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(2-(diethylamino)-4-methyl-1,3,2l5-dioxaphosphinan-2-yl)copper(II) bromide | 473576-53-3

中文名称
——
中文别名
——
英文名称
(2-(diethylamino)-4-methyl-1,3,2l5-dioxaphosphinan-2-yl)copper(II) bromide
英文别名
——
(2-(diethylamino)-4-methyl-1,3,2l5-dioxaphosphinan-2-yl)copper(II) bromide化学式
CAS
473576-53-3
化学式
C8H18BrCuNO2P
mdl
——
分子量
334.66
InChiKey
XIQJDFCYKQSAKX-YJUVXMIUSA-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):
    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:
    tetrabutoxytitanium(2-(diethylamino)-4-methyl-1,3,2l5-dioxaphosphinan-2-yl)copper(II) bromide 在 acetylacetone 作用下, 以 乙醇 为溶剂, 生成
    参考文献:
    名称:
    摘要:
    The relationship of the structural organization and acid-base properties of the surface of phosphorus titanate oxides prepared from tetra-n-butoxytitanium and phosphorous esters with the catalytic activity and selectivity of these materials in ethylene glycol oxyethylation was studied. Single-phase phosphorus-containing oxides synthesized from 2-diethylamido-4-methyl-1,3,2-dioxophosphorinane and diphenyl(methano)phosphocane have strong surface aprotic acid sites and exhibit high catalytic activity with respect to oxyethylation and a record-breaking selectivity in the formation of the lower homolog, diethylene glycol. The last-mentioned fact is a consequence of the sieve effect exerted by the homogeneous porous structure of supermicropores (8-10 Angstrom) of the oxides. An increase in the concentration of the strong acid sites (greater than or equal to130 kJ mol(-1)) on the oxide surface enhances the catalytic activity. On the basis of the temperature programmed desorption of ammonia and CO2 and kinetic measurements, a concerted acid-base mechanism was proposed for the catalytic addition of ethylene oxide to ethylene glycol on the phosphorus-titanate surface.
    DOI:
    10.1023/a:1019601332563
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