cadmium diisopropyldithiocarbamate

• 分子结构分类: 有机化合物 - 有机盐 - 有机金属盐
• 英文名称: cadmium diisopropyldithiocarbamate
• 英文别名: Cd2(N,N-di-iso-propyldithiocarbamate)4；[Cd2(S2CN(iso-C3H7)2)4]
• 化学式: 4C₇H₁₄NS₂*2Cd
• 分子量: 930.127
• InChiKey: OFDUBVGCWAWQHM-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  1.93
• 重原子数：
  11.0
• 可旋转键数：
  2.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  3.24
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  cadmium diisopropyldithiocarbamate 以 乙腈 为溶剂， 生成 cadmium di(isopropyl)dithiocarbamate
  参考文献：
  名称：

  A binuclear cadmium(II) complex: bis[bis(N,N-diisopropyldithiocarbamato)cadmium(II)]

  摘要：

  The title compound, bis[mu-(N, N-diisopropyldithiocarbamato)-S,S':S][bis(N,N-diisopropyldithiocarbamato-S,S')-cadmium(II)], [Cd-2(C7H14NS2)(4)], a binuclear complex, consists of two bis(N, N-diisopropyldithiocarbamato)-cadmium complex units bridged by Cd-S bonds. Each Cd-II atom has a distorted tetragonal pyramidal environment and the inversion-related complex forms an edge-shared tetragonal pyramidal geometry with a Cd Cd distance of 3.6049 (6) Angstrom.

  DOI：

  10.1107/s0108270198012062
• 作为产物：
  描述：

  cadmium(II) perchlorate hexahydrate 、 sodium di-iso-propyldithiocarbamate trihydrate 以 not given 为溶剂， 生成 cadmium diisopropyldithiocarbamate
  参考文献：
  名称：

  使用二硫代氨基甲酸镉（II）从溶液中固定金（III）的方式。多核和杂多核金（III）配合物的制备，超分子结构和热行为：双（N，N-二烷基二硫代氨基甲酸酯-S，S '）金（III）多氯金属金属盐，[Au（S 2 CNR 2）2 ] n X（n  = 1：X = [AuCl 4 ] -；n  = 2：X = [CdCl 4 ] 2−，[Cd 2 Cl 6 ] 2−）

  摘要：

  通式[Au（S 2 CNR 2）2 ] 2 X（X = [CdCl 4 ] 2−，R = CH 3（1）; X = [Cd 2 Cl 6 ] 2−的四种新颖的杂多核和多核配合物，R = C 3 H 7（2））和[Au（S 2 CNR 2）2 ] [AuCl 4 ]（R = 异-C 3 H 7（3）； R = 异-C 4 H 9（4））是使用适当新鲜沉淀的双核二烷基二硫代氨基甲酸镉（II）与AuCl 3在2 M盐酸中的非均相反应制备的。通过13 C CP / MAS NMR光谱，单晶X射线衍射和氩气气氛下的同时热分析（STA）对分离的配合物进行了研究。在所有的分子结构（1 - 4），金原子坐标之一在两个二烷基二配体小号，小号'-bidentate模式，形成一个正方形平面协调多边形[AUS 4 ]，而其他金原子（在3和4）具有四个相邻的氯原子[AuCl 4 ]。在超分子水平上，化合物1和2包含双核阳离子[Au

  DOI：

  10.1016/j.poly.2012.03.043

文献信息

• Gold(III) preconcentration from acid solutions by cadmium diisopropyldithiocarbamate: Gold(III)-binding species, supramolecular structure, and thermal properties of the heteropolynuclear complex ([Au{S2CN(iso-C3H7)2}2]2[CdCl4] · 1/2C3H6O) n
  作者：A. V. Ivanov、S. A. Zinkin、V. I. Sergienko、A. V. Gerasimenko、A. S. Zaeva、O. V. Loseva

