TY - JOUR
T1 - Two Silver Coordination Network Compounds with Colorful Photoluminescence
AU - Yang, Dandan
AU - Xu, Wenlong
AU - Cao, Xiaowei
AU - Zheng, Shaojun
AU - He, Jiangang
AU - Ju, Qiang
AU - Fang, Zhenlan
AU - Huang, Wei
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/8/15
Y1 - 2016/8/15
N2 - The excitation-wavelength-dependent photoluminescence (EWDP) property of flexible organic ligand 1,4-bis(2-methyl-imidazol-1-yl)butane (Bmib) was observed. Herein, Bmib was chosen as a bridge linker to react with AgX (X = Br and I) to synthesize novel coordination network compounds (CNCs) with interesting EWDP properties. As anticipated, under the same hydrothermal synthesis conditions, two new isomorphic CNCs, i.e. [Ag2(Bmib)Br2]∞ (IAM16-1) and [Ag2(Bmib)I2]∞ (IAM16-2), as the first examples of CNCs showing EWDP properties, have been obtained. The EWDP properties may be attributed to the stretch and rotation of the long -(CH2)4- chains of Bmib and the spatial orientation adjustment of the methyl group of each imidazole ring at different excitation wavelengths. It is a great challenge to point out the emission mechanisms of CNCs merely from the experimental results due to their multiple charge transfer routes. To address this issue, we adopt DFT calculations to pursue in-depth investigation of the emission mechanisms for IAM16-1 and IAM16-2, respectively.
AB - The excitation-wavelength-dependent photoluminescence (EWDP) property of flexible organic ligand 1,4-bis(2-methyl-imidazol-1-yl)butane (Bmib) was observed. Herein, Bmib was chosen as a bridge linker to react with AgX (X = Br and I) to synthesize novel coordination network compounds (CNCs) with interesting EWDP properties. As anticipated, under the same hydrothermal synthesis conditions, two new isomorphic CNCs, i.e. [Ag2(Bmib)Br2]∞ (IAM16-1) and [Ag2(Bmib)I2]∞ (IAM16-2), as the first examples of CNCs showing EWDP properties, have been obtained. The EWDP properties may be attributed to the stretch and rotation of the long -(CH2)4- chains of Bmib and the spatial orientation adjustment of the methyl group of each imidazole ring at different excitation wavelengths. It is a great challenge to point out the emission mechanisms of CNCs merely from the experimental results due to their multiple charge transfer routes. To address this issue, we adopt DFT calculations to pursue in-depth investigation of the emission mechanisms for IAM16-1 and IAM16-2, respectively.
UR - http://www.scopus.com/inward/record.url?scp=84982151644&partnerID=8YFLogxK
U2 - 10.1021/acs.inorgchem.6b00999
DO - 10.1021/acs.inorgchem.6b00999
M3 - 文章
AN - SCOPUS:84982151644
SN - 0020-1669
VL - 55
SP - 7954
EP - 7961
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 16
ER -