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[N((C3H7)C(2,6-diisopropylphenyl)N)2]H | 799811-79-3

中文名称
——
中文别名
——
英文名称
[N((C3H7)C(2,6-diisopropylphenyl)N)2]H
英文别名
——
[N((C3H7)C(2,6-diisopropylphenyl)N)2]H化学式
CAS
799811-79-3
化学式
C32H35F14N3
mdl
——
分子量
727.6
InChiKey
MYSYYJZMDBWUTN-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):
    12.4
  • 重原子数:
    49
  • 可旋转键数:
    12
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    36.8
  • 氢给体数:
    1
  • 氢受体数:
    15

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    空间上需要的氟化三氮杂戊二烯基配体[N((C3F7)C(Dipp)N)2]-(Dipp = 2,6-二异丙基苯基)的银(I)配合物。
    摘要:
    立体要求高的三氮杂戊二烯[N((C3F7)C(Dipp)N)2] H可分离热稳定的二配位和三配位的银配合物。游离配体[N((C3F7)C(Dipp)N)2] H具有固态的W形配体骨架。[N((C3F7)C(Dipp)N)2] H与银(I乙腈中的氧化物)导致CH(3)CNAg [N((C3F7)C(Dipp)N)2] HIt具有两个配位的银中心和一个与kappa(1)配位的三氮杂戊二烯基配体。该乙腈银络合物是获得热稳定的异氰酸银t-BuNCAg [N((C3F7)C(Dipp)N)2]手工银膦[[N((C3F7)C(Dipp)N)2]的极佳前体。 ] HAgPPh(3)加合物。异氰酸银(I)t-BuNCAg [N((C3F7)C(Dipp)N)2] H的红外光谱数据显示nu(CN)在2219 cm(-)(1)处。银离子通过中心氮原子配位至三氮杂戊二烯基配体。PPh(3)银加合物[N((C3F7)C(Dipp)N)2]
    DOI:
    10.1021/ic0491231
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文献信息

