The flexible coordination modes of guanidine ligands in Zn alkyl and halide complexes: chances for catalysis
Due to their high basicity, guanidines are versatile ligand systems. In principal, they could use both their imino and amino nitrogen to establish a dative metal-N bond. However, generally only the imino N of a guanidine ligand is bound to a metal. Herein we present some examples in which both the i...
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| Hauptverfasser: | , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2011
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| In: |
European journal of inorganic chemistry
Year: 2011, Heft: 1, Pages: 83-90 |
| ISSN: | 1099-0682 |
| DOI: | 10.1002/ejic.201000775 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/ejic.201000775 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ejic.201000775 
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| Verfasserangaben: | Matthias Reinmuth, Christiane Neuhäuser, Petra Walter, Markus Enders, Elisabeth Kaifer, and Hans-Jörg Himmel |
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| 520 | |a Due to their high basicity, guanidines are versatile ligand systems. In principal, they could use both their imino and amino nitrogen to establish a dative metal-N bond. However, generally only the imino N of a guanidine ligand is bound to a metal. Herein we present some examples in which both the imino and amino groups of guanidine ligands are directly engaged in the bonding to a metal ion. Under certain conditions the amino group could establish an additional link to a metal center acting as a hemilabile ligand. This result is likely to be of relevance for catalytic reactions, demonstrating the possibility to stabilize a vacancy at the metal (for instance generated by ligand dissociation). | ||
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