草酸钯 | 57592-57-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: 草酸钯
• 英文名称: palladium oxalate
• 英文别名: palladium (II) oxalate；Palladium(II) oxalate；oxalate;palladium(2+)
• CAS: 57592-57-1
• 化学式: C₂O₄*Pd
• 分子量: 194.44
• InChiKey: YKUNZXXSTMDFIY-UHFFFAOYSA-L

物化性质

• 熔点：
  144 °C (dec.)(lit.)

计算性质

• 辛醇/水分配系数(LogP)：
  -3.52
• 重原子数：
  7
• 可旋转键数：
  0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  80.3
• 氢给体数：
  0
• 氢受体数：
  4

安全信息

• 危险品标志：
  Xn
• 安全说明：
  S24/25
• 危险类别码：
  R21/22

反应信息

• 作为产物：
  描述：

  、 草酸 以 水 为溶剂， 反应 1.0h， 生成 草酸钯
  参考文献：
  名称：

  Effect of precursor acidity on zeolite supported Pd catalyst properties and hydrodeoxygenation activity for the production of biofuel

  摘要：

  In this study, two different zeolite (ZLT) supported palladium catalysts (Pd/Zs) of varying acidity were synthesized, characterized and tested for biofuel production. The first Pd/Z was synthesized via the incorporation of palladium oxalate complex (PdOxC) prepared from the functionalization of H2PdCl4 with oxalic acid at pH 5.3 into ZLT. The PdOxC was further modified with drops of HF until pH 3.7 and incorporated into ZLT to synthesize zeolite supported fluoride ion modified PdOxC catalyst (FPd/Z). Their characterization results showed that there is considerable crystallinity loss in Pd/Z, while FPd/Z showed drastic crystallinity loss according to the SEM and XRD results. In addition, the specific surface area and porosity of ZLT increased from 202 m(2)/g and 0.13 cm(3)/g to 371 m(2)/g and 0.23 cm(3)/g in Pd/Z, and 427 m(2)/g and 0.29 cm(3)/g in FPd/Z catalysts, respectively. Pd/Z catalyst produces 56% n-C18H38 and 11% iso-C18H38, while FPd/Z produces 58% n-C18H38 and 28% iso-C18H38 in the hydrodeoxygenation (HDO) and isomerization (ISO) steps, respectively. The enhancements in the catalysts properties are due to the acidic effect of OxA via the incorporation of PdOxC, while the additional enhancements in the properties and the ISO activity of FPd/Z was ascribed to the acidic effect of fluoride ion modification. It is obvious that OxA functionalization and subsequent fluoride ion modification are highly invaluable toward biofuel production. (C) 2015 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.molcata.2015.01.033

文献信息

• Thermodynamics for complex formation between palladium(<scp>ii</scp>) and oxalate
  作者：Radomír Pilný、Přemysl Lubal、Lars I. Elding

  DOI：10.1039/c4dt01062k

  日期：——

  Specific Ion Interaction Theory from spectrophotometric titrations with initial hydrogen ion concentrations of 1.00, 0.100 and 0.0100 mol dm−3 and ionic strengths of 1.00, 2.00 or 3.00 mol dm−3. The values derived together with literature data give estimated overall stability constants for Pd(II) compounds such as [Pd(en)(ox)] and cis-[Pd(NH3)2Cl2], some of them analogs to Pt(II) complexes used in cancer

  [Pd（H 2 O）4 ] 2+与草酸盐（ox = C 2 O 4 2-）之间的络合物形成已在水溶液中，在可变温度，离子强度和pH下分光光度法进行了研究。络合物形成[Pd（H 2 O）4 ] 2+ + H 2 ox for [Pd（H 2 O）2（ox）] + 2H 3在298.2 K和1.00 mol dm -3 HClO 4离子介质中的热力学参数具有平衡常数K 1，H（以mol dm -3表示）的O +为log由分光光度平衡滴定法在15.0确定， 10 K 1，H = 3.38±0.08， ΔH 0 1 = -33±3 kJ mol -1， ΔS 0 1 = -48±11 JK -1 mol -1， 20.0、25.0和31.0°C。热力学整体稳定性常数β 0 Ñ（在（摩尔分米-3） - ñ， Ñ = 1,2）为[钯（H 2 O） 2（OX）]和[钯（OX） 2 ] 2-零离子强度和298
• Effect of precursor acidity on zeolite supported Pd catalyst properties and hydrodeoxygenation activity for the production of biofuel
  作者：O.B. Ayodele、Hamisu U. Farouk、Jibril Mohammed、Yoshimitsu Uemura、W.M.A.W. Daud

  DOI：10.1016/j.molcata.2015.01.033

  日期：2015.5

  In this study, two different zeolite (ZLT) supported palladium catalysts (Pd/Zs) of varying acidity were synthesized, characterized and tested for biofuel production. The first Pd/Z was synthesized via the incorporation of palladium oxalate complex (PdOxC) prepared from the functionalization of H2PdCl4 with oxalic acid at pH 5.3 into ZLT. The PdOxC was further modified with drops of HF until pH 3.7 and incorporated into ZLT to synthesize zeolite supported fluoride ion modified PdOxC catalyst (FPd/Z). Their characterization results showed that there is considerable crystallinity loss in Pd/Z, while FPd/Z showed drastic crystallinity loss according to the SEM and XRD results. In addition, the specific surface area and porosity of ZLT increased from 202 m(2)/g and 0.13 cm(3)/g to 371 m(2)/g and 0.23 cm(3)/g in Pd/Z, and 427 m(2)/g and 0.29 cm(3)/g in FPd/Z catalysts, respectively. Pd/Z catalyst produces 56% n-C18H38 and 11% iso-C18H38, while FPd/Z produces 58% n-C18H38 and 28% iso-C18H38 in the hydrodeoxygenation (HDO) and isomerization (ISO) steps, respectively. The enhancements in the catalysts properties are due to the acidic effect of OxA via the incorporation of PdOxC, while the additional enhancements in the properties and the ISO activity of FPd/Z was ascribed to the acidic effect of fluoride ion modification. It is obvious that OxA functionalization and subsequent fluoride ion modification are highly invaluable toward biofuel production. (C) 2015 Elsevier B.V. All rights reserved.