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1,1,10,10-tetraphenyl-4,7-diaza-1,10-diphosphadecane | 102915-40-2

中文名称
——
中文别名
——
英文名称
1,1,10,10-tetraphenyl-4,7-diaza-1,10-diphosphadecane
英文别名
N,N'-bis(2-diphenylphosphanylethyl)ethane-1,2-diamine
1,1,10,10-tetraphenyl-4,7-diaza-1,10-diphosphadecane化学式
CAS
102915-40-2
化学式
C30H34N2P2
mdl
——
分子量
484.561
InChiKey
LSPRWOPMRQGZOV-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):
    5
  • 重原子数:
    34
  • 可旋转键数:
    13
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    24.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    tris(triphenylphosphine)ruthenium(II) chloride1,1,10,10-tetraphenyl-4,7-diaza-1,10-diphosphadecane异丙醇甲苯 为溶剂, 反应 6.0h, 以0.594 g的产率得到RuCl2((Ph2PCH2CH2NHCH2)2)
    参考文献:
    名称:
    [EN] CATALYTIC CONVERSION OF CARBON DIOXIDE TO METHANOL
    [FR] CONVERSION CATALYTIQUE DU DIOXYDE DE CARBONE EN MÉTHANOL
    摘要:
    本公开涉及一种从二氧化碳生产甲醇的新催化过程,包括:(1)将二氧化碳和氢转化为甲酸或甲酸盐;(2)将甲酸或甲酸盐转化为二醇的二甲酸酯;(3)加氢二甲酸酯以制备甲醇和二醇。从加氢反应中产生的二醇可以回收并重新用于制备二甲酸酯。
    公开号:
    WO2019193483A1
  • 作为产物:
    描述:
    N,N'-di(β-diphenylphosphorylethyl)ethylenediamine 在 lithium aluminium tetrahydride 、 cerium(III) chloride 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以92%的产率得到1,1,10,10-tetraphenyl-4,7-diaza-1,10-diphosphadecane
    参考文献:
    名称:
    二氨基二膦四齿配体、其钌络合物及上述两者 的制备方法和应用
    摘要:
    本发明公开了一种二氨基二膦四齿配体、其钌络合物及上述两者的制备方法和应用。本发明提供一种如式I所示的钌络合物,其中L为如式II所示的二氨基二膦四齿配体,X和Y各自独立地为氯离子、溴离子、碘离子、氢负离子或BH4‑。该钌络合物在酯类化合物催化氢化反应中表现出非常优异的催化活性,不仅收率高,而且反应的化学选择性也非常高,可以兼容共轭和非共轭的碳碳双键、碳碳三键、环氧、卤素及羰基等官能团,具有很大的应用前景。
    公开号:
    CN110357923B
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文献信息

  • Preparation and Stereochemistry of Cobalt(III) Complexes Containing 1,1,10,10-Tetraphenyl-4,7-diaza-1,10-diphosphadecane or 2,11-Dimethyl-5,8-diaza-2,11-diphosphadodecane, R<sub>2</sub>PCH<sub>2</sub>CH<sub>2</sub>NHCH<sub>2</sub>CH<sub>2</sub>NHCH<sub>2</sub>CH<sub>2</sub>PR<sub>2</sub>(R=C<sub>6</sub>H<sub>5</sub>or CH<sub>3</sub>)
    作者:Masamichi Atoh、Kazuo Kashiwabara、Junnosuke Fujita
    DOI:10.1246/bcsj.58.2793
    日期:1985.10
    NaPR2 (R=C6H3, CH3) and purified through their Ni(II) complexes. Seven new cobalt(III) complexes containing the phosphine ligand were prepared: [CoX2(pp- or mm-PNNP)]n+(X2=(Cl)2, (NCS2), C5H7O2−(2,4-pentanedionate ion), and CO32−). Four complexes of [CoX2(pp- or mm-PNNP)]+ (X=Cl, NCS) afforded only a trans(X,X) isomer, and [Co(acac)(pp- or mm-PNNP)]2+ and [Co(CO3)(pp-PNNP)]+ complexes yielded a cisβ
    新的四齿膦配体,1,1,10,10-tetraphenyl-4,7-diaza-1,10-diphosphadecane (pp-PNNP) 和 2,11-dimethyl-5,8-diaza-2,11-diphosphadodecane ( mm-PNNP),由 (ClCH2CH2NHCH2)·2HCl 和 NaPR2(R=C6H3,CH3)制备,并通过它们的 Ni(II) 配合物进行纯化。制备了七种含有膦配体的新钴 (III) 配合物:[CoX2(pp- 或 mm-PNNP)]n+(X2=(Cl)2, (NCS2), C5H7O2-(2,4-pentanedionate ion), 和CO32-)。[CoX2(pp- 或 mm-PNNP)]+ (X=Cl, NCS) 的四种复合物仅提供反式 (X,X) 异构体,而 [Co(acac)(pp- 或 mm-PNNP)]2+和 [Co(CO3)(pp-PNNP)]+
  • Method for Producing Aromatic Compound Polymer
    申请人:Higashimura Hideyuki
    公开号:US20090018309A1
    公开(公告)日:2009-01-15
    A method for producing an aromatic compound polymer comprising oxidatively polymerizing one or more of aromatic compound(s) having two or more hydrogen atoms directly connected to aromatic ring(s), in the presence of an oxidizing agent, wherein the method employs a catalyst composed of a transition metal complex or a catalyst prepared from a transition metal complex and an activating agent, and said catalyst has a parameter P defined by the following formula (A) of 0.50 or more, and a parameter Eo defined by the following formula (B) of 0.50 [V] or more: P=Af/Ai (A) and Eo =( Epa+Epc )/2[V]  (B).
