• 농업과학연구
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• 제11권1호
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• pp.176-181
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• 1984

살충성 O,O-diethylphenylphosphate (A)와 3,5-dimethylphenyl-O,O-diethylphosphate 유도체 (B)에 의한 acetylcholinesterase(Ach E)의 phosphorylation 반응에 미치는 정량적인 자유에너지 관계(LFER)를 알아보기 위하여 Ach E의 두 작용점인 esteratic-anionic site에 대응하는 (A) 및 (B)의 P원자 및 meta 위치간의 공간직선 거리 및 알짜전하를 확장 H$\ddot{u}$ckel이론(EHT)에 의한 MO 계산 방법으로 계산하고 여러 가지 치환기상수와 $pI_{50}$ 상수를 Hammett 및 Okamoto-Brown식, Taft와 Swaln-Lupton의 DSP식에 적용한 회귀분석 결과로부터 살충작용에 미치는 정량적인 자유에너지 관계, %R과 %F를 계산하여 검토하였다. 즉, (A) 및 (B)의 살충효과는 서로 비슷하였으며 blending coefficient (${\lambda}$)는 모두 ${\lambda}$<1의 값을 나타내었다. (A) 및 (B)의 resonance effect (%R)와 field effect (%F)는 각각 %R=33.5, %F=66.5 그리고 %R=2, %F=98로 각각 계산되었는데(B)와 같이 phenyl group에 bulky한 소수성의 methyl group이 결합될수록 resonance effect($R_{\pi}$)보다는 direct through space field effect ($F_D$)가 아닌 through space field effect가 더 크게 영향을 미치게 된다는 사실을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제30권10호
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• pp.2393-2397
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• 2009

Second-order rate constants ($k_{HOO}$‒) have been measured spectrophotometrically for nucleophilic substitution reactions of Y-substituted phenyl benzenesulfonates (1a-g) with $HOO^-$ ion in $H_2O$ at $25.0\;{\pm}\;0.1\;{^{\circ}C}$. The Br$\phi$nsted-type plot is linear with ${\beta}_{lg}$ = ‒0.73. The Hammett plot correlated with with ${\sigma}^-$ constants results in much better linearity than ${\sigma}^o$ constants, indicating that expulsion of the leaving group occurs in the rate-determining step (RDS) either in a stepwise mechanism or in a concerted pathway. However, a stepwise mechanism in which departure of the leaving group occurs in the RDS has been excluded since $HOO^-$ ion is more basic and a poorer leaving group than the leaving Y-substituted phenoxide ions. Thus, the reactions of 1a-g with $HOO^-$ ion have been concluded to proceed through a concerted mechanism. The $\alpha$-nucleophile $HOO^-$ ion is more reactive than its reference nucleophile $OH^-$ ion although the former is ca. 4 p$K_a$ units less basic than the latter (i.e., the $\alpha$-effect). TS stabilization through intramolecular H-bonding interaction has been suggested to be irresponsible for the $\alpha$-effect shown by $HOO^-$ ion, since the magnitude of the $\alpha$-effect is independent of the electronic nature of substituent Y in the leaving group. GS destabilization through desolvation of $HOO^-$ ion has been concluded to be responsible for the $\alpha$-effect found in the this study.

• 대한화장품학회지
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• 제40권4호
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• pp.383-390
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• 2014

기질 분자로서 2-[(2,6-dioxocyclohexyl)methyl]cyclohexane-1,3-dione 유도체(1-23)들의 분자 내 치환기($R_1$ 및 $R_2$)가 변화함에 따른 tyrosinase 수용체의 저해활성에 관한 2D-QSAR 모델로부터 다음과 같은 결론을 얻었다. 유도된 최적의 2D-QSAR 모델은 $Obs.pI_{50}=-0.295({\pm}0.031)TDM$ $-0.120({\pm}0.014)DMZ+0.135({\pm}0.050)DMX$. $R_2+6.382({\pm}0.17)$이었으며, 예측성($q^2=0.843$)보다는 상관성($r^2=0.905$)이 큰 모델이었다. Tyrosinase 저해활성은 TDM > $DMX.R_2{\geq}DMZ$ 순으로 영향을 미치었으며, 기질분자의 소수성(ClogP > 0)이 크고, $R_1$-치환기의 입체적 크기가 클수록 더욱 증가하는 경향을 나타내었다. 모델을 분석한 결과, 분자 내 $R_2$-치환기 상 X-축 성분의 쌍극자능률($DMX.R_2$)이 클수록, 그리고 분자 전체의 쌍극자능률(TDM; Total Dipole Moment)과 Z-성분의 쌍극자능률(DMZ; Dipole Moment of Z-Component)이 작을수록 기질분자의 tyrosinase 저해활성이 높아짐을 암시하였다. 따라서 tyrosinase 저해활성은 기질분자 및 $R_2$-치환기의 전자 친화력에 기인한 것으로 예상되었다. 그러므로 저해활성을 증가시키려면 분자 내 극성 그룹을 소수성에 기여하는 비극성 작용기로 대체함이 바람직할 것으로 예측되었다.

