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Tris<(diphenylphosphanyl)methyl>methan | 155850-41-2

中文名称
——
中文别名
——
英文名称
Tris<(diphenylphosphanyl)methyl>methan
英文别名
1,1,1-tris-((diphenylphosphanyl)methyl)methane;1,1,1-tris(diphenylphosphinomethyl)methane;1,1,1-tris(diphenylphosphinomethyl)ethane;tdppmm;Tris[(diphenylphosphanyl)methyl]methan;[3-Diphenylphosphanyl-2-(diphenylphosphanylmethyl)propyl]-diphenylphosphane
Tris<(diphenylphosphanyl)methyl>methan化学式
CAS
155850-41-2
化学式
C40H37P3
mdl
——
分子量
610.655
InChiKey
CFYZYTMLFDEFRD-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

物化性质

  • 沸点:
    704.6±55.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    9
  • 重原子数:
    43
  • 可旋转键数:
    12
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    调制所述螺旋桨状的一个三角架C(CH的形状2 PPH 2)3通过取代基的大小在macrobicyclic枢碳原子片段三λ 5 -phosphazenes
    摘要:
    手性macrobicyclic三λ 5个由三球三角架三(3-叠氮基苄)胺和1,1,1-三耦合形成-phosphazenes [(二苯基膦基)甲基]甲烷本螺旋拓扑作为将两个螺旋桨形的结果三脚架碎片具有相同的扭曲感。在低级叔丁烷片段R piv –C(CH 2 PPh 2)3的枢轴碳处引入一系列尺寸逐渐增加的R piv取代基,导致下部螺旋桨的螺旋度逐渐降低。这种现象被揭示在他们的CDCL 3溶液的NMR谱,和活化能为三λ的外消旋化过程5-磷腈通过聚结VT-NMR实验计算。
    DOI:
    10.1016/j.tet.2007.03.076
  • 作为产物:
    描述:
    2-羟甲基-1,3-丙二醇二苯基膦吡啶氯化亚砜potassium tert-butylate 作用下, 以 四氢呋喃 为溶剂, 反应 22.0h, 以42%的产率得到Tris<(diphenylphosphanyl)methyl>methan
    参考文献:
    名称:
    Center-to-propeller and propeller-to-propeller stereocontrol in a series of macrobicyclic tri-λ5-phosphazenes
    摘要:
    Center-to-propeller stereocontrol in a family of macrobicyclic, double-propeller shaped tri-lambda(5)-triphosphazenes remains constant in the upper tribenzylamine fragment as the size of the pivotal group at the lower tris(phosphane) fragment is gradually increased. In contrast the propeller-to-propeller stereocontrol diminishes as a result of the increasing conformational lability in the lower hemisphere. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.03.087
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文献信息

