Stannylium ions cationic

In the field of stannylium ions, n-BusSn B (C6F5)3H , synthesized by the oxidation of stannyl hydride with B(CgF5)3 (Section 2.1.2.2, Scheme 2.2, D), was characterized by Lambert et al. as a tricoordinate stannyl cation becanse of its low-field Sn NMR resonance of 360ppm. The same n-BusSn cation, having a TPFPB connterion, exhibited a less deshielded valne of +263 ppm (at room temperature), which, however, was corrected in snbseqnent stndies to +434ppm (at -Bn3Sn+ TFPB, ... 

In recent years, examples of stannylium ions, R3Sn+, and of stannylalkyl cations, R3SnCC+, have been isolated and characterized. 

The straightforward access to stable radicals opened the avenue for the synthesis of the corresponding cations by one-electron oxidations. Thus, the stable radicals (t-Bu2MeSi)3E (E = Si, Ge, Sn) can be oxidized by trityl cation in benzene, and for germanium and tin the free germylium, 22, and stannylium ion, 23, could be... 

The intramolecular n-electron donation from the remote double bond to the stannylium ion center in the stannanorbornyl cation, 62 (8 Sn = 336 in CeDg), also leads to a significant shielded tin nucleus compared to what is expected for a free trialkylstannylium ion. As already shown for the sila compounds 55-58, the coordination of the C = C double bond to the electron-deficient tin center in 62 is indicated by a low-field shift of the resonance of the vinylic carbon atoms by 11.1 ppm. Additionally, the small scalar Sn-C coupling constant J(SnC) = 26 Hz gives clear evidence for the intramolecular Ti-complexation." ... 

Similarly, the cationic character of the germylium ion MessGe", 76, was estimated by comparison of the low-field shift of the C NMR resonances of the aryl carbon atoms upon ionization with those low-field shifts found for the homologous silylium and stannylium ions." The deshielding of the aryl carbon atoms in 76 is comparable to that found for 1 and 65. This is consistent with charge development on germanium in 76 that is comparable to that on silicon in MessSi, 1, and tin in Mes3Sn, 65. 

The next landmark was the synthesis of the germylium, 22, and the stannylium ion, 23, by one-electron oxidations from the corresponding stable radicals with trityl TPFPB by Sekiguchi and co-workers. As in the case of the allyl cleavage to generate the mesityl-substituted cations, the reaction, in this case the oxidation, occurs at the periphery of the molecule and gives the possibility for efficient steric protection of the incipient cation. Both trivalent cations were obtained as their TPFBP salts and the crystal structure show well separated anions and cations. 

While for silyl and germyl cation complexes tetracoordination of the element prevails, stannyl cations favor pentacoordination. That is, the trigonal-bipyramidal environment of the Sn atom in the diwater complex of the stannylium ion Me3Sn ... 

Recently, catalytic amounts of Lewis acids have been used in the reaction of allyllic tri- -butyltins with carbonyl compounds. Maruoka et al. report the remarkably chemoselective allylstannation of o-anisaldehyde over/>-anisaldehyde, catalyzed by BlCgFsL.1 z Piers et al. report that the chemoselectivity observed does not rely on classical chelation control. They conclude that stannylium ion pair [Bu3Sn(o-anisaldehyde)2]+[o-ArCH(allyl)OB(G6Fs)3] is the active species which is preferentially formed over the complex of/>-anisaldehyde with BlCgFsL (Equation (44)).143 Lambert et al. report a similar formation of stannyl cation from allyltri- -butyltin and trityl (CgFsLB-.144... 

While for silyl and germyl cation complexes tetracoordination of the element prevails, stannyl cations favor pentacoordination. That is, the trigonal-bipyramidal environment of the Sn atom in the diwater complex of the stannylium ion Me3Sn + [Me3Sn(H20)2]+ 84178 has its counterpart in the tetrahedral structure of the pro-tonated silanol 85.116 The structure of the bis(acetonitrile)tricyclohexyltin hexa-fluoroantimonate 86 SbF6179 reveals pentacoordination for the tin atom,180 while all... 

Tin(IV) compounds are known with tin coordination numbers of 3,4, 5, 6, and in some cases >6. The search for free triorganotin cations (stannylium ions) continues, and a few examples (e.g. 25 and have been reported where three-coordinate tin atoms are likely to be present both in the solid state and in solution (Scheme 2.1.6). The extreme " Sn nuclear deshielding in the tris(silyl)stannylium ion 26 is caused by Bo-induced currents involving a -tt magnetic dipole-allowed transitions, for which the energy difference is much smaller when compared with the triarylstannylium ion 25. Examples of another new class of organotin compounds are also shown in Scheme 2.1.6. The positively charged tin centers in these zwitterionic species 27 and 28 are stabilized by coordination with C C bonds. ... 

Free stannylium cations and stannylium ions stabilized by side-on coordination with C=C... 

Coordination with solvent or anion can generate several different geometries. When a stannylium ion coordinates with a neutral solvent molecule S, either a tetracoordinate species (3, referred to as a solvated stannyl cation) or a pentacoordinate species (4) can form. Although these materials qualify as stannyl... 

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