Abstract

Secondary interactions stabilize coordinatively demanding complexes of s-block metals [...]

Highlights

  • Complexes of the electropositive alkali and alkalino-earth metals are characterized by ionic bonding between the cation and the ligands and co-ligands

  • This is perhaps best epitomized in the structure of the arene complex [1]4, where the four potassium centers display different coordination environments

  • The potassium–alkyne complex described here is the only one of this type. This is in line with the recent account of the utilization of π ligands in alkaline-earth chemistry [19,20]

Read more

Summary

Introduction

Complexes of the electropositive alkali and alkalino-earth metals are characterized by ionic bonding between the cation and the ligands and co-ligands. The concept of so-called secondary interactions, which are essentially weak donor–acceptor interactions between the cation and charge-neutral Cπ , halide, H, or other neutral atom or group of atoms, was highlighted in a landmark article by Ruhlandt-Senge and coworkers in 2010 [1] This and other groups have in particular prepared many a compound of alkali metals (M) featuring one or more M+ ···F [2,3,4,5,6] and, perhaps more prominently, M+ ···Cπ (arene) [4,7] intramolecular interactions. Many such complexes have been structurally characterized; there are nearly 300 referenced X-ray structures to date in the Cambridge Structural Database (CSD) for η6 -coordinated K+ ···Cπ (arene) compounds alone

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.