  DOI：10.1134/s0036023611030107

  日期：2011.3

  The reaction of binuclear cadmium diisopropyldithiocarbamate with a solution of AuCl3 in 2 M HCl was studied. The heterogeneous reaction of gold(III) binding follows a chemisorption scenario (in combination with partial ion exchange) and yields a heteropolynuclear gold(III)-cadmium complex. The molecular and crystal structure of a solvated species of the compound, namely ([AuS2CN(iso-C3H7)(2)}(2)](2)[CdCl4] center dot 1/2C(3)H(6)O) (n) (I), was solved by X-ray crystallography. The structure of complex I contains (in the ratio 1: 1) structurally nonequivalent molecular cations [AuS2CN(iso-C3H7)(2)}(2)](+); the differences between these cations allow them to be classified as conformational isomers (cations A and B). The specifics of the supramolecular organization of complex I consist of the alternation of layers of [Au-2S2CN(iso-C3H7)(2)}(4)](2+) binuclear cations (formed by cations A), ([AuS2CN(iso-C3H7)(2)}(2)](+)) (n) polymer chains (formed by cations B), and [CdCl4](2-) anions. The chemisorption capacity of the precursor cadmium diisopropyldithiocarbamate as calculated from the gold(III) binding reaction is 423.5 mg Au3+ per gram of sorbent. The thermal properties of complex I were studied by simultaneous thermal analysis (STA) in order for the parameters of sorbed gold recovery to be determined. The multistep thermal destruction process involves desorption of solvating acetone molecules, thermolysis of the dithiocarbamate part of the complex and [CdCl4](2-) with release of metallic gold and cadmium chloride and formation of CdS, as well as vaporization of CdCl2 and CdS. The only final product of thermal conversions is reduced metallic gold.
• Fixation modes of gold(III) from solutions using cadmium(II) dithiocarbamates. Preparation, supramolecular structure and thermal behaviour of polynuclear and heteropolynuclear gold(III) complexes: Bis(N,N-dialkyldithiocarbamato-S,S′)gold(III) polychlorometallates, [Au(S2CNR2)2]nX (n=1: X=[AuCl4]−; n=2: X=[CdCl4]2−, [Cd2Cl6]2−)
  作者：Tatyana A. Rodina、Alexander V. Ivanov、Andrey V. Gerasimenko、Olga V. Loseva、Oleg N. Antzutkin、Valentin I. Sergienko

  DOI：10.1016/j.poly.2012.03.043

  日期：2012.6

  single-crystal X-ray diffraction and simultaneous thermal analysis (STA) under an argon atmosphere. In all molecular structures (1–4), one of the gold atoms coordinates two dialkyldithiocarbamate ligands in the S,S′-bidentate mode, forming a square-planar coordination polygon [AuS4], while the other gold atom (in 3 and 4) has four neighbouring chlorine atoms [AuCl4]. At the supramolecular level, compounds 1 and

  通式[Au（S 2 CNR 2）2 ] 2 X（X = [CdCl 4 ] 2−，R = CH 3（1）; X = [Cd 2 Cl 6 ] 2−的四种新颖的杂多核和多核配合物，R = C 3 H 7（2））和[Au（S 2 CNR 2）2 ] [AuCl 4 ]（R = 异-C 3 H 7（3）； R = 异-C 4 H 9（4））是使用适当新鲜沉淀的双核二烷基二硫代氨基甲酸镉（II）与AuCl 3在2 M盐酸中的非均相反应制备的。通过13 C CP / MAS NMR光谱，单晶X射线衍射和氩气气氛下的同时热分析（STA）对分离的配合物进行了研究。在所有的分子结构（1 - 4），金原子坐标之一在两个二烷基二配体小号，小号'-bidentate模式，形成一个正方形平面协调多边形[AUS 4 ]，而其他金原子（在3和4）具有四个相邻的氯原子[AuCl 4 ]。在超分子水平上，化合物1和2包含双核阳离子[Au
• A binuclear cadmium(II) complex: bis[bis(<i>N,N</i>-diisopropyldithiocarbamato)cadmium(II)]
  作者：F.-F. Jian、Z.-X. Wang、H.-K. Fun、Z.-P. Bai、X.-Z. You

  DOI：10.1107/s0108270198012062

  日期：1999.2.15

  The title compound, bis[mu-(N, N-diisopropyldithiocarbamato)-S,S':S][bis(N,N-diisopropyldithiocarbamato-S,S')-cadmium(II)], [Cd-2(C7H14NS2)(4)], a binuclear complex, consists of two bis(N, N-diisopropyldithiocarbamato)-cadmium complex units bridged by Cd-S bonds. Each Cd-II atom has a distorted tetragonal pyramidal environment and the inversion-related complex forms an edge-shared tetragonal pyramidal geometry with a Cd Cd distance of 3.6049 (6) Angstrom.