Abstract
The dimetallacyclic complex H2C(Me2SiC≡CAuPMe2)2CH2 has been synthesized, in which the two gold centers are bridged by the diphosphine dmpme (= bis(dimethylphosphino)methane) and a diethynyl ligand providing “full support” for the possible transannular Au–Au contact (3). This compound and its “semi-” and “unsupported” analogues (2, 1) have been characterized by NMR spectroscopy and elemental analysis. The monomeric nature of complex 3 in solution has been established using diffusion coefficients measured by DOSY-NMR spectroscopy and comparing the data with those of complexes 1 and 2 as references.
Acknowledgements
The authors thank Barbara Teichner for performing the CHN analyses and Dr. Jens Spross for measuring the accurate mass.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved submission.
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Research funding: None declared.
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Conflict of interest statement: The authors declare no conflict of interest regarding this article.
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Supplementary Material
This article contains supplementary material (https://doi.org/10.1515/znb-2023-0022).
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Articles in the same Issue
- Frontmatter
- In this issue
- Research Articles
- Cobalt(II) and nickel(II) complexes based on 2,5-di(pyridine-4-yl)thiazolo[5,4-d]thiazole and dicarboxylate ligands: synthesis, structures and properties
- Crystal structure of the oxidotechnetate(V) complex Na2[(TcVO)(OTf)5] · 2(TfOH) with TfOH = trifluoromethanesulfonic acid
- Design, synthesis, and in-silico study of new letrozole derivatives as prospective anticancer and antioxidant agents
- Understanding formation of the InPd3 polymorphs: a DFT study
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