• 대한화학회지
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• 제44권3호
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• pp.229-236
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• 2000

6-Chloro-2-hydrazinoquinoxaline4-oxide(10)를 아세틸아세톤 또는 디벤조일메탄과 반응시켜 분자내 고리화반응에 의한 6-chloro-2-(3,5-disubstituted pyrazol-1-yl) quinoxaline 4-oxide류(11)를 합성하였다. 화합물 11을 phosphoryl chloride로 염소와 반응시켜 3,6-dichloro-2-(3,5-disubstituted pyrazol-1-yl)quino-xaline류(12)를 합성한 다음 hydrazine hydrate 반응시켜 6-chloro-3-hydrazino-2-(3,5-disubstituted pyrazol-1-yl)quinoxaline류(13)를 합성하였다. 화합물 13을 치환 벤즈알데히드류, benzenesulfonyl chloride, 치환 benzoyl chloride류 및 acyl chlorid 류와 반응시켜 새로운 pyrazolylquinoxaline류(14-17)를 각각 합성하였다.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2002년도 International Meeting on Information Display
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• pp.762-765
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• 2002

The bilayer organic light-emitting diode using Al (DBM) $_3$ (DBM=Dibenzoylmethane) as an emitting material and poly (N-vinylcarbazole) (PVK) as hole-transport material, emitted bright blue-green light instead of blue light. The blue-green emission is attributed to exciplex formation at the solid interface between Al (DBM) $_3$ and the hole-transport material. The exciplex formation was evidenced by the measurement of the photoluminescence spectra and lifetimes of Al (DBM) $_3$, PVK and an equimolar amount of mixture of Al (DBM) $_3$ and PVK.

• 분석과학
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• 제11권2호
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• pp.79-87
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• 1998

최근의 소비자들은 waterproof 기능을 가진 광범위한 UV 차단 제품을 선호하며, 피부 안전성에도 많은 관심을 가지고 있다. NR method로 세포 자극성(in-vitro)을 실험한 결과, UV-B의 자외선 차단제들은 0.08 w/v% 이상에서 세포의 생존율이 떨어졌고, UV-A의 자외선 차단제들은 0.06 w/v% 이상에서 세포의 생존율이 떨어졌다. 무기 자외선 차단제들의 patch-test는 각각 10.5와 11.25 이하로 피부에 자극성은 없었다. UV 흡수 곡선, UV-B는 octyl methoxycinnamate(OMC), UV-A는 butyl methoxy dibenzoylmethane(BMDM) 가장 적합하였다. 따라서, 유기 자외선 차단제는 OMC와 BMDM이 nylon과 polyethylene에 코팅된 원료인 $Nylonpoly^{TM}$ UVA/UVB을 사용하였다. 무기 자외선 차단제는 zinc oxide(ZnO)와 titanium dioxide($TiO_2$)를 사용하였다. ZnO와 $TiO_2$의 혼합 비율은 6:4가 적당하였다. 총 UV차단제의 함량은 ZnO 6%, $TiO_2$ 4%와 $Nylonpoly^{TM}$ UVA/UVB 5%를 썬 스크린 크림에 혼합하였다. In-vi-tro의 SPF값은 38.9이었다. 응용으로, 동일 함량을 넣은 O/W type과 W/S type의 썬 스크린 크림을 만들어 시간 경과에 따른 SPF를 측정한 결과, SPF가 O/W type보다 W/S type이 5배 이상 오래 지속되었다. 이것은 해수욕, 등산, 스키를 탈 경우에 효과적이다. 본 연구는 자외선 차단제의 피부 트러블을 최소화하고자 하였으며, 매끄러움성, 피부 안전성과 자외선 차단 효과가 우수한 화장품이라고 생각되어진다.

• 대한화장품학회지
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• 제23권3호
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• pp.134-146
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• 1997

Consumers have recently preferred to purchase extensive UV intercepting products, which are waterproof and free from side effects on skin. Testing Cytoroxicity in SR method, cell survivial ratio of UV-B interceptors decreased above 0.08W/V%, and so did that of UV-A interceptors above 0.06W/V%. Also, Patch-test of inorganic UV interceptors resulted in no skin irritation even below 10.0 and 11.25. UV interceptors in the sunlight showed yellowish discoloration in 5 to 14 days. In absorption curves, UV-B was most suitable for Octyl methoxycinnamate and UV-A for Butyl methoxy dibenzoylmethane. Fro this reason, Nylonpoly UVA/UVB the material of OMC and BMDM coated with Nylon & polyethylene, was used as the organic UV interceptor. And zinc oxide and titanium dioxide was used as inorganic UV ibterceptors. The appropriate mixture ratio of ZnO and TiO2 was 6 to 4.6% of ZnO, 4% of TiO2 and 5% of Nylonpoly UVA/UVB were all combined with our sunscreen cream. The SPF value of in-vivo applied to a guinea pig was 34.9 and that of in-vivo was 38.5. Cyclomerhicone and dimerthicone were used in water-in-Silicone system. Ceryl diverhicone and sorbitan sesquioleate were used as emulsifiers and MgSO4, 7H2O, Mg-stearate/Mg-Al-stearate copolymer as emulsification stabilizers. In practical application, each SPF duration of O/W type and W/S type containing sunscreen cream of the same content showed that W/S type of sunscreen cream was 5 times as durable as the other. This product is fit for using in swimming, climbing or skiing. This research is to minimize skin trouble used by UV interceptors and to make one with proper softness, skin safety and UV intercepting efficiency.

• Bulletin of the Korean Chemical Society
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• 제34권2호
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• pp.399-405
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• 2013

Two series of new green phosphorescent polymers bearing a bis(2-phenyl-pyridine)iridium(III)(dibenzoylmethane) [$(ppy)_2Irdbm$] complex were designed and synthesized. Poly-carbazole (PCbz) derivative or polyfluorene with pendant carbazole groups (PFCbz) were employed as host polymers for the iridium complex. The iridium complex monomer was copolymerized with the host monomers using varying monomer ratios via a Yamamoto coupling reaction. Efficient energy transfer from host to dopant unit was observed by increasing the ratio of the iridium guest in the copolymers. Electroluminescent devices with the configuration ITO/PEDOT:PSS/polymer/BmPyPB/LiF/Al were fabricated and characterized. The phosphorescent polymers composed of the iridium complex guest and polyfluorene with carbazole pendants as a host performed better than the polymers composed of the same guest and the main chain polycarbazole host. A maximum external quantum efficiency of 0.73%, a luminous efficiency of 1.21 cd/A, and a maximum luminance of 372 $cd/m^2$ were obtained from a device fabricated using one of the synthesized copolymers.