42983-07-3Relevant articles and documents
Effect of ligand deuteration on the decay of Eu3+(5D0) in tris(2,2,6,6-tetramethyl-3,5-heptanedionato)europium(III)
Schwendemann, Todd C.,May, Paul S.,Berry, Mary T.,Hou, Yuqing,Meyers, Cal Y.
, p. 8690 - 8694 (1998)
Contributions to the first-order rate constant for the decay of the Eu3+(5D0) state of tris(2,2,6,6-tetramethyl-3,5-heptanedionato)europium(III), Eu(thd)3, from radiative and multiphonon mechanisms are evaluated independently by measuring the luminescence decay rates in undeuterated Eu(thd)3, fully deuterated Eu(thd-d19)3, and α-deuterated Eu(thd-d1)3, which is also designated Eu(α-D,thd)3. In the latter case, deuterium substitution is at the α-carbon, between the carbonyl groups of the β-diketonate ligand. These measurements yield a multiphonon contribution of 332 s-1, of which 157 s-1 is attributed to relaxation via the Cα-H stretching vibration and 175 s-1 to relaxation via the C-H stretching modes of the tert-butyl groups. By use of the measured total Eu3+(5D0) relaxation rate constant and the multiphonon rate constants given above, the Eu3+(5D0) radiative relaxation rate constant is inferred to be 1930 s-1. It is suggested that this unusually high radiative rate constant may be due to an increased allowedness in the 5D0 → 7FJ transitions due to contributions to the predominantly 4f crystal-field wave functions from a low-lying ligand-to-metal charge-transfer state.
Deuterated Benzene Sulfonamide Thiazole Compounds
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Paragraph 0070, (2013/03/26)
Deuterated forms of N-{3-[5-(2-Amino-4-pyrimidinyl)-2-(1,1-dimethylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide and pharmaceutical compositions containing the same.
Change in reaction pathway induced by deuteration: Thermal decomposition of neopentyl groups on Pt(111) surfaces
Janssens,Jin,Zaera
, p. 1169 - 1170 (2007/10/03)
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