• 대한화학회지
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• 제18권3호
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• pp.194-201
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• 1974

네자리 schiff리간드는 salicylaldehyde와 m-phenylenediamine을 Duff-반응 시킴으로써 N,N-bis(salicylaldehyde)-m-phenylenediimine을 합성하고 이 리간드와 Cu(II), Ni(II), Co(II) 및 Zn(II) 이온들과의 새로운 착물 Cu(II)$[C_{20}H_{14}O_2N_2]{\cdot}2H_2O, Co(II)[C_{20}H_{14}O_2N_2]{\cdot}2H_2O$ 및 Zn(II)$[C_{20}H_{14}O_2N_2]{\cdot}4H_2O$들을 합성하였다. 이들 착물에 대하여 가시부 흡수스펙트럼, 적외선스펙트럼, TGA, X-ray 회절 및 원소분석 결과에 의하여 Cu(II), Ni(II) 및 Co(II) 착물들은 리간드와 금속이 1:1 몰비 및 2수화물의 6배위 착물로 주어지며 Zn(II) 착물은 1:2 몰비 4배위 착물로 주어짐을 알았다

• 분석과학
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• 제9권4호
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• pp.345-354
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• 1996

산소-질소를 포함하는 여러 자리 시프염기 리간드인 비스-살리실알데히드-에틸렌디이민(SED), 비스-살리실알데히드-프로필렌디이민(SPD), 비스-살리실알데히드-디에틸렌트리이민(SDT), 비스-살리실알데히드-트리에틸렌테트라이민(STT) 및 비스-살리실알데히드-테트라에틸 렌펜타이민(STP) 등을 합성하고 이들 리간드들을 에탄올과 70% 디옥산 수용액에서 전위차법으로 넷, 다섯 및 여섯 단계의 양성자 해리상수값을 구하였다. 구리(II)-시프염기 착물의 안정도상 수값의 크기는 Cu(II)-SPD${\leq}$Cu(II)-SED~STT${\leq}$Cu(II)-STP 순서로 음전위쪽으로 이동하였다. Cu(II)-시프염기 착물의 산화-환원 과정은 일전자 반응이었다.

• 대한화학회지
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• 제56권3호
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• pp.357-362
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• 2012

5-Nonylsalicylaldoxime and salicylaldehyde are two derivatives of phenolic compounds which are very applicable materials in industries. Formerly the formylation of phenolic derivatives were carried out by Rimer-Tiemann method. In this work both of these two materials were synthesized by magnesium meditated formylation technique and their structural characterizations were compared by instrumental analysis technique. In order to achieve a selectively orthoformylated product, the hydroxyl group of nonylphenol (or phenol) was first modified by magnesium methoxide. The nonylphenol magnesium salt was then formylated by paraformaldehyde. The oximation reaction was finally applied to the prepared nonylsalicylaldehyde magnesium salt by liquid extracting via water and acid washing and other extractions. The solvent was finally removed by evaporation under reduced pressure. Some instrumental analysis such as $^1H$-NMR, GC/MS and FT-IR spectra were taken on the product in order to interpret the reaction characterization quantitatively and qualitatively. The formaldehyde and oxime functional groups of two compounds were investigated through $^1H$-NMR and FT-IR spectra and were compared. The yield of methoxilation was very good and the yields of formylation and oximation reactions were about 90%and 85% respectively. The orthoselectivity of formylation reaction were evaluated by comparing of the relevant spectra. The GC/MS spectra also confirmed the obtained results.

• Bulletin of the Korean Chemical Society
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• 제20권10호
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• pp.1225-1228
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• 1999

• Bulletin of the Korean Chemical Society
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• 제21권4호
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• pp.405-411
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• 2000

Electrochemical and spectroelectrochemical studies of cobalt-Schiff (Co-SB) base complexes, Co(salen) [N-N'-bis(salicylaldehyde)-ethylenediimino cobalt(II)] and Co(salophen) [N-N'-bis(salicylaldehyde)-1,2-pheny-lenediimino cobalt(II)], have been c arried out to test them as oxygen reduction catalysts. Both compounds were found to form an adduct with oxygen and exhibit catalytic activities for oxygen reduction. Comparison of spec-tra obtained from electrooxidized complexes with those from Co-SB complexes equilibrated with oxygen in-dicates that the latter are consistent with the postulated complex formed with oxygen occupying the coaxial ligand position, namely, Co(III)-SB·O2 - .The catalysis of oxygen reduction is thus achieved by reducing Co(III) in the oxygen-Co-SB adduct, releasing the oxygen reduction product, e.g., O2 - ., from the Co(II)-SB complex.

