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8-methyl(phenyl)phosphino-quinoline | 80127-37-3

中文名称
——
中文别名
——
英文名称
8-methyl(phenyl)phosphino-quinoline
英文别名
methylphenyl-(8-quinolyl)phosphine;(8-quinolyl)methylphenylphosphane;Methyl-phenyl-quinolin-8-ylphosphane
8-methyl(phenyl)phosphino-quinoline化学式
CAS
80127-37-3;80183-97-7;80183-96-6
化学式
C16H14NP
mdl
——
分子量
251.268
InChiKey
NNPSBKICJUNOQS-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):
    3.3
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    12.9
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    双(乙腈)氯化钯(II)8-methyl(phenyl)phosphino-quinoline二氯甲烷 为溶剂, 以87%的产率得到{SP-4-3}-(+/-)dichloro{methylphenyl(8-quinolyl)phosphine-P,N}palladium(II)*1.5water
    参考文献:
    名称:
    Salem, Geoffrey; Wild, S. Bruce, Inorganic Chemistry, 1992, vol. 31, # 4, p. 581 - 586
    摘要:
    DOI:
  • 作为产物:
    描述:
    8-喹啉三氟甲烷磺酸二苯基甲氧基膦 在 palladium diacetate 作用下, 反应 72.0h, 以18%的产率得到8-methyl(phenyl)phosphino-quinoline
    参考文献:
    名称:
    Palladium-catalyzed phosphination of functionalized aryl triflates
    摘要:
    Catalytic user-friendly approach to the syntheses of various functionalized aromatic phosphines from their corresponding substituted aryl triflates and triarylphosphines was accomplished. This method is carried out in neutral media and compatible with many functional groups including aldehyde, keto, ester, nitrile, ether and pyridyl groups. (C) 2003 Elsevier Ltd. All fights reserved.
    DOI:
    10.1016/j.tet.2003.10.061
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文献信息

  • [EN] BIARYL LIGANDS<br/>[FR] LIGANDS BIARYLE
    申请人:UNIV FLORIDA
    公开号:WO2015038872A1
    公开(公告)日:2015-03-19
    Embodiments of the present disclosure provide for biaryl ligands (also referred to herein as "biaryl compound"), biaryl complexes, methods of making biaryl compounds, methods of making single enantiomers of these biaryl compounds, methods of use (e.g., catalysis) and the like.
    本公开的实施例提供了联苯配体(在本文中也称为“联苯化合物”)、联苯配合物的制备方法、制备这些联苯化合物的单对映体的方法、使用方法(例如催化)等。
  • Preparation, Crystal Structures, and Spectroscopic and Redox Properties of Nickel(II) Complexes Containing Phosphane–(Amine or Quinoline)‐Type Hybrid Ligands and a Nickel(I) Complex Bearing 8‐(Diphenylphosphanyl)quinoline
    作者:Akira Hashimoto、Hiroshi Yamaguchi、Takayoshi Suzuki、Kazuo Kashiwabara、Masaaki Kojima、Hideo D. Takagi
    DOI:10.1002/ejic.200900767
    日期:2010.1
    Nickel(II) complexes containing P―N-type bidentate hybrid ligands of 2-aminoethylphosphanes (RR'Pea; RR' = Ph 2 or MePh) or 8-quinolylphosphanes (RR'Pqn), namely [Ni(P―N) 2 ]-(BF 4 ) 2 [P―N = Ph 2 Pea (1), MePhPea (2), Ph 2 Pqn (3), or MePhPqn (4)] have been prepared, and their structural, spectroscopic, and electrochemical properties determined. The crystal structure analysis indicates that the 2
    (II)配合物含有2-氨基乙基膦(RR'Pea;RR' = Ph 2 or MePh)或8-喹啉基膦(RR'Pqn)的P-N型双齿杂化配体,即[Ni(P-N) 2 ]-(BF 4 ) 2 [P―N = Ph 2 Pea (1), MePhPea (2), Ph 2 Pqn (3), or MePhPqn (4)] 已被制备,及其结构、光谱和电化学性质决定。晶体结构分析表明,2-基乙基-膦配合物(1 和 2)在 Ni II 中心周围具有方形平面配位几何结构,具有顺式(P,P)构型,而 8-喹啉基膦配合物(3 和 4) ) 表现出严重的四面体畸变,因为相互顺式定位的喹啉环中的邻位 H 原子之间存在空间排斥。配合物 1 和 2 在乙腈溶液中保持其抗磁性方形平面四坐标结构,而配合物 3 和 4 则表现出顺磁性。光谱和电化学测量表明,这四种 PN配体配体场强度以 Ph 2 Pqn (3) <
  • Biaryl ligands, methods of making biaryl ligands, and methods of use thereof
    申请人:University of Florida Research Foundation, Inc.
    公开号:US10618922B2
    公开(公告)日:2020-04-14
    Embodiments of the present disclosure provide for biaryl ligands (also referred to herein as “biaryl compound”), biaryl complexes, methods of making biaryl compounds, methods of making single enantiomers of these biaryl compounds, methods of use (e.g., catalysis), and the like.
    本公开的实施方案提供了双芳基配体(此处也称为 "双芳基化合物")、双芳基络合物、双芳基化合物的制造方法、这些双芳基化合物的单一对映体的制造方法、使用方法(例如催化)等。
  • Biaryl ligands, methods of making biarlyl ligands, and methods of use thereof
    申请人:University of Florida Research Foundation, Inc.
    公开号:US11198701B2
    公开(公告)日:2021-12-14
    Embodiments of the present disclosure provide for biaryl ligands (also referred to herein as “biaryl compound”), biaryl complexes, methods of making biaryl compounds, methods of making single enantiomers of these biaryl compounds, methods of use (e.g., catalysis), and the like.
    本公开的实施方案提供了双芳基配体(此处也称为 "双芳基化合物")、双芳基络合物、双芳基化合物的制造方法、这些双芳基化合物的单一对映体的制造方法、使用方法(例如催化)等。
  • Allen, David G.; Mclaughlin, George M.; Robertson, Glen B., Inorganic Chemistry, 1982, vol. 21, # 3, p. 1007 - 1014
    作者:Allen, David G.、Mclaughlin, George M.、Robertson, Glen B.、Steffen, William L.、Salem, Geoffrey、Wild, Stanley Bruce
    DOI:——
    日期:——
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