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SYNTHESIS-STUTTGART · 2019 ·Vol. 52 ·期 02 ·297-303 · IF 2.867

DMSO-Mediated Synthesis of Methylene-Bridged Unsymmetrical Bisamides in the Presence of AcOH

Yi Zhang,Dongheng Zhou,Yongmin Ma,Jing Chen

A simple and efficient procedure for the synthesis of N-[(methylthio)methyl]benzamides and methylene-bridged unsymmetrical bisamides was achieved mediated by DMSO in the presence of acetic acid. DMSO plays a dual role in the transformation, as not only a solvent, but also an environmentally benign methylene source. The protocol provides new strategies for effective synthesis of unsymmetrical bisamides and avoids the use of transition-metal catalysts.

研究领域: 有机化学 · 绿色化学
✓ 已验证 DOI 高影响因子
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INORGANICA CHIMICA ACTA · 2021 · IF 2.545

Anthraquinone functionalized pseudocalixarene for high lithium loading and chromogenic ion-pair recognition in DMSO

Yiwen Yao,Feifei Xing,Shourong Zhu

The [2 + 2] condensation between 1,8-dihydroxyanthraquinone diester and 1,3-diamino-2-propanol in ethanol affords pseudocalixarene macrocyclic L2 in high yield. Heating L2 to 200 °C in DMSO can generate much smaller [1 + 1] macrocycle L1 . Crystal structure of L1 shows that all non-hydrogen atoms are coplanar except one carbon from 1,3-diamino-2-propanol. L1 is quite inert, but L2 can interact with alkaline, alkaline-earth, as well as Zn 2+ , Cu 2+ , Fe 3+ and Al 3+ cation (chloride) evidenced by their CV and 1 H NMR. With a L2 :M (1:2), there are discernable UV–vis spectrum/ 1 H NMR changes in the presence Cu 2+ , Fe 3+ , Al 3+ . Anion plays a key role in the cation binding process as the chromogenic response to Li + , Na + , K + , Ba 2+ and TBA + hydroxide. L2 forms 1:1 complex with TBAOH and 2:3 complex with NaOH, KOH, Ba(OH) 2 in DMSO. L2 reacts with LiOH in 1:4 stoichiometric and is one of the highest lithium loading ligand. The reaction is second-order with t 1/2  ~ 30 min for 0.25 mM L2 in the presence of 4.0 eq. LiOH. Besides hydroxide, L2 can interact with TBAF to form 1:1 host–guest complexes evidenced by their color and NMR change. With bulky cation, TBAOH shifts E p(II) more negative, while other cations shift E p(II) to positive. L2 is an ion pair acceptor that binds hydroxide and fluoride salt chromogenic.

CAS / MDL: 616-29-5 105-36-2
研究领域: 化学 · 材料科学
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AIP Advances · 2021 ·Vol. 11 ·期 11 · IF 1.548

Effect of chlorine dioxide with NaH2PO4 and DMSO on bleaching of kraft pine pulp

Huang Lijie,Wei Zhehao,Wang Yanan,Han Xiaoxue,Chen Haobin,Huang Chongxing,Wei Yingnan

