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[(4,4′-dinitro-2,2′-bipyridine)PtMe2] | 1430851-50-5

中文名称
——
中文别名
——
英文名称
[(4,4′-dinitro-2,2′-bipyridine)PtMe2]
英文别名
[(4,4′-dinitro-2,2′-bipyridine)PtMe2]
[(4,4′-dinitro-2,2′-bipyridine)PtMe2]化学式
CAS
1430851-50-5
化学式
C12H12N4O4Pt
mdl
——
分子量
471.332
InChiKey
XRQGRPVKICTIOV-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:
    苯乙烯 、 Brookhart's acid 、 [(4,4′-dinitro-2,2′-bipyridine)PtMe2]二氯甲烷 为溶剂, 以96%的产率得到[(4,4′-dinitro-2,2′-bipyridine)Pt(Me)(η2-styrene)][B(3,5-bis(trifluoromethyl)phenyl)4]
    参考文献:
    名称:
    Platinum(II)-Catalyzed Ethylene Hydrophenylation: Switching Selectivity between Alkyl- and Vinylbenzene Production
    摘要:
    The series of Pt-II complexes [((x)bpy)Pt(Ph)(THF)][BAr'(4)] ((x)bpy=4,4'-X-2,2'-bipyridyl, X = OMe, Bu-t, H, Br, CO2Et, NO2; Ar' = 3,5-bis(trifluoromethyl)phenyl) are catalyst precursors for ethylene hydrophenylation. The bipyridyl substituent provides a tunable switch for catalyst selectivity that also has significant influence on catalyst activity and longevity. Less electron donating 4,4'-substituents increase the propensity toward styrene formation over ethylbenzene.
    DOI:
    10.1021/om400306w
  • 作为产物:
    描述:
    [(Me)2Pt(μ-SEt2)]24,4-二硝基-2,2-联吡啶乙醚 为溶剂, 反应 16.0h, 以94%的产率得到[(4,4′-dinitro-2,2′-bipyridine)PtMe2]
    参考文献:
    名称:
    Platinum(II)-Catalyzed Ethylene Hydrophenylation: Switching Selectivity between Alkyl- and Vinylbenzene Production
    摘要:
    The series of Pt-II complexes [((x)bpy)Pt(Ph)(THF)][BAr'(4)] ((x)bpy=4,4'-X-2,2'-bipyridyl, X = OMe, Bu-t, H, Br, CO2Et, NO2; Ar' = 3,5-bis(trifluoromethyl)phenyl) are catalyst precursors for ethylene hydrophenylation. The bipyridyl substituent provides a tunable switch for catalyst selectivity that also has significant influence on catalyst activity and longevity. Less electron donating 4,4'-substituents increase the propensity toward styrene formation over ethylbenzene.
    DOI:
    10.1021/om400306w
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