1,3-dipolar cycloaddition of CS2 to the coordinated azide in the cyclopalladated [Pd(bzan)(mu-N-3)](2). Crystal and molecular structure of di(mu-N,S-1,2,3,4-thiatriazole-5-thiolate)bis[(benzylideneaniline-C-2,N)palladium(II)]
Am. Santana et al., 1,3-dipolar cycloaddition of CS2 to the coordinated azide in the cyclopalladated [Pd(bzan)(mu-N-3)](2). Crystal and molecular structure of di(mu-N,S-1,2,3,4-thiatriazole-5-thiolate)bis[(benzylideneaniline-C-2,N)palladium(II)], J COORD CH, 53(2), 2001, pp. 163-172
The compound [Pd(bzan)(mu -N-3)](2) 1, bzan = benzylideneaniline, was prepa
red from [Pd(bzan) (mu -OOCCH3)](2) by an anion exchange reaction. The 1,3-
dipolar cycloaddition of carbon disulfide to the bridged coordinated azide
in the cyclometallated compound I was investigated. The species resulting f
rom this reaction, di(mu -N,S-1,2,3,4-thiatriazol-5-thiolate)bis[(benzylide
neaniline)palladium(II)] 2, was characterized by IR spectroscopy and X-ray
diffraction. The compound 2 is a dimer containing two [Pd(benzylideneanilin
e)] moieties connected by two vicinal bridging N,S-1,2,3,4-thiatriazole-5-t
hiolate anions in a square-planar coordination geometry for the palladium a
toms.