LCST-type liquid–liquid phase separation behaviour of poly(ethylene oxide) derivatives in an ionic liquid
文献信息
Ryohei Tsuda, Koichi Kodama, Takeshi Ueki, Hisashi Kokubo, Shin-ichiro Imabayashi, Masayoshi Watanabe
We present a new series of polymer–ionic liquid solutions exhibiting LCST-type liquid–liquid phase separation behaviour, and reveal their phase behaviour and intermolecular interactions based on phase diagrams and NMR analysis.
相关文献
Effects of incorporation of Ag into a kesterite Cu2ZnSnS4 thin film on its photoelectrochemical properties for water reduction
Riku Okamoto, Mikas Remeika, Imane Abdellaoui, Muhammad M. Islam, Takashi Harada, Ryu Abe, Takeaki Sakurai
DOI: 10.1039/D1CP04075H
The determination of the HOR/HER reaction mechanism from experimental kinetic data
Karen Chan
DOI: 10.1039/D1CP04134G
Estimation of electrochemical cell potentials and reaction energies using Fermi energies
Mohammad Mahdi Kalantarian, Amir Haghipour
DOI: 10.1039/D1CP04800G
Spectroscopy and photoisomerization of protonated Schiff-base retinal derivatives in vacuo
Anne P. Rasmussen, Elisabeth Gruber, Ricky Teiwes, Mordechai Sheves, Lars H. Andersen
DOI: 10.1039/D1CP04501F
Fragmentation and rearrangement of Breslow intermediates: branches to both radical and ionic pathways
Ming-Hsiu Hsieh, Jen-Shiang K. Yu
DOI: 10.1039/D1CP03118J
Exploration of chromophores for a VCD couplet in a spectrally transparent infrared region for biomolecules
Tohru Taniguchi, Mohamad Zarif Mohd Zubir, Nobuyuki Harada, Kenji Monde
DOI: 10.1039/D1CP04074J
Direct evaluation of hole effective mass of SnS–SnSe solid solutions with ARPES measurement
Issei Suzuki, Zexin Lin, Sakiko Kawanishi, Kiyohisa Tanaka, Yoshitaro Nose, Takahisa Omata, Shin-Ichiro Tanaka
DOI: 10.1039/D1CP04553A
Time-resolved relaxation and cage opening in diamondoids following XUV ultrafast ionization
Alexie Boyer, Marius Hervé, Audrey Scognamiglio, Vincent Loriot, Franck Lépine
DOI: 10.1039/D1CP03502A
Questioning the orbital picture of magnetic spin coupling: a real space alternative
A. Martín Pendás, E. Francisco
DOI: 10.1039/D1CP03485E
Hydrogen-bond-dominated mechanical stretchability in PVA films: from phenomenological to numerical insights
Zhen-zhen Fu, Sheng-jie Guo, Chen-xi Li, Ke Wang, Qin Zhang, Qiang Fu
DOI: 10.1039/D1CP03893A
您可能还喜欢
3 - (二氟甲基)-1 -氟苯(CAS号:26029-52-7)适用哪些法规指南?
3 - (二氟甲基)-1 -氟苯需遵循联合国全球化学品统一分类和标签制度(GHS),包括急性毒性、皮肤腐蚀/刺激、严重眼损伤/眼刺激等分类。同时,该化合物还需符...
3,5-二甲基苯胺(CAS号:108-69-0)通常如何合成?
3,5-二甲基苯胺通常通过乙苯的氨解反应合成。反应中使用硫酸作为催化剂,反应温度为120-130°C。乙苯在硫酸存在下与氨反应,生成3,5-二甲基苯胺和苯胺副产...
3-甲基异噻唑-5-胺(CAS号:24340-76-9)安全吗?
3-甲基异噻唑-5-胺在适当使用和储存条件下是相对安全的,但在操作时应注意防护措施。应避免吸入粉尘,避免与皮肤和眼睛直接接触。在操作过程中,应穿戴适当的防护装备...
3-(1,3-Thiazol-2-yl)-1H-indole(CAS号:135531-86-1)通常如何合成?
3-(1,3-噻唑-2-基)-1H-吲哚通常通过多步合成方法制备。首先,由噻唑-2-基溴化物和吲哚进行偶联反应,得到中间体。然后,通过还原反应将中间体转化为所需...
4-溴-2-氟苯甲基氯(CAS号:85510-82-3)的主要用途是什么?
4-溴-2-氟苯甲基氯主要用于有机合成中间体,特别是在医药、农药和染料等领域。作为一种具有特定结构的化合物,它在合成复杂有机分子时扮演重要角色。
处理Fmoc-β-(3-噻吩基)-D-Ala-OH(CAS号:220497-90-5)时应注意哪些实验室安全事项?
处理Fmoc-β-(3-噻吩基)-D-Ala-OH时,应佩戴防护手套、护目镜和实验服。操作应在通风橱内进行。如发生泄露,应立即用大量水冲洗,并通知实验室管理人员...
氮化硅(CAS号:12033-89-5)通常如何合成?
氮化硅通常通过氮化硅的直接反应合成,即在高温下将四氯化硅与氨气反应。具体步骤是将四氯化硅和氨气混合并加热至1300-1700℃,在该条件下,四氯化硅与氨气反应生...
Cetirizine EP Impurity B DiHCl(CAS号:1000690-91-4)通常如何合成?
Cetirizine EP Impurity B DiHCl通常通过一锅法合成,首先将4-氯苯基-苯甲基氯甲酸酯与1-哌嗪乙酸反应,生成相应的酸,然后与盐酸反应...
如何储存1-哌啶-4-基丁-1-酮(CAS号:3509-15-7)?
1-哌啶-4-基丁-1-酮应储存在阴凉、干燥的地方,避免阳光直射。存储容器应密封,并确保通风良好。建议储存温度不超过25℃,湿度保持在相对较低的水平。
如何处理含有VORUCICLIB(CAS号:1000023-04-0)的废料?
含有VORUCICLIB的废料应进行专业的收集和处理,包括使用适当的容器进行隔离,避免与其他化学品接触。处理方法通常包括化学中和、沉淀反应或吸附过程,随后进行焚...
来源期刊
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry











![4-Chloro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine structure 4-Chloro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine structure](https://cnstatic.chemtradehub.com/structs/869/869335-75-1-a9d0.webp)


