1992
DOI: 10.1107/s010827019101096x
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cis-Dichloro[2-(4-ethoxyphenyltelluro)ethyl methyl sulfide-S,Te]platinum(II) cis-PtCl2[Te(C6H4OC2H5)CH2CH2(CH3)S]

Abstract: another Te or to a P atom.

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Cited by 20 publications
(11 citation statements)
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“…The coordination geometry around Pt is substantially square planar, and the chlorine atom deviates the most 2+ . [10] The chelate rings are in the puckered conformation, and the carbon atoms are slightly offset from the coordination plane, www.eurjic.org [14] this can be attributed to the weaker donor property of Se relative to that of Te. By contrast, the Pt-Se2 [2.3699(9) Å] bond is obviously shorter than the other two Pt-Se bonds [2.4126(9) and 2.4158(9) Å], and it is also out of the range of other Pt-Se bond lengths formed by trans Se pairs, such as the 2.4274(5) and 2.4386(7) Å distances found for [Pt{FcSe(CH 2 ) 3 -SeFc} 2 ](PF 6 ) 2 ·2MeCN, [10] the 2.414(2) and 2.421(2) Å distances in [Pt{MeSe(CH 2 ) 3 SeMe} 2 ](PF 6 ) 2 ·2MeCN [15] and the 2.420(3) and 2.417(3) Å ones in [Pt({16}aneSe 4 )](PF 6 ) 2 · 2MeCN.…”
Section: Crystal Structuresmentioning
confidence: 97%
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“…The coordination geometry around Pt is substantially square planar, and the chlorine atom deviates the most 2+ . [10] The chelate rings are in the puckered conformation, and the carbon atoms are slightly offset from the coordination plane, www.eurjic.org [14] this can be attributed to the weaker donor property of Se relative to that of Te. By contrast, the Pt-Se2 [2.3699(9) Å] bond is obviously shorter than the other two Pt-Se bonds [2.4126(9) and 2.4158(9) Å], and it is also out of the range of other Pt-Se bond lengths formed by trans Se pairs, such as the 2.4274(5) and 2.4386(7) Å distances found for [Pt{FcSe(CH 2 ) 3 -SeFc} 2 ](PF 6 ) 2 ·2MeCN, [10] the 2.414(2) and 2.421(2) Å distances in [Pt{MeSe(CH 2 ) 3 SeMe} 2 ](PF 6 ) 2 ·2MeCN [15] and the 2.420(3) and 2.417(3) Å ones in [Pt({16}aneSe 4 )](PF 6 ) 2 · 2MeCN.…”
Section: Crystal Structuresmentioning
confidence: 97%
“…[30] Hydrogen atoms were in geometrically generated positions, riding, with the constraint U H = 1.2 U C eq on thermal parameters. The absolute structure was assigned on the basis of Flack's test [31] [0.008 (14) parameter value] in the case of FcSe(CH 2 ) 3 -Se(CH 2 ) 3 SeFc, which crystallises in an acentric space group. For graphics ORTEP-3 was employed.…”
Section: Syntheses Of Fce(ch 2 ) 3 Eј(ch 2 ) 3 Efc (E Eј = Se or Te)mentioning
confidence: 99%
“…The trans influence of telluroether donor sites has been presumed most of the time as some what lower or at the most, nearly equal to that of thioether one. We have recently observed 18 that Pt-Cl trans to SMe is 2⋅324(4) Å, whereas in the same molecule of complex, [PtCl 2 (4-EtOC 6 H 4 TeCH 2 CH 2 SMe)], Pt-Cl trans to ArTe is 2⋅336(3) Å. This observation prompted us to synthesize a palladium complex of the same (Te, S) ligand and study further the more general status of relative trans influence of telluro and thioethers.…”
Section: Trans-influence Of Tellurium Ligandsmentioning
confidence: 99%
“…In three [89,326,327] [330] contains two CI atoms and a bidentate (S, Te) ligand to give the square planar PtCljSTe chromophore. In three [89,326,327] [330] contains two CI atoms and a bidentate (S, Te) ligand to give the square planar PtCljSTe chromophore.…”
Section: Fig5 Structure Of «I-[ptcl 2^2 -Mptcp)]2chcb [325]mentioning
confidence: 99%