• Bulletin of the Korean Mathematical Society
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• v.61 no.1
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• pp.1-12
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• 2024

In this paper, we introduce the notion of Gorenstein (m, n)-flat modules as an extension of (m, n)-flat left R-modules over a ring R, where m and n are two fixed positive integers. We demonstrate that the class of all Gorenstein (m, n)-flat modules forms a Kaplansky class and establish that (𝓖𝓕_m,n(R),𝓖𝓒_m,n(R)) constitutes a hereditary perfect cotorsion pair (where 𝓖𝓕_m,n(R) denotes the class of Gorenstein (m, n)-flat modules and 𝓖𝓒_m,n(R) refers to the class of Gorenstein (m, n)-cotorsion modules) over slightly (m, n)-coherent rings.

• Journal of KSNVE
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• v.11 no.2
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• pp.301-306
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• 2001

Electro-Rheological (ER) fluid is applied to a controllable squeeze film damper (SFD) for stabilizing a flexibly supported rotor system. ER fluid is a class of functional fluid whose yield stress varies according to the applied electric field strength, which is observed as viscosity variation of the fluid. In applying ER fluid to a SFD, a pair of rings of the damper can be used as electrodes. When the electrodes are divided into a horizontal pair and a vertical one, the SFD can produce damping force in each direction independently. A prototype of the directionally controllable SFD was constructed and its performance was experimentally and numerically investigated in the present work.

• Proceedings of the Korean Society for Noise and Vibration Engineering Conference
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• 2000.11a
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• pp.256-261
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• 2000

Electro-Rheological(ER) fluid is applied to a controllable squeeze film damper(SFD) for stabilizing a flexible rotor system. ER fluid is a class of functional fluid whose yield stress varies according to the applied electric field strength, which is observed as viscosity variation of the fluid. In applying ER fluid to a SFD, a pair of rings of the damper can be used as electrodes. When the electrodes are divided into a horizontal pair and a vertical one, the SFD can produce damping force in each direction independently. A prototype of the directionally controllable SFD was constructed and its performance was experimentally and numerically investigated in the present work.

• Bulletin of the Korean Chemical Society
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• v.9 no.5
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• pp.311-317
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• 1988

The surface-enhanced Raman scattering(SERS) of methoxybenzonitrile in a silver sol was investigated. All of ortho-, meta-, and para-substituted benzonitriles were found to adsorb on the silver surface via the nitrogen lone pair electrons. The benzene ring of meta derivative seemed likely to stand perpendicular to the silver surface, while the benzene rings of both otho and para derivatives assumed tilted stances with respect to the surface. The SERS technique appeared to be a useful means to study the substituent electronic effects.

• Korean Journal of Environmental Biology
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• v.40 no.4
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• pp.477-496
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• 2022

During a survey of free-living marine nematodes of Korea, two new marine desmoscolecid nematodes belonging to subgenus Quadricoma Filipjev, 1922 were discovered. Tricoma (Q.) jejuensis sp. nov. and T.(Q.) unipapillata sp. nov. are described based on specimens obtained from washings of coarse sediments from eastern and southern coasts of Korea. Tricoma (Q.) jejuensis sp. nov. is characterized by having 33 quadricomoid body rings and inversion at main ring 23, pentagonal head with truncated anterior end, a pair of ocelli situated at main ring 6, somatic setae comprising of 8 pairs of subdorsal setae and 12 pairs of subventral setae, and relatively short spicules (42-46 ㎛ long). Tricoma (Q.) unipapillata sp. nov. is characterized by 44 quadricomoid body rings and inversion at main ring 32, somatic setae comprising of 7 pairs of subdorsal setae and 10 pairs of subventral setae, globular head truncated anterior end, relatively short and stumpy cephalic setae with cuticular flange, one single naked ventral median genital papillae situated on main ring 20, and spicules with a proximally marked capitulum. Detailed morphological descriptions and illustrations of these two new species are provided in this study.

• Bulletin of the Korean Chemical Society
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• v.32 no.3
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• pp.768-778
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• 2011

Calixpyrroles and related macrocycles are non-planer synthetic anion receptors that have attracted considerable attentions in recent years. Although the synthesis of calix[4]pyrrole (known as meso-octamethylporphyrinogen) was reported more than 100 years ago, the anion binding properties were first discovered in 1996. The simple calix[4]pyrroles can be synthesized in single step in high yield by condensation of pyrrole with acetone. The compounds showed preferential binding for halide anions including fluoride, phosphate, carboxylate, and chloride in organic media. Efforts to improve the anion affinity of calix[4]pyrrole and to enhance its selectivity have led to the synthesis of a variety of new calixpyrrole derivatives. Among the various modifications, introduction of straps on one side of the calix[4]pyrroles are the most effective. Incorporation of aromatic rings other than pyrroles also exhibited interesting binding behaviour. Introduction of signalling units as part of the strapping element enable to detect the anions on chromogenic or fluorogenic fashion. Finding of the anion transport properties across the membrane and cytotoxic effects of the calix[4]pyrroles open new window for calixpyrrole-related research. The polymer-incorporated systems have also been employed as anion complexants in solvent-solvent extraction. These old, yet easy-to-make macrocycles have well advanced more recently with the discovery of the ion-pair complexation properties. In this review, the synthetic developments and anion binding properties of calixpyrroles for the last decades will be discussed and will cover the advances in calixpyrrole chemistry.