In this paper, the effect of D 0 temperature, Kappa factor and the final pH value on bleaching sulfate bleached pine wood pulp was studied. The results showed that the bleaching efficiency was better when the pH value was 4, and the amount of absorbable organic halogen (AOX) in the bleaching wastewater was decreased. The Kappa factor is linear with the whiteness in the range of 0–0.15. With the increase of the Kappa factor, the amount of AOX in bleaching wastewater of D 0 and Ep gradually increases. High temperature bleaching can reduce AOX production, but some fibers are hydrolyzed, leading to a decrease in pulp viscosity. The effects of chlorine dioxide solution adding sodium dihydrogen phosphate (NaH 2 PO 4 ) and dimethylsulfoxide (DMSO) on pulp bleaching were investigated. The results showed that both solutions could reduce the amount of AOX in bleaching wastewater. Among them, the addition of NaH 2 PO 4 in chlorine dioxide increased pulp whiteness, while the addition of DMSO was the opposite. Scanning electron microscope showed that a small amount of hollow cracks and more voids appeared on the surface of pulp fibers after the addition of NaH 2 PO 4 . Pulp fibers bleached by the chlorine dioxide adding DMSO have more folds and less voids on the surface. The surface wrinkles of pulp fibers increased with the addition of DMSO and the voids were less. FT-IR showed that the number of chromophore groups in the pulp bleached by chlorine dioxide adding NaH 2 PO 4 were decreased. However, the lignin characteristic absorption peak in the pulp bleached by chlorine dioxide adding DMSO increased at the intensity of 1062 and 1160 cm −1 , which indicated that there were more residual chromophore groups.

研究领域: 制浆造纸工程 · 环境科学
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JOURNAL OF MOLECULAR LIQUIDS · 2018 · IF 4.513

NMR studies of the tautomer distributions of d‑fructose in lower alcohols/DMSO‑d6

Kemeng Shi,Christian Marcus Pedersen,Zhaohui Guo,Yanqiu Li,Hongyan Zheng,Yan Qiao,Tuoping Hu,Yingxiong Wang

The tautomer distributions of d ‑fructose, a popular model compound for biorefinery , in various lower alcohols and DMSO‑ d 6 (ROHs/DMSO‑ d 6 ) mixtures at 298 K were investigated by quantitative 13 C NMR. The tautomer distributions of d ‑fructose in ethanol/DMSO‑ d 6 and methanol/DMSO‑ d 6 with different volume ratios of alcohols to DMSO‑ d 6 were also examined. For these normal alcohols (methanol, ethanol, n ‑propanol and n ‑butanol)/DMSO‑ d 6 , the tautomer distribution of d ‑fructose in methanol/DMSO‑ d 6 exhibited the shortest equilibration time (46 h) and the lowest concentration of β‑furanose (39.0%) at equilibrium. The fraction of fructofuranose (α‑furanose and β‑furanose) at equilibrium and time needed to reach equilibrium in branched chain alcohols/DMSO‑ d 6 obey the following order: 2‑propanol/DMSO‑ d 6 (62.2%, 320 h) >  tert ‑butanol/DMSO‑ d 6 (61.6%, 307 h) > 2‑butanol/DMSO‑ d 6 (60.6%, 216 h) > isobutanol/DMSO‑ d 6 (57.8%, 134 h). For the diols/DMSO‑ d 6 , the time for the tautomer distribution of d ‑fructose to reach the equilibrium was found to be: 1,4‑butanediol/DMSO‑ d 6 (113 h) > 1,2‑propanediol/DMSO‑ d 6 (38 h) > ethylene glycol/DMSO‑ d 6 (36 h). For ethanol/DMSO‑ d 6 and methanol/DMSO‑ d 6 with respectively different volume ratios, the experimental results showed that the high concentration of ethanol or methanol increases the conversion rate of tautomers.

研究领域: 生物化学 · 分析化学
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Journal of Environmental Chemical Engineering · 2021 · IF 5.909

Microfluidic synthesis of ZnWO4 nanoparticles and its performance in DMSO-containing wastewater treatment

