[Sm(1,10-phenanthroline)(N,N-diethyldithiocarbamate)3] | 152046-31-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: [Sm(1,10-phenanthroline)(N,N-diethyldithiocarbamate)3]
• 英文别名: [Sm(diethyldithiocarbamate)3(1,10-phenanthroline)]；[Sm(diethyldithiocarbamato)3(1,10-phenanthroline)]；[Sm(diethyldithiocarbamate)3(o-phenanthroline)]；[Sm(S2CNEt2)3(1,10-phenanthroline)]；[Sm(S2CNEt2)3(Phen)]；[Sm(phen)(Et2dtc)3]
• CAS: 152046-31-6
• 化学式: C₂₇H₃₈N₅S₆Sm
• 分子量: 775.388
• InChiKey: MNPXWEYXCKFADA-UHFFFAOYSA-K

物化性质

• 熔点：
  215 °C(Solvent: Ethanol)

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：

  [Sm(1,10-phenanthroline)(N,N-diethyldithiocarbamate)3] 以 solid 为溶剂， 生成 samarium diethyldithiocarbamate
  参考文献：
  名称：

  Malkerova; Alikhanyan; Kuz'mina, Russian Journal of Inorganic Chemistry, 2005, vol. 50, # 8, p. 1243 - 1246

  摘要：

  DOI：
• 作为产物：
  描述：

  二乙基二硫代氨基甲酸二乙铵盐 、 邻菲罗啉 、 samarium(III) trifluoromethanesulfonate 以 乙腈 为溶剂， 以90%的产率得到[Sm(1,10-phenanthroline)(N,N-diethyldithiocarbamate)3]
  参考文献：
  名称：

  一种新的连续两步分子前体路线制备稀土氧硫化物Ln 2 O 2 S

  摘要：

  设计了一个连续的两步式分子前体途径，用于制备稀土氧硫化物Ln 2 O 2 S（Ln = Y，La，Pr，Nd，Sm-Lu）。该新路线涉及第一步氧化步骤，该氧化步骤导致了稀土氧硫酸盐Ln 2 O 2 SO 4，随后通过切换至H 2 -Ar气氛而还原为稀土氧硫化物Ln 2 O 2 S。整个过程的温度大大低于通常的固态合成（T≤650°C），避免使用危险的硫基气体，为合成整个Ln 2 O 2 S系列提供了便捷的途径。分子前体由杂二硫代氨基甲酸酯复合物组成[ Ln（Et 2 dtc）3（phen）]和[ Ln（Et 2 dtc）3（bipy）]（Et 2 dtc = N，N-二乙基二硫代氨基甲酸酯; phen = 1,10-菲咯啉; bipy = 2,2'-联吡啶）并通过a新的高产高纯度合成路线。分子前体的性质决定了最低合成温度，因此影响了最终Ln 2 O的纯度2 S结晶相。

  DOI：

  10.1016/j.jssc.2012.03.017

文献信息

• Chen; Gao; Wei, Russian Journal of Physical Chemistry, 2005, vol. 79, # 7, p. 1022 - 1028
  作者：Chen、Gao、Wei、Xie、Shi

  DOI：——

  日期：——
• Luminescence of Ln(III) Dithiocarbamate Complexes (Ln = La, Pr, Sm, Eu, Gd, Tb, Dy)
  作者：Michelle D. Regulacio、Michele H. Pablico、Joan Acay Vasquez、Peter N. Myers、Stuart Gentry、Michael Prushan、Suk-Wah Tam-Chang、Sarah L. Stoll

  DOI：10.1021/ic701974q

  日期：2008.3.1

  We have discovered room temperature photoluminescence in SM3+ and Pr3+ dithiocarbamate complexes. Surprisingly, these complexes exhibit more intense emission than those of the Eu3+, Tb3+, and Dy3+ analogues. The electronic absorption, excitation, and emission spectra are reported for the complexes [Ln(S2CNR2)(3)L] and NH2Et2[Ln(S2CNEt2)(4)], where Ln = Sm, Pr; R = ethyl, butyl, benzyl; and L = 1,10-phenanthroline, 2,2'-bipyridine, and 5-chloro-1,10-phenanthroline. The lowest ligand-localized triplet energy level (T-1) of the complexes are determined from the phosphorescence spectra of analogous La3+ and Gd3+ chelates. The luminescence decay curves were measured to determine the excited-state lifetimes for the Pr3+ and Sm3+ complexes. X-ray crystal structures of Sm((S2CNBu2)-Bu-i)(3)phen, Pr(S2CNEt2)(3)phen, and Pr((S2CNBu2)-Bu-i)(3)phen are also reported.
• Thermolysis of lanthanide dithiocarbamate complexes
  作者：William L. Boncher、Michelle D. Regulacio、Sarah L. Stoll

  DOI：10.1016/j.jssc.2009.10.003

  日期：2010.1

  Polycrystalline lanthanide sulfide materials were formed at low temperatures using a single-source precursor based on the lanthanide dithiocarbamate complex. The synthesis temperatures aye generally lower than standard solid state preparations, avoid toxic sulfurizing gases and provide a convenient route to prepare lanthanide chalcogenide nanoparticles. Depending on the reaction conditions and oxophilicity of the lanthanide, the Sulfide material was formed with oxidized products including oxysulfides, oxysulfates and the oxide. (C) 2009 Elsevier Inc. All rights reserved.