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cis-N(PPh3)2[Mn(CO)4(TePh)2] | 164990-79-8

中文名称
——
中文别名
——
英文名称
cis-N(PPh3)2[Mn(CO)4(TePh)2]
英文别名
cis-[PPN][Mn(CO)4(TePh)2]
cis-N(PPh3)2[Mn(CO)4(TePh)2]化学式
CAS
164990-79-8
化学式
C16H10MnO4Te2*C36H30NP2
mdl
——
分子量
1114.98
InChiKey
WOJABWAIOVGXIQ-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):
    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:
    cis-N(PPh3)2[Mn(CO)4(TePh)2]四氢呋喃 为溶剂, 以90%的产率得到[PPN][(CO)3Mn(.mu-TePh)3Mn(CO)3]
    参考文献:
    名称:
    Oxidative Addition of Diorganyl Ditellurides to [Mn(CO)5]-: Crystal Structures of cis-[Na-18-crown-6-ether.cntdot.2THF][Mn(CO)4(TePh)2], [PPN][(CO)3Mn(.mu.-TePh)3Mn(CO)3], (CO)3Mn(.mu.-TePh)3Co(CO)(.mu.-TePh)2Mn(CO)4, and (CO)4Mn(.mu.-TePh)2Mn(CO)4
    摘要:
    Oxidative addition of diphenyl ditellurides to organometallic fragment [Mn(CO)(5)](-) produced cis-[Mn(CO)4(TePh)(2)](-). This complex crystallized in monoclinic space group P2(1)/n with a = 12.876(6) Angstrom, b = 18.001(7) Angstrom, c = 18.670(7) Angstrom, beta = 93.77(3)degrees, V= 4318(3) Angstrom(3), Z = 4, final R = 0.035, and R(w) = 0.034. Thermolytic conversion of cis-[Mn(CO)(4)(TePh)(2)](-) to [(CO)(3)Mn(mu-TePh)(3)Mn(CO)(3)](-) was accomplished in high yield by refluxing [Mn(CO)(4)(TePh)(2)](-) in THF solution. Crystal data: triclinic space group P (1) over bar, a = 10.820(2) Angstrom, b = 15.038(4) Angstrom, c = 19.697(7) Angstrom, alpha = 107.67(3)degrees beta = 96.23(3)degrees, gamma = 107.63(2)degrees, V =2838(1) Angstrom(3), Z = 2, R = 0.025, and R(w) = 0.026. Oxidation of Co2+ by diphenyl ditelluride in the presence of ''chelating metalloligand'' cis-[Mn(CO)(4)(TePh)(2)](-), followed by carbonyl shift from Mn to Co and a benzenetellurolate group rearranging to bridge two metals, led directly to (CO)(3)Mn(mu-TePh)(3)Co(CO)(mu-TePh)(2)Mn(CO)(4). Crystal data: triclinic space group P (1) over bar, a = 11.689(4) Angstrom, b = 12.509(5) Angstrom, c = 15.930(9) Angstrom, alpha = 82.85(5)degrees, beta = 74.87(5)degrees, gamma = 70.56(4)degrees, V = 2119(2) Angstrom 3, Z = 2, R = 0.074, and R(w) = 0.091. Addition of [Ph(3)C][BF4] to [(CO)(3)Mn(mu-TePh)3Mn(CO)(3)](-) resulted in formation of the well-known (CO)(4)Mn(mu-TePh)(2)Mn(CO)(4) dimer. This complex crystallized in the monoclinic space group P2(1)/n with a = 18.852(4) Angstrom, b = 7.094(4) Angstrom, c 18.604(6) Angstrom, beta = 106.29(2)degrees, V = 2388(2) Angstrom(3), Z = 4, final R = 0.048, and R(w) = 0.047.
