Ligand emission

In a subsequent investigation, the luminescence properties of Pd(ppy)2 have been compared with those of the isomeric Pd(bphXbpy) complex [76]. The structured emission of Pd(bphXbpy) is red shifted from the free ligand emission of 1900cm-1 and exhibits a radiative lifetime of 10-3s. This situation does not allow a clear-cut assignment and points again towards a LC-MLCT mixture [76]. 

Photoexcited fluorescence from spread monolayers may be studied [158,159] if the substance has both a strong absorption band and a high emission yield as in the case for chlorophyll [159]. Gaines and co-workers [160] have reported on the emission from monolayers of Ru(bipyridine)3, one of the pyridine ligands having attached C g aliphatic chains. Ruorescence depolarization provides information about the restriction of rotational diffusion of molecules in a monolayer [161], Combining pressure-area... 

The concentration of aluminum in serum can be determined by adding 2-hydroxy-1-naphthaldehyde p-methoxybenzoyl-hydrazone and measuring the initial rate of the resulting complexation reaction under pseudo-first-order conditions.The rate of reaction is monitored by the fluorescence of the metal-ligand complex. Initial rates, with units of emission intensity per second, were measured for a set of standard solutions, yielding the following results... 

Hahde complexes of Cu with nitrogen base ligands are known to exhibit another form of reversible spectral change known as fluorescence thermochromism. The example of Cu4l4(Py)4 from Table 1 is typical and shows red shifting ia the visible emission spectmm while the sample is both cooled and irradiated with a 364 nm ultraviolet source (7). 

Metal-centered emission is found in several rare-earth complexes, for example europium diketone chelates [29]. These compounds emit relatively narrow spectra associated with the d-f transitions of the metal ion. Relatively few comprehensive studies of this class have been carried out to date, but the available evidence [30] seems to indicate that the photoluminescent efficiencies are somewhat lower than the ligand-centered emitters. 

Basis. The rotational mobility of a small ligand is relatively unrestricted in solution (anisotropy approaches 0). The mobility is restricted when the ligand binds to a large immobilized molecule such as the receptor. In a T-format fluorometer, the parallel and perpendicular components of the emission can be examined simultaneously. While precautions must be exercised in working with turbid suspensions, it is nonetheless practical to make continuous measurements of binding and dissociation. 

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