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tetrakis(aminopropoxy)calix[4]arene | 1354344-59-4

中文名称
——
中文别名
——
英文名称
tetrakis(aminopropoxy)calix[4]arene
英文别名
2-[2-(dioctylamino)-2-oxoethoxy]-N-[3-[[5,11,17,23-tetratert-butyl-26,27,28-tris[3-[[2-[2-(dioctylamino)-2-oxoethoxy]acetyl]amino]propoxy]-25-pentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(24),3,5,7(28),9,11,13(27),15(26),16,18,21(25),22-dodecaenyl]oxy]propyl]acetamide
tetrakis(aminopropoxy)calix[4]arene化学式
CAS
1354344-59-4
化学式
C136H232N8O16
mdl
——
分子量
2235.38
InChiKey
QWELSGWYMVMZIE-UHFFFAOYSA-N
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):
    37.9
  • 重原子数:
    160
  • 可旋转键数:
    96
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    272
  • 氢给体数:
    4
  • 氢受体数:
    16

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    4-nitrophenyl 2-(2-(dioctylamino)-2-oxoethoxy)acetate 、 5,11,17,23-tetra(t-butyl)-25,26,27,28-tetrakis(3-aminopropoxy)calix[4]arene三乙胺 作用下, 以 氯仿 为溶剂, 反应 48.0h, 以74%的产率得到tetrakis(aminopropoxy)calix[4]arene
    参考文献:
    名称:
    Remarkable acidity independent actinide extraction with a both-side diglycolamide-functionalized calix[4]arene
    摘要:
    室温离子液体中含有一种新合成的双面二甘醇酰胺功能化钙[4]炔(L-I)的新型溶剂系统显示出对锕系元素的高效萃取,而且对三价锕系元素 Am3+ 的萃取显著不受酸浓度的影响,这表明该系统可用于高放射性废物的修复。通过斜率分析、发光光谱研究和热力学参数确定了复合物的性质。此外,还研究了溶剂系统在长期应用中的可持续性。
    DOI:
    10.1039/c3dt50557j
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文献信息

