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Long-lived triplet excited state in a platinum(ii) perylene monoimide complex

Journal Article · · Dalton Transactions
DOI:https://doi.org/10.1039/c8dt02496k· OSTI ID:1633630
We report here the synthesis and solution based photophysical properties of a new Pt(II)-terpyridine complex coupled to a perylene monoimide (PMI) chromophoric unit through an acetylene linkage. This structural arrangement resulted in quantitative quenching of the highly fluorescent PMI chromophore by introducing metal character into the lowest energy singlet state, thereby leading to the formation of a long-lived PMI-ligand localized triplet excited state (τ = 8.4 μs). Even though the phosphorescence from this triplet state was not observed, highly efficient quenching of this excited state by dissolved oxygen and the observation of singlet oxygen photoluminescence in the near-IR at 1270 nm initially pointed towards triplet excited state character. Furthermore, the coincidence of the excited state absorbance difference spectra from the sensitized PMI ligand using a triplet donor and the Pt-PMI complex provided strong evidence for this triplet state assignment, which was further supported by TD-DFT calculations.
Research Organization:
North Carolina State Univ., Raleigh, NC (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
Grant/Contract Number:
SC0011979
OSTI ID:
1633630
Alternate ID(s):
OSTI ID: 1476959
Journal Information:
Dalton Transactions, Journal Name: Dalton Transactions Journal Issue: 42 Vol. 47; ISSN 1477-9226; ISSN ICHBD9
Publisher:
Royal Society of ChemistryCopyright Statement
Country of Publication:
United States
Language:
English

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