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[Co{N(SiMe3)2}2(py)2] | 518061-54-6

中文名称
——
中文别名
——
英文名称
[Co{N(SiMe3)2}2(py)2]
英文别名
[Co{N(SiMe3)2}2(py)2]
[Co{N(SiMe3)2}2(py)2]化学式
CAS
518061-54-6
化学式
C22H46CoN4Si4
mdl
——
分子量
537.969
InChiKey
BCUUWDNUNBMAEB-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:
    [Co{N(SiMe3)2}2(py)2] 以 neat (no solvent, solid phase) 为溶剂, 以69%的产率得到[Co{N(SiMe3)2}2(py)]
    参考文献:
    名称:
    Reactions of M{N(SiMe3)2}2 (M=Mn, Fe or Co) with pyridine and 4,4′-bipyridyl: structural and magnetic studies
    摘要:
    The reactions of the aromatic nitrogen donor ligands pyridine (py) and 4,4'-bipyridyl (4,4-bipy) with the transition metal silylamides M{N(SiMe3)(2)}(2) (M = Mn, Fe or Cc) were investigated. Treatment of the metal amides with pyridine afforded the bispyridine complexes M{N(SiMe3)(2)}(py)(2) (M = Mn, 1a; Fe, 2a; Co, 3a). Distillation or sublimation of 2a or 3a afforded the monopyridine complexes M{N(SiMe3)(2)}(2)(py) (M = Fe, 2b; Co, 3b). The addition of pyrazine (prz) to Mn{N(SiMe3)(2)}(2) also yielded the bispyrazine adduct Mn{N(SiMe3)(2)}(2)(prz)(2), 1b. However, the reaction of 4,4'-bipyridyl with Fe{N(SiMe3)(2)}(2) or Co{N(SiMe3)(2)}(2) afforded the polymeric chain-like complexes {M{N(SiMe3)(2)}(2)(4,4'-bipy)}(infinity) (M = Fe, 4; Co, 5). With the exception of 2b, all complexes were characterized by X-ray crystallography. The complexes la, 1b, 2a and 3a displayed monomeric structures and metal geometries that are based on a tetrahedron with interligand angles that deviate markedly from idealized values. Complex 3b was found to have a distorted trigonal planar geometry. In contrast, complexes 4 and 5 displayed polymeric zig-zag chain structures which have four coordinate metal centers connected by 4,4'-bipyridyl ligands. Magnetic studies indicated that complexes 1-3b have high-spin electron configurations and that the paramagnetic centers in 4 and 5 did not interact with each other through the 4,4'-bipyridyl ligands. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0277-5387(02)01264-0
  • 作为产物:
    描述:
    吡啶cobalt(II) bis(trimethylsilyl)amide正己烷 为溶剂, 以62%的产率得到[Co{N(SiMe3)2}2(py)2]
    参考文献:
    名称:
    Reactions of M{N(SiMe3)2}2 (M=Mn, Fe or Co) with pyridine and 4,4′-bipyridyl: structural and magnetic studies
    摘要:
    The reactions of the aromatic nitrogen donor ligands pyridine (py) and 4,4'-bipyridyl (4,4-bipy) with the transition metal silylamides M{N(SiMe3)(2)}(2) (M = Mn, Fe or Cc) were investigated. Treatment of the metal amides with pyridine afforded the bispyridine complexes M{N(SiMe3)(2)}(py)(2) (M = Mn, 1a; Fe, 2a; Co, 3a). Distillation or sublimation of 2a or 3a afforded the monopyridine complexes M{N(SiMe3)(2)}(2)(py) (M = Fe, 2b; Co, 3b). The addition of pyrazine (prz) to Mn{N(SiMe3)(2)}(2) also yielded the bispyrazine adduct Mn{N(SiMe3)(2)}(2)(prz)(2), 1b. However, the reaction of 4,4'-bipyridyl with Fe{N(SiMe3)(2)}(2) or Co{N(SiMe3)(2)}(2) afforded the polymeric chain-like complexes {M{N(SiMe3)(2)}(2)(4,4'-bipy)}(infinity) (M = Fe, 4; Co, 5). With the exception of 2b, all complexes were characterized by X-ray crystallography. The complexes la, 1b, 2a and 3a displayed monomeric structures and metal geometries that are based on a tetrahedron with interligand angles that deviate markedly from idealized values. Complex 3b was found to have a distorted trigonal planar geometry. In contrast, complexes 4 and 5 displayed polymeric zig-zag chain structures which have four coordinate metal centers connected by 4,4'-bipyridyl ligands. Magnetic studies indicated that complexes 1-3b have high-spin electron configurations and that the paramagnetic centers in 4 and 5 did not interact with each other through the 4,4'-bipyridyl ligands. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0277-5387(02)01264-0
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