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[HC(C(Me)N(2,6-(i)Pr2C6H3))2]Al(SH)2 | 501081-97-6

中文名称
——
中文别名
——
英文名称
[HC(C(Me)N(2,6-(i)Pr2C6H3))2]Al(SH)2
英文别名
[HC(C(Me)N(2,6-i-Pr-C6H3))2]Al(SH)2;(HS)2Al(HC(C(CH3)N(2,6-iPr2C6H3)2)
[HC(C(Me)N(2,6-(i)Pr2C6H3))2]Al(SH)2化学式
CAS
501081-97-6
化学式
C29H43AlN2S2
mdl
——
分子量
510.787
InChiKey
LJSHEPGROIKZBG-IEBALEEYSA-L
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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Unusual Anions [LAl(SH)(S)]- and [LAl(S)2]2- Stabilized by Weakly Coordinating Imidazolium Cations. Synthesis of LAl(SSiMe2)2O (L = HC[C(Me)N(Ar)]2, Ar = 2,6-iPr2C6H3)
    摘要:
    Deprotonation of an Al-SH moiety has been achieved easily by using N-heterocyclic carbene as the base. Monomeric mono- and bis-imidazolium salts [CtH+][LAI(SH)(S)](-) ([CtH+] = N,N'-bis-tert-butylimidazolium), [CmH+][LAI(SH)(S)](-), and [CmH+](2)[LAI(S)(2)](2) ([CmH+] = N,N'-bismesitylimidazolium), containing unusual anions [LAI(SH)(S)](-) and [LAI(S)(2)](2-), have been synthesized in nearly quantitative yields, Furthermore, [CmH+](2)[LAI(S)(2)](2) has been successfully used for the preparation of LAI(SSiMe2)(2)O containing the [O(Me2SiS)(2)](2-) ligand.
    DOI:
    10.1021/ic050693q
  • 作为产物:
    描述:
    1,2,3,4,5,6,7,8-八硫杂环辛烷[(HC(CMeN(2,6-i-Pr2C6H3))2)AlH2]三(二甲胺基)膦 作用下, 以 甲苯 为溶剂, 以90%的产率得到[HC(C(Me)N(2,6-(i)Pr2C6H3))2]Al(SH)2
    参考文献:
    名称:
    The First Structurally Characterized Aluminum Compound with Two SH Groups:  [LAl(SH)2] (L = N(Ar)C(Me)CHC(Me)N(Ar), Ar = 2,6-i-Pr2C6H3) and the Catalytic Properties of the Sulfur P(NMe2)3 System
    摘要:
    Surprisingly stable is the bis(hydrogen sulfide) of aluminum LAl(SH)(2) with two terminal arranged SH groups. The insertion of sulfur into the Al-H bonds is catalyzed by SP(NMe(2))(3). A possible mechanism is discussed.
    DOI:
    10.1021/ja028801k
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文献信息

  • Phosphane‐Catalyzed Reactions of LAlH <sub>2</sub> with Elemental Chalcogens; Preparation of [LAl(μ‐E) <sub>2</sub> AlL] [E = S, Se, Te, L = HC{C(Me)N(Ar)} <sub>2</sub> , Ar = 2,6‐ <i>i</i> Pr <sub>2</sub> C <sub>6</sub> H <sub>3</sub> ]
    作者:Vojtech Jancik、Monica M. Moya Cabrera、Herbert W. Roesky、Regine Herbst‐Irmer、Dante Neculai、Ana M. Neculai、Mathias Noltemeyer、Hans‐Georg Schmidt
    DOI:10.1002/ejic.200400062
    日期:2004.9
    Addition of catalytic amounts of a phosphane to a reaction mixture containing LAlH2 [2; L = HCC(Me)N(Ar)}2, Ar = 2,6-iPr2C6H3] and elemental Se or Te resulted in the formation of poorly soluble [LAl(μ-Se)2AlL] (3) and [LAl(μ-Te)2AlL] (4), respectively. The sulfur analogue [LAl(μ-S)2AlL] (5) could not be obtained from the direct reaction of 2 with elemental sulfur; consequently, its synthesis was successfully
    向含有 LAlH2 的反应混合物中加入催化量的烷 [2; L = HCC(Me)N(Ar)}2, Ar = 2,6-iPr2C6H3] 和元素 Se 或 Te 导致形成难溶性 [LAl(μ-Se)2AlL] (3) 和 [LAl (μ-Te)2AlL] (4),分别。2与元素直接反应不能得到类似物[LAl(μ-S)2AlL](5);因此,通过[LAlH2]和[LAl(SH)2]的反应成功合成了它。讨论了形成[LAl(μ-Se)2AlL]和[LAl(μ-Te)2AlL]的可能机制。化合物3-5的分子结构通过X射线结构分析确定。(© Wiley-VCH VerLAg GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)
