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Silver complexes with carbenes

An extension of the research on silver complexes with Lewis base-functionalized mono(A-heterocyclic carbene) ligands has been made toward the better-studied and stronger coordinating phosphine systems. The reaction of a diphenylphosphine-functionalized imidazolium salt with silver oxide in dichloromethane affords a trinuclear silver carbene complex 50, as confirmed by electrospray-ionization mass spectrometry.96,97 Metathesis reaction of 50 in methanol using silver nitrate gives 51 in 33% yield. The crystal structures of 51 were found to be different when different solvents were used during crystallization (Scheme 12).97 One NO3- anion was found to be chelated to... [Pg.213]

Although the main emphasis with imino functionalised carbene hgands is on their silver complexes, as carbene transfer agents, and on late transition metal complexes - palladium. [Pg.85]

The fact that pentacarbonyl carbene complexes react with enynes in a chemo-selective and regiospecific way at the alkyne functionality was successfully applied in the total synthesis of vitamins of the Kj and K2 series [58]. Oxidation of the intermediate tricarbonyl(dihydrovitamin K) chromium complexes with silver oxide afforded the desired naphthoquinone-based vitamin K compounds 65. Compared to customary strategies, the benzannulation reaction proved to be superior as it avoids conditions favouring (E)/(Z)-isomerisation within the allylic side chain. The basic representative vitamin K3 (menadione) 66 was synthesised in a straightforward manner from pentacarbonyl carbene complex 1 and propyne (Scheme 38). [Pg.143]

In 2007, Fernandez et al. demonstrated that transition-metal complexes with heterobidentate S/C ligands based on imidazopyridin-3-ylidene and thioether functionalities could be readily prepared from the corresponding azolium salts by reaction with Ag20 and transmetalation of the resulting silver carbenes with appropriate metal sources. The cationic Pd(allyl)(carbene-S) complexes have proven to be active catalysts in the test reaction, reaching enantioselectivities of... [Pg.40]

The reaction of A-benzyl-C-imidazolyllithium with [Ag(N03)(SMe)2] affords the corresponding C-imidazolylsilver (Equation (3)), which has been proposed by molecular weight determination to be trimeric.297 A-Functionalized C-imidazolylsilver compounds or carbene-type silver complexes are obtained by reaction of the imidazolium salt with Ag20 or Ag2C03 some of these are shown in Figure 4 298,299... [Pg.924]

Carbene complexes have also been prepared by transmetallation reactions. Lithiated azoles react with gold chloride compounds and after protonation or alkylation the corresponding dihydro-azol-ylidene compounds, e.g., (381) or (382), are obtained.22 9-2264 Silver salts of benz-imidazol have also been used to obtain carbene derivatives.2265 Mononuclear gold(I) carbene complexes also form when trimeric gold(I) imidazolyl reacts with ethyl chlorocarbonate or ethyl idodate.2266,2267 The treatment of gold halide complexes with 2-lithiated pyridine followed by protonation or alkylation also yields carbene complexes such as (383).2268 Some of these carbene complexes show luminescent properties.2269-2271... [Pg.1032]

Reports on the coordination chemistry of A-heterocyclic carbene-containing metal complexes started to appear as long ago as 1968,50,51 while metal-free carbenes have only been isolated very recently.52 In view of the fact that the general chemistry and applications of organic carbenes and related metal complexes in chemical synthesis have been reviewed several times recently,53-57 examples limited only to those carbene complexes with silver(i) have been discussed. Nevertheless, it is worth mentioning that the developments in silver(i) A-heterocyclic carbenes have also been reviewed recently by Lin.5... [Pg.204]

In spite of the fact that silver(i) X-heterocyclic carbene complexes were widely employed as carbene-transfer reagents for the synthesis of other transition metal carbene complexes, their synthesis could also be achieved by the reaction of silver salts with relatively more labile carbene metal complexes, albeit rare. Complexes 71a-71c were reported to be synthesized from the reaction of the corresponding pentacarbonyl(carbene)chromium(i) complexes with silver(i) hexafluorophosphate in CDC13 under inert atmosphere (Scheme 17).117... [Pg.221]

