• 공업화학
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• 제33권3호
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• pp.289-295
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• 2022

본 연구에서는 동종의 thiophene계 고분자를 전극과 전해질 재료로 적용하여 고체 전해질과 전극이 맞닿은 계면 저항을 감소시킨 고분자 전지를 제작하였다. 먼저 poly(3,4-ethylenedioxy thiophene) (PEDOT) 기반 전극과의 계면 저항을 최소화하기 위해 3,4-ethylenedioxy thiophene (EDOT) 올리고머[oligo(EDOT)]를 고체 전해질에 도입하고, oligo(EDOT)의 부족한 리튬 염 해리능력을 향상시키기 위해서 poly(vinylidene fluoride) (PVdF)와 블렌딩한 oligo(EDOT)/PVdF 블렌드 기반 고체 전해질을 제작하였다. 그 결과, oligo(EDOT)에 PVdF를 도입함으로써 고체 고분자 전해질의 이온 전도도는 증가하였다. 또 PEDOT 기반 전극과 oligo(EDOT)/PVdF 블렌드 기반 고체 전해질로 이루어진 전 고체 고분자 전지의 전기화학적 특성을 평가한 결과, 동종의 thiophene계 고분자 물질을 전극과 전해질에 도입함으로써 계면 저항이 크게 감소함을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제33권8호
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• pp.2585-2591
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• 2012

A series of heterocyclic chalcone derivatives bearing heterocycles such as thiophene or furan ring as an isostere of benzene ring were carefully prepared, and the influence of heterocycles on 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activities was systematically investigated. Structure-activity relationships (SAR) analysis showed that the activities of thiophene ring-containing chalcones were higher than those of furan ring-containing chalcones, and the presence of methyl substituent of heterocyclic ring distinctly affected the activities compared with non-substituted heterocycles in an opposite manner, with the 4'-methyl group of thiophene ring increasing activity and the 3'-methyl group of the furan ring decreasing activity. The distinct isosteric effect of heterocycles (i.e., thiophene or furan ring) on radical scavenging activities of heterocyclic chalones was distinctly demonstrated in our work.

• 농약과학회지
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• 제5권2호
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• pp.33-36
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• 2001

2-Chloromethyl-1,3-dioxolane기가 치환된 새로운 thiophene sulfonylurea계 유도체들을 합성하였고, 신규 합성된 화합물을 발아전 토양처리와 발아후 경엽처리를 통하여 문제잡초 9종의 제초활성을 규명하였으며, 답작 조건의 이앙벼 및 주요 잡초에 대한 제초활성도 시험하였다. 이 화합물들의 제초활성은 헤테로고리의 치환기에 따라 매우 다르게 나타났는데, 4, 6 위치에 각각 dimethoxy, 혹은 methyl, methoxy가 치환된 pyrimidine, 혹은 triazine이 붙어있는 sulfonylurea들이 활성이 좋았다. 그러나 이들은 2-fluoromethyl-1,3-dioxolane기가 치환된 thiophene sulfonylurea계 유도체보다 일반적으로 제초활성이 약하게 나타났다.

• Fibers and Polymers
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• 제1권1호
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• pp.25-31
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• 2000

Poly(3-hexyl thiophene)(P3HT) and poly(3-dodecyl thiophene)(P3DT) were polymerized by oxidative coupling with ferric chloride. The P3HT light-emitting device emitted red light and it could be observable in the ordinary indoor light. The device had the turn-on electric field of about 3$\times$$10^7$ V/m. The maximum electroluminescene (EL) intensity was obtained when the thickness of polymer layer was about 130 nm in IT0/P3HT/Al device. The maximum external quantum yield was 0.002%. The maximum luminance was 21 cd/$m^2$. The EL intensity decreases with increasing the crystallinity of the polymer layer. By using the oriented poly(3-alkyl thiophene)(PAT) layer as an electroluminescent layer in the ITO/polymer/Al light-emitting devices, the polarized EL light emission was observed. The EL intensity ratio of parallel to perpendicular direction to the stretch direction for P3HT was about 1.40.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.202.2-202.2
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• 2014

We have studied the bonding structures of five membered aromatic ring heterocyclic molecules, such as furan, thiophene, and selenophene, adsorbed on the Si(100) surface at room temperature with density functional theory. Additionally, we have investigated the evolution upon annealing of thiophene and selenophene molecules on the Si(100) surface by the core-level photoemission spectroscopy and near-edge X-ray absorption fine structure (NEXAFS). The core-level-spectra measured at different temperatures are consistently interpreted in terms of various adsorption structures suggested by theoretical calculations. In this study, we found the most suitable structures by theoretical and experimental results considering room temperature and mild thermal annealing.

• Rapid Communication in Photoscience
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• 제1권2호
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• pp.27-29
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• 2012

Noble diamine monomers containing thiophene moiety were prepared, such as 2,5'''-diamino-2, 2':5', 2'':5'', 2'''-quaterthiophene (4TDA) and 2, 5'''''-diamino-3'', 4'''-dihexyl-2,2':5', 2'':5'', 2''':5''', 2'''':5'''', 2'''''-sexithiophene (6TDA). Then, these monomers were utilized to prepare polyimides with 3,6-diphenylpromellitic dianhydride (DPPMDA), 3,6-di(4'-trifluoro-methylphenyl) pyromellitic dianhydride (6FPMDA) or 3,6-di(3',5'-bis (trifluoromethyl)phenyl) pyromellitic dianhydride (12FPMDA) via a conventional two-step process. The polyimides were characterized by FT-IR, TGA and DSC, and then subjected CV, UV-vis and PL measurements. The polyimides containing thiophene moiety exhibited high glass transition temperatures ($280{\sim}310^{\circ}C$) and excellent thermal stability (> $420^{\circ}C$) in air as well as green emission (535~586 nm).

• Bulletin of the Korean Chemical Society
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• 제25권5호
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• pp.754-756
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• 2004

• 한국환경성돌연변이발암원학회:학술대회논문집
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• 한국환경성돌연변이발암원학회 2002년도 Current Trends in Toxicological Sciences
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• pp.92-92
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• 2002

• Bulletin of the Korean Chemical Society
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• 제30권12호
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• pp.2871-2872
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• 2009

• Bulletin of the Korean Chemical Society
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• 제34권1호
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• pp.306-308
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• 2013