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bis(acetylacetonato)manganese(II) dihydrate | 14024-80-7

中文名称
——
中文别名
——
英文名称
bis(acetylacetonato)manganese(II) dihydrate
英文别名
manganse(II) acetylacetonate dihydrate;[Mn(Acetylacetonato)2]*2H2O;[Mn(acetylacetonate)2]*2H2O;[Mn(II)(acac)2]*2H2O
bis(acetylacetonato)manganese(II) dihydrate化学式
CAS
14024-80-7
化学式
C10H14MnO4*2H2O
mdl
——
分子量
289.187
InChiKey
HITFXGZOLUQCFD-SUKNRPLKSA-L
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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    bis(acetylacetonato)manganese(II) dihydrate 在 P2O5 作用下, 以 neat (no solvent) 为溶剂, 生成 bis(acetylacetonato)manganese(II)
    参考文献:
    名称:
    Shibata, Shuzo; Onuma, Shigeki; Inoue, Hironao, Inorganic Chemistry, 1985, vol. 24, # 11, p. 1723 - 1725
    摘要:
    DOI:
  • 作为产物:
    描述:
    三乙酰甲烷manganese (II) acetate tetrahydratesodium carbonate 作用下, 以 乙醇 为溶剂, 以15%的产率得到bis(3-acetylpentane-2,4-dionato)manganese(II)
    参考文献:
    名称:
    Coordinating properties of the anionic ligand (MeCO)2C(−)C(X)Me (X=O or NH) toward transition metal(II) centers
    摘要:
    The exchange reaction between transition metal(II) acetates and the protic nucleophiles 3-(1-aminoethylidene) pentane-2,4-dione (Hampd) or 3-acetylpentane-2,4-dione (Hacpd) affords the corresponding [M(ampd)(2)] (M = Ni (1), Pd (2)) or [M(acpd)(2)] (M = Mn (5), Fe (6), Ni (7), Cu (8), Pd (9)) complexes in fair to good yields. The reaction is performed in ethanol at room temperature, with addition of sodium carbonate in some cases. This last new synthetic procedure is applied for those complexes which easily undergo an extensive deacylation process. The factors determining the success of the exchange reaction and the resulting N, O or O, O coordination are fully discussed. (C) 2008 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2008.11.017
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文献信息

  • Reaction of the framework 3d-organometallosiloxanes with acetylacetone
    作者:N. V. Sergienko、N. V. Cherkun、V. D. Myakushev、A. A. Korlyukov、B. G. Zavina
    DOI:10.1007/s11172-010-0248-3
    日期:2010.7
    A reaction of acetylacetone with the framework sandwich-type metallosiloxanes (MOS) of general formula [PhSiO2]6M6[PhSiO2]6, where M = Cu, Ni, Mn, was studied by GPC, 1H and 29Si NMR spectroscopy, X-ray diffraction, elemental and functional analysis. The reaction involved replacement of the metal atoms with the hydrogen atoms and is accompanied by the formation of the corresponding chelate complexes M(acac)2. Displacement of the metal from the framework MOS leads to the destruction of molecular skeleton and formation of phenylsiloxanes containing Si-OH groups. The yield and composition of the reaction products considerably depend on the nature of the metal in [PhSiO2]6M6[ThSiO2]6. A selective substitution of the metal leads to the stereoregular hexahydroxyhexaphenylcyclohexasiloxane, [PhSiO(PH)]6, cis-isomer. The structure and composition of the crystalline hexahydroxyhexaphenylcyclohexasiloxane obtained were confirmed by 29Si NMR spectroscopy, X-ray diffraction study, and functional analysis, while its TMS derivative was studied with 1H NMR spectroscopy and GPC. Using a framework manganese phenylsiloxane as an example, a reversible character of the process has been established and an alternative synthesis of this compound from hexahydroxyhexaphenylcyclohexasiloxane and Mn(acac)2 has been accomplished for the first time.
