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1,3-bis(methyltelluro)propane | 105598-32-1

中文名称
——
中文别名
——
英文名称
1,3-bis(methyltelluro)propane
英文别名
1,3-bis(methyltellanyl)propane;2,6-ditelluraheptane;1,3-bis(methyltelluranyl)propane;MeTeCH2CH2CH2TeMe;Propane, 1,3-bis(methyltelluro)-
1,3-bis(methyltelluro)propane化学式
CAS
105598-32-1
化学式
C5H12Te2
mdl
——
分子量
327.35
InChiKey
QCASWOQTQQLFJQ-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):
    1.72
  • 重原子数:
    7
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

SDS

SDS:24574bf45e5512117fd4379342194f66
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反应信息

  • 作为反应物:
    描述:
    1,3-bis(methyltelluro)propane碘甲烷 作用下, 以 丙酮 为溶剂, 生成 1,3-Bis[iodo(dimethyl)-lambda4-tellanyl]propane
    参考文献:
    名称:
    螯合二铁醚醚配体RTeCH2CH2CH2TeR(R = Me,Ph)的合成
    摘要:
    DOI:
    10.1021/om00144a045
  • 作为产物:
    描述:
    二甲基二碲化物1,3-二溴丙烷氢氧化钾一水合肼 作用下, 反应 1.5h, 以80%的产率得到1,3-bis(methyltelluro)propane
    参考文献:
    名称:
    Reaction of 1-bromo-3-chloropropane with tellur and dimethyltelluride in the system of hydrazine hydrate-alkali
    摘要:
    A synthesis of oligomeric substance of thiocol type, the poly(trimethyleneditelluride), from 1-bromo-3-chloropropane and elemental tellurium is performed using a hydrazine hydrate-alkali system. Reductive splitting of the tellurocol followed by alkylation with methyl iodide give rise to preparation of bis(methyltelluro)propane, which was synthesized also from dimethyltelluride and 1,3-dihalopropanes using the (N2H4H2O)-H-./KOH system. Mass spectra of the synthesized low molecular weight organotellurium compounds are considered.
    DOI:
    10.1134/s1070363206050112
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文献信息