    一种生产芳香族化合物聚合物的方法,包括在氧化剂存在下氧化聚合具有两个或更多氢原子直接连接到芳香环的一个或多个芳香族化合物,其中该方法采用由过渡金属配合物或由过渡金属配合物和活化剂制备的催化剂,所述催化剂具有以下公式(A)定义的参数P,P的值为0.50或更高,并且具有以下公式(B)定义的参数Eo,Eo的值为0.50 [V]或更高:P=Af/Ai(A)和Eo=(Epa+Epc)/2[V](B)。
  • METHOD FOR PRODUCING AROMATIC COMPOUND POLYMER
    申请人:Sumitomo Chemical Company, Limited
    公开号:EP1767560A1
    公开(公告)日:2007-03-28
    A method for producing an aromatic compound polymer comprising oxidatively polymerizing one or more of aromatic compound(s) having two or more hydrogen atoms directly connected to aromatic ring(s), in the presence of an oxidizing agent, wherein the method employs a catalyst composed of a transition metal complex or a catalyst prepared from a transition metal complex and an activating agent, and said catalyst has a parameter P defined by the following formula (A) of 0.50 or more, and a parameter Eo defined by the following formula (B) of 0.50 [V] or more: P=Af/Ai (wherein Ai represents an absorbance at an absorption maximum belonging in an absorption band located at the longest wavelength side in an absorption spectrum obtained for a solution containing the catalyst, in a ultraviolet to near-infrared wavelength region from 200 nm to 800 nm, and Af represents an absorbance at the same wavelength applied to the Ai, in an absorption spectrum in the above wavelength region obtained for a solution prepared by adding 3 equivalent of water per mole of the metal contained in the catalyst to the solution), and Eo=Epa+Epc/2V (wherein, Epa represents a peak potential at the oxidation side of an oxidation-reduction potential derived from the transition metal contained in the catalyst, at a potential of 0.50 [V] or more based on oxidation-reduction potential of ferrocene/ferrocenium ion measured with a cyclic voltammetry for the solution containing the catalyst, and Epc represents a peak potential at the reduction side corresponding to Epa by the same measurement).
