Sudheendran, Mavila3; Horecha, Marta4; Kiriy, Anton4; Gevorgyan, Suren1; Krebs, Frederik C1; Buchmeiser, Michael R.5
1 Department of Energy Conversion and Storage, Technical University of Denmark2 Functional organic materials, Department of Energy Conversion and Storage, Technical University of Denmark3 University of Suttgart4 Leibniz-Institut für Polymerforschung Dresden e.V.5 Universität Stuttgart
The synthesis of AB-type block copolymers of 4,4-bis(octyloxymethyl)-1,6-heptadiyne (M1) and dipropargyl malonodinitrile (M2) via metathesis-based cyclopolymerization using well-defined molybdenum- and ruthenium-based initiators is described. While backbiting reactions were observed in the case where polymerizations were triggered by [Ru(NCO)2(IMesH2)(]CH-2-(2-PrO)–C6H4] (I2) and [Ru(NCO)2(3-Br-Py)2(IMesH2)(CHPh)] (I3), (IMesH2 ¼ 1,3-dimesitylimidazolin-2-ylidene, 3-Br-Py ¼ 3-bromopyridine), the use of RuCl2(Py)2(IMesH2)(CHPh) (I1) in THF allowed for the synthesis of poly(M1) without any backbiting, though with a broad PDI. Block copolymers, i.e. poly(M1)-b-poly(M2), could be prepared in a living manner without any backbiting by the use of the Mo-based Schrock-type initiator Mo(N-2,6-i-Pr2C6H3)(CHCMe2Ph)(OCH(CH3)2)2 (I4) and THF as solvent. Poly(M1)-b-poly(M2) was characterized by UV and fluorescence spectroscopy and used for the construction of a photovoltaic device.