Electronically activated

Noncyclic photophosphorylation has been the focus of our discussion and is represented by the scheme in Figure 22.21, where electrons activated by quanta at PSII and PSI flow from HgO to NAJDP, with concomitant establishment of the proton-motive force driving ATP synthesis. Note that in noncyclic photophosphorylation, Og is evolved and NADP is reduced. 

The effect of a carboxy group is illustrated by the reactivity of 2-bromopyridine-3- and 6-carboxylic acids (resonance and inductive activation, respectively) (cf. 166) to aqueous acid under conditions which do not give hydroxy-debromination of 2-bromopyridine and also by the hydroxy-dechlorination of 3-chloropyridine-4-car-boxylic acid. The intervention of intermolecular bifunctional autocatalysis by the carboxy group (cf. 237) is quite possible. In the amino-dechlorination (80°, 4 hr, petroleum ether) of 5-carbethoxy-4-chloropyrimidine there is opportunity for built-in solvation (167) in addition to electronic activation. This effect of the carboxylate ion, ester, and acid and its variation with charge on the nucleophile are discussed in Sections I,D,2,a, I,D,2,b, and II,B, 1. A 5-amidino group activates 2-methylsulfonylpyridine toward methanolic am-... 

Besides the classical search for linear, one-dimensional electronically active materials, synthetic approaches are now also focussed on the generation and characterization of two- and three-dimensional structures, especially shape-persistent molecules with a well-defined size and geometry on a nanometer-scale. It is therefore timely and adequate to extend concepts of materials synthesis and processing to meet the needs defined by nanochcmislry since the latter is now emerging as a subdiscipline of material sciences. 

Thus, it seems that the concept of anomeric electronic activation-deactivation at the anomeric center taking precedence over armed-disarmed in the remainder of the pyranose ring might have reasonable validity, but, in many instances, the difference in reactivity of the p-nitrophenyl thioglycoside versus the p-acetamidophenyl thioglycoside is not enough to make this work (Scheme 1l).94... 

An alternative could be steric activation-deactivation at the anomeric centers of the donor and acceptor. An example using this concept is shown in Scheme 12. In the electronic activation-deactivation concept, deactivated p-nitrophenyl thioglycosides can, after functioning as glycosyl acceptors, be transformed into... 

Whereas electronically activated 2-pyrones can react thermally in both normal and inverse electron-demand Diels-Alder cycloaddition, 2-pyrone by itself requires thermal conditions that are so vigorous that they cause spontaneous extrusion of carbon dioxide from the bicyclic cycloadduct [61]. 

As an alternative, the tendency for a reduction to occur may also be expressed in terms of a h)q)othetical electron activity based on the standard hydrogen electrode. Activity was functionally defined in Equation (9). The free energy of an electron is related to chemical activity of the electron by... 

Hostettler (1984) discusses issues involved in associating ps with electron activity. 

These pe values actually represent electron activities for a new set of half-cell reactions derived from reactions 1, 2, and 3 ... 

The COMPACT (computer-optimized molecular parametric analysis of chemical toxicity) procedure, developed by Lewis and co-workers [92], uses a form of discriminant analysis based on two descriptors, namely, molecular planarity and electronic activation energy (the difference between the energies of the highest occupied and lowest unoccupied molecular orbitals), which predict the potential of a compound to act as a substrate for one of the cytochromes P450. Lewis et al. [93] found 64% correct predictions for 100 compounds tested by the NTP for mutagenicity. 

Supported metal catalysts, M°/S, are typically two-components materials built up with a nanostructured metal component, in which the metal centre is in the zero oxidation state (M°), and with an inorganic support (S), quite various in its chemical and structural features [1], M° is the component typically deputed to the electronic activation of the reagents involved in the catalyzed reactions. S is typically a microstructured component mainly deputed to the physical support and to the dispersion of M° nanoclusters. 

Thorstenson, D. C., 1984, The concept of electron activity and its relation to redox potentials in aqueous geochemical systems. US Geological Survey Open File Report 84—072,45 p. 

The reaction can be extended to more elaborate systems as shown in the reactions of the substituted pyrrolidines (Equations (25) and (26)).85,86 Even though the 2-substituted pyrrolidine 8 has three electronically activated sites, two are sterically crowded. Furthermore, the Rh2(5-DOSP)4-catalyzed C-H insertion exhibited extreme stereodifferentiation, such that only one enantiomer of 8 was reactive under the reaction conditions. Consequently, a high level of kinetic resolution was observed, and the C-H insertion product was produced with 98% ee (Equation (25)).85 Similar reactivity was seen in the reaction of the 3-substituted pyrrolidine 9. In some regards, this reaction is even more impressive, because there was selective insertion into one of the two available methylene groups adjacent to nitrogen (Equation (26)).85... 

Based on this work, Itoh and co-workers developed ruthenium(n)-catalyzed [2 + 2 + 2]-cyclotrimerizations of 1,6-diynes 174 and electron-deficient nitriles (Equation (34)),368>368a These partially intramolecular cycloadditions proceed through ruthenacycle intermediates as well. The importance of using electronically activated nitriles is underlined by the fact that acetonitrile and benzonitrile gave only very low yields. 

In contrast to the information transduction mechanism based on conformational change, the information transduction may effectively be performed through the electron transfer if the integrated molecular systems are composed of electronically active molecules. 

The prototypes of electronically active molecules are linear conjugated chains made from olefinic and aromatic repeat units (Scheme 1). 

Many other PF copolymers, which do not contain a particularly electron-active moiety, but nevertheless, can improve the performance of the material in PLED have been synthesized. The Huang group [364,365] at Institute of Materials Research and Engineering (IMRE, Singapore) synthesized deep-blue copolymer 272 by Suzuki copolymerization of fluorene-diboronic acid with dibromobenzene. The emission band of 272 has a peak at 420 nm and a well-defined vibronic feature at 448 nm with a fwhm of 69 nm, and virtually no green emission,... 

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