Cobalt phthalocyanine complex

The study just described is in accordance with the observation that electrochemical reduction of the (highly conjugated) phthalocyanine (5) complex of Mn(n) also gives no evidence for the formation of a Mn(i) species (in contrast to the corresponding iron and cobalt complexes which, on reduction, yield Fe(i) and Co(i) products) (Lever, Minor Wilshire, 1981). 

In abroad sense, the model developed for the cobaloxime(II)-catalyzed reactions seems to be valid also for the autoxidation of the alkyl mercaptan to disulfides in the presence of cobalt(II) phthalocyanine tetra-sodium sulfonate in reverse micelles (142). It was assumed that the rate-determining electron transfer within the catalyst-substrate-dioxygen complex leads to the formation of the final products via the RS and O - radicals. The yield of the disulfide product was higher in water-oil microemulsions prepared from a cationic surfactant than in the presence of an anionic surfactant. This difference is probably due to the stabilization of the monomeric form of the catalyst in the former environment. 

At present, synthetic routes to more than 40 metal complexes other than the copper complex are known. Apart from a cobalt phthalocyanine pigment (P.B.75) which was introduced to the market just recently, none of the resulting products, however, has stimulated commercial interest as a pigment. Nickel complexes, however, are found in reactive dyes, while cobalt complexes of this basic structure are employed as developing dyes. 

Porphyrins, 21 14, 36, 135 -based manganese complexes, 46 400-402 as cobalt complex ligants, 44 284-290 compared to phthalocyanines, 7 75 complexes, 19 144, 145, 147 complex stability, 42 135-137 degeneracy lifting, 36 206 metalloporphyrins, DNA cleavage and, 45 271-283... 

By running a potentiometric precipitation titration, we can determine both the compositions of the precipitate and its solubility product. Various cation- and anion-selective electrodes as well as metal (or metal amalgam) electrodes work as indicator electrodes. For example, Coetzee and Martin [23] determined the solubility products of metal fluorides in AN, using a fluoride ion-selective LaF3 single-crystal membrane electrode. Nakamura et al. [2] also determined the solubility product of sodium fluoride in AN and PC, using a fluoride ion-sensitive polymer membrane electrode, which was prepared by chemically bonding the phthalocyanin cobalt complex to polyacrylamide (PAA). The polymer membrane electrode was durable and responded in Nernstian ways to F and CN in solvents like AN and PC. 

Cobalt complexes find various applications as additives for polymers. Thus cobalt phthalocyanine acts as a smoke retardant for styrene polymers,31 and the same effect in poly(vinyl chloride) is achieved with Co(acac)2, Co(acac)3, Co203 and CoC03.5 Co(acac)2 in presence of triphenyl phosphite or tri(4-methyl-6- f-butylphenyl) phosphite has been found to act as an antioxidant for polyenes.29 Both cobalt acetate and cobalt naphthenate stabilize polyesters against degradation,73 and the cobalt complex of the benzoic acid derivative (12) (see Section 66.4) acts as an antioxidant for butadiene polymers.46 Stabilization of poly(vinyl chloride)-polybutadiene rubber blends against UV light is provided by cobalt dicyclohexyldithiophosphinate (19).74 Here again, the precise structure does not appear to be known. 

Cobalt complexes of dendritic phthalocyanines (Fig. 6.37) showed a 20% lower catalytic activity (TON 339 min-1 for G2 dendrons) as catalysts for the oxidation of 2-mercaptoethanol than non-dendritic phthalocyanines [56]. By way of compensation, however, the dendritic catalysts proved to be more stable than non-dendritic ones, which is probably attributable to enclosure of the metallo-phthalocyanine core unit by the dendrons. This also prevents molecular aggregation of the phthalocyanines in polar solvents and thin films. 

A poly(propylenamine) dendrimer (11, Fig. 6.37) functionalised with poly-(N-isopropylacrylamide) (PIPAAm) (see Section 4.1.2) was used as dendritic host for anionic cobalt(II)-phthalocyanine complexes (a, b) as guests, which are held together by supramolecular (electrostatic and hydrophobic) interactions [57]. These dendritic complexes were investigated as catalysts in the above-mentioned oxidation of thiols, where they show a remarkable temperature dependence the reaction rate suddenly increases above 34°C. One attempted explanation assumes that the dendritic arms undergo phase separation and contraction above the Lower Critical Solubility Temperature (LCST). At this temperature the phthalocyanine complex site is more readily accessible for substrates and the reaction rate is therefore higher. 

