• 접착 및 계면
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• 제1권1호
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• pp.38-46
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• 2000

Phosphine oxide와 불소를 함유하는 단량체(bis(3-aminophenyl) 3,5-bis (trifluoromethyl) phenyl phosphine oxide (mDA6FPPO))를 Grignard 반응에 의하여 합성한 다음, 이를 PMDA, 6FDA, BTDA 또는 ODPA와 함께 폴리이미드 합성에 사용하였다. 폴리이미드는 폴리아믹산을 합성한 후 이를 이미드화시키는 방법을 사용하였으며, FT-IR, NMR, DSC 및 점도측정기를 이용하여 분석하였다. 또한 T-peel 시험으로 접착강도를 측정하였다. Phosphine oxide를 함유하는 bis(3-aminophenyl) phenyl phosphine oxide (mDAPPO) 및 상용의 3.3'-diamino diphenyl sulfone (mDDS)로부터 합성된 폴리이미드와 비교하였다. 본 연구에서 합성된 mDA6FPPO를 사용하여 만들어진 폴리이미드는 높은 $T_g$, 우수한 용해도 및 접착성을 보였다.

• Macromolecular Research
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• 제8권5호
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• pp.215-223
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• 2000

A novel diamine monomer, containing fluorine and phosphine oxide, bis(3-aminophenyl) 3,5-bis(trifluoromethyl)phenyl phosphine oxide (mDA6FPPO), was prepared via Grignard reaction, and utilized to prepare polyimides with dianhydrides such as PMDA, 6FDA, BTDA or ODPA, by the conventional two-step route; preparation of poly(amic acid), followed by solution imidization. The polyimides were characterized by FT-IR, NMR, and DSC with intrinsic viscosity and refractive index also being evaluated. A phosphine oxide containing monomer, bis(3-aminophenyl)phenyl phosphine oxide (mDAPPO) and a commercial 3,3-diaminodiphenyl sulfone (mDDS) were also used for comparison. The polyimides derived from mDA6FPPO exhibited high T$\sub$g/, excellent solubility and low birefringence.

• 대한화학회지
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• 제49권2호
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• pp.161-166
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• 2005

• 대한화학회지
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• 제52권4호
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• pp.445-449
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• 2008

• 대한화학회지
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• 제45권3호
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• pp.264-267
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• 2001

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2009년도 9th International Meeting on Information Display
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• pp.188-191
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• 2009

A high efficiency deep blue phosphorescent organic light-emitting diode (PHOLED) was developed using a new wide triplet bandgap host material (PPO1) with a phenylcarbazole and a phosphine oxide unit. The wide triplet bandgap host material was synthesized by a phosphornation reaction of 2-bromo-Nphenylcarbazole with chlorodiphenylphosphine. A deep blue emitting phosphorescent dopant, tris((3,5-difluoro-4-cyanophenyl)pyridine)iridium (FCNIr), was doped into the PPO1 host and a high quantum efficiency of 17.1 % and a current efficiency of 19.5 cd/A with a color coordinate of (0.14,0.15) were achieved in the blue PHOLED. The quantum efficiency of the deep blue PHOLED was better than any other quantum efficiency value reported up to now.

• 대한화학회지
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• 제7권4호
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• pp.245-250
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• 1963

TBPO와 TOPO와의 混合溶媒(稀釋制 : toluene)에 依한 三假狀態의 4f 稀土類元素의 抽出에 있어 相乘效果(synerigistic effect)가 나타남을 알았으며 이것은 各 單獨溶媒系에 있어서 生成抽出되는 $M(NO_3)_3\;(TBPO)_3$ 및 $M(NO_3)_3\;(TOPO)_3$型 外에 $M(NO_3)_3\;(TBPO)_2\;(TOPO)$型이 새로히 追加生成됨을 起因된 것으로 認定된다.

