ACS Applied Materials & Interfaces
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2012
·
IF 4.525
Jinxing Yu,Na Xu,Zhengping Liu,Liyuan Wang
Maleopimaric acid, cycloaddition reaction product of rosin with maleic anhydride, was reacted with hydroxylamine to afford N-hydroxy maleopimarimide, which was then further esterified with 2-diazo-1-naphthoquinone-4-sulfonyl chloride (2,1,4-DNQ-Cl) to give N-hydroxy maleopimarimide sulfonate. The carboxylic acid group of the compound was then protected by the reaction of this compound with vinyl ether compounds to give the corresponding molecular glass compounds. Upon irradiation to 365 nm light, the 2,1,4-DNQ group undergo photolysis not only to be converted into indene carboxylic acid but also generate a few amount of sulfonic acid which can catalyze the deprotection of the acid labile group. So, novel one-component positive-tone chemically amplified i-line photoresists can be formed by the molecular glass compounds. The lithographic performance of the resists was evaluated using i-line exposure system with high photosensitivity and resolution.
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高影响因子
NEW JOURNAL OF CHEMISTRY
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2019
·Vol. 43
·期 47
·18685-18694
·
IF 3.069
Rui-Xue Liu,Ying-Shu Wu,Yan-Cheng Liu,Ru-Yi Luo,Li-Dong Yang,Meng-Ting Tang,Zhen-Feng Chen,Hong Liang
Based on the characteristic anthrahydrazone pharmacophore, two new anthrahydrazone derivatives (9-PMAH and APMAH) were synthesized, which further afforded two corresponding cisplatin-like Pt(II) complexes (9-PMAH-Pt and APMAH-Pt). Their chemical structures were characterized by IR, ESI-MS, elemental analysis and X-ray single crystal diffraction method. Their in vitro cytotoxicity towards a series of human tumor cell lines and the normal liver cell line HL-7702 were screened and shown in IC50 values and compared with that of cisplatin. 9-PMAH-Pt showed higher cytotoxicity against MGC-803 and HepG-2 than the other tested compounds including cisplatin, while it showed lower toxicity on HL-7702 than cisplatin. The structure–activity relationship from the in vitro cytotoxicity study indicated that the substitution of –CHO on the opposite C10 of anthrahydrazone was unfavorable to higher cytotoxicity, which might be due to its steric hindrance considering the planar aromatic anthracene. Further studies demonstrated that 9-PMAH-Pt induced cell apoptosis in both MGC-803 and T-24 cells by arresting the cell cycle at the G2/M phase, which was totally different for cisplatin, suggesting the different antitumor efficacies of this platinum complex and cisplatin. On the molecular level, it was suggested that 9-PMAH-Pt could bind with DNA via an intercalative mode, likely competing with GelRed in similar intercalative binding sites. 9-PMAH-Pt also effectively inhibited the activity of TOPO I, acting as a TOPO I suppressor. The results of this work suggest a new type of platinum complex bearing anthrahydrazone ligands to form a new bifunctional antitumor candidate in comparison with the classic platinum drugs.
研究领域:
药物化学
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肿瘤学
·
分子生物学
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高影响因子
FOOD CHEMISTRY
·
2024
·
IF 8.5
Jiefen Cui,Dan Liu,Yuyang Zhang,Mengyu Ma,Mengshan Shang,Cheng Zhao,Xingmiao Lu,Chengying Zhao,Jinkai Zheng
Due to the excellent health benefits of rhamnogalacturonan I (RG-I)-enriched pectin, there has been increasing research interest in its gelling properties. To elucidate its structure–gelation relationship, chemical modifications were used to obtain RG-I-enriched pectin (P11). Then, enzymatic modification was performed to obtain debranched pectins GP11 and AP11, respectively. The effects of RG-I side chains on structural characteristics (especially spatial conformation) and gelling properties were investigated. Among the low-methoxylated pectins (LMPs), AP11, with a loose conformation (Dmax 52 nm) showed the poorest gelling, followed by GP11. In addition to primary structure , spatial conformation (Dmax and Rg) also showed strong correlations ( r 2 > 0.8) with gelation . We speculate that compact conformation may shorten distance between pectin chains and reduces steric hindrance , contributing to formation of strong gel network. This is particularly important in LMPs with abundant side chains. The results provide novel insights into relationship between spatial conformation and gelling properties of RG-I-enriched pectin.
