• Journal of the Korean Chemical Society
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• v.29 no.4
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• pp.372-381
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• 1985

Oxo molybdenum (V) complexes of substituted 8-quinolinols were synthesized and characterized by means of the investigation of elemental analysis, infrared spectra, electron spectra, electric conductivity and mass spectrometry compared with oxo molybdenum (VI) complexes. Oxo molybdenum(V) complexes were nonelectrolyte and one strong band of stretching mode of molybdenum and terminal oxygen appeared approximately $940cm^{-1}$. Oxo molybdenum(VI) complexes gave two peaks corresponding molybdenum containing ions, a molecular ion (I) of a 2 : 1 (ligand : metal) chelate and a fragment ion (II) of a 1:1 chelate due to the loss of ligand radical from ion (I). Molybdenum(V) complexes were observed the fragment ion(II) of a 1 : 1 chelate partly. The electronic spectra corresponding to d-d transition and charge transfer transition were observed and interpreted.

• Journal of the Korean Chemical Society
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• v.29 no.5
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• pp.482-489
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• 1985

The substituted quinolinium salts of pentachlorooxomolybdate (V) have been synthesized and characterized by means of the investigation of elemental analysis, infrared spectra, electron spectra, electric conductivity. The results of elemental analysis were well coincided with the theoretical value and all prepared salts were mononuclear complexes. The complexes were binary univalent electrolytes and analyzed d-d transition and charge transfer transition.

• Proceedings of the Optical Society of Korea Conference
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• 1991.06a
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• pp.80-80
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• 1991

1 GW급 옥소레이저를 직경과 깊이가 각각 0.5 mm에서 1.5 mm 사이에 있는 12 종류의 몰리브덴(Mo, Z=42) 홈 표적에 집속시켜서 발생하는 X-선의 세기를 측정하였다. 이때의 X-선 세기를 평면 표적의 경우와 비교하여 홈 표적에서의 효과를 조사하였다. X-선의 세기는 20 A 이하의 단파장을 통과시키는 필터뒤에 X-선 두어 측정하였으며 홈 표적에서의 X-선 세기는 평면 표적의 약 2 배가 됨을 보았다. 이 결과는 홈 표적에서의 플라즈마 감금효과에 의해 정성적으로ㅅ 성명 되었다.

• Journal of the Korean Chemical Society
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• v.25 no.3
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• pp.177-182
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• 1981

Benzoylpyridinium and lutidinium salts containing$ [MoO(NCS)_5]^{2-}$ have been synthesized. The complexes have been characterized by spectroscopic, magnetic susceptibility and conductivity studies. Benzoylpyridinium and lutidinium oxopentaisothiocyanatomolybdates(Ⅴ) arise from d-d and charge transfer transitions. The magnetic moments of the complexes are close to the spin-only values. The complex anions are mononuclear containing N-bonded $NCS^-$ ligand.

• Journal of the Korean Chemical Society
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• v.34 no.2
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• pp.171-178
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• 1990

The rates of the reaction Of $[MoO_2(S_2CNC_4H_8)_2]$ with triphenylphosphine in 1,2-dichloroethane have been by the spectrophotometric method. The increase in absorbance at 514 nm has been interpreted as a result of production of $[Mo_2O_3(S_2CNC_4H_8)_4]$ and the decrease in absorbance then corresponds to the reduction of $[Mo_2O_3(S_2CNC_4H_8)_4]$. The data suggest mechanisms involving the formation of $\mu$-oxo dimer in the first stage and molybdenum(IV) in the second stage.

• Journal of the Korean Chemical Society
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• v.26 no.6
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• pp.383-388
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• 1982

$Mo_2O_4Cl_2$$(X-py)_4{\cdot}2H_2$O and $(X-pyH)_4$[$Mo_2O_4(NCS)_6)$]${\cdot}H_2$O have been prepared. The infrared, electronic and reflectance spectra, molar conductances and magnetic susceptibility data of complexes are reported. $Mo_2O_4Cl_2$$(X-py)_4{\cdot}2H_2$O (X-py were 3-and 4-cyanopyridine, nicotinamide, 3,5-lutidine and 2-amino-4-picoline) were obtained by hydrolysis of the corresponding substituted pyridinium oxopentachloromolybdates(Ⅴ). Addition of water and substituted pyridines to molybdenum(Ⅴ)-thiocyanate ethylacetate extract yielded brown compounds, $(X-pyH)_4$[$Mo_2O_4(NCS)_6)$]${\cdot}H_2$O where X-py were pyridine, ${\alpha}$, 3-bromopyridine 3,5-lutidine, 3-benzoylpyridine and 4-acetylpyridine. Binuclear, $Mo_2O_4Cl_2(X-py)_4{\cdot}2H_2$ prepared from hydrolysis of $(X-pyH)_2[MoOCl_5]{\cdot}H_2O$ were diamagnetic and nonelectrolytes. The anion of $(X-pyH)_4$[$Mo_2O_4(NCS)_6)$]${\cdot}H_2$O was formulated as dimer and electrolyte.

