N-(diisopropoxyphosphoryl)-N',N'-diethyl-thiocarbamide | 902146-68-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机磷酸及其衍生物
• 英文名称: N-(diisopropoxyphosphoryl)-N',N'-diethyl-thiocarbamide
• 英文别名: N,N-diethyl-N'-(diisopropoxyphosphoryl)thiocarbamide；(Et2N)-C(S)-N(H)-P(O)(OiPr)2；[Et2NC(S)NP(O)(OPri)2]；3-Di(propan-2-yloxy)phosphoryl-1,1-diethylthiourea；3-di(propan-2-yloxy)phosphoryl-1,1-diethylthiourea
• CAS: 902146-68-3
• 化学式: C₁₁H₂₅N₂O₃PS
• 分子量: 296.371
• InChiKey: LIKJLQYCYDVZJM-UHFFFAOYSA-N

物化性质

• 熔点：
  107-108 °C(Solv: dichloromethane (75-09-2); hexane (110-54-3))
• 沸点：
  332.3±25.0 °C(Predicted)
• 密度：
  1.102±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  18
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  82.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-(diisopropoxyphosphoryl)-N',N'-diethyl-thiocarbamide 、 zinc(II) chloride 在 氢氧化钾 作用下， 以 乙醇 、 水 为溶剂， 以92%的产率得到bis[N,N-diethyl-N'-(diisopropoxyphosphoryl)thiocarbamido-O,S]zinc(II)
  参考文献：
  名称：

  Specific Features of the Structure of Chelate Complexes of N-Thiocarbamoylamidophosphates with Zn(II) and Cd(II) Cations

  摘要：

  N-硫代氨基甲酰氨基磷酸钾盐的反应 RC(S)NHP(O)(OPr-i)2X [X = PhNH, p-MeOPhNH, p-BrPhNH, i-PrNH, t-BuNH, Et2N, C5H10N, OC4H8N, C6H11NH] 与 Zn(II) 阳离子生成组成为 Zn(L-O,S)2 的络合物。 Cd(II) 配合物由于其水解不稳定性而无法在类似条件下分离。硫脲 (X = PhNH, p-MeOPhNH) 与乙酸 Cd(II) 在 DMF 中反应，得到组成为 Cd(DMF)2L2 的稳定溶剂化配合物。通过IR、1H和31P NMR光谱以及EI和ESI质谱研究了所得化合物的结构。

  DOI：

  10.1007/s11176-006-0014-2
• 作为产物：
  描述：

  diisopropoxyphosphoryl isothiocyanate 、 二乙胺 以 二氯甲烷 为溶剂， 反应 0.5h， 以48%的产率得到N-(diisopropoxyphosphoryl)-N',N'-diethyl-thiocarbamide
  参考文献：
  名称：

  Specific Features of the Structure of Chelate Complexes of N-Thiocarbamoylamidophosphates with Zn(II) and Cd(II) Cations

  摘要：

  N-硫代氨基甲酰氨基磷酸钾盐的反应 RC(S)NHP(O)(OPr-i)2X [X = PhNH, p-MeOPhNH, p-BrPhNH, i-PrNH, t-BuNH, Et2N, C5H10N, OC4H8N, C6H11NH] 与 Zn(II) 阳离子生成组成为 Zn(L-O,S)2 的络合物。 Cd(II) 配合物由于其水解不稳定性而无法在类似条件下分离。硫脲 (X = PhNH, p-MeOPhNH) 与乙酸 Cd(II) 在 DMF 中反应，得到组成为 Cd(DMF)2L2 的稳定溶剂化配合物。通过IR、1H和31P NMR光谱以及EI和ESI质谱研究了所得化合物的结构。

  DOI：

  10.1007/s11176-006-0014-2

文献信息

• The influence of the intramolecular hydrogen bond on the 1,3-N,S- and 1,5-O,S-coordination of N-phosphoryl-N′-(R)-thioureas with Ni(ii) and Pd(ii)
  作者：Felix D. Sokolov、Sergey V. Baranov、Damir A. Safin、F. Ekkehardt Hahn、Maria Kubiak、Tania Pape、Maria G. Babashkina、Nail G. Zabirov、Joanna Galezowska、Henryk Kozlowski、Rafael A. Cherkasov

  DOI：10.1039/b702896b

  日期：——

  Reaction of the potassium salts of N-phosphorylated thioureas of common formula R1–N(H)–C(S)–N(H)–P(O)(OiPr)2 (HA) with NiII and PdII cations leads to [MA2] chelate complexes (M = NiII, R1 = p-MeOC6H4, p-BrC6H4, t-Bu, c-Hex; M = PdII, R = iPr). In both the NiII and PdII complexes, the metal center is found in a square-planar N2S2 environment formed by the CS sulfur atoms and the P–N nitrogen atoms of two deprotonated ligands A−. The PdII atoms in [PdB2] complexes with deprotonated thioureas of common formula R2–C(S)–N(H)–P(O)(OiPr)2 (HB) (R2 = Et2N, morpholine-N-yl) are coordinated in a square-planar fashion by the CS sulfur atoms and the PO oxygen atoms of two anionic ligands. Molecular structures of four complexes [M(A-N,S)2] (M = NiII, R1 = p-MeOC6H4, p-BrC6H4, t-Bu; M = PdII, R1 = iPr) and the palladium(II) 1,5-O,S-chelate of formula [Pd(B-O,S)2] (R2 = morpholine-N-yl) were elucidated by X-ray diffraction.

