Tributyltin cation

Similarly, the reaction of photoexcited 9,10-dicyanoanthracene (DCA) with a benzylstannane yields the contact ion pair in which the cation radical undergoes rapid mesolytic cleavage of the C—Sn bond to afford benzyl radical and tributyltin cation (which then adds to DCA- )77 (Scheme 14). When such unimolecular processes are faster than the energy-wasting back electron transfer (/cbet) within the contact ion pair, the D/A reactions occur rapidly despite unfavorable driving forces for electron transfer. 

If fcf > feBET- the overall transformation can occur rapidly despite unfavorable driving forces for the electron transfer itself. Only follow-up reactions with high kf can compete with back electron transfer. Different kinds of such unimolecular processes can drive the equilibria toward the final product. A representative example is the mesolytic cleavage of the C-Sn bond in the radical cation resulting from the oxidation of benzylstannane by photoexcited 9,10-dicyanoanthracene (DCA). This is followed by the addition of the benzyl radical and the tributyltin cation to the reduced acceptor DCA [59]. In the arene/nitrosonium system, [ArH, NO+] complexes can exist in solution in equilibrium with a low steady-state concentration of the ion-radical pair. However, the facile deprotonation or fragmentation of the arene cation radical in the case of bifunctional donors such as octamethyl(diphenyl)methane and bicumene can result in an effective (ET) transformation of the arene donor [28, 59]. Another pathway involves collapse of the contact ion pair [D+, A- ] by rapid formation of a bond between the cation radical and anion radical (which effectively competes with the back electron transfer), as illustrated by the examples in Chart 5 [59]. 

The allylstannane 474 is prepared by the reaction of allylic acetates or phosphates with tributyltin chloride and Sml2[286,308] or electroreduction[309]. Bu-iSnAlEt2 prepared in situ is used for the preparation of the allylstannane 475. These reactions correspond to inversion of an allyl cation to an allyl anion[3l0. 311], The reaction has been applied to the reductive cyclization of the alkenyl bromide in 476 with the allylic acetate to yield 477[312]. Intramolecular coupling of the allylic acetate in 478 with aryl bromide proceeds using BuiSnAlEti (479) by in situ formation of the allylstannane 480 and its reaction with the aryl bromide via transmetallation. (Another mechanistic possibility is the formation of an arylstannane and its coupling with allylic... 

Radical Diels-Alder reactions have been used mainly to synthesize polycyclic molecules. These reactions, like those that involve cations and anions as components, proceed quickly but generally do not give high yields. Thus, the tricyclic enone 14 is the result of an intramolecular Diels-Alder reaction of quenched vinyl radical intermediate 13 obtained by treating the iododienynone 12 with n-tributyltin hydride/2,2 -azobisisobutyronitrile (AIBN) [28] (Equation 1.11). 

Mono-, di- and tributyltin ion species (in water) have been determined by cation exchange IC-ICP-MS at 0.2 ng detection limits [856]. IC is also particularly useful for HSE purposes, such as the determination of acid gases in the workplace. Applications of IC have been reviewed [857]. 

Ion chromatography using a weak cation-exchange column with direct conductivity detection was applied in the determination of aqueous tributyltin ions, with short elution times LOD 0.01 ppm, without preconcentration or derivatization. No organotin remains adsorbed on the column94. 

Ionization of the substrates to cation-radicals is affected by means of tris(4-bromophenyl) ammoniumyl hexachloroantimonate (see Section 1.7.11). Subsequent reduction of the cation-radicals is accomplished by tributyltin hydride. For example, l,l-di(anisyl)ethylene was efficiently (93%) reduced essentially at the time of mixing (less than 1 min). Scheme 7.4. 

A high degree of stereoselectivity was achieved in reductive radical cyclizations with Coordination of the oxime function (e.g. 108) with samarium cation seems to play an important role, since the identical reaction with a tributyltin hydride/radical initiator system produces poor stereoselectivity (equation 79). ... 

Fig. 8. ESI(+)-MS of the Stille reaction of 3,4-dichloroiodobenzene and vinyl-tributyltin in acetonitrile mediated by Pd(PPh3)4. A radical cation intermediate undergoing transmetallation is observed at m/z 958.

Various monohalides of triorganotin derivatives have been shown by NMR spectroscopy to ionize in polar solvents, providing the corresponding coordinated cations . Solutions of tributyltin or triphenyltin chloride, perchlorate and tetrafluoroborate have been studied by Edlund and coworkers in dichloromethane, sulfolane, acetonitrile, pyridine, DMPU, DMSO and HMPA (Table 6). They reported the most downfield Sn NMR chemical shift of 220 ppm for n-Bu3Sn+ C104 in dichloromethane and showed that the Sn NMR... 

Indolyl radicals can be generated under standard conditions by reacting 2-bromoindole with tributyltin hydride. 3-Methyl-1-tosylindole can be cyanated at C-2 in good yield by a mixture of TMSCN and PIFA via oxidation of the indole to a cation radical, then addition of cyanide anion. ... 

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