containing 1,4-dihydroxyanthracene-9,10-dione
含有1,4-二羟基蒽醌-9,10-二酮
analyzing 1,4-dihydroxyanthracene-9,10-dione
分析1,4-二羟基蒽醌-9,10-二酮
synthesizing 1,4-dihydroxyanthracene-9,10-dione
合成1,4-二羟基蒽醌-9,10-二酮
detecting 1,4-dihydroxyanthracene-9,10-dione
检测1,4-二羟基蒽醌-9,10-二酮
1,4-dihydroxyanthracene-9,10-dione derivative
1,4-二羟基蒽醌-9,10-二酮衍生物
modified 1,4-dihydroxyanthracene-9,10-dione
修饰的1,4-二羟基蒽醌-9,10-二酮
using 1,4-dihydroxyanthracene-9,10-dione
使用1,4-二羟基蒽醌-9,10-二酮
identifying 1,4-dihydroxyanthracene-9,10-dione
鉴定1,4-二羟基蒽醌-9,10-二酮
1,4-dihydroxyanthracene-9,10-dione compound
1,4-二羟基蒽醌-9,10-二酮化合物
researchers synthesized 1,4-dihydroxyanthracene-9,10-dione for potential solar cell applications.
研究人员为潜在的太阳能电池应用而合成了1,4-二羟基蒽醌-9,10-二酮。
the fluorescence of 1,4-dihydroxyanthracene-9,10-dione was investigated under different ph conditions.
在不同的ph条件下研究了1,4-二羟基蒽醌-9,10-二酮的荧光性。
1,4-dihydroxyanthracene-9,10-dione derivatives showed promise as chemosensors for metal ions.
1,4-二羟基蒽醌-9,10-二酮衍生物显示出作为金属离子化学传感器的潜力。
the compound 1,4-dihydroxyanthracene-9,10-dione exhibited strong absorption in the visible region.
化合物1,4-二羟基蒽醌-9,10-二酮在可见光区域表现出强烈的吸收性。
a novel synthesis route for 1,4-dihydroxyanthracene-9,10-dione was developed in the lab.
实验室开发了一种1,4-二羟基蒽醌-9,10-二酮的新型合成路线。
the stability of 1,4-dihydroxyanthracene-9,10-dione solutions was assessed over time.
随时间推移评估了1,4-二羟基蒽醌-9,10-二酮溶液的稳定性。
1,4-dihydroxyanthracene-9,10-dione's redox properties were studied using cyclic voltammetry.
使用循环伏安法研究了1,4-二羟基蒽醌-9,10-二酮的氧化还原性质。
the interaction of 1,4-dihydroxyanthracene-9,10-dione with biomolecules was analyzed.
分析了1,4-二羟基蒽醌-9,10-二酮与生物分子的相互作用。
modifications to the structure of 1,4-dihydroxyanthracene-9,10-dione are ongoing.
对1,4-二羟基蒽醌-9,10-二酮的结构进行修改正在进行中。
1,4-dihydroxyanthracene-9,10-dione was used as a building block in a supramolecular assembly.
1,4-二羟基蒽醌-9,10-二酮被用作超分子组装的结构单元。
the optical properties of 1,4-dihydroxyanthracene-9,10-dione are highly dependent on the solvent.
1,4-二羟基蒽醌-9,10-二酮的光学性质在很大程度上取决于溶剂。
containing 1,4-dihydroxyanthracene-9,10-dione
含有1,4-二羟基蒽醌-9,10-二酮
analyzing 1,4-dihydroxyanthracene-9,10-dione
分析1,4-二羟基蒽醌-9,10-二酮
synthesizing 1,4-dihydroxyanthracene-9,10-dione
合成1,4-二羟基蒽醌-9,10-二酮
detecting 1,4-dihydroxyanthracene-9,10-dione
检测1,4-二羟基蒽醌-9,10-二酮
1,4-dihydroxyanthracene-9,10-dione derivative
1,4-二羟基蒽醌-9,10-二酮衍生物
modified 1,4-dihydroxyanthracene-9,10-dione
修饰的1,4-二羟基蒽醌-9,10-二酮
using 1,4-dihydroxyanthracene-9,10-dione
使用1,4-二羟基蒽醌-9,10-二酮
identifying 1,4-dihydroxyanthracene-9,10-dione
鉴定1,4-二羟基蒽醌-9,10-二酮
1,4-dihydroxyanthracene-9,10-dione compound
1,4-二羟基蒽醌-9,10-二酮化合物
researchers synthesized 1,4-dihydroxyanthracene-9,10-dione for potential solar cell applications.
研究人员为潜在的太阳能电池应用而合成了1,4-二羟基蒽醌-9,10-二酮。
the fluorescence of 1,4-dihydroxyanthracene-9,10-dione was investigated under different ph conditions.
在不同的ph条件下研究了1,4-二羟基蒽醌-9,10-二酮的荧光性。
1,4-dihydroxyanthracene-9,10-dione derivatives showed promise as chemosensors for metal ions.
1,4-二羟基蒽醌-9,10-二酮衍生物显示出作为金属离子化学传感器的潜力。
the compound 1,4-dihydroxyanthracene-9,10-dione exhibited strong absorption in the visible region.
化合物1,4-二羟基蒽醌-9,10-二酮在可见光区域表现出强烈的吸收性。
a novel synthesis route for 1,4-dihydroxyanthracene-9,10-dione was developed in the lab.
实验室开发了一种1,4-二羟基蒽醌-9,10-二酮的新型合成路线。
the stability of 1,4-dihydroxyanthracene-9,10-dione solutions was assessed over time.
随时间推移评估了1,4-二羟基蒽醌-9,10-二酮溶液的稳定性。
1,4-dihydroxyanthracene-9,10-dione's redox properties were studied using cyclic voltammetry.
使用循环伏安法研究了1,4-二羟基蒽醌-9,10-二酮的氧化还原性质。
the interaction of 1,4-dihydroxyanthracene-9,10-dione with biomolecules was analyzed.
分析了1,4-二羟基蒽醌-9,10-二酮与生物分子的相互作用。
modifications to the structure of 1,4-dihydroxyanthracene-9,10-dione are ongoing.
对1,4-二羟基蒽醌-9,10-二酮的结构进行修改正在进行中。
1,4-dihydroxyanthracene-9,10-dione was used as a building block in a supramolecular assembly.
1,4-二羟基蒽醌-9,10-二酮被用作超分子组装的结构单元。
the optical properties of 1,4-dihydroxyanthracene-9,10-dione are highly dependent on the solvent.
1,4-二羟基蒽醌-9,10-二酮的光学性质在很大程度上取决于溶剂。
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