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Ir(2-phenylpyridinato)(PPh3)2(H)(Cl) | 1042659-29-9

中文名称
——
中文别名
——
英文名称
Ir(2-phenylpyridinato)(PPh3)2(H)(Cl)
英文别名
Ir(ppy)(PPh3)2(H)(Cl);chloro(hydrido)(2-phenylpyridinato)bis(triphenylphosphine)iridium(III)
Ir(2-phenylpyridinato)(PPh<sub>3</sub>)<sub>2</sub>(H)(Cl)化学式
CAS
1042659-29-9
化学式
C47H39ClIrNP2
mdl
——
分子量
907.454
InChiKey
OCIMPODQSWGZLR-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

  • 作为产物:
    描述:
    2-苯基吡啶sodium carbonate 作用下, 反应 3.0h, 以65%的产率得到Ir(2-phenylpyridinato)(PPh3)2(H)(Cl)
    参考文献:
    名称:
    在环金属化铱(iii)配合物的通用框架中轻松调节聚集诱导的发射波长:细胞成像中的胶束封装探针†
    摘要:
    开发了一个简单的包括两个步骤的合成方案,用于合成一系列单环金属化铱(III)配合物。最初,中间,[IrHCl [(ø -C 6 ħ 3 X)P(AR)X -(PAR X - [R ÿ)2 ] [ A(I,J,K,L)],六配铱(III)分离出涉及4元螯合物的复合物。然后,将其转化为单环金属化铱(III)络合物[[(C ^ N)Ir(PAr x -1 R y)2(Cl(H)](1–12),用5元环金属盐代替4元螯合物。通过FTIR,1 H,13 C和31 P NMR光谱学对中间体和配合物进行结构表征。对于Ir(八面体配位III)在2,8和9通过单晶X射线衍射确定。光物理实验和量子化学计算揭示了所有这些在固态中发出亮光的配合物的最低激发态的混合LC / MLCT / LLCT性质。通过发色环金属盐和非发色芳基膦配体的适当组合,可以在整个可见光范围内对发射波长进行微调。更有趣的是,所有研究的复合
    DOI:
    10.1039/c4tc00466c
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文献信息

  • One-pot synthesis of strong solid state emitting mono-cyclometalated iridium(iii) complexes: study of their aggregation induced enhanced phosphorescence
    作者:Parvej Alam、Maheswararao Karanam、Angshuman Roy Choudhury、Inamur Rahaman Laskar
    DOI:10.1039/c2dt30771e
    日期:——
    solid-state greenish-blue emitting, mono-cyclometalated iridium complexes, [Ir(ppy)(PPh3)2(H)(Cl)], 2a and [Ir(F2ppy)(PPh3)2(H)(Cl)], 2b [ppyH = 2-phenylpyridine; F2ppyH = 2-(2′,4′-difluoro)phenylpyridine], have been synthesized by a convenient route. The ‘aggregation induced enhanced phosphorescence (AIEP)’ activity exhibited by these complexes has been rationalized.
    发出强固态绿蓝光的单环属化络合物[Ir(ppy)(PPh 3)2(H)(Cl)],2a和[Ir(F 2 ppy)(PPh 3)2(H) (Cl)],2b [ppyH =2-苯基吡啶; F 2 ppyH = 2-(2',4'-二)苯基吡啶]是通过方便的途径合成的。这些配合物表现出的“聚集诱导的增强的光(AIEP)”活性已得到合理化。
  • Induced Aggregation of AIE-Active Mono-Cyclometalated Ir(III) Complex into Supramolecular Branched Wires for Light-Emitting Diodes
    作者:Subrata Maji、Parvej Alam、Gundam Sandeep Kumar、Sandip Biswas、Piyush Kanti Sarkar、Bidisa Das、Ishita Rehman、Benu Brata Das、Nikhil Ranjan Jana、Inamur Rahaman Laskar、Somobrata Acharya
    DOI:10.1002/smll.201603780
    日期:2017.4
    Aggregationinduced emission (AIE) is commonly observed in irregular bulk form. Herein, unique aggregation properties of an AIE‐active complex into branched supramolecular wires are reported for the first time. Mono‐cyclometalated Ir(III) complex shows in‐plane J‐aggregation at the air–water interface owing to the restriction of intramolecular vibration of bidentate phenylpyridinato and intramolecular
    聚集诱导发射 (AIE) 通常以不规则的块状形式观察到。在此,首次报道了 AIE 活性复合物独特的聚集特性成支链超分子线。由于双齿苯基吡啶的分子内振动和单齿三苯基膦配体在空气-界面的分子内旋转受到限制,单环属化 Ir(III) 配合物在空气-界面显示出面内 J 聚集。结果,从超分子线的单层获得了与固态相当的发光的大增强。这种独特的特性可用于使用超分子线作为有源层来制造具有低阈值电压的发光二极管。
  • Ligand Effects on Luminescence of New Type Blue Light-Emitting Mono(2-phenylpyridinato)iridium(III) Complexes
    作者:Min-Sik Eum、Chong Shik Chin、Song yi Kim、Choongil Kim、Sung Kwon Kang、Nam Hwi Hur、Ji Hoon Seo、Gu Young Kim、Young Kwan Kim
    DOI:10.1021/ic800376e
    日期:2008.7.1
    Newly prepared hydrido iridium(III) complexes [Ir(ppy)(PPh3)(2)(H)L](0,+) (ppy = bidentate 2-phenylpyridinato anionic ligand; L = MeCN (1b), CO (1c), CN- (1d); H being trans to the nitrogen of ppy ligand) emit blue light at the emission lambda(max) (452-457, 483-487 nm) significantly shorter than those (468, 495 nm) of the chloro complex Ir(ppy)(PPh3)(2)(H)(Cl) (1a). Replacing ppy of 1a-d with F(2)ppy (2,4-difluoro-2-phenylpyridinato anion) and F(2)Meppy (2,4-difluoro-2-phenyl-m-methylpyridinato anion) brings further blue-shifts down to the emission lambda(max) at 439-441 and 465-467 nm with CIE color coordinates being x = 0.16 and y = 0.18-0.20 to display a deep-blue photoemission. No significant blue shift is observed by replacing PPh3 of 1a with PPh2Me to produce Ir(ppy)(PPh2Me)(2)(H)(Cl) (1aPPh(2)Me), which displays emission lambda(max) at 467 and 494 nm. The chloro complexes, [Ir(ppy)(PPh3)(2)(Cl)(L)](0,+) (L = MeCN (2b), CO (2c), CN- (2d)) having a chlorine ligand trans to the nitrogen of ppy also emit deep-blue light at emission lambda(max) 452-457 and 482-487 nm.
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