    一种生产芳香族化合物聚合物的方法,包括在氧化剂存在下,氧化聚合一种或多种具有两个或两个以上氢原子直接连接到芳香环上的芳香族化合物,其中该方法采用由过渡金属络合物组成的催化剂或由过渡金属络合物和活化剂制备的催化剂,所述催化剂的参数P由下式(A)定义为0.50或以上,参数Eo由下式(B)定义为0.50[V]或以上:P=Af/Ai (其中,Ai 表示在含有催化剂的溶液的吸收光谱中,在 200 纳米至 800 纳米的紫外至近红外波长区域内,属于最长波长侧的吸收带的吸收最大值处的吸光度;Af 表示在通过向溶液中加入每摩尔催化剂所含金属 3 当量的水而制备的溶液的吸收光谱中,在上述波长区域内,与 Ai 相同波长处的吸光度),以及 Eo=Epa+Epc/2V (其中,Epa 代表由催化剂所含过渡金属衍生的氧化还原电位的氧化侧峰值电位,电位值为 0.50 [V] 或更高,该电位值基于对含有催化剂的溶液用循环伏安法测得的二茂铁/二茂铁离子的氧化还原电位;Epc 代表与 Epa 相对应的还原侧峰值电位,该测量值与 Epa 相同)。
  • Method for producing aromatic compound polymer
    申请人:Sumitomo Chemical Company, Limited
    公开号:EP2241547A1
    公开(公告)日:2010-10-20
    A method for producing an aromatic compound polymer by oxidatively polymerizing an aromatic compound in the presence of an oxidizing agent, wherein the method employs (a) a catalyst composed of a transition metal complex or (b) a catalyst prepared from a transition metal complex and an activating agent, and said transition metal complex is a vanadium di-nuclear complex represented by the following general formula (1-3): wherein A1, A2, A3 and A4 each independently represent an oxygen atom, or NR11, and B1, B2, B3 and B4 each independently represent -O- or NR12-; R1, R2, R3, R4, R5, R6, R7 and R8 each independently represent a C1-30 hydrocarbon group optionally substituted by a C1-50 alkoxy, nitro, cyano or halogen group; or a C1-40 hydrocarbonoxy group optionally substituted by a C1-50 alkoxy, nitro, cyano or halogen group; R9 and R10 each independently represent a C1-20 alkylene group optionally substituted by a C1-50 alkoxy, nitro, cyano or halogen group; or R9 and R10 represent a C6-60 arylene group optionally substituted by a C1-50 alkyl, C7-50 aralkyl, C1-50 alkoxy, nitro, cyano or halogen group; or R9 and R10 represent -O-, -S--SO2- or NR13-; and when R9 and R10 exist in a plural number respectively, they may be the same or different; m and n each independently represent an integer of 1 to 7; R11, R12 and R13 each independently represent a hydrogen atom or a C1-30 hydrocarbon group optionally substituted by a C1-50 alkoxy, nitro, cyano or halogen group; when R11, R12 and R13 exist in a plural number respectively, they may be the same or different; when both of A1 and A2 and/or both of A3 and A4 are together NR11 respectively, two R11s may combine to form a C1-20 divalent hydrocarbon group optionally substituted by a C1-30 hydrocarbon, C1-40 hydrocarbonxy, nitro, cyano or halogen group which connects A1 and A2 and/or A3 and A4 to each other; and when both of B1 and B2 and/or both of B3 and B4 are together -NR12- respectively, two R12s may combine to form a C1-20 divalent hydrocarbon group optionally substituted by a C1-30 hydrocarbon, C1-40 hydrocarbonxy, nitro, cyano or halogen group which connects B1 and B2 and/or B3 and B4 to each other.
    一种在氧化剂存在下通过氧化聚合芳香族化合物生产芳香族化合物聚合物的方法,其中该方法采用(a)由过渡金属络合物组成的催化剂或(b)由过渡金属络合物和活化剂制备的催化剂,所述过渡金属络合物是由以下通式(1-3)表示的钒二核络合物: 其中 A1、A2、A3 和 A4 各自独立地代表氧原子或 NR11,B1、B2、B3 和 B4 各自独立地代表 -O- 或 NR12-; R1、R2、R3、R4、R5、R6、R7 和 R8 各自独立地代表被 C1-50 烷氧基、硝基、氰基或卤素基团任选取代的 C1-30 烃基;或被 C1-50 烷氧基、硝基、氰基或卤素基团任选取代的 C1-40 烃氧基;R9 和 R10 各自独立地代表被 C1-50 烷氧基、硝基、氰基或卤素基团任选取代的 C1-20 亚烷基;或 R9 和 R10 代表任选被 C1-50 烷基、C7-50 芳基、C1-50 烷氧基、硝基、氰基或卤素基团取代的 C6-60 芳烯基团;或 R9 和 R10 代表 -O-、-S--SO2- 或 NR13-;当 R9 和 R10 分别以复数存在时,它们可以相同或不同;m 和 n 各自独立地代表 1 到 7 的整数;R11、R12 和 R13 各自独立地代表氢原子或任选被 C1-50 烷氧基、硝基、氰基或卤素取代的 C1-30 烃基;当 R11、R12 和 R13 分别以复数形式存在时,它们可以相同或不同;当 A1 和 A2 和/或 A3 和 A4 分别都是 NR11 时,两个 R11 可结合形成一个 C1-20 二价烃基,该烃基可选择被 C1-30 烃、C1-40 烃氧基、硝基、氰基或卤素基取代,该烃基将 A1 和 A2 和/或 A3 和 A4 连接在一起;当 B1 和 B2 和/或 B3 和 B4 分别为-NR12-时,两个 R12 可结合形成一个 C1-20 二价烃基,该烃基可选择被 C1-30 烃、C1-40 烃氧基、硝基、氰基或卤素基取代,该烃基将 B1 和 B2 和/或 B3 和 B4 连接在一起。
