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(bicyclicamylamine)diiodoplatinum(II) | 850940-74-8

中文名称
——
中文别名
——
英文名称
(bicyclicamylamine)diiodoplatinum(II)
英文别名
cis-{Pt(cyclopentylNH2)2I2};cis-[diiodobis(cyclopentylamino)platinum(II)];cis-bis(cyclopentylamine)platinum(II) iodide;cis-PtI2(cpa)2;cis-Pt(cyclopentylamine)2I2;cis-PtI2(cyclopentylamine)2
(bicyclicamylamine)diiodoplatinum(II)化学式
CAS
850940-74-8
化学式
C10H22I2N2Pt
mdl
——
分子量
619.187
InChiKey
CIUQZOUGRHHQRH-UHFFFAOYSA-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:
    描述:
    (bicyclicamylamine)diiodoplatinum(II) 为溶剂, 生成 cis-(2-(4-diethylaminobutyl)malonato)(dicyclopentylamine)platinum(II) acetate
    参考文献:
    名称:
    PLATINUM COMPOUND OF MALONIC ACID DERIVATIVE HAVING LEAVING GROUP CONTAINING AMINO OR ALKYLAMINO
    摘要:
    公开号:
    EP2924044B1
  • 作为产物:
    描述:
    tetrakis(cyclopentylamine)platinum(II) iodide 以 乙醇 为溶剂, 以59%的产率得到(bicyclicamylamine)diiodoplatinum(II)
    参考文献:
    名称:
    研究的Pt(II)的种类-环状胺络合物的顺式-和反式-Pt(胺)2我2和顺-和反式-Pt(胺)2(NO 3)2和它们的含水产品通过
    摘要:
    合成了含顺式和反式-Pt(胺)2 I 2型环胺的配合物,并主要通过IR和多核NMR光谱学进行了研究。将该化合物转化为顺式和反式-Pt(胺)2(NO 3)2,也对其进行了研究。然后在不同的pH条件下,在D 2 O中研究了后者化合物的水解和水合反应。在酸性介质中,水性产物为[Pt(胺)2(D 2 O)2 ] 2+,对于一些胺,其为[Pt(胺)2检测到(D 2 O)(NO 3)] +。在碱性pH下,主要产物为Pt(胺)2(OD)2和Pt(胺)2(OD)(NO 3)被检测出。在中性pH中,在新鲜溶液中,顺式异构体形成2至4种。在195 Pt NMR中,最受保护的物质是一水合一羟基复合物顺式[[Pt(胺)2(D 2 O)(OD)] +,而受保护程度较小的化合物是二氢桥联的二聚体[Pt(胺)2( μ-OD)2 Pt(胺)2 ] 2+,所有化合物均已观察到。对于一些胺,检测到单羟基桥接的二聚体[Pt(D
    DOI:
    10.1016/j.ica.2004.12.030
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文献信息

