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tris[1-(4-pyridyl)butane-1,3-dionato]aluminium | 1195938-76-1

中文名称
——
中文别名
——
英文名称
tris[1-(4-pyridyl)butane-1,3-dionato]aluminium
英文别名
[tris(1-(4-pyridyl)acetylacetonato)aluminum(III)]
tris[1-(4-pyridyl)butane-1,3-dionato]aluminium化学式
CAS
1195938-76-1
化学式
C27H24AlN3O6
mdl
——
分子量
513.486
InChiKey
WNRNBMKQKFDXBI-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):
    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:
    ethylenediamine palladium(II) nitrate 、 tris[1-(4-pyridyl)butane-1,3-dionato]aluminium甲醇 为溶剂, 以25%的产率得到[(palladium(2+))6(tris(1-(4-pyridyl)acetylacetonato)aluminum(III))8](NO3)12
    参考文献:
    名称:
    用三脚架金属配体构建异金属笼
    摘要:
    更换笼子:所含金属的配位偏好决定了使用AlL 3(HL = 1-(4-吡啶基)丁烷-1,3-二酮)作为金属配体组装而成的杂金属笼子的几何形状。分离出一个三角双锥和一个巨大的带帽八面体(见图;绿色Al,红色O,蓝色N,紫色Pd)。的手性三角双锥复合体M的空前自发分辨率2 M' 3大号6与d 3,观察到的对称。
    DOI:
    10.1002/anie.200903575
  • 作为产物:
    描述:
    aluminum(III) nitrate nonahydrate4-hydroxy-4-(pyridin-4-yl)but-3-en-2-one 在 NaHCO3 作用下, 以 甲醇 为溶剂, 以55.5%的产率得到tris[1-(4-pyridyl)butane-1,3-dionato]aluminium
    参考文献:
    名称:
    用三脚架金属配体构建异金属笼
    摘要:
    更换笼子:所含金属的配位偏好决定了使用AlL 3(HL = 1-(4-吡啶基)丁烷-1,3-二酮)作为金属配体组装而成的杂金属笼子的几何形状。分离出一个三角双锥和一个巨大的带帽八面体(见图;绿色Al,红色O,蓝色N,紫色Pd)。的手性三角双锥复合体M的空前自发分辨率2 M' 3大号6与d 3,观察到的对称。
    DOI:
    10.1002/anie.200903575
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文献信息

  • [MIII2MII3]<sup>n+</sup> trigonal bipyramidal cages based on diamagnetic and paramagnetic metalloligands
    作者:S. Sanz、H. M. O'Connor、V. Martí-Centelles、P. Comar、M. B. Pitak、S. J. Coles、G. Lorusso、E. Palacios、M. Evangelisti、A. Baldansuren、N. F. Chilton、H. Weihe、E. J. L. McInnes、P. J. Lusby、S. Piligkos、E. K. Brechin
    DOI:10.1039/c7sc00487g
    日期:——
    [MIII2PdII3](OTf)6. The metallic skeleton of all cages describes a trigonal bipyramid with the MIII ions occupying the two axial sites and the MII ions sitting in the three equatorial positions. Direct current (DC) magnetic susceptibility, magnetisation and heat capacity measurements on 1 reveal weak antiferromagnetic exchange between the FeIII and CoII ions. EPR spectroscopy demonstrates that the distortion imposed
    五个[M III 2 M II 3 ] n +三角双锥体笼子的一个族(M III =和铝; M II =;n = 0表示1–3,n = 6表示4– 5)式的[Fe 2共3大号66 ](1),的[Fe 2的Zn 3大号66 ](2),[CR 2的Zn 3大号66 ](3),[Cr 2 Pd 3 L 6(dppp)3 ](OTf)6(4)和[Al 2 Pd 3 L 6(dppp)3 ](OTf)6(5)(其中HL为1-(4报道了-吡啶基)丁烷-1,3-二酮和dppp为1,3-双(二苯基膦基丙烷)。中性笼1-3是使用三位[M III L 3 ]配体与盐Co II Cl 2和Zn II Br 2结合合成的,它们都充当四面体连接体。用[M III L 3 ]进行顺式保护的[Pd II(dppp)(OTf)2 ]的组装,得到通式[M III 2 Pd II 3 ](OTf)
  • Coordination-Driven Self-Assembly of M<sub>3</sub>L<sub>2</sub> Trigonal Cages from Preorganized Metalloligands Incorporating Octahedral Metal Centers and Fluorescent Detection of Nitroaromatics
    作者:Ming Wang、Vaishali Vajpayee、Sankarasekaran Shanmugaraju、Yao-Rong Zheng、Zhigang Zhao、Hyunuk Kim、Partha Sarathi Mukherjee、Ki-Whan Chi、Peter J. Stang
    DOI:10.1021/ic1020719
    日期:2011.2.21
    The design and preparation of novel M3L2 trigonal cages via the coordination-driven self-assembly of preorganized metalloligands containing octahedral aluminum(III), gallium(III), or ruthenium(II) centers is described. When tritopic or dinuclear linear metalloligands and appropriate complementary subunits are employed, M3L2 trigonal-bipyramidal and trigonal-prismatic cages are self-assembled under mild conditions. These three-dimensional cages were characterized with multinuclear NMR spectroscopy (H-1 and P-31) and high-resolution electrospray ionization mass spectrometry. The structure of one such trigonal-prismatic cage, self-assembled from an arene ruthenium metalloligand, was confirmed via single-crystal X-ray crystallography. The fluorescent nature of these prisms, due to the presence of their electron-rich ethynyl functionalities, prompted photophysical studies, which revealed that electron-deficient nitroaromatics are effective quenchers of the cages' emission. Excited-state charge transfer from the prisms to the nitroaromatic substrates can be used as the basis for the development of selective and discriminatory turn-off fluorescent sensors for nitroaromatics.
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