Sequential Electrophilic Substitution Reactions of Tungsten-Coordinated Phosphenium Ions and Phosphine Triflates

被引:12
|
作者
Jayaraman, Arumugam [1 ,2 ]
Nilewar, Shrikant [1 ]
Jacob, Tyler V. [1 ]
Sterenberg, Brian T. [1 ]
机构
[1] Univ Regina, Dept Chem & Biochem, 3737 Wascana Pkwy, Regina, SK S4S 0A2, Canada
[2] Univ Laval, Dept Chim, Pavillon Alexandre Vachon,1045 Ave Med, Quebec City, PQ G1V 0A6, Canada
来源
ACS OMEGA | 2017年 / 2卷 / 11期
关键词
N-HETEROCYCLIC PHOSPHENIUM; EFFECTIVE CORE POTENTIALS; BIDENTATE DIPHOSPHINE LIGANDS; MOLECULAR-ORBITAL METHODS; BASIS-SET; ASYMMETRIC-SYNTHESIS; BOND FORMATION; X-RAY; COMPLEXES; PHOSPHORUS;
D O I
10.1021/acsomega.7b01424
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Abstraction of chloride from [W(CO)(5){PPhCl2}] with AgOSO2CF3 leads to the phosphine triflate complex [W(CO)(5){PPhCl(OSO2CF3)}] which undergoes electrophilic substitution reactions with N,N-diethylaniline, anisole, N,N-dimethyl-p-toluidine, toluene, biphenyl, naphthalene, 2,7,9,9-tetramethyl xanthene, and allyltrimethylsilane to form the chlorophosphine complexes [W(CO)(5){PPhClR}], where R = p-diethylanilinyl, p-anisyl, 2-(N,N-dimethyl-4-methylphenyl), p-tolyl, p-phenylphenyl, 1-naphthyl, 4-(2,7,9,9-tetramethylxanthyl), and allyl. Abstraction of the second chloride with AgOSO2CF3 leads, in most cases, to the respective phosphine triflates [W(CO)(5){PPhR(OSO2CF3)}], which react with ferrocene to form the ferrocenyl phosphine complexes [W(CO)(5){PPhR(C10H9Fe)}]. The W(CO)(5) unit can be removed via photolysis in the presence of bis(diphenylphosphino)ethane to form metal-free phosphines.
引用
收藏
页码:7849 / 7861
页数:13
相关论文
共 30 条