• 한국응용과학기술학회지
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• 제7권1호
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• pp.93-105
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• 1990

Semicarbazone formation of nine monosubstituted benzaldehydes was studied kinetically in 20% methanol buffer solution at 15, 25, 35, and $45^{circ}C$. The rate of p-nitrobenzaldehyde semicarbazone formation is 2.7 times as fast as that of benzaldehyde, while p-hvdroxybenzaldehyde is 3.6 times as slow as that of benzaldehyde. Activation energies for p-chlorobenzaldehyde, benzaldehyde, p-methylbenzaldehyde, p-methoxybenzaldshyde, p-hydroxybenzaldehyde, and p-dimethylaminobenzaldehyde semicarbazone formation are calculated as 5.80, 6.19, 6.57, 7.06, 8.03, and 6.46 kcal/mol respectively. It is concluded from the effect of ionic strength that the reaction is affected by not ions but neutral molecules involving hydrogen bonding between oxygen atom of carbonyl group and hydrogen atom of acid-catalyst, and concerted attack of the necleophilic reagent, free base on carbonyl compound. Also, the effect of solvent composition is small in 20% and 50% methanol (and ethanol) aqueous solutions. The ${\rho}-{\sigma}$ plots for the rates of semicarbazone formation at pH 7.1 show a linear ${\rho}-{\sigma}$ relationship (${\rho}=0.14l$, in contrast to that at pH 2.75 and pH 5.4 corresponding to ${\rho}-{\sigma}$ correlations reparted by Jencks. The rate of semicarbazone formation at pH 5.4 show a relationship which is convex upward, resulting in a break in the curve but at pH 2.75, slight difference from a linear relationship. As a result of studying citric acid catalysis, second-order rate constants increase linearly with citric acid concentration and show a 2 times increase as the catalyst concentration is varied from 0.025 to 0.1 mol/1 at pH 2,9, but slight increase at pH 5.3. The rate-determining step is addition below pH 5 but is dehydration between pH 5 and 7. Conclusively, the rate-determining step of the reaction changes from dehydration to addition in respect to hydrogen ion activity near pH 5. The ortho: para rate ratio of the hydroxybenzaldehydes for semicarbazone formation is about 17 at $15^{\circ}C$. It is concluded that the results constitute strong evidence in favor of greater stabilization of p- than o-hydroxybenzaldehyde by substituent which donate electrons by resonance and is due to hydrogen bonding between the carbon-bound hydrogen of the-CHO group and the oxygen atom of the substituent.

• 농약과학회지
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• 제13권2호
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• pp.63-69
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• 2009

