• Bulletin of the Korean Chemical Society
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• v.33 no.5
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• pp.1675-1680
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• 2012

Three new cyanide-bridged $Cr^{III}Mn^{II}$ binuclear complexes, $[Mn(phen)_2Cl][Cr(bpmb)(CN)_2]{\cdot}H_2O$ ($\mathbf{1}$) (phen = 1,10-phenanthroline, $bpdmb^{2-}$ = 1,2-bis(pyridine-2-carboxamido)-4-methyl-benzenate), $[Mn(phen)_2Cl][Cr(bpmb)-(CN)_2]{\cdot}H_2O$ ($\mathbf{2}$) ($bpdmb^{2-}$ = 1,2-bis(pyridine-2-carboxamido)-4,5-dimethyl-benzenate), and $[Mn(phen)_2Cl]-[Cr(bpClb)(CN)_2]{\cdot}CH_3OH{\cdot}H_2O$ ($\mathbf{3}$) ($bpClb^{2-}$ = 1,2-bis(pyridine-2-carboxamido)-4-chloro-benzenate) were obtained based on $Mn(phen)_2Cl_2$ and a series of dicyanidechromate(III) building blocks. Single crystal X-ray diffraction analysis shows the structures of the three complexes are dimeric type with two different metal centers linked by a cyanide group from corresponding dicyanidechromate(III) building block. Magnetic investigations indicate the existence of relatively weak antiferromagnetic coupling between Cr(III) and Mn(II) ions with best-fit constants $J_{CrMn}=-2.78(5)cm^{-1}$ for $\mathbf{1}$, $J_{CrMn}=-3.02(2)cm^{-1}$ for $\mathbf{2}$ and $J_{CrMn}=-2.27(3)cm^{-1}$ for $\mathbf{3}$ based on the spin exchange Hamiltonian = $-2J_{CrMn}\hat{S}_{Cr}\hat{S}_{Mn}$. The magneto-structural correlation of cyanide-bridged $Cr^{III}Mn^{II}$ complexes has been discussed at last.

• Journal of the Korean Magnetics Society
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• v.5 no.3
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• pp.175-178
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• 1995

The temperature dependence of $^{23}Na$ nuclear magnetic resonance in a $NaMnCl_{3}$ single crystal grown by the Czochralski method has been investigated by employing a Bruker FT NMR spectrometer operating at 4.7 T. The quadrupole coupling constant of $^{23}Na$ in $NaMnCl_{3}$ increases as the temperature increases. The temperature dependence of $e^{2}qQ/h$ may be fitted with a linear equation of the form $e^{2}qQ/h=155+0.117(T-T_{r})\;kHz$ for the temperature range of 140-380 K.

• Bulletin of the Korean Chemical Society
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• v.17 no.2
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• pp.138-142
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• 1996

The transition metal carbonylate, PPN+(${\eta}^5-MeCp)Mn(CO)_2Cl^-$ undergoes a novel ligand substitution reaction with PR3 (R=Me, Et, OEt, $C_6H_5$ in THF at elevated temperatures (40 $^{\circ}C$ up to 60 $^{\circ}C)$ under the pseudo-first-order reaction conditions (usually 20-fold excess of PR3 with respect to metal carbonylate concentrations) where chloride is displaced by PR3. The reaction follows overall first order dependence on [(${\eta}^5-MeCp)Mn(CO)_2Cl^-$]; however, the negative entropy changes of activation (${\Delta}S^{\neq}$=-19.3 e.u. for $P(OEt)_3$; ${\Delta}S^{\neq}$=-16.4 e.u. for $PPh_3$) suggest the existence of the intermediate, ((η3-MeCp)Mn(CO)2(THF)Cl-, which eventually transforms to the product (${\eta}^5-MeCp)Mn(CO)_2(PR_3)$.

• Journal of the Korean Vacuum Society
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• v.15 no.5
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• pp.541-546
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• 2006

In this study we have investigated cathodoluminescence (CL) and structural properties of thin film $ZnGa_2O_4:Mn$ oxide phosphor by using field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), photoluminescence (PL), and cathodoluminescence. PL emission peaked at 506 nm was observed from the $ZnGa_2O_4:Mn$ phosphor target and it was attributed to the $^4T_1-^6A_1$ transition in $Mn^{2+}$ ion. The color coordinates of the emission were x = 0.09 and y = 0.67. The $ZnGa_2O_4:Mn$ films showed the excitation spectrum peaked at 294 nm by $Mn^{2+}$ ion absorption. It was found that the higher intensity of CL emission at 505 nm appears to result from the denser and closely-packed structure in $ZnGa_2O_4:Mn$ phosphor films deposited at lower pressures. The CL intensity did not show any systematic dependence on film surface roughness.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
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• v.20 no.4
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• pp.363-366
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• 2007

[ $Zn_2SiO_4:Mn$ ] green phosphors doped with $NH_4Cl$ and Al for PDP were synthesized by solid state reaction method. The luminescence of 532 nm in $Zn_2SiO_4:Mn$ phosphors was associated with $^4T_1{\to}^6A_1$ transition. Photoluminescence intensity of $Zn_2SiO_4:Mn$ doped with $NH_4Cl$ 15 mol% increased about two times as compared with that of $NH_4Cl$ non-doped sample. The color of the emission of Al-doped $Zn_2SiO_4:Mn$ phosphors changed to yellowish green.

