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calcium bromide hydride | 10024-43-8

中文名称
——
中文别名
——
英文名称
calcium bromide hydride
英文别名
——
calcium bromide hydride化学式
CAS
10024-43-8
化学式
BrCa
mdl
——
分子量
119.982
InChiKey
NJBLGWVFUHAPEF-UHFFFAOYSA-M
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):
    0.46
  • 重原子数:
    2.0
  • 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:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为产物:
    描述:
    calcium 、 calcium bromide 以 neat (no solvent) 为溶剂, 生成 calcium bromide hydride
    参考文献:
    名称:
    Electric quadrupole refocusing of CaBr: Differential transmission of hyperfine levels and assignment of low-J lines in optical spectra
    摘要:
    DOI:
    10.1016/0301-0104(84)87013-5
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文献信息

  • Steric effects in chemiluminescent reactions of metastable Ca∗, Sr∗ atoms with isomeric propyl halides
    作者:B. Pranszke、P. Kierzkowski、A. Kowalski
    DOI:10.1016/s0009-2614(99)00676-4
    日期:1999.8
    Reactions of metastable alkaline earth atoms with normal and branched propyl halides were studied in a beam-gas arrangement. Chemiluminescence spectra of alkaline earth monohalides were observed for calcium and strontium reactions. Some differences in the CaX () branching ratio were found with isomeric variation of the targets. Total collision cross-sections for Mg∗ and Ca∗ reactions are independent
    在束流-气体装置中研究了亚稳碱土原子与正卤和支链丙基卤的反应。观察到反应的碱土属卤化物的化学发光光谱。发现CaX()支化比率存在一些差异,这与靶标的异构体变异有关。Mg *和Ca *反应的总碰撞截面与异构体取代无关。对于异丙基的值比正常丙靶的值高50%。发现与丙化物和丙的反应在化学发光横截面上存在差异。
  • Radiative lifetimes of the A2Π, B2Σ+, C2Π and D2Σ+ states of the CaBr and CaI radicals
    作者:C. Bahrini、F. Augé-Rochereau、J. Rostas、G. Taïeb
    DOI:10.1016/j.chemphys.2006.08.003
    日期:2006.11
    The lifetimes of the A2Π, B2Σ+, C2Π and D2Σ+ states of the CaBr and CaI radicals have been measured directly from the time rate of fluorescence decay using an appropriate pulsed dye laser as an excitation source. The zero pressure radiative lifetimes determined for the first time for the C2Π1/2 state of CaI and D2Σ+ state of CaBr were (50.5 ± 1.5) ns and (21.0 ± 2.6) ns, respectively. The measured
    在A的寿命2 Π,B 2 Σ +,C 2 Π和d 2 Σ +的CABR与CAI自由基的状态已经从使用适当的脉冲染料激光作为激发源的荧光衰减的时间速率直接测量。零压力辐射寿命确定首次用于C 2 Π 1/2 Cai和d的状态2 Σ +分别CABR的状态分别为(50.5±1.5)NS和(21.0±2.6)纳秒。测得的寿命与配体场(LF)模型预测的趋势非常吻合。对于蔡Ç 2 Π 3/2状态(τ = 31.2纳秒在1mbar压力)和d 2 Σ +状态(τ  <11纳秒),异常短的寿命中观察到,表明这些状态预离解。
  • State selective reactions prepared through the excitation of orbital states in van der Waals complexes of Ca–HX*
    作者:B. Soep、S. Abbès、A. Keller、J. P. Visticot
    DOI:10.1063/1.462884
    日期:1992.1
    We have observed the chemiluminescent reaction Ca*+HX→CaX*+H, where the reactants are prepared in a van der Waals complex formed in a supersonic expansion. This preparation, combined with tunable laser excitation, allows access to well-defined electronic states of the reaction complex corresponding to different orientations of the calcium excited orbital. In the case of the Ca–HBr complex, a remarkable effect of this preparation is observed on the branching ratio to the final excited states A 2Π and B 2Σ of CaBr: Depending upon the selected state of the complex, the A/B ratio varies by a factor of 2. This is interpreted by the conservation of the orbital orientation during the reaction involving the departure of the hydrogen.
  • Electronic branching in reactions of calcium (3P,1D) and magnesium(3P) with fluorine, chlorine, and bromine: experiments and global model
    作者:Andrzej. Kowalski、Michael. Menzinger
    DOI:10.1021/j100368a034
    日期:1990.3
  • Hyperfine and spin–rotational structure of CaBr X <sup>2</sup>Σ (v = 0) by molecular‐beam laser‐rf double resonance
    作者:W. J. Childs、David R. Cok、G. L. Goodman、L. S. Goodman
    DOI:10.1063/1.442057
    日期:1981.7.15
    The molecular-beam, laser–rf, double-resonance technique has been used to make high-precision measurements of the spin–rotation and hyperfine interactions in the X 2Σ (v = 0) electronic ground state of Ca79Br and Ca81Br. The spin–rotation interaction is found to have a strong N dependence. The Frosch–Foley magnetic hyperfine parameters b and c and the electric–quadrupole hfs parameter eqQ are determined for both molecules.
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