Electron transfer reactions chemiluminescence

Exchange Electron Transfer Reactions Chemiluminescent and Electrogenerated Chemilum... 

Chain processes, free radical, in aliphatic systems involving an electron transfer reaction, 23,271 Charge density-NMR chemical shift correlation in organic ions, 11,125 Chemically induced dynamic nuclear spin polarization and its applications, 10, 53 Chemiluminescence of organic compounds, 18,187... 

Special review articles published since 1968 on these topics are one by E. H. White and D. F. Roswell 2> on hydrazide chemiluminescence M. M. Rauhut 3) on the chemiluminescence of concerted peroxide-decomposition reactions and D. M. Hercules 4 5> on chemiluminescence from electron-transfer reactions. The rapid development in these special fields justifies a further attempt to depict the current status. Results of bioluminescence research will not be included in this article except for a few special cases, e.g. enzyme-catalyzed chemiluminescence of luminol, and firefly bioluminescence 6>. 

Chemiluminescence is defined as the production of light by chemical reactions. This light is cold , which means that it is not caused by vibrations of atoms and/or molecules involved in the reaction but by direct transformation of chemical into electronic energy. For earlier discussions of this problem, see 7 9h Recent approaches towards a general theory of chemiluminescence are based on the relatively simple electron-transfer reactions occurring in aromatic radical-ion chemiluminescence reactions 10> and on considerations of molecular orbital symmetry as applied to 1.2-dioxetane derivatives, which very probably play a key role in a large number of organic chemiluminescence reactions 11>. 

R. A. Marcus for simple electron-transfer reactions 10> which, in appropriate modification, appears to be theoretically valid for more complex chemiluminescence reactions, too (e.g. 13>. 

In complex organic molecules calculations of the geometry of excited states and hence predictions of chemiluminescent reactions are very difficult however, as is well known, in polycyclic aromatic hydrocarbons there are relatively small differences in the configurations of the ground state and the excited state. Moreover, the chemiluminescence produced by the reaction of aromatic hydrocarbon radical anions and radical cations is due to simple one-electron transfer reactions, especially in cases where both radical ions are derived from the same aromatic hydrocarbon, as in the reaction between 9.10-diphenyl anthracene radical cation and anion. More complex are radical ion chemiluminescence reactions involving radical ions of different parent compounds, such as the couple naphthalene radical anion/Wurster s blue (see Section VIII. B.). 

The importance of radical ions and electron-transfer reactions has been pointed out in the preceding sections (see also p. 128). Thus, in linear hydrazide chemiluminescence (p. 103) or acridine aldehyde or ketone chemiluminescence, the excitation steps consist in an electron transfer from a donor of appropriate reduction potential to an acceptor in such a way that the electron first occupies the lowest antibonding orbital, as in the reaction of 9-anthranoyl peroxide 96 with naphthalene radical anion 97 142> ... 

R. Bezman and L. R. Faulkner 189> developed methods for defining a concise set of parameters which quantitatively describe the efficiencies of chemiluminescent electron-transfer reactions (see Section VIII. A.) by means of analysis of chemiluminescence decay curves. 

A.J. Bard, University of Texas The fact that one can generate chemiluminescence in polymer films containing Ru-(bpy)3 2 implies that the excited state may not be quenched completely by electron transfer reactions. Are the photoreactions you describe thermodynamically uphill (i.e., with chemical storage or radiant energy) or are they photocatalytic ... 

Electrochemiluminescence Emission occurring in solution, from an electronically excited state produced by high-energy electron transfer reactions Electrogenerated chemiluminescence Emission produced at an electrode surface Oxyluminescence Emission from polymers caused by oxidative processes (presence of oxygen is required)... 

Electrogenerated chemiluminescence (ECL) is the process whereby a chemiluminescence emission is produced directly, or indirectly, as a result of electrochemical reactions. It is also commonly known as electrochemiluminescence and electroluminescence. In general, electrically generated reactants diffuse from one or more electrodes, and undergo high-energy electron transfer reactions either with one another or with chemicals in the bulk solution. This process yields excited-state molecules, which produce a chemiluminescent emission in the vicinity of the electrode surface. 

