A5032232050- Particle physics theoretical and experimental studies
- High-Energy Particle Collisions Research
- Particle Detector Development and Performance
- Quantum Chromodynamics and Particle Interactions
- Molecular Sensors and Ion Detection
- Sulfur Compounds in Biology
- Dark Matter and Cosmic Phenomena
- Catalytic C–H Functionalization Methods
- Catalytic Cross-Coupling Reactions
- Asymmetric Hydrogenation and Catalysis
- Cosmology and Gravitation Theories
- Luminescence and Fluorescent Materials
- Computational Physics and Python Applications
- Pesticide Exposure and Toxicity
- X-ray Diffraction in Crystallography
- Crystallization and Solubility Studies
- Synthetic Organic Chemistry Methods
- Chaos-based Image/Signal Encryption
- Coding theory and cryptography
- Advanced biosensing and bioanalysis techniques
- Sulfur-Based Synthesis Techniques
- Cryptographic Implementations and Security
- Neutrino Physics Research
- Cyclopropane Reaction Mechanisms
- Polyamine Metabolism and Applications
Luoyang Normal University
2019-2024
Institute of Information Engineering
2020-2023
University of Michigan–Ann Arbor
2015-2022
Tsinghua University
2015-2022
Chinese Academy of Sciences
2009-2020
University of Chinese Academy of Sciences
2020
Brookhaven National Laboratory
2013-2016
Institute of High Energy Physics
2013-2016
Boğaziçi University
2016
Istituto Nazionale di Fisica Nucleare, Sezione di Bologna
2016
In the presence of TBAB, CuI-catalyzed Suzuki−Miyaura cross-coupling vinyl halides and aryl with arylboronic acids was conducted smoothly to afford corresponding diarylethenes polyaryls in moderate good yields using DABCO (1,4-diazabicyclo[2.2.2]octane) as ligand. We also found that inexpensive CuI/DABCO catalytic system effective for Sonogashira cross-couplings halides. A variety including activated chlorides underwent coupling terminal alkynes excellent yields.
We reported a reactive probe for HSO3(-), which showed colorimetric and ratiometric fluorescence response to HSO3(-) with fast (t1/2 = 20 s), good specificity low detection limit (3.0 nM). The was cell membrane permeable successfully used visualizing trace SO2 derivatives in living cells.
A novel fluorescent probe displayed a colorimetric response to ClO<sup>−</sup> with high selectivity, fast and low detection limit (0.08 μM).
This paper describes that a simple and readily available chain diene (3R,4R)-hexa-1,5-diene-3,4-diol (L1) was successfully utilized as novel steering ligand for Rh(I)-catalyzed asymmetric conjugated additions. Encouraging yields ee's have been achieved, which may provide new practical direction designing chiral ligands in the future.
A variety of readily accessible vicinal-diamine-based chiral chain dienes were successfully synthesized and utilized as steering ligands for rhodium-catalyzed conjugated additions organoboronic acids to α,β-unsaturated carbonyl compounds afford the desired adducts in good excellent yields ee's.
Abstract A variety of acyclic chiral dienes were synthesized in a single step via palladium(0)‐catalyzed asymmetric allylic and homoallylic CH diamination terminal olefins. The applications such simple as steering ligands for rhodium(I)‐catalyzed 1,4‐additions afforded the corresponding adducts excellent yields up to 85% ee .
Nerve agents are the most toxic chemical warfare that pose severe threat to human health and public security. In this work, we developed a novel fluorescent probe NZNN based on naphthylimide
A novel pH probe based on hemi-cyanine was synthesized, which displays extremely large Stokes shift (122 nm) and good photostability. The responds to basic (pKa 8.32) with a colorimetric fluorescence turn-on signal. Interestingly, the has cell membrane permeability could selectively stain nuclei in living cells.