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nitritophthalocyaninato(2-)manganese(III) | 351413-82-6

中文名称
——
中文别名
——
英文名称
nitritophthalocyaninato(2-)manganese(III)
英文别名
Nitritophthalocyaninato(2-)mangan(III)
nitritophthalocyaninato(2-)manganese(III)化学式
CAS
351413-82-6
化学式
C32H16MnN9O2
mdl
——
分子量
613.476
InChiKey
HIDCUORBTOQKMN-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):
    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:
    nitritophthalocyaninato(2-)manganese(III)四丁基亚硝酸铵 在 n-Bu4NOH 、 CS2 作用下, 以 二氯甲烷 为溶剂, 生成 tetra(n-butyl)ammonium-trans-di(nitrosyl)phthalocyaninato(2-)manganate
    参考文献:
    名称:
    Mononitrosyl- undtrans-Dinitrosyl-Komplexe von Phthalocyaninaten des Mangans und Rheniums
    摘要:
    Tetra(n-butyl)ammonium or di(triphenylphosphane)iminium nitrosylacidophthalocyaninato(2-)manganate, (cat)[Mn(NO)(X)pc(2-)] (X = ONO, NCO, N-3: cat = (Bu4N)-Bu-n, PNP) is prepared from acidophthalocyaninato(2-)manganese, [Mn(X)pc(2-)], (cat)NO2 and ((Bu4N)-Bu-n)BH4 in CH2Cl2 or from nitrosylphthalocyaninato(2-)manganese. [Mn(NO)pc(2-)] and ((Bu4N)-Bu-n)X (X = ONO, NCO, N-3, NCS) at T < 120 degreesC. respectively. [Mn(NO)(X)pc(2-)](-) dissociates in methanol. and [Mn(NO)pc2-] precipitates. Nitrito(O)phthalocyaninato(2-)manganese, (cat)NO2 and hydrogensulfide yield trans-di(nitrosyl)phthalocyaninato(2-)manganate. (trans)[Mn(NO)(2)pc(2-)](-) isolated as red violet (PNP) and ((Bu4N)-Bu-n) complex salt. Nitrosyl(triphenylphosphane oxide)phthalocyaninato(2-)manganese, [Mn(NO)(OPPh3)pc(2-)] is obtained by addition of OPPh3 to [Mn(NO)pc(2-)] at 200 degreesC. Di(triphenylphosphane)phthalocyaninato(2-)rhenium(II) and (PNP)NO2 in CH2Cl2 or in molten (PNP)NO2 and PPh3 at 100 degreesC yields green blue l-di( triphenylphosphane) iminium nitrosylnitrito(O)phthalocyaninato(2-)rhenate. (l)(PNP)[Re(NO)(ONO)pc2-]. Similarly, but with ((Bu4N)-Bu-n)NO2 red plates of tetra-(n-butyl) ammonium trans-di(nitrosyl)phthalocyaninato(2-)rhenate, ((Bu4N)-Bu-n)(trans)[Re(NO)(2)pc(2-)] is isolated. Addition of (PNP)Br or (PNP)PF6 to a concentrated solution of ((Bu4N)-Bu-n)(trans)[Re (NO)(2)pc(2-)] in pyridine precipitates (l)(PNP)(trans)[Re(NO)(2)pc(2-)]. ((Bu4N)-Bu-n)(trans)[Re(NO)(2)pc(2-)] and PPh3 at 300 degreesC yield blue green nitrosyl(triphenylphosphane oxide)phthalocyaninato(2-)rhenium, [Re(NO)(OPPh3)pc2-], that is oxidised with iodine precipitating nitrosyl(triphenylphosphane oxide)phthalocyaninato(2-)rhenium triiodide, [Re(NO)(OPPh3)pc(2-)]I-3. The crystal structures of (l)(PNP)[Mn(NO)(ONO)pc(2-)] (1), (l)(PNP)[Mn(NO)(NCO)pc(2-)] (2), (l)(PNP)(trans)[Mn(NO)(2)pc(2-)] (3),l(PNP)(trans)[Re(NO)(2)pc(2-)] (4) [Mn(NO)(OPPh3)pc(2-)] (5), [Re(NO)(OPPh3)pc(2-)] (6), and [Re(NO)(OPPh3)pc(2-)]I-3. CH2Cl2 (7) have been determined. The M-N(NO) distance varies between 1.623(12)Angstrom in 5 and 1.846(3)Angstrom in 3. The M-N-O moiety is almost linear. The UV-Vis spectra with the B band at ca. 14500 cm(-1) and the Q band at 30400 cm(-1) do not dependent significantly on the axial ligand and the metal atom and its oxidation state. N-O stretching vibrations are observed in the IR spectra between 1701 cm(-1) in 3 and 1753 cm(-1) in [Mn(NO)pc(2-)] or for the Re series between 1571 cm(-1) in 4 and 1724 cm(-1) in 7. M-N(NO) stretching and M-N-O deformation vibrations are assigned in the IR spectra and resonance Raman spectra between 486 cm(-1) in 4 and 620 cm(-1) in 1.
