1998
DOI: 10.1002/(sici)1521-3773(19980518)37:9<1291::aid-anie1291>3.3.co;2-o
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New Iron–Mercury Clusters: [Hg7{Fe(CO)4}5(StBu)3Cl], [Hg14Fe12{Fe(CO)4}6S6(StBu)8Br18], and [Hg39Fe8{Fe(CO)4}18S8(StBu)14Br28]

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Cited by 5 publications
(9 citation statements)
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“…Thus, while the Cu 6 In 3 cluster is described as having a central [Cu 6 S 4 ] core, 3 has an inner [In 8 S 13 ] framework. The structure of 3 is very similar to that of two recently reported copper−indium−selenide clusters [Cu 6 In 8 Se 13 Cl 4 (PPh 3 ) 6 (CH 8 O)] and [Cu 6 In 8 Se 13 Cl 4 (P n Pr 2 Ph) 12 ] ( II ) 6a…”
Section: Resultssupporting
confidence: 79%
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“…Thus, while the Cu 6 In 3 cluster is described as having a central [Cu 6 S 4 ] core, 3 has an inner [In 8 S 13 ] framework. The structure of 3 is very similar to that of two recently reported copper−indium−selenide clusters [Cu 6 In 8 Se 13 Cl 4 (PPh 3 ) 6 (CH 8 O)] and [Cu 6 In 8 Se 13 Cl 4 (P n Pr 2 Ph) 12 ] ( II ) 6a…”
Section: Resultssupporting
confidence: 79%
“…The UV spectrum for a solution of 3 displays a weak maximum at 400 nm, with the onset of absorption at 490 nm, mirroring observations for the related selenium complex [Cu 6 In 8 Se 13 Cl 4 (PPh 3 ) 6 (OC 4 H 8 )] 6a. Solid-state diffuse reflectance spectra of 3 display a similar profile.…”
Section: Resultssupporting
confidence: 62%
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“…The method of interest to our research can be depicted by eq 4, where use of the trimethylsilyl moiety allows for favorable thermodynamic release of X−SiMe 3 13 (X can be a halide, acetate, amide, or any other adequate leaving group). In this case the substituent “R” is typically an alkyl (butyl) or aryl (phenyl, mesityl) moiety. Tanaka and co-workers have illustrated recently that a terminal trimethylsilytellurolate ligand can be accessed via the oxidative addition of Te(SiMe 3 ) 2 to a Pt(0) center .…”
Section: Introductionmentioning
confidence: 99%