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manganese(II) propionate | 21129-18-0

中文名称
——
中文别名
——
英文名称
manganese(II) propionate
英文别名
manganese propionate;manganese(II) propanoate;Mn(O2CEt)2;manganese dipropionate;manganese(2+);propanoate
manganese(II) propionate化学式
CAS
21129-18-0
化学式
2C3H5O2*Mn
mdl
——
分子量
201.081
InChiKey
ZQVQDMPMXVIBOO-UHFFFAOYSA-M
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.86
  • 重原子数:
    6.0
  • 可旋转键数:
    1.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    40.13
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

安全信息

  • 海关编码:
    2915509000

SDS

SDS:e727cb64b58ef5ab30994971236e99bc
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反应信息

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文献信息

  • Metal carboxylate salts
    申请人:Goh Swee-Keng
    公开号:US20080033196A1
    公开(公告)日:2008-02-07
    A dietary source of mineral in the form of a metal carboxylate is prepared using the acid-base-like reaction. A salt of a carboxylate anion and a by-product cation is reacted in aqueous solution with a salt of a metal cation and a by-product anion under conditions which form a metal carboxylate and the by-product salt. Solutions formed in the reaction may be applied directly to a dry carrier to produce a dry dietary supplement or, alternatively, the solutions may be filtered to remove precipitated by-product salt and the filtrate used as a liquid dietary supplement. Preferably, a reducing agent, such as ascorbic acid, is added to help prevent the oxidation of divalent to trivalent form of a metal salt, when an easily oxidized divalent metal is used as starting material.
    使用酸碱类似反应制备以金属羧酸盐形式存在的矿物质的膳食来源。通过在水溶液中使羧酸盐阴离子和副产物阳离子的盐与金属阳离子的盐和副产物阴离子在条件下反应,形成金属羧酸盐和副产物盐。反应中形成的溶液可以直接应用于干载体上制备干燥膳食补充剂,或者可以将溶液过滤以去除沉淀的副产物盐,然后将滤液用作液体膳食补充剂。最好在使用易被氧化的二价金属作为起始材料时,添加还原剂,如抗坏血酸,以帮助防止金属盐从二价氧化为三价的氧化。
  • Thermal decomposition of freeze-dried μ-oxo-carboxylates of manganese and iron
    作者:H Langbein、S Christen、G Bonsdorf
    DOI:10.1016/s0040-6031(98)00611-x
    日期:1999.3
    Abstract The decomposition of freeze-dried mixed carboxylates of manganese and iron was investigated by means of DTA, TG, mass spectroscopy and X-ray powder diffractometry. The three main steps of decomposition are characterized as release of (a) H 2 O, (b) carboxylic acid and CO 2 /CO, and (c) the corresponding carbonyl compound and CO 2 . In particular, the course of process (b) strongly depends
    摘要 采用差热分析(DTA)、热重分析(TG)、质谱法和X射线粉末衍射法研究了冻干锰铁混合羧酸盐的分解过程。分解的三个主要步骤的特征在于释放 (a) H 2 O,(b) 羧酸和 CO 2 /CO,以及 (c) 相应的羰基化合物和 CO 2 。特别是,过程 (b) 的过程在很大程度上取决于三种研究的羧酸盐中金属-羧酸盐连接的稳定性。通过适当组成的甲酸盐的分解和分解产物在600°C下的热处理,同时保持ap (O 2 )在锰铁氧体的共存场内,可以获得结晶良好的单相铁酸锰。
  • Molecular Wheels: New Mn<sub>12</sub> Complexes as Single-Molecule Magnets
    作者:Sonali J. Shah、Christopher M. Ramsey、Katie J. Heroux、Antonio G. DiPasquale、Naresh S. Dalal、Arnold L. Rheingold、Enrique del Barco、David N. Hendrickson
    DOI:10.1021/ic801374u
    日期:2008.10.20
    Hz indicates an S = 7 ground state for 1, 2, and 3. Magnetization hysteresis data were collected on a single crystal of 1 in the 0.27-0.9 K range and on single crystals of 2 and 3 in the 0.1-0.9 K temperature range. Discrete steps in the magnetization curves associated with resonant quantum tunneling of magnetization (QTM) confirm these complexes to be single-molecule magnets. The appearance of extra
