • Advanced Chemical Sensor Technologies
  • Advanced biosensing and bioanalysis techniques
  • Electrochemical sensors and biosensors
  • TiO2 Photocatalysis and Solar Cells
  • Lanthanide and Transition Metal Complexes
  • Analytical Chemistry and Sensors

Pusan National University
2009-2018

Government of the Republic of Korea
2015-2018

Busan Medical Center
2014

Korea Basic Science Institute
2008-2012

Busan National University of Education
2010

Pohang University of Science and Technology
2007-2009

Chonnam National University
2009

Ewha Womans University
2007

Chungnam National University
2002

University of Illinois Urbana-Champaign
1985-1987

The postsynthetic modification strategy is adopted to demonstrate for the first time syntheses of catalytically active chiral MOPMs from a preassambled achiral framework, MIL-101, by attaching L-proline-derived catalytic units open metal coordination sites host framework. Various characterization techniques (including PXRD, TGA, IR, and N(2) absorption measurements) indicated that are successfully incorporated into keeping parent framework intact. new show remarkable activities in asymmetric...

10.1021/ja901440g article EN Journal of the American Chemical Society 2009-05-12

Signal amplification by enzyme labels in enzyme-linked immunosorbent assays (ELISAs) is not sufficient for detecting a low number of bacterial pathogens. It useful to employ approaches that involve multiple signal such as enzymatic plus redox cycling. An advantageous combination an product [for fast electrochemical-chemical-chemical (ECC) cycling involves the product] and substrate (for slow side reactions ECC substrate) has been developed obtain detection limit E. coli O157:H7...

10.1021/ac3028855 article EN Analytical Chemistry 2013-01-17

The authors herein report optimized conditions for ultrasensitive phosphatase-based immunosensors (using redox cycling by a reducing agent) that can be simply prepared and readily applied to microfabricated electrodes. were the detection of cardiac troponin I in human serum. preparation an immunosensing layer was based on passive adsorption avidin (in carbonate buffer (pH 9.6)) onto indium–tin oxide (ITO) allows very low levels nonspecific binding proteins. optimum enzymatic reaction...

10.1021/ac200447b article EN Analytical Chemistry 2011-04-13

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTA chiral stationary phase for the facile resolution of amino acids, alcohols and amines as N-3,5-dinitrobenzoyl derivativesWilliam H. Pirkle Myung Ho HyunCite this: J. Org. Chem. 1984, 49, 17, 3043–3046Publication Date (Print):August 1, 1984Publication History Published online1 May 2002Published inissue 1 August 1984https://pubs.acs.org/doi/10.1021/jo00191a001https://doi.org/10.1021/jo00191a001research-articleACS PublicationsRequest reuse...

10.1021/jo00191a001 article EN The Journal of Organic Chemistry 1984-08-01

Crown ether-based HPLC chiral stationary phases (CSPs) have been successfully utilized in the resolution of various racemic compounds containing a primary amino group. Especially, CSPs based on crown ethers incorporating binaphthyl unit or tartaric acid and phenolic pseudo shown high recognition efficiency. In this account paper, review development etherbased CSPs, their structural characteristics applications to including drugs secondary group with variation type content mobile phase...

10.5012/bkcs.2005.26.8.1153 article EN Bulletin of the Korean Chemical Society 2005-08-20

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTA chiral recognition model for the chromatographic resolution of N-acylated 1-aryl-1-aminoalkanesWilliam H. Pirkle, Christopher J. Welch, and Myung Ho HyunCite this: Org. Chem. 1983, 48, 25, 5022–5026Publication Date (Print):December 1, 1983Publication History Published online1 May 2002Published inissue 1 December 1983https://pubs.acs.org/doi/10.1021/jo00173a045https://doi.org/10.1021/jo00173a045research-articleACS PublicationsRequest reuse...

10.1021/jo00173a045 article EN The Journal of Organic Chemistry 1983-12-01

Two new anthracene thiourea derivatives, 1 and 2, were investigated as fluorescent chemosensors for the chiral recognition of two enantiomers alpha-amino carboxylates. Especially, host 2 displayed K(L)/K(D) values high 10.4 with t-Boc alanine. Furthermore, D/L selectivity hosts is opposite, even though both bear same glucopyranosyl units. These intriguing opposite binding affinities by obtained without/with H-pi interaction between anthrancene moiety methyl groups, which explained extensive...

