Dimerization arene

Intramolecular acylnitrene-induced ring expansions of arenes are of great interest for the synthesis of novel 1//-azepines. Benzyl azidoformates, when subjected to spray-vacuum pyrolysis (SVP),152 yield l//,3//-oxazolo[3,4-a]azepin-3-ones which dimerize spontaneously 153,154 however, 2,6-dichlorobenzyl azidoformate yields the thermally stable (< 100 C) 5,9-dichloro-1 //,3//-oxazolo[3,4-a]azepin-3-one (8).154... 

Recently Noble s group (Haub et al., 1992) showed that sulfidomolybdenum dimer anion complexes react with arenediazonium ions and form complexes (Mo)2S — N2 — Ar. Synthesis and (homolytic) dediazoniation reflect characteristics of arene-diazosulfide anions (see Zollinger, 1995, Sec. 10.1). 

A set of oxygen donor atoms, providing both a and tt donation to a metal center, is not appropriate to stabilize any low oxidation state of a metal.19 This is, however, a synthetic advantage since very reactive, unstable, low-valent metalla-calix[4]arenes can be generated in situ and intercepted by an appropriate substrate. In the absence of a suitable substrate, the reactive fragment, however, can collapse to form metal-metal bonded dimers. The formation of metal-metal bonds has been, however, so far observed in the case of Group V and VI metals only. The most complete sequence so far reported has been for tungsten, molybdenum, and niobium. 

As will be discussed in detail in the next section, when the reduction of the parent compound 6 was conducted at low temperature (—20 °C) with 2 equiv. of Na in tetrahydrofuran (THF) saturated with ethylene, complete salt removal was achieved, and the r 2-ethylene complex 20 was isolated.22 Upon irradiation, the latter released ethylene, behaving as a source of the d2 [W / -Bu -calix[4]-(0)4 ] carbenoid, which coupled to give a new W=W dimer [W=W, 2.582(1) A], isolated as the bis-Bu NC adduct 21. In H NMR, 21 exhibits a C5-symmetric pattern of signals for the calix[4]arene moiety. 

The conversion of functionalized arenes as represented by the general formula 97, into isothiazolium compounds (99) has been achieved by the sequence shown in Scheme 117.180 From a synthetic viewpoint, transformation of cyclopalladated products into thiocyanate derivatives is more efficiently achieved using monomeric dithiocarbamato complexes (98) rather than dimeric compounds. The generation of analogous dithiolylium perchlorates by a related procedure is described later (see Section IV,H). 

Solution studies of the complexes outlined in Table 3 are in general agreement that they remain aggregated in solution, with the most common form being dimers.325 Solution studies of 300 in arene solvent indicate that at least two independent aggregates coexist.322 The most likely scenario from the data available is that a dimer-hexamer equilibrium is present in solution. Gas-phase studies of the hydrazides have proved to be problematic due to decomposition of the complexes on volatilization. 

Loss of Coordinated Arene. We previously stated that the arene ligand in ruthenium(II)-arene complexes is relatively inert towards displacement under physiological conditions. While this is generally true, there are a few exceptions to this rule and this type of reactivity can be used to advantage. Weakly bound arenes, for instance, can be thermally displaced, a property convenient for the synthesis of ruthenium-arene complexes that are not readily available through more common synthetic routes. This way, the reaction of a precursor dimer, [RuCl2(etb)]2 (etb, ethylbenzoate) (68), with either 3-phenyl-1-propylamine or... 

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