研究领域:
食品科学
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生物化学
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ACS Sustainable Chemistry & Engineering
·
2025
·
IF 7.3
Xiaoyan Han,Shan Wang,Tingting Cui,Yumin Yang,Haixiang Li,Haiwen Zhang,Huanhuan Zhou,Xiaoxia Li
Aristolochic acid I (AA-I), a known nephrotoxin and carcinogen, is commonly found in certain medicinal plants, posing significant safety concerns. In this work, defect-engineered, molecularly imprinted UiO-66-NH2 was synthesized via a one-pot hydrothermal method using indomethacin (IND) as a green alternative template. The resulting imprinted metal–organic framework effectively mitigates matrix interference, enabling highly selective recognition and the efficient adsorption of AA-I. Structural characterization confirmed that the imprinting process and template removal did not compromise the framework integrity of UiO-66-NH2. Spectroscopic analysis revealed that AA-I recognition was governed by Zr coordination, electrostatic interactions, and spatially confined recognition sites within the porous framework. Density functional theory calculations further elucidated the interaction mechanisms involved in the adsorption process. The imprinted UiO-66-NH2 exhibited a maximum adsorption capacity of 42.74 mg/g and an imprinting factor of 2.48. In real sample analysis, the material achieved recovery rates of 96.7–103.5% and excellent selectivity in Clematis armandii extracts. The adsorption efficiency remained above 80% after five adsorption–desorption cycles, indicating good structural stability and reusability. This work offers a promising and sustainable strategy for improving herbal medicine safety through the rational design of ecofriendly MOF-based adsorbents.
研究领域:
药用植物学
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材料科学
·
分析化学
·
环境科学
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高影响因子
JOURNAL OF SOLID STATE CHEMISTRY
·
2021
·
IF 3.498
Mei Yan,Wen-Dong Yao,Wenfeng Zhou,Wenlong Liu,Ru-Ling Tang
Inorganic gallates are attractive owing to their abundant structures and wide applications for nonlinear optics, magnetism , molecular sieve and catalysis. Herein, a new cesium cadmium gallate, CsCdGa 3 O 6 , has been synthesized by a solid-state reaction, which is the first I-II-III-O (I = alkali metals, II = divalent metals, III = Al, Ga, In) type oxide. It crystallizes in the centrosymmetric space group P 2 1 / c , and the three-dimensional Ga–O polyanionic framework is constructed by [Ga 4 O 14 ] 16− helical belts linked [Ga 6 O 6 ] 6+ and [Ga 8 O 8 ] 8+ cages. Thermal analysis indicates that it possesses high thermal stability. Various characterizations and results analysis including XRD , TG-DSC, IR, Raman spectrum , as well as electronic structure calculations were performed.
研究领域:
无机化学
·
材料科学
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DOI
高影响因子
MATERIALS LETTERS
·
2016
·
IF 2.437
Huan Zhou,Shiqin Kong,Zhiwei Liu,Yan Pan,Yang Liu,Mingzhi Luo,Linhong Deng
Calcium polyphosphate (CPP) incorporated calcium alginate (CA) composite beads were prepared via adding sodium polyphosphate (STPP) contained sodium alginate (SA) solution dropwise to calcium chloride (CaCl 2 ) solution. In the process Ca 2+ ion may attach to the -COO − in SA because of electrostatic attraction. Additionally, there is an interaction of PP to Ca 2+ to generate CPP, inducing intermolecular crosslinkages between CA and CPP. The rotational rheometer showed STPP addition had no significant impacts on the rheological properties of SA solution. While a combination of SEM, AFM, FTIR and swelling behavior study demonstrated CPP was successfully formed within the gel network of CA gel beads and played an active role in restricting the movability of the alginate polymer chains. The in vitro study implied CPP can promote the expression of ALP , Col-I, OCN and OPN of osteoblasts.
