1982
DOI: 10.1021/om00064a007
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Reaction of (1-3-.eta.-vinylcarbene)iron complexes with enneacarbonyldiiron. Formation of a (ferracyclopentadiene)iron (Fe-Fe) complex and a vinylcarbenediiron (Fe-Fe) complex

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Cited by 13 publications
(9 citation statements)
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“…At −60 °C this broad singlet split into three sharp signals, at 208.1, 208.5, and 219.8 ppm, showing that the Fe(CO) 3 group is fluxional at ambient temperature. A similar temperature dependence was observed for 6 . In a comparison of the spectral data of 7 with those of 6 , which are also summarized in Table , 7 is deduced to be a heterobinuclear Fe−Ru vinylcarbene complex, [μ-(1-methoxy- anti -2-(methoxycarbonyl)-μ-3-(methoxycarbonyl)-1−3-η-prop-2-en-1-ylidene)]hexacarbonyl(Fe−Ru).…”
Section: Resultssupporting
confidence: 60%
See 1 more Smart Citation
“…At −60 °C this broad singlet split into three sharp signals, at 208.1, 208.5, and 219.8 ppm, showing that the Fe(CO) 3 group is fluxional at ambient temperature. A similar temperature dependence was observed for 6 . In a comparison of the spectral data of 7 with those of 6 , which are also summarized in Table , 7 is deduced to be a heterobinuclear Fe−Ru vinylcarbene complex, [μ-(1-methoxy- anti -2-(methoxycarbonyl)-μ-3-(methoxycarbonyl)-1−3-η-prop-2-en-1-ylidene)]hexacarbonyl(Fe−Ru).…”
Section: Resultssupporting
confidence: 60%
“…For the past two decades, much attention has been focused on the chemistry of mononuclear 1 and binuclear transition-metal vinylcarbene complexes 2 , (η 4 -metallabutadiene)metal complexes 2 ‘, or η 3 :η 1 -allylidene complexes 2 ‘‘ (Chart ). Especially, heterobinuclear vinylcarbene complexes are of interest; however, methods of preparation of these complexes are not completely established. As for the preparation of (μ-vinylcarbene)(M 1 −M 2 ) complexes, the following two representative methods are reported: (1) reaction of (μ-methylene)(M 1 −M 2 ) 3 with alkynes (eq 1); (2) reaction of (η 1 -vinylcarbene)M 1 or 1-metallabutadiene 4 with M 2 (eq 2) .…”
Section: Introductionmentioning
confidence: 99%
“…1976, 421, 97 NMR spectrum of this product shows aromatic and ethyl resonances in a 3:1 ratio (o-H, 7.43 (d, 6, J = 8 Hz); m-H, 7.13 (t, 6, J = 8 Hz); p-H, 7.20 (t, 3, J = 7 Hz); CH2, 1.34 (q, 2, J = 8 Hz); CH3, 0.92 (t, 3, -7=8 Hz)). If the initial reaction solution is stirred at room temperature for 4 h and then refluxed for 20 h and worked up as described above, both Ge(SePh) 4 and EtGe(SePh)3 were isolated in yields of 20.5% and 64.2%, respectively. The 77Se NMR spectrum (2)* 0 Parameters with an asterisk were refined isotropically.…”
Section: Resultsmentioning
confidence: 99%
“…In spite of this extensive application of Superhydride over the past 10 years few examples of ethyl incorporation in an organometallic product resulting from the use of this 0.241 (5) 0.393 ( 5) 8 (1)* H3C2 -0.066 (6) 0.110 (6) 0.306 ( 6) 11 (2)* H4 0.324 ( 4 5) 9 (1)* H20 0.377 (4) 0.021 (4) 0.650 (4) 6 (D* a Parameters with an asterisk were refined isotropically. Anisotropically refined atoms are given in the form of the isotropic equivalent thermal parameter defined as C/3)[a2B(l,l) + 62B(2,2) + c2B(3,3) + a6(cos ) (1,2) + oc(cos 0)B( 1,3) + 6c(cos a)B(2,3)].…”
Section: Resultsmentioning
confidence: 99%
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