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caesium phenoxide | 1120-91-8

中文名称
——
中文别名
——
英文名称
caesium phenoxide
英文别名
cesium phenoxide;Cs-Phenolat;Cesium phenolate;cesium;phenoxide
caesium phenoxide化学式
CAS
1120-91-8
化学式
C6H5O*Cs
mdl
——
分子量
226.011
InChiKey
NHGGJRABQHWCGJ-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):
    -2.24
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    23.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    caesium phenoxide二甲基亚砜 为溶剂, 生成 苯氧基自由基 、 alkaline earth salt of/the/ methylsulfuric acid
    参考文献:
    名称:
    Template effects. 4. Ion pairing of aryloxide ions with alkali cations in 99% dimethylsulfoxide: influence on the rate of formation of benzo-18-crown-6 and of other Williamson-type reactions
    摘要:
    DOI:
    10.1021/ja00341a041
  • 作为产物:
    描述:
    苯氧基自由基caesium 作用下, 以 二甲基亚砜 为溶剂, 生成 caesium phenoxide
    参考文献:
    名称:
    Template effects. 4. Ion pairing of aryloxide ions with alkali cations in 99% dimethylsulfoxide: influence on the rate of formation of benzo-18-crown-6 and of other Williamson-type reactions
    摘要:
    DOI:
    10.1021/ja00341a041
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文献信息

  • Chemical shifts of phenolic monomers in solution and implications for addition and self-condensation
    作者:Robert A. Haupt、Scott Renneckar
    DOI:10.1002/mrc.3914
    日期:2013.2
    Alkali metal counter-cations alter the electron density of phenolates in solution by electrostatic interactions. This change in electron density affects their reactivity toward formaldehyde, hydroxymethylphenols, and isocyanates during polymerization. The electronic perturbation of phenolic model compounds in the presence of alkali metal hydroxides was investigated with (13)C and (1)H nuclear magnetic
    碱金属抗衡阳离子通过静电相互作用改变溶液中酚盐的电子密度。电子密度的这种变化会影响它们在聚合过程中对甲醛,羟甲基苯酚和异氰酸酯的反应性。相对于非离子对照物,在极性溶剂中用(13)C和(1)H核磁共振研究了碱金属氢氧化物存在下酚类化合物的电子扰动,从而改变了模型化合物的化学位移,从而表明以化学位移为代表的电子密度变化。这些变化归因于抗衡阳离子与酚醛阴离子的库仑静电相互作用,该相互作用与水合离子半径和溶剂介电常数有关。基于酚模型的(13)C核磁共振的电子密度等级,将甲醛添加的预计相对反应速率与文献值进行了比较。由化学位移对2-和4-羟甲基苯酚的缩合反应的预测与已发表的结果一致。结果允许预测酚类化合物用于形成热固性聚合物材料的反应。
  • Process For Producing Phosphonitrilic Acid Ester
    申请人:Kuwata Kotaro
    公开号:US20080091050A1
    公开(公告)日:2008-04-17
    A process for producing a cyclic and/or linear phosphonitrilic acid ester from a cyclic and/or linear phosphonitrile dichloride is provided, wherein the reaction time is shorter and the content of monochloro phosphazenes is very small. When phosphonitrile dichloride is reacted with a metal arylolate and/or a metal alcoholate in the presence of a reaction solvent, a metal arylolate and/or a metal alcoholate composed of at least two different metals having different ionization energies is used and also a specific compound is used as a catalyst.
    <待解决问题> 提供一种从环状和/或线性磷氮化物二氯化物中生产环状和/或线性磷氮化物酸酯的方法,其中反应时间更短,单氯磷氮烷的含量非常小。 <解决方案> 当磷氮化物二氯化物与金属芳氧基和/或金属醇盐在反应溶剂的存在下反应时,使用由至少两种具有不同电离能的不同金属组成的金属芳氧基和/或金属醇盐,并且使用特定化合物作为催化剂。
  • Benzylic C–H activation and C–O bond formation via aryl to benzylic 1,4-palladium migrations
    作者:Tanay Kesharwani、Richard C. Larock
    DOI:10.1016/j.tet.2008.01.144
    日期:2008.6
    A procedure for benzylic C-H activation has been developed using a palladium 1,4-aryl to benzylic migration as a key step. Carboxylates and phenoxides readily trap the resulting benzylic palladium intermediates obtained from palladium 'through space' migration. Aryl bromides and iodides have been successfully employed in this reaction, furnishing moderate to good yields. The mechanism of this reaction has been studied by deuterium-labeling experiments, which suggest that the migration of palladium from an aryl to a benzylic position occurs reversibly. The reaction conditions developed for the migration process also oxidize the neighboring benzylic alcohols to the corresponding aldehydes and ketones. (C) 2008 Elsevier Ltd. All rights reserved.
  • Direct Arylation of 2-Pyridones; Photostimulated SRN1 Reaction between Cesium Phenoxides and Chloro-2-pyridones
    作者:Shigeru Ohmiya、Hiroyuki Higuchi、Masayo Hattori
    DOI:10.3987/com-99-s18
    日期:——
  • Template effects. 4. Ion pairing of aryloxide ions with alkali cations in 99% dimethylsulfoxide: influence on the rate of formation of benzo-18-crown-6 and of other Williamson-type reactions
    作者:Gabriello Illuminati、Luigi Mandolini、Bernardo Masci
    DOI:10.1021/ja00341a041
    日期:1983.2
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