π-Conjugated stannole copolymers synthesised by a tin-selective Stille cross-coupling reaction.

The synthesis of four well-defined conjugated polymers containing unusual heterocycle units in the main chain, namely stannole units as building blocks, is reported. The stannole-thiophenyl copolymers were generated by tin-selective Stille coupling reactions in nearly quantitative yields of 94% to 98%. NMR data show that the tin atoms in the rings remain unaffected.

The influence of the formal replacement of thiophenes by stannoles in terthiophene and sexithiophene on the optoelectronic properties and electrochemical behavior.

Polystannoles with thienyl co-monomers are in many ways similar to polythiophenes, but they display much reduced band gaps. However, their polymerization processes are not well researched. Thiophene can be oxidatively electropolymerized, but as stannoles are organometallic, the fundamental question arises whether their inclusion in a conjugated backbone can protect them sufficiently to be able to perform an oxidative electropolymerization.

Experimental and Theoretical Studies of a Spirostannole and Formation of a Pentaorganostannate.

A new spirostannole, 1,1',3,3'-tetrakis(5-methylthiophen-2-yl)-4,4',5,5',6,6',7,7'-octahydro-2,2'-spirobi[benzo[]stannole] (), is synthesised and the molecular structure is compared with the optimised geometry from DFT calculations. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) are twice degenerated and show a small HOMO-LUMO energy gap of 3.2 eV.

Aggregation induced emission - emissive stannoles in the solid state.

The optoelectronic and structural properties of six stannoles are reported. All revealed extremely weak emission in solution at 295 K, but intensive fluorescence in the solid state with quantum yields (ΦF) of up to 11.1% in the crystal, and of up to 24.

Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes.

Zirconacyclopentadienes are versatile precursors for a large number of heteroles, which are accessible by Zr-element exchange reactions. The vast majority of reports describe their preparation by the use of Negishi's reagent, which is a species that is formed in situ. The zirconacyclopentadiene is then formed by the addition of one equivalent of a diyne or two equivalents of a monoyne moiety to this Negishi species.

Tuning the Optoelectronic Properties of Stannoles by the Judicious Choice of the Organic Substituents.

Stannoles are organometallic rings in which the heteroatom is involved in a form of conjugation that is called σ*-π* conjugation. Only very little is known about how the substituents on the Sn atom or substituents on the stannole ring determine the optoelectronic properties of these heterocycles. In this work, this question has been studied experimentally and theoretically.

Syntheses and Properties of Tin-Containing Conjugated Heterocycles.

Heterocycles that contain tin atoms can be aromatic in a similar sense to well-known aromatic compounds such as benzene or thiophene, but such examples are rare. However, due to the low-lying σ*-orbitals of the tin-substituent bond in stannoles, they are capable of σ*-π* conjugation in a way that is exclusive to heavier element containing heterocycles. This makes stannoles very interesting alternatives for purely organic heterocycles in material applications, in which optoelectronic properties are of interest.