Porphyrins reviews

Table 2. Specification of the porphyrin part (P) of the general metalloporphyrin formula M(P)LX [4] and other abbreviations used (abbreviations in accord with the recent porphyrin review literature (21, 22) R, M, L, X specified in the text)...

Given stringent requirements for effective sensitizers and the desire to use wavelengths further to the red for therapeutic appHcations, definition of newer sensitizers has been a principal area of research since about 1987. Expanded theoretical and experimental understanding of photophysics has been a key element in identifying new classes of potential sensitizers (93—98). Research has focused on cationic derivatives of Nile Blue (93), metaHo-phthalocyanines (94), naphthalocyanines (95), chlorin-type compounds (96), expanded ring porphyrinoids (97), as well as porphyrins other than hematoporphyrin and its derivatives (98). This work has also been reviewed (10,91). Instmmentation for photodynamic therapy has been reviewed (99). 

To date, the most extensively studied polyboron hydride compounds in BNCT research have been the icosahedral mercaptoborane derivatives Na2[B22H22SH] and Na [(B22H22S)2], which have been used in human trials with some, albeit limited, success. New generations of tumor-localizing boronated compounds are being developed. The dose-selectivity problem of BNCT has been approached using boron hydride compounds in combination with a variety of deUvery vehicles including boronated polyclonal and monoclonal antibodies, porphyrins, amino acids, nucleotides, carbohydrates, and hposomes. Boron neutron capture therapy has been the subject of recent reviews (254). 

Porphyrin, 5,10,15,20-tetraphenyl-, 4, 386 Porphyrin, vinyl-synthesis, 4, 278, 279 Porphyrin coenzymes in biochemical pathways, 1, 258-260 Porphyrinogen, mcso-tetraaryl-synthesis, 4, 230 Porphyrinogens, 4, 378, 394 pyrazoles, 5, 228 synthesis, 4, 231 Porphyrins, 4, 377-442 acetylation, 4, 395 aromatic ring current, 4, 385 basicity, 4, 400 biosynthesis, reviews, 1, 99... 

Tliere are several reasons for this great interest in the tautomerism of porphyrins (which could justify its own review) (1) their biological significance, (2) their applications in material science ( hole burning is related to their tautomerism), (3) the simplicity of the system (annular tautomerism involving intramolecular proton transfer both in solution and in the solid state), and (4) the possibility of elucidating the kinetic processes in great detail. 

It should be noted here that expanded porphyrins, namely [22]porphyrin(4.0.4.0) and (22]porphyrin(6.0.6.0), have been prepared in Vogel s laboratory.1 1 The work on these porphyrins was only briefly reviewed in ref 1 e based on information from doctoral theses. Neither communications nor a full publication has appeared on this topic so the work is not reviewed here. 

Chemical transformations at the macroeyclic chromophorc of expanded porphyrins are still not known. The complexation behavior of expanded porphyrins is very different from that of nonexpanded porphinoid macrocycles. The coordination hole of the expanded porphyrins is often too big for the complexation of a single metal ion, so in fact two metal ions can be chelated. With some expanded porphyrins, anion binding is observable, a striking difference to the nonexpanded porphyrins. The complexation behavior and the host-guest chemistry of expanded porphyrins is a rapidly growing field of research. The work in this field has been reviewed. Ie f... 

Enikolopyan et al.til found that certain Co11 porphyrin complexes (eg. 87) function as catalytic chain transfer agents. Later work has established that various square planar cobalt complexes (e.g. the cobaloximes 88-92) are effective transfer agents.Ij2 m The scope and utility of the process has been reviewed several times,1 lt>JM ns most recently by Hcuts et al,137 Gridnev,1 3X and Gridnev and Ittel."0 The latter two references1provide a historical perspective of the development of the technique. 

Many catalysts have been screened for activity in catalytic chain transfer. A comprehensive survey is provided in Gridnev and Ittel s review."0 The best known, and to date the most effective, are the cobalt porphyrins (Section 6.2.5.2.1) and cobaloximes (Sections 6.2.5.2.2 and 6.2.5.2.3). There is considerable discrepancy in reported values of transfer constants. This in part reflects the sensitivity of the catalysts to air and reaction conditions (Section 6.2.5.3). 