벼 도열병균에 대하여 2-페닐이미노-1,3-티아졸린-4-아세트아닐리드 유도체의 NH수소가 항균력에 미치는 영향을 조사하기 위하여 2-페닐이미노-1,3-티아졸린 골격의 C-4 곁가지에 모르포리닐, 피페리디닐 등의 기능기가 도입된 4-모르포리 닐카르보닐메틸-2-페닐이미노-1,3-티아졸린 2(X=O), 피페리디닐카르보닐메틸-2-페닐이미노-1,3-티아졸린 3(X=C) 등의 새로운 화합물을 합성하였다. 합성된 30종 화합물의 대표적인 식물병원균 6종에 대한 항균력 시험을 수행하였다. 키틴 이합체를 염소로 처리한 다음 생성된 중간체, 아세토아세틸클로라이드의 분리없이 모르폴린 또는 피페리딘과 반응시켜 각각 상응하는 감마-클로로-베타-케토 유도체를 얻었다. 이들을 각각 티오우레아 유도체와 반응시켜 4-모르포리닐카르보닐메틸-2-페닐이미노-1,3-티아졸린 2, 피페리디닐카르보닐메틸-2-페닐이미노-1,3-티아졸린 3을 좋은 수율(27-98%)로 합성하였다. 화합물 3의 벼 도열병원균에 대한 항균력은 피페리디닐기가 C-4 위치에 치환되어 있고 2-페닐이미노기의 페닐기의 ortho 및 para 위치에 불소가 포함된 화합물의 경우(3j)에 가장 높았다 (100 ppm, 90%). 이것으로 미루어보아 2-페닐이미노-1,3-티아졸린 계열의 C-4위치의 치환체는 이 계열 화합물의 벼도열병균에 대한 항균활성을 나타내는데 보조적인 역할을 하는 것으로 생각된다.

• Bulletin of the Korean Chemical Society
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• 제30권12호
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• pp.2913-2917
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• 2009

Second-order rate constants (k$_{Nu–}$) have been measured for nucleophilic substitution reactions of Y-substituted phenyl benzoates (1a-i) with butane-2,3-dione monoximate ($Ox^-\;an\;\alpha$-nucleophile) and Z-substituted phenoxides in 80 mol% H$_2$O/20 mol% DMSO at 25.0${\pm}$0.1$^{\circ}C$. Hammett plots correlated with ${\sigma}^o$ and ${\sigma}^-$ constants for reactions of 1a-h with Ox$^–$ exhibit many scattered points. In contrast, the Yukawa-Tsuno plot results in a good linear correlation with ${\rho}_Y$ = 2.20 and r = 0.45, indicating that expulsion of the leaving group occurs in the rate-determining step (RDS). A stepwise mechanism with expulsion of the leaving-group being the RDS has been excluded, since Y-substituted phenoxides are less basic and better nucleofuges than Ox$^–$. Thus, the reactions have been concluded to proceed through a concerted mechanism. Ox$^–$ is over 10$^2$ times more reactive than its reference nucleophile, 4-chlorophenoxide (4-ClPhO$^–$). One might suggest that stabilization of the transition-state (TS) through intramolecular general acid/base catalysis is responsible for the ${\alpha}$-effect since such general acid/base catalysis is not possible for the corresponding reactions with 4-ClPhO$^–$. However, destabilization of the ground-state (GS) of Ox$^–$ has been concluded to be mainly responsible for the ${\alpha}$-effect found in this study on the basis of the fact that the magnitude of the ${\alpha}$-effect is independent of the nature of the substituent Y.

• Bulletin of the Korean Chemical Society
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• 제35권8호
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• pp.2448-2452
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• 2014

Second-order rate constants ($k_N$) have been measured spectrophotometrically for $S_NAr$ reactions of Y-substituted-phenoxy-2,4-dinitrobenzenes (1a-1g) with hydrazine and glycylglycine in 80 mol % $H_2O$/20 mol % DMSO at $25.0{\pm}0.1^{\circ}C$. Hydrazine is 14.6-23.4 times more reactive than glycylglycine. The magnitude of the ${\alpha}$-effect increases linearly as the substituent Y becomes a stronger electron-withdrawing group (EWG). The Br${\o}$nsted-type plots for the reactions with hydrazine and glycylglycine are linear with ${\beta}_{lg}=-0.21$ and -0.14, respectively, which is typical for reactions reported previously to proceed through a stepwise mechanism with expulsion of the leaving group occurring after rate-determining step (RDS). The Hammett plots correlated with ${\sigma}^{\circ}$ constants result in much better linear correlations than ${\sigma}^-$ constants, indicating that expulsion of the leaving group is not advanced in the transition state (TS). The reaction of 1a-1g with hydrazine has been proposed to proceed through a five-membered cyclic intermediate ($T_{III}$), which is structurally not possible for the reaction with glycylglycine. Stabilization of the intermediate $T_{III}$ through intramolecular H-bonding interaction has been suggested as an origin of the ${\alpha}$-effect exhibited by hydrazine.

