Despite the widespread use of tris(pyrazolyl)borate ligands, their isoelect
ronic, neutral analogs, tris(pyrazolyl)methane Ligands, have not been exten
sively studied. By use of appropriate starting materials, such as [Cu(NCMe)
(4)]PF6 or [Cd-2(thf)(5)](BF4)(4), stable cationic complexes of the ligands
HC(3,5-Me(2)pz)(3), HC(3-Phpz)(3) and HC(3-Bu(t)pz)(3) can be prepared wit
h the metals copper(I), silver(I), cadmium(ll), lead(II) and thallium(I). I
n many cases isoelectronic groups of complexes, such as [HB(3,5-Me(2)pz)(3)
](2)Cd, {[HC(3,5-Me(2)pz)(3)]Cd[HB(3,5-Me(2)pz)(3)]}(+), and {[HC(3,5-Me(2)
pz)(3)](2)Cd}(2+), have been prepared and shown to have very similar struct
ures. The Cd-113 NMR chemical shifts of the three complexes are also very s
imilar. The isoelectronic complexes {[HC(pz)(3)](2)Pb}(2+) and [HB(pz)(3)](
2)Pb have similar distorted six-coordinate structures. The isoelectronic pa
ir {[HC(3,5-Me(2)pz)(3)](2)Pb}(2+) and [HB(3,5-Me(2)pz)(3)](2)Pb have very
similar octahedral structures in which the lone pair on the lead(ll) is ste
reochemically inactive. Thus, for most cases the tris(pyrazolyl)methane and
tris(pyrazolyl)borate ligands bond to these metals in a similar fashion.