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[iron(II) (chloride)2 (2-propanol)4] | 685569-57-7

中文名称
——
中文别名
——
英文名称
[iron(II) (chloride)2 (2-propanol)4]
英文别名
[FeCl2(HOPr(i))4]
[iron(II) (chloride)2 (2-propanol)4]化学式
CAS
685569-57-7;837387-40-3
化学式
C12H32Cl2FeO4
mdl
——
分子量
367.137
InChiKey
PYIRVGRIWNHAHE-UHFFFAOYSA-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:
    参考文献:
    名称:
    Fe(II)在2-丙醇中的辐射还原
    摘要:
    通过脉冲辐射分解技术研究了铁(II)在2-丙醇中的第一步还原步骤。溶剂化电子与铁(II)的反应的速率常数为4.8×10 9  dm 3  mol -1  s -1。确定了Fe(I)在350 nm处的最大吸收光谱。Fe II在惰性气氛下在2-丙醇中的辐射还原导致形成非常小的铁纳米颗粒,而在CO气氛下则形成稳定的Fe(CO)5络合物。
    DOI:
    10.1016/j.cplett.2006.09.055
  • 作为产物:
    描述:
    iron(II) chloride 、 [V(OiPr)4]2 以 not given 为溶剂, 生成 [iron(II) (chloride)2 (2-propanol)4]
    参考文献:
    名称:
    The first hetero-binuclear alkoxide of iron and vanadium: structural and spectroscopic features
    摘要:
    The immediate reaction between [V-2(mu-OPri)(2)(OPri)6] (A) and [Fe-2(mu-I)(2)I-2(HOPri)(4)] (B) in toluene/propan-2-ol gives the novel mixed-metal [FeI2(mu-OPri)(2)V(0Pr(i))(2)(HOPri)] (C). Structural, spectroscopic and magnetochemical characterisation are all consistent with a non-oxo vanadium(IV)/high-spin iron(II) formulation; variable-temperature X-band EPR spectra reveal an S = 1/2 <----> S = 1 equilibrium involving the vanadium centres in propan-2-ol solution. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/s1387-7003(03)00250-8
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文献信息

  • Iron(<scp>iii</scp>) and titanium(<scp>iv</scp>) oxoalkoxide chemistry: synthetic, structural, magnetochemical and spectroscopic studies of [Ti<sub>3</sub>(μ<sub>3</sub>-OPr<sup>i</sup>)<sub>2</sub>(μ-OPr<sup>i</sup>)<sub>3</sub>(OPr<sup>i</sup>)<sub>6</sub>][FeCl<sub>4</sub>] and [Fe<sub>5</sub>(μ<sub>5</sub>-O)(μ-OPr<sup>i</sup>)<sub>8</sub>Cl<sub>5</sub>]
    作者:Dayane M. Reis、Giovana G. Nunes、Eduardo L. Sá、Geraldo R. Friedermann、Antonio S. Mangrich、David J. Evans、Peter B. Hitchcock、G. Jeffery Leigh、Jaísa F. Soares
    DOI:10.1039/b403899a
    日期:——
    Two synthetic routes were employed for the preparation of iron(III) haloalkoxides in the presence of titanium(IV). Three crystalline products (A, B and C) were isolated and characterised by chemical and physical techniques including X-ray diffractometry, Mössbauer and EPR spectroscopies and variable-temperature magnetic susceptibility measurements. Products B and C are common to both synthetic routes
    (IV)存在下,采用两种合成途径制备卤代(III)的卤化物。分离出三种结晶产物(A,B和C)并通过化学和物理技术进行了表征,包括X射线衍射,Mössbauer和EPR光谱学和可变温度磁化率测量。产物B和C对于两种合成路线都是共同的。产品A是单核(II)络合物,反式-[FeCl 2(HOPr i)4 ],可能是通过氧化丙-2-醇通过FeCl 3在反应介质中。乙是离子,混合[Ti 3(μ 3 -OPr我)2(μ-OPR我)3(OPR我)6 ] [的FeCl 4 ],而Ç是一种高收率氧代haloalkoxide,[5(μ 5 -O)(μ-OPR我)85 ]。在[ 2 H 8 ]-四氢呋喃溶液中从323至173 K的磁矩测量结果表明,C中含有反磁耦合的(III)处于中间(S = 3/2)自旋配置的中心。C是固态的多晶型物,在单斜晶系或四方晶系中分别结晶为非溶剂化物和单溶剂化物
  • New FeII starting materials: preparation, characterisation and structural features of iron halide complexes with alcohol ligands
    作者:Giovana G Nunes、Rúbia C.R Bottini、Dayane M Reis、Pedro H.C Camargo、David J Evans、Peter B Hitchcock、G Jeffery Leigh、Eduardo L Sá、Jaı́sa F Soares
    DOI:10.1016/j.ica.2003.10.004
    日期:2004.3
    The new mononuclear [FeCl2(HOPri)(4)] (1), polymeric [Cl3Fe(mu-Cl)Fe(HOPri)(4)}(n)] (2) and binuclear [I2Fe(mu-I)(2)Fe((PrOH)-O-i)(4)] (3) iron(II) complexes have been synthesized in high yields in propan-2-ol or toluene/propan-2-ol mixtures at room temperature. Magnetic moment measurements, Fe-57 Mossbauer spectroscopy data and the results of semi-empirical quantum mechanical calculations confirmed the high-spin configuration of the iron(II) centres, which were shown to be four- and/or six-coordinate by single crystal X-ray diffraction analyses. Intermolecular hydrogen bonding was observed in the solid state structure of 1, intramolecular interactions in 2, while both intra- and intermolecular association was seen in 3. Long iron-(mu-halide) bonds suggest the possibility of complex dissociation in solution and facile ligand substitution in 2 and 3. (C) 2003 Elsevier B.V. All rights reserved.
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