  • Fluorinated triazapentadienyl ligand supported ethyl zinc(<scp>ii</scp>) complexes: reaction with dioxygen and catalytic applications in the Tishchenko reaction
    作者:Naveen V. Kulkarni、Animesh Das、Shawn G. Ridlen、Erin Maxfield、Venkata A. K. Adiraju、Muhammed Yousufuddin、H. V. Rasika Dias
    DOI:10.1039/c6dt00257a
    日期:——
    bridging-ethoxy or -ethylperoxy groups. The ethyl zinc complexes catalyze the Tishchenko reaction of benzaldehyde under solventless conditions affording benzyl benzoate. The reaction of ethyl zinc complexes with dioxygen and their catalytic behaviour in the Tishchenko reaction are affected by the electronic and steric factors of the triazapentadienyl ligand. [N(C3F7)C(Cy)N}2]ZnOOEt}2 is an excellent reagent
    乙基络合物[N (C 3 F 7)C(Dipp)N} 2 ] ZnEt,[N (C 3 F 7)C(Cy)N} 2 ] ZnEt,[N (CF 3)C(由2,4,6-Br 3 C 6 H 2)N} 2 ] ZnEt和[N (C 3 F 7)C(2,6-Cl 2 C 6 H 3)N} 2 ] ZnEt合成相应的1,3,5-三氮杂戊二烯二乙基。X射线数据显示[N (C 3 F 7)C(Dipp)N} 2] ZnEt在中心具有变形的三角形平面几何形状。所述triazapentadienyl配体结合到在κ 2 -mode。[N (C 3 F 7)C(Dipp)N} 2 ] ZnEt,[N (C 3 F 7)C(Cy)N} 2 ] ZnEt,[N (CF 3)C(2,4,6-Br 3 C 6 H 2)N} 2 ] ZnEt和[N (C 3 F 7)C(2,6-Cl 2 C
  • Copper(I) Complexes of Fluorinated Triazapentadienyl Ligands:  Synthesis and Characterization of [N{(C<sub>3</sub>F<sub>7</sub>)C(Dipp)N}<sub>2</sub>]CuL (Where L = NCCH<sub>3</sub>, CNBu<sup>t</sup>, CO; Dipp = 2,6-Diisopropylphenyl)
    作者:H. V. Rasika Dias、Shreeyukta Singh
    DOI:10.1021/ic049229w
    日期:2004.9.1
    features a W-shaped ligand backbone in the solid state. [N[(C3F7)C(Dipp)N]2]H reacts with copper(I) oxide in acetonitrile leading to [N[(C3F7)C(Dipp)N]2]CuNCCH3. This copper adduct serves as an excellent precursor to obtain thermally stable [N[(C3F7)C(Dipp)N]2]CuCNBut and [N[(C3F7)C(Dipp)N]2]CuCO. IR spectroscopic data of these copper(I) isocyanide (CN = 2176 cm(-1)) and copper(I) carbonyl (CO = 2109
    立体要求高的三氮杂戊二烯[N [(C3F7)C(Dipp)N] 2] H的合成产率很高。它具有固态的W型配体骨架。[N [( )C(Dipp)N] 2] H与乙腈中的氧化铜(I)反应,生成[N [( )C(Dipp)N] 2] CuNCCH3。该加合物是获得热稳定的[N [( )C(Dipp)N] 2] CuCNBut和[N [( )C(Dipp)N] 2] CuCO的极好前体。这些异氰酸(I)(CN = 2176 cm(-1))和羰基(I)(CO = 2109 cm(-1))的红外光谱数据表明,[N [( )C(Dipp) N] 2]-配体是相当弱的供体。
  • Synthesis and catalytic activity of an electron-deficient copper–ethylene triazapentadienyl complex
    作者:Jaime A. Flores、Vivek Badarinarayana、Shreeyukta Singh、Carl J. Lovely、H. V. Rasika Dias
    DOI:10.1039/b911981g
    日期:——
    The copper(I) ethylene complex [N(C3F7)C(Dipp)N}2]Cu(C2H4) (Dipp = 2,6-diisopropylphenyl) has been synthesized by treating [N(C3F7)C(Dipp)N}2]Cu(NCCH3) with ethylene at room temperature. [N(C3F7)C(Dipp)N}2]Cu(C2H4) is an air stable, yellow solid. X-Ray crystallographic data of [N(C3F7)C(Dipp)N}2]Cu(C2H4) show that the 1,3,5-triazapentadienyl ligand coordinates to copper in κ2-fashion. The copper atom adopts a trigonal-planar geometry. [N(C3F7)C(Dipp)N}2]Cu(C2H4) and [N(C3F7)C(Dipp)N}2]Cu(NCCH3) effectively catalyze carbene and nitrene transfer to a variety of substrates in high efficiencies.
    通过在室温下用乙烯处理 [N(C3F7)C(Dipp)N}2]Cu(NCCH3) 合成了(I)乙烯络合物 [N( )C(Dipp)N}2]Cu(C2H4)(Dipp = 2,6-二异丙基苯基)。N( )C(Dipp)N}2]Cu( )是一种在空气中稳定的黄色固体。[N( )C(Dipp)N}2]Cu( )的 X 射线晶体学数据显示,1,3,5-三氮杂戊二烯配体以δ2 方式与配位。原子采用了三方平面几何。N( )C(Dipp)N}2]Cu( )和[N( )C(Dipp)N}2]Cu(NCCH3)能有效催化碳烯和腈向多种底物的高效转移。
  • Monomeric lithium triazapentadienyl complexes
    作者:H. V. Rasika Dias、Shreeyukta Singh
    DOI:10.1039/b518464a
    日期:——
    5-triazapentadienes [N(C3F7)C(Mes)N}2]H and [N(C3F7)C(Dipp)N}2]H (where Mes = 2,4,6-Me3C6H2; Dipp = 2,6-Pri2C6H3) with n-BuLi in hexane, followed by the crystallization from hexane–THF mixture afforded the corresponding lithium 1,3,5-triazapentadienyl complexes as their THF solvates. X-Ray crystallographic analyses revealed that [N(C3F7)C(Mes)N}2]Li(THF)2 and [N(C3F7)C(Dipp)N}2]Li(THF) are monomeric
    1,3,5-三氮杂戊二烯类[N (C 3 F 7)C(Mes)N} 2 ] H和[N (C 3 F 7)C(Dipp)N} 2 ] H(其中Mes = 2,4,6-Me 3 C 6 H 2; Dipp = 2,6-Pr i 2 C 6 H 3),其中n -BuLi正己烷,然后从 正己烷-THF混合物作为THF溶剂化物提供相应的1,3,5-三氮杂戊二烯配合物。X射线晶体分析表明,[N (C 3 F 7)C(Mes)N} 2 ] Li(THF)2和[N (C 3 F 7)C(Dipp)N} 2 ] Li(THF) )是固态的单体。[N (C 3 F 7)C(Mes)N} 2 ] Li(THF)2具有四坐标的中心,具有扭曲的四面体几何形状,并且具有船形的C 2 N 3 Li属环。[N (C 3 F 7)C(Dipp)N} 2] Li(THF)具有三配位的原子和平面的U形C 2
  • Gold(I) Complexes [N{(C <sub>3</sub> F <sub>7</sub> )C(Dipp)N} <sub>2</sub> ]AuL (L = Ethylene, <i>tert</i> ‐Butyl Isocyanide, Tetrahydrothiophene, Triphenylphosphine) and Different Triazapentadienyl Ligand Coordination Modes
    作者:Shreeyukta Singh、Guocang Wang、James X. Mao、Jaime A. Flores、Xiaodi Kou、Charles Campana、Peter Kroll、H. V. Rasika Dias
    DOI:10.1002/ejic.201600878
    日期:2016.12
    Fluorinated 1,3,5-triazapentadienyl ligand [N(C3F7)C(Dipp)N}2] (Dipp = 2,6-iPr2C6H3) has been used in the synthesis of monomeric gold(I)-ethylene, tBuNC, tetrahydrothiophene (THT), and PPh3 complexes. X-ray crystal structures show a rich diversity of coordination modes in which gold coordinates to the central nitrogen atom of 1,3,5-triazapentadienyl ligand in tBuNCAu[N(C3F7)C(Dipp)N}2] and (THT)
    化 1,3,5-三氮杂戊二烯配体 [N(C3F7)C(Dipp)N}2] (Dipp = 2,6-iPr2C6H3) 已用于合成单体 (I)-乙烯、tBuNC、四氢噻吩(THT) 和 PPh3 复合物。X 射线晶体结构显示出丰富多样的配位模式,其中与 tBuNCAu[N( )C(Dipp)N}2] 和 (THT) 中 1,3,5-三氮杂戊二烯配体的中心氮原子配位Au[N( )C(Dipp)N}2] 或 [N( )C(Dipp)N}2]Au(THT) 和 [N( )C 中的两个末端氮原子之一(Dipp)N}2]Au(PPh3) 或螯合 [N( )C(Dipp)N}2]Au(C2H4) 中的两个末端氮原子。因此,三氮杂戊二烯配体作为 κ1-N 或 κ2-NN 供体,N3C3 骨架采用扭曲的 W 或 U 形构象。 (I) THT 加合物以固
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