    对通式为[PhSiO2]6M6(其中M = Cu, Ni, Mn)的框架夹心型硅氧烷(MOS)与乙酰乙酮的反应进行了研究,使用了GPC、1H和29Si NMR光谱、X射线衍射、元素分析和功能分析。反应过程涉及属原子被氢原子取代,并伴随形成相应的配位化合物M(acac)2。从框架MOS中取代属会导致分子骨架的破坏,并形成含有Si-OH基团的苯基硅氧烷。反应产物的产率和组成显著依赖于[PhSiO2]6M6中属的性质。属的选择性取代导致了立体规律性的六羟基六苯基环己硅氧烷[PhSiO(PH)]6的顺异构体的形成。所获得的结晶六羟基六苯基环己硅氧烷的结构和组成通过29Si NMR光谱、X射线衍射研究及功能分析得到了确认,而其TMS衍生物则通过1H NMR光谱和GPC进行了研究。以框架苯基硅氧烷为例,确立了该过程的可逆特征,并首次完成了从六羟基六苯基环己硅氧烷和Mn(acac)2合成该化合物的替代合成。
  • Synthese, Charakterisierung und Magnetische Eigenschaften eines tetranuklearen, Thiacalix[4]aren-stabilisierten Mangankomplexes
    作者:Jürgen Zeller、Ian J. Hewitt、Udo Radius
    DOI:10.1002/zaac.200600209
    日期:2006.11
    Synthesis, Characterization and Magnetic Properties of a Tetranuclear, Thiacalix[4]aren stabilized Manganese Complex Synthesis, characterization and magnetic properties of the compound [(TCA)(TCAH)Mn4(acac)] (1) are reported, the first tetranuclear thiacalix[4]aren stabilized manganese complex synthesized under conventional conditions.
    四核萼 [4] 的合成、表征和磁性能是稳定的络合物 化合物 [(TCA) (TCAH) Mn4 (acac)] (1) 的合成、表征和磁性能被报道,这是第一个四核萼 [ 4] 是在常规条件下合成的稳定配合物。
  • Tanase, Tomoaki; Yun, Joanne W.; Lippard, Stephen J., Inorganic Chemistry, 1996, vol. 35, # 12, p. 3585 - 3594
    作者:Tanase, Tomoaki、Yun, Joanne W.、Lippard, Stephen J.
    DOI:——
    日期:——
  • Synthesis and Characterization of Some New Manganese(II) Complexes, Manganese(III) Heterochelates, and µ‐Dioxo‐dimanganese(IV) Complexes Involving Tetradentate Schiff Bases
    作者:Kamalendu Dey、Susobhan Biswas、Saikat Sarkar
    DOI:10.1081/sim-200026605
    日期:2004.11
    Condensation of 1,3-diaminopropane-2-ol with diacetylmonoxime and acetylacetone yielded the tetradentate Schiff bases N,N'-(2-hydroxy) propylene-bis(2-imino-3-oximino)butane} (H2L2) and N,N'-(2-hydroxy) propylene-bis(acetylacetoneimine) (H2L2), respectively. The ligands form mononuclear manganese(II) complexes of the type [Mn(II)(L-1)] (1) and [Mn(II)(L-2)] (3), which are used for the formation of the manganese(III) heterochelates of the type [Mn(III)(L)(L-L)] (where H2L = H2L1 or H2L2; L-L = anion of acetylacetone or salicylaldehyde). Cationic heterochelates of the type [Mn(L)(L-L)]ClO4 where H2L = H2L1 or H2L2 and L-L = ethylenediamine and N,N'-propylene-bis(benzaldimine) (L-3) have been synthesized by the reactions of bis(acetylacetonato)manganese(II) or bis(salicylaldehydato)manganese(H) with the preformed Schiff bases or by the reactions of [Mn(II)(L-1)] or [Mn(II)(L-2)] with L-L in absolute alcohol under reflux. Some of the complexes, synthesized here, may be used as precursors in the synthesis of higher nuclearity manganese complexes. Air oxidation of [Mn(II)(L-1)] (1) and [Mn(II)(L-2)] (3) in DMF yielded the dark-brown mu-dioxo-bis-[N,N'-(2-hydroxy)propylene-bis(2-imino-3-oximino)butane}]dimangenese(IV) (2) and mu-dioxo-bis[N,N'-(2-hydroxy)propylenebis(acetylacetoneimine)}]dimangenese(IV) (4) complexes, respectively. All of the complexes have been characterized with the help of elemental analyses, molar conductance values, molecular weights, magnetic moments, and spectroscopic (IR, UV-VIS, ESR) data.
  • JP2023/176615
    申请人:——
    公开号:——
    公开(公告)日:——
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