Variable co-ordination numbers in 1∶1 adducts of silver(I) tetrakis(pyrazolyl)borates with tertiary phosphines

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Effendy , Giancarlo Gioia Lobbia, Claudio Pettinari, Carlo Santini, Brian W. Skelton and Allan H. White


Abstract

Silver(I) derivatives containing tertiary phosphines and anionic tetrakis(pyrazol-1-yl)borates were prepared from AgO3SCF3, PR3 (R = phenyl, benzyl, cyclohexyl, 2,4,6-Me3C6H2, o-, m- or p-tolyl) or PPh2R′ (R′ = methyl or ethyl) and K[B(pz)4] or K[B(mpz)4] (Hpz = pyrazole, Hmpz = 3-methylpyrazole) and characterized through analytical and spectral (IR, 1H, 13C and 31P NMR) measurements. These compounds are stable, soluble in chlorinated solvents, and non-electrolytes in CH2Cl2 and acetone. Room-temperature single-crystal structural characterizations were made for several of them. The pyrazolyl ligand is potentially maximally tridentate, and the maximally four-co-ordinate array about the silver potentially of threefold symmetry (excepting the fourth pz moiety) where the symmetry of the phosphine permits. The variation in the silver(I) co-ordination number and environment in various combinations of various degrees of steric interaction among the above entities has been explored. The reactivity of [{AgB(pz)4}{P(C6H4Me-m)3}] and [{AgB(pz)4}{P(C6H4Me-o)3}] towards unidentate N-, S- and P-donors was also investigated.


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