• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.218-218
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• 2006

A number of new ideas have been implemented to control the droplet morphology and electrooptic properties of holographic polymer dispersed liquid crystal (HPDLC). Doping of conductive fullerene particles to the conventional HPDLC induced dual effects of reducing both droplet coalescence and operating voltage. Chain transfer agent gave higher gel content with lower crosslink density, less dark reactions and less grating shrinkage with much smooth LC-polymer interfaces. Addition of octanoic acid (OA) to the formulation of HPDLC gave a decrease in droplet size and monotonic increase of the off state diffraction throughout the OA content.

• Macromolecular Research
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• 제17권8호
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• pp.557-562
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• 2009

The free radical polymerization of styrene was initiated with azobis(isobutyronitrile) in the presence of benzene sulfonyl chloride. Analysis of the terminal structures of the obtained polystyrene with $^1H$ NMR spectroscopy revealed the presence of a phenyl sulfonyl group at the ${\alpha}$-end and a chlorine atom at the ${\omega}$-end of each polystyrene chain. The terminal chlorine atom in the polystyrene chains was further confirmed through atom transfer radical polymerization (ATRP) of styrene and methyl acrylate using the obtained polystyrenes as macroinitiators and CuCl/2,2'-bipyridine as the catalyst system. GPC traces of the products obtained in ATRP at different reaction times were clearly shifted to higher molecular weight direction, indicating that nearly all the macroinitiator chains initiated ATRP of the second monomers. In addition, the number-average molecular weights of the polystyrenes increased directly proportional to the monomer conversions, and agreed well with the theoretical ones.

• Macromolecular Research
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• 제15권1호
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• pp.31-38
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• 2007

Pentamethylcyclopentadienyltitanium trichloride, bis(cyclopentadienyl)titanium dichloride ($Cp_2TiCl_2$), and bis(pentamethylcyclopentadienyl)titanium dichloride were used in the polymerization of styrene without the aid of Group I-III cocatalysts. The properties of the resulting polymer indicated that polymerization was more controlled than in thermal polymerization. The kinetic studies indicated that a lower level of termination is present and that the polymer chain can be extended by adding an additional monomer. To elucidate the mechanism of polymerization, a series of experiments was performed. All results supported the involvement of a radical mechanism in the polymerization using $Cp_2TiCl_2$. The possibility of atom transfer radical polymerization (ATRP) mechanism was investigated by isolating the intermediate species. We could confirm the activation step from the reaction of 1-PEC1 with $Cp_2TiCl$ by detecting the coupling product of the generated active radicals. However, the reversible deactivation reaction competes with other side reactions, and it detection was difficult with our model system.

• 폴리머
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• 제32권6호
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• pp.566-572
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• 2008

메탈로센 [(TMDS)$Cp_2$]$ZrCl_2$, 촉매 1과 Exxon 촉매인 [$(n-Bu)_2Cp_2$]$ZrCl_2$, 촉매 2를 사용하여 폴리에틸렌 왁스를 제조하였다. 분자량을 조절하기 위하여 수소를 연쇄이동제로 사용하였다. 실험결과 수소의 주입량이 증가할수록 중합활성의 감소 생성된 폴리에틸렌 왁스의 분자량과 분자량 분포의 감소 그리고 폴리에틸렌 왁스의 융점 저하가 관찰되었다. 수소의 주입으로 폴리에틸렌의 분자량은 1500, 융점은 60 $^\circ$C까지 조절이 가능하였다. 수소의 양을 조절함으로써 메탈로센을 통해 분자량분포가 좁고 융점이 낮은 고품질의 폴리에틸렌 왁스의 제조가 가능하였다. 본 연구실에서 개발된 촉매 1은 알려진 가장 우수한 메탈로센인 촉매 2와 폴리에틸렌 왁스 제조에서 경쟁이 가능한 유사한 특성을 보였다.

• 한국전기전자재료학회논문지
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• 제18권5호
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• pp.407-413
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• 2005

Ion implantation provides a unique way to modify the mechanical, optical and electrical properties of polymer by depositing the energy of ions in the material on the atomic scale. Implantation of ions into the polymers generally leads to a radiation damage, which, in many cases, modifies the properties of the surface and bulk of the material. These modifications result from the changes of the chemical structure caused in their turn by changing the chemical bonding when the incident ions cut the polymer chains, breaks covalent bonds, promotes cross-linking, and liberates certain volatile species. We studied the relation among the linear energy transfer (LET) and changes of surface microstructure and surface resistivity on PPS material using the high current ion implantation technology The surface resistivity of nitrogen implanted PPS decreased to $10^{7}{\Omega}/cm^{2}$ due to the chain scission, cross linking, ${\pi}$ electron creation and mobility increase. In this case, the surface conductivity depend on the 1-dimensional hopping mechanism.

