个人信息Personal Information
副教授
硕士生导师
性别:女
毕业院校:大连理工大学
学位:博士
所在单位:化学学院
学科:物理化学. 化学工艺
办公地点:主校区化学楼225房间
联系方式:0411-84708901
电子邮箱:fptian@dlut.edu.cn
Metal-ion-dependent, Solvent-mediated Structural Transformation and Simultaneous Partial Transmetalation of ansrsFramework into Desulfurization-efficient Co-Cu-HKUST-1
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论文类型:期刊论文
发表时间:2021-03-26
发表刊物:ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
卷号:646
期号:17
页面范围:1437-1443
ISSN号:0044-2313
关键字:Metal-organic framework; Metal-organic framework; Structural transformation; Metal-organic framework; Structural transformation; Transmetalation; Metal-organic framework; Structural transformation; Transmetalation; HKUST-1; Metal-organic framework; Structural transformation; Transmetalation; HKUST-1; Desulfurization
摘要:[Co-2(BTC)(Cl)(DMA)(3)] (1) (BTC3-= benzene-1,3,5-tricarboxylate, DMA =N,N-dimethylacetamide) obtained from the reaction between Co(2+)and H3BTC in DMA features a three-dimensionalsrsframework built of 3-connected {Co-2(COO)(3)} as secondary building units and BTC(3-)as spacers. When exposed to DMA solution of Cu(NO3)(2),1was progressively transformed into the first heterometallic Co-Cu-HKUST-1 ([Co0.14Cu2.86(BTC)(2)]) (2) of such kind via unusually solvent-mediated structural transformation and simultaneous partial transmetalation. While the mechanism for such conversion is proposed based on systematic studies,2was revealed to be an equally efficient desulfurization adsorbent as the homometallic Cu-HKUST-1 in removing thiophene (0.142 mmol S per gram of adsorbent). However, when exposed to Zn(NO3)(2)solution in DMA for longer time,1retained its framework with limited metal-ion exchange, resulting in the formation of [Co1.93Zn0.07(BTC)(Cl)(DMA)(3)] (3). Possible reasons responsible for the formation of2and3through different routes could be due to the less solubility and more thermodynamic stability of2in comparison with those of1, and the different coordination geometries which Co2+, Zn(2+)and Cu(2+)prefer.