• 한국세라믹학회지
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• 제51권5호
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• pp.472-476
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• 2014

In this work, a new method that utilizes L-cysteine salicylaldehyde Schiff-base modified macroporous polystyrene resin (PS-CSC) as an effective sorbent has been developed for preconcentration of trace cadmium and lead in environmental water samples. The effect of pH, the contact time, the elution conditions, the flow rate, the initial concentration of target metal ions, and the effects of interfering ions on the preconcentration of the analytes were investigated. The maximum adsorption capacity of PS-CSC under optimum conditions for cadmium and lead were found to be 6.03 - 18.17 mg/g and 12.58 - 36.13 mg/g when the initial concentration of metal ions between 5.0 - 90 mg/L. The limits of detection for cadmium and lead were 2.46 ng/L and $0.52{\mu}g/L$, with a preconcentration factor of 200. The developed method has been validated by analyzing certified reference material and successfully applied for the enrichment and determination of trace cadmium and lead from environmental water samples.

• Journal of Applied Biological Chemistry
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• 제59권2호
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• pp.159-164
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• 2016

Plant growth regulator is an essential pesticide to date while the available active ingredient is not well understood unlike fungicide, insecticide and herbicide. This study was aimed to evaluate a new chemical class of plant growth regulator, and the total of 92 benzene derivatives were screened for their germination and early stage of the root growth regulation on Brassica campestris. Thirty benzaldehydes, nine acids, one amide, and one ester showed potent root growth inhibitory activity (>70 % inhibition) while only salicylaldehyde showed potent germination inhibition ($IC_{50}=81.2mg/L$) suggesting that benzaldehyde was a key module candidate for the growth inhibition. Benzaldehydes were further evaluated for root growth inhibition. 2,3-Dihydroxybenzaldehyde and salicylaldehyde showed $IC_{50}$ values of 8.0 and 83.9 mg/L, respectively. On the other hand, salicylaldehyde, and 2,4,5-trihydroxybenzaldehyde were found to have root growth promotion effects less than 10 mg/L. This result suggests that the benzaldehyde is a new class candidate for plant growth regulator.

• 대한화학회지
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• 제38권6호
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• pp.461-464
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• 1994

• Bulletin of the Korean Chemical Society
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• 제29권9호
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• pp.1819-1822
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• 2008

• 대한화학회지
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• 제58권2호
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• pp.193-197
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• 2014

Dibenzo-18-crown-6, dibenzo-21-crown-7 and dihydroxy dibenzo-18-crown-6 were synthesized by Bayer-Villiger oxidation strategy. Dibenzo-18-crown-6 and dibenzo-21-crown-7 could be synthesized through a three-step protocol starting from salicylaldehyde. Salicylaldehyde was reacted with bis-(2-chloroethyl)ether using $K_2CO_3$ in acetonitrile to link the two phenolic groups with the oxyethylene bridge followed by conversion of the formyl group to the hydroxy group via a Baeyer-Villiger reaction and finally linking the two phenolic group with appropriate oxyethylene bridge. The two target crown ethers were obtained in overall yield, 24% and 30%, respectively. This method has a great potential for synthesis of symmetrical as well as unsymmetrical dibenzo crowns with varying oxyethylene bridges. Baeyer-Villiger oxidation could be used to prepare dihydroxy derivative of dibenzo-18-crown-6 through acetylation of dibenzo-18-crown-6 followed by Baeyer-Villiger oxidation. The Baeyer-Villiger oxidation could be substantially accelerated using trifluoroacetic acid.