    [Mn12(Adea)8(CH3COO)14] x 7 CH3CN(1 x 7CH3CN),[Mn12(Edea)8(CH3CH2COO)14] [3]三种新的轮状十二烷核锰配合物的制备,结构和磁性能)和[Mn12(Edea)8(CH3COO)2(CH3CH2COO)12](3),其中Adea(2-)和Edea(2-)是N-烯丙基二乙醇胺和N-乙基二乙醇胺的二价阴离子配体。每个络合物具有六个Mn(II)和六个Mn(III)离子,呈轮状拓扑交替排列,带有八个n-取代的二乙醇胺二价阴离子。所有的温度可变直流(DC)磁化率数据都是在1、0.1或0.01 T磁场以及1.8-300 K的温度范围内收集的。在0-9 T的应用场和1.8-100 K的温度范围内收集的热容数据表明,由于1和3的长距离磁排序,没有相变。在1.8-10 K和0.1-5 T范围内获得了温度可变,磁场可变的直流磁化率数据。所有复合
  • New Mixed-Valent Mn Clusters from the Use of <i>N</i>,<i>N</i>,<i>N′</i>,<i>N′</i>-Tetrakis(2-hydroxyethyl)ethylenediamine (edteH<sub>4</sub>): Mn<sub>3</sub>, Mn<sub>4</sub>, Mn<sub>6</sub>, and Mn<sub>10</sub>
    作者:Arpita Saha、Khalil A. Abboud、George Christou
    DOI:10.1021/ic201916d
    日期:2011.12.19
    The syntheses, crystal structures, and magnetochemical characterization are reported for the new mixed-valent Mn clusters [(Mn2MnIII)-Mn-II(O2CMe)(2)(edteH(2))(2)](ClO4) (1), [(Mn2Mn2III)-Mn-II(edteH(2))(2)- (hmp)(2)cl(2)](Mn(II)cl(4)) (2), [(Mn6O2)-O-III(O2CBut)(6)(edteH)(2)(N-3)(2)] (3), [(Na2Mn8Mn2O4)-Mn-III-O-II(OMe)(2)(O2CEt)(6)(edte)(2)(N-3)(6)] (4), and (NEt4)(2)- [(Mn8Mn2O4)-Mn-III-O-II(OH)(2)-(O2CEt)(6)(edte)(2)(N-3)(6)](5), where edteH(4) is N,N,N',N'-tetrakis-(2-hydroxyethyl)ethylenediamine and hmpH is 2-(hydroxymethyl)pyridine. 1-5 resulted from a systematic exploration of the effect of different Mn sources, carboxylates, the presence of azide, and other conditions, on the Mn/edteH(4) reaction system. The core of 1 consists of a linear (MnMnMnII)-Mn-II-Mn-III unit, whereas that of 2 is a planar Mn-4 rhombus within a [(Mn2Mn2III)-Mn-II(mu(3)-OR)(2)] incomplete-dicubane unit. The core of 3 comprises a central [Mn-4(III)(OR)(2)] incomplete-dicubane on either side of which is edge-fused a triangular [Mn-3(III)(mu(3)-O)] unit. The cores of 4 and S are similar and consist of a central [(Mn2Mn2III)-Mn-II(mu(3)-OR)(2)] incomplete-dicubane on either side of which is edge-fused a distorted [(MnMn3III)-Mn-II(mu(3)-O)(2)(mu(3)-OR)(2)] cubane unit. Variable-temperature, solid-state direct current (dc) and alternating current (ac) magnetization studies were carried out on 1-5 in the 5.0-300 K range, and they established the complexes to have ground state spin values of S = 3 for 1, S = 9 for 2, and S = 4 for 3. The study of 3 provided an interesting caveat of potential pitfalls from particularly low-lying excited states. For 4 and 5, the ground state is in the S = 0-4 range, but its identification is precluded by a high density of low-lying excited states.
  • ——
    作者:T. Vlase、G. Vlase、A. Chiriac、N. Doca
    DOI:10.1023/a:1025066131365
    日期:——
    The thermal decomposition in non-isothermal conditions of formates, acetates, propionates and butyrates of Mn, Co, Zn, Cd, Eu, Sm and Ni was studied. The observed compensation effect allows us to calculate the isokinetic temperature. A selective activation mechanism was suggested. This leads to a good agreement between kinetic and spectroscopic data.
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