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Issue 25, 2010
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Synthesis and stabilization—advances in organoalkaline earth metal chemistry

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Abstract

The last decade has seen an impressive growth in alkaline earth metal chemistry, with applications ranging from synthetic organic and polymer chemistry to materials science. As a consequence, alkaline earth metal chemistry has made a leap from obscurity into the spotlight of modern organometallic chemistry. Much of this rapid development was made possible by the establishment of novel synthetic procedures that allowed facile access to the target compounds, as many conventional synthetic routes posed and continue to pose significant limitations. Novel approaches have allowed the preparation of a multitude of compounds, initiating progress not thought possible just five years ago. Examination of the new compounds delineates several factors responsible for their structure and function. Key elements in the coordination, aggregation behavior, and reactivity of these systems have been linked to secondary interactions, including M–Cπ, M–Nπ, M–F, and M–H(agostic) interactions. This feature article will provide a very brief overview of established synthetic procedures, including a brief discussion on specific shortcomings. This will be followed by a detailed presentation of novel methodologies that are the core of the rapid development of alkaline earth metal chemistry. The second part of the article will be concerned with the analysis of various secondary interactions and their role in the further development of this rapidly emerging field of chemistry.

Graphical abstract: Synthesis and stabilization—advances in organoalkaline earth metal chemistry

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Publication details

The article was received on 08 Feb 2010, accepted on 07 Apr 2010 and first published on 06 May 2010


Article type: Feature Article
DOI: 10.1039/C002600J
Citation: Chem. Commun., 2010,46, 4449-4465

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    Synthesis and stabilization—advances in organoalkaline earth metal chemistry

    W. D. Buchanan, D. G. Allis and K. Ruhlandt-Senge, Chem. Commun., 2010, 46, 4449
    DOI: 10.1039/C002600J

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