10.1021/jo7022813 article EN The Journal of Organic Chemistry 2007-12-06

Abstract Two novel alternating π‐conjugated copolymers, poly[2,8‐(6,6′,12,12′‐tetraoctyl‐6,12‐dihydroindeno‐[1,2b]fluorene‐ alt ‐5(1‐(2,6‐diisopropylphenyl)‐2,5‐di(2‐thienyl)pyrrole) ( P1 ) and ‐5(1‐(p‐octylphenyl)‐2,5‐di(2‐thienyl)pyrrole) P2 ), were synthesized via the Suzuki coupling method their optoelectronic properties investigated. The resulting polymers completely soluble in various common organic solvents weight‐average molecular weights M w 5.66 × 10 4 (polydispersity: 1.97) 2.13×...

10.1002/pola.24101 article EN Journal of Polymer Science Part A Polymer Chemistry 2010-06-14

We report an interference-free electrochemical lateral-flow immunoassay that enables one-step ultrasensitive detection with serum.

10.1039/c3an02328a article EN The Analyst 2014-01-01

Abstract Crown ether‐based chiral stationary phases (CSPs) have been known to be quite useful for the liquid chromatographic resolution of racemic compounds containing a primary amino group. Chiral separations on crown CSPs are characterized by several factors. In this paper, structural characteristics five selected CSPs, analyte and factors characterizing such as mobile phase modifiers column temperature were reviewed. Among various factors, inorganic modifier in influence equally CSPs....

10.1002/jssc.200390030 article EN Journal of Separation Science 2003-03-01

Pyrrolo[3,4-c]pyrrole-1,3(2H,5H)-dione (DPPD)-based large band gap polymers, P(BDT-TDPPDT) and P(BDTT-TDPPDT), are prepared by copolymerizing electron-rich 4,8-bis(2-ethylhexyloxy)benzo[1,2-b:4,5-b′]dithiophene (BDT) or 4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophene (BDTT) unit with novel electron deficient 2,5-dioctyl-4,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,3(2H,5H)-dione (TDPPDT) unit. The absorption bands of polymers P(BDTT-TDPPDT) cover the region from 300 to...

10.1002/pola.27424 article EN Journal of Polymer Science Part A Polymer Chemistry 2014-09-01

A chiral stationary phase (CSP) prepared by bonding (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid to silica gel was used for the direct resolution of β-amino acids. To determine optimum mobile composition, two acids were selected and their resolutions on CSP performed with variation types contents organic acidic modifiers in aqueous phase. The chromatographic behaviors found be dependent From results these experiments, a possible composition proposed mixed solvent 50% methanol water...

10.1002/1615-9314(20020701)25:10/11<648::aid-jssc648>3.0.co;2-d article EN Journal of Separation Science 2002-07-01

Abstract The preparation of 3,5-dinitrophenyl carbamates and ureas from chiral alcohols amines 3,5-dinitrobenzoyl azide is described. These have been observed to resolve on α-arylalkylamine based stationary phases 1 2. A mechanism for the resolution these presented compared thereof analogous series 3,5-dinitrobenzamides phases.

10.1080/01483918608076646 article EN Journal of Liquid Chromatography 1986-02-01

Abstract Liquid chromatographic chiral stationary phases (CSPs) based on crown ethers have been successfully utilized in the separation of enantiomers various racemic compounds containing a primary amino group. Especially, CSPs incorporating binaphthyl unit or tartaric acid most successful. In this review, development unit, their applications to resolution and non‐primary with variation type content organic, acidic, inorganic modifiers an aqueous mobile phase non‐aqueous efforts improve...

10.1080/10826070701191136 article EN Journal of Liquid Chromatography &amp Related Technologies 2007-02-01

Magnetic silica nanoparticles modified by a chiral selector were demonstrated to be useful in magnetic field induced separation of enantiomers.

10.1039/b908349a article EN Chemical Communications 2009-01-01
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