• Bulletin of the Korean Chemical Society
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• v.17 no.10
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• pp.929-934
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• 1996

The electrochemistry and the reaction of non-μ-oxo dimer-forming [5,10,15,20-tetrakis(2,6-dichlorophenyl)porphyrinato] manganese(Ⅲ) chloride [(Cl8TPP)MnⅢCl] with tetraethylammonium hydroxide in water [-OH(H2O)] have been investigated by electrochemical and spectroscopic methods under anaerobic conditions. The stronger autoreduction of (C18TPP)MnⅢCl by -OH(H2O) in comparison with (Me12TPP)MnⅢCl by -OH(CH3OH) in MeCN is explained as the influence of electronic effects on substituted phenyl groups bonded to meso-position of porphyrin ring and the positive shift of reduction potential (-0.11 V) for (C18TPP)MnⅢCl. The autoreduction of manganese(Ⅲ) porphyrin to manganese (Ⅱ) by this process is only observed when one axial position is occupied by a ligating solvent and OH- coordinates the other axial site. The results are discussed in relation to the mechanisms for the reduction of manganese(Ⅲ) porphyrin.

• Bulletin of the Korean Chemical Society
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• v.25 no.7
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• pp.1036-1040
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• 2004

$Mn_{12}O_{12}(O_2CCH_2CH_2CH_2Cl)_{16}(H_2O)_4]$ (noted as $Mn_{12}$-BuCl), a new polynuclear complex of manganese chlorobutyrate has been successfully prepared by substitution of acetate with 4-chlorobutyric acid. The $Mn_{12}-BuCl$ crystallizes into triclinic space group P-1 with a = 14.5560(11) ${\AA}$, b = 14.5819(11) TEX>${\AA}$, c = 27.265(2) ${\AA}$, ${\alpha}\;=\;84.1140(10)^{\circ}\;,\;{\beta}\;=\;88.805(2)^{\circ},\;{\gamma}\;=\;89.8820(10)^{\circ}$, and Z = 2. The local environments of manganese 3+ and 4+ ions of the title compound are close to those of other $Mn_{12}$ compounds. The electrochemical data for $Mn_{12}-BuCl$ involve reversible reactions of two-electron reductions. The $Mn_{12}-BuCl$ also presents magnetic relaxation below 10 K implying that each molecule behaves as a single molecule magnet.

• Journal of Energy Engineering
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• v.4 no.1
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• pp.67-75
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• 1995

50 kW 냉방용 화학열펌프에 관한 전산설계를 하기 위하여 반응기 모사용 부프로그램을 작성하였으며 전체 시스템을 위하여 상용모사기인 ASPEN PLUS를 이용하였다. 반응물로 각각 SrCl2-8/1 NH3 그리고 MnCl2-6/2 NH3를 사용하는 두 시스템에 대하여 비교 연구하였으며, 조작조건에 따라 시스템 설계치의 변화를 관찰하였다. 이로부터 향후 실용화될 화학열펌프 시스템에 대한 기본 설계자료를 제시할 수 있었다. SrCl2-8/1 NH3를 반응물로 한 경우 반응기의 UA는 6,868.2 J/(s·K), 출력은 95.2 kW이었고, 제한 성능 계수는 0.40이었다. MnCl2-6/2 NH3의 경우 UA는 1,569.7 J/(s·K), 출력은 109.0 kW이었으며 제한 성능계수는 0.34이었다. 이로부터 SrCl2-8/1 NH3을 반응물로 한 시스템이 MnCl2-6/2 NH3를 사용한 시스템보다 유리함을 알 수 있었다.

• Proceedings of the Korean Vacuum Society Conference
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• 2010.02a
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• pp.233-233
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• 2010

Magnetic random access memory (MRAM), based on magnetic tunnel junction (MTJ) and CMOS, is a prominent candidate among prospective semiconductor memories because it can provide nonvolatility, fast access time, unlimited read/write endurance, low operating voltage and high storage density. The etching of MTJ stack with good properties is one of a key process for the realization of high density MRAM. In order to achieve high quality MTJ stack, the use of CoFeB and IrMn magnetic films as free layers was proposed. In this study, inductively coupled plasma reactive ion etching of CoFeB and IrMn thin films masked with Ti hard mask was investigated in a $Cl_2$/Ar gas mix. The etch rate of CoFeB and IrMn films were examined on varying $Cl_2$ gas concentration. As the $Cl_2$ gas increased, the etch rate monotonously decreased. The effective of etch parameters including coil rf power, dc-bais voltage, and gas pressure on the etch profile of CoFeB and IrMn thin film was explored, At high coil rf power, high dc-bais voltage, low gas pressure, the etching of CoFeB and IrMn displayed better etch profiles. Finally, the clean and vertical etch sidewall of CoFeB and IrMn free layers can be achieved by means of thin Ti hard mask in a $Cl_2$/Ar plasma at the optimized condition.

• Proceedings of the Korean Magnestics Society Conference
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• 2008.12a
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• pp.38.2-38.2
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• 2008