• Journal of Photoscience
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• 제12권3호
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• pp.119-122
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• 2005

The photophysical properties of coumarin 6 laser dye have been studied in two solvents; ethanol and acetonitrile using steady-state fluorescence depolarization technique. The experimentally measured reorientation time of coumarin 6 is more or less the same in given solvents at particular temperature. It is found that coumarin 6 rotates slower in acetonitrile than in ethanol especially at higher values of viscosity over temperature. We also measure the ground and excited state dipole moments of coumarin 6 by solvent perturbation method. The results found that excited state dipole moment is greater than ground state dipole moment, which indicates that excited state is more polar than the ground state.

• 대한화학회지
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• 제52권6호
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• pp.649-656
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• 2008

• 한국산업융합학회 논문집
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• 제6권2호
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• pp.109-113
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• 2003

We report herein synthetic results obtained new types of crown ethers containing coumarin group. Crown ethers containing coumarin group 1~3 are hydroxymethyl-15-crown-5-ether linked with 4-hydroxy coumarin-4-acetic acid by esterification reaction. Crown ethers containing coumarin group 1~3 have different cavity in each crown ether rings. The 12-crown-4 ether with coumarin 1 has the smallest cavity size. The 15-crown-5 ether with coumarine 2 has the medium cavity size. The 18-crown-6 ether with coumarin 3 has the largest cavity size. Therefore each crown ether with coumarin group will recognize different ionic radius meta. Because of different hole size in crown ethers, these crown ethers seem to be had different selectivity in luminescent sensors. The crown ethers with coumarine 1~3 synthesized hydroxymethyl-15-crown-5-ether and 4-hydroxy coumarin-4-acetic acid same ratio at one to one. The synthesized crown ethers were characterized respectively by IR, NMR. GC-Mass.

• 한국식품영양학회지
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• 제10권1호
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• pp.6-13
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• 1997

여러 종류의 coumarin 유도체가 광화학 반응에 의하여 OH·라디칼을 생성하는 반응을 ESR 및 레이저 섬광분해 반응으로 진행시키고 반응속도 상수를 구하여 반응성가 메카니즘을 알아보았다. 본 연구에서 사용된 9종류의 coumarin 유도체는 모두 OH·라디칼 생성반응 메카니즘으로 반응이 진행되었으나 1-ethy1-3-nitro-1-nitrosoguanidine은 광조사에 의해 OH·라디칼 생성반응이 일어나기 전에 분해하여 카르벤 중간체로 변하였다. 9개의 coumarin 유도체는 DMPO-OH 스핀부가 생성물에 해당하는 시그날을 나타내었다. OH·라디칼을 소진시키는 NaN3, EtOH, HCOONa 등은 강한 광증감제로 작용하였다. 수화된 전자의 소멸 THRE 상수는 N20을 첨가했을 때가 K3Fe(CN)6을 첨가했을 때보다 크게 나타났다.

• Elastomers and Composites
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• 제44권4호
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• pp.416-422
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• 2009

Benzyl 4-Hydroxybenzoate와 1,6-Dibromohexane을 반응시켜 4-(6-bromohexyloxy)benzoic acid를 합성하였다. 이것을 하이드로퀴논과 반응시켜 브롬 그룹을 갖는 새로운 mesogenic ester를 합성하였다. Mesogenic ester를 자외선에 민감한 coumarin과 반응시켜 새로운 형태의 광응답성 coumarin 화합물을 합성 하였다. 합성된 화합물의 구조는 FT-IR 및 $^1H$-NMR에 의해 확인 하였으며, 그들의 열적 상전이온도 및 안정성들은 DSC, 편광현미경 및 X-선 회절에 의해 조사 하였다. 한편 합성된 새로운 화합물은 광학 편광 현미경 관찰에 의해 스멕틱 및 네마틱 구조를 갖는 쌍방성 액정성을 보였다.

