固相微萃取-气相色谱法测定醒脑静注射剂中的麝香酮

中药制剂醒脑静注射剂中的麝香酮含量较低,采用水蒸气蒸馏法需要长时间的提取富集才能进行含量测定.本文采用固相微萃取-气相色谱法（SPME-GC）对醒脑静注射剂中的麝香酮含量进行测定,集样品采集、萃取、浓缩、进样和分析于一体,完成测定的整个过程仅需十几分钟,操作简单,测定结果准确可靠.     

SiO2 film electret with high surface potential stability

The plasma surface treatment and ion implantation were utilized to improve the stability of charge storage in the SiO₂ film electret. It was found that the SiO₂ films treated by argon plasma with the arcing at 700 V for 15 min, or implanted by 150 keV (kilo electron volt) Ar⁺ with a dose of 2 × 10¹¹ cm⁻², after being negatively charged, showed a remnant negative potential as large as 90% of the primary value after being stored in a glass container with desiccant for 10 days. It was also found that after being negatively charged at room temperature and aged at 200-350 °C for several times, the SiO₂ films implanted by 150 keV Ar⁺ had a relatively high remnant potential and it did not decay significantly even after being heated at the aging temperature of 200-350 °C in room atmosphere for 60 min.     

A novel approach to the synthesis of 11,11-dimethyl-bisbenzopyran-5-ones

A facile route for the synthesis of 11,11-dimethyl-bisbenzopyran-5-ones ring system is described. The key step, the late stage oxidation of the allylic methylene group was achieved by benzyl(triethyl)ammonium permanganate in CH₂Cl₂.     

Defect mitigation using d-penicillamine for efficient methylammonium-free perovskite solar cells with high operational stability

Trap-dominated non-radiative charge recombination is one of the key factors that limit the performance of perovskite solar cells (PSCs), which was widely studied in methylammonium (MA) containing PSCs. However, there is a need to elucidate the defect chemistry of thermally stable, MA-free, cesium/formamidinium (Cs/FA)-based perovskites. Herein, we show that d-penicillamine (PA), an edible antidote for treating heavy metal ions, not only effectively passivates the iodine vacancies (Pb²⁺ defects) through coordination with the –SH and –COOH groups in PA, but also finely tunes the crystallinity of Cs/FA-based perovskite film. Benefiting from these merits, a reduction of non-radiative recombination and an increase in photoluminescence lifetime have been achieved. As a result, the champion MA-free device exhibits an impressive power conversion efficiency (PCE) of 22.4%, an open-circuit voltage of 1.163 V, a notable fill factor of 82%, and excellent long-term operational stability. Moreover, the defect passivation strategy can be further extended to a mini module (substrate: 4 × 4 cm², active area: 7.2 cm²) as well as a wide-bandgap (∼1.73 eV) Cs/FA perovskite system by delivering PCEs of 16.3% and 20.2%, respectively, demonstrating its universality in defect passivation for efficient PSCs.

Iodine vacancy defects in MA-free perovskite are effectively passivated through the interaction between Pb²⁺ and the functional groups in d-penicillamine, resulting in an impressive efficiency of 22.4% along with excellent operational stability.     

Multienzyme Biocatalytic Cascade Systems in Porous Organic Frameworks for Biosensing

Multienzyme biocatalytic cascade systems (MBCS) have attracted widespread research in the field of biosensing due to selective substrate transformations and signal amplification function. However, the poor stability of enzymes significantly restricts their effectiveness in practical applications. The spatial organization of MBCS within porous organic frameworks (POFs), such as metal–organic frameworks, covalent organic frameworks, and hydrogen-bonded organic frameworks, is regarded as a promising strategy to overcome these challenges. This advanced biotechnology sets up a POFs microenvironment for enzymes immobilization, and thus make it possible to shield the enzyme from the external stimulus by POFs-guided structural confinement. Simultaneously, the tailorable porous structure of POFs shell allows for the selective transport of substrates into interior enzymes, thereby accelerating the sensing process. Herein, we present the concept of this POFs-confined MBCS, wherein enzymes were completely encapsulated into, rather than adsorption onto, the POFs. We highlight the new strategies for MBCS spatial organization through rational POFs support, and describe how this new bio-nanosystem that integrates framework and enzymes functions can be designed as a versatile biosensing platform. In addition, the challenges and outlooks are also discussed.     

Halogen- and N-haloimide-promoted homo- and heterocoupling of alpha-(N-carbamoyl)alkylcuprates and alpha-(alkoxy)alkylcuprates

Both homo- and mixed lithium di-alpha-(heteroatom)alkylcuprates readily dimerize upon addition of halogens (e.g., I(2), Br(2)) or N-halosuccinimides to afford the coupled products in excellent yields. Higher yields result when the requisite alpha-(heteroatom)alkyllithium reagents are generated via deprotonation rather than by transmetalation of the corresponding stannanes. Mixed lithium dialkyl- or alkyl(aryl)cuprate reagents containing one alpha-(heteroatom)alkyl ligand and one simple alkyl or aryl ligand give significantly lower yields of coupled product. Low enantioselectivity has been achieved in the oxidative coupling of lithium (n-Bu)(2-pyrrolidinyl)cuprate.     

Single‐Walled Carbon Nanotube Based Real‐Time Organophosphate Detector

A novel single‐walled carbon nanotube (SWNT) based biosensor for real‐time detection of organophosphate has been developed. Horizontally aligned SWNTs are assembled to desirable electrodes using AC dielectrophoresis technique. Organophosphorus hydrolase (OPH) immobilized on the SWNTs by nonspecific binding triggers enzymatic hydrolysis of organophosphates (OPs), such as paraoxon, consequently causing a detectable change in the conductance of the SWNTs. The conductance change is found to be correlated to the concentration of organophosphate. Our results suggest the novel biosensor has great potential to serve as a simple and reusable platform of sensing organophosphate on a real‐time basis.