• 공업화학
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• 제1권2호
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• pp.168-175
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• 1990

1, 2-Disubstituted imidazoline 화합물인 1-behenoylaminoethyl-1-glycidyl-2-heneicosylimidazolinium chloride(BHIC), 1-behen oylbis(aminoethyl)-1-glycidyl-2-heneicosylimidazolinium chloride(BBIC) 및 1-behenoyltris(aminoethyl)-1-glycidyl-2-heneicosylimidazolinium chloride(BTIC)로부터 유연제 원액인 BHICS, BBICS, BTICS를 각각 제조하여 아크릴섬유에 유연처리를 한 후 유연성, 평활성 및 대전방지성을 측정한 결과 유연제 모두 유연성과 평활성이 양호하였으며 약간의 대전방지성도 보유하였다. 또한 BBICS와 BTICS의 초기강연도는 5 grade, 5회 세탁후는 3~4 grade로 각각 나타나 내수성을 지닌 양호한 유연효과를 나타내었다. 아울러 처리온도에 따른 촉감의 내세탁성 및 pH 변화에 따른 촉감의 내세탁성 시험결과 등을 통하여 제조된 유연제가 내구성 유연제임을 입증하였다.

• 한국응용과학기술학회지
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• 제11권2호
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• pp.113-120
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• 1994

Amphoteric surfactants were synthesized by the cyclization of 1-(2-hydroxyethyl)-2-undecyl-2-imidazoline [I] with acrylic acid ethyl ester. Compound [I] was easily hydrolyzed with water, especially in the presence of a alkali, to afford amidoamines. After [I] was hydrolyzed, the reaction mixture was allowed to react with acrylic acid ethyl ester and then soapoinfied. Only sodium salts of N- -(2-carboxyethyl)-N'-(2-hydroxyethyl)aminoethyl]dodecanoyl amide[III] was obtained. However, when the reacton of [I] with acrylic acid ethyl ester was carried out in the presence of water, followed by soapnification, ring cleavage of [I] occurred at 2, 3 position, different from hydrolysis of [I] where the cleavage occurred at 1, 2 position, to give sodium salts of N-[N'-(2-carboxyethyl)aminoethyl]-N-(2-hydroxyethyl)dodecanoyl amide [IV] and N-[N', N'-bis(2-carboxyethyl)aminoethyl]-N(2-hydroxyethyl)dodecanoyl amide [V] as main products.

• Bulletin of the Korean Chemical Society
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• 제17권4호
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• pp.331-334
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• 1996

New copper(Ⅱ) complex of the pentaaza non-macrocyclic ligand 1-(2-aminoethyl)-3-(N-{2-aminoethyl}aminomethyl)-1,3-diazacyclohexane (2) and a dinuclear copper(Ⅱ) compex of the bis(macrocyclic) ligand 3, in which two 1,5,8,10,12,15-hexaazabicyclo[11.3.11.5]heptadecane subunits are linked together by an ethylene chain through the uncoordinated nitrogen (N10) atoms, have been prepared selectively by the reaction of the metal ion, 1,4,8-triazaoctane, ethylenediamine, and formaldehyde. The dinuclear complex [Cu2(3)]4+ has been also prepared by the reaction of [Cu(2)]2+ with ethylenediamine and formaldehyde. The reaction products largely depend on the molar ratio of the reactants employed. The mononuclear complex or each macrocyclic subunit of the dinuclear complex contains one 1,3-diazacyclohexane ring and has a square-planar geometry with a 5-6-5 or 5-6-5-6 chelate ring sequence. In acidic solution, the copper(Ⅱ) complex of 2 dissociates more slowly than those of other related non-cyclic polyamines.

• Bulletin of the Korean Chemical Society
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• 제7권1호
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• pp.82-83
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• 1986

• Bulletin of the Korean Chemical Society
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• 제22권1호
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• pp.107-109
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• 2001

• Bulletin of the Korean Chemical Society
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• 제20권7호
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• pp.846-848
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• 1999

• Bulletin of the Korean Chemical Society
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• 제20권8호
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• pp.961-964
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• 1999

• Bulletin of the Korean Chemical Society
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• 제34권7호
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• pp.2125-2130
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• 2013