  • Synthesis, characterisation and structures of thio-, seleno- and telluro-ether complexes of indium(III) halides
    作者:Chitra Gurnani、Marek Jura、William Levason、Raju Ratnani、Gillian Reid、Michael Webster
    DOI:10.1039/b816148h
    日期:——
    [(InCl(3))(2)micro(2)-o-C(6)H(4)(CH(2)SMe)(2)}] and [(InCl(3))(2)micro(2)-MeTe(CH(2))(3)TeMe}] are formed even from a 1:1 In:ligand ratio. Key structure types were confirmed from crystal structures of [InCl(2)RSe(CH(2))(2)SeR}(micro-Cl)(2)InCl(2)RSe(CH(2))(2)SeR(2)}] (R = Me or (n)Bu), trans-[InX(2)(i)PrS(CH(2))(2)S(i)Pr}(2)][InX(4)] (X = Cl or Br), trans-[InBr(2)MeSe(CH(2))(2)SeMe}(2)][InBr(4)]
    铟(III)卤桥八面体二聚体[InX(2)(LL)(mu-X)(2)InX(2)(LL)](X = Cl:LL = MeS(CH(2))(2 )SMe,MeSe(CH(2))(2)SeMe,(n)BuSe(CH(2))(2)Se(n)Bu),离子反式-[InX(2)(LL)(2) ] [InX(4)](X = Cl:LL =(i)PrS(CH(2))(2)S(i)Pr; X = Br:LL = MeS(CH(2))(2)SMe ,(i)PrS(CH(2))(2)S(i)Pr,MeSe(CH(2))(2)SeMe),顺式[InCl(2)(thiamacrocycle)] [InCl(4)] (硫杂大环= [12] aneS(4)或[14] aneS(4))和中性八面体[InCl(3)([9] aneS(3))]和[InCl(3)MeC(CH( 2)SMe)(3)}]是通过在无水CH(2)C
  • Synthesis, characterisation and structures of thio-, seleno- and telluro-ether complexes of gallium(iii)
    作者:Chitra Gurnani、William Levason、Raju Ratnani、Gillian Reid、Michael Webster
    DOI:10.1039/b810005e
    日期:——
    of the gallium as the halide co-ligands become heavier. Multinuclear NMR studies suggest that in chlorocarbon solutions partial dissociation of the ligands occur, which increases with the halide co-ligand Cl < Br < I. The o-xylyl dithioether, o-C6H4(CH2SMe)2, despite being pre-organised for chelation, also forms [(GaCl3)2(mu-L-L)]. The corresponding diselenoether complex decomposes in solution with C-Se
    GaX3(X = Cl,Br或I)与SMe2,SeMe2和TeMe2(L)在非配位溶剂中的反应仅产生伪四面体[GaX3L],其特征在于IR,拉曼光谱和多核NMR(1H ,71Ga,77Se或125Te)光谱,以及[GaCl3(SeMe2)]的晶体结构。随着中性施主从S-> Se-> Te的变化,固定卤化物的71Ga NMR共振显示出较小的低频位移。包括MeS(CH2)2SMe,PhS(CH2)2SPh,MeSe(CH2)2SeMe,nBuSe(CH2)2Se(n)Bu和MeTe(CH2)3TeMe(LL)的双齿配体也产生具有4个配位镓中心的配合物,[ ([GaX3)2(mu-LL)],由[(GaI3)2(mu-MeS(CH2)2SMe)],[(GaCl3)2(mu-PhS(CH2)2SPh)]和[ (GaCl3)2(mu-nBuSe(CH2)2Se(n)Bu)]。结构数据与卤化物共配体变重
  • Synthesis and structural properties of the first bismuth(iii) telluroether complex
    作者:William Levason、Nicholas J. Hill、Gillian Reid
    DOI:10.1039/b209321a
    日期:2002.11.25
    The first donor–acceptor complexes of Sb(III) and Bi(III) with telluroether ligands are reported, together with the crystal structure of [BiBr3(PhTeMe)].
    首次报道了Sb(III)和Bi(III)与碲醚配体的首例供体-受体配合物,以及[BiBr3(PhTeMe)]的晶体结构。
  • Co-ordination chemistry of higher oxidation states. Part 27. Synthesis, properties, and electrochemistry of some cis-tetrahalogenoiridium(IV) complexes: crystal structure of [Ir(phen)Cl4]
    作者:Robert A. Cipriano、Lyall R. Hanton、William Levason、Derek Pletcher、Nigel A. Powell、Michael Webster
    DOI:10.1039/dt9880002483
    日期:——
    The iridium(IV) complexes cis-[Ir(L–L)Cl4][L–L = MeSCH2CH2SMe, MeSeCH2CH2SeMe, 2,2′-bipyridyl (bipy), or 1,10-phenanthroline (phen)] have been prepared by Cl2 or HNO3 oxidation of the corresponding IrIII anions [Ir(L–L)Cl4]–. Dark green cis-[Ir(L–L)Br4](L–L = bipy or phen) and cis-[Ir(py)2X4](X = Cl or Br) are also described. Iridium(III) complexes [IrRTe(CH2)3TeR}Cl4]–(R = Me or Ph), [Ir[Me2Sb(CH2)3SbMe2]Cl3}n]
    铱(IV)络合物为顺式-[Ir(L–L)Cl 4 ] [L–L = MeSCH 2 CH 2 SMe,MeSeCH 2 CH 2 SeMe,2,2'-联吡啶(bipy)或1,10-菲咯啉(phen)是通过Cl 2或HNO 3氧化相应的Ir III阴离子[Ir(L–L)Cl 4 ] –制备的。还描述了深绿色的顺式-[Ir(L-L)Br 4 ](L = L = bipy或phen)和顺式-[Ir(py)2 X 4 ](X = Cl或Br)。铱(III)配合物[Ir RTe(CH 2)3 TeR} Cl 4 ] –(R = Me或Ph),[Ir [Me 2 Sb(CH 2)3 SbMe 2 ] Cl 3 } n ],反式-[Ir(L–L)2 Cl 2 ] + [L–L = Ph 2 PCH 2 CH 2 PPh 2(dppe),Me 2 PCH 2 CH 2 PMe 2(dmpe)或o -C
  • Systematics of boron halide complexes with dichalcogenoether ligands – Synthesis, structures and reaction chemistry
    作者:Coco K.Y.A. Okio、William Levason、Francesco M. Monzittu、Gillian Reid
    DOI:10.1016/j.jorganchem.2017.11.018
    日期:2018.1
    [BF3(μ-L−L)BF3], [(BF3)2o-C6H4(SMe)2}] and [(BF3)2o-C6H4(SeMe)2}], made from BF3 and the neat ligands, are viscous oils which have a significant vapour pressure of BF3 at ambient temperatures. X-ray crystal structures are reported for [BX3μ-EtS(CH2)2SEt}BX3] (X = Cl, Br, I), [BBr3μ-MeSe(CH2)2SeMe}BBr3], [BCl3o-C6H4(SMe)2}] and [(BBr3)2μ-o-C6H4(SeMe)2}]. The complexes [(BX3)2MeTe(CH2)3TeMe}] (X = F,
    配合物[BX 3(μ-L-L)BX 3 ](X =氯,溴,I; L-L = ETS(CH 2)2组,MESE(CH 2)2 SEME),[BX' 3 ø -C 6 ħ 4(SME)2 }](X” =氯,I),[(的BBr 3)2 ø -C 6 ħ 4(SME)2 }],[(的BBr 3)2 ø - C 6 H 4(SeMe)2 }]和[BI 3 o -C 6H 4(SeMe)2 }]已通过使适当的BX 3与二卤代醚在无水正己烷中反应制备成对湿气敏感的浅色固体,并进行了微分析,IR和多核分析(1 H,11 B,77 Se 1 H})NMR光谱。相反,[BF 3(μ-L-L)BF 3 ],[(BF 3)2 o -C 6 H 4(SMe)2 }]和[(BF 3)2 o -C 6 H 4(SEME)2 }],自BF制成3和纯的配体,是具有BF的显著蒸汽压粘稠油3在环境温度下。报告了[BX
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