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Diseleno[2,3‑b:3′,2′‑d]selenophene and Diseleno[2,3‑b:3′,2′‑d] thiophene: Building Blocks for the Construction of [7]Helicenes

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Figshare2017-10-06 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Diseleno_2_3_i_b_i_3_2_i_d_i_selenophene_and_Diseleno_2_3_i_b_i_3_2_i_d_i_thiophene_Building_Blocks_for_the_Construction_of_7_Helicenes/5478526
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New building blocks, 2,5-di­(trimethylsilanyl)­diseleno­[2,3-b:3′,2′-d]­selenophene ((TMS)2-DSS) and 2,5-di­(trimethylsilanyl)­diseleno­[2,3-b:3′,2′-d]­thiophene ((TMS)2-DST), for helicenes were obtained from selenophene with total yields of 54 and 61%. From (TMS)2-DSS and (TMS)2-DST, selenophene-based hetero[7]­helicenes, 5,5′-di­(trimethylsilanyl)­benzo­[1,2-b:3,4-b′]­bis­(diseleno­[2,3-b:3′,2′-d]­thiophene) (rac-1), and 5,5′-di­(trimethylsilanyl)­benzo­[1,2-b:3,4-b′]­bis­(diseleno­[2,3-b:3′,2′-d]­selenophene) (rac-2) were prepared. The overall yields from selenophene were approximately 6.5 and 6.1%, respectively. Intermolecular interactions such as C–Se, C–S, and Se–Se were observed in the crystal packings of rac-1 and rac-2. In addition, the absorption behaviors of rac-1 and rac-2 were investigated.
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2017-10-06
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