基于萘啶类配体,我们得到了具有单分子磁体行为的热稳定镝配合物(inset of Fig.1)。零场下自旋翻转有效能垒为38波数,1000 Oe直流场下为93波数。单晶/粉末X射线衍射、交流磁化率、荧光光谱[1]的测试表明,升华后化合物的结构和磁学性质...
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基于萘啶类配体,我们得到了具有单分子磁体行为的热稳定镝配合物(inset of Fig.1)。零场下自旋翻转有效能垒为38波数,1000 Oe直流场下为93波数。单晶/粉末X射线衍射、交流磁化率、荧光光谱[1]的测试表明,升华后化合物的结构和磁学性质与升华前一致。第一原理计算确认了升华前后有效能垒和磁易轴方向相近。另外,磁场下荧光光谱首次应用于稀土单分子磁体的研究。在强磁场下
The aspartate receptor (Tar) in ***, a crucial component in the bacterial sensory systems that mediate chemotaxis, has been intensively studied for years[1].However the kinetics of Tar-ligand binding in vivo is still ...
The aspartate receptor (Tar) in ***, a crucial component in the bacterial sensory systems that mediate chemotaxis, has been intensively studied for years[1].However the kinetics of Tar-ligand binding in vivo is still not clear due to lack of labeling.
D-3-phosphoglycerate dehydrogenase (PGDH) from Escherichia coli catalyzes the first critical step in serine biosynthesis[1], and can be allosterically inhibited by serine[2].
D-3-phosphoglycerate dehydrogenase (PGDH) from Escherichia coli catalyzes the first critical step in serine biosynthesis[1], and can be allosterically inhibited by serine[2].
Intrinsically disordered proteins (IDPs) show little ordered structures under physiological *** 10% of proteins in various genomes have been predicted to be fully *** occur more often in disease related genes and may ...
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Intrinsically disordered proteins (IDPs) show little ordered structures under physiological *** 10% of proteins in various genomes have been predicted to be fully *** occur more often in disease related genes and may be used as potential drug design targets.
The heat-shock protein DegP is essential for the survival of Escherichia coli cells at elevated *** binding transforms hexameric DegP into large, catalytically active multimers.
The heat-shock protein DegP is essential for the survival of Escherichia coli cells at elevated *** binding transforms hexameric DegP into large, catalytically active multimers.
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