• 폴리머
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• 제39권2호
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• pp.256-260
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• 2015

우레탄 아크릴레이트에 montmorillonite(MMT)를 첨가한 UV 경화형 나노복합체 제조 시 사용하는 광개시제의 종류에 따른 기계적 성질 및 내흡수성을 조사하였다. 1 wt%의 MMT가 첨가될 경우 가장 우수한 인장강도와 내흡수성을 나타내었으며, 광개시제의 경우 기존의 benzyldimethylketal 계열 광개시제와 bisacyl phosphine oxide 계열의 광개시제를 함께 사용할 경우 3 wt%의 MMT 함량에서도 사용된 UV 램프의 방출 파장대인 340~450 nm에서의 광흡수가 강화되어 나노복합체의 경화거동에 보다 효과적인 것으로 확인되었다.

• Bulletin of the Korean Chemical Society
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• 제30권2호
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• pp.327-333
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• 2009

For the Pt-catalyzed nucleophilic addition of enones, Pt complexes were employed in the presence of various phosphine ligands and $H_2\;(or\;Et_3SiH),$ affording inter- and intra-molecular coupling products in good to modest yield. Depending on reaction protocols, different phosphine ligands were required to optimize the conditions. In the aldol reaction, the Pt catalyst involving $P(2,4,6-(OMe)_3C_6H_2)3\;or\;P(p-OMeC_6H_4)_3$ was chosen. Michael reaction proceeds in good yields in the presence of $P(p-CF_3C_6H_4)_3$. Regarding the activity of the reductants, $H_2$ exhibited superior activity to $Et_3SiH$, resulting in a shorter reaction time and higher yield in the aldol and Michael reaction. In light of the deuterium labeling studies, the catalytic cycle including the hydrometalation of the enones by the platinum hydride species was proposed.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2009년도 9th International Meeting on Information Display
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• pp.767-770
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• 2009

We synthesized a spirobenzofluorene type phosphine oxide (SPPO2) as a new triplet host and an universal electron transport material for phosphorescent organic light-emitting diodes(PHOLEDs). Red PHOLEDs with the SPPO2 host material showed a high quantum efficiency of 14.3 % with a current efficiency of 20.4 cd/A. In addition, the SPPO2 could be applied as an electron transport material which can be matched with any host material due to the lowest unoccupied molecular orbital of 2.4 eV. Electron injection from a cathode to the SPPO2 electron transport layer was better than common electron transport materials. In particular, the SPPO2 was effective as the electron transport material in blue PHOLEDs and the quantum efficiency was more than doubled and driving voltage was lowered by more than 3 V using the SPPO2 instead of common electron transport material.

• 대한화학회지
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• 제57권6호
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• pp.726-730
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• 2013

Complexes synthesized by reacting alkyl and aryl phosphines with different transition metals are of great interest due to their catalytic properties. Many of the phosphine complexes are soluble in polar solvents as a result they find applications in homogeneous catalysis. In our present work we report, four transition metal complexes of Ni(II), Pd(II), Pt(II) and Ru(II) with an asymmetrical ditertiaryphosphine ligand. The synthesized ligand bears a less electronegative substituent such as methyl group on the aromatic nucleus hence makes it a strong ${\sigma}$-donor to form stable complexes and thus could effectively used in catalytic reactions. The complexes have been completely characterized by elemental analyses, FTIR, $^1HNMR$, $^{31}PNMR$ and FAB Mass Spectrometry methods. Based on the spectroscopic evidences it has been confirmed that Ni(II), Pd(II) and Pt(II) complexes with the ditertiaryphosphine ligand showed cis whereas the Ru(II) complex showed trans geometry in their molecular structure.