Zhiquan Chen,Qingwei Song,Lei Ni,Juncheng Jiang,Yuan Yu

A systematic comparison between batch and continuous microfluidics systems was conducted for the synthesis of ZnWO 4 nanoparticles . A series of ZnWO 4 nanoparticles were prepared by different operating modes, initial concentration of reactants and residence time. The features of ZnWO 4 nanoparticles including microscopic morphology, particle size distribution and chemical structure were systematically characterized. The results showed that the continuous microfluidics system could obtain ZnWO 4 nanoparticles with a more uniform particle size compared with batch system. The size of ZnWO 4 are reduced from 92.6 to 65.2 nm by changing the reaction system. Besides, a low concentration of reactants is more suitable for preparing smaller particles ZnWO 4 nanoparticles. The average diameters of prepared ZnWO 4 nanoparticles was reduced to 50 nm in the condition that the residence time was 20 s and the concentration of reactants was 0.1 mol/L. Afterward, the degradation of dimethyl sulfoxide (DMSO) in the wastewaters was used as a probe reaction to evaluate the catalysis performance of prepared ZnWO 4 nanoparticles. This work indicates the potential opportunity of versatile continuous microfluidics technique for the fabrication of various multifunctional metal tungstates nanoparticles.

研究领域: 材料科学 · 环境科学 · 化学工程
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APPLIED OPTICS · 2024 ·Vol. 63 ·期 9 ·2279-2285 · IF 1.7

DMSO synergized with sugars: optical clearing agent modulation of optical coherence tomography of skin tissues

Yuelin Wang,Wenhui Fang,Wenhui Fang,Kai Zhang,Zhiwei Men,Zhiwei Men

The stratum corneum of the outermost skin is an important barrier impeding transdermal permeation, and permeation enhancers can reduce the barrier resistance of the stratum corneum and enhance the permeation of drugs in tissues. The optical imaging depth, signal intensity, and scattering coefficient variation rules of skin tissues in time dimension are obtained by using optical coherence tomography (OCT). The effect of optical clearing agents (OCAs) on OCT imaging is obtained by quantitatively analyzing the changes in the optical properties of tissues. D-fructose, one of the monosaccharides, and sucrose, one of the disaccharides, were selected for the ex vivo optical clearing experiments on pig skin tissues utilizing the dimethyl sulfoxide (DMSO) carrier effect. We find that DMSO synergized with sugars applied to skin tissue has a more significant increase in the optical imaging depth and signal intensity, and a reduction in the scattering coefficient with an increasing concentration of DMSO. DMSO with a high concentration and D-fructose with saturated concentration (10:1; v/v) effectively reduce light attenuation in OCT imaging and improve the image quality. This operation will also shorten the application time to minimize skin damage from hyperosmotic agents.

研究领域: 生物医学工程 · 药学
✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY · 2021 ·Vol. 21 ·期 12 ·6196-6204 · IF 0

Effect of Superparamagnetic DMSO@γ-Fe2O3 Combined with Carmustine on Cervical Cancer

Wen Shu,Xing Weiping,Gao Lingxue,Zhao Shuping

This study aimed to investigate the effects of DMSO@γ-Fe2O3 nanomagnetic fluid thermotherapy combined with the chemotherapy drug carmustine on cervical cancer cells under a certain intensity of alternating magnetic field. And the role of Mir-590-3P in the development and progression of cervical cancer. The optimal thermotherapy concentration of γ-Fe2O3 nanomaterials on cervical cancer cells was determined by in vitro heating. In addition, the MTT colorimetric method was used to evaluate the toxic effect of γ-Fe2O3 magnetic nanoparticles on cervical cancer cells, and the optimal therapeutic concentration of carbachol on cervical cancer cells was optimized (0.015 g · L−1). The cervical cancer cells were divided into control, γ-Fe2O3 hyperthermia, chemotherapy, and DMSO@γ-Fe2O3 combined chemotherapy groups. After 2 h exposure to hypothermic conditions, flow cytometry was used to assess cell apoptosis for each group. The heating effect of the γ-Fe2O3 magnetic nanomaterials was apparent. When the concentration of γ-Fe2O3 was ≥6 g· L−1, the temperature rise above 41 °C. γ-Fe2O3 is non-toxic to cervical cancer cells and has good biocompatibility. Taking the drug concentration of IC25 as the working concentration of this study, the working concentration of carmustine was 0.015 g · L−1. Both the 41 °C heat treatment and chemotherapy alone had a killing effect on glioma and cervical cancer cells (P < 0.05). Additionally, the combined inhibitory effect of DMSO@γ-Fe2O3 nanomagnetic fluid thermotherapy and drugs at this temperature was significantly stronger than that of thermotherapy and chemotherapy alone (P < 0.05). For the control, gamma-Fe2O3 hyperthermia, chemotherapy, and DMSO@γ-Fe2O3 combined chemotherapy groups, the apoptosis rates of the cervical cancer cells were 1.4%, 18.6%, 24.12%, and 38.97%, respectively. DMSO@γ-Fe2O3 nanomagnetic fluid thermotherapy combined with the chemotherapeutic drug carmustine exerted a noticeable toxic effect on the cervical cancer cells, and DMSO@γ-Fe2O3 significantly enhanced the killing effect of carmustine on cervical cancer cells.

