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PPh4[FeIII(8-(2-quinoline-2-carboxamido)quinoline)(CN)3] | 1134942-52-1

中文名称
——
中文别名
——
英文名称
PPh4[FeIII(8-(2-quinoline-2-carboxamido)quinoline)(CN)3]
英文别名
PPh4[Fe(8-(2-quinoline-2-carboxamido)quinoline)(CN)3];[PPh4][iron(III)(8-(2-quinoline-2-carboxamido)quinoline)(cyanide)3];PPh4[FeIII(qcq)(CN)3];PPh4[Fe(qcq)(CN)3];[PPh4][Fe(qcq)(CN)3]
PPh<sub>4</sub>[Fe<sup>III</sup>(8-(2-quinoline-2-carboxamido)quinoline)(CN)<sub>3</sub>]化学式
CAS
1134942-52-1
化学式
C22H12FeN6O*C24H20P
mdl
——
分子量
771.62
InChiKey
MJQKQVZWPYUNKL-UHFFFAOYSA-M
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:
    [Cu(3,10-dipropyl-1,3,5,8,10,12-hexaazacyclotetradecane)](ClO4)2PPh4[FeIII(8-(2-quinoline-2-carboxamido)quinoline)(CN)3]甲醇 为溶剂, 生成 {[Cu(3,10-dipropyl-1,3,5,8,10,12-hexaazacyclotetradecane)][mer-Fe(8-(2-quinoline-2-carboxamido)quinoline)(CN)3]2}*4.75H2O
    参考文献:
    名称:
    Low dimensional cyano-bridged heterobimetallic M–FeIII(M = NiII, CuII) complexes constructed from Mer-[FeIII(qcq)(CN)3]building blocks: syntheses, structures and magnetic properties
    摘要:
    四种氰桥杂二金属三核配合物,{[Ni(en)2][Fe(qcq)(CN)3]2}Â-2H2O (1) [en = 1,2-乙二胺;qcqâ = 8-(2-喹啉-2-甲酰胺基)喹啉阴离子],{[Ni(teta)][Fe(qcq)(CN)3]2}Â-2DMFÂ-2H2O (2) (teta = 5、5,7,12,12,14-六甲基-1,4,8,11-四氮杂环十四烷,DMF = N,N-二甲基甲酰胺),{[CuL1][Fe(qcq)(CN)3]2}Â-0.61H2O(3)(L1 = 3,10-二丁基-1,3,5,8,10,12-六氮杂环十四烷)和{[CuL2][Fe(qcq)(CN)3]2}Â-4.75H2O(4)(L2 = 3,10-二丙基-1,3,5,8,10,12-六氮杂环十四烷)进行了合成,并进行了结构和磁学表征。结构分析表明,1â4 都是三核中心对称团簇,团簇间的 ÏâÏ 相互作用和氢键将 1â4 扩展成高维超分子网络。磁学研究表明,1 和 2 表现出簇内铁磁耦合,并伴有显著的磁各向异性。与此相反,3 和 4 显示出不寻常的簇内反铁磁耦合,甚至可以在强外加磁场的作用下解耦。
    DOI:
    10.1039/c3ra45218b
  • 作为产物:
    描述:
    四苯基溴化膦K[FeIII(8-(2-quinoline-2-carboxamido)quinoline)(CN)3] 为溶剂, 以72%的产率得到PPh4[FeIII(8-(2-quinoline-2-carboxamido)quinoline)(CN)3]
    参考文献:
    名称:
    氰化桥联的Fe III -Mn III双金属配合物,由新型mer -Fe三氰化物构造而成:结构和磁性
    摘要:
    通过使Mn Schiff碱与新的分子前体(PPh 4)[Fe(qcq)(CN)3 ] [ 1 ]制备四种氰化物连接的Fe III -Mn III配合物。qcq = 8-(2-喹啉羧酰胺基)喹啉阴离子]。它们包括二聚体分子,[Fe(qcq)(CN)3 ] [Mn(3-MeOsalen)(H 2 O)]·2H 2 O [ 2 ·2H 2 O; 3-MeOsalen = N,N'-亚乙基双(3-甲氧基水杨基亚胺基)双阴离子]和三个1D锯齿形链[Fe(qcq)(CN)3 ] [Mn(5-Clsalen)]·3H 2 O [ 3 ·2MeOH ; 5-Clsalen = N,N'-亚乙基双(5-氯水杨基亚氨基)二价阴离子],[Fe(qcq)(CN)3 ] [Mn(5-Brsalen)]·2MeOH [ 4 ·2MeOH; 5-Brsalen = N,N′-亚乙基双(5-溴水杨基亚胺基二氨基)二价阴离子]和Fe(qcq)(CN)3
    DOI:
    10.1021/ic802033q
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文献信息

  • Tuning the structures of manganese(III) (Schiff base) complexes: Syntheses, crystal structures and magnetic properties
    作者:Hongbo Zhou、Yingying Wang、Xiaoping Shen、Yashu Liu、Aihua Yuan
    DOI:10.1016/j.ica.2014.07.070
    日期:2014.11
    structurally and magnetically. The results reveal that complexes 1 and 2 are mononuclear MnIII structures crystallizing in different space groups, while 3 and 4 are dinuclear MnIII–NC–FeIII entities with different local arrangement of the subunits. Interestingly, the structures of these complexes are highly dependent on the reaction conditions though the reaction precursors are the same. Magnetic investigation
