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neptunyl(V) nitrate | 17118-09-1

中文名称
——
中文别名
——
英文名称
neptunyl(V) nitrate
英文别名
neptunoyl nitrate;neptunyl nitrate;Np(V) nitrate
neptunyl(V) nitrate化学式
CAS
17118-09-1
化学式
NO3*NpO2
mdl
——
分子量
331.052
InChiKey
OKXKFUGESFNZQM-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):
    -0.48
  • 重原子数:
    7.0
  • 可旋转键数:
    0.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    100.34
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    硝酸ept
    摘要:
    水合neptunium-(IV), - (V),和- (VI)的硝酸盐,NP(NO 3)4,2H 2 O(灰色),NPO 2 NO 3,H 2 O(绿色),NPO(NO 3)3,3H 2 O(粉红色)和NPO 2(NO 3)2,6H 2 O(粉红色),已经从含水硝酸制备。溶剂化-- (IV)和-(VI)硝酸盐Np(NO 3)4,x N 2 O 5(X〜1·2)(灰白色)和NPO 2(NO 3)2,N 2 ø 5,H 2 O(淡粉色),已被镎三氧化水合物,分别和制备由四氯化镎反应,与一氧化二五氧化物。通过使二水合物与配体反应,或由相应的氯化物络合物和硝酸银在氰化甲基中的反应,制得了四硝酸二甲基乙酰胺(DMA)络合物Np(NO 3)4,2 ·5DMA(灰绿色)。尝试制备nitr (V)硝酸根合和羟硝根合络合物均未成功。磁性能,红外光谱和一些X还介绍了射线衍射测量。
    DOI:
    10.1039/j19660000780
  • 作为产物:
    描述:
    neptunyl(VI) nitrate hydrate 在 NaNO2 作用下, 以 为溶剂, 生成 neptunyl(V) nitrate
    参考文献:
    名称:
    Chaikorskii, A. A.; Leikina, E. V., Radiokhimiya, 1982, vol. 24, p. 288 - 295
    摘要:
    DOI:
  • 作为试剂:
    描述:
    参考文献:
    名称:
    Chaikorskii, A. A.; Leikina, E. V., Radiokhimiya, 1982, vol. 24, p. 288 - 295
    摘要:
    DOI:
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文献信息

  • Synthesis of New Crystalline Pu(V) Compounds from Solutions: III. Synthesis and Study of NaPuO2C2O4·nH2O with n = 3, 1, and 0
    作者:N. N. Krot、A. A. Bessonov、M. S. Grigor’ev、I. A. Charushnikova、V. I. Makarenkov
    DOI:10.1007/s11137-005-0059-9
    日期:2005.3
    NaPuO2C2O4·3H2O was isolated from a freshly prepared oxalate solution of Pu(VI) by reduction with a stoichiometric amount of hydrazine hydrate. Heating of the compound results in its stepwise dehydration with successive formation of the monohydrate and anhydrous salt. According to powder X-ray patterns, NaPuO2C2O4· n H2O ( n = 3, 4) is isostructural to the corresponding analogs NaNpO2C2O4· n H2O. The
    NaPuO 2 c ^ 2 Ò 4 ·3H 2 O的从浦(VI)的还原与化学计量量的新鲜制备的草酸溶液中分离。化合物的加热导致其逐步脱,并依次形成一合物和无盐。根据粉末X射线图,NaPuO 2 C 2 O 4 · n H 2 O( n = 3,4)与相应的类似物NaNpO 2 C 2 O 4 · n H 2 O同构。NaNpO的晶胞参数2确定了C 2 O 4 ·H 2 O和NaPuO 2 C 2 O 4 · n H 2 O( n = 3,1)。X射线分析的结果以及庚基(V)和p基(V)结晶化合物的电子和IR光谱表明,NaPuO 2 C 2 O 4 · n H 2 O( n = 1,0)。
  • Synthesis of New Crystalline Pu(V) Compounds from Solutions: IV. Double Pu(V) Malonates of the Composition Co(NH3)6[PuO2C3H2O4]2A ⋅ nH2O, A = NO3, ClO4, Cl, and Br
    作者:N. N. Krot、A. A. Bessonov、I. A. Charushnikova、M. S. Grigor’ev、V. I. Makarenkov
    DOI:10.1007/s11137-005-0081-y
    日期:2005.5
    New crystalline compounds of the composition Co(NH3)6[PuO2L]2A ⋅ nH2O, where L = C3H2O4 and A = NO3, ClO4, Cl, and Br, were obtained by addition of a small excess of Co(NH3) 6 3+ ions to freshly prepared neutral malonate solutions of Pu(V). They are fairly stable in storage in air and isostructural to the corresponding Np(V) compounds. Thermal behavior of the compounds synthesized was studied, and their IR spectra were measured.