  • Solubilizing functionalized molecular aluminosilicates
    作者:Fernando Rascón-Cruz、Raúl Huerta-Lavorie、Vojtech Jancik、Rubén Alfredo Toscano、Raymundo Cea-Olivares
    DOI:10.1039/b815291h
    日期:——
    aluminosilicate Al(SH)(micro-O)Si(OH)(O(t)Bu)(2) ( = [HCC(Me)N(Ar)}(2)](-), Ar = 2,6-(i)Pr(2)C(6)H(3)) has been prepared from Al(SH)(2) and ((t)BuO)(2)Si(OH)(2) in high yield. When reacted with one equiv. of water, the unique aluminosilicate containing two terminal hydroxy groups Al(OH.THF)(mu-O)Si(OH)(O(t)Bu)(2) can be isolated. However, when is reacted with the bulkier silanol ((t)BuO)(3)SiOH, no reaction is
    分子铝硅酸盐Al(SH)(micro-O)Si(OH)(O(t)Bu)(2)(= [HC C(Me)N(Ar)}(2)](-),Ar = 2由Al(SH)(2)和((t)BuO)(2)Si(OH)(2)高产率地制备了6,6-(i)Pr(2)C(6)H(3)) 。当与一个当量反应时。对于,可以分离出包含两个末端羟基的独特铝硅酸盐Al(OH.THF)(mu-O)Si(OH)(O(t)Bu)(2)。但是,当与较大的硅烷醇((t)BuO)(3)SiOH反应时,未观察到反应。所需的Al(SH)(micro-O)Si(O(t)Bu)(3)可以在AlH(2)和((t)BuO)(3)SiOH之间进行两步合成制备,得到第一个Al (H)(micro-O)Si(O(t)Bu)(3),它进一步与元素反应生成唯一产物。进行直接解以获得Al(OH)(micro-O)Si(O(t)Bu)(3),但是,这种
  • Soluble, reactive and stable – unique aluminosilicate ligands and a heterobimetallic derivative [LAl(SLi)(µ-O)Si(OLi·2thf)(OtBu)2]2
    作者:Vojtech Jancik、Fernando Rascón-Cruz、Raymundo Cea-Olivares、Rubén A. Toscano
    DOI:10.1039/b707895a
    日期:——
    The heterobimetallic aluminosilicate [LAl(SLi)(micro-O)Si(OLi.2thf)(O(t)Bu)(2)](2) was prepared from the LAl(SH)(micro-O)Si(OH)(O(t)Bu)(2) (L = [HCC(Me)N(Ar)}(2)](-), Ar = 2,6-di-(i)Pr(2)C(6)H(3)) ligand, which can also be hydrolyzed to LAl(OH.thf)(micro-O)Si(OH)(O(t)Bu)(2)- leading to the first aluminosilicate-dihydroxide soluble in organic solvents.
    杂双硅铝酸盐[LAl(SLi)(micro-O)Si(OLi.2thf)(O(t)Bu)(2)](2)由LAl(SH)(micro-O)Si(OH)制备(O(t)Bu)(2)(L = [HC C(Me)N(Ar)}(2)](-),Ar = 2,6-di-(i)Pr(2)C( 6)H(3))配体,也可以解为LAl(OH.thf)(micro-O)Si(OH)(O(t)Bu)(2)-生成可溶于有机溶剂。
  • Preparation of [LAl(?-S)2MCp2] (M=Ti, Zr) from the Structurally Characterized Lithium Complexes [{LAl(SH)[SLi(thf)2]}2] and [{LAl[(SLi)2(thf)3]}2]?2 THF
    作者:Vojtech Jancik、Herbert W. Roesky、Dante Neculai、Ana M. Neculai、Regine Herbst-Irmer
    DOI:10.1002/anie.200461254
    日期:2004.11.19
  • An Unknown Coordination Mode of the Phosphite Unit and a Carbon-Free Heterocycle in Two Different Heterobimetallic Alumophosphites
    作者:A. Paulina Gómora-Figueroa、Vojtech Jancik、Raymundo Cea-Olivares、Rubén A. Toscano
    DOI:10.1021/ic701614c
    日期:2007.12.1
    The unique alumophosphite reagent LAI(SH)(mu-O)P(OEt)(2) was prepared and used for the synthesis of the heterobimetallic alumophosphites [kappa(2)-S,P-LAI(S)(mu-O)P(OEt)(2)}(2)Zn] and [kappa(4)-S,O,O-LAI(SLi)(mu-O)P(OEt)(2)}(2)]. The first contains a rare example of two carbon-free five-membered heterocycles (Al-S-Zn-P-O) connected in a spiro fashion through the zinc atom, whereas the second possesses an unknown example of a coordination environment of a phosphite unit M-O-P(mu-OEt)(2)M with an uncoordinated lone electron pair on the phosphorus center.
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