摘要
One new complex [Cu3(L1)I2]n (1; L1 = 3,5-bis(3-pyridyl)-1,2,4-triazolate) has been obtained through unprecedented in situ copper-mediated conversion of 2,5-bis(3-pyridyl)-1,3,4-oxadiazole (L2) into L1 with aqueous ammonia under solvothermal conditions. It is very remarkable that, if considering the weak bond of Cu2-I2 [2.97 Å], the whole neutral framework adopts an unprecedented 6,8-connected 2-nodal 3-D network; while regarding [(Cu1)(I2)2]1- aggregates as cavity anionic pieces, the host cationic framework adopts a 6-connected uninodal net of α-Po primitive cubic topology. The new complex 1 exhibits strong fluorescence emission with long multicomponent fluorescent lifetimes at room temperature. Its emissive excited state is primarily attributed to the (M + X)LCT based on the results of the DFT calculation.
源语言 | 英语 |
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页(从-至) | 6243-6250 |
页数 | 8 |
期刊 | CrystEngComm |
卷 | 13 |
期 | 20 |
DOI | |
出版状态 | 已出版 - 21 10月 2011 |
已对外发布 | 是 |