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While I agree with the conclusion the authors have made, it will be instructive to the reader if the authors can acquire lifetime and quantum yield data that correspond to direct excitation. Where direct excitation is distinct from ligand absorption (e.g., at ~ 525-540 nm), a mono-exponential decay and low quantum yield should be obtained. Where direct excitation is merged with ligand absorption at its tail red end (e.g., at ~ 450-470 nm for compounds 1 and 2), a bi-exponential decay and high quantum yield should be obtained.

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