    DOI:
    10.1021/ic00118a023
  • 作为产物:
    参考文献:
    名称:
    Oxidative Addition of Diorganyl Ditellurides to [Mn(CO)5]-: Crystal Structures of cis-[Na-18-crown-6-ether.cntdot.2THF][Mn(CO)4(TePh)2], [PPN][(CO)3Mn(.mu.-TePh)3Mn(CO)3], (CO)3Mn(.mu.-TePh)3Co(CO)(.mu.-TePh)2Mn(CO)4, and (CO)4Mn(.mu.-TePh)2Mn(CO)4
    摘要:
    Oxidative addition of diphenyl ditellurides to organometallic fragment [Mn(CO)(5)](-) produced cis-[Mn(CO)4(TePh)(2)](-). This complex crystallized in monoclinic space group P2(1)/n with a = 12.876(6) Angstrom, b = 18.001(7) Angstrom, c = 18.670(7) Angstrom, beta = 93.77(3)degrees, V= 4318(3) Angstrom(3), Z = 4, final R = 0.035, and R(w) = 0.034. Thermolytic conversion of cis-[Mn(CO)(4)(TePh)(2)](-) to [(CO)(3)Mn(mu-TePh)(3)Mn(CO)(3)](-) was accomplished in high yield by refluxing [Mn(CO)(4)(TePh)(2)](-) in THF solution. Crystal data: triclinic space group P (1) over bar, a = 10.820(2) Angstrom, b = 15.038(4) Angstrom, c = 19.697(7) Angstrom, alpha = 107.67(3)degrees beta = 96.23(3)degrees, gamma = 107.63(2)degrees, V =2838(1) Angstrom(3), Z = 2, R = 0.025, and R(w) = 0.026. Oxidation of Co2+ by diphenyl ditelluride in the presence of ''chelating metalloligand'' cis-[Mn(CO)(4)(TePh)(2)](-), followed by carbonyl shift from Mn to Co and a benzenetellurolate group rearranging to bridge two metals, led directly to (CO)(3)Mn(mu-TePh)(3)Co(CO)(mu-TePh)(2)Mn(CO)(4). Crystal data: triclinic space group P (1) over bar, a = 11.689(4) Angstrom, b = 12.509(5) Angstrom, c = 15.930(9) Angstrom, alpha = 82.85(5)degrees, beta = 74.87(5)degrees, gamma = 70.56(4)degrees, V = 2119(2) Angstrom 3, Z = 2, R = 0.074, and R(w) = 0.091. Addition of [Ph(3)C][BF4] to [(CO)(3)Mn(mu-TePh)3Mn(CO)(3)](-) resulted in formation of the well-known (CO)(4)Mn(mu-TePh)(2)Mn(CO)(4) dimer. This complex crystallized in the monoclinic space group P2(1)/n with a = 18.852(4) Angstrom, b = 7.094(4) Angstrom, c 18.604(6) Angstrom, beta = 106.29(2)degrees, V = 2388(2) Angstrom(3), Z = 4, final R = 0.048, and R(w) = 0.047.
    DOI:
    10.1021/ic00118a023
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文献信息

  • An Approach to Heterometallic Complexes with Selenolate and Tellurolate Ligands: Crystal Structures of <i>cis</i>-[Mn(CO)<sub>4</sub>(SePh)<sub>2</sub>]<sup>-</sup>, [(CO)<sub>3</sub>Mn(μ-SeMe)<sub>3</sub>Mn(CO)<sub>3</sub>]<sup>-</sup>, (CO)<sub>4</sub>Mn(μ-TePh)<sub>2</sub>Co(CO)(μ-SePh)<sub>3</sub>Mn(CO)<sub>3</sub>, and (CO)<sub>3</sub>Mn(μ-SePh)<sub>3</sub>Fe(CO)<sub>3</sub>
    作者:Wen-Feng Liaw、Chih-Yuan Chuang、Way-Zen Lee、Chen-Kang Lee、Gene-Hsiang Lee、Shie-Ming Peng
    DOI:10.1021/ic951487t
    日期:1996.1.1
    cis-[Mn(CO)(4)(SePh)(2)](-) and cis-[Mn(CO)(4)(TePh)(2)](-), followed by a bezenselenolate ligand rearranging to bridge two metals and a labile carbonyl shift from Mn to Co, led directly to [(CO)(4)Mn(&mgr;-TePh)(2)Co(CO)(&mgr;-SePh)(3)Mn(CO)(3)]. Crystal data: triclinic space group P&onemacr;, a = 11.712(3) Å, b = 12.197(3) Å, c = 15.754(3) Å, alpha = 83.56(2) degrees, beta = 76.13(2) degrees, gamma = 72.69(2) degrees
    二有机基二化物的氧化加成到不饱和配位的低价过渡属羰基片段[Mn(CO)(5)](-)产生的顺式[Mn(CO)(4)(SeR)(2)] [ -)。在三斜晶空间群P&onemacr中结晶的顺式[PPN] [Mn(CO)(4)(SePh)(2)]络合物;其中a = 10.892(8)Å,b = 10.992(7)Å,c = 27.021(4)Å,alpha = 101.93(4)度,beta = 89.79(5)度,γ= 116.94(5)度,V = 2807(3)Å(3),Z = 2; 最终R = 0.085,R(w)= 0.094。顺式[Mn(CO)(4)(SeMe)(2)](-)的热转化为[(CO)(3)Mn(&mgr; -SeMe)(3)Mn(CO)(3)]( -)在室温下以高收率在THF中完成。[Na-18-crown-6-ether] [(CO)(3)Mn(&mgr; -SeMe
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