| 貨號 |
名稱 |
CAS |
規格 |
| B34105 |
硝酸異山梨酯 |
87-33-2 |
分析標準品,HPLC≥98% |
摘要：High-energy-density lithium–metal batteries (LMBs) coupling lithium–metal anodes and high-voltage cathodes are hindered by unstable electrode/electrolyte interphases (EEIs), which calls for the rational design of efficient additives. Herein, we analyze the effect of electron structure on the coordination ability and energy levels of the additive, from the aspects of intramolecular electron cloud density and electron delocalization, to reveal its mechanism on solvation structure, redox stability, as-formed EEI chemistry, and electrochemical performances. Furthermore, we propose an electron reconfiguration strategy for molecular engineering of additives, by taking sorbide nitrate (SN) additive as an example. The lone pair electron-rich group enables strong interaction with the Li ion to regulate solvation structure, and intramolecular electron delocalization yields further positive synergistic effects. The strong electron-withdrawing nitrate moiety decreases the electron cloud density of the ether-based backbone, improving the overall oxidation stability and cathode compatibility, anchoring it as a reliable cathode/electrolyte interface (CEI) framework for cathode integrity. In turn, the electron-donating bicyclic-ring-ether backbone breaks the inherent resonance structure of nitrate, facilitating its reducibility to form a N-contained and inorganic Li2O-rich solid electrolyte interface (SEI) for uniform Li deposition. Optimized physicochemical properties and interfacial biaffinity enable significantly improved electrochemical performance. High rate (10 C), low temperature (?25 °C), and long-term stability (2700 h) are achieved, and a 4.5 Ah level Li||NCM811 multilayer pouch cell under harsh conditions is realized with high energy density (462 W h/kg). The proof of concept of this work highlights that the rational ingenious molecular design based on electron structure regulation represents an energetic strategy to modulate the electrolyte and interphase stability, providing a realistic reference for electrolyte innovations and practical LMBs.
https://pubs.acs.org/doi/abs/10.1021/acsnano.4c04517
Nature Communications（IF=16.6)
| 貨號 |
名稱 |
CAS |
規格 |
| B20660 |
咖啡酸 |
331-39-5 |
分析標準品,HPLC≥98% |
| B29008 |
3-(3,4-二羥基苯基)丙酸 |
1078-61-1 |
分析標準品,HPLC≥98% |
| B20291 |
地骨皮乙素 |
164991-67-7 |
分析標準品,HPLC≥98% |
摘要：Lycibarbarspermidines are unusual phenolamide glycosides characterized by a dicaffeoylspermidine core with multiple glycosyl substitutions, and serve as a major class of bioactive ingredients in the wolfberry. So far, little is known about the enzymatic basis of the glycosylation of phenolamides including dicaffeoylspermidine. Here, we identify five lycibarbarspermidine glycosyltransferases, LbUGT1-5, which are the first phenolamide-type glycosyltransferases and catalyze regioselective glycosylation of dicaffeoylspermidines to form structurally diverse lycibarbarspermidines in wolfberry. Notably, LbUGT3 acts as a distinctive enzyme that catalyzes a tandem sugar transfer to the ortho-dihydroxy group on the caffeoyl moiety to form the unusual ortho-diglucosylated product, while LbUGT1 accurately discriminates caffeoyl and dihydrocaffeoyl groups to catalyze a site-selective sugar transfer. Crystal structure analysis of the complexes of LbUGT1 and LbUGT3 with UDP, combined with molecular dynamics simulations, revealed the structural basis of the difference in glycosylation selectivity between LbUGT1 and LbUGT3. Site-directed mutagenesis illuminates a conserved tyrosine residue (Y389 in LbUGT1 and Y390 in LbUGT3) in PSPG box that plays a crucial role in regulating the regioselectivity of LbUGT1 and LbUGT3. Our study thus sheds light on the enzymatic underpinnings of the chemical diversity of lycibarbarspermidines in wolfberry, and expands the repertoire of glycosyltransferases in nature.
https://www.nature.com/articles/s41467-024-49010-9
CHEMICAL ENGINEERING JOURNAL（IF=15.1)
| 貨號 |
名稱 |
CAS |
規格 |
| B25673 |
嘧菌酯 |
131860-33-8 |
分析標準品,HPLC≥99% |
摘要：Foliar washoff by rainfall is a major factor inducing the inefficient utilization of pesticides. Enhancing the adhesion and retention of pesticide on plant foliage has long been of interest. The presence of waxy platelets on most plant foliage surfaces renders them rough and hydrophobic. This reduces the area of contact between pesticide particle and plant foliage, which decreases the adhesion. In this study, we developed a pesticide nanocarrier (PANI/HACC) with sea urchin-like surface morphology based on polyaniline (PANI) doped with biodegradable 2-hydroxypropyltrimethyl ammonium chloride chitosan (HACC). Then, azoxystrobin (AZOX) loaded nanoparticles (AZOX@PANI/HACC) was synthesized by physical adsorption. It exhibited retention rates of 61.4% on rice leaves and 64.6% on cucumber leaves, which were higher than that of commercially available azoxystrobin water dispersible granules (AZOX-WDG, 42.1% and 24.5%, respectively) and suspension concentrates (AZOX-SC, 23.1% and 58.8%, respectively). Additionally, pot experiments demonstrated that the control efficacy of AZOX@PANI/HACC on rice against Rhizoctonia solani was 1.64-fold and 3.0-fold of that of AZOX-WDG and AZOX-SC, respectively. The higher retention performance of AZOX@PANI/HACC was attributed to the stable adhesion by fitting nanometer-sized spikes into the spaces between the waxy platelets. Overall, the pesticide nanocarrier with spiky surface morphology provides an effective strategy for improving pesticide retention and reducing pesticide loss in agricultural production.
https://www.sciencedirect.com/science/article/pii/S1385894724033886