    DOI:
    10.1002/1521-3749(200105)627:5<935::aid-zaac935>3.0.co;2-j
  • 作为产物:
    描述:
    iodophthalocyaninato(2-)manganese(III)四丁基亚硝酸铵二氯甲烷 为溶剂, 以99%的产率得到nitritophthalocyaninato(2-)manganese(III)
    参考文献:
    名称:
    Mononitrosyl- undtrans-Dinitrosyl-Komplexe von Phthalocyaninaten des Mangans und Rheniums
    摘要:
    Tetra(n-butyl)ammonium or di(triphenylphosphane)iminium nitrosylacidophthalocyaninato(2-)manganate, (cat)[Mn(NO)(X)pc(2-)] (X = ONO, NCO, N-3: cat = (Bu4N)-Bu-n, PNP) is prepared from acidophthalocyaninato(2-)manganese, [Mn(X)pc(2-)], (cat)NO2 and ((Bu4N)-Bu-n)BH4 in CH2Cl2 or from nitrosylphthalocyaninato(2-)manganese. [Mn(NO)pc(2-)] and ((Bu4N)-Bu-n)X (X = ONO, NCO, N-3, NCS) at T < 120 degreesC. respectively. [Mn(NO)(X)pc(2-)](-) dissociates in methanol. and [Mn(NO)pc2-] precipitates. Nitrito(O)phthalocyaninato(2-)manganese, (cat)NO2 and hydrogensulfide yield trans-di(nitrosyl)phthalocyaninato(2-)manganate. (trans)[Mn(NO)(2)pc(2-)](-) isolated as red violet (PNP) and ((Bu4N)-Bu-n) complex salt. Nitrosyl(triphenylphosphane oxide)phthalocyaninato(2-)manganese, [Mn(NO)(OPPh3)pc(2-)] is obtained by addition of OPPh3 to [Mn(NO)pc(2-)] at 200 degreesC. Di(triphenylphosphane)phthalocyaninato(2-)rhenium(II) and (PNP)NO2 in CH2Cl2 or in molten (PNP)NO2 and PPh3 at 100 degreesC yields green blue l-di( triphenylphosphane) iminium nitrosylnitrito(O)phthalocyaninato(2-)rhenate. (l)(PNP)[Re(NO)(ONO)pc2-]. Similarly, but with ((Bu4N)-Bu-n)NO2 red plates of tetra-(n-butyl) ammonium trans-di(nitrosyl)phthalocyaninato(2-)rhenate, ((Bu4N)-Bu-n)(trans)[Re(NO)(2)pc(2-)] is isolated. Addition of (PNP)Br or (PNP)PF6 to a concentrated solution of ((Bu4N)-Bu-n)(trans)[Re (NO)(2)pc(2-)] in pyridine precipitates (l)(PNP)(trans)[Re(NO)(2)pc(2-)]. ((Bu4N)-Bu-n)(trans)[Re(NO)(2)pc(2-)] and PPh3 at 300 degreesC yield blue green nitrosyl(triphenylphosphane oxide)phthalocyaninato(2-)rhenium, [Re(NO)(OPPh3)pc2-], that is oxidised with iodine precipitating nitrosyl(triphenylphosphane oxide)phthalocyaninato(2-)rhenium triiodide, [Re(NO)(OPPh3)pc(2-)]I-3. The crystal structures of (l)(PNP)[Mn(NO)(ONO)pc(2-)] (1), (l)(PNP)[Mn(NO)(NCO)pc(2-)] (2), (l)(PNP)(trans)[Mn(NO)(2)pc(2-)] (3),l(PNP)(trans)[Re(NO)(2)pc(2-)] (4) [Mn(NO)(OPPh3)pc(2-)] (5), [Re(NO)(OPPh3)pc(2-)] (6), and [Re(NO)(OPPh3)pc(2-)]I-3. CH2Cl2 (7) have been determined. The M-N(NO) distance varies between 1.623(12)Angstrom in 5 and 1.846(3)Angstrom in 3. The M-N-O moiety is almost linear. The UV-Vis spectra with the B band at ca. 14500 cm(-1) and the Q band at 30400 cm(-1) do not dependent significantly on the axial ligand and the metal atom and its oxidation state. N-O stretching vibrations are observed in the IR spectra between 1701 cm(-1) in 3 and 1753 cm(-1) in [Mn(NO)pc(2-)] or for the Re series between 1571 cm(-1) in 4 and 1724 cm(-1) in 7. M-N(NO) stretching and M-N-O deformation vibrations are assigned in the IR spectra and resonance Raman spectra between 486 cm(-1) in 4 and 620 cm(-1) in 1.
    DOI:
    10.1002/1521-3749(200105)627:5<935::aid-zaac935>3.0.co;2-j
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