Abstract
The cyclopalladated [Pd(C6)Cl]2 and [Pd(C6)En]PF6 complexes based on Coumarin 6 are studied by 1H NMR spectroscopy and electronic absorption and emission spectroscopy. It is shown that cyclopalladation leads both to a long-wavelength shift of the spin-allowed intraligand absorption bands of coumarin and to the formation of a characteristic metal-ligand absorption band. It is found that, in comparison with coumarin, the complexes are characterized by a bathochromic shift and by a decrease in the fluorescence quantum yield due to more efficient intersystem crossing to the lower excited triplet state responsible for the low-temperature (77 K) phosphorescence of the complexes.
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Original Russian Text © O.A. Rodionova, M.V. Puzyk, K.P. Balashev, 2008, published in Optika i Spektroskopiya, 2008, Vol. 105, No. 1, pp. 70–74.
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Rodionova, O.A., Puzyk, M.V. & Balashev, K.P. Effect of cyclopalladation on the spectroscopic properties of a Coumarin dye. Opt. Spectrosc. 105, 62–66 (2008). https://doi.org/10.1134/S0030400X08070102
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DOI: https://doi.org/10.1134/S0030400X08070102