• Journal of the Korean Chemical Society
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• v.31 no.6
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• pp.527-533
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• 1987

Kinetic studies on the complexing of aquamolybdenum(Ⅳ) trimer with thiocyanate have been carried out using the spectrophotometric method. The observed rate constant, $k_{obsd}$ is given by $k_{obsd}\;=\;{k_O + k_H[H^+]^2}(SCN^-) + k_r$. At 25$^{\circ}$C and ionic strength of 2.30 the values of $k_f$ and $k_r$ are $(3.78 {\pm} 0.61) {\times} 10^{-4}M^{-1}s^{-1}$ and $(6.93 {\pm} 2.39) {\times} 10^{-4}s^{-1}$, respectively. Activation parameters are ${\Delta}H^* = 50.71{\pm}6.91 kJmol^{-1}$ and ${\Delta}S^* = -121.65JK^{-1}mol^{-1}$. The mechanism is proposed and discussed.

• Journal of the Korean Chemical Society
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• v.26 no.6
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• pp.378-382
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• 1982

Green crystalline salts of substituted pyridinium oxopentachloromolybdates(V) were obtained from concentrated hydrochloric acid solution of molybdenum(V)-thiocyanate extract. $MoOCl_3(X-py)_2$ (X-py were 4-and 3-cyanopyridine, 2-amino-4-picoline and 4-acetylpyridine) were obtained by reflux of the corresponding substituted pyridinium salts of oxopentachloromolybdates(Ⅴ) in absolute ethanol. ($X-pyH_2$)[$MoOCl_5$]$H_2$O containing the $MoO^{3+}$ group are dissolved and hydrolysed in water but $MoOCl_3(X-py)_2$ are insoluble in water, alcohol and acetone. The complexes are paramagnetic compounds.

• Journal of the Korean Chemical Society
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• v.46 no.1
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• pp.26-36
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• 2002

A solid-state reaction of $MoO_3$ with as-synthesized H-SAPO-34 generated paramagnetic Mo(V) species. The dehydration resulted in weak Mo(V) species, and subsequent activation resulted in the formation of Mo(V) species such as $Mo(V)_{5c}$ and $Mo(V)_{6c}$ that are characterized by ESR. The data of ESR and ESEM show the oxomolybdenum species, to be $(MoO_2)^+$ or $(MoO)^{3+}$. The $(MoO_2)^+$ species seems to be more probable. Since H-SAPO-34 has a low framework negative charge, $(MoO)^{3+}$ with a high positive charge can not be easily stabilized. A solution reaction between the solution of silico-molybdic acid and calcined H-SAPO-34 resulted in only $(MoO_2)^+$ species. A rhombic ESR signal is observed on adsorption of $D_2O$, $CD_3OH$, $CH_3Ch_2OD$ and $ND_3$. The Location and coordination structure of Mo(V) species has been determined by three-pulse electron spin-echo modulation data and their simulations. After the adsorption of methanol, ethylene, ammonia, and water for MoH-SAPO-34, three molecules, one molecule, one and one molecule, respectively, are directly coordinated to $(MoO_2)^+)$.

• Journal of the Korean Chemical Society
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• v.33 no.5
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• pp.477-477
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• 1989

The rates of the reaction of $[MoO_2(S_2CNEt_2)_2]$ with triphenylphosphine in 1,2-dichloroethane have been determined by the spectrophotometric method. The increase in the initial absorbance has been interpreted as a result of the production of $[Mo_2O_3(S_2CNEt_2)_4]$ and the decrease in absorbance then corresponds to the reduction of $[M_2O_3(S_2CNEt_2)_4]$. The data suggest mechanisms involving the enzymatic reaction in the first stage and the decay of intermediate, ${\mu}$-oxo molybdenum (V) dimer in the second stage.