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)]

Citation
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
Citations number
36
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF COORDINATION CHEMISTRY
ISSN journal
00958972 → ACNP
Volume
53
Issue
2
Year of publication
2001
Pages
163 - 172
Database
ISI
SICI code
0095-8972(2001)53:2<163:1COCTT>2.0.ZU;2-L
Abstract
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.