2008
DOI: 10.1016/j.jorganchem.2008.05.016
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Cyclopentadienyl chromium and tungsten complexes with halide, methyl and σ-phenylethynyl ligands: Structures of (η5-C5H5)Cr(NO)2(–CC–C6H5), (η5-C5H5)Cr(NO)2I and [(η5-C5H4)-COOCH3]W(CO)3Cl

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Cited by 13 publications
(1 citation statement)
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“…[55,56] In light of these applications we were curious as to the ability of 1 to serve as a synthon to form a new σ-bond via a salt metathesis reaction with LiC 2 Ph. We reasoned this substrate a good choice to evaluate the electrophilic reactivity of 1 as lithium phenylacetylide is readily prepared, [57] phenlacetylide complexes of Cr are known to the crystallographic record, [58][59][60][61][62][63][64][65][66][67][68][69] and the steric demands of the square-capping pentadentate NHC ought not prohibit access by the phenylacetylide anion. We observed no change to the paramagnetic 1 H NMR spectrum over the course of 24 hr upon charging a J-young NMR tube with 1 and 1.2 equivalents of lithium phenylacetylide using THF-d8 solvent.…”
Section: Mementioning
confidence: 99%
“…[55,56] In light of these applications we were curious as to the ability of 1 to serve as a synthon to form a new σ-bond via a salt metathesis reaction with LiC 2 Ph. We reasoned this substrate a good choice to evaluate the electrophilic reactivity of 1 as lithium phenylacetylide is readily prepared, [57] phenlacetylide complexes of Cr are known to the crystallographic record, [58][59][60][61][62][63][64][65][66][67][68][69] and the steric demands of the square-capping pentadentate NHC ought not prohibit access by the phenylacetylide anion. We observed no change to the paramagnetic 1 H NMR spectrum over the course of 24 hr upon charging a J-young NMR tube with 1 and 1.2 equivalents of lithium phenylacetylide using THF-d8 solvent.…”
Section: Mementioning
confidence: 99%