    摘要四种新的配位化合物,[MnIII(3-EtO-salpn)(H2O)(CH3OH)] ClO4(1),[MnIII(3-EtO-salpn)( )2]· · (2), [MnIII(3-EtO-salpn)( )] [FeIII(qcq)(CN)3]}·3 ·CH3OH·CH3CN(3)和[MnIII(3-EtO-salpn)( )] [FeIII (qcq)(CN)3]}·3 ·CH3CN(4)(salpn = N,N'-1,2-亚丙基双(杨基亚基)双阴离子; qcq = 8-(2-喹啉-2-羧酰胺基)喹啉阴离子)合成并在结构和磁性上进行了表征。结果表明,复合物1和2是在不同空间群中结晶的单核MnIII结构,而复合物1和2是具有不同亚基局部排列的双核MnIII–NC–FeIII实体。有趣的是,尽管反应前体相同,但这些配合物的结构高度依赖于反应条件
  • Syntheses, Crystal Structures, and Magnetic Properties of Four New Cyano-Bridged Bimetallic Complexes Based on the<i>mer</i>-[Fe<sup>III</sup>(qcq)(CN)<sub>3</sub>]<sup>−</sup>Building Block
    作者:Xiaoping Shen、Hongbo Zhou、Jiahao Yan、Yanfeng Li、Hu Zhou
    DOI:10.1021/ic401753y
    日期:2014.1.6
    and [MnII(phen)2}FeIII(qcq)(CN)3}2]·CH3CN·2H2O (4) (phen = 1,10-phenanthroline) have been synthesized and characterized both structurally and magnetically. The structures of 1 and 2 are both unique 1-D linear branch chains with additional structural units of MnIII(salen/salpn)}FeIII(qcq)(CN)3} dangling on the sides. In contrast, 3 and 4 are cyano-bridged bimetallic hexanuclear and trinuclear clusters
    四个新的基桥联双属配合物[Mn III(salen)} 2 Fe III(qcq)(CN)3 } 2 ] n ·3 n CH 3 CN· n H 2 O(1)[salen = N,N′-亚乙基双(杨基亚胺基)二价阴离子; qcq – = 8-(2-喹啉-2-甲酰胺基)喹啉阴离子],[Mn III(salpn)} 2 Fe III(qcq)(CN)3 } 2 ] n ·4 n H 2 O(2)[salpn = Ñ,Ñ '-1,2-亚丙基(杨)二价阴离子],[II(联吡啶)(CH 3 OH)} 的Fe III(qcq)(CN)3 } 2 ] 2 ·2H 2 O·2CH 3 OH(3)(bipy = 2,2'-bipyridine)和[Mn II(phen)2 } Fe III(qcq)(CN)3 } 2 ]·CH 3 CN·2H 2 O (4)(phen = 1,10
  • Structures and magnetic studies of two new bimetallic chain complexes constructed by manganese(III)–(Schiff-base) and mer-tricyanidoferrate building block
    作者:Yingying Wang、Hongbo Zhou、Xiaoping Shen、Aihua Yuan
    DOI:10.1016/j.ica.2014.01.046
    日期:2014.4
    Two new cyano-bridged bimetallic complexes, [Mn-III(5-CH3)salen][Fe-III(qcq)(CN)(3)]}(n)center dot 1.85H(2)O (1) [salen = N,N'-ethylenebis(salicylideneiminato) dianion; qcq = 8-(2-quinoline-2-carboxamido)quinoline anion] and [Mn-III(acphen)][Fe-III(qcq)(CN)(3)]}(n)center dot 6.46H(2)O (2) (acphen = bis(o-hydroxyacetophenone) ethylenediiminate), have been synthesized and characterized both structurally and magnetically. The structures of 1 and 2 are both 1-D zigzag chains connected through pi center dot center dot center dot pi stacking and short contact interactions to form extended supramolecular networks. The magnetic measurements revealed the presence of antiferromagnetic Fe-III center dot center dot center dot Mn-III interactions in 1 and 2. Interestingly, weak slow magnetic relaxation was only detected for 1, indicating the intermolecular antiferromagnetic interactions in 2 are stronger than that in 1 and lead to the disappearance of the 1-D magnetic behavior. (C) 2014 Elsevier B. V. All rights reserved.
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