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Volumn 15, Issue 37, 2009, Pages 9375-9386

On the electronic impact of abnormal C4-bonding in n-heterocyclic carbene complexes

Author keywords

Coordination modes; Electronic tuning; Metal nucleophilicity; N heterocyclic carbene ligands; Palladium

Indexed keywords

ANALYTICAL INVESTIGATIONS; BONDING MODES; CARBENE COMPLEXES; CARBENE LIGANDS; CARBENES; CATALYTIC PROCESS; COORDINATION MODES; ELECTRON DENSITIES; ELECTRONIC IMPACT; ELECTRONIC TUNING; HYDROGENATION OF OLEFINS; LEWIS ACID; METAL CENTERS; N-HETEROCYCLIC CARBENE COMPLEX; N-HETEROCYCLIC CARBENE LIGANDS; NEUTRAL DONOR; OXIDATIVE ADDITIONS; REACTIVITY PATTERN; REDUCTIVE ELIMINATION; STEREOELECTRONIC EFFECT; STRUCTURAL ANALOGIES; X-RAY PHOTOELECTRONS;

EID: 70349300137     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200900249     Document Type: Article
Times cited : (99)

References (106)
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    • [10b,c] For clarity and consistency, the term carbene is therefore preserved,
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    • Formally, the dicarbene in complex B features C5-bound imidazolylidene ligands. In analogy to previous reports on this type of imidazolylidene bonding, we refer to this bonding mode as C4 bonding throughout this manuscript. See also refs. [6d, 7, 10]
    • Formally, the dicarbene in complex B features C5-bound imidazolylidene ligands. In analogy to previous reports on this type of imidazolylidene bonding, we refer to this bonding mode as C4 bonding throughout this manuscript. See also refs. [6d, 7, 10].
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    • See Supporting Information for details
    • See Supporting Information for details.
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