研究领域:
材料科学
·
生物医学工程
·
细胞生物学
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DOI
高影响因子
INTERNATIONAL BIODETERIORATION & BIODEGRADATION
·
2021
·
IF 4.32
Liangzhong Li,Chang Liu,Ruixue Ma,Yunjiang Yu,Zhaofeng Chang,Xiaohui Zhang,Chengyu Yang,Da Chen,Yang Yu,Wei Li,Yongdi Liu
Thallium contamination has raised global concern due to its high toxicity and treatment difficulties. In this study, the magnetic adsorbent rGO-Fe 3 O 4 @TiO 2 was synthesized for the effective removal of thallium(I) from water. The stable magnetism of the adsorbent before and after the adsorption ensured the facile magnetic separation from treated streams. The abundant hydroxyl groups on the surface of nano-sized TiO 2 particles served as adsorptive sites for the Tl(I) ions. The adsorbent performed a fast adsorption rate of Tl(I), achieving approximately 50% of ultimate adsorbed amount within the initial 10 min at near neutral condition (pH 7.0). Tl(I) removal was significantly enhanced by increasing solution pH value due to the electrostatic attraction between Tl(I) ions and the adsorbent surface. Isotherm study showed that the adsorption process was favorable, with the maximum adsorption capacity of 141.8 mg g −1 . The presence of co-existing cations might interfere and compete with the adsorption sites of Tl(I) ions. The prepared magnetically responsive adsorbent with good regeneration ability could be used as a competitive alternative to address the sudden thallium pollution incidents considering its rapid rate and high efficiency for Tl(I) adsorption and removal from aqueous systems.
研究领域:
环境科学
·
材料科学
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DOI
高影响因子
ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Xuzheng Feng,Xing Li,Zhuoxin Li,Yufei Xue,Xianggang Chen,Xiaoxu Sun,Jixiang Tang,Shuyi Liu,Zishuo Wang,Yuhang Xie,Rui Jia,Songyuan Dai,Guoping Gao,Molang Cai
Wide-bandgap perovskite solar cells (WBG PSCs) have been receiving increasing focus due to the ideal application in tandem photovoltaics. Nonetheless, WBG perovskites tend to form high-density trap states, causing serious nonradiative recombination and phase segregation, which is detrimental to the efficiency and stability of WBG PSCs. In this work, a dual-field passivation strategy facilitated by isopropylamine hydroiodide (i-PAI) is introduced, in effect, showing both the molecular dipole field passivation and interface electric field passivation. This strategy reduces the charge trap density of WBG perovskite and suppresses the phase segregation, which is supported by the analysis of the experimental data and simulation results. Moreover, the dual functional passivation mitigates the open-circuit-voltage (VOC) deficit of the WBG (1.65 eV) PSCs to 0.39 V and increases the efficiency to a competitive value of 22.21%. The device also exhibits excellent photostability, maintaining 84.2% of the initial efficiency after 1080 h of illumination under 1-sun white LED. This work showcases a pivotal pathway to defect passivation that can markedly enhancing both the efficiency and stability of wide-bandgap perovskite solar cells.
研究领域:
材料科学
·
能源技术
·
光伏研究
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高影响因子
Frontiers in Chemistry
·
2020
·
IF 3.693
Xu Yubing,Wang Xin,Pan Yuzhu,Li Yuwei,Emeka Elemike Elias,Li Qing,Zhang Xiaobing,Chen Jing,Zhao Zhiwei,Lei Wei
Organic-inorganic hybrid perovskite single crystals (PSCs) have been emerged as remarkable materials for some optoelectronic applications such as solid-state photodetectors, solar cells and light emitting diodes due to their excellent optoelectronic properties. To decrease the dark current, function layers based on spin-coating method are frequently requested for intrinsic PSCs to block the injected current by forming energy barrier. However, the amorphous function layers suffer from small carrier mobility and high traps density, which limit the speed of the photoelectric response of perovskite devices. This work supposes to grow thick MAPbBr3 and MAPbI3 mono-crystalline thin films on the surface of intrinsic MAPbBr2.5Cl0.5 PSCs substrate by a heteroepitaxial growth technique to act as electron-blocking layers. Meanwhile, C60 and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) layers are deposited on the opposite surface of substrate PSCs by spin-coating method to block injected holes. This Au-MAPbI3-MAPbBr3-MAPbBr2.5Cl0.5PSCs-C60-PCBM-Ag heterostructure can be used as excellent X-ray photodetector (XPD) due to its low dark current density of 6.97 × 10−11 A cm−2 at −0.5 V bias, high responsivity of 870 mA/W at −100 V bias and X-ray sensitivity as high as 59.7 μC mGy−1 cm−2 at −50 V bias.
