Thallium III Derivatives

The dimeric thallium(III) amide [( fo (pentafluorophenyl) Tl(dpa))]2 (where Hdpa = 2,2 -dipyridylamine) comprises distorted trigonal bipyramidal thallium(III) ions that are coordinated by two pentafluorophenyl groups (TI—C distances are 2.12(4) and 2.16 

---

Reactions of Me3P=CH2 with MeaMCl (M = Ga, In, or Tl) form the new dimethylmetaldimethylphosphonium-bis(methylides), [Me2MCH2PMe2CH2] . Dimers (n = 2) may be isolated, and these possess eight-membered ring structures (76). This structure stabilizes the inherently labile thallium(iii) derivative." ... 

Complex supramolecular architectures have been established for dimethyl-thallium(III) derivatives of polyfunctional nitrogen ligands, e.g. the cyanide, the azide, the cyanate, the thiocyanate [177], the dicyanamide, and the tricyanomethide [178], The cyanide, Me2TlCN, 53, contains layers of nearly coplanar CN groups... 

Thallium(III) acetate reacts with alkenes to give 1,2-diol derivatives (see p. 128) while thallium(III) nitrate leads mostly to rearranged carbonyl compounds via organothallium compounds (E.C. Taylor, 1970, 1976 R.J. Ouelette, 1973 W. Rotermund, 1975 R. Criegee, 1979). Very useful reactions in complex syntheses have been those with olefins and ketones (see p. 136) containing conjugated aromatic substituents, e.g. porphyrins (G. W. Kenner, 1973 K.M. Smith, 1975). 

Monoalkylthallium(III) compounds are unstable (73, 79), and very few examples of this class have been isolated. A number of alkylthallium diacetates have been obtained either from oxythallation of olefins with thallium-(III) acetate (see below) or from exchange reactions such as that shown in Eq. (11) (74, 75). Only four alkylthallium dihalides have been isolated so far, namely a neopentylthallium dihalide (60) [Eq. (12)] and the isomeric 2-, 3-, and 4-pyridiomethylthallium dichlorides (20) [Eq. (13)]. Monoaryl-and monovinylthallium(III) derivatives are considerably more stable than... 

Monoalkylthallium(III) compounds can be prepared easily and rapidly by treatment of olefins with thallium(III) salts, i.e., oxythallation (66). In marked contrast to the analogous oxymercuration reaction (66), however, where treatment of olefins with mercury(II) salts results in formation of stable organomercurials, the monoalkylthallium(III) derivatives obtained from oxythallation are in the vast majority of cases spontaneously unstable, and cannot be isolated under the reaction conditions employed. Oxythallation adducts have been isolated on a number of occasions (61, 71,104,128), but the predominant reaction pathway which has been observed in oxythallation reactions is initial formation of an alkylthallium(III) derivative and subsequent rapid decomposition of this intermediate to give products derived by oxidation of the organic substrate and simultaneous reduction of the thallium from thallium(III) to thallium(I). The ease and rapidity with which these reactions occur have stimulated interest not only in the preparation and properties of monoalkylthallium(III) derivatives, but in the mechanism and stereochemistry of oxythallation, and in the development of specific synthetic organic transformations based on oxidation of unsaturated systems by thallium(III) salts. 

Oxidation of the steroidal olefin (XXVII) with thallium(III) acetate gives mainly the allylic acetates (XXXI)-(XXXIII) (Scheme 15), again indicating that trans oxythallation is the preferred reaction course (19). Addition of the electrophile takes place from the less-hindered a-side of the molecule to give the thallinium ion (XXVIII), which by loss of a proton from C-4 would give the alkylthallium diacetate (XXIX). Decomposition of this intermediate by a Type 5 process is probably favorable, as it leads to the resonance-stabilized allylic carbonium ion (XXX), from which the observed products can be derived. Evidence in support of the decomposition process shown in Scheme 15 has been obtained from a study of the exchange reaction between frawr-crotylmercuric acetate and thallium(III) acetate in acetic acid (Scheme 16) (142). 

In a new reaction of the pyrano[2,3-c]azepines 40 with hydrazine hydrate, the first derivatives of the pyridazino[4,3-c]azepine system 42 (for example R1 = R2 = Me) have been described (Scheme 10). The rearrangement probably involves initial ring opening to the intermediate 41. Aromatisation of this system was achieved by further oxidation with thallium (III) nitrate or copper(II) acetate . 

Oxidative phenolic coupling. Biosynthesis of the alkaloid narwedine (3) is known to involve oxidative phenolic coupling of norbelladine derivatives (1), but the usual oxidants for such coupling in vitro convert 1(R = H) into the oxomaritidine skeleton (4) rather than 3. A new biomimetic synthesis of 3 involves the palladacycle 2, formed by reaction of 1(R = CH3) with Li2PdCl4, which is known to form complexes with allylic amines or sulfides (8,176-177). Oxidation of 2 with thallium(III) trifluoroacetate effects the desired coupling to give 3. 

Dialkyl and diarylthallium(III) derivatives are stable, crystalline solids that melt at 180—300°C. The dimethyl thallium derivatives of CN", C10 4, BF 4, and NO 3 contain linear (CH3)2T1 cations and the free anions (19). In aqueous solutions, they ionize to the (CH3)2T1(H20)+ ions, except those derivatives containing alkoxide, mercaptide, or amide anions, which yield dimeric structures (20,21). 

RTIX2 derivatives are covalent compounds, generally soluble in organic solvents. The aryl and vinyl derivatives are more stable than the corresponding alkyl compounds. This type of compound has been postulated to be an intermediate in many organic synthetic reactions involving thallium(III) species. 

Thallium (III) Compounds. Thallium (ITT) derivatives have been used extensively as oxidants in oiganic synthesis. In particular, thallic acetate and trifluoroacetate are extremely effective as electrophiles in oxythallation and thallation reactions. For example, ketones can be prepared from terminal acetylenes by means of Tl(OOCCH3)3 in acetic acid (oxythallation) (30) ... 

In addition to the halide systems there are a number of thallium(I) salts of thallium(III) complex anions in which the overall stoichiometry implies, incorrectly, the presence of thallium(II) species. These include the sulfate, selenate,369 acetate370 and oxalate371 derivatives. An X-ray determination has confirmed that Tl(OAc)2 is indeed Tl[Tl(OAc)4], in which the anions are linked through seven-coordinate Tl+, with some evidence for a stereochemically active inert pair.370 In T1[T1(0H)(S04)2], the structure consists of sheets of linked anions with Tl+ ions.372... 

The porphyrin derivative of thallium(III) has been found437 to have the metal atom above the N4 plane by 0.9 A. Electrochemical two-electron reduction results in reduction to Tl L-(L = porphyrin), and subsequent protonation gives H2L and Tl+ in aqueous solution.438... 

Nickel(III) complexes, with alkyls and aryls, 8, 117 Nickel(IV) complexes, with alkyls and aryls, 8, 117 Nickel coordination complexes, thallium(I) derivatives,... 

---