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(bis(2-hydroxyl-naphthalene-carboxaldehyde) benzil dihydrazonato)copper(II) acetonitrile adduct (1/1) | 1034051-08-5

中文名称
——
中文别名
——
英文名称
(bis(2-hydroxyl-naphthalene-carboxaldehyde) benzil dihydrazonato)copper(II) acetonitrile adduct (1/1)
英文别名
——
(bis(2-hydroxyl-naphthalene-carboxaldehyde) benzil dihydrazonato)copper(II) acetonitrile adduct (1/1)化学式
CAS
1034051-08-5
化学式
C2H3N*C36H24CuN4O2
mdl
——
分子量
649.211
InChiKey
FNLTXFQAOZCNIG-ZDJILPSNSA-L
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

反应信息

  • 作为产物:
    描述:
    copper(II) perchlorate hexahydrate 、 bis(2-hydroxyl-naphthalene-carboxaldehyde) benzil dihydrazone 、 乙腈甲醇二氯甲烷 为溶剂, 生成 (bis(2-hydroxyl-naphthalene-carboxaldehyde) benzil dihydrazonato)copper(II) acetonitrile adduct (1/1)
    参考文献:
    名称:
    “Turn-On” Fluorescent Sensor for Hg2+ via Displacement Approach
    摘要:
    A new Cu2+ compound Cu-NB, (where H2NB is bis(2-hydroxyl-naphthalene-carboxaldehyde) benzil dihydrazone) was synthesized as a highly selective fluorescence chemosensor for the detection of Hg2+ in aqueous media through a displacement "turn-on" signaling strategy. Whereas the coordination of Cu2+ resulted in a considerable quenching of the typical luminescence of the naphthol rings in Cu-NB, the addition of Hg2+ ion led to a dramatic increase in the emission intensity of Cu-NB at about 530 nm (excitation at 430 nm). The competitive fluorescent experiments showed that alkali, alkaline earth metal ions, the group 12 metals Zn2+, Cd2+, the first-row transition-metal ions such as Mn2+, Fe2+, Co2+, and Ni2+, as well as Pb2+ could not inhibit the Hg2+-binding fluorescent enhancement. It is postulated that the existence of Cu2+ in the luminescent probe Cu-NB could turn away the interferences of other metal cations from Hg2+ detection. The optical responses of the free ligand upon addition of Cu2+ ion, and of the Hg-H2NB compound upon the addition of Cu2+ were also investigated for comparisons.
    DOI:
    10.1021/ic702494s
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