Hysteresis Photomodulation within photochromic assemblies of [Dy(Tp2-py)F]+ Single-Molecule Magnets : Influence of the supramolecular magnetic couplings.

A 1D coordination compound made of a photochromic dithienylethene linker and [Dy(Tp2-py)F]+ units (with Tp2-py = tris(3-(2-pyridyl)pyrazolyl)hydroborate) and having tetrakis[3,5-bis(trifluoromethyl)phenyl]borate counterions is reported. Full photoconversion from the closed isomer to the open isomer of the dithienyethene within single crystals allow for monitoring of the transformation by photocrystallography. Magnetic slow relaxation as well as magnetic hysteresis are observed and can be both modulated upon light irradiation.

Phosphorus-containing polycarbosilazanes: synthesis dehydrocoupling catalysis and flame-retardant properties.

The barium complex [Ba{N(SiMe)}] has been used to catalyse the dehydropolymerisation of the phosphine-functionalised hydrosilane 4-PhP-CHSiH (A) with the α,ω-diamine 1,4-(CHNHMe)-CH (C), for the production of -[Si(4-CHPPh)H-N(Me)CH-CH-CHN(Me)]- polycarbosilazanes that contain dangling phosphino groups along the polymer backbone. The comonomers A and C, specifically prepared for this purpose and comprehensively characterised, lend themselves well to barium-promoted dehydrocoupling catalysis. They allow for the formation of linear, amine-capped polymers with molecular weights in the range 4000-8000 g mol, as estimated by DOSY and H end-group NMR analyses.

Regiospecific Methylalumination of Silacyclopropenes: The Access to Z-1-Silyl-2-Aluminyl-Disubstituted Olefins.

A methodology to access Z-1-silyl-2-aluminyl-disubstituted olefins is developed. It relies on the uncatalyzed ring opening of silacyclopropenes in the presence of a stoichiometric amount of trimethylaluminum. The resulting heterosubstituted alkenes exhibit a particular interaction between the electron-rich [Si-CH] moiety and the electron-deficient diorganoaluminyl group, resulting in similar geometrical features due to the proximity of these two centers.

Luminescence Thermochromism of a Noncluster Copper Iodide Complex.

Hybrid copper(I) halide materials are currently attracting significant attention due to their exceptional luminescence properties, offering great potential for the development of multifunctional emissive materials with, in addition, eco-friendly features. A binuclear copper iodide complex, based on the [CuIL] motif with phosphite derivatives as ligands, has been synthesized and structurally characterized. Photophysical investigations indicate that this complex displays luminescence thermochromic properties, which are characterized by a temperature-dependent change in the relative intensity of two emission bands.