mu-Acetylide and mu-alkenylidene ligands in "click" triazole syntheses
In a computational investigation, dinuclear and tetranuclear copper acetylide complexes display both superior stability and higher reactivity in the CuAAC reaction than do mononuclear complexes due to favored dicopper(I,III) mu-alkenylidene fragments, instead of ring strain in a Cu=C=C intermediate.
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2007-01 (37), p.3868-3870 |
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Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | In a computational investigation, dinuclear and tetranuclear copper acetylide complexes display both superior stability and higher reactivity in the CuAAC reaction than do mononuclear complexes due to favored dicopper(I,III) mu-alkenylidene fragments, instead of ring strain in a Cu=C=C intermediate. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/b706926j |