Molecule-Enhanced Electrocatalysis of Sustainable Oxygen Evolution Using Organoselenium Functionalized Metal-Organic Nanosheets.

Remolding the reactivity of metal active sites is critical to facilitate renewable electricity-powered water electrolysis. Doping heteroatoms, such as Se, into a metal crystal lattice has been considered an effective approach, yet usually suffers from loss of functional heteroatoms during harsh electrocatalytic conditions, thus leading to the gradual inactivation of the catalysts. Here, we report a new heteroatom-containing molecule-enhanced strategy toward sustainable oxygen evolution improvement. An organoselenium ligand, bis(3,5-dimethyl-1H-pyrazol-4-yl)selenide containing robust C-Se-C covalent bonds equipped in the precatalyst of ultrathin metal-organic nanosheets Co-SeMON, is revealed to significantly enhance the catalytic mass activity of the cobalt site by 25 times, as well as extend the catalyst operation time in alkaline conditions by 1 or 2 orders of magnitude compared with these reported metal selenides. A combination of various in situ/ex situ spectroscopic techniques, ab initio molecular dynamics, and density functional theory calculations unveiled the organoselenium intensified mechanism, in which the nonclassical bonding of Se to O-containing intermediates endows adsorption-energy regulation beyond the conventional scaling relationship. Our results showcase the great potential of molecule-enhanced catalysts for highly efficient and economical water oxidation.

Structural data of highly luminescent lanthanide complexes constructed by bis-tridentate ligand and as sensor for Et2O.

In this data article, we present the structural and PXRD data of the lanthanide complexes constructed by bis-tridentate ligand tppz (2,3,5,6-tetra-2-pyridinylpyrazine). Detailed structure, luminescence and sensing properties were discussed in "highly luminescent lanthanide complexes constructed by bis-tridentate ligand and as sensor for Et2O" (Zheng et al., 2018). The data includes the structure of Tb-complex, PXRD of Tb-complex, and also detailed structure information listed in Table 1, Table 2, Table 3.

A preliminary study of neck-stomach syndrome.

AIM: To determine the expression of c-Fos, caspase-3 and interleukin-1beta (IL-1beta) in the cervical cord and stomach of rats with cervical spondylosis, to analyze their relationship, and to offer an explanation of one possible cause for functional dyspepsia (FD) and irritable bowel syndrome (IBS) caused by cervical spondylosis. METHODS: The cervical spondylosis model in rats was established by destroying the stability of cervical posterior column. The cord segments C4-6 and gastric antrum were collected 3 mo and 5 mo after the operation. Rats with the sham operation were used as controls. The expressions of c-Fos, caspase-3 and IL-1beta in the cervical cord and gastric antrum were determined by immunohistochemistry and/or Western blot. RESULTS: Immunohistochemical staining showed a few c-Fos, caspase-3 and IL-1beta-positive cells in the cervical cord and antrum in the control. There was a significant increase in c-Fos, caspase-3 and IL-1beta expression in model groups compared to the control groups at 3 mo and 5 mo after operation. More importantly, there was a significant (P < 0.05) increase in c-Fos, caspase-3 and IL-1beta expression in the model group rats at 3 mo compared to those at 5 mo after the operation (c-Fos: 11.20 +/- 2.26 vs 27.68 +/- 4.36 in the cervical cord, 11.3 +/- 2.3 vs 29.3 +/- 4.6 in the gastric antrum; caspase-3: 33.83 +/- 3.71 vs 36.32 +/- 4.01 in the cervical cord, 13.23 +/- 3.21 vs 26.32 +/- 4.01 in the gastric antrum; IL-1beta: 42.06 +/- 2.95 vs 45.91 +/- 3.98 in the cervical cord, 26.56 +/- 2.65 vs 32.01 +/- 2.98 in the gastric antrum). Western blot analysis showed time-dependent changes of caspase-3 and IL-1beta protein in the cervical cord and gastric antrum of rats with cervical spondylosis; there was no significant expression of caspase-3 and IL-1beta protein in the control group at 3 mo and 5 mo after the sham operation, whereas there was a significant difference in caspase-3 and IL-1beta protein levels between the model group rats followed up for 3 mo and those for 5 mo (P < 0.05). CONCLUSION: There is a significant association of c-Fos, caspase-3 and IL-1beta expressions in the gastric antrum with that in the spinal cord in rats with cervical spondylosis, suggesting that the gastrointestinal function may be affected by cervical spondylosis.