铈
硝基
化学
转身(生物化学)
荧光
组合化学
叠氮化物
无机化学
光化学
材料科学
纳米技术
有机化学
生物化学
烷基
物理
量子力学
作者
Amlan Buragohain,Shyam Biswas
出处
期刊:CrystEngComm
[Royal Society of Chemistry]
日期:2016-01-01
卷期号:18 (23): 4374-4381
被引量:101
摘要
A new and an existing Ce-based metal–organic framework (MOF) having a UiO-66 framework topology and incorporating azide and nitro functional groups in their frameworks have been successfully used as turn-on fluorescent probes for the sensing of H2S under physiological conditions. The azide (1-N3) and nitro (2-NO2) functionalized Ce MOFs have been synthesized under similar solvothermal conditions (100 °C, 15 min) using ammonium cerium(IV) nitrate and H2BDC-X (BDC = 1,4-benzenedicarboxylate; X = –N3 for 1-N3 and –NO2 for 2-NO2) linkers in DMF/H2O (DMF = N,N-dimethylformamide) mixtures. The phase purity of both compounds has been confirmed by X-ray powder diffraction (XRPD) analyses, infrared spectroscopy and thermogravimetric (TG) analyses. The thermally activated forms of both compounds (1′-N3 and 2′-NO2) show fast response time, excellent selectivity and sensitivity for the detection of H2S under physiological conditions (HEPES buffer, pH 7.4) through the fluorescence 'turn-on' mechanism. The detection limits (12.2 μM for 1′-N3 and 34.8 μM for 2′-NO2) of both materials lie within the range of the H2S concentration observed in biological systems. The materials can selectively detect H2S even in the presence of other competing biomolecules. Apart from the sensing of H2S, both compounds exhibit high uptake of CO2 (2.6 mmol g−1 for 1′-N3 and 3.7 mmol g−1 for 2′-NO2) at 0 °C and 1 bar. Thus, the materials are promising candidates in the fields of H2S sensing and CO2 capture.
科研通智能强力驱动
Strongly Powered by AbleSci AI