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Published in 2020 at "Inorganic chemistry"
DOI: 10.1021/acs.inorgchem.0c01554
Abstract: The heterometallic complex [MoReCp(μ-PR*)(CO)6] (3) was prepared in 60% overall yield from syn-[MoCp(PHR*)(CO)2] via a three-step procedure involving complexes syn-[MoCp(PClR*)(CO)2] and [MoReCp(μ-PR*)(CO)7] as intermediate species (R* = 2,4,6-C6H2tBu3). The PR* ligand in 3 displays a…
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Keywords:
morecp;
efficient synthesis;
bridged complex;
phosphinidene ... See more keywords
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Published in 2022 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.2c02236
Abstract: Cage-opening reactions of the highly strained tri-tert-butylphosphatetrahedrane (1), shown here to function as a synthon of (tri-tert-butylcyclopropenyl)phosphinidene, are described. Treatment of 1 with a base-stabilized silylene led to the corresponding phosphasilene, which was isolated in…
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Keywords:
transfer;
nickel catalyzed;
phosphinidene;
tert butylphosphatetrahedrane ... See more keywords
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Published in 2018 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.7b11032
Abstract: Reactions of trinuclear rare-earth metal complexes bearing functionalized phosphinidene ligand [L3Ln3(μ2-Me)2(μ3-Me)(μ3-η1:η2:η2-PC6H4-o)] (L = [PhC(NC6H4iPr2-2,6)2]-, Ln = Y (1a), Lu (1b)) with phenylacetylene, CO2, diisopropyl carbodiimide, isocyanide, or PhSSPh lead to the formation of a series…
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Keywords:
rare earth;
reaction mode;
phosphorus;
phosphinidene ... See more keywords
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Published in 2019 at "Dalton transactions"
DOI: 10.1039/c9dt00012g
Abstract: The stable base-free terminal phosphinidene thorium metallocene, [η5-1,2,4-(Me3C)3C5H2]2Th[double bond, length as m-dash]P-2,4,6-tBu3C6H2 (2), can be isolated from the reaction of the thorium dichloride complex [η5-1,2,4-(Me3C)3C5H2]2ThCl2 (1) with 2 equiv. of 2,4,6-(Me3C)3C6H2PHK in THF. The reactivity…
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Keywords:
thorium;
complex me3c;
3c5h2 2th;
phosphinidene ... See more keywords