Hoveyda and co-workers also tested optically active A-heterocyclic carbenes and their silver complexes in copper-catalyzed reactions of allylic phosphates with dialkylzincs.402 The ratios of Sn2 SN2 products were higher than 98 2 and the ee varied from 34% to 98%. [Pg.405]

Bis(butadiene) complexes, with tantalum, 5, 173 Bis(z-butanethiolato) complexes, with bis-Cp Ti(IV), 4, 601 Bis(calixarene) complexes, as organic molecule hosts, 12, 799 Bis(carbene) complexes with gold(I), 2, 287-288 with manganese, 5, 780, 5, 826 with mercury, 2, 429 with palladium, 8, 230 with silver , 2, 206... [Pg.63]

Bis(guanidinato)bis(benzyl) complexes, with Zr(IV), 4, 776 Bis(heteroarene) vanadium complexes, preparation, 5, 48 Bis(heteroatom) polysilanes, synthesis, 3, 584 Bis(iV-heterocyclic carbene) ligands, in silver(I) complexes,... [Pg.65]

Imidazolium ligands, in Rh complexes, 7, 126 Imidazolium salts iridium binding, 7, 349 in silver(I) carbene synthesis, 2, 206 Imidazol-2-ylidene carbenes, with tungsten carbonyls, 5, 678 (Imidazol-2-ylidene)gold(I) complexes, preparation, 2, 289 Imidazopyridine, in trinuclear Ru and Os clusters, 6, 727 Imidazo[l,2-a]-pyridines, iodo-substituted, in Grignard reagent preparation, 9, 37—38 Imido alkyl complexes, with tantalum, 5, 118—120 Imido-amido half-sandwich compounds, with tantalum, 5,183 /13-Imido clusters, with trinuclear Ru clusters, 6, 733 Imido complexes with bis-Gp Ti, 4, 579 with monoalkyl Ti(IV), 4, 336 with mono-Gp Ti(IV), 4, 419 with Ru half-sandwiches, 6, 519—520 with tantalum, 5, 110 with titanium(IV) dialkyls, 4, 352 with titanocenes, 4, 566 with tungsten... [Pg.125]

In addition to participating in [2 + l]-cycloaddition reactions, divalent reactive intermediates can form ylides in the presence of carbonyl or other Lewis basic functionalities.108 These ylides participate in cycloaddition or other pericyclic reactions to furnish products with dramatically increased complexity. While carbenes (or metal carbenoids) are well known to participate in these pericyclic reactions, silylenes, in contrast, were reported to react with aldehydes or ketones to form cyclic siloxanes109,110 or enoxysilanes.111,112 Reaction of silylene with an a,p-unsaturated ester was known to produce an oxasilacyclopentene.109,113,114 By forming a silver silylenoid reactive intermediate, Woerpel and coworkers enabled involvement of divalent silylenes in pericyclic reactions involving silacarbonyl ylides115 to afford synthetically useful products.82,116,117... [Pg.207]


See other pages where Silver complexes with carbenes is mentioned: [Pg.174]    [Pg.206]    [Pg.210]    [Pg.293]    [Pg.254]    [Pg.333]    [Pg.118]    [Pg.140]    [Pg.207]    [Pg.225]    [Pg.41]    [Pg.208]    [Pg.209]    [Pg.210]    [Pg.210]    [Pg.211]    [Pg.214]    [Pg.217]    [Pg.218]    [Pg.218]    [Pg.218]    [Pg.286]    [Pg.289]    [Pg.6]    [Pg.264]    [Pg.101]    [Pg.33]    [Pg.145]    [Pg.705]    [Pg.230]    [Pg.233]    [Pg.243]    [Pg.252]    [Pg.254]    [Pg.221]   


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Silver carbene

Silver complexes

With Carbenes

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