The effect of some thiosemicarbazide derivatives on corrosion of aluminium in 2M sodium hydroxide has been studied using thermometric, weight loss and hydrogen evolution techniques. The rate of the corrosion depends on the nature of the inhibitor and its concentration, heated of hydrogenation, mode of interaction with the metal surface and formation of metallic complexes. The compounds are weakly adsorbed on the surface of aluminium and form a monolayer of the adsorbate. Values of the Arrhenius activation energies indicate agreement with those obtained for an activation controlled process.

(-)-(1R, 2R) and (+)-(1S, 2S)-menthyl-trans-2-phenylcyclopropanecarboxylat e have been synthesized with the aid of chiral Cu(II) complex catalyst by the addition reaction of l-menthyldiazoacetate to styrene. The yield was 75%, with the purity of trans isomer over 95% and the optical purity of 95%.

Several new palladium(II) complexes of aminophosphines, $(Pd(L)X_2)$, (L = $Ph_2PNH$ ++ $NR_2$; R = $CH_3(L_1)$, $C_2H_5(L_2)$ : X = Cl, Br, I, and NCS) that contain two different donor atoms of nitrogen and phosphorus as ${\pi}$-electron acceptor, were synthesized and characterized by conductivity measurement, ir, and UV/Vis-spectra. For the dithiocyanatopalladium(II) complexes with aminophosphines, it was confirmed that the thiocyanate group trans to phosphorus is coordinated as Pd-NCS mode and the one trans to nitrogen as Pd-SCN mode, and the aminophosphines form six-membered chelate ring. The spectra of dihalogenopalladium(II) complexes with aminophosphines show that the band maxima are shifted to the short wavelengths as the concentration is decreased.

In order to investigate the oligomerization state of the plasma membrane proteolipid apoprotein purified from the bovine kidney, fluorescence polarization experiment was carried out in the two different solvent systems, i.e., water and organic solvent(chloroform-methanol). The molecular volumes of the proteins estimated from the Perrin equation, were to be 45,258$A^3$ and 17,608$A^3$ in water and organic solvent, respectively. These values indicate that a trimerization is possibly occurring in the aqueous environment. As an auxiliary experiment for the calculation of the molecular volume using Perrin equation, fluorescence quenching constants ($K_q$) with the quencher acrylamide and fluorescence lifetimes (${\tau}_F$) of the intrinsic fluorophore tryptophan residue were estimated in the two different solvent systems. $K_q$ in water was 18.21$M^{-1}$ and it was 46.24$M^{-1}$ in organic solvent. Fluorescence lifetimes of tryptophan residue were calculated to be 2.80 nsec. in water and 3.81 nsec. in organic solvent, respectively.

2,7,7-Trimethyl-1,5-dicarboethoxybicyclo[3.3.0]oct an-2-ol(5) is synthesized as a synthetic intermediate for hirsutene by use of dianion methodology.

The hydrophobic interaction leading to the formation of ion-pair between $MB^+$ and $TPB^-$ was investigated spectroscopically by varying the medium with the addition of 1,A-dioxane or urea. Beyond 0.01 mole fraction of 1,A-dioxane in water or above 2.0M urea the ion-pair appeared to be completely dissociated into individual ions. The ion-pair was not observed in common organic solvents and the absorption maxima of $MB^+$ were correlated relatively well with the ${\pi}^{\ast}$-scale.

A new paradigm for the viscosity of fluid is presented by considering the fact that the viscosity is equal to the shear stress divided by the shear rate. The shear stress is obtained from the sum of kinetic and internal pressures of fluid, and the shear rate is found from the phonon velocity divided by the mean free path of the phonon. The calculated viscosities for various simple substances are in excellent agreements with those of the observed data through the wide temperature range covered both of liquid and gas phase.

The surface-enhanced Raman scattering of L-phenylalanyl-glycine (L-Phe-Gly), L-phenylalanyl-glycyl-glycine (L-Phe-Gly-Gly), glycyl-glycyl-L-phenylalanine (Gly-Gly-L-Phe), L-tyrosyl-glycine (L-Tyr-Gly), and L-tyrosyl-glycyl-glycine (L-Tyr-Gly-Gly) adsorbed on silver colloidal particles have been investigated. More detailed investigations on the surface-enhanced Raman scattering from L-phenylalanine (L-Phe), glycyl-L-phenylalanine (Gly-L-Phe), L-tyrosine (L-Tyr), and glycyl-L-tyrosine (Gly-L-Tyr) than in ref. 17 have also been made. It has been found that the above molecules adsorb on the surface via both the carboxylate ($COO^-$) and amino ($NH_2$) groups.

