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Fluorinated Tetraarylethenes: Universal Tags for the Synthesis of Solid State Luminogens

Rosario Scopelliti, Kay Severin, Farzaneh Fadaei Tirani, Euro Solari, Albert Ruggi, Abdusalom Suleymanov, Thibault Jacques Marie Damiens Vanrapenbusch, Barbara Maja Kraus

The aggregation-induced emission properties of tetraarylethenes (TAEs) have led to numerous applications in chemistry, biology, and materials science. Herein, we describe two fluorinated tetraarylethenes, which can be employed as universal tags for the synthesis of solid state luminogens. The tags are accessible in one or two steps from commercially available starting materials. Facile coupling reactions with ubiquitous substrates such as thiols, alcohols, amines, phosphines, aldehydes, and enamines allow preparing a wide range of TAE conjugates, including tagged amino acids, peptides, carbohydrates, steroids, and commercial polymers.

2022

A Mesoionic Diselenolene Anion and the Corresponding Radical Dianion

Rosario Scopelliti, Kay Severin, Farzaneh Fadaei Tirani, Andrzej Sienkiewicz, Abdusalom Suleymanov, Zhaowen Dong, Cesare Berton

Dichalcogenolenes are archetypal redox non-innocent ligands with numerous applications. Herein, we describe a diselenolene ligand with fundamentally different electronic properties. By selenation of a C2-protected imidazolium salt, we have prepared a mesoionic diselenolene. This ligand is diamagnetic, which is in contrast to the paramagnetic nature of standard dichalcogenolene monoanions. The new ligand is also redox-active, as demonstrated by isolation of a stable diselenolene radical dianion. The unique electronic properties of the new ligand give rise to unusual coordination chemistry. Thus, we were able to prepare a hexa-coordinate aluminum tris(diselenolene) complex, and a Lewis acidic aluminate complex with two ligand-centered unpaired electrons.

2022

Synthesis of Four-Membered BN3 Heterocycles by the Borylation of Triazenes

Rosario Scopelliti, Kay Severin, Abdusalom Suleymanov

Borylated triazenes were synthesized by the dehydrocoupling of triazenes with 9-borabicyclo(3.3.1)nonane, by the condensation of triazenes with BEt3, or by the reaction of sodium triazenides with dialkyl- or diarylboron halides. The structures of the products were found to depend on the size of the substituents. Sterically demanding mesityl groups at boron or nitrogen gave rise to open-chain structures, whereas smaller substituents led to the formation of novel BN3 heterocycles.

2022