• Composites Research
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• 제12권4호
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• pp.55-61
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• 1999

Poly(arylene ether phosphine oxide)(PEPO)로 코팅된 탄소섬유의 계면접착력을 microdroplet 시험으로 측정하였으며, 이 결과를 poly(arylene ether sulfone) (PES), Udel$^{\circledR}$ P-1700 and Ultem$^{\circledR}$ 1000으로 코팅된 탄소섬유의 결과와 비교하였다. 또한 코팅에 사용된 고분자와 탄소섬유와의 계면접착력을 탄소섬유와 고분자의 접착 메카니즘을 규명하기 위하여 측정하였다. PEPO로 코팅된 탄소섬유가 가장 높은 계면접착력을 보였으며, Udel, PES 그리고 Ultem 고분자 코팅 순으로 감소하였다. 고분자와 탄소섬유의 계면접착력 또한 비슷한 경향을 보였다. SEM 분석결과 PEPO로 코팅된 탄소섬유에서는 비닐에스터 수지 내에서 파괴가 일어난 것으로 보여지나, 다른 고분자로 코팅된 탄소섬유에서는 계면 또는 계면에서 가까운 곳에서 파괴가 일어난 것으로 판단된다. PEPO 코팅에 의한 계면접착력 향상은 PEPO내에 존재하는 P=O 때문으로 사료된다.

• Macromolecular Research
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• 제17권10호
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• pp.739-745
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• 2009

N,N'-(bicyclo[2,2,2]oct-7-ene-tetracarboxylic)-bis-L-amino acids 3a-g were synthesized by the condensation reaction of bicyclo[2,2,2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride 1 with two equimolars of Lalanine 2a, L-valine 2b, L-leucine 2c, L-isoleucine 2d, L-phenyl alanine 2e, L-2-aminobutyric acid 2f and L-histidine 2g in an acetic acid solution. Seven new poly(amide-imide)s PAIs 5a-g were synthesized through the direct polycondensation reaction of seven chiral N,N'-(bicyclo[2,2,2]oct-7-ene-tetracarboxylic)-bis-L-amino acids 3a-g with bis(3-amino phenyl) phenyl phosphine oxide 4 by two different methods: direct polycondensation in a medium consisting of N-methyl-2-pyrrolidone (NMP)/triphenyl phosphite (TPP)/calcium chloride ($CaCl_2$/pyridine (py), and direct polycondensation in a tosyl chloride (TsCl)/pyridine (py)/N,N-dimethylformamide (DMF) system. The polymerization reaction produced a series of flame-retardant and thermally stable poly(amide-imide)s 5a-g with high yield. The resulted polymers were fully characterized by FTIR, $^1H$ NMR spectroscopy, elemental analyses, inherent viscosity, specific rotation and solubility tests. Data obtained by thermal analysis (TGA and DTG) revealed that the good thermal stability of these polymers. These polymers can be potentially utilized in flame retardant thermoplastic materials.

• Bulletin of the Korean Chemical Society
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• 제27권8호
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• pp.1140-1144
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• 2006

A macrocyclic ligand, N,N',N'-tribenzyl-2,11,20-triaza[3,3,3](2,6)pyridinophane (BAPP), was used to prepare an iron(II) complex as a nonheme model complex, $[(BAPP)Fe]^{+2}$ (1). X-ray crystallography of a colorless crystal of 1 revealed that BAPP acted as a pentadentate ligand due to geometrical strain for the formation of a six-coordinate iron(II) complex by BAPP. As a result, the iron center revealed a significantly distorted square pyramidal geometry similar to that found in the active site of taurine dioxygenase (tauD). In the reaction of 1 with PhIO, no intermediate was observed in the UV-visible region of spectrometer at low temperatures. Catalytic oxidations of triphenyl phosphine with PhIO at ${-40^{\circ}C}$ revealed that 1 was able to convert triphenyl phosphine to triphenyl phosphine oxide.23; SSOCHKThioanisole was also oxidized to the corresponding methylphenyl sulfoxide under the same conditions.