[Pt(4′-(methylamino)-2,2′:6′,2″-terpyridine)Cl]PF₆ | 1448366-44-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: [Pt(4′-(methylamino)-2,2′:6′,2″-terpyridine)Cl]PF₆
• CAS: 1448366-44-6
• 化学式: C₂₄H₁₉N₄Pt*F₆P
• 分子量: 703.486
• InChiKey: FYILDBQWHSWRIU-UHFFFAOYSA-N

反应信息

• 作为产物：
  描述：

  [Pt(4′-(methylamino)-2,2′:6′,2″-terpyridine)Cl]PF₆ 、 苯乙炔 在 copper(l) iodide 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 [Pt(4′-(methylamino)-2,2′:6′,2″-terpyridine)Cl]PF₆
  参考文献：
  名称：

  π Donation and Its Effects on the Excited-State Lifetimes of Luminescent Platinum(II) Terpyridine Complexes in Solution

  摘要：

  Introducing electron-donating groups extends the excited-state lifetimes of platinum(II) terpyridine complexes in fluid solution. Such systems are of interest for a variety of applications, viz., as DNA binding agents or as components in luminescence-based devices, especially sensors. The complexes investigated here are of the form [Pt(4'-X-T)Y], where 4'-X-T denotes a 4' substituted 2,2':6',2 ''-terpyridine ligand and Y denotes the coligand. The pi-donating abilities of X and Y increase systematically in the orders NHMe < -NMe2 < (pyrrolidin-l-yl) and -CN < -Cl < -CCPh, respectively. The results presented include crystal structures of two new 4'-NHMe-T complexes of platinum, as well as absorption, emission, and excited-state Lifetime data for nine complexes. Excited-state lifetimes obtained in deoxygenated dichloromethane vary by a factor of 100, ranging from 24 mu s for [Pt(4'-pyrr-T)CN](+) to 0.24 mu s for [Pt(4'-ma-T)Cl]+, where ma-T denotes 4'(methylamino)-2,2':6',2 ''-terpyridine and pyrr-T denotes 4'-(pyrrolidin-l-y)-2,2':6',2 ''-terpyridine. Analysis of experimental and computational results shows that introducing a simple amine group on the terpyridine and/or a pi-donating coligand engenders the emitting state with intraligand charge transfer (ILCT) and/or ligand ligand charge transfer (LLCT) character. The excited state lifetime increases when the change in orbital parentage lowers the emission energy, suppresses quenching via d-d states, and encourages delocalization of the excitation onto the ligand(s). At some point, however, the energy is low enough that direct vibronic coupling to the ground-state surface becomes important, and the lifetime begins to decrease again.

  DOI：

  10.1021/ic4004643