  • Vanadium di-nuclear complex
    申请人:Sumitomo Chemical Company, Limited
    公开号:EP2241548A1
    公开(公告)日:2010-10-20
    A vanadium di-nuclear complex represented by the following general formula (1-3): wherein A1, A2, A3 and A4 each independently represent an oxygen atom, or NR11, and B1, B2, B3 and B4 each independently represent -O- or NR12-; R1, R2, R3, R4, R5, R6, R7 and R8 each independently represent a C1-30 hydrocarbon group optionally substituted by a C1-50 alkoxy, nitro, cyano or halogen group; or a C1-40 hydrocarbonoxy group optionally substituted by a C1-50 alkoxy, nitro, cyano or halogen group; R9 and R10 each independently represent a C 1-20 alkylene group optionally substituted by a C1-50 alkoxy, nitro, cyano or halogen group; or R9 and R10 represent a C6-60 arylene group optionally substituted by a C1-50 alkyl, C7-50 aralkyl, C1-50 alkoxy, nitro, cyano or halogen group; or R9 and R10 represent -O-, -S--SO2- or NR13-; and when R9 and R10 exist in a plural number respectively, they may be the same or different; m and n each independently represent an integer of 1 to 7; R11, R12 and R13 each independently represent a hydrogen atom or a C1-30 hydrocarbon group optionally substituted by a C1-50 alkoxy, nitro, cyano or halogen group; when R11, R12 and R13 exist in a plural number respectively, they may be the same or different; when both of A1 and A2 and/or both of A3 and A4 are together NR11 respectively, two R11s may combine to form a C1-20 divalent hydrocarbon group optionally substituted by a C1-30 hydrocarbon, C1-40 hydrocarbonxy, nitro, cyano or halogen group which connects A1 and A2 and/or A3 and A4 to each other; and when both of B1 and B2 and/or both of B3 and B4 are together -NR12- respectively, two R12s may combine to form a C1-20 divalent hydrocarbon group optionally substituted by a C1-30 hydrocarbon, C1-40 hydrocarbonxy, nitro, cyano or halogen group which connects B1 and B2 and/or B3 and B4 to each other.
    由以下通式(1-3)表示的二核钒络合物: 其中 A1、A2、A3 和 A4 各自独立地代表氧原子或 NR11,B1、B2、B3 和 B4 各自独立地代表 -O- 或 NR12-; R1、R2、R3、R4、R5、R6、R7 和 R8 各自独立地代表被 C1-50 烷氧基、硝基、氰基或卤素基团任选取代的 C1-30 烃基;或被 C1-50 烷氧基、硝基、氰基或卤素基团任选取代的 C1-40 烃氧基;R9 和 R10 各自独立地代表被 C1-50 烷氧基、硝基、氰基或卤素基团任选取代的 C 1-20 亚烷基;或 R9 和 R10 代表任选被 C1-50 烷基、C7-50 芳基、C1-50 烷氧基、硝基、氰基或卤素基团取代的 C6-60 芳烯基团;或 R9 和 R10 代表 -O-、-S--SO2- 或 NR13-;当 R9 和 R10 分别以复数存在时,它们可以相同或不同;m 和 n 各自独立地代表 1 到 7 的整数;R11、R12 和 R13 各自独立地代表氢原子或任选被 C1-50 烷氧基、硝基、氰基或卤素取代的 C1-30 烃基;当 R11、R12 和 R13 分别以复数形式存在时,它们可以相同或不同;当 A1 和 A2 和/或 A3 和 A4 分别都是 NR11 时,两个 R11 可结合成一个 C1-20 二价烃基,该烃基可选择被 C1-30 烃、C1-40 烃氧基、硝基、氰基或卤素基取代,该烃基将 A1 和 A2 和/或 A3 和 A4 连接在一起;当 B1 和 B2 和/或 B3 和 B4 分别都是-NR12-时,两个 R12 可结合成一个 C1-20 二价烃基,该烃基可选择被 C1-30 烃、C1-40 烃氧基、硝基、氰基或卤素基取代,该烃基将 B1 和 B2 和/或 B3 和 B4 连接在一起。
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(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