• 대한화학회지
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• 제29권3호
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• pp.277-282
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• 1985

N-benzylideneaniline 유도체의 C-phenyl group 파라위치에 치환기가 변화함에 따라 imidoyl양성자의 화학적 이동 (H${\alpha}$-SCS)에 미치는 자유에너지 직선관계(LFER)를 검토하기 위하여 치환기별 H$_{\alpha}$-SCS와 ${\sigma}$,${\sigma}^+$, ${\sigma}_I$,${\sigma}_R$, F 및 R등의 여러가지 자유에너지 관계 파라미터를 Hammett, Okamoto-Brown식과 그리고 Taft, Swain-Lupton의 DSP식에 적용한 바, 2.8∼3.2의 섞임계수(blending coefficient values, ${\lambda}$)값을 얻음으로써 공명효과(R)가 유발효과(I)나 장효과(F)보다 H_${\sigma}$-SCS에 크게 영향을 미친다는 사실을 알 수 있었으며 Swain-Lupton의 식으로 구한 %R = 66.6 and %F = 33.4의 값으로 부터 H$_{\sigma}$-SCS에 미치는 공명효과(R)와 장효과(F)의 비가 2:1이라는 정량적인 관계를 알았다.

• Bulletin of the Korean Chemical Society
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• 제23권5호
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• pp.688-692
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• 2002

The aminomethylation of phenols with para-substituents by the Mannich reaction has successfully been accomplished to produce the Mannich bases 2-6. The compounds 7-8 have also been synthesized in order to identify the effect of the side arms and t he macrocycle in the complex formation. Protonation constants and stability constants of the double armed diaza-18-crown-6 ethers 2-7 with metal ions have been determined by potentiometric method at 25 $^{\circ}C$ in 95 % methanol solution. Under a basic condition (pH > 8.0), the double-armed crown ethers 2-6 revealed stronger interaction with divalent metal ions than the simple diazacrown ether 1. The stability constants with these metal ions were Co 2+ < Ni2+ < Cu2+ > Zn 2+ in increasing order, which are in accordance with the order of the Williams-Irving series. The stability constants with alkali earth metal ions were Ca 2+ < Sr 2+ < Ba 2+ in increasing order, which may be explained by the concept of size effect. It is noteworthy that the hosts 2-6, which have phenolic side arms and a macrocycle, bind stronger with metal ions than the hosts 1 and 7. On the other hand, the host 8, which has phenolic side arms with a pyperazine ring,provided comparable stability constants to those with the host 3. These facts demonstrate that phenolic side arms play a more important role than the azacrown ether ring in the process of making a complex with metal ions especially in a basic condition. In particular, the log KML values for complexation of divalent metal ions with the hosts 2-6 had the sequence, i.e., 2 (R=OCH3) < 3 (R=CH3) < 4 (R=H) < 5 (R=Cl) < 6 (R=CF3). The stability constants of the hosts 5 and 6 containing an electron-withdrawing group are larger than those of the hosts 2 and 3 containing an electron-donating group. This substituent effect is attributed to the solvent effect in which the aryl oxide with an electron-donating group has a tendency to be tied strongly with protic solvents.

• 대한화학회지
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• 제34권5호
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• pp.430-437
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• 1990

금속원자 반응기를 사용하여 몰리브덴 금속증기와 1,3-butadiene 유도체를 반응시켜서 (${\eta}^4$-CH$_2$CRCR'CH$_2$)$_3$Mo(R, R'= H 또는 CH$_3$)를 합성하였으며, 이 때 생성된 유기금속화합물에 대한 1,3-butadiene 유도체의 메틸치환기 효과에 대하여 논의하였다. 그리고 몰리브덴 금속증기와 다른 몇 가지 알카디엔화합물을 반응시켜서 유기금속화합물이 형성됨을 확인하였으며 이들은 공기 중의 실온에서 쉽게 분해 되었다. 또한 (${\eta}^4$-CH$_2$CCH$_3$CCH$_3$CH$_2$)$_3$Mo와 일산화탄소를 반응시켜서 (C$_6$H$_{10}$)$_2$(CO)$_3$Mo를 합성하였으며 이 화합물의 금속-리간드 결합에 관하여 논하였다.