Zobrazeno 1 - 10
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pro vyhledávání: '"Carlo Floriani"'
Autor:
Carlo Floriani
Publikováno v:
CHIMIA, Vol 50, Iss 12 (1996)
The absence of the meso-hydrogen atoms in meso-octaalkylporphyrinogens enable the generation of novel forms of the oxidized porphyrinogen, 'artificial porphyrins'. A stepwise four-electron oxidation of meso-octaalkylporphyrinogen transitionmetal comp
Externí odkaz:
https://doaj.org/article/b0fcd11eb5bc4c86bfd0957cf17d574c
Autor:
Nazzareno Re, Federico Franceschi, Philip Pattison, Henrik Birkedal, Geoffroy Guillemot, Euro Solari, Carlo Floriani
Publikováno v:
Chemistry. 7:1468-1478
A novel class of dinucleating ligands has been introduced into manganese chemistry to study the reactivity of this metal towards dioxygen under strictly controlled conditions. Such N4 ligands combine some of the major peculiarities of tetradentate Sc
Publikováno v:
Chemistry. 7:1322-1332
The full metallation of meso-octaalkylporphyrinogens [R8N4H4] (R=Et, 1; nBu, 2; CH2Ph, 3; (CH2)4, 4) with heavy alkali metals (M=K, Rb, Cs) leads to the porphyrinogen-M4 compounds, in which the solvation of the alkali cations is largely assured by th
Publikováno v:
Inorganic chemistry (Chichester, England) 40 (2001): 1544–1549. doi:10.1021/ic0004028
info:cnr-pdr/source/autori:Simona Fantacci, Antonio Sgamellotti, Nazzareno Re, Carlo Floriani/titolo:Density Functional Study of Tetraphenolate and Calix[4]arene Complexes of Early Transition Metals/doi:10.1021%2Fic0004028/rivista:Inorganic chemistry (Chichester, England)/anno:2001/pagina_da:1544/pagina_a:1549/intervallo_pagine:1544–1549/volume:40
info:cnr-pdr/source/autori:Simona Fantacci, Antonio Sgamellotti, Nazzareno Re, Carlo Floriani/titolo:Density Functional Study of Tetraphenolate and Calix[4]arene Complexes of Early Transition Metals/doi:10.1021%2Fic0004028/rivista:Inorganic chemistry (Chichester, England)/anno:2001/pagina_da:1544/pagina_a:1549/intervallo_pagine:1544–1549/volume:40
Density functional calculations have been performed on some calix[4]arenes complexes of early transition metals. Particular emphasis has been placed on the comparison of the main properties of these metal complexes with the analogous metal complexes
Publikováno v:
Angewandte Chemie. 113:793-796
Publikováno v:
Organometallics. 20:607-615
The [{calix[4]-(O)4}W(η2-C6H10)], 2, has been used as a source of WIV-d2 center-bonded to an oxo surface, which has been modeled by the calix[4]arene tetraanion in the reaction with diazoalkanes and organic azides. The olefin is easily displaced by
Publikováno v:
Scopus-Elsevier
Density functional calculations have been carried out on a series of model hypothetical intermediates in the six-electron oxidation of porphyrinogen (5,10,15,20,22,24-hexahydroporphyrin) to porphyrin. Two possible reaction pathways have been investig
Publikováno v:
Chemistry. 6:4518-4531
The availability of the parent compound, meso-hexaethylporphodimetheneiron(II), [(Et6N4)Fe] (2), of this report results from a novel synthetic methodology that makes [Et6N4Li2] (1) easily available. The major focus is on how the axial positions, whic
Publikováno v:
Organometallics. 19:5218-5230
This report deals with the deprotonation of [W(η2-alkene)] complexes to the corresponding 1-metallacyclopropene, which can be equally well obtained via hydride addition to the corresponding [W(η2-alkyne)]. The ancillary ligand supporting the metal
Publikováno v:
Journal of the American Chemical Society. 122:5312-5326
The general synthetic methods presented in this paper make available, on a preparative scale, unprecedented porphyrinogen-derived skeletons, including their functionalization at the meso positions. The stepwise dealkylation of meso-octaalkylporphyrin