Silver complexes isocyanide

Silver(I) isocyanide complexes have been known for a long time and they were usually prepared by alkylation of silver cyanide.226 More recent reports include the study of steric effects of ligands... 

Synthesis and Properties of Isocyanide and Carbonyl Complexes of Silver 2.04.2.3.1 Silver(i) isocyanide complexes... 

Reaction of the Schiff base ligand A,Ar -bis(o-diphenylphosphinobenzylidene)(ethylene-diamine (49 en=P2) with AgBF4 produced a pale yellow salt. The IR spectrum of this complex showed strong bands due to the imino and BF4 group (v(C=N) 1653 cm-1, v(BFj) 1080 cm-1). The crystal structure of the Cu1 analogue was reported and the copper ion was found to adopt a severely distorted tetrahedral geometry. This strain was manifested in its reactivity since both the copper and silver complex reacted with f-butyl isocyanide. In the case of silver(I) a five-coordinate adduct was obtained, [Ag(en=P2)(Bu NC)]BF4.396... 

The ferrocenylphosphine-silver complex catalyzes the aldol-type reaction of tosylmethyl isocyanide 71 with aldehydes with higher stereoselectivity than the gold complex (Scheme 2-59) [84]. The reaction with several aldehydes produces trans-4-tosyloxazolines 72 in up to 86% ee, which can be converted into optically active l-alkyl-2-aminoethanols by reduction with LiAlH4. 

Gold and silver isonitriles complexes were investigated recently ((168) M = Au, Ag X = N03, PFg, BF4 = 4, 8, 12). Overall, the phenyl and biphenyl gold derivatives showed an SmA phase, whereas the analogous silver complexes displayed an additional SmC phase (Figure 74). Electrostatic interactions thus seem to favor and stabilize lamellar arrangements, since phenyl isocyanides... 

Benouazzane, M., Coco, S., EspineL P., Martm-Alvarez, J. and Barbera J. (2002) Liquid crystalline behavior in gold(I) and silver(I) ionic isocyanide complexes smectic and columnar mesophases. Journal of Materials Chemistry, 12, 691-696. 

Imidazolines are also formed in silver cyanide-catalyzed cyclization of alkyl isocyanides with aliphatic diamines (Scheme 103).169 This simple synthesis can be applied in a general way with difunctional nucleophiles and has been used to prepare benzimidazoles, oxazoles, thiazoles, and oxazines.169 It is suggested that transient carbene complexes are formed in these reactions (cf. 87 in Scheme 103) but further work is required to ascertain the mechanism and scope of these processes. 

A more conventional pathway uses the halide complexes (RNC)AuX which are reacted with 1 equiv. of the isocyanide, preferentially in the presence of a silver salt (AgS03CF3, AgBF4) for removal of the halide X as AgX (Equation (44)).222... 

The cyanide ion is an ambident nucleophile and isocyanides may be side products. If the preparation of isocyanides is desired, they can be made the main products by the use of silver or copper(I) cyanide1577 (p. 368). Vinylic bromides can be converted to vinylic cyanides with CuCN,1578 with KCN, a crown ether, and a Pd(0) complex,1579 with KCN and a Ni(0) catalyst,15 1 or with K4Ni2(CN)6.1581 Tertiary halides can be converted to the corresponding nitriles by treatment with trimethylsilyl cyanide in the presence of catalytic amounts of SnCl4 RjCCl + Me3SiCN — R3CCN.1582... 

The asymmetric aldol-type addition of tosylmethyl isocyanide (99) to aldehydes can also be catalyzed by the chiral silver(I) complex, giving almost exclusively trans-S-alkyl-4-tosyl-2-oxazolines 98 [E = S02(p-Tol)] with up to 86 % ee as shown in Sch. 26 [52]. The slow addition method described above is not necessary for this reaction system. 

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