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Anion-driven Ag(I) coordination architectures: structural diversity and photoluminescence behaviors

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Version 2 2016-02-15, 20:34
Version 1 2015-12-23, 10:05
journal contribution
posted on 2016-02-15, 20:34 authored by Jiyong Hu, Junshuai Zhang, Jin’an Zhao, Liangliang Hu, Shufang Chen

To observe anion impact on structural diversity of coordination architectures, three 1-D Ag(I) complexes with distinct features have been prepared, {[Ag(bpbib)2(NO3)]·C3NH9O)}n (1), [Ag2(bpbib)2·(BF4)2]n (2), and [Ag2(bpbib)2·(ClO4)2]n (3), by the reactions of 4,4′-bis((2-(pyridin-2-yl)-1H-benzo[d]imidazol-1-yl)methyl)biphenyl (bpbib) with Ag(I) salts. Complex 1 is a 1-D helical chain, whereas 2 and 3 bear ligand-unsupported Ag(I)···Ag(I) interaction-directed 1-D structural motif, with synergetic working of flexible organic linker and anions. All complexes exhibit strong triplet state emission at cryogenic temperatures, which profits from the reduction of nonradiative transitions.

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