  • Molecular interaction fields vs. quantum-mechanical-based descriptors in the modelling of lipophilicity of platinum(<scp>iv</scp>) complexes
    作者:Giuseppe Ermondi、Giulia Caron、Mauro Ravera、Elisabetta Gabano、Sabrina Bianco、James A. Platts、Domenico Osella
    DOI:10.1039/c2dt32360e
    日期:——
    We report QSAR calculations using VolSurf descriptors to model the lipophilicity of 53 Pt(IV) complexes with a diverse range of axial and equatorial ligands. Lipophilicity is measured using an efficient HPLC method. Previous models based on a subset of these data are shown to be inadequate, due to incompatibility of whole molecule descriptors between carboxylato and hydroxido ligands. Instead, the interaction surfaces of complexes with various probes are used as independent descriptors. Partial least squares modelling using three latent variables results in an accurate (R2 = 0.92) and robust model (Q2 = 0.87) of lipophilicity, that moreover highlights the importance of size and hydrophobicity terms and the modest relevance of hydrogen bonding.
    我们使用VolSurf描述符进行定量结构-性质关系(QSAR)计算,以模拟53种具有多样轴向和赤道配体的Pt(IV)配合物的亲脂性。亲脂性采用高效液相色谱(HPLC)方法进行测量。基于这些数据子集的先前模型因羧酸根与羟基配体之间的全分子描述符不兼容而被证明是不充分的。相反,我们使用配合物与各种探针的相互作用表面作为独立描述符。采用包含三个潜变量的偏最小二乘建模法,我们得到了一个准确(R² = 0.92)且稳健(Q² = 0.87)的亲脂性模型,该模型进一步突显了尺寸和合性质项的重要性以及氢键作用的适度相关性。
  • Synthesis, multinuclear magnetic resonance and crystal structures of Pt(II) complexes containing amines and bidentate carboxylate ligands
    作者:Fernande D. Rochon、Gassan Massarweh
    DOI:10.1016/j.ica.2006.04.014
    日期:2006.9
    synthetic method for the synthesis of the complexes cis-Pt(amine)2R(COO)2 is compared to two other methods involving the use of either barium dicarboxylate or sodium carboxylate. Pt(II) compounds with monodentate and bidentate amines were studied. The reaction involves the use of a silver dicarboxylato complex, which is the intermediate in the new synthetic procedure. The crystal structure of the silver intermediate
    摘要将一种新颖的合成顺式-Pt(胺)2R(COO)2配合物的合成方法与另外两种涉及使用二羧酸羧酸的合成方法进行了比较。研究了含单齿和双齿胺的Pt(II)化合物。该反应涉及使用二羧酸配合物,该配合物是新的合成方法的中间体。通过X射线衍射测定具有配体1,1-环丁烷羧酸酯(1,1-CBDCA)的中间体的晶体结构。晶体Ag2(1,1-CBDCA)具有非常有趣的3-D扩展结构。通过多核(1H,13C和195Pt)磁共振波谱研究了溶液中的顺式-Pt(胺)2R(COO)2配合物,但溶解度很低。发现D2O是最好的溶剂。在195Pt NMR中,与含有单齿胺的那些相比,在更高的视野下观察到了含有二齿胺形成五元螯合物的配合物。NH3化合物的共振也比伯胺配合物的共振场低。除1,2-CBDCA以外,所有二羧基配体均形成六元螯合物,其Pt(II)化合物在比其他化合物更低的电场下观察到。通过X射线衍射法确认了Pt(en)(1
  • A rapid method for the synthesis of water-soluble platinum(II) amine and pyridine complexes
    作者:Jean-Pierre Souchard、Franz L. Wimmer、Tam T. B. Ha、Neil P. Johnson
    DOI:10.1039/dt9900000307
    日期:——
    Seventeen cis-[Pt(am)2(ONO2)2] complexes (am = methylamine, cycloalkylamines, substituted pyridines, aniline, or benzylamine; 2am = 2,2′-bipyridyl) were synthesized by reaction of cis-[Pt(am)2l2] with silver nitrate in acetone. The reaction was rapid (5–20 min at room temperature) with a yield of about 85%. The complexes appear to be stable in acetone with respect to isomerization. Thus, after 1 h
    十七顺- [PTAM)2(ONO 2)2 ]配合物(AM =甲胺,环烷基,取代的吡啶苯胺苄胺或;上午02点= 2,2'-联吡啶),通过反应合成顺式- [AM)2 l 2 ],用硝酸银丙酮溶液。反应迅速(室温下5–20分钟),产率约85%。相对于异构化,该络合物在丙酮中似乎是稳定的。因此,在25°C下1小时后,顺式-[PTAM)2 X 2 ](AM =环己胺或4-甲基吡啶; X = I或ONO 2)的丙酮溶液显示1没有判断异构化。这些化合物及其相应的反式异构体的1 H nmr光谱。
  • Synthesis and NMR characterization of the novel mixed-ligands Pt(II) complexes Pt(amine)(pyrimidine)X2 and trans,trans-X2(amine)Pt(μ-pyrimidine)Pt(amine)X2 (X=I and Cl)
    作者:Fernande D. Rochon、Hyem Titouna
    DOI:10.1016/j.ica.2009.12.010
    日期:2010.5
    Pt(amine)(pm)I 2 , (pm = pyrimidine) were synthesized and characterized by IR spectroscopy and by multinuclear ( 195 Pt, 1 H and 13 C) magnetic resonance spectroscopy. The cis compounds were prepared from the reaction of I(amine)Pt(μ-I) 2 Pt(amine)I with pyrimidine (1:2 proportion) in water, while the trans isomers were synthesized from the isomerization of the cis complexes in acetone. The cis isomers
    摘要合成了Pt(胺)(pm)I 2(pm =嘧啶)型混合配体配合物,并通过红外光谱和多核(195 Pt,1 H和13 C)磁共振波谱进行了表征。顺式化合物是由I(胺)Pt(μ-I)2 Pt(胺)I与嘧啶(1:2的比例)在中反应制得的,而反式异构体是由顺式配合物在中的异构化反应合成的。丙酮。顺式异构体不能用几种胺,尤其是较笨重的胺来分离。在1 H NMR中,发现顺式化合物的嘧啶质子比反式类似物的场低,并且J(195 Pt– 1 H)耦合常数在顺式几何中稍大。对于正丁胺,反应还产生了I 2(正丁胺)Pt(μ-pm)Pt(正丁胺)I 2。这样的二聚体不能与其他胺分离。还使用过量的嘧啶由离子络合物K [Pt(胺)Cl 3]制备了化合物Pt(胺)(pm)Cl 2(胺=甲胺叔丁胺)。IR和NMR表征表明,甲胺化合物为顺式-反式混合物,而只有叔-丁胺分离出反式异构体。当以2:1的Pt:pm比率进行相同的反应时,分离出Cl
  • Iodo-bridged complexes of platinum(II) and synthesis of <i>cis</i> mixed-amine platinum(II) compounds
    作者:F. D. Rochon、P. C. Kong
    DOI:10.1139/v86-312
    日期:1986.9.1

    Iodo-bridged platinum(II) dimers, [Pt(L)I2]2 with ligands (L) containing nitrogen as the donor atom, have been synthesized from the reactions of cis-[Pt(L)2I2] with perchloric acid. The dimers can be cleaved in aqueous media by a second nitrogen ligand to produce isometrically pure cis-[Pt(L)(L′)I2].These compounds can finally be converted to the chloro or carboxylato compounds by precipitating the iodo ligands with a silver salt and adding KCl or a carboxylate salt. Several compounds of the types cis-[Pt(L)(L′)Cl2] and cis-[Pt(L)(L′)(dicarboxylate)] were thus prepared. A few dimers of the type [(L)(L′)Pt(tetra-carboxylate)Pt(L)(L′)] were also synthesized.

    桥联的(II)二聚体,[Pt(L)I2]2,其中配体(L)含有氮作为供体原子,已经通过顺式-[Pt(L)2I2]与高氯酸反应合成。这些二聚体可以在介质中通过第二个氮配体裂解,产生等摩尔的顺式-[Pt(L)(L′)I2]。这些化合物最终可以通过用盐沉淀配体并加入KCl或羧酸盐来转化为羧酸酯化合物。因此,几种类型的化合物 cis-[Pt(L)(L′)Cl2] 和 cis-[Pt(L)(L′)(二羧酸盐)] 被制备出来。还合成了几种类型的二聚体 [(L)(L′)Pt(四羧酸盐)Pt(L)(L′)]。
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