Much of the study of ECL reactions has centered on two areas electron transfer reactions between certain transition metal complexes, and radical ion-annihilation reactions between polyaromatic hydrocarbons. ECL also encompasses the electrochemical generation of conventional chemiluminescence (CL) reactions, such as the electrochemical oxidation of luminol. Cathodic luminescence from oxide-covered valve metal electrodes is also termed ECL in the literature, and has found applications in analytical chemistry. Hence this type of ECL will also be covered here. 

The assumptions, equations and several applications of a recently formulated theory of electron transfer reactions of solvated electrons are outlined. The relationship of the reorganization terms to those of ordinary electron exchange and electrochemical reactions is described, together with the role played by an effective standard free energy of reaction. Applications include prediction of conditions under which chemiluminescence might be found and description of conditions under which reactions might not be diffusion-controlled. 

In a series of papers between 1956 and 1965, Marcus solved much of the mystery by outlining a description of the probability of fluctuations in the geometry of reactants and their solvents. These fluctuations lead to changes in the energy barriers that the reactants must surmount before an electron can be transferred from one molecule to another. Marcus extended the theory to other systems, such as electrochemical rate constants at electrodes, and to chemiluminescent electron transfer reactions. The by-now famous inverted effect is a consequence of his theory after a certain point, adding more energy to an electron transfer reaction actually slows the process. Scientists believe photosynthesis can occur because of the inverted effect. 

A theoretical treatment of chemiluminescent reactions has been presented by Marcus (1965, 1970). Although developed for electron-transfer reactions, this treatment appears to be applicable to other chemiluminescent reactions when... 

The second general mechanism for chemical light formation is one-electron transfer (Faulkner, 1976 Faulkner, 1978 Hercules, 1969). The simplest of bimolecular reactions, energetic electron-transfer reactions possess several additional characteristics which make them intuitively perhaps the most reasonable choice for a general mechanistic class of chemiluminescent reactions. 

The electron-transfer chemiexcitation is shown schematically in molecular orbital terms in Fig. 2. Although other electron-transfer reactions are potentially chemiluminescent (Tokel-Takvoryan et al., 1973), the charge annihilation reaction of oppositely charged aromatic radical ions is the prototypical case and has been most extensively studied. This is due to the convenient preparation of the radical ions by electrochemical means, the large range of redox potentials which are available, and the high fluorescence... 

Elect regenerated chemiluminescence (ECL) — (-> electrochemiluminescence or electrochemically generated chemiluminescence) The generation of light in an electrochemical cell by an energetic electron transfer reaction, often between radical ions in an aprotic solvent. In a typical experiment in a solution of rubrene (R) and N,N,N, N -tetramethyl-p-phenylenediamine (TMPD) in dimethylformamide initially radical anions of rubrene are formed by electroreduction... 

CIEEL (Chemically initiated Electron Exchange Luminescence) A type of luminescence resulting from a thermal electron-transfer reaction. Also called catalyzed chemiluminescence. 

Recently,the electron-transfer theory was extended in order to incorporate the slow and reversible chemically induced electron-exchange reactions, as observed for the fluorescer-catalyzed chemiluminescent decomposition of a-peroxylactones. It was argued that electron transfer is complete in the transition state for such a slow and irreversible endergonic electron-transfer reaction, but that the typically small slopes (— a/RT where a is about 0.3) of the In (intensity) vs. oxidation potential plot was due to the fact that only a fraction (a) of the total free-energy change manifests itself in the activation energy. 

As mentioned above, the formation of excited states in chemical reactions may be understood in the context of an electron transfer model for chemiluminescence, first proposed by Marcus [2]. According to this model the formation of excited states is competitive with the formation of the ground state, even though the latter is strongly favored thermodynamically. Thus, understanding the factors that determine the electron transfer rate is of considerable importance. The theory of electron transfer reactions in solution has been summarized and reviewed in many reviews (e.g., [30-36]). Therefore, in this chapter the relevant ideas and equations are only briefly summarized, to serve as a basis for description of the ECL experiments. 

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