Reactions of a quintuply bonded chromium dimer with alkynes
Quintuply bonded [(H)L(iPr)Cr](2) reacts with alkynes RC≡CR (R = Me, Et, Ph, CF(3)) to form exclusively 1 : 1 adducts [(H)L(iPr)Cr](2)(RCCR). All products feature relatively short Cr-Cr distances (1.919-1.962 Å) and elongated C-C bonds (1.315-1.436 Å), consistent with [2+2] cycloaddition reactions....
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Published in | Chemical communications (Cambridge, England) Vol. 47; no. 44; pp. 12191 - 12193 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
28.11.2011
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Subjects | |
Online Access | Get full text |
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Summary: | Quintuply bonded [(H)L(iPr)Cr](2) reacts with alkynes RC≡CR (R = Me, Et, Ph, CF(3)) to form exclusively 1 : 1 adducts [(H)L(iPr)Cr](2)(RCCR). All products feature relatively short Cr-Cr distances (1.919-1.962 Å) and elongated C-C bonds (1.315-1.436 Å), consistent with [2+2] cycloaddition reactions. The hydrocarbon adducts are 4-membered metallacycles, the bridging alkynes of which are progressively skewed with respect to the Cr-Cr axis. In contrast, perfluoroalkyne adds across the metal ligand moiety. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c1cc15218a |