    在新制备的(V)的中性丙二酸盐溶液中加入少量过量的 Co(NH3) 6 3+ 离子,得到了组成为 Co(NH3)6[PuO2L]2A⋅nH2O 的新晶体化合物,其中 L = C3H2O4,A = NO3ClO4、Cl 和 Br。它们在空气中储存相当稳定,与相应的(V)化合物结构相同。对合成化合物的热行为进行了研究,并测量了它们的红外光谱。
  • Crystal structure of new complexes of Np(V) and Pu(V) propionates with 2,2’-bipyridine, [AnO2(C10H8N2)(OOCC2H5)(H2O)]
    作者:N. N. Krot、I. A. Charushnikova、M. S. Grigor’ev、A. A. Bessonov、I. N. Polyakova
    DOI:10.1134/s1066362210010030
    日期:2010.2
    The crystal structure of new complexes of Np(V) and Pu(V) propionates with 2,2’-bipyridine (Bipy) was studied. The compounds are isostructural. Their crystals are built of electrically neutral complexes [AnO2 (C10H8N2)(OOCC2H5)(H2O)] (An = Np, Pu). The equatorial surrounding of the actinyl(V) group consists of two nitrogen atoms of Bipy, two oxygen atoms of the propionateion, and oxygen atom of the
    研究了丙酸Np(V)和Pu(V)与2,2'-联吡啶(Bipy)的新配合物的晶体结构。这些化合物是同构的。它们的晶体由电中性络合物[AnO 2(C 10 H 8 N 2)(OOCC 2 H 5)(H 2O)](An = Np,Pu)。in基(V)的赤道周围由Bipy的两个氮原子,丙酸酯的两个氧原子和分子的氧原子组成。An(V)原子的配位周围是五边形双锥体。从Np(V)到Pu(V),the系化合物的收缩表现为五边形双锥体的键长有规律地减少。An(V)配位球中的分子与相邻配合物[AnO 2(Bipy)(OOCC2H 5)(H 2 O)]的“ yl”氧原子形成牢固的氢键。结果,晶体中的络合物被束缚在沿[100]方向取向的无限链中。
  • Periodic Trends in Hexanuclear Actinide Clusters
    作者:Juan Diwu、Shuao Wang、Thomas E. Albrecht-Schmitt
    DOI:10.1021/ic2023242
    日期:2012.4.2
    described and compared with other clusters of containing An(IV) or Ce(IV). All of the clusters share the common formula M6(H2O)m[C6H3(PO3)(PO3H)]6(NO3)n(6–n) (M = Ce, Th, U, Np, Pu). The metal centers are normally nine-coordinate, with five oxygen atoms from the ligand and an additional four either occupied by NO3– or H2O. It was found that the Ce, U, and Pu clusters favor both C3i and Ci point groups
    通过在室温下自组装制备了四个新的具有1,2-苯二膦酸酯作为桥联配体的Th(IV),U(IV)和Np(IV)六核簇。Th 6 Tl 3 [C 6 H 4(PO 3)(PO 3 H)] 6(NO 3)7(H 2 O)6 ·(NO 3)2 ·4H 2 O(Th6-3)的结构, (NH 4)8.11 Np 12 Rb 3.89 [C 6 H 4(PO 3)(PO 3 H)] 12(NO 3)24 ·15H 2 O(Np6-1),(NH 4)4 U 12 Cs 8 [C 6 H 4(PO 3)(PO 3 H)] 12(NO 3)24 ·18H 2 O(U6-1)和(NH 4)4 U 12 Cs 2 [C 6 H 4(PO 3)(PO 3 H)] 12描述(NO 3)18 ·40H 2 O(U6-2)并与其他包含An(IV)或Ce(IV)的簇进行比较。所有簇均具有共同的公式M 6(H 2 O)m [C
  • Nitrate Complexes of Neptunium(V) with Alkali Metal Cations in the Outer Sphere
    作者:I. A. Charushnikova、M. S. Grigor’ev、A. M. Fedoseev、A. A. Bessonov、K. A. Lysenko
    DOI:10.1134/s1066362220020022
    日期:2020.2
    AbstractNitrate complexes of pentavalent neptunium with alkali cations in the outer sphere, with composition Li[NpO2(NO3)2]·2H2O (I), Na[NpO2(NO3)2]·2H2O (II), Cs3[NpO2(NO3)2]3·H2O (III), NaRb5[NpO2(NO3)2]6·4H2O (IV) were isolated in the crystalline form and examined by the method of X-ray diffraction analysis. The cation–cation (CC) interaction of NpO2+ ions occurs in the complexes to give square (I
    摘要Li [NpO 2(NO 3)2 ]·2H 2 O(I),Na [NpO 2(NO 3)2 ]·2H 2 O(II)组成的五价n与外层球中的碱性阳离子的硝酸盐络合物,Cs 3 [NpO 2(NO 3)2 ] 3 ·H 2 O(III),NaRb 5 [NpO 2(NO 3)2 ] 6 ·4H 2 O(IV)以结晶形式分离并通过X射线衍射分析方法检查。NpO 2 +离子的阳离子-阳离子(CC)相互作用发生在配合物中,从而形成正方形(I,II)或三角六边形(II,IV)阳离子网络。I–IV结构中的Np原子具有六方双锥形式的配位环境,其双峰平面由两个二齿环状硝酸根离子和两个相邻的NpO 2 +阳离子的氧原子形成。化合物II单晶的高质量使得可以进行高精度X射线衍射实验(最大2θ= 120°)并首次研究Np化合物的电子密度分布ρ(r)。给出了化合物Ⅱ的红外光谱和电子吸收光谱。
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