Arene-platinum complex

Bis(arene)zirconium complexes, characteristics, 4, 697 Bis(arylamido)pyridines, with Hf(IV), 4, 792 Bis(aryl) bridges, in complexes with chromium(VI), 5, 346... 

Alkanes and arenes can also be activated to other reactions by platinum complexes in aqueous solution (57,58). For arenes in the presence of H2PtCl5, reduction from Pt(IV) to Pt(II) occurs and the arene undergoes chlorination. The reaction is catalyzed by platinum(II) (59). Similarly, if a platinum(IV) catalyst such as HjPtClg is used, chloroalkanes are formed from alkanes. As an example, chloromethane is formed from methane (Eq. 23) (60-62). Linear alkanes preferentially substitute at the methyl... 

Vinyl halides add to allylic amines in the presence of Ni(cod)2 where cod=l, 5-cyclooctodine, followed by reduction with sodium borohydride. Aryl iodides add to alkynes using a platinum complex in conjunction with a palladium catalyst. A palladium catalyst has been used alone for the same purpose, and the intramolecular addition of a arene to an aUcene was accomplished with a palladium or a GaCl3 catalyst, " AUcyl iodides add intramolecularly to aUcenes with a titanium catalyst, or to alkynes using indium metal and additives. The latter cyclization of aryl iodides to alkenes was accomplished with indium and iodine or with Sml2. " ... 

Little is known about the chemical nature of the recently isolated carbon clusters (C o> C70, Cg4, and so forth). One potential application of these materials is as highly dispersed supports for metal catalysts, and therefore the question of how metal atoms bind to C40 is of interest. Reaction of C o with organometallic ruthenium and platinum re nts has shown that metals can be attached directly to the carbon framework. Ihe native geometry of transition metal, and an x-ray difi action analysis of the platinum complex [(CgHg)3P]2Pt( () -C6o) C4HgO revealed a structure similar to that known for [(C4Hs)3P]2Pt( n -ethylene). The reactivity of C40 is not like that of relatively electron-rich planar aromatic molecules su( as benzene. The carbon-carbon double bonds of C40 react like those of very electron-deficient arenes and alkcnes. 

In this chapter, we will consider the reactions of C-H compounds, such as alkanes, arenes as well as some others, with platinum complexes containing mainly chloride ligands. The reactions of alkanes with platinum(II) complexes have been the first examples of true homogeneous activation of saturated hydrocarbons in solution. Complexes of Pt(II) exhibit both nucleophilic and electrophilic properties, they do not react with alkanes via a typical oxidative addition mechanism nor can they be regarded as typical oxidants. Due to this, it is reasonable to discuss their reactions in a special chapter which is a bridge between previous chapters (devoted to the low-valent complexes) and further sections of the book that consider mainly complexes in a high oxidation state. Chloride cortplexes of platinum(IV) are oxidants and electrophiles and they will constitute the first subjects in our discussion of processes of electrophilic substitution in arenes and alkanes as well as their oxidation. 

Reactions between the sulfur-containing amino acids cysteine and methionine (Fig. 2.18) and rufhenium(II) arene anticancer complexes are of much interest in view of the strong influence of sulfur amino acids on the intracellular chemistry of platinum drugs, their involvement in detoxification and resistance mechanisms [100]. We found [101] that [(ri -biphenyl)Ru(en)Cl][PF 5] reacts slowly with the thiol amino add L-cysteine in aqueous solution at 310 K, pH 2-5, and only to about 50% completion at a 1 2 mM ratio. Reactions appeared to involve aquation as the first step followed by initial formation of 1 1 adducts via substitution of water by S-bound or O-bound cysteine. Two dinuclear complexes were also detected as products from the reaction. In these reactions half or all of the chelated ethylene-diamine had been displaced and one or two bridging cysteines were present The unusual cluster species (biphenyl) Ru g was also formed espedaUy at higher cysteine concentrations. The reaction was suppressed in 50 mM triethylammo-nium acetate solution at pH > 5 or in 100 mM NaCl suggesting that thiols may not readily inactivate Ru(II)-en arene complexes in blood plasma or in cells. Similarly, reactions with the thioether sulfur of methionine appeared to be relatively weak. Only 27% of [(r -biphenyl)Ru(en)Cl][PF5] reacted with L-methionine (L-MetH) at an initial pH of 5.7 after 48 h at 310 K, and gave rise to only one adduct [(ri -biphenyl) Ru(en) (i-MetH -S)]. ... 

Most platinum complexes with arene ligands show coordination of the Pt atom to two adjacent C-C bonds (rf), and... 

Asymmetric hydroformylation of vinylarenes allows access to the 2-aryl propionic acids, an important family of nonsteroidal anti-inflammatory agents, known as the profen drugs (Scheme 14.6). For the reactions of vinyl arenes, early platinum-based catalysts again provided higher enan-tioselectivities than the rhodium catalysts available up to the early 1990s. However, the platinum complexes suffered from poor chemo- and regioselectivities. 

