• Journal of Photoscience
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• 제8권2호
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• pp.79-82
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• 2001

2-(p-Diethylaminostyryl)pyrrole (I) and 2-[5-diethylaminothienyl]vinyl]pyrrole (II) derivatives with systematic variation of the acceptors have been synthesized and their first hyperpolarizabilities were measured. The $\beta$ values increased systematically as the aromatic resonance energy decreased. Moreover, the value of $\beta$ for the former increased gradually as the acceptor strength increased. The opposite trend observed in the latter series of compounds has been attributed to the distorted structure caused by the steric hindrance between the N-methyl group and the acceptor moiety.

• Bulletin of the Korean Chemical Society
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• 제33권1호
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• pp.305-308
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• 2012

• Bulletin of the Korean Chemical Society
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• 제29권3호
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• pp.679-681
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• 2008

• 폴리머
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• 제26권5호
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• pp.568-574
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• 2002

호스트 분자로서 환형 폴리옥시에틸렌을 사용한 inclusion 화합물을 이용하여 수용액상에서 피롤의 화학적 중합을 수행하였다. 이와 같은 합성 전략은 수용액상에서 화학적 산화방법에 의해 견고한 방향족 고분자의 사슬을 성장시킬 수 있는 가능성을 나타내며, 수용성 올리고 또는 폴리피롤을 손쉽게 얻을 수 있는 방법을 제시하고 있다. 본 연구에서는 부분적으로 고분자 주사슬에 환형 폴리옥시에틸렌을 함유한 수용성 폴리피롤을 얻었으며, NMR, IR, UV 및 MALDI-TOF MS 분석 등을 통하여 그 구조를 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제11권1호
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• pp.41-44
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• 1990

The rates of electropolymerization of pyrrole from aqueous solutions containing p-toluenesulfonic acid were studied as functions of the concentration of the surfactant anions and of temperature for the polymerization on the electrode surface immersed in the solution and also for the polymerization along the solution surface. In the case of the solution-surface polymerization, the polymerization rate showed maximum as the concentration of the p-toluenesulfonic acid changed at a fixed temsperature or as the temperature was varied at a fixed concentration. The decrease of the polymerization rate with increasing concentration or with rising temperature beyond the values at the maxima is interpreted as resulting from micelle formation.

• Bulletin of the Korean Chemical Society
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• 제17권6호
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• pp.515-520
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• 1996

Simple conditions were discovered to afford tripyrranes by reaction of 2,5-bis(α-hydroxymethyl)furan or 2,5-bis(α-hydroxy-α-phenylmethyl)thiophene with excess pyrrole in the presence of acid catalyst. Stepwise synthesis of porphyrins with core-ligand modification and synthesis of meso-tetraarylporphyrins bearing two different substituents in cis orientation have developed as building blocks for the various porphyrin-based model systems. Consequently, 21-thia-23-oxa-10,15-diphenylporphyrin (28), 21-oxa-10,15-diphenylporphyrin (29) and 21-oxa-23-carba-12-aza-10,15-diphenylporphyrin (30) were synthesized by acid-catalyzed [3+1] condensation between tripyrranes and 2,5-bis(α-hydroxymethyl)pyrrole or 2,5-bis(α-hydroxy-α-phenylmethyl)thiophene. The synthetic pathway described here gave regioisomerically pure porphyrins and thus overcame the synthetic problems associated with separation and purification of regioisomeric mixture.

• 한국자기공명학회논문지
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• 제22권4호
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• pp.115-118
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• 2018

Dipyrromethane 2 functionalized with 3-chloropropyl group on the meso carbon undergoes an unusual intramolecular electrophilic aromatic substitution reaction in the presence of $NaN_3$ instead of a simple nucleophilic substitution reaction. As a result, a new chiral dipyrromethane 1 was synthesized. In this reaction, the ${\beta}$-carbon of the pyrrole ring functions as a nucleophile while the carbon next to the chlorine atom acts as an electrophile. Interestingly, this reaction progresses even in the absence of an acid catalyst. Compound 1 was fully characterized by $^1H-^1H$ and $^1H-^{13}C$ COSY NMR spectroscopic analyses and the high resolution EI mass spectrometry.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1991년도 제1차 학술발표초록집
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• pp.39-39
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• 1991

• Bulletin of the Korean Chemical Society
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• 제18권10호
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• pp.1043-1045
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• 1997

• Bulletin of the Korean Chemical Society
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• 제9권6호
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• pp.413-414
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• 1988