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Deuteroporphyrin IX dimethyl ester

Table 5 Basicity of Substituted Deuteroporphyrin-IX Dimethyl Esters... Table 5 Basicity of Substituted Deuteroporphyrin-IX Dimethyl Esters...
Mossbauer data for 2,4 diacetyl deuteroporphyrin IX dimethyl ester and Fe(II) protoporphyrin IX obtained at 77 °K show isomer shifts... [Pg.14]

Not only has binding of imidazoles and pyridines to Fe protoporphyrin IX been studied, as discussed in Section 4.1.2, but also photodissociation of axial ligands such as pyridines, imidazoles, or piperidines from six-coordinate, low-spin Fe porphyrins, in which the porphyrin is derived from protoporphyrin IX, or proto- or deuteroporphyrin IX dimethyl ester, has been investigated in nonaqueous solvents using picosecond transient absorption spectroscopy (see Photochemistry of Transition Metal Complexes). It has been shown that photodissociation leads to the formation of five-coordinate complexes, that is, only one ligand appears to be released upon excitation of the six-coordinate complex. ... [Pg.2117]

Janson, T. R., Katz, J. J. (1972). An Examination of the 220 MHz NMR Spectra of Meso-porphyrin IX Dimethyl Ester, Deuteroporphyrin IX Dimethyl Ester, and Protoporphyrin IX Dimethyl Ester, J. Magn. Resonance, 6 209. [Pg.551]

Table I. Spectroscopic Properties of Deuteroporphyrin IX Dimethyl Ester Iron (III) Compounds... Table I. Spectroscopic Properties of Deuteroporphyrin IX Dimethyl Ester Iron (III) Compounds...
Figure 2. Absorption spectra for deuteroporphyrin IX dimethyl ester iron-fill) derivatives in chloroform ligands correspond to X of Figure I... Figure 2. Absorption spectra for deuteroporphyrin IX dimethyl ester iron-fill) derivatives in chloroform ligands correspond to X of Figure I...
Figure 5. Proton magnetic resonance spectra at 60 MHz of 2,4-dipropionyU deuteroporphyrin IX dimethyl ester at different concentrations in CDCl at 35°C. Arrows indicate ester methyls. Figure 5. Proton magnetic resonance spectra at 60 MHz of 2,4-dipropionyU deuteroporphyrin IX dimethyl ester at different concentrations in CDCl at 35°C. Arrows indicate ester methyls.

See other pages where Deuteroporphyrin IX dimethyl ester is mentioned: [Pg.594]    [Pg.92]    [Pg.2098]    [Pg.2111]    [Pg.2172]    [Pg.594]    [Pg.594]    [Pg.2097]    [Pg.2110]    [Pg.2171]    [Pg.59]    [Pg.116]    [Pg.181]    [Pg.181]    [Pg.181]    [Pg.187]    [Pg.209]    [Pg.390]    [Pg.75]    [Pg.41]    [Pg.471]    [Pg.64]    [Pg.771]    [Pg.901]    [Pg.901]    [Pg.230]    [Pg.322]    [Pg.2788]   
See also in sourсe #XX -- [ Pg.187 , Pg.189 ]




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