• Bulletin of the Korean Chemical Society
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• 제30권3호
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• pp.551-555
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• 2009

The ytterbium catalyst immobilized on the cross-linked poly(4-vinylpyridine/styrene) copolymer (P/S-Yb) was applied in the Mannich-type, three component one-pot synthesis of $\beta$-aminoketones. This catalytic system showed excellent catalytic activity and selectivity which resulted in the exclusive formation of $\beta$-aminoketone. The applicability of this immobilized catalyst system was shown by the reusability test and again highlighted by the synthesis of a $\beta$-aminoketone library using a broad range of substrates.

• 공업화학
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• 제19권3호
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• pp.316-321
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• 2008

Styrene과 4-vinylpyridine의 공중합체(poly(st-co-4vp)) 입자를 무유화제 유화중합에 의해 합성하고 이 입자 내부에 iron pentacarbonyl을 침투시킨 후 열분해 시켜 입자의 표면과 내부에 산화철 나노입자를 갖는 자성 poly(st-co-4vp) 입자를 제조하였다. 얻어진 자성 poly(st-co-4vp) 입자의 크기와 분포, 열적 특성 및 자성 특성에 대해서 조사하였다. 자성 poly(st-co-4vp) 입자는 크기가 약 250 nm 정도로 매우 균일하였으며 약 14%의 산화철을 가졌다. 산화철은 XRD 시험에 의해 대부분 $Fe_3O_4$임이 확인되었으며 superconducting susceptometer (SQUID) 시험에 의해 자성 poly(st-co-4vp) 입자가 초상자성을 가짐을 확인하였다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2008년도 추계학술대회 논문집 Vol.21
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• pp.61-61
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• 2008

Nanocomposites of metal (gold and silver) nanoparticles and multi-walled carbon nanotubes (MWNTs) were prepared with the assistance of various stabilizers for metals and MWNTs. Especially common surfactants such as poly(4-vinylpyridine) (PVP), sodium dodecyl sulfate (SDS), poly(sodium 4-styrene sulfonate) (PSS), and poly(diallyldimethylammonium) chloride (PDDA) were used for the sample preparation. Metal/MWNT nanocomposites were structurally characterized in by transmission electron microscopy (TEM), x-ray photoelectron spectroscopy (XPS), x-ray diffraction (XRD), UV/Vis spectroscopy. In addition, the electrical properties of the nanocomposites were studied by cyclic voltammetry (CV).

• 분석과학
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• 제8권4호
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• pp.561-568
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• 1995

Two methods, precipitation and ultrafiltration, were applied in order to recover platinum group metals(PGM) by complexing them with water-soluble polyelectrolytes, e.g., polyethyleneimine [PEl], poly(2-vinylpyridine) [2-PVP], poly (4-vinylpyridine) [4-PVP], and poly (styrene sulfonic acid) [PSSA]. In the precipitation method, the PGM-polyelectrolyte complex that was formed by mixing first with polybase, e.g.,4-PVP at pH 1 was precipitated by further mixing with polyacid, e.g., PSSA. However, the recovery of PGM obtained by this method was not quantitative(less than 70%). The "sandwiching" binding between the metal anions and two polyelectrolytes was examined by X-ray photoelectron spectroscopy(XPS). The XPS studies indicated that the PGM atom was bound with the acdic and basic polyelectrolyte via its oxygen and nitrogen atom, respectively. The recovery of PGM using polyelectrolyte was further studied by ultrafiltration methods as follows : The PGM ions, eomplexed at pH 1 with polyelectrolyte, allowed the applicntion of membrane filtration by virtue of the great differences in molecular weights between PGM and other low molecular weight species. By applying this method, Pd and Pt (ca. $10^{-4}M$) were selectively separated almost quantitatively from coexisting metal ions, e.g., $Cu^{2+}$ and $Ni^{2+}$. The EPR spectra and viscosity measurements indicated that these polyelectrlytes were not bound to $Cu^{2+}$ and $Ni^{2+}$ ions at this pH, which provided the basis for selective separation of PGM(Pd, Pt and Rh) from these coexisting ions.

