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lithium tris(1-pyrazolyl)methanesulfonate | 292136-23-3

中文名称
——
中文别名
——
英文名称
lithium tris(1-pyrazolyl)methanesulfonate
英文别名
lithium tris(pyrazol-1-yl)methanesulfonate;Li(Tpms);Lithium;tri(pyrazol-1-yl)methanesulfonate
lithium tris(1-pyrazolyl)methanesulfonate化学式
CAS
292136-23-3
化学式
C10H9LiN6O3S
mdl
——
分子量
300.227
InChiKey
YZYHUHROLGFMNB-UHFFFAOYSA-M
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):
    -3.51
  • 重原子数:
    21
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    119
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    lithium tris(1-pyrazolyl)methanesulfonateN,N-二甲基甲酰胺异丙醇乙腈 为溶剂, 生成 [tricyano(tris(pyrazolyl)methanesulfonate)iron(II)][bis( N,N-dimethylformamide)diaquamanganese(II)]-N,N-dimethylformamide (1/1)
    参考文献:
    名称:
    Long-range superexchanged magnetic interaction observed in heterometallic complex: {[FeII(Tpms)(CN)3][MnII(H2O)2(DMF)2]}·DMF
    摘要:
    A new tri-cyanometalate building block for heterometallic complexes, [PPh4](2)[Fe-II(Tpms)(CN)(3)] (2) (PPh4 = tetraphenylphosphonium; Tpms = tris(pyrazolyl) methanesulfonate), has been prepared. Using it as a building block, a one-dimensional chain compound, {[Fe-II(Tpms)(CN)(3)][Mn-II(H2O)(2)( DMF)(2)]}. DMF (3), has been synthesized and structurally characterized. The magnetic properties of 3 correspond to a ferromagnetic chain with weak long-range superexchanged magnetic interaction between the high-spin manganese(II) ions. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2005.06.060
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文献信息

  • Synthesis, Antimicrobial and Antiproliferative Activity of Novel Silver(I) Tris(pyrazolyl)methanesulfonate and 1,3,5-Triaza-7-phosphadamantane Complexes
    作者:Claudio Pettinari、Fabio Marchetti、Giulio Lupidi、Luana Quassinti、Massimo Bramucci、Dezemona Petrelli、Luca A. Vitali、M. Fátima C. Guedes da Silva、Luísa M. D. R. S. Martins、Piotr Smoleński、Armando J. L. Pombeiro
    DOI:10.1021/ic201714c
    日期:2011.11.7
    (ESI-MS), and IR spectroscopic techniques. The single crystal X-ray diffraction study of 3 shows the Tpms ligand acting in the N3-facially coordinating mode, while in 2 and 5 a N2O-coordination is found, with the SO3 group bonded to silver and a pendant free pyrazolyl ring. Features of the tilting in the coordinated pyrazolyl rings in these cases suggest that this inequivalence is related with the cone