• 대한화학회지
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• 제29권3호
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• pp.287-294
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• 1985

Acrylamide, N-alkyl substituted acrylamides and N,N-diethylacrylamide를 트리에틸아민과 palladium acetate-triorthotolyl phosphine 촉매 존재하에서 브롬화 방향족화합물들과 비닐화 반응을 실시하여 여러 기능기로 치환된 aryl conjugated enamides를 합성하였다. 이들 반응은 모두 선택적으로 진행되어 (E)-이성질체의 aryl conjugated enamides를 생성하였다. N-alkyl substituted acrylamides는 브롬화 방향족화합물들과의 반응에서 acrylamide와 N,N-diethylacrylamide보다 더 좋은 반응성을 나타내어 생성물들을 높은 수득율로 얻을 수 있었다. 또한 브롬화 방향족화합물이 전자받기 기능기로 치환된 경우에 좋은 반응성을 나타냈으며 전자 주기 기능기를 갖는 경우 acrylamide와 N,N-diethylacrylamide와의 반응에서는 반응이 전혀 진행되지 않거나 낮은 반응성을 나타냈다.

• Bulletin of the Korean Chemical Society
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• 제12권3호
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• pp.332-334
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• 1991

The reaction and coordination chemistry of chiral ferrocenylaminophosphines such as 2-(diphenylphosphino)-1-(N,N-dimethylaminoethyl) ferrocene (PPFA), and 1',2-bis(diphenylphosphino)-l-(N,N-dimethylaminoe thyl) ferrocene (BPPFA), with various iron carbonyls have been investigated. PPFA reacted with iron carbonyls, Fe$(CO)_5$, $Fe_2(CO)_9$, or $Fe_3(CO)_{12}$ to give an iron complex of the type (${\eta}^1$-PPFA-P)Fe$(CO)_4$ (1) as a single product regardless the choice of the iron carbonyls. The bisphosphine ligand BPPFA afforded two products (${\eta}^1$-BPPFA-P)Fe$(CO)_4$ (2) and (${\mu}$,${\eta}^1$-BPPFA-P,P)$Fe_2(CO)_8$ (3) in which BPPFA acts as a monodentate and a bridging ligand, respectively. In all cases coordination to the -Fe$(CO)_4$ moiety is made through the phosphine rather than the amino group and, in the case of 2, the coordination is made through the phosphine substituted at the $C_5H_4$ ring to reduce the steric congestion.

• 에너지공학
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• 제25권4호
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• pp.176-183
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• 2016

본 연구는 연료전지용 고분자 전해질 막의 성능 향상에 관한 것으로서 연료전지를 구동하기 위해 요구되는 전해질 막의 특성에 대하여 연구하였다. Bis(4-fluorophenyl)phenyl phosphine oxide를 발연 황산을 이용하여 양이온($H^+$)을 전도할 수 있는 술폰산기를 치환시켜 주었다. 친수성 올리고머와 소수성 올리고머를 각각 합성하고, 블록 공중합체는 친수성 올리고머와 소수성 올리고머를 방향족 친핵성 치환반응에 의해 제조하였다. 블록 공중합체의 구조 및 술폰화도(DS)는 $^1H$-NMR, 겔 침투 크로마토그래피 (GPC) 분석에 의해 확인하였다. 열적 안정성은 열중량 분석(TGA)을 통해 확인하였으며, 본 연구에서 제조한 블록 코폴리머는 $200^{\circ}C$ 이상의 온도 조건에서 내열성을 나타내었다. 또한, 이온전도성은 연료전지 전해질 막으로서의 성능을 증명하기 위해 이온전도도 시험을 수행하였다. 제조한 막은 온도가 증가할수록 발달된 이온클러스터의 영향으로 최대 58 mS/cm의 이온전도성을 보였다. 블록 코폴리머의 미세 상 분리의 특성은 AFM분석을 통해 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제31권3호
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• pp.697-699
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• 2010

• Bulletin of the Korean Chemical Society
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• 제29권8호
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• pp.1624-1626
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• 2008

• 대한화학회지
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• 제13권2호
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• pp.141-147
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• 1969

Organophosphorous compounds can be reduced by zinc metal in acidic solution after alkaline hydrolysis. Although phosphates and phosphonates did not evolve any gas, dithioates did evolve hydrogen sulfide and phosphine, thionates and thiolates did evolve only hydrogen sulfide. The evolved gases were qualitatively detected by means of lead acetate and silver nitrate or mercuric bromide papers and determined by spectrophotometrically. The reduction mechanism and analytical method of dithioates were proposed.