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Bipyridines/bipyridinium derivatives

Bipyridine resembles nicotine in its pharmacological properties but is not as active. The 3,4 -bipyridine derivative 113 known as amrinone and its relatives are of interest as cardiotonic agents. 4,4 -Bipyridine has been tested as an insecticide, but it is not of practical value.It is used in the study of the electrochemistry of cytochrome c and acts as a polymerization catalyst or hardening agent for various resins. l-Hexyl-4,4 -bipyridinium salts are especially effective as electron carriers in photochemical hydrogen producing systems. l,l -Dimethyl-4,4 -bipyridinium (92 R = R = CHj) and l,l -dibenzyl-4,4 -bipyridinium... [Pg.373]

The most widely used electron acceptors in inorganic chromophore-quencher systems have been bipyridinium dications, often called viologens (quatemarized derivatives of 4,4 -bipyridine) or diquat (cyclic quatemarized derivatives of 2,2 -bipyridine). The classical studies of Elliott, Schmehl, and Mallouk have been concentrated on dyads of types (4) and (5). For dyads (4) [168, 169], oxidative PET takes place, with forward processes in the 80 to 1700-ps time scale and very fast (<30 ps) charge recombination. The main observations are that (i) electron transfer to the diquat quencher occurs from the directly linked bipyridine ligand (ii) fast equilibration between the MLCT excited states on the three bipyridine ligands precedes electron transfer (iii) the electron transfer rates are in the normal Marcus... [Pg.2037]

Fig. 27 Elecriochemical synthesis of supramolecular porphyrin arrays by nucleophilic attack of pyridine and bipyridine derivatives to porphyrin C-atoms at me o-positions leading to formation of C-N(pyridinium) bonds generating a a meio-bipiridinium OEP b a cw-few-bipyridinium OEP c a mew-pyridinium bridged feii-porphyrin d a few-bipyridinium bridged OEP multiarray and e trans-bis- yndimma (POM) bridged OEP arrays... Fig. 27 Elecriochemical synthesis of supramolecular porphyrin arrays by nucleophilic attack of pyridine and bipyridine derivatives to porphyrin C-atoms at me o-positions leading to formation of C-N(pyridinium) bonds generating a a meio-bipiridinium OEP b a cw-few-bipyridinium OEP c a mew-pyridinium bridged feii-porphyrin d a few-bipyridinium bridged OEP multiarray and e trans-bis- yndimma (POM) bridged OEP arrays...

See other pages where Bipyridines/bipyridinium derivatives is mentioned: [Pg.117]    [Pg.388]    [Pg.43]    [Pg.82]    [Pg.168]    [Pg.174]    [Pg.498]    [Pg.106]   
See also in sourсe #XX -- [ Pg.125 , Pg.239 , Pg.248 , Pg.251 , Pg.257 , Pg.258 , Pg.259 , Pg.278 , Pg.354 , Pg.412 , Pg.521 ]




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2,2 -Bipyridine derivatives

Bipyridinium

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