4.6 Article

Accessing the Long-Lived Triplet Excited States in Transition-Metal Complexes: Molecular Design Rationales and Applications

Journal

CHEMICAL RECORD
Volume 16, Issue 1, Pages 173-188

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/tcr.201500237

Keywords

chromophores; photochemistry; sensitizers; transition metals; triplet states

Funding

  1. NSFC [21273028, 21421005, 21473020]
  2. Ministry of Education [SRFDP-20120041130005]
  3. Program for Changjiang Scholars and Innovative Research Team in University [IRT_13R06]
  4. Fundamental Research Funds for the Central Universities [DUT14ZD226]
  5. Dalian University of Technology [DUT2013TB07]

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Transition-metal complex triplet photosensitizers are versatile compounds that have been widely used in photocatalysis, photovoltaics, photodynamic therapy (PDT) and triplet-triplet annihilation (TTA) upconversion. The principal photophysical processes in these applications are the intermolecular energy transfer or electron transfer. One of the major challenges facing these triplet photosensitizers is the short triplet-state lifetime, which is detrimental to the above-mentioned photophysical processes. In order to address this challenge, transition-metal complexes showing long-lived triplet excited states are highly desired. This review article summarizes the development of this fascinating area, including the molecular design rationales, the principal photophysical properties, and the applications of these complexes in PDT and TTA upconversion.

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