• Macromolecular Research
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• 제15권6호
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• pp.541-546
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• 2007

The combination of atom transfer radical polymerization (ATRP) and click chemistry was employed for the efficient preparation of well-defined block copolymers. Bromo terminated poly(methyl acrylate) (pMA-Br) was prepared by an ATRP initiator, ethyl-2-bromoisobutyrate (EBiB). Subsequently, the bromine chain end of pMA-Br was converted to an azide group by simple nucleophilic substitution reaction. ${\alpha}-Alkyn-{\omega}-bromo-functionalized$ polystyrene was also synthesized by ATRP using the alkyn-functionalized initiator, propargyl-2-bromoisobutyrate (PgBiB). In both cases, the conversion was limited to a low level to ensure a high degree of chain end functionality. Then the coupling reaction between the azide end group in $pMA-N_3$ and alkyn-functionalized PgBiB-pSt was performed by Cu(I)catalysis. This coupling reaction was monitored by gel permeation chromatography (GPC). The synthesized block copolymer was characterized by FT-IR, $^1H-NMR$ spectroscopy and $^1H-^1H$ COSY correlation spectroscopy.

• Bulletin of the Korean Chemical Society
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• 제17권1호
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• pp.16-19
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• 1996

The bulk photopolymerization of methyl methacrylate (MMA) with disilanes such as 1,2-diphenyldisilane and 2-phenyl-1,3-disilapropane was carried out to yield poly(MMA)s containing the corresponding disilyl moiety presumably as an end group. It was found that while the polymerization yields and the polymer molecular weights decreased as the relative disilane concentration increased, the TGA residue yields and the relative intensities of SiH IR stretching bands increased with increment of molar ratio of disilane over MMA. The photopolymerization of MMA with 2-phenyl-1,3-disilapropane produced higher-molecular-weight polymer with lower TGA residue yield when compared to the photopolymerization of MMA with 1,2-diphenyldisilane. The disilanes seemed to significantly influence on the photopolymerization as both chain initiation and chain transfer agents.

• Bulletin of the Korean Chemical Society
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• 제21권3호
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• pp.291-294
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• 2000

The bulk photopolymerization of methyl methacrylate(MMA) with bis(silane)s such as 1,4-$C_6H_4(SiH_3)_2$ (1) and 1,4-$C_6H_4(SiH_2Me)_2$ (2) was performed to produce poly(MMA)s possessing the corresponding bis(silyl) moiety as an end group. For the bis(silane)s, while the polymerizaiton yields and the polymer molecular weights decreased, the TGA residue yields and the relative intensities of Si-H IR stretching bands increased as the relative bis(silane) concentration over MMA increased. The polymerizaion yield, polymer molecular weight, and TGA residue yield of MMA with 1 were found to be higher than those with 2. The bis(silane)s appears to influence significantly upon the photopolymerization of MMA as both chain initiation and chain transfer agents.

• 통합자연과학논문집
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• 제2권1호
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• pp.1-12
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• 2009

This miniaccount presents the selective examples of our recent discoveries in the photopolymerization of vinyl monomers using the organic initiators such as hydrosilanes, poly(hydroarylsilane)s, benzoin silyl ethers, and thianthrene cation radical. In the photopolymerization of vinyl monomers with silanes polysilanes, while the polymerization yields and polymer molecular weights of the poly(MMA)s containing the silyl moieties decreased, the TGA residue yields and intensities of SiH stretching IR bands increased as the mole ratio of the silanes over MMA increased. The hydroarylsilane and poly(hydroarylsilane) seemed to influence strongly on the photopolymerizaiton of olefinic monomers as both chain initiation and chain transfer agents. For the photohomopolymerization and photocopolymerization of MA and AA, the similar trends were observed. Benzoin silyl ethers and thianthrene cation radical also exhibit the photoinitiating ability in the photopolymerization of MMA.

• 접착 및 계면
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• 제21권4호
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• pp.129-134
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• 2020

공액분자반도체와 고분자절연체 계면에서 전하트래핑을 이해하는 것은 장시간 구동가능한 안정성 높은 유기전계효과 트랜지스터(이하 유기트랜지스터) 개발을 위해 중요하다. 본 연구에서는 다양한 분자량의 고분자절연체를 이용한 유기트랜지스터의 전하이동 특성을 평가하였다. Polymethyl methacrylate (PMMA) 표면 위에 적층된 펜타센 공액반도체의 모폴로지와 결정성은 PMMA 분자량에 무관함이 나타났다. 그 결과 트랜지스터 소자의 초기 트랜스퍼 곡선과 전하이동도는 분자량에 상관없었다. 하지만, 적정한 상대습도 환경에서 소자에 바이어스가 인가되었을 경우, 바이어스 스트레스 효과로 불리는 드레인전류 감소와 트랜스퍼 곡선 이동은 PMMA 분자량이 감소할수록 증대됨이 관찰되었다(분자량 효과). 분자량 효과에 의한 전하트래핑은 회복이 매우 어려운 비가역적인 과정임을 밝혀 내었다. 이러한 분자량 효과는 PMMA 존재하는 고분자사슬 말단의 밀도 변화에 의한 것으로 판단된다. 즉, PMMA 고분자사슬 말단이 가지는 자유부피가 전하트랩으로 작용하여 분자량에 민감한 바이어스 스트레스 효과를 일으킨 것으로 판단된다.