研究领域: 肿瘤学 · 纳米医学 · 分子生物学 · 癌症治疗
✓ 已验证 DOI PubMed
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SOLAR ENERGY MATERIALS AND SOLAR CELLS · 2024 · IF 6.3

Enhancing the performance of CZTSSe solar cells via an alternate spin-coating process with DMSO and DMF

Yunjie Bai,Yiming Wang,Ruijian Liu,Yu He,Yuhao Zhang,Chu Liu,Hongmei Luan,Yanchun Yang,Chengjun Zhu

The CZTSSe absorber layer prepared with DMSO exhibits extensive cavities at its bottom, and a prominent double-layer structure is frequently observed within the CZTSSe absorber synthesized using DMF , both of which have a detrimental impact on the device performance. In this paper, an alternate spin-coating process using DMSO and DMF solvent systems is proposed, which eliminates the double-layer structure of CZTSSe and reduces the number of cavities at the bottom of the absorber layer, thereby enhancing its overall quality. This method outperforms the traditional single-solution spin-coating technique by combining the advantages of two solvent systems, allowing for the preparation of an ideal CZTSSe film without disturbing the elemental ratio, ultimately resulting in a single-layer absorber composed of large grains. After three repetitions of an identical alternate spin-coating process, the average grain size of the absorber layer increased from 0.83 to 1.21 μm. This innovative process leads to a reduction in carrier recombination and an improvement in the short-circuit current density, ultimately raising the photoelectric conversion efficiency from 7.40% to 8.88%.

研究领域: 材料科学 · 能源技术
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SYNTHESIS-STUTTGART · 2022 ·Vol. 54 ·期 09 ·2258-2266 · IF 2.969

DMSO-Mediated Difunctionalization of Electron-Deficient Olefins to Access β-Hydroxysulfides with High Chemoselectivity

Bao Gao,Xiaojun Liu,Qian Yan,Ruiting Yang,Tao Jiang,Xiuli Zhang

A novel and convenient method for the highly chemoselective synthesis of β-hydroxysulfides mediated by DMSO is reported. This eco-friendly reaction was amenable to a broad range of substrates and provided the desired β-hydroxysulfides in moderate to good yields with high selectivity via radical process. Moreover, several pharmaceutical and bioactive molecules were also suitable substrates for this reaction conditions to afford the targeted products in good yields.

研究领域: 有机化学 · 药物化学
✓ 已验证 DOI 高影响因子
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INORGANICA CHIMICA ACTA · 2020 · IF 2.304

Synthesis of 1,8-anthraquinone functionalized aza 18/20-crown-5 macrocycles and their chromogenic ion-pair recognition of hydroxides in DMSO

