Porphyrin hydrophilic

The first synthesis of amphiphilic porphyrin molecules involved replacement of the phenyl rings in TPP with pyridine rings, quaternized with C2QH 2Br to produce tetra(3-eicosylpyridinium)porphyrin bromide (3) (36). The pyridinium nitrogen is highly hydrophilic the long C2Q hydrocarbon serves as the hydrophobic part. Tetra[4-oxy(2-docosanoic acid)]phenyl-porphyrin (4) has also been used for films (37). 

The highly evolved catalyst 20 combines several features that have proved successful in simpler cases. The ionic sulfonate groups make the substrate sufficiently soluble for the reaction to be run in water. (The four hydrophilic cyclodextrins perform the same service for the catalyst.) The target reaction, the seledive oxidation of the steroid skeleton, goes back to the early days of enzyme models,1711 and the choice of porphyrin and of manganese as the metal cation are based on many years experience. The aryl groups are perfluorinated because an earlier version of the catalyst suffered self-oxidation. 

Other aspects of solvation have included the use of surfactants (SDS, CTAB, Triton X-100), sometimes in pyridine-containing solution, to solubilize and de-aggregate hemes, i.e., to dissolve them in water (see porphyrin complexes, Section 5.4.3.7.2). An example is provided by the solubilization of an iron-copper diporphyrin to permit a study of its reactions with dioxygen and with carbon monoxide in an aqueous environment. Iron complexes have provided the lipophilic and hydrophilic components in the bifunctional phase transfer catalysts [Fe(diimine)2Cl2]Cl and [EtsBzNJpeCU], respectively. 

We are primarily concerned with several typical modes of the Chi interfacial layer relevant to photoelectric and photoelectro-chemical systems. Since the Chi molecule, a surfactant pigment consisting of a partially hydrophilic porphyrin ring and a totally hydrophobic phytol chain, is insoluble in water, it is generally employed for photoelectric and photoelectrochemical measurements in the form of a solid (or quasi-solid) film deposited on an electrode surface. Such Chi films are divided into three typical modes according to molecular configuration. 

Porphyrin dendrimers are suitable as sensors for small molecular and ionic analytes. Unsubstituted metal-free porphyrins often show poor solubility in water. However, if it proves possible to envelop them in hydrophilic dendrimers they can be used in water as fluorescent pH indicators because they exhibit distinct changes of their absorption and emission bands owing to protonation of... 

Adding polar functional groups to cross-linked, apolar polymeric resins by covalent chemical modification has developed particularly for generation of SPE sorbents suitable for recovery of polar compounds. Hydrophilic functional groups such as acetyl, benzoyl, o-carboxybenzoyl, 2-carboxy-3/4-nitrobenzoyl, 2,4-dicarboxybenzoyl, hydroxymethyl, sulfonate, trimethyl-ammonium, and tetrakis(/>-carboxyphenyl)porphyrin have been chemically... 

Ru(II)-trls-bipyridine, Ru(bipy) +(JO and Zn-porphyrins, such as Zn-meso-tetraphenylporphyrins (2) o water-soluble derivatives ( ) and ( ) have been widely explored. Different structural modi-fTcations such as hydrophobic substituents and charged headgroups have also been Introduced. Thus, control of electrostatic interactions and precise location of the sensitizer in hydrophilic or hydrophobic environments can be achieved. 

An interesting attempt to overcome this problem is the design of simplified systems which try to reproduce the activity of natural enzymes (biomimetic catalysts). This approach has produced, e.g., impressive advances in the chemistry of synthetic porphyrins and in understanding the activity of some enzymes e.g. cytochrome P-450) which catalyzes oxidation reactions by an iron-porphyrin centre. Furthermore, interesting similarities have been noticed between enzymes and completely different catalysts. For instance, selective adsorption in the channels of some zeolites provide a confined, relatively hydrophobic medium even in aqueous solvent (Annex 2). This strongly resembles the active sites of several enzymes (including cytochrome P-450) that are deeply buried in hydrophobic pockets where lipophilic substrates are readily oxidized. The more hydrophilic reaction products are promptly released into... 

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