261903-03-1Relevant articles and documents
Synthesis and spectroscopic study of silacyclyne-substituted phenyleneethynylenes
Mao, Guoliang,Orita, Akihiro,Matsuo, Daisuke,Hirate, Takayoshi,Iwanaga, Tetsuo,Toyota, Shinji,Otera, Junzo
supporting information; experimental part, p. 2860 - 2864 (2009/09/06)
A series of 1,1-dimethyl-4,5:8,9-dibenzo-1-silacycloundeca-4,8-diene-2,6,10-triyne (DST)-substituted phenyleneethynylenes were successfully synthesized by reaction of Me2SiCl2 with dimagnesium dianions which had been prepared from 2,
A High-Spin and Durable Polyradical: Poly(4-diphenylaminium-1,2-phenylenevinylene)
Murata, Hidenori,Takahashi, Masahiro,Namba, Kazuaki,Takahashi, Naoki,Nishide, Hiroyuki
, p. 631 - 638 (2007/10/03)
A purely organic, high-spin, and durable polyradical molecule was synthesized: It is based on the non-Kekule- and non-disjoint design of a φ-conjugated poly(1,2-phenylenevinylene) backbone pendantly 4-substituted with multiple robust arylaminium radicals. 4-N,N-Bis(4-methoxy- and -tert-butylphenyl)amino-2-bromostyrene 5 were synthesized and polymerized with a palladium-phosphine catalyst to afford the head-to-tail-linked polyradical precursors (1). Oxidation of 1 with the nitrosonium ion solubilized with a crown ether gave the aminium polyradicals (1+) which were durable (half-life > 1 month) at room temperature in air. A high-spin ground state with an average S = (4.5)/2 for 1a+ was proved even at room temperature by magnetic susceptibility, magnetization, ESR, and NMR measurements.