Li Li,Feifei Xing,Shourong Zhu

Two N 3 O 3 macrocyclic compounds with rigid chromogenic 1,8-dihydroxylenanthraquione and flexible diethylenetriamine/dipropenetriamine (L1 and L2), were synthesized and characterized. L1/L2 can interact with alkaline, alkaline-earth, as well as Zn 2+ , Pb 2+ , and Al 3+ chloride/perchloride evidenced by their DPV change and 1 H NMR spectra. Unexpectedly, both L1 and L2 can show chromogenic response to Na + , K + , and TBA + hydroxide (but not LiOH). Large cavity L2 can show chromic response to Ca(OH) 2 and Ba(OH) 2 , but L1 can only respond to Ca(OH) 2 in DMSO. L1 and L2 form 1:1 and 2:1 (Host:Guest) complex respectively with NaCl, NaOH, TBAOH in DMF/DMSO. Both hosts bind smaller Zn 2+ and Al 3+ in 2:1 in DMSO. L2 can form L2·TBAOH greenish yellow complex that gradually transformed to red L2 2 ·TBAOH in two steps in DMSO. Different from other macrocycles, L1 and L2 are ion-pair hosts that recognize cation and OH − via carbonyl groups.

研究领域: 有机化学 · 分析化学
✓ 已验证 DOI 高影响因子
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ACS Applied Energy Materials · 2018 · IF 0

Enhanced Cycling Performance of Li–O2 Battery by Using a Li3PO4-Protected Lithium Anode in DMSO-Based Electrolyte

Huanhuan Guo,Guangmei Hou,Jianguang Guo,Xiaohua Ren,Xiaoxin Ma,Linna Dai,Shirui Guo,Jun Lou,Jinkui Feng,Lin Zhang,Pengchao Si,Lijie Ci

Lithium–oxygen batteries (LOBs) have attracted increasing interest because of their superior theoretical specific energy. However, the stability of lithium metal anode is one of the obstacles limiting their practical applications. Here, we introduce an artificial Li3PO4 solid electrolyte interphase (SEI) film to protect the lithium anode in LOB with LiI/LiNO3/DMSO (dimethyl sulfoxide) electrolyte. The Li3PO4-protected Li anode exhibits excellent electrochemical stability during the Li stripping/plating process and leads to a relatively uniform and featureless surface in LOB after cycling. Our research demonstrates that superior electrochemical performance can be achieved in the Li–O2 battery with the synergistic combination of the DMSO-based electrolyte, the LiI redox mediator, and the Li3PO4-protected Li anode. The LOB with a Li3PO4-protected Li anode exhibits a prolonged cycling life span of 152 cycles with a fixed capacity of 1000 mA h g–1 at 2 A g–1. The results in this work provide knowledge for the development of a robust strategy for protecting the Li anode in the applications of Li–O2 batteries.

研究领域: 材料科学 · 电化学 · 能源存储技术
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Energy Storage Materials · 2022 · IF 20.831

A high-energy dual-ion battery based on chloride-inserted polyviologen cathode and LiCl/DMSO electrolyte

Feng Wang,Junxiao Wang,Gaofeng Li,Zhihua Guo,Jun Chu,Xinping Ai,Zhiping Song

To improve the energy density of dual-ion batteries (DIBs), for the first time we employ a Cl – -insertable p-type polymer, poly(butyl viologen dichloride) (PBV-Cl 2 ), as cathode material , and low-cost LiCl/DMSO (dimethyl sulfoxide) solution as electrochemically favorable electrolyte. Benefiting from the highest reversible capacity of the PBV-Cl 2 cathode among all p-type polymers (183 mAh g –1 based on the weight involving anion), and greatly lowered Li + /Li potential (by 0.5 V) in DMSO compared to that in conventional ester solvents, the Li–PBV-Cl 2 DIB achieves the highest actual energy density of 470 Wh kg –1 . After adding fluoroethylene carbonate (FEC) additive in the electrolyte for better Li anode compatibility, it also exhibits an excellent cycling stability (88% after 300 cycles) and a superior rate capability (75% at 5000 mA g –1 ). The concepts of Cl – charge carrier, polyviologen cathode, and LiCl-based electrolyte provide significant insights for the development of high-energy, low-cost, and sustainable DIBs.

研究领域: 材料科学 · 电化学
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