• Bulletin of the Korean Chemical Society
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• v.26 no.3
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• pp.467-469
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• 2005

• Journal of the Korean Chemical Society
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• v.19 no.1
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• pp.38-42
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• 1975

Chloral-2-acetothienone was synthesized from the condensation of 2-acetothienone with chloral, and trichloroethylidene-2-acetothienone was obtained from the dehydration of chloral-2-acetothienone. From the reaction of trichloroethylidene-2-acetothienone with phenylhydrazine or substituted phenylhydrazines 2-aryl-6-(2-thienyl)-3(2H)-pyridazinones were obtained. 3-(2-Thienyl)-5-trichloromethyl-2-pyrazoline was synthesized from the reaction of trichloroethylidene-2-acetothienone with hydrazine hydrate.

• Journal of the Korean Chemical Society
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• v.67 no.4
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• pp.306-310
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• 2023

• Bulletin of the Korean Chemical Society
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• v.27 no.7
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• pp.1083-1085
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• 2006

• Journal of the Korean Chemical Society
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• v.61 no.5
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• pp.291-295
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• 2017

• Bulletin of the Korean Chemical Society
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• v.23 no.12
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• pp.1715-1718
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• 2002

Treatment of ethyl 5-hydroxy-3,4-diphenylthieno[2,3-c]pyridazine-6-carboxylate (1a) with hydrazine hydrate in ethanol gave the carbohydrazide 2,. Some derivatives of the latter compound have been synthesized. Also, 6-acetyl-3,4-diphenyl-5-hydroxythieno[2.3-c]pyridazine (1b) was subjected to some reactions to produce other new thienopyridazine derivatives.

• Journal of the Korean Chemical Society
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• v.48 no.3
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• pp.331-334
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• 2004

• Journal of the Korean Chemical Society
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• v.17 no.1
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• pp.25-30
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• 1973

2,6-Disubstituted-3-pyridazinones were synthesized by the reactions of $\gamma$,$\gamma$,$\gamma$-trichloroethylidene-m-nitroacetophenone with phenylhydrazine and substituted phenylhydrazines, and hydrazone was isolated as an intermediate from the reaction with 2, 4-dinitrophenylhydrazine. From the reaction with hydrazine hydrate 3-(m-nitrophenyl)-5-trichloromethyl-2-pyrazoline was obtained in good yield. The effect of substituents on phenyl group in the reaction of $\gamma$,$\gamma$,$\gamma$-trichloroethylidene-m-nitroacetophenone with substituted phenylhydrazines was also discussed.

• Journal of the Korean Graphic Arts Communication Society
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• v.21 no.2
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• pp.101-108
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• 2003

We synthesised 1,3-Diphenyl-5-pyren-2-yl-4,5-dihydro-1H-pyrazole(DPP) and investigated its optical properties. The structure of DPP was confirmed by GC-Mass and elemental analysis. The absorption and photoluminescent spectra of DPP were measured at both hydrophobic and hydrophilic solvents and by the stokes shifts of DPP Lippert's equation could be applied. The results showed linear relation between $[{\varepsilon}-1/2{\varepsilon}+1)-(n^2-1/2n^2+1)]$ and $({\mu}_g\;-\;{\mu}_2)^2$.

• Bulletin of the Korean Chemical Society
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• v.28 no.9
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• pp.1539-1544
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• 2007

1-Phenyl-3-p-fluorophenyl-5-p-chlorophenyl-2-pyrazoline has been synthesized and characterized by elemental analysis, IR, UV-Vis and X-ray single crystal diffraction. Density functional calculations show that B3LYP/6-311G** method can reproduce the structural parameters. The electronic absorption spectra have been predicted based on the optimized structure by using 6-311G** and 6-311++G** basis sets and compared with the experimental values. The results indicate that TD-DFT method can only predict the electronic absorption spectra of the system studied here approximately. On the basis of vibrational analyses, the thermodynamic properties of the title compound at different temperatures have been calculated, revealing the correlations between ,C0p,m,S0m,H0m and temperature.