This review essentially comprises a survey of the developments in the organometallic chemistry of porphyrin complexes over the last decade, continuing on from the three reviews published during 1986-1988. Literature since the mid-1980s has been surveyed, and work reported prior to this will be touched on primarily to put the more recent developments into context and will not be described in depth. A new multivolume set encompassing the entire range of porphyrin chemistry has been recently published, and this contains a chapter on organometallic porphyrin chemistry. ... 

For the purposes of this review the criterion has been refined to include only those porphyrin complexes where there is direct structural or spectroscopic evidence for a metal-carbon interaction. This interaction will not, however, be limited to covalent bonds. The last decade has seen the rise in importance of supramolecular chemistry and non-covalent interactions, and a small set of examples involving porphyrin complexes will be included as the last section in the review. 

One family of porphyrin complexes that will be treated in the review, even though they do not contain metal-carbon bonds, are metalloporphyrin hydride and dihydrogen complexes. As in classical organometallic chemistry, hydride complexes play key roles in some reactions involving porphyrins, and the discovery of dihydrogen complexes and their relationship to metal hydrides has been an important advance in the last decade. 

The synthesis, reactivity, spectroscopy, and electrochemi.stry of organometallic iron porphyrins was de.scribed in some detail in the three reviews published in the period from 1986 to I988. Although a brief synopsis of the early chemistry will be given here, this review will focus on more recent developments. 

Over the last decade a number of high oxidation state ruthenium porphyrin complexes containing 0x0 or imido ligands have been reported and have been thoroughly studied for their role in oxidation and atom-transfer chemistry. Although comparisons can be drawn with organometallic species (carbene, imido. and 0x0 ligands are formally isolobal) the chemistry of the 0x0 and imido complexes is beyond the scope of the review and will not be covered here. 

The syntheses and spectroscopic and electrochemical characterization of the rhodium and iridium porphyrin complexes (Por)IVI(R) and (Por)M(R)(L) have been summarized in three review articles.The classical syntheses involve Rh(Por)X with RLi or RMgBr, and [Rh(Por) with RX. In addition, reactions of the rhodium and iridium dimers have led to a wide variety of rhodium a-bonded complexes. For example, Rh(OEP)]2 reacts with benzyl bromide to give benzyl rhodium complexes, and with monosubstituted alkenes and alkynes to give a-alkyl and fT-vinyl products, respectively. More recent synthetic methods are summarized below. Although the development of iridium porphyrin chemistry has lagged behind that of rhodium, there have been few surprises and reactions of [IrfPorih and lr(Por)H parallel those of the rhodium congeners quite closely.Selected structural data for rr-bonded rhodium and iridium porphyrin complexes are collected in Table VI, and several examples are shown in Fig. 7. ... 

In this review, CPOs constructed by covalent bonds are mainly focused on however, stable coordination bonds comparable to the stability of the covalent bonds have potential for future enhanced molecular design of novel CPOs. One representative is the bond between pyridine-type nitrogen and metal, which is widely used in supramolecular chemistry, that is, the cyclic supramolecular formation reaction between pyridine-substituted porphyrin and metal salts (Fig. 6d) [27,28]. Palladium salts are frequently used as the metal salts. From the viewpoint of the hard and soft acid and base theory (HSAB), this N-Pd coordination bond is a well-balanced combination, because the bonds between nitrogen and other group X metals, N-Ni and Ni-Pt coordination bonds, are too weak and too strong to obtain the desired CPOs, respectively. For the former, the supramolecular architectures tend to dissociate into pieces in the solution state, and for the latter. 

CPOs are best characterized by the following three features 1) axial coordination to the incorporated metals, 2) specific nano-sized space created by rigid porphyrin panels, and 3) specific (photo-induced) redox reactions associated with the porphyrin s rr-electron system. In this chapter, some examples are reviewed based on these properties. 

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