119171-18-5Relevant articles and documents
Ionothermal synthesis, structures, properties of cobalt-1,4-benzenedicarboxylate metal-organic frameworks
Zhang, Zong-Hui,Xu, Ling,Jiao, Huan
, p. 217 - 222 (2016)
Eight kinds of 1-methyl-3-alkylimidazolium halide [RMI]X (R=ethyl (E), propyl (P), butyl (B) and amyl (A); MI = imidazolium; X= Cl-, I-) ionic liquids (ILs) were used as reaction media and obtained a series of 2D [RMI]2[Co3(BDC)3X2] frameworks through the ionothermal reactions of 1,4-benzenedicarboxylic acid (H2BDC) with Co(NO3)2·6H2O. The 2D [RMI]2[Co3(BDC)3X2] frameworks exhibit a same (3,6) topology network with [RMI]+ cations locating in the interlayer space. [RMI]+ cations play a template role in the structure constructions, whose influence combining with the effect of X- anions pass to the TG behaviors. The decomposition temperatures of the [RMI]2[Co3(BDC)3X2] frameworks decrease with the alkyl chains in [RMI]+ cations, and the compounds containing Cl- show higher thermal stabilities than those with I-. However, compounds 1-8 exhibit two similar broad emissions at ca. 380 and 390 nm, assigned to ILCT. The RMI+ templates and the X- anions do not exert their influence on the fluorescence.
Towards Safer Rocket Fuels: Hypergolic Imidazolylidene-Borane Compounds as Replacements for Hydrazine Derivatives
Huang, Shi,Qi, Xiujuan,Liu, Tianlin,Wang, Kangcai,Zhang, Wenquan,Li, Jianlin,Zhang, Qinghua
, p. 10187 - 10193 (2016)
Currently, toxic and volatile hydrazine derivatives are still the main fuel choices for liquid bipropellants, especially in some traditional rocket propulsion systems. Therefore, the search for safer hypergolic fuels as replacements for hydrazine derivatives has been one of the most challenging tasks. In this study, six imidazolylidene-borane compounds with zwitterionic structure have been synthesized and characterized, and their hypergolic reactivity has been studied. As expected, these compounds exhibited fast spontaneous combustion upon contact with white fuming nitric acid (WFNA). Among them, compound 5 showed excellent integrated properties including wide liquid operating range (?70–160 °C), superior loading density (0.99 g cm?3), ultrafast ignition delay times with WFNA (15 ms), and high specific impulse (303.5 s), suggesting promising application potential as safer hypergolic fuels in liquid bipropellant formulations.
A Cation-Tethered Flowable Polymeric Interface for Enabling Stable Deposition of Metallic Lithium
Huang, Zhuojun,Choudhury, Snehashis,Gong, Huaxin,Cui, Yi,Bao, Zhenan
, p. 21393 - 21403 (2020)
A fundamental challenge, shared across many energy storage devices, is the complexity of electrochemistry at the electrode-electrolyte interfaces that impacts the Coulombic efficiency, operational rate capability, and lifetime. Specifically, in energy-dense lithium metal batteries, the charging/discharging process results in structural heterogeneities of the metal anode, leading to battery failure by short-circuit and capacity fade. In this work, we take advantage of organic cations with lower reduction potential than lithium to build an electrically responsive polymer interface that not only adapts to morphological perturbations during electrodeposition and stripping but also modulates the lithium ion migration pathways to eliminate surface roughening. We find that this concept can enable prolonging the long-term cycling of a high-voltage lithium metal battery by at least twofold compared to bare lithium metal.
PEGylated imidazolium ionic liquid electrolytes: Thermophysical and electrochemical properties
Ganapatibhotla, Lalitha V.N.R.,Zheng, Jianping,Roy, Dipankar,Krishnan, Sitaraman
, p. 6347 - 6360 (2010)
We report the synthesis and characterization of a series of imidazolium iodide ionic liquids (ILs) containing monomethoxy-terminated poly(ethylene glycol) (mPEG), and n-alkyl groups. These PEGylated ILs contain 7, 12, or 16 ethylene glycol units in the si
Poly(ionic liquid)/ionic liquid/graphene oxide composite quasi solid-state electrolytes for dye sensitized solar cells
Lin, Bencai,Feng, Tianying,Chu, Fuqiang,Zhang, Shuai,Yuan, Ningyi,Qiao, Gang,Ding, Jianning
, p. 57216 - 57222 (2015)
Poly(ionic liquid)/ionic liquid/graphene oxide (poly(IL)/IL/GO) composite gel electrolytes containing poly(1-butyl-3-vinylimidazolium bis(trifluoromethanesulfonyl)imide), 1-propyl-3-methylimidazolium iodide and graphene oxide are prepared for dye-sensitized solar cells (DSSCs), without any volatile organic solvent. The conductivity of the composite electrolyte is significantly increased by adding an appropriate amount of GO, and the DSSCs based on composite electrolytes containing