• Bulletin of the Korean Chemical Society
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• 제17권4호
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• pp.373-376
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• 1996

The bulk thermal and photopolymerization of methyl methacrylate(MMA) with phenylsilane were performed to produce poly(MMA)s containing phenylsilyl moiety presumably as an end group. It was found for both thermal and photopolymerization that while the polymerization yields and polymer molecular weights decreased as the relative phenylsilane concentration increases, the TGA residue yields and the relative intensities of SiH IR stretching bands increased with increasing molar ratio of phenylsilane over MMA. The polymerization yield, molecular weight, and TGA residue yield for the thermal polymerization were higher than those for the photopolymerization. Thus, the phenylsilane seemed to significantly influence on the polymerization as both chain initiation and chain transfer agents. However, an appreciable silane effect was not observed on the thermal and photopolymerization of 4-vinylpyridine, acrylonitrile, styrene, and vinyltrimethoxysilane.

• KSBB Journal
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• 제6권3호
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• pp.241-247
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• 1991

본 연구에서는 고정전달자를 갖는 poly(4-vinylpyridine-co-styrene) 고분자막을 합성하여 이를 특성화하고, $Cl^-$ 및 $CCl_3COO$ 의 $H^+$ 및 $OH^-$ 농도차에 따른 능동전달 기구에 대하여 고찰하였다. 시험 범위 내에서 $Cl^-$의 능동전달은 주로 $H^+$ 농도차를 구동력으로 한 병류수송(symprot)이 주가 되었으며 반면에 $CCl_3COO^{-}$의 능동전달은 $OH^-$의 농도차에 의한 향류 수성(antiport)의 영향이 큼을 알 수 있었다. $H^+$ 농도와 $OH^-$ 농도에 의한 음이온의 초기플럭스를 관찰함으로서, 고정전달자와 이온간의 엄형성계수, K와 이온의 막내 확산계수, D는 $Cl^-$의 경우 각각 $4.60{\times}10^2\;mol^{-1}{\cdot}\textrm{cm}^3$ 및 $1.57{\times}10^3{\textrm{cm}^2}/h$, $CCl_3COO^{-}$의 경우 각각 $1.10{\times}10^4\;mol^{-1}{\cdot}\textrm{cm}^3$ 및 $1.44{\times}10^4{\textrm{cm}^2}/h$ 이었다.

• 대한화학회지
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• 제38권2호
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• pp.136-145
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• 1994

Poly(4-vinylpyridine-co-styrene)[PVPS]리간드에 monomer착물인 M(Ⅱ)(SND) 및 M(Ⅱ)(SOPD)[M: Co(Ⅱ), Ni(Ⅱ) 및 Cu(Ⅱ)]들을 반응시켜 새로운 polymer다섯자리 Schiff base착물인 M(Ⅱ)(PVPS)(SND), M(Ⅱ)(PVPS)(SOPD)들을 합성하였다. 이들 착물들의 원소분석, IR-spectra, UV-visible spectra 및 T.G.A.측정결과에 의하여 Co(Ⅱ), Ni(Ⅱ) 및 Cu(Ⅱ) 착물들은 polymer 5배위 착물로 주어짐을 알았다. 또한 0.1M TEAP-DMF용액에서 순환 전압-전류법과 시차펄스 포라로그래피에 의한 이들의 전기화학적 성질은 Co(Ⅱ)(PVPS)(SND) 및 Co(Ⅱ)(PVPS)(SOPD)는 Co(Ⅲ)/Co(Ⅱ) 와 Co(Ⅱ)/Co(Ⅰ)의 두단계의 환원과정이 비가역적으로 일어나고, Ni(Ⅱ)(PVPS)(SND) 와 Ni(Ⅱ)(PVPS)(SOPD)는 Ni(Ⅱ)/Ni(Ⅰ)의 비가역적인 일단계 환원과정으로, 그리고 Cu(Ⅱ)(PVPS)(SND)와 Cu(Ⅱ)(PVPS)(SOPD)는 Cu(Ⅱ)/Cu(Ⅰ)의 비가역적인 일단계 환원과정으로 일어남을 알았다.