ORGANOTIN COMPOUNDS CONTAINING A BULKY (ME3SI)(3)C OR RELATED LIGAND - CRYSTAL-STRUCTURES OF ((ME3SI)(3)CME(O2NO)SN)(2)O, (PHME2SI)(3)CSNMECL2 AND (PHME2SI)(3)CSNCL3
Ss. Aljuaid et al., ORGANOTIN COMPOUNDS CONTAINING A BULKY (ME3SI)(3)C OR RELATED LIGAND - CRYSTAL-STRUCTURES OF ((ME3SI)(3)CME(O2NO)SN)(2)O, (PHME2SI)(3)CSNMECL2 AND (PHME2SI)(3)CSNCL3, Journal of organometallic chemistry, 564(1-2), 1998, pp. 215-226
Some compounds having very bulky ligands, mainly (Me3Si)(3)C (denoted
by Tsi) or (PhMe2Si)(3)C (denoted by Tpsi), attached to functional tin
centres have been studied. Treatment of TsiSnR(2)Cl, R = Me or Ph, wi
th one equivalent of ICl gave the corresponding chloride TsiSnRCl(2),
and use of an excess of ICI gave TsiSnCl(3) in both cases. Reaction of
either chloride with one equivalent of Br-2 gave the dibromide TsiSnR
Br(2); when an excess of Br-2 was used TsiSnMe(2)Cl still gave the dib
romide but TsiSiPh(2)Cl gave the tribromide TsiSnBr(3). Reaction of Ts
iSnMe(2)Br with AgSCN or Ag2O gave TsiSnMe(2)NCS and (TsiSnMe(2))(2)O,
respectively, but when the crude product from the reaction of TsiSnMe
Br(2) with AgNO3 was recrystallized from MeOH the nitrate-oxide {TsiMe
(O2NO)Sn}(2)O was obtained. In a seemingly previously unreported type
of reaction, the alkoxide TsiSnMe(2)OEt reacted with ICl, Br-2, or I-2
to give TsiSnMe(2)X, X = Cl, Br, or I, respectively, and Bu3SnOEt lik
ewise reacted with ICl to give Bu3SnCl. The chlorides TsiSnMe(2)Cl and
TsiSnMeCl(2) gave the hydrides TsiSnMe(2)H and TsiSnMeH(2) on treatme
nt with LiAlH4, but in the case of TpsiSnMe(2)Cl the Tpsi-Sn bond was
cleaved to give TpsiH. The compound (Me3Si)(2)C(SnMe2Ph)(SiMe2Cl) reac
ted with a 1 M proportion of AgBF4 in CH2Cl2 with cleavage of the Sn-P
h bond to give the difluoride (Me3Si)(2)C(SnMe2F)(SiMe2F). The crystal
structures of the monomeric compounds {TsiMe(O2NO)Sn}(2)O, TpsiSnMeCl
(2) and TpsiSnCl(3) are reported; {TsiMe(O2NO)Sn}(2)O provides the fir
st example of unidentate bonding of an NO, group to four-coordinate ti
n. (C) 1998 Elsevier Science S.A. All rights reserved.