• 한국환경과학회지
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• 제25권9호
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• pp.1283-1288
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• 2016

In this study, we synthesized fluorescent sensors from rhodamine 6G derivatives and hydroxy coumarin. The synthetic routes to the rhodamine 6G derivatives containing hydroxy coumarin are shown in Fig. 1. Two derivatives were synthesized through Schiff base reactions. The structures of the new compounds were confirmed by melting point, $^1H$-NMR, and GC-MS analyses. The compounds were found to selectively bind to tin ($Sn^{2+}$) ion by fluorescence titration using various metal cations. Longer carbon chains gave more sensitivity. $Sn^{2+}$ ions exhibited the strongest fluorescence among the nime ions. The binding analysis using Job plots suggested that compounds form 1:1 complexes with the $Sn^{2+}$ ions.

• Natural Product Sciences
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• 제4권1호
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• pp.51-52
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• 1998

From the chloroform extract of the defatted seeds of jute a new coumarin $C_9H_6O_4$, $m.p.\;178-179^{\circ}C$, was isolated. The structure of the compound was established as 4,7-dihydroxy coumarin on the basis of physical methods viz. $^1H\;NMR,\;^{13}C\;NMR$ and Ms.

• 한국수산과학회지
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• 제46권1호
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• pp.53-58
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• 2013

The active antifouling compounds coumarin and its derivatives were isolated from the cinnamon tree Cinnamomum loureiroi. The antifouling activities were determined using representative soft fouling organisms: the seaweed Ulvapertusa and diatom Navicula annexa. The chemical constituents with antifouling activities were identified as coumarin, hydroxylcoumarin, coumaric acid, and cinnamaldehyde by interpreting nuclear magnetic resonance, and high-resolution mass spectroscopy data. These compounds were isolated from 1.09 g of crude Cinnamomum sp. methanol extract, yielding approximately 18.4, 6.3, 9.8, and 14.7 mg of coumarin, hydroxylcoumarin, coumaric acid, and cinnamaldehyde, respectively. The compounds inhibited U. pertusa zoospores with $EC_{50}$ values of $0.13-0.25{\mu}g/mL$, and the diatom N. annexa with $EC_{50}$ of $0.21-0.81{\mu}g/mL$.

• Applied Biological Chemistry
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• 제42권3호
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• pp.210-217
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• 1999

전통민속주 제조에 이용되는 부재료 가운데 휘발성 향기성분인 asarone, coumarin, thujone등 식품에 허용기준이 제한된 독성 관련 향기성분을 함유하고 있는 식물성 방향재료 및 약용재료를 확인, 분류하기 위하여 이들의 20% ethanol 추출액으로부터 고상추출(solid phase extraction) 방법을 이용하여 각 성분을 흡착, 용리시킨 후 GC-FID와 GC/MS로 검출, 확인하였다. 조사대상 87종의 식물성재료 중 창포(Acorus asiaticus Nakai), 석창포(Acorus gramineus Solander), 당귀(Angelica gigus Nakai), 백단향(Santalum album) 등 6종에서 asarone이 검출되었으며, coumarin은 소회향(Anethum graveolens), 회향(Foeniculum vulgare Gaertner), 자초(Lithosperum erythrorhizon Siebold et Zuccarinii) 등 22종에서 검출되었다. 한편, 우실(Achyranthes japonica Nakai), 사인(Amomum xanthiodes Wallich), 약쑥(Artemisia asiatia Nakai), 대마자(Cannabis sativa L.)씨, 골담초(Caragana sinica R.), 국화(Chrysanthem morifolium Ramat), 사삼(Codonopsis lanceolata Bentham et flooker), 회향(Foeniculum vulgare Gaertner) 등 24종에서는 thujone을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제18권6호
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• pp.594-599
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• 1997

A number of complexes of transition metal ions with some coumarin derivatives have been prepared and their structures were elucidated with the help of conductometric, photometric and infrared studies. The stability constants of various complexes were determined, in aqueous medium, at different temperatures potentiometrically. The thermodynamic characteristics, ΔG, ΔH and ΔS, were calculated. The electrical behaviour of prepared compounds was followed.