• Polymer(Korea)
• /
• v.34 no.2
• /
• pp.159-165
• /
• 2010

Dipyridine-terminated polystyrenes and polybutadienes were synthesized by the chain endfunctionalization reaction of polystyryllithium (PSLi) and polybutadienyllithium (PBDLi) with di(2-pyridyl) ketone(DPK) using a living anionic polymerization method in the Ar-glove box. Living polymeric lithiums with low molecular weights (Mw=1000~2000 g/mol) were used to investigate the chain end-functionalization yield with DPK and the degree of coupling reaction by the attack of organolithium to the pyridine ring in the presence of TMEDA using GPC, $^1H$-NMR, $^{13}C$ analysis. DPK-terminated PBD exhibited much higher functionalization yield and less amount of coupling reaction compared with DPK-terminated PS. 86% functionalization yield with 9% degree of coupling was obtained when the PBDLi was added dropwise to DPK solution at room temperature. The functionalization yield was increased as the reaction temperature decreased, however, no LiCl effect was observed in this chain end-functionalization reaction with DPK.

• Carbon letters
• /
• v.11 no.4
• /
• pp.298-303
• /
• 2010

A method of functionalization of multi-walled carbon nanotube (MWNT) at room temperature using dry ozone gas is described. The resulting MWNT were characterized by Fourier transform infrared, x-ray photoelectron spectroscopy, and scanning electron microscopy. Combined to these analyses and solubility in liquids, it could be concluded that the dry ozone gas exposure introduces polar functional groups such as carboxylic groups to MWNT similar to acidic modification of MWNT. Particularly, the stable dispersion of MWNT in water after ozone treatment above a critical level could be obtained, implying potential bio-application. The hydrophilic functional groups on the MWNT introduced by ozone oxidation were helpful in improving the interaction with functional groups in PA6 such as $-NH_2$ and -CONH- resulting in improved mechanical properties.

• Bulletin of the Korean Chemical Society
• /
• v.26 no.6
• /
• pp.871-877
• /
• 2005

Recent progress in the filed of transition-metal mediated C-H bond activation has had a great influence on organic synthesis. Among such transition-metal catalyzed reactions, ortho-functionalization via the chelationassisted strategy has been paid great attentions as one of the powerful methodologies for converting aromatic compounds into ones that are more functionalized at the exclusively ortho-position. In this context, various transition metal-catalyzed ortho-functionalizations such as alkylation, alkenylation, silylation and carbonylation are described briefly and their prospects are suggested.

• Bulletin of the Korean Chemical Society
• /
• v.24 no.11
• /
• pp.1702-1704
• /
• 2003

• Macromolecular Research
• /
• v.11 no.5
• /
• pp.347-351
• /
• 2003

The hydrophobic ligand-containing hollow polypropylene (PP) membranes were synthesized by the mutual radiation induced graft copolymerization with glycidylmethacrylate (GMA) onto hollow PP membrane followed by the subsequent functionalization with L-phenylalanine. FT-IR, elemental analysis and UV spectroscopy were utilized to characterize copolymer composition, and degree of grafting, functionalization conversion and ${\gamma}$-globulins adsorption. The degree of grafting on the PP surface increased with the reaction time and total dose of E-beam. In the subsquent functionalization, the amount of L-phenylalanine increased with the increase in the degree of grafting and the degree of conversion was about 30%. The ${\gamma}$-globulins adsorption experiments showed that adsorption capacity had a maximum value at pH 8. The ${\gamma}$-globulins adsorption capacity in the basic pH region was higher than in the acidic pH region.

• Journal of Radiation Industry
• /
• v.4 no.4
• /
• pp.341-345
• /
• 2010

The surface functionalization of a fluoropolymer by ion beam-induced graft polymerization was described in this research. The surface of poly(tetrafluoroethylene) (PTFE) films were irradiated by a 150 keV $H^+$ ions, and 4-vinyl pyridine (4VP) as a functional monomer was then thermally graft polymerized on the irradiated surface. The surface properties of poly(4-vinyl pyridine) (P4VP)-grafted PTFE films were investigated in terms of grafting degree, wettability, chemical structure, and morphology. The results revealed that the surface of PTFE films was successfully functionalized by ion beam-induced graft polymerization of 4VP.

• Elastomers and Composites
• /
• v.55 no.4
• /
• pp.339-346
• /
• 2020

We functionalized a wear-resistant carbon-based MoS2 filler to solve its limited wear condition problem. The filler exhibits excellent lubricative properties. The surface modification of MoS2 was carried out using a (3-glycidyloxypropyl)trimethoxysilane (GPTMS) silane coupling agent to improve the low compatibility and dispersibility of the filler that generally degrade the performance of composites. A silane coupling agent was employed for the functionalization of MoS2, and its effect on the wear resistance of MoS2/Polyamide-6,6 was investigated. The silanization of MoS2 was identified by contact angle analysis and Fourier-transform infrared, energy dispersive X-ray, and X-ray photoelectron spectroscopies. The wear resistance of the composite was found to be improved significantly by the surface functionalization of MoS2.

• Journal of the Korean Society of Manufacturing Process Engineers
• /
• v.12 no.4
• /
• pp.29-33
• /
• 2013

Here we report a partially aminated micropattern via direct functionalization and examine eleven different solution-phase probe DNAs hybridizing with the same target DNA on both hydrogen and oxygen terminated diamond. The hybridization intensities determined by epifluorescence microscopy were compared and are influenced strongly by the negatively charged surface and mismatched position of its sequence with immobilized probe DNA.

• Bulletin of the Korean Chemical Society
• /
• v.32 no.9
• /
• pp.3473-3476
• /
• 2011

• Bulletin of the Korean Chemical Society
• /
• v.35 no.1
• /
• pp.253-256
• /
• 2014

Functionalization of zigzag graphene nanoribbon (ZGNR) segment containing 120 C atoms with pyridine (3NV-ZGNR) defects was investigated on the basis of density-functional theory (DFT) calculations, results show that edge-modified ZGNRs by Sc can adsorb multiple hydrogen molecules in a quasi-molecular fashion, thereby can be a potential candidate for hydrogen storage. The stability of Sc functionalization is dictated by a strong binding energy, suggesting a reduction of clustering of metal atoms over the metal-decorated ZGNR.