Allyl Complexes. Allyl complexes of thorium have been known since the 1960s and are usually stabilized by cyclopentadienyl ligands. AEyl complexes can be accessed via the interaction of a thorium haUde and an aHyl grignard. This synthetic method was utilized to obtain a rare example of a naked aHyl complex, Th(Tj -C2H )4 [144564-74-9] which decomposes at 0°C. This complex, when supported on dehydroxylated y-alumina, is an outstanding heterogeneous catalyst for arene hydrogenation and rivals the most active platinum metal catalysts in activity (17,18). 

Platinum mediated regioselective H-B addition of H-B(cat) to vinyl arenes and alkynes has been realised using the complexes 79 and 80 (Fig. 2.12). The reactions... 

The coordination chemistry of tertiary phosphine-functionalized calix[4]arenes have been described.279 Treatment of a bis(diphenylphosphino) or bis(dimethylphosphino) derivative of calix[4]arene with [PtCl2(COD)] leads to the formation of the corresponding dichloroplatinum(II) complex. The related diplatinum(II) species has also been reported with the tetrafunctionalized calix[4]arene.280 The mononuclear derivative is susceptible to oligomerization if the two free phosphine ligands are not oxidized or complexed to another metal center such as gold(I).279 The platinum(II) coordination chemistry of a mono-281 and diphosphite282 derived calix[ ]arene (n = 4 and 6, respectively) has also been described. 

Yordanov, A. T. Mague, J. T. Roundhill, D. M. Solvent extraction of divalent palladium and platinum from aqueous solutions of their chloro complexes using an N,N- dimethyldithiocarbamoylethoxy substituted calix 4 arene. Inorg. Chim. Acta 1995, 240, 441 146. 

Alternatively, arene displacement can also be photo- rather than thermally-induced. In this respect, we studied the photoactivation of the dinuclear ruthenium-arene complex [ RuCl (rj6-indane) 2(p-2,3-dpp)]2+ (2,3-dpp, 2,3-bis(2-pyridyl)pyrazine) (21). The thermal reactivity of this compound is limited to the stepwise double aquation (which shows biexponential kinetics), but irradiation of the sample results in photoinduced loss of the arene. This photoactivation pathway produces ruthenium species that are more active than their ruthenium-arene precursors (Fig. 18). At the same time, free indane fluoresces 40 times more strongly than bound indane, opening up possibilities to use the arene as a fluorescent marker for imaging purposes. The photoactivation pathway is different from those previously discussed for photoactivated Pt(IV) diazido complexes, as it involves photosubstitution rather than photoreduction. Importantly, the photoactivation mechanism is independent of oxygen (see Section II on photoactivatable platinum drugs) (83). 

The University of Edinburgh (former employer of Peter J. Sadler) has filed patent applications relating to the ruthenium-arene, and platinum diazido complexes and University of Warwick for osmium-arene complexes under study in the Peter J. Sadler laboratory. 

Denmark pursued intramolecular alkyne hydrosilylation in the context of generating stereodefined vinylsilanes for cross-coupling chemistry (Scheme 21). Cyclic siloxanes from platinum-catalyzed hydrosilylation were used in a coupling reaction, affording good yields with a variety of aryl iodides.84 The three steps are mutually compatible and can be carried out as a one-pot hydro-arylation of propargylic alcohols. The isomeric trans-exo-dig addition was also achieved. Despite the fact that many catalysts for terminal alkyne hydrosilylation react poorly with internal alkynes, the group found that ruthenium(n) chloride arene complexes—which provide complete selectivity for trans-... 

The reactivity of the closely related system TpMe2PtMeH2 toward electrophiles in arene solvents has also been reported recently (68). The boron-based Lewis acid B(C6F5)3 induced elimination of methane and formation of an aryl(dihydrido) platinum(IV) complex via arene C-H activation (Scheme 17, A -> C). The active acid may be either B(C6F5)3 or alternatively a proton generated from B(C6F5)3 and trace water. It was proposed that the acid coordinates to a pyrazole nitrogen (shown in Scheme 17, B) forming an intermediate five-coordinate platinum(IV) complex, which readily eliminates methane. 

Section III.E Barriers for Arene C-H Bond Activation in Platinum(II) r 2-Arene Intermediates (227) were measured for the complex shown in Scheme 26 (B) and similar derivatives. 

For each case we will also present catalytic analogues, namely (1) the activation of methane to form methanol with platinum, the reaction of certain aromatics with palladium to give alkene-substituted aromatics, and (2) the alkylation of aromatics with ruthenium catalysts, and the borylation of alkanes and arenes with a variety of metal complexes. 

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