• Bulletin of the Korean Chemical Society
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• v.19 no.4
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• pp.439-444
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• 1998

The protonation of tetraphenylporphyrin (TPP) in acidic organic solutions was analyzed by acid titrimetric and temperature-dependent absorption measurements. Competition between the protonation of free base TPP $(TPPH_2)$ and the solvation of proton by near solvent molecules determines the equilibrium of the diprotonated TPP $(TPPH_4^{2+})$ formation. The diprotonated TPP exists as an ion pair complex with the acid counterions, which are found to affect the degree of red shift of the Soret band. The rotation of the phenyl rings also plays an important role in the diprotonation, as suggested by the decrease in the degree of diprotonation for the fluorophenyl TPP derivatives whose phenyl ring rotation is significantly hindered relative to normal TPP. The difference of fluorescence lifetime between $TPPH_2 \;({\pi}_{FL}=19.6\;ns)\; and\; TPPH_4^{2+} \;({\pi}_{FL}=2.1 \;ns)$ was used advantageously to measure the rate of protonation in the excited state. The protonation of TPPH2 are found to occur much slower than the diffusion of protons from bulk solution to the porphyrin ring. The monoprotonated TPP is suggested to be the transient species for the diprotonation process.

• Bulletin of the Korean Mathematical Society
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• v.20 no.1
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• pp.31-36
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• 1983

Let R be a commutative ring with 1, and A a unitary commutative R-algebra. By a derivation module of A, we mean a pair (M, d), where M is an A-module and d: A.rarw.M and R-derivation, i.e., d is an R-linear mapping such that d(ab)=a)db)+b(da). A derivation module homomorphism f:(M,d).rarw.(N, .delta.) is an A-homomorphism f:M.rarw.N such that f.d=.delta.. A derivation module of A, (U, d), there exists a unique derivation module homomorphism f:(U, d).rarw.(M,.delta.). In fact, a universal derivation module of A exists in the category of derivation modules of A, and is unique up to unique derivation module isomorphisms [2, pp. 101]. When (U,d) is a universal derivation module of R-algebra A, the A-module U is denoted by U(A/R). For out convenience, U(A/R) will also be called a universal derivation module of A, and d the R-derivation corresponding to U(A/R).

• Bulletin of the Korean Chemical Society
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• v.32 no.12
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• pp.4179-4184
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• 2011

The nucleophilic substitution reactions of bis(2,6-dimethylphenyl) chlorophosphate (5), containing the four ortho-methyl substituents, with X-pyridines are investigated kinetically in MeCN at $65.0^{\circ}C$. The free energy correlations for substituent X variations in the nucleophiles exhibit biphasic concave upwards with a breakpoint at a X = 3-Cl. Unusual positive ${\rho}_X$ (= +5.40) and negative ${\beta}_X$ (= -0.83) values are obtained with the weakly basic pyridines. The pyridinolysis rate of 5 is hundreds times slower compared to that of bis(phenyl) chlorophosphate because of the steric hindrance of the four ortho-methyl substituents in the two phenyl rings. Ion-pair mechanism is proposed and positive ${\rho}_X$ and negative ${\beta}_X$ values are substantiated by an imbalance of the transition state.

• YAKHAK HOEJI
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• v.24 no.3_4
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• pp.151-157
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• 1980

Color transition mechanism of shikonin as an acid-alkali indicator was studied. It was confirmed that the presence of phenolic hydroxy radical was essential for the color change of shikonin. But in accordance with shikonin sodium salt (blue color), which was presumed to make chelation as six membered rings. Shikonin in alkaline solution, by dissociated phenolic protons of naphthoquinone nucleous, converted to the corresponding anion and instead of disappearance tautomerization, electron delocalization occurred and an additional pair of nonbonding electrons in the anion was available for interaction with .phi. electron system of the ring with further extension of the conjugation. It was responsible for its blue color(corresponding color: orange) with needs less energy difference (${\phi}{\rarw}{\phi}^{*}$) because of conjugation extension. Shikonin sodium salt seems to have similar nuclear structure as shikonin anion.