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Os(5dmb)2Cl2 | 128471-98-7

中文名称
——
中文别名
——
英文名称
Os(5dmb)2Cl2
英文别名
(5,5'-Me2bpy)2OsCl2;Dichloroosmium;5-methyl-2-(5-methylpyridin-2-yl)pyridine;dichloroosmium;5-methyl-2-(5-methylpyridin-2-yl)pyridine
Os(5dmb)<sub>2</sub>Cl<sub>2</sub>化学式
CAS
128471-98-7
化学式
C24H24Cl2N4Os
mdl
——
分子量
629.587
InChiKey
PAFILMLAWCVWOP-UHFFFAOYSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    6.9
  • 重原子数:
    31
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    Os(5dmb)2Cl21,2-双(4'-甲基-2,2'-联吡啶-4-基)乙烷乙醇 为溶剂, 反应 13.5h, 以61%的产率得到[(5dmb)2Os(bpyC2bpy)](PF6)2
    参考文献:
    名称:
    Red-Light-Driven Photocatalytic Reduction of CO2 using Os(II)–Re(I) Supramolecular Complexes
    摘要:
    The novel supramolecular complexes, which are composed of an [Os(5dmb)(2)(BL)](2+)-type complex (5dmb = 5,5'-dimethyl-2,2'-bipyridine; BL = 1,2-bis(4'-methyl-[2,2'-bipyridin]-4-yl)ethane) as a photosensitizer and cis,trans-[Re(BL)(CO)(2){P(p-X-C6H4)(3)}(2)](+)-type complexes (X = F, Cl) as a catalyst, have been synthesized. They photocatalyzed selective reduction of CO2 to CO under red-light irradiation (lambda > 620 nm). The photocatalytic abilities were affected by the phosphine ligands on the Re unit, and the supramolecule with P(p-Cl-C6H4)(3) ligands exhibited better photocatalysis (Phi(CO) = 0.12, TONCO = 1138, TOFCO = 3.3 min(-1)). The detailed studies clarified the electron balance and material balance; i.e., one molecule of the sacrificial electron donor (1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]-imidazole (BIH)) donated two electrons, one molecule of CO2 accepted the two electrons, and another CO2 molecule served as an "O2-" acceptor to give each molecule of the two-electron oxidized compound of BIH, CO, and HCO3-.
    DOI:
    10.1021/ic4015543
  • 作为产物:
    描述:
    5 5'-二甲基-2,2'-二吡啶 、 ammonium hexachloroosmate(IV) 以 N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 生成 Os(5dmb)2Cl2
    参考文献:
    名称:
    Red-Light-Driven Photocatalytic Reduction of CO2 using Os(II)–Re(I) Supramolecular Complexes
    摘要:
    The novel supramolecular complexes, which are composed of an [Os(5dmb)(2)(BL)](2+)-type complex (5dmb = 5,5'-dimethyl-2,2'-bipyridine; BL = 1,2-bis(4'-methyl-[2,2'-bipyridin]-4-yl)ethane) as a photosensitizer and cis,trans-[Re(BL)(CO)(2){P(p-X-C6H4)(3)}(2)](+)-type complexes (X = F, Cl) as a catalyst, have been synthesized. They photocatalyzed selective reduction of CO2 to CO under red-light irradiation (lambda > 620 nm). The photocatalytic abilities were affected by the phosphine ligands on the Re unit, and the supramolecule with P(p-Cl-C6H4)(3) ligands exhibited better photocatalysis (Phi(CO) = 0.12, TONCO = 1138, TOFCO = 3.3 min(-1)). The detailed studies clarified the electron balance and material balance; i.e., one molecule of the sacrificial electron donor (1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]-imidazole (BIH)) donated two electrons, one molecule of CO2 accepted the two electrons, and another CO2 molecule served as an "O2-" acceptor to give each molecule of the two-electron oxidized compound of BIH, CO, and HCO3-.
    DOI:
    10.1021/ic4015543
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文献信息

  • Johnson, Susan R.; David Westmoreland; Caspar, Jonathan V., Inorganic Chemistry, 1988, vol. 27, # 18, p. 3195 - 3200
    作者:Johnson, Susan R.、David Westmoreland、Caspar, Jonathan V.、Barqawi, Khaled R.、Meyer, Thomas J.
    DOI:——
    日期:——
  • Electrochemiluminescence of Osmium Complexes: Spectral, Electrochemical, and Mechanistic Studies
    作者:Héctor D. Abruña
    DOI:10.1149/1.2113970
    日期:1985.4.1
  • Red-Light-Driven Photocatalytic Reduction of CO<sub>2</sub> using Os(II)–Re(I) Supramolecular Complexes
    作者:Yusuke Tamaki、Kazuhide Koike、Tatsuki Morimoto、Yasuomi Yamazaki、Osamu Ishitani
    DOI:10.1021/ic4015543
    日期:2013.10.21
    The novel supramolecular complexes, which are composed of an [Os(5dmb)(2)(BL)](2+)-type complex (5dmb = 5,5'-dimethyl-2,2'-bipyridine; BL = 1,2-bis(4'-methyl-[2,2'-bipyridin]-4-yl)ethane) as a photosensitizer and cis,trans-[Re(BL)(CO)(2)P(p-X-C6H4)(3)}(2)](+)-type complexes (X = F, Cl) as a catalyst, have been synthesized. They photocatalyzed selective reduction of CO2 to CO under red-light irradiation (lambda > 620 nm). The photocatalytic abilities were affected by the phosphine ligands on the Re unit, and the supramolecule with P(p-Cl-C6H4)(3) ligands exhibited better photocatalysis (Phi(CO) = 0.12, TONCO = 1138, TOFCO = 3.3 min(-1)). The detailed studies clarified the electron balance and material balance; i.e., one molecule of the sacrificial electron donor (1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]-imidazole (BIH)) donated two electrons, one molecule of CO2 accepted the two electrons, and another CO2 molecule served as an "O2-" acceptor to give each molecule of the two-electron oxidized compound of BIH, CO, and HCO3-.
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