    五个新的式[Ag(Tpms)](1),[Ag(Tpms)(PPh 3)](2),[Ag(Tpms)(PCy 3)](3),[Ag( PTA)] [BF 4 ](4)和[Ag(Tpms)(PTA)](5)Tpms =三(吡唑-1-基)甲磺酸盐,PPh 3 =三苯基膦,PCy 3 =三环己基膦,PTA = 1 1,3,5-triaza-7-phosphaadamantane}已合成并通过元素分析,1 H,13 C和31 P NMR,电喷雾电离质谱(ESI-MS)和IR光谱技术进行了全面表征。单晶的X射线衍射研究图3显示了Tpms配体以N 3表面配位方式起作用,而在2和5中发现了N 2 O配位,其中SO 3基团键合至银和无侧基的吡唑基环。在这些情况下,配位吡唑基环中倾斜的特征表明,这种不等式与膦的锥角有关。已经对所有化合物的抗分枝杆菌和抗增殖特性进行了详细的研究。筛选了它们对标准菌株粪肠球菌(ATCC
  • Oxorhenium Complexes Bearing the Water-Soluble Tris(pyrazol-1-yl)methanesulfonate, 1,3,5-Triaza-7-phosphaadamantane, or Related Ligands, as Catalysts for Baeyer–Villiger Oxidation of Ketones
    作者:Luísa M. D. R. S. Martins、Elisabete C. B. A. Alegria、Piotr Smoleński、Maxim L. Kuznetsov、Armando J. L. Pombeiro
    DOI:10.1021/ic400024r
    日期:2013.4.15
    New rhenium(VII or III) complexes [ReO3(PTA)2][ReO4] (1) (PTA = 1,3,5-triaza-7-phosphaadamantane), [ReO3(mPTA)][ReO4]I (2) (mPTA = N-methyl-1,3,5-triaza-7-phosphaadamantane cation), [ReO3(HMT)2][ReO4] (3) (HMT = hexamethylenetetramine), [ReO3(η2-Tpm)(PTA)][ReO4] (4) [Tpm = hydrotris(pyrazol-1-yl)methane, HC(pz)3, pz = pyrazolyl], [ReO3(Hpz)(HMT)][ReO4] (5) (Hpz = pyrazole), [ReO(Tpms)(HMT)] (6) [Tpms
    新的((VII或III)络合物[ReO 3(PTA)2 ] [ReO 4 ](1)(PTA = 1,3,5-三氮杂-7-磷酸金刚烷),[ReO 3(mPTA)] [ReO 4 ] I(2)(mPTA = N-甲基-1,3,5-三氮杂-7-磷酸金刚烷阳离子),[ReO 3(HMT)2 ] [ReO 4 ](3)(HMT =六亚甲基四胺),[ReO 3( η 2 -Tpm)(PTA)] [REO 4 ](4)[Tpm时=氢三(吡唑-1-基)甲烷,HC(PZ)3,PZ =吡唑基],[REO 3(HPZ)(HMT)] [ReO 4](5)(Hpz =吡唑),[ReO(Tpms)(HMT)](6)[Tpms =三(吡唑-1-基)甲磺酸盐,O 3 SC(pz)3 – ]和[ReCl 2 N 2 C(O)PH}(PTA)3 ](7)已经从重新制备(VII)氧化物重新2 ö 7(1 - 6),或在的情况
  • A new amido-phosphane as ligand for copper and silver complexes. Synthesis, characterization and catalytic application for azide–alkyne cycloaddition in glycerol
    作者:Abdallah G. Mahmoud、M. Fátima C. Guedes da Silva、Armando J. L. Pombeiro
    DOI:10.1039/d1dt00992c
    日期:——
    it a very versatile ligand that could be used in a variety of reaction systems. To assess the coordination characteristics of the new phosphane, seven copper complexes of formulas [Cu(DBPTA)4]BF4 (2), [CuX(DBPTA)3] X = Br (3) and I (4)}, [Cu(μ-X)(DBPTA)2]2 X = Br (5) and I (6)}, [Cu(bpy)(DBPTA)2]Y Y = BF4 (7) and BPh4 (8)} bpy = 2,2′-bipyridine}, and three silver complexes with formulas [Ag(DBPTA)4]NO3