  • Ring slippage in indenyl derivatives of molybdenum and tungsten
    作者:JoséR. Ascenso、Isabel S. Gonçalves、Eberhardt Herdtweck、Carlos C. Romão
    DOI:10.1016/0022-328x(95)05859-n
    日期:1996.2
    Ring slippage of the indenyl occurs upon dissolution of the complexes [η5-IndM(CO)2L2]BF4 (M=Mo of W; L=NCMe or dimethylformamide) in an excess of L, to give [(η3-Ind)M(CO)2L3]Bf4. Other ring-slipped complexes synthesized are [(η3-Ind)Mo(CO)2L3]BF4 (L3=HC(pz)3, [HB(pz)3]−, Me3tacn or en(NCMe)}). Addition of NCMe or an excess of L failed to give ring slippage in [η5-IndMo(CO)2L2]BF4 (L2=bipy, dppe
    基的环滑动时发生的复合物的溶解[ η 5 -IndM(CO)2大号2 ] BF 4(W的M =; L = NCMe或二甲基甲酰胺)在过量的升,得到[(η 3 -Ind)M(CO)2 L 3 ] Bf 4。其他环滑落合成络合物[(η 3 -Ind)的Mo(CO)2大号3 ] BF 4(L 3 = HC(PZ)3,[HB(PZ)3 ] -中,Me 3 TACN或EN( NCMe)})。添加NCMe或过量的L未能在[η 5 -IndMo(CO)2大号2 ] BF 4(L 2 =联吡啶DPPE,(PME 3)2,P(OME)3 } 2或三磷酸)。NMR和X射线研究揭示了大量折叠的η 3 -基环。
  • [EN] PROCESS FOR THE PRODUCTION OF ACETALS FROM CARBON DIOXIDE<br/>[FR] PROCÉDÉ DE PRODUCTION D'ACÉTALS À PARTIR DE DIOXYDE DE CARBONE
    申请人:BASF SE
    公开号:WO2020161175A1
    公开(公告)日:2020-08-13
    The invention relates to a process for the preparation of acetals from carbon dioxide. The invention also relates to a mixture of phosphorus containing ligands comprising least one polydentate ligand and at least one monodentate ligand. Further, the invention also relates to the use of mixtures comprising at least one polydentate ligand and at least one monodentate ligand in transition metal complexes for the preparation of acetals.
    该发明涉及一种从二氧化碳制备缩醛的方法。该发明还涉及一种含配体混合物,包括至少一种多牙配体和至少一种单牙配体。此外,该发明还涉及在过渡属配合物中使用至少一种多牙配体和至少一种单牙配体的混合物以制备缩醛
  • Bonding and Activation of N<sub>2</sub>in Mo(0) Complexes Supported by Hybrid Tripod Ligands with Mixed Dialkylphosphine/Diarylphosphine Donor Groups: Interplay of Steric and Electronic Factors
    作者:Ludger Söncksen、Christian Gradert、Jan Krahmer、Christian Näther、Felix Tuczek
    DOI:10.1021/ic400582v
    日期:2013.6.3
    Molybdenum dinitrogen complexes are presented which are supported by novel hybrid tripod ligands of the type Me-C(CH2PPh2)2(CH2PiPr2) (trpd-1) and H–C(CH2PPh2)(CH2PiPr2)2 (trpd-2) having mixed dialkylphosphine/diarylphosphine donor groups. Reaction of the ligand trpd-1 with [MoI3(thf)3] followed by sodium amalgam reduction in the presence of the dppm gives the dinitrogen complex [Mo(N2)(trpd-1)(dmpm)]
    提出了二氮配合物,这些配合物由新型Me-C(CH 2 PPh 2)2(CH 2 P i Pr 2)(trpd-1)和H-C(CH 2 PPh 2)混合三脚架配体支持CH 2 P我2)2(trpd-2具有)混合二烷基膦/二芳基供体基团。配体trpd-1与[MoI 3(thf)3 ]的反应,然后在DPPM存在下还原钠汞齐,得到二氮配合物[Mo(N 2)(trpd-1)(DMPM)]其中trpd-1在一个κ协调3方式。该复合物表现出适度的N 2活化,这使得其在保留五膦连接的情况下能够质子化。发现用空间要求更高的大肠菌素DPPM代替DMPm会阻碍N 2的配位,并导致[Mo(trpd-1)(DPPM)],这是第一个具有结构特征的仅具有磷化氢的五配位Mo(0)配合物配体球。采用配体trpd-2沿着与二膦DMPM和DPPM以类似的合成路线导致双(二氮)的混合物中复合物的反式[沫(N - 2)2(κ 2-trpd-2)(二膦)]和反式-
  • METHOD FOR PRODUCING ALCOHOL BY HYDROGENATING LACTONE AND CARBOXYLIC ACID ESTER IN LIQUID PHASE
    申请人:Maeda Hirofumi
    公开号:US20100113842A1
    公开(公告)日:2010-05-06
    Disclosed is a method for producing an alcohol from a lactone or a carboxylic acid ester, which enables to produce an alcohol from a lactone or a carboxylic acid ester under relatively mild conditions with high yield and high catalytic efficiency. This method also enables to produce an optically active alcohol from an optically active lactone or an optically active carboxylic acid ester. Specifically disclosed is a method for producing an alcohol by hydrogen reducing a lactone or a carboxylic acid ester in the presence of a catalyst containing ruthenium and a phosphine compound represented by the following general formula (1): wherein R 1 represents a spacer; R 2 , R 3 , R 4 , R 5 , R 6 and R 7 independently represent a hydrogen atom, an alkyl group having 1-12 carbon atoms, an aryl group or a heterocyclic group; and R 8 , R 9 , R 10 , R 11 , R 12 and R 13 independently represent an alkyl group having 1-12 carbon atoms, an aryl group or a heterocyclic group.
    本发明公开了一种从内酯或羧酸酯中制备醇的方法,该方法可以在相对温和的条件下高收率、高催化效率地从内酯或羧酸酯中制备醇。该方法还可以从手性内酯或手性羧酸酯中制备手性醇。具体公开了一种通过在催化剂中加入和以下通式(1)所代表的膦化合物的存在下,氢化还原内酯或羧酸酯制备醇的方法:其中R1代表间隔物,R2、R3、R4、R5、R6和R7分别独立地代表氢原子、具有1-12个碳原子的烷基、芳基或杂环基,R8、R9、R10、R11、R12和R13分别独立地代表具有1-12个碳原子的烷基、芳基或杂环基。
  • POLYMER ELECTROLYTE COMPOSITION, AND POLYMER ELECTROLYTE MEMBRANE, MEMBRANE ELECTRODE ASSEMBLY AND SOLID POLYMER FUEL CELL EACH USING SAME
    申请人:TORAY INDUSTRIES, INC.
    公开号:US20140377686A1
    公开(公告)日:2014-12-25
    Provided are: a practically excellent polymer electrolyte composition having excellent chemical stability of being resistant to strong oxidizing atmosphere during operation of fuel cell, and achieving excellent proton conductivity under low-humidification conditions, excellent mechanical strength and physical durability; a polymer electrolyte membrane, a membrane electrode assembly, and a polymer electrolyte fuel cell each using the same. The polymer electrolyte composition of the present invention comprises at least an ionic group-containing polymer (A) and a phosphorus-containing additive (B), the phosphorus-containing additive (B) being at least one of a phosphine compound and a phosphinite compound. The polymer electrolyte membrane, the membrane electrode assembly, and the polymer electrolyte fuel cell of the present invention are structured by the polymer electrolyte composition.
    提供了一种具有优异化学稳定性,在燃料电池操作期间对强氧化气氛具有抗性,并在低加湿条件下实现优异的质子传导性、优异的机械强度和物理耐久性的实用优良聚合物电解质组成物;以及使用相同组成物的聚合物电解质膜、膜电极组件和聚合物电解质燃料电池。本发明的聚合物电解质组成物包括至少一种离子基团含有的聚合物(A)和一种含添加剂(B),该含添加剂(B)至少为膦化合物和膦酸酯化合物中的一种。本发明的聚合物电解质膜、膜电极组件和聚合物电解质燃料电池由聚合物电解质组成物构成。
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