A new nickel(II) complex $[NiL^1]^{2+}$ ($L^1$ = 1-(2-aminoethyl)-3-(N-{2-aminoethyl}aminomethyl-1,3-diazacyclohexane) containing one 1,3-diazacyclohexane ring has been prepared selectively by the metal-template condensation of formaldehyde with N-(2-aminoethyl)-1,3-propanediamine and ethylenediamine at room temperature. The complex reacts with nitroethane and formaldehyde to yield the pentaaza macrocyclic complex $[NiL^2]^{2+}$ ($L^2$ = 8-methyl-8-nitro-1,3,6,10,13-pentaazabicyclo[13.3.1]heptadecane) bearing one C-$NO_2$ pendant arm. The reduction of $[NiL^2]^{2+}$ by using Zn/HCl produces $[NiL^3(H_2O)]^{2+}$ ($L^3$ = 8-amino-8-methyl-1,3,6,10,13-pentaazabicyclo[13.3.1]heptadecane) bearing one coordinated C-$NH_2$ pendant arm that is readily protonated in acid solutions. The hexaaza macrocyclic complex $[NiL^4]^{2+}$ ($L^4$ = 8-phenylmethyl-8-nitro-1,3,6,8,10,13-hexaazabicyclo[13.3.1]heptadecane) bearing one N-$CH_2C_6H_5$ pendant arm has also been prepared by the reaction of $[NiL^1]^{2+}$ with benzylamine and formaldehyde. The nickel(II) complexes of $L^1$, $L^2$, and $L^4$ have square-planar coordination geometry in the solid states and in nitromethane. However, they exist as equilibrium mixtures of the square-planar $[NiL]^{2+}$ (L = $L^1$, $L^2$, or $L^4$) and octahedral $[NiL(S)_2]^{2+}$ species in various coordinating solvents (S); the proportion of the octahedral species $[NiL(S)_2]^{2+}$ is strongly influenced by the ligand structure and the nature of the solvent. Synthesis, spectra, and chemical properties of the nickel(II) complexes of $L^1-L^4$ are described.

• Journal of Plant Biotechnology
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• 제5권1호
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• pp.33-41
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• 2003

Microspore-derived cell lines resistant to 5-methyltryptophan (5MT, a tryptophan analog) or S-(2-aminoethyl)-L-cysteine (AEC, a Iysine analog) were selected in rice by in vitro mutagenesis. For selection of 5MT or AEC resistant cell lines, suspension-cultured cells were irradiated with gamma rays. Thirteen 5MT resistant cell lines were selected and they were able to grow stably at 2 times higher 5MT concentration. A feedback insensitive form of anthranilate synthesis, the pathway specific control enzyme for tryptophan synthesis, was detected from the 5MT resistant lines. Contents of the free amino acids in five resistant lines (MR12-1 to MR12-5) showed a 7.4 to 46.6 times greater level than that in the control culture. Tryptophan, phenylalanine, and tyrosine levels in the shikimate pathway were 28.1 and 22.5 times higher in MR12-3 and MR12 4, respectively, than that measured in the control cells. Four AEC resistant cell lines were isolated from cultures grown on medium containing 1 mM AEC, They were able to grow stably with 2 mM AEC, while sensitive calli were inhibited by 0.5 mM AEC. Aspartate kinase activities of the resistant lines were insensitive to the natural inhibitor, Iysine, and accumulated 2.2 to 12.9-fold higher levels of free Iysine than that of the control cells. Especially, the levels of aspartate, asparagine, and methionine in the aspartate pathway showed higher accumulation in the AEC resistant lines than that in the control cells.

• Journal of Radiation Protection and Research
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• 제7권1호
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• pp.11-16
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• 1982

Cysteamine(Mercaptoethylamine, MEA), S-2-Aminoethyl isothionronium Bromide HBr(AET) 및 S-2(2-Aminoethyl) Dihydrogen phosphorothioate(WR-638)들을 합성(合成)하고 이들 각각(各各) 또는 그들의 혼합물(混合物)의 $^{60}Co$ ${\gamma}$-선(線) 방사선(放射線)에 대(對)한 장해방호효과(障害防護效果)를 ICR생쥐를 사용(使用)하여 검토(檢討)하였다. 조사전(照射前) 15분(分)에 복강내(腹腔內)에 약제(藥劑)를 투여(投與)하고 그 효과(效果)를 검토(檢討)한바 MEA, AET 및 그들 혼합물(混合物)에 있어서는 약독작용(藥毒作用)이 관찰(觀察)되었으나 WR-638 및 AET와의 혼합물(混合物)에서는 약독작용(藥毒作用)이 경미(輕微)하거나 또는 거의 없었다. 시험(試驗)한 각각(各各)의 화합물(化合物) 및 그 혼합물(混合物)들은 $^{60}Co$ $\gamma$-선(線) 방사선(放射線)에 대(對)한 방호효과(防護效果)를 나타냈으며 AET와 WR-638의 혼합물(混合物)에 있어서는 부가(附加)된 방사선(放射線) 방호효과(防護效果)가 관찰(觀察)되었다.