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rdf:type
lifeskim:mentions
pubmed:issue
23
pubmed:dateCreated
2005-11-7
pubmed:abstractText
A new type of an o-phenylene-bridged tetrathioether ligand tethered with extremely bulky substituents, 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl (Tbt) groups, at its terminal sulfur atoms, TbtS[(o-phenylene)S]3Tbt (1), was synthesized by taking advantage of the coupling reaction of thiols with iodobenzenes using Cu2O in 2,4,6-trimethylpyridine. Complexation of 1 with Na2PdCl4 gave the corresponding dichloropalladium(II) complex, [PdCl2(1)] (7). The X-ray structural analysis of 7 indicated that the central palladium metal is in a distorted octahedral environment, where the two inner sulfur atoms of 1 and the two chlorine atoms form a square planar arrangement around the palladium metal and the two terminal sulfur atoms of 1 weakly coordinate to the palladium center at the axial positions. In addition, a phenyl analogue of 1, PhS[(o-phenylene)S]3Ph (2), was synthesized by a method similar to that for 1. Reaction of 2 with Na2PdCl4 gave the corresponding dichloropalladium(II) complex, [PdCl2(2)] (8). X-ray crystallography of 8 showed a type of the structure different from the distorted octahedral structure in 7, i.e., a square planar arrangement around the central palladium atom with the one terminal sulfur atom of 2, its neighboring sulfur atom, and the two chlorine atoms. The results of the NMR studies on 8 in a CDCl3 solution were not consistent with the results of the X-ray crystallography and suggested the coordination of the two inner sulfur atoms of 2 to the palladium metal, although a possibility of the existence of the rapid interconversion among isomers could not be excluded.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Nov
pubmed:issn
0020-1669
pubmed:author
pubmed:issnType
Print
pubmed:day
14
pubmed:volume
44
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
8561-8
pubmed:year
2005
pubmed:articleTitle
Synthesis and structure of a distorted octahedral palladium(II) complex coordinated with a tetrathioether ligand tethered with bulky substituents.
pubmed:affiliation
Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan.
pubmed:publicationType
Journal Article