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Chlorin ring

Since iron phthalocyanine complexes can be activated and stabilized by a chlorine ring substitution (12), the activity of iron hexadecachlorophthalocyanine (7b) immobilized on silica was examined for the synthesis of 4, 5, and 6 with TBHP as oxidant. [Pg.436]

Insertion of metals into the porphyrin and chlorin ring occurs with variable ease (and difficulty) commonly employed metals such as zinc(II), copper(II) and nickel(II) are simply chelated using the corresponding metal acetate in methanol, but others such as mag-nesium(II) and iron(III) require specialized conditions. Since a full description of the best method for any particular case is outside the scope of this Chapter, readers are advised to consult recent reviews (B-75MI30703, B-75MI30704). [Pg.391]

JCS(P1)1972). The intermediate (524) was isolated, confirming that the initial electrophilic attack occurs on the brominated rather than the chlorinated ring. [Pg.839]

Figure 6.18 Stop-flow 2D WET-TOCSY spectrum of 3,5-dichloro-2-hydroxybiphenyl. Protons (H4.H6) of the chlorinated ring can be identified due to the magnetization transfer between the signals at 7.23 (H4) and 7.41 (H6) ppm. Conditions spectrometer, Bruker DRX 600 probe head, 4mm z-gradient LC probe. 13C decoupling was applied during the WET-pulse train and acquisition. The spectral size was 8k x 512 data points, with 16 scans per increment, and a 64 ms TOCSY mixing time... Figure 6.18 Stop-flow 2D WET-TOCSY spectrum of 3,5-dichloro-2-hydroxybiphenyl. Protons (H4.H6) of the chlorinated ring can be identified due to the magnetization transfer between the signals at 7.23 (H4) and 7.41 (H6) ppm. Conditions spectrometer, Bruker DRX 600 probe head, 4mm z-gradient LC probe. 13C decoupling was applied during the WET-pulse train and acquisition. The spectral size was 8k x 512 data points, with 16 scans per increment, and a 64 ms TOCSY mixing time...
Dihydropyran 395 can undergo a hypochlorite-acetic acid promoted chlorination-ring expansion process to afford the tetrahydropyran 396 in high yield (Scheme 93) <2002OL3899>. [Pg.507]

Answer Since we are limited to starting with monosubstituted cyclic molecules we have the option of adding the carbons to the chlorinated ring or adding the Cl to the aromatic alcohol. In the lab it is easier to do the former, so we shall proceed along that line. Thus, we have to add carbons. [Pg.81]

Hydroxylation is favoured at the para position in the least chlorinated ring unless this site is sterically hindered. [Pg.102]

PS II and PS I, and the 28 kDa protein of LHC II, show a number of possible a-helical regions in each case (see Chapter 11). Given the size of the chlorin ring (= 15 X 15 A) and the fact that each apoprotein binds many pigment molecules, it is not surprising that these apoproteins are associated with the membrane o-helical regions, since protease digestions of intact thylakoids or vesicles do not release any of the chlorophyll of the PS II complex [27], the PS I complex [28,29] or LHC II [27,28], Moreover, as neither the chlorophyll or xanthophyll molecules of LHC II are accessible to proton attack, they are likely to be located within the hydrophobic interior of the membrane [30],... [Pg.280]

Chlorophenoxyalkanoic compounds of different molecular structure do not show any definite order of reactivity for the coupling to the various HAs as a function of type of alkanoic chain. An approximate trend is shown in relation to the number of chlorine ring-atoms, in the order monochlorinated > dichbrinated > trichlorinated. [Pg.195]

Chlorinated ring systems, such as cyclodiene insecticides dieldrin and aldrin react to CO2 and HCl during irradiation with UVdight (X > 290 nm). By using... [Pg.261]

Hydrodechlorination. With nascent Raney nickel generated from Ni-Al alloy in dilute aqueous alkaline solutions, chlorinated biaryls can be dechlorinated or have the chlorinated ring completely converted to a cyclohexane moiety. [Pg.254]

Figure 10. Dielectric model of the protein. Within this model, the protein medium (i.e., the medium with the refractive index of n = 1.2) is represented with a set of cylinders. The cross section of these cylinders is shown with white circles. The real location of the transmembrane part of a-helices in PSI are indicated by coiled structures. Chlorophylls are presented as Mg-chlorin rings, lacking the phytyl tail. Chlorophyll Mg atoms are shown in van der Waals representation. See color insert. Figure 10. Dielectric model of the protein. Within this model, the protein medium (i.e., the medium with the refractive index of n = 1.2) is represented with a set of cylinders. The cross section of these cylinders is shown with white circles. The real location of the transmembrane part of a-helices in PSI are indicated by coiled structures. Chlorophylls are presented as Mg-chlorin rings, lacking the phytyl tail. Chlorophyll Mg atoms are shown in van der Waals representation. See color insert.
We are dealing with a highly ordered array of substances. What that array is on the molecular level—i.e., how the plane of the chlorin ring is located with respect to these layers or with respect to the spherical globules of which the layers seem to be composed—is still a matter of controversy and remains one of the areas which this writer would like to see the physical chemists explore. It is necessary to bridge the gap between ordinary statistical molecular behavior and individual structures that can be seen. We do not know, for example, what the arrangement of the chlorophyll molecules is in the lamellar layers. Order is, however, the major factor with which we are left. [Pg.9]

Figure 8 Schematic cross-section of a chloroplast membrane showing an intrinsic protein spanning the membrane, with hydrophilic regions located at the membrane surfaces and a hydrophobic portion shaded) embedded within the non-polar interior of the lipid bilayer. Anderson 55 postulates that the chlorophyll molecules represented above with the hydrophobic portion of the chlorin ring shaded) are located as part of the boundary lipid of a chlorophyll-protein complex (Reproduced by permission from Nature, 1975, 253, 536)... Figure 8 Schematic cross-section of a chloroplast membrane showing an intrinsic protein spanning the membrane, with hydrophilic regions located at the membrane surfaces and a hydrophobic portion shaded) embedded within the non-polar interior of the lipid bilayer. Anderson 55 postulates that the chlorophyll molecules represented above with the hydrophobic portion of the chlorin ring shaded) are located as part of the boundary lipid of a chlorophyll-protein complex (Reproduced by permission from Nature, 1975, 253, 536)...
All forms of chlorophyll have a similar chemical structure. They have a complex system of rings made of carbon and nitrogen known as a chlorin ring. The five forms of... [Pg.218]

CHLORIN RING A ring of carbon and nitrogen atoms bonded to each other. [Pg.220]


See other pages where Chlorin ring is mentioned: [Pg.234]    [Pg.164]    [Pg.114]    [Pg.1302]    [Pg.1702]    [Pg.10]    [Pg.179]    [Pg.359]    [Pg.94]    [Pg.2099]    [Pg.2100]    [Pg.2105]    [Pg.2182]    [Pg.3865]    [Pg.3870]    [Pg.369]    [Pg.183]    [Pg.194]    [Pg.308]    [Pg.1481]    [Pg.393]    [Pg.124]    [Pg.170]    [Pg.5]    [Pg.389]    [Pg.578]    [Pg.219]    [Pg.2098]    [Pg.2099]    [Pg.2104]    [Pg.2181]   
See also in sourсe #XX -- [ Pg.44 ]




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Chlorin ring system

Chlorination of aromatic rings

Chlorins, oxidative ring opening

RING-CHLORINATED TOLUENES

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