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Porphyrins 77—77* transitions

On the other hand, phthalocyanines and porphyrins transition metal complexes have been adsorbed on activated carbon fiber nanopouros support in the form of gas diffusion electrodes The loading of the complexes in the support involve the dissolution of the macrocycles in the proper solvent and then the addition of the (activated carbon fibers ACF). The mixtures were stirred on a magnetic stirrer for 3-4 days at room temperature and then vacuum filtered. The ACF with... [Pg.231]

George, R.G. and M.P.D.H. Padmanabhan (2003). Studies on iron(III) and man-ganese(III) derivatives of new meso-aryl substituted and brominated porphyrins. Transit Met. Chem. 28, 858-863. [Pg.463]

An Arrhenius plot of the rate constant, consisting of the three domains above, is schematically shown in fig. 45. Although the two-dimensional instanton at Tci < < for this particular model has not been calculated, having established the behavior of fc(r) at 7 > Tci and 7 <7 2, one is able to suggest a small apparent activation energy (shown by the dashed line) in this intermediate region. This consideration can be extended to more complex PES having a number of equivalent transition states, such as those of porphyrines. [Pg.108]

Construction of one-dimensional multicomponent molecular arrays, transition metal complexes with terpyridines and/or porphyrins as ligands 98EJI1. [Pg.206]

Cis, trans and metal effects in transition metal porphyrins. J. W. Buchler, W. Kokisch and P. D. Smith, Struct. Bonding (Berlin), 1978, 34, 80-134 (158). [Pg.42]

The transition state of concerted Diels-Alder reactions has stringent regio- and stereochemical requirements and can assume settled configurations if the reaction is carried out in a molecular cavity. Cyclodextrins, porphyrin derivatives and cyclophanes are the supramolecular systems that have been most investigated. [Pg.170]

Brothers, Penelope J., Organometallic Chemistry of Transition Metal Porphyrin... [Pg.465]

Buchler JW, Kokisch W, Smith PD (1978) Cis, Trans, and Metal Effects in Transition Metal Porphyrins. 34 79-134... [Pg.243]

Organometallic Chemistry of Transition Metai Porphyrin Compiexes... [Pg.223]

A particular feature of transition metal porphyrin chemistry is that the energies of the metal d orbitals and the frontier orbitals of the porphyrin ligand arc often quite close, with the result that the redox chemistry of the porphyrin ligand and the... [Pg.228]

Bis(cyclopentadienyl) complexes are central to the organometallic chemistry of the early transition metals and feature in applications such as alkene polymerization chemistry. Parallels can be drawn between a porphyrin ligand and two cyclopentadienyl ligands, in that they both contribute a 2— formal charge and exert a considerable steric influence on other ligands in the same molecule. Several of the metalloporphyrin complexes discussed below have bis(cyclopentadienyl) counterparts, and authors in some ca.ses have drawn quite detailed comparisons, although these discussions will not be repeated here. [Pg.232]

The last decade has seen the development of a rich and varied chemistry for or-ganometallic porphyrin complexes of the early transition metals (groups 3 and 4). However, there have been many fewer developments in the organometallic chemistry of the middle transition elements. Despite the paucity of its organometallic porphyrin compounds, molybdenum has played a very important role in... [Pg.240]


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