1997
DOI: 10.1021/ic9609867
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A Carbidoheptarhenate Complex of Thallium(I)

Abstract: The reaction of TlPF6 with [Re7C(CO)21]3- in dichloromethane produces [Re7C(CO)21(μ3-Tl]2-, isolated in high yield as PPN+ or PPh4 + salts. The complex is strongly dissociated in acetone. Treatment of the complex with AuCl(PPh3) gives [Re7C(CO)21(AuPPh3)]2- and TlCl.

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Cited by 10 publications
(9 citation statements)
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“…The average of 2.87 Å is identical to that found for the arenethiolate complex [Re 7 C(CO) 21 HgSC 6 H 4 Br] 2- . The Re−Re distances in the hydrosulfide complex 2 are closely comparable to those found in other carbidoheptarhenate clusters of the type [Re 7 C(CO) 21 ML n ] 2- . , …”
Section: Resultssupporting
confidence: 72%
See 1 more Smart Citation
“…The average of 2.87 Å is identical to that found for the arenethiolate complex [Re 7 C(CO) 21 HgSC 6 H 4 Br] 2- . The Re−Re distances in the hydrosulfide complex 2 are closely comparable to those found in other carbidoheptarhenate clusters of the type [Re 7 C(CO) 21 ML n ] 2- . , …”
Section: Resultssupporting
confidence: 72%
“…The solvents used were distilled from appropriate drying agents and degassed before use. The compounds [PPh 4 ] 3 [Re 7 C(CO) 21 ] , and [PPh 4 ] 2 [Re 7 C(CO) 21 HgOH] 2 were prepared as reported. The reagents 4-bromothiophenol (Aldrich), 4-mercaptopyridine (Aldrich), 3-mercaptopropionic acid (Aldrich), and cysteamine (Fluka) were used as received.…”
Section: Methodsmentioning
confidence: 99%
“…In another carbonyl mixed metal cluster, [Re 7 C(CO) 21 Tl] 2Ϫ , dissociation of µ 3 -Tl I was followed by infrared spectroscopy in acetone and a dissociation constant K ϭ 2.1 · 10 Ϫ3  was calculated. [13] Also for the related cyano metal clusters equilibrium data are very scarce. A study of a stepwise coordination of cyanide to MoϪMo and WϪW bonded clusters has been published, but a formation of the metalϪmetal bond is not involved in the qualitative description of the equilibria.…”
Section: Resultsmentioning
confidence: 99%
“…The data on reversible equilibrium processes for metalϪmetal bonded compounds is practically non-existent. [11] [12] [13] Also for metalϪcarbon bonded compounds (excluding cyano complexes) the information is very scarce. [14] [15] Equilibrium models, which are routinely used in coordination chemistry, would provide obvious advantages also for cluster chemistry, e.g.…”
Section: Introductionmentioning
confidence: 99%
“…A variety of interesting cluster compounds results formally from the interaction of the octahedral [Re 6 (μ 6 -C)(CO) 18 ] 4- cluster core with one or more electrophilic moieties. The set for one added electrophile (X + = H + , Re(CO) 3 + , M(CO) n 2+ , Re(CO) 3 L 3+ ) includes the clusters [HRe 6 C(CO) 18 ] 3- , [Re 7 C(CO) 21 ] 3- , [Re 6 C(CO) 18 M(CO) n ] 2- (M = Ru, n = 3; M = Mo, n = 4), and [Re 7 C(CO) 21 P(OPh) 3 ] 1- [HRe 7 C(CO) 21 ] 2- , , [Re 8 C(CO) 24 ] 2- , and [Re 7 C(CO) 21 ML n ] 2- (M = Rh, , Ir, 9,11 Pd, 9,12 Pt, Cu, Ag, Au, 6,13 Hg, Tl 15 ), and the only previously reported example of three added electrophiles (X + , Y + , Z + = H + , H + , Re(CO) 3 + ) is [H 2 Re 7 C(CO) 21 ] 1- …”
Section: Introductionmentioning
confidence: 99%