  • A highly efficient solvent system containing functionalized diglycolamides and an ionic liquid for americium recovery from radioactive wastes
    作者:Arijit Sengupta、Prasanta K. Mohapatra、Mudassir Iqbal、Jurriaan Huskens、Willem Verboom
    DOI:10.1039/c2dt12364a
    日期:——
    Three room temperature ionic liquids (RTILs), viz. C4mim+·PF6−, C6mim+·PF6− and C8mim+·PF6−, were evaluated as diluents for the extraction of Am(III) by N,N,N′,N′-tetraoctyl diglycolamide (TODGA). At 3 M HNO3, the DAm-values by 0.01 M TODGA were found to be 102, 34 and 74 for C4mim+·PF6−, C6mim+·PF6− and C8mim+·PF6−, respectively. The extraction of Am(III) decreased with increasing feed acidity for all three diluents, indicating an ion exchange mechanism for the extraction. The stoichiometry of the extracted species suggested that two TODGA molecules were associated with Am(III) during the extraction for all three RTILs and the conditional extraction constants have been determined. The DM-values for different metal ions followed the order: 75 (Am(III)) > 30.7 (Pu(IV)) > 3.9 (Np(IV)) > 1.19 (Pu(VI)) > 0.52 (U(VI)) > 0.12 (Cs(I)) > 0.024 (Sr(II)). The distribution behaviour of Am(III) was also studied with a recently synthesized calix[4]arene-4DGA (C4DGA) extractant dissolved in C8mim+·PF6−. Using this extractant diluent combination, the DAm-value was 194 at 3 M HNO3 using 5 × 10−5 M C4DGA, suggesting a very high distribution coefficient at very low extractant concentrations. The stoichiometry of the extracted species containing Am was found to be 1 : 2 (M : L) in C8mim+·PF6−. The thermodynamics of the extraction was also studied for both extractants in C8mim+·PF6−. The use of RTILs gives rise to significantly improved extraction properties than the commonly used n-dodecane and an unusual increase in separation factor values was seen for the first time which can lead to selective separation of Am from wastes containing a mixture of U, Pu and Am.
    评估了三种室温离子液体(RTILs),即 C4mim+-PF6-、C6mim+-PF6- 和 C8mim+-PF6-,作为 N,N,N′,N′-四辛基二乙二醇酰胺(TODGA)萃取 Am(III)的稀释剂。在 3 M HNO3 条件下,0.01 M TODGA 对 C4mim+-PF6-、C6mim+-PF6- 和 C8mim+-PF6- 的 DAm 值分别为 102、34 和 74。在所有三种稀释剂中,Am(III)的萃取率随着进样酸度的增加而降低,这表明萃取过程中存在离子交换机制。萃取物的化学计量学表明,在所有三种 RTIL 的萃取过程中,都有两个 TODGA 分子与 Am(III) 结合,并确定了条件萃取常数。不同金属离子的 DM 值依次为75 (Am(III))> 30.7(Pu(IV)> 3.9 (Np(IV)1.19 (Pu(VI)) > 0.52 (U(VI))> 0.52(U(VI)> 0.12(铯(I)>0.024(Sr(II))。我们还利用最近合成的溶于 C8mim+-PF6- 的钙[4]炔-4DGA(C4DGA)萃取剂研究了 Am(III) 的分布行为。使用这种萃取剂稀释剂组合,在3 M HNO3中使用5 × 10-5 M C4DGA时,DAm值为194,这表明在萃取剂浓度很低的情况下,分布系数非常高。在 C8mim+-PF6- 中,含有 Am 的萃取物的化学计量为 1 : 2 (M : L)。还研究了 C8mim+-PF6- 中两种萃取剂的萃取热力学。与常用的正十二烷相比,RTILs 的使用大大提高了萃取性能,分离因子值也首次出现了不寻常的增长,从而可以从含有铀、钚和镅混合物的废物中选择性地分离出镅。
  • Complexation of novel diglycolamide functionalized calix[4]arenes: Unusual extraction behaviour, transport, and fluorescence studies
    作者:Prasanta K. Mohapatra、Mudassir Iqbal、Dhaval R. Raut、Willem Verboom、Jurriaan Huskens、Shrikant V. Godbole
    DOI:10.1039/c1dt11561h
    日期:——
    functionalized calix[4]arenes (calix[4]-nDGA) were synthesized and evaluated for their extraction behaviour towards lanthanide/actinide ions. Exceptionally high DAm and DPu values indicate these radiotoxic elements can be selectively removed from nuclear waste solutions. Transport and laser induced fluorescence studies indicated strong complexation of the trivalent metal ions with the calix[4]-4DGA ligand
    合成了三甘醇酰胺官能化的杯[4]芳烃(杯[4] -nDGA),并评估了它们对镧系//系离子的萃取行为。极高的D Am和D Pu值表示可以从核废料溶液中选择性去除这些放射性元素。运输和激光诱导的荧光研究表明三价金属离子与杯[4] -4DGA配体的强络合。
  • Remarkable acidity independent actinide extraction with a both-side diglycolamide-functionalized calix[4]arene
    作者:Prasanta K. Mohapatra、Arijit Sengupta、Mudassir Iqbal、Jurriaan Huskens、Shrikant V. Godbole、Willem Verboom
    DOI:10.1039/c3dt50557j
    日期:——
    A novel solvent system containing a newly synthesized both-side diglycolamide-functionalized calix[4]arene (L-I) in a room temperature ionic liquid showed highly efficient extraction of actinides and a remarkable acid concentration independent extraction of trivalent actinide ion, Am3+ suggesting its possible use for high level radioactive waste remediation. The nature of the complexes was ascertained by slope analysis, luminescence spectroscopic investigations and from the thermodynamic parameters. The sustainability of the solvent system for long term applications was also investigated.
    室温离子液体中含有一种新合成的双面二甘醇酰胺功能化钙[4]炔(L-I)的新型溶剂系统显示出对锕系元素的高效萃取,而且对三价锕系元素 Am3+ 的萃取显著不受酸浓度的影响,这表明该系统可用于高放射性废物的修复。通过斜率分析、发光光谱研究和热力学参数确定了复合物的性质。此外,还研究了溶剂系统在长期应用中的可持续性。
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