课题基金 / 基金详情

Achieving NIR circularly polarized luminescence (CPL) by triad change of d10 systems

Achieving NIR circularly polarized luminescence (CPL) by triad change of d10 systems
通过 d10 系统的三元组变化实现近红外圆偏振发光 (CPL)
批准号:
495031819
负责人:
Professorin Dr. Christel M. Marian
金额:
$0.0万
依托单位国家:
德国
项目类别:
Priority Programmes
财政年份:
--
资助国家:
德国
项目状态:
未结题
起止时间:

项目摘要

项目成果

Professorin Dr. Christel M. Marian的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Chiral photoactive compounds that exhibit circularly polarized luminescence (CPL) in the near-IR (λem > 700 nm) from triplet excited states have the potential to greatly influence the development of possibly game-changing technologies, such as quantum computing and cryptography, spintronics, and biosensors. The challenges to design molecular systems suitable for such applications based on electroluminescence are manifold, with a particularly intriguing intellectual dilemma related to the mutually exclusive prerequisites for simultaneously high luminescence efficiency and high dissymmetry of left and right polarized emission. Molecular low-energy emitters typically suffer significantly from non-radiative decay according to the energy gap law, and thus high radiative rate constants k(r) (i.e. high electric transition dipole moments) are mandatory to outcompete k(nr). However, CPL with a high dissymmetry factor g(lum) requires a large magnetic transition dipole moment, that is detrimental to k(r). Thus, a very fine balance needs to be found between these two properties to efficiently harvest triplet states in the NIR for chiroptical applications. While d10 metal complexes of group 11 typically exhibit LLCT/MLCT excited states, group 12 compounds are dominated by LLCT/LMCT electronic structures and it has been found that there are severe limitations to achieve NIR emission with high k(r). In contrast, group 10 complexes bearing strongly donating ligands benefit from high oxidation potentials, allowing for very low energy MLCT states with high spin-orbit coupling. Thus, within this collaborative project, we aim to combine our expertise in the fields of synthetic chemistry, spectroscopy and theoretical chemistry to construct chiral highly efficient (Ni0/Pd0/Pt0) luminophores in linear and trigonal coordination geometries, of which the dissymmetry of the triplet state emission is fine-tuned by the ligand environment. Suitable candidate compounds will be tested in proof-of-concept applications such as NIR-CPL-OLEDs or non-classical single-photon sources.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Exploration of Zn(II) complexes for efficient phosphorescence and TADF
  • 批准号:
    404381916
  • 项目类别:
    Priority Programmes
  • 资助金额:
    $0.0万
  • 财政年份:
    2018
  • 负责人:
    Professorin Dr. Christel M. Marian
  • 依托单位:
Understanding Thermally Activated Delayed Fluorescence in Cu(I) Complexes and Metal-Free Donor-Acceptor Systems: A Quantum Chemical Approach
  • 批准号:
    323603989
  • 项目类别:
    Research Grants
  • 资助金额:
    $0.0万
  • 财政年份:
    2016
  • 负责人:
    Professorin Dr. Christel M. Marian
  • 依托单位:
Design and Parameterization of a DFT/MRCI Hamiltonian for Radicals with Odd Numbers of Electrons
  • 批准号:
    245515727
  • 项目类别:
    Research Grants
  • 资助金额:
    $0.0万
  • 财政年份:
    2013
  • 负责人:
    Professorin Dr. Christel M. Marian
  • 依托单位:
Mechanisms of light-induced triplet activation: MELITA
  • 批准号:
    194304672
  • 项目类别:
    Research Grants
  • 资助金额:
    $0.0万
  • 财政年份:
    2011
  • 负责人:
    Professorin Dr. Christel M. Marian
  • 依托单位:
国内基金
海外基金
青蒿琥酯协同TROP2/线粒体级联靶向的NIR-II多模态诊疗用于晚期TNBC精准诊断与治疗的机制研究
  • 批准号:
    2026JJ30126
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
    杨沙
  • 依托单位:
基于NIR光热/超声压电协同效应构建多功能水凝胶支架在皮肤黑色素瘤相关创面愈合中的作用和机制研究
  • 批准号:
    2026JJ81814
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
    李敏
  • 依托单位:
医工融合策略下的新型NIR-II有机探针用于中晚期肝癌精准诊断与协同治疗
  • 批准号:
    2026JJ30093
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
    陈国栋
  • 依托单位:
用于肺纤维化实时动态监测的NIR-II稀土纳米探针研究
  • 批准号:
    JCZRLH202600246
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
  • 依托单位: