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Important milestone on the way to transition metal catalysis with aluminum

Date:
August 12, 2022
Source:
University of Freiburg
Summary:
Chemists have succeeded in synthesizing the low-valent cationic aluminum complex by a metathesis reaction.
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The chemists Philipp Dabringhaus, Julie Willrett and Prof. Dr. Ingo Krossing from the Institute of Inorganic and Analytical Chemistry at the University of Freiburg have succeeded in synthesizing the low-valent cationic aluminum complex [Al(AlCp*)3]+ by a metathesis reaction. The team presents their research work in the journal Nature Chemistry.

"In chemistry, cationic low-valent aluminum compounds are highly sought after due to their potential transition metal-like ambiphilic reactivity. However, numerous previous attempts to synthesize cationic low-valent aluminum compounds by oxidative or reductive methods have been largely unsuccessful," Krossing explains. So far, he said, there has been only one example of a cationic, low-valent aluminum compound, but it cannot be prepared by rational synthesis. "We now show that there is an unexpectedly easy access to low-valent aluminum complexes with metathesis after all," Krossing says. In metathesis, partial structures are simply exchanged between the reaction partners.

Aluminum as a cheaper alternative for catalysis

The Freiburg chemists prepared the salt [Al(AlCp*)3]+[Al(OC{CF3)3}4]- from the Schnöckel tetramer (AlCp*)4, in which aluminum is already present in the +1 oxidation state. The (AlCp*)4 reacted with Li[Al{OC(CF3)3}4] and the reaction mixture immediately turned from yellow to red. When the reaction mixture was crystallized, the scientists obtained the [Al(AlCp*)3]+[Al(OC{CF3)3}4]--salt as dark purple crystals. "X-ray crystallographic, UV spectrometric and computational studies indicate the presence of the dimeric structure both in the solid state and in solution at high concentration and low temperature, but at low concentration and room temperature the monomer forms. This clearly indicates ambiphilic reactivity of the cation," Dabringhaus said.

"Consequently, this salt can potentially be used as a building block for an [:Al(L)3]+-salt that, due to its cationic nature, might be able to perform reversible oxidative additions and reductive eliminations of small molecules," Krossing explains. "This brings us one step closer to our long-term goal of achieving catalysis -- currently done with expensive and rare transition metals -- with aluminum. Aluminum is the second most abundant element in the Earth's crust and capable of doing so in principle, as our work shows. But unfortunately, it will probably be at least another 20 years before our research on this is applied."


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Materials provided by University of Freiburg. Note: Content may be edited for style and length.


Journal Reference:

  1. Philipp Dabringhaus, Julie Willrett, Ingo Krossing. Synthesis of a low-valent Al4+ cluster cation salt. Nature Chemistry, 2022; DOI: 10.1038/s41557-022-01000-4

Cite This Page:

University of Freiburg. "Important milestone on the way to transition metal catalysis with aluminum." ScienceDaily. ScienceDaily, 12 August 2022. <www.sciencedaily.com/releases/2022/08/220812113301.htm>.
University of Freiburg. (2022, August 12). Important milestone on the way to transition metal catalysis with aluminum. ScienceDaily. Retrieved December 26, 2024 from www.sciencedaily.com/releases/2022/08/220812113301.htm
University of Freiburg. "Important milestone on the way to transition metal catalysis with aluminum." ScienceDaily. www.sciencedaily.com/releases/2022/08/220812113301.htm (accessed December 26, 2024).

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