Henan Normal University

About: Henan Normal University is a education organization based out in Xinxiang, China. It is known for research contribution in the topics: Catalysis & Ionic liquid. The organization has 10863 authors who have published 11077 publications receiving 166773 citations.

Observation of Zc (3900)0 in e+e- →π0π0J/ψ

Abstract: Using a data sample collected with the BESIII detector operating at the BEPCII storage ring, we observe a new neutral state Z(c)(3900)(0) with a significance of 10.4 sigma. The mass and width are measured to be 3894.8 +/- 2.3 +/- 3.2 MeV/c(2) and 29.6 +/- 8.2 +/- 8.2 MeV, respectively, where the first error is statistical and the second systematic. The Born cross section for e(+)e(-) -> pi(0)pi(0) J/Psi and the fraction of it attributable to pi(0)Z(c)(3900)(0) -> pi(0)pi(0) J/Psi in the range E-c.m. = 4.19-4.42 GeV are also determined. We interpret this state as the neutral partner of the four-quark candidate Z(c)(3900)(+/-).

Time-dependent density functional theory study on electronically excited States of coumarin 102 chromophore in aniline solvent: reconsideration of the electronic excited-state hydrogen-bonding dynamics.

Abstract: The time-dependent density functional theory method was performed to investigate the electronically excited states of the hydrogen-bonded complex formed by coumarin 102 (C102) chromophore and the hydrogen-donating aniline solvent. At the same time, the electronic excited-state hydrogen-bonding dynamics for the photoexcited C102 chromophore in solution was also reconsidered. We demonstrated that the intermolecular hydrogen bond C═O···H—N between C102 and aniline molecules is significantly strengthened in the electronically excited-state upon photoexcitation, since the calculated hydrogen bond energy increases from 25.96 kJ/mol in the ground state to 37.27 kJ/mol in the electronically excited state. Furthermore, the infrared spectra of the hydrogen-bonded C102−aniline complex in both the ground state and the electronically excited state were also calculated. The hydrogen bond strengthening in the electronically excited-state was confirmed for the first time by monitoring the spectral shift of the stretching...

Dual-locked spectroscopic probes for sensing and therapy

Abstract: Optical imaging probes allow us to detect and uncover the physiological and pathological functions of an analyte of interest at the molecular level in a non-invasive, longitudinal manner. By virtue of simplicity, low cost, high sensitivity, adaptation to automated analysis, capacity for spatially resolved imaging and diverse signal output modes, optical imaging probes have been widely applied in biology, physiology, pharmacology and medicine. To build a reliable and practically/clinically relevant probe, the design process often encompasses multidisciplinary themes, including chemistry, biology and medicine. Within the repertoire of probes, dual-locked systems are particularly interesting as a result of their ability to offer enhanced specificity and multiplex detection. In addition, chemiluminescence is a low-background, excitation-free optical modality and, thus, can be integrated into dual-locked systems, permitting crosstalk-free fluorescent and chemiluminescent detection of two distinct biomarkers. For many researchers, these dual-locked systems remain a ‘black box’. Therefore, this Review aims to offer a ‘beginner’s guide’ to such dual-locked systems, providing simple explanations on how they work, what they can do and where they have been applied, in order to help readers develop a deeper understanding of this rich area of research. Dual-locked optical probes change their optical signals when they respond to two biomarkers of interest. This facilitates real-time imaging of multiple interrelated biomarkers in living systems and, thus, provides opportunities to better understand pathological events and enhanced diagnostic specificity.