3,4-Dithiaphosphole and 3,3',4,4'-Tetrathia-1,1'-Biphosphole [pi]-Conjugated Systems: S Makes the Impact

• Published in: Chemistry : a European journal Vol. 16; no. 37; p. 11340
• Main Authors: Fadhel, Omrane, Benko, Zoltán, Gras, Michael, Deborde, Valérie, Joly, Damien, Lescop, Christophe, Nyulaszi, László, Hissler, Muriel, Reau, Régis
• Format: Journal Article
• Language: English
• Published: Weinheim Wiley Subscription Services, Inc 04.10.2010
• Subjects: Chemistry; Electrons
• ISSN: 0947-6539; 1521-3765
• DOI: 10.1002/chem.201001463

Conjugated systems based on phospholes and 1,1'-biphospholes bearing 3,4-ethylenedithia bridges have been prepared using the Fagan-Nugent route. The mechanism of this organometallic route leading to intermediate zirconacyclopentadienes has been investigated by using theoretical calculations. This study revealed that the oxidative coupling leading to zirconacyclopentadienes is favored over oxidative addition within the SCC bond both thermodynamically and kinetically. The impact of the presence of the S atoms on the optical and electrochemical behavior of the phospholes and 1,1'-biphospholes has been systematically evaluated both experimentally and theoretically. A comparison with their "all-carbon" analogues is provided. Of particular interest, this comparative study revealed that the introduction of S atoms has an impact on the electronic properties of phosphole-based conjugated systems. A decrease of the HOMO-LUMO separation and a stabilization of the LUMO level were observed. These general trends are also observed with 1,1'-biphospholes exhibiting σ-π conjugation. The P atom of the 3,4-ethylenedithiaphospholes can be selectively oxidized by S8 or O2. These P modifications result in a lowering of the HOMO-LUMO separation as well as an increase of the reduction and oxidation potentials. The S atoms of the 3,4-ethylenedithia bridge of the 2,5-phosphole have been oxidized using m-chloroperoxybenzoic acid. The resulting 3,4-ethylenesulfoxide oxophosphole was characterized by an X-ray diffraction study. Experimental and theoretical studies show that this novel chemical manipulation results in an increase of the HOMO-LUMO separation and an important decrease of the LUMO level. The electropolymerization of 2-thienyl-capped 3,4-ethylenedithiathioxophosphole and 1,1'-biphosphole is reported. The impact of the S substituents on the polymer properties is discussed.