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2,2′-(2-hydroxy-3-methoxy-5-methylbenzylazanediyl)diethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1198601-74-9

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1198601-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198601-74-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,6,0 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1198601-74:
(9*1)+(8*1)+(7*9)+(6*8)+(5*6)+(4*0)+(3*1)+(2*7)+(1*4)=179
179 % 10 = 9
So 1198601-74-9 is a valid CAS Registry Number.

1198601-74-9Downstream Products

1198601-74-9Relevant academic research and scientific papers

Synthesis, structure, and magnetic properties of a new family of tetra-nuclear {Mn2IIILn2}(Ln = Dy, Gd, Tb, Ho) clusters with an arch-type topology: Single-molecule magnetism behavior in the dysprosium and terbium analogues

Chandrasekhar, Vadapalli,Bag, Prasenjit,Speldrich, Manfred,Van Leusen, Jan,Koegerler, Paul

, p. 5035 - 5044 (2013)

Sequential reaction of Mn(II) and lanthanide(III) salts with a new multidentate ligand, 2,2′-(2-hydroxy-3-methoxy-5-methylbenzylazanediyl) diethanol (LH3), containing two flexible ethanolic arms, one phenolic oxygen, and a methoxy group afforded heterometallic tetranuclear complexes [Mn2Dy2(LH)4(μ-OAc)2](NO 3)2·2CH3OH·3H2O (1), [Mn2Gd2(LH)4(μ-OAc)2](NO 3)2·2CH3OH·3H2O (2), [Mn2Tb2(LH)4(μ-OAc)2](NO 3)2·2H2O·2CH 3OH·Et2O (3), and [Mn2Ho 2(LH)4(μ-OAc)2]Cl2· 5CH3OH (4). All of these dicationic complexes possess an arch-like structural topology containing a central MnIII-Ln-Ln-MnIII core. The two central lanthanide ions are connected via two phenolate oxygen atoms. The remaining ligand manifold assists in linking the central lanthanide ions with the peripheral Mn(III) ions. Four doubly deprotonated LH2- chelating ligands are involved in stabilizing the tetranuclear assembly. A magnetochemical analysis reveals that single-ion effects dominate the observed susceptibility data for all compounds, with comparably weak Ln...Ln and very weak Ln...Mn(III) couplings. The axial, approximately square-antiprismatic coordination environment of the Ln3+ ions in 1-4 causes pronounced zero-field splitting for Tb3+, Dy3+, and Ho3+. For 1 and 3, the onset of a slowing down of the magnetic relaxation was observed at temperatures below approximately 5 K (1) and 13 K (3) in frequency-dependent alternating current (AC) susceptibility measurements, yielding effective relaxation energy barriers of ΔE = 16.8 cm-1 (1) and 33.8 cm-1 (3).

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