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[trans-Pt(C6F5)2(phenylethynyl)2Cd(2,2'-bipyridine)2] | 1159374-07-8

中文名称
——
中文别名
——
英文名称
[trans-Pt(C6F5)2(phenylethynyl)2Cd(2,2'-bipyridine)2]
英文别名
——
[trans-Pt(C6F5)2(phenylethynyl)2Cd(2,2'-bipyridine)2]化学式
CAS
1159374-07-8
化学式
C48H26CdF10N4Pt
mdl
——
分子量
1156.24
InChiKey
XXKJFNBEEQJFGP-UHFFFAOYSA-N
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

反应信息

  • 作为产物:
    描述:
    2,2'-联吡啶cadmium(II) perchlorate hexahydrate 、 (tetrabutylammonium)2[trans-Pt(pentafluorophenyl)2(C*C-Ph)2] 以 丙酮 为溶剂, 以62%的产率得到[trans-Pt(C6F5)2(phenylethynyl)2Cd(2,2'-bipyridine)2]
    参考文献:
    名称:
    Self-Assembly of Luminescent Alkynyl-Based Platinum−Cadmium Complexes Containing Auxiliary Diimine or Terpyridine Ligands.
    摘要:
    Reaction of different "Cd(N-N)(2)(2+n), (N-N = bpy, dmby, phen) or "Cd(trpy)(2+") fragments with cis- or trans- (5) dianionic bis(alkynyl)platinate substrates [Pt(C6F5)(2)(C CR)(2)](2-) (R = Ph a, Tol b) leads to the generation of novel bimetallic neutral Platinum-Cadmium derivatives, which show photoluminescence (PL) strongly influenced by the structure and the media. In complexes [cis-Pt(C6F5)(2)(C CR)(2)Cd(N-N)(2)] (N-N = bpy (1), dmbpy (2), phen (3)), the dianionic cis-bis (alkynyl)platinate fragment interacts with the "Cd(N-N)(2)(+2n) unit mainly through both the C-alpha atoms (d(Cd-C-alpha) = 2.417 (5)-2.554(5) angstrom) and the Pt center (d(Pt-Cd) similar to 3.10 angstrom); while in complexes [cis-Pt(C6F5)(2)(C CR)(2)Cd(trpy)] (4), probably because of the presence of only three Cd-N bonds, the Pt-Cd interaction is enhanced (d(Pt-Cd) similar to 3.00 angstrom), the Cd(II) atom being additionally solvated with acetone or H2O. By contrast, in complexes [trans-Pt-(C6F5)(2)(C CR)(2)Cd(bpy)(2)] (6) the Cd center is found to be in a distorted trigonal-bipyramid coordination, interacting with one of the Pt-C-alpha bonds of the platina-bis(alkynyl) unit with very short Cd-C-alpha (2.376(10) angstrom) and Pt-Cd (2.8931 (6) angstrom) bond distances. Bimetallic complexes 1-4, having cis-configured platinum fragments, exhibit, in solid state, blue and/or green phosphorescence with contribution of close emissive states of different natures: metal (Pt, Cd) perturbed pi pi* intraligand (alkynyl, polyimine) manifolds mixed, to a greater (trpy complexes 4) or lesser extent, with (Pt-Cd) charge transfer (MM'CT). In glassy state (2-MeTHF, 77 K), complexes 1b-4b exhibit structured emissions mainly ascribed to (diimine 1b-3b, trpy 4b) (3)pi pi phosphorescence, likely mixed with some ligand (alkyne) to ligand (imine) charge transfer (3LL'CT). Complexes 6 are not emissive in solid state at room temperature. At 77 K they display a high energy (IL)-I-3/(MLCT)-M-3 (L = C CR) blue-shifted emission relative to 5 and, in the case of 6b, an additional low energy feature, tentatively ascribed to pi pi stacking interactions, in accordance with the presence of very short pi center dot center dot center dot pi contacts (3.25 angstrom) found in the extended lattice of 6b.
    DOI:
    10.1021/ic9002109
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