1989
DOI: 10.1016/s0277-5387(00)83834-6
|View full text |Cite
|
Sign up to set email alerts
|

Group 10 telluride and polytelluride complexes: Synthesis and structures of Pd(Te4)22− and (Ph3P)2Pt(μ-Te)2Pt(PPh3)2

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
10
0

Year Published

1994
1994
2017
2017

Publication Types

Select...
5
3

Relationship

0
8

Authors

Journals

citations
Cited by 44 publications
(11 citation statements)
references
References 14 publications
1
10
0
Order By: Relevance
“…The bond lengths and angles in the Se 4 2- chains lie within the expected range (Table ) and are similar to values observed in other Se x 2- chains of known Pd polyselenides. The Pd−Se(1)−Se(2) angle with 106.31(3)° is slightly higher than the Se−Se−Se angles within the chain.…”
Section: Resultssupporting
confidence: 82%
See 1 more Smart Citation
“…The bond lengths and angles in the Se 4 2- chains lie within the expected range (Table ) and are similar to values observed in other Se x 2- chains of known Pd polyselenides. The Pd−Se(1)−Se(2) angle with 106.31(3)° is slightly higher than the Se−Se−Se angles within the chain.…”
Section: Resultssupporting
confidence: 82%
“…In this respect the Pd polyselenide system is interesting because it is highly responsive to changes in countercations. For example, K 4 [Pd(Se 4 ) 2 ][Pd(Se 6 ) 2 ] (=K 2 PdSe 10 ), Cs 2 [Pd(Se 4 ) 2 ] (=Cs 2 PdSe 8 ), K 2 (enH 2 ) 2 [Pd(Se 4 ) 2 ·2Se 4 ], {(CH 3 )N(CH 2 CH 2 ) 3 N} 2 [Pd(Se 6 ) 2 ], (enH) 2 [Pd(Se 5 ) 2 ], (NEt 4 ) 5 [Pd(Se 4 ) 2 ·0.5Pd(Se 5 ) 2 ], and (Ph 4 P) 2 [Pd(Se 4 ) 2 ] all contain [Pd(Se x ) 2 ] frameworks which feature different architectures. The structural analysis of all compounds clearly shows a trend to form lower-dimensional structures with an increasing cation size, while the Pd atom always maintains a square-planar geometry.…”
Section: Introductionmentioning
confidence: 99%
“…A structural database search reveals the existence of three analogous complexes of Cu or Ni with dichalcogenide bridges (X = S, Te) with a structure of type 1a for which the corresponding 1b isomers are not known. Conversely, there are many compounds of the general formula [L 2 M(μ-X) 2 ML 2 ] (M = Rh(I), Ir(I), Pd(II), Pt(II), Au(III); X = Cl, Br, S, Se, Te) which crystallize in structures of type 1b but whose 1a isomers are not known. In this contribution, we wish to take a qualitative, delocalized view of the bonding and electronic structures of these compounds in order to understand the existence of isomerism in the copper−oxygen compounds, the analogies and differences with other existing dichalcogenide-bridged compounds, and the influence of several structural parameters on the isomerization process.…”
mentioning
confidence: 99%
“…Cluster compounds like [PPh 4 ] 2 [Pd(Te 4 ) 2 ] were synthesized by reuxing the palladium precursor with tellurium powder. 148 This intriguing complex exists in two crystallographic forms: the a and b forms. The triclinic a and orthorhombic b forms were separated using ethylene diamine and ether solvents, respectively.…”
Section: Metal Telluridesmentioning
confidence: 99%
“…The triclinic a and orthorhombic b forms were separated using ethylene diamine and ether solvents, respectively. [148][149][150] Similarly, the complex [ 151 Contrary to the palladium precursors, the platinum analog resulted in the cluster complex [Pt 4 Te 4 (Te 3 ) 6 ] 4À , which was comprised of a Pt 4 Te 4 cubane core with a distorted octahedral conguration around the platinum atom. 152 Recently, several platinum group cluster complexes were isolated by reuxing TeCl 4 with the corresponding metal precursors.…”
Section: Metal Telluridesmentioning
confidence: 99%