Solvent dyes for solvent based ink-jet inks and hot melt ink-jet systems are selected 1 2 chromium or cobalt complex azo (C.I. Solvent Yellow 83 1 [61116-27-6], C.I. Solvent Red 91 [61901-92-6]), anthraquinone (C.I. Solvent Blue 45 [37229-23-5]), or phthalocyanine (C.I. Solvent Blue 44 [61725-69-7]) dyes. 

N.m.r. line-broadening and shift effects have been investigated for CoL [L = (12)] in H2O, MeOH, and DMT. " Crystalline and molecular susceptibilities and their orientations of cobalt(ii) phthalocyanine [Co(pc)], bis(pentane-2,4-dithionate)cobalt(ii) [Co(pdt)2], and the analogous copper(ii) complexes have been reported. E.s.r. has been used to show that addition of DMF or DMSO to aqueous solutions of cobalt(ii)tetraphenylporphyrintetrasulphonate [Co(tpps)] results in a... 

Phthalocyanines and their metal complexes have interesting catalytic, electronic, and optical properties.172 Kimura et al.173 synthesized a phthalocyanine-centered dendrimer possessing Newkome-type dendrons,174 and subsequently used the second-generation cobalt-metalated phthalocyanine dendrimer as the catalyst for the oxidation of mercaptoethanol by dioxygen... 

The porphyrin cobalt complex in radical polymerization of methylmethacrylate catalyzes the chain transfer to the monomer without affecting the polymerization rate. The phthalocyanine cobalt complex catalyzes the chain termination. 

Attempts to oxidize cobalt phthalocyanine to a cobalt(III) derivative in neutral or basic solvent were unsuccessful 213). However, it is reported 80) that cobalt phthalocyanine is oxidized to nitratocobalt(III) phthalocyanine by nitric acid in nitrobenzene at 10°-20°C. Unfortunately no data were presented which excluded the alternative formulation of the complex as a nitric acid adduct of cobalt(II) phthalocyanine, which seems more likely. 

Synthesis of the phthalocyanine-2,9,16,23-tetracarboxylic acid tetrachloride cobalt complex 48 (R = -COCl M = Co(II)) 0.5 g of the tetracarboxylic acid was added to 1.5 mL thionyl chloride containing 2 drops of pyridine. The mixture was heated for 20 h under reflux at 80 °C. After centrifugation the blue-colored acid chloride was dried at 100 °C in vacuo over P4O10. Yield 0.48 g (88%). IR (KBr) 1657, 1522, 1323, 1091, 749, 719 cm". ... 

Cobalt complexes of polymeric phthalocyanines have been employed in aqueous alkaline solution as heterogenous catalysts in the oxidation of thiols to disulfides (MEROX, mercaptan oxidation process in the petroleum industry, Eq. 6-12, see Sections 5.2 and 5.4, Experiments 5-11 and 5-12). The catalytic activities of the polymer 31 (M = Co(II)) are higher than those of dissolved low molecular weight phthalocyanines, and both complexes exhibit better activities on charcoal than on Si02 as carrier. This is the result of better electrical contact between different reaction centers, which facilitates a multi-electron process in the oxidation of R-S to R-S-S-R and reduction of O2 to H2O [95]. Another advantage of the heterogeneous catalysts in comparison to the dissolved low molecular weight phthalocyanines is their easy re-use. 

It has been shown that this catalyst is selective in epoxidation of linear alkenes the linear epoxide yield was two to four times higher than in catalysis by ordinary porphyrin. It was also demonstrated that, in catalysis by the dendrimers, cyclic alkenes are oxidized three times more rapidly than similar linear 1-alkenes are. The catalyst activity decreases only by 10% at a turnover number (TON) of 1000, which is much higher than that for the monomolecular analogue. A cobalt complex with dendrimer phthalocyanine was much more stable, while remaining active, in... 

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