  通式为 R1âN(H)âC(S)âN(H)âP(O)(OiPr)2 (HA) 的 N-磷酸化硫脲的钾盐与 NiII 和 PdII 阳离子反应生成 [MA2] 螯合物（M = NiII，R1 = p-MeOC6H4、p-BrC6H4、t-Bu、c-Hex；M = PdII，R = iPr）。在 NiII 和 PdII 复合物中，金属中心都位于由 CS 硫原子和两个去质子化配体 Aâ 的 PâN 氮原子形成的方形平面 N2S2 环境中。[PdB2]配合物中的钯二原子与通式为 R2âC(S)âN(H)âP(O)(OiPr)2 (HB)（R2 = Et2N，吗啉-N-基）的去质子化硫脲以方形平面的方式由 CS 硫原子和两个阴离子配体的 PO 氧原子配位。通过 X 射线衍射阐明了四种配合物 [M(A-N,S)2]（M = NiII，R1 = p-MeOC6H4、p-BrC6H4、t-Bu；M = PdII，R1 = iPr）和式为 [Pd(B-O,S)2]（R2 = 吗啉-N-基）的 1,5-O,S-螯合钯（II）的分子结构。
• Monodentate S-vs. bidentate 1,5-O,S-coordination of N-phosphoryl-N′-(R)-thioureas with Pd(II)
  作者：Damir A. Safin、Felix D. Sokolov、Łukasz Szyrwiel、Sergey V. Baranov、Maria G. Babashkina、Timur R. Gimadiev、Henryk Kozlowski

  DOI：10.1016/j.poly.2008.03.012

  日期：2008.6

  Reaction of N-phosphorylated thioureas of common formula RNHC(S)NHP(O)(OiPr)(2) (R = rBu, HL1:R = Ph, HLII; R = 4'-benzo- I 5-crown-5, HLIII) with Pd(PhCN)(2)Cl-2 in acetonitrile leads to complexes of the structure Pd(HL1-S)(2)Cl-2 (1), Pd(HLII-S)(2)Cl-2 (2) and Pd(HLIII-S)(2)Cl-2 (3). Reaction of N-phosphorylated thioureas of common formula RC(S)NHP(O)(OiPr)(2) (R = Et2N, HLIV; R = morpholine-N-yl, HLV) in the same conditions leads to complexes Pd(L-IV-O,S)(2) (4) and Pd(L-V-O,S)(2) (5), where the palladium(II) atoms are coordinated in a square-planar fashion by the C=S sulfur atoms and the P=O oxygen atoms of two anionic ligands. The crystal structure of complex I has been investigated by X-ray crystallography. It was established that the thiourea ligands are in a trans-configuration and the palladium(II) cation is coordinated by the sulfur atoms of the C=S groups and the chlorine atoms. Complex 1 is the first example of palladium(II) complex in which the potentially chelating N-phosphorylated thiourea ligand is bound through the sulfur atom only. (C) 2008 Elsevier Ltd. All rights reserved.
• Studies on cobalt(II) complexes with N-thioacylamido(thio)phosphates: X-ray crystal structure of the Co[PhC(S)NP(S)(OPri)2]2
  作者：Damir A. Safin、Felix D. Sokolov、Nail G. Zabirov、Vasiliy V. Brusko、Dmitry B. Krivolapov、Igor A. Litvinov、Robert C. Luckay、Rafael A. Cherkasov

  DOI：10.1016/j.poly.2006.06.005

  日期：2006.12

  Reaction of the potassium salts of N-thioacylamidophosphates RC(S)NHP(O)(OPri)(2) (R = Ph, PhNH, p-MeOPhNH, p-BrPhNH, iPrNH, tBuNH, Et2N, c-C5H10N, c-OC4H8N, C-C5HIINH) with Co(II) cation in aqueous EtOH leads to the complexes of Co(L-S)(2) type structure. Complexes Co(B)L-2 were obtained by the reaction of chelate complexes CoL2 (R = Ph, PhNH) with 2,2'-bipyridine and 1,10-phenanthroline. Structures of the compounds obtained were investigated by EIMS, IR, UV-Vis spectroscopy and microanalysis. Complex Co[PhC(S)NP(S)(OPri)](2) was investigated by single crystal X-ray diffraction. (c) 2006 Elsevier Ltd. All rights reserved.