Some pattern recognition methods have been used to characterize Korean ancient porcelainsherds using their elemental composition as analyzed by instrumental neutron activation analysis. A combination of analytical data by means of statistical linear discriminant analysis(SLDA) has resulted in removal of redundant variables, optimal linear combination of meaningful variables and formulation of classification rules. The plot in the first-to-second discriminant scores has shown that the three distinct territorial regions exist among porcelainsherds of Kyungki, Chunbuk-Chungnam, and Chunnam, with respective efficiencies of 20/30, 22/27 and 14/15. Similar regions have been found to exist among punchong porcelain and ceradonsherds of Kyungki, Chungnam and Chunbuk, with respective efficiencies of 7/9, 15/16 and 6/6. Classification has been further attempted by statistical isolinear multiple component analysis(SIMCA), using the sample set selected appropriately through SLDA as training set. For this purpose, all analytical data have been used. An agreement has generally been found between two methods, i.e., SLDA and SIMCA.

Through the Bucherer-Berg method, new 5-alkylthiomethyl or 5-alkylsulfonylmethylhydantoins were prepared. The reaction of ethyl chloroacetate with these compounds gave 3-acetate and the subsequent hydrolysis with dilute sodium hydroxide resulted in 3-hydantoinacetic acid derivatives. These products are expected to exhibit anti-inflammatory and analgestic activities.

A thioamide, N-5-trifluoromethyl-6-methoxy-1-thionaphthoyl-N-m ethylglycine, undergoes trans${\rightleftharpoons}$cis photoisomerization around C-N bound in solution. Azulene quenching studies showed the photoisomerization to proceed via both singlet and triplet excited states.The total quantum yield of the trans${\rightarrow}$cis photoisomerization is about 0.26, 0.14 from the singlet excited state and 0.12 from the triplet excited state. Intersystem crossing and internal conversion quantum yields were calculated from sensitized photostationary state and a plausible mechanism is proposed.

Degradation of the 90 K superconductor $YBa_2Cu_3O_{7-{\delta}}$ in water and humid atmosphere were studied and its decomposition products were identified as $BaCO_3$, CuO, $Y_2(CO_3)_3{\cdot}3H_2O$ and $O_2$. XRD analysis, iodometric titration and IR-spectroscopy of the degraded samples suggest that the $YBa_2Cu_3O_{7-{\delta}}$ decomposes in three steps such as the reduction of $Cu^{3+}$ to $Cu^{2+}$, followed by the hydroxylation of $Ba^{2+}$ and $Y^{3+}$ via hydration and finally the formation of carbonates through the uptake of ambient $CO_2$.

Multilayer adsorption isotherms of nitrogen on hexagonal boron nitride, ${\gamma}$-alumina, and silica-gel powders are determined at the liquid nitrogen temperature using a gravimetric adsorption apparatus. The volume (V) of the adsorbed gas are plotted against the statistical thickness(t) of the adsorbed layer, and the t-method area are calculated from the slope of these V-t plots to compare with the BET area. A number of universal adsorption isotherms and the Frenkel-Halsey-Hill equation are used one after another in calculating the statistical thickness. The appropriateness of the FHH equation as an universal adsorption isotherm is discussed finally.

Mechanism of electrochemical polymerization of pyrrole (Py) on a Pt electrode in acidic aqueous solutions was studied by means of potentiostatic measurements, cyclic voltammetry and chronopotentiometry. Pyrrole molecule appeared to be initially oxidized via two-electron transfer step to produce oxidized pyrrole ion ($Py^+$), which was coupled with a non-oxidized pyrrole to yield a dimerized species, Py-Py. The Py-Py thus formed was further oxidized again via two-electron transfer step, which was followed by coupling with non-oxidized monomer and by concomitant expulsion of a $H^+$. Then the latter chain extension process was repeated. The chain extension and polypyrrole oxidation reactions occurred competitively.