    新的位阻酰胺基膦1,3,7-三氮杂-5-磷杂双环[3.3.1]壬烷-3,7-二基双(苯甲酮)DBPTA(1)是通过开笼双N-获得的。使用苯甲酸酐酰化1,3,5-triaza-7-phosphadamantane(PTA)。DBPTA是PTA唯一包含芳族附件的酰基衍生物。由于苯甲酰基C(O)Ph基团的大体积性质,它们表现出互为反构型,如溶液NMR和单晶X射线衍射所证实的。化合物1易溶于常见的极性有机和绿色溶剂,使其成为一种用途广泛的配体,可用于各种反应系统。为了评估新膦的配位特性,需要七个式[Cu(DBPTA)4 ] BF 4(2),[CuX(DBPTA)3 ] X = Br(3)和I(4)},[ Cu(μ-X)(DBPTA)2 ] 2 X = Br(5)和I(6)},[Cu(bpy)(DBPTA)2 ] Y Y = BF 4(7)和BPh 4(8}} bpy = 2,2'-bipy
  • Synthesis, characterization and antioxidant activity of new copper(<scp>i</scp>) complexes of scorpionate and water soluble phosphane ligands
    作者:Maura Pellei、Giancarlo Gioia Lobbia、Carlo Santini、Riccardo Spagna、Mercedes Camalli、Donatella Fedeli、Giancarlo Falcioni
    DOI:10.1039/b407061e
    日期:——
    New copper(I) complexes have been synthesised from the reaction of CuCl with potassium hydrotris(4-bromo-1H-pyrazol-1-yl)borate, KTp4Br or lithium bis(3,5-dimethylpyrazol-1-yl)acetate, Li[L2CO2] ligands and 4- or 2-(diphenylphosphane)benzoic acid or tris(m-sulfonatophenyl)posphine trisodium salt (TPPTS) coligands. The complexes obtained have been characterized by elemental analyses and FT-IR in the
    由CuCl与氢三(4-溴-1H-吡唑-1-基)硼酸钾,KTp4Br或双(3,5-二甲基吡唑-1-基)乙酸锂Li合成新的铜(I)配合物[L2CO2]配体和4-或2-(二苯基膦)苯甲酸或三(间磺基苯基)正膦三钠盐(TPPTS)大分子配体。通过元素分析和固态FT-IR以及溶液中的NMR(1H和31P [1H])和电喷雾质谱(ESI-MS)对所得复合物进行了表征。对[Cu [PPh2(4-C6H4COOH)](Tp4Br)]衍生物(一种有趣的二聚超分子组装体)进行了单晶结构表征。化学发光研究表明,这些新的铜络合物具有超氧化物清除活性。彗星试验用于评估暴露于不同活性氮物种的大鼠上皮细胞中DNA的损伤。此外,本研究还包括相同的复合物,以确定它们作为抗氧化剂的功效,可减轻DNA的氧化损伤。用作DNA损伤指标的参数尾矩表明,复合物[Cu [PPh2(4-C6H4COOH)](Tp4Br)]显着抑制了不同氮
  • Rhenium complexes of tris(pyrazolyl)methanes and sulfonate derivative
    作者:Elisabete C. B. Alegria、Lu?sa M. D. R. S. Martins、Matti Haukka、Armando J. L. Pombeiro
    DOI:10.1039/b611209a
    日期:——
    The trioxo [ReO(3)SO(3)C(pz)(3)}] (1) (pz = pyrazolyl) and oxo [ReOClSO(3)C(pz)(3)}(PPh(3))]Cl (2) compounds with tris(pyrazolyl)methanesulfonate were obtained by treatment of Re(2)O(7) or [ReOCl(3)(PPh(3))(2)], respectively, with Li[SO(3)C(pz)(3)], whereas [ReCl(3)HC(pz)(3)}] (3), [ReCl(3)HC(3,5-Me(2)pz)(3)}] (4) and [ReCl(4)eta(2)-HC(pz)(3)}] (5) were prepared by reaction of [ReOCl(3)(PPh(3))(2)]
    三氧[ReO(3)SO(3)C(pz)(3)}](1)(pz =吡唑基)和氧代[ReOCl SO(3)C(pz)(3)}(PPh(3 ))]分别用Re [2] O(7)或[ReOCl(3)(PPh(3))(2)]和Li [SO]处理带有三(吡唑基)甲磺酸盐的Cl(2)化合物(3)C(pz)(3)],而[ReCl(3)HC(pz)(3)}](3),[ReCl(3)HC(3,5-Me(2)pz) (3)}](4)和[ReCl(4)eta(2)-HC(pz)(3)}](5)通过[ReOCl(3)(PPh(3))(2 )](3,4)或[ReCl(4)(NCMe)(2)](5)与氢化三(吡唑基)甲烷HC(pz)(3)(3,5)或氢化三(3,5-二甲基- 1-吡唑基)甲烷HC(3,5-Me(2)pz)(3)(4)。[ReO SO(3)C(pz)(3)} OC(CH(3))(2)pz}] [ReO(4)]
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