2021
DOI: 10.1039/d1dt00707f
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A unique series of chromium(iii) mono-alkynyl complexes supported by tetraazamacrocycles

Abstract: Aiming for donor–bridge–acceptor dyads based on dissymmetric bis-alkynyl CrIII complexes, a high yield synthetic route for mono-alkynyl CrIII complexes has been developed.

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Cited by 2 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%