研究领域:
材料科学
·
光电子学
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DOI
PubMed
高影响因子
CHEMISTRY OF MATERIALS
·
2023
·
IF 8.6
Zong Chang,Liangjian Liu,Jingying Zhai,Chenchen Liu,Xiao Wang,Chengbo Liu,Xiaojiang Xie,Qinchao Sun
Molecular electronic coupling has been found to play a crucial role in the light-induced processes of natural and artificial systems. The light-induced acoustic process (photoacoustic) is also considered to be one of the most essential characters of the light-absorbing molecules. Herein, we report an interesting observation of the molecular electronic coupling-induced photoacoustic effect (MECPA) in which the PA intensity is dominated by the molecular electronic coupling, rather than the absorption intensity as usually concerned. The molecular electronic coupling effect results in a significant exciton absorption suppression from the monomer to pentamer. However, the corresponding PA efficiency was found to be approximately 2 orders of magnitude greater for the latter. A well-behaved linear correlation between the molecular exciton absorbance and PA efficiency was observed. The surprisingly significant MECPA effect was realized via novel NIR-II squaraine-benzothiopyrylium dyes. Excellent photophysical properties of the novel NIR-II dyes were achieved, such as a large absorption extinction coefficient and high photostability. In vivo duplex PA imaging was demonstrated for tumor tissue and macrophage cells and blood and lymphoid vessels. The MECPA effect would open a new window for the design of PA contrast agent systems for in vivo imaging.
研究领域:
生物医学工程
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光学成像
·
分子生物学
·
材料科学
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DOI
高影响因子
POLYMER DEGRADATION AND STABILITY
·
2021
·
IF 5.03
Pingping Tang,Tingting Zheng,Lirui Shen,Guoying Li
Collagen hydrogels with a three-dimensional network structure were prepared through self-assembly of collagen molecules, and incubated in laccase-catalyzed gallic acid solutions (L-GA) with different concentrations (0.5–10%, w/v, calculated from the L-GA mother solution). UV-visible spectroscopy and Fourier transform infrared spectrometry suggested that quinones and cross-links between the quinones and the collagen molecules had formed. With an increase in L-GA concentration from 0.5 to 5%, the degree of cross-linking increased from 8.78% to 19.13%; when the L-GA concentration exceeded 5%, the degree of cross-linking increased slightly. At L-GA concentrations ≤ 5%, the thermal denaturation temperature (from 67.4to 74.7°C), the storage modulus (from 90 to 251.42 Pa) and the ABTS• + free radical scavenging activity (from 4.89 to 98.92%) significantly increased, and a distinct decrease was observed in the degree of enzymatic degradation (from 81.48 to 49.34%). At L-GA concentrations >5%, only a slight improvement in these properties was observed. The gel strength of the modified collagen hydrogels reached a maximum value of 1346 g, which was more than twice that of the native collagen hydrogel (656 g) at 5%L-GA. Furthermore, afterthe concentration of L-GA exceeded 1%, the pore sizes observed by scanning electron microscopy began to diminish and showed denser network structures. These data indicated that the properties of collagen hydrogels can be substantially improved by modification with an appropriate concentration of L-GA.
研究领域:
生物材料
·
材料科学
·
生物化学
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DOI
高影响因子
Acta Pharmaceutica Sinica B
·
2021
·
IF 11.614
Wenjuan Liu,Zhenqiang Li,Simeng Chu,Xiaoyao Ma,Xiaoying Wang,Min Jiang,Gang Bai
Hyperaldosteronism is a common disease that is closely related to endocrine hypertension and other cardiovascular diseases. Cytochrome P450 11B2 (CYP11B2), an important enzyme in aldosterone (ALD) synthesis, is a promising target for the treatment of hyperaldosteronism. However, selective inhibitors targeting CYP11B2 are still lacking due to the high similarity with CYP11B1. In this study, atractylenolide-I (AT-I) was found to significantly reduce the production of ALD but had no effect on cortisol synthesis, which is catalyzed by CYP11B1. Chemical biology studies revealed that due to the presence of Ala320, AT-I is selectively bound to the catalytic pocket of CYP11B2, and the C8/C9 double bond of AT-I can be epoxidized, which then undergoes nucleophilic addition with the sulfhydryl group of Cys450 in CYP11B2. The covalent binding of AT-I disrupts the interaction between heme and CYP11B2 and inactivates CYP11B2, leading to the suppression of ALD synthesis; AT-I shows a significant therapeutic effect for improving hyperaldosteronism.
研究领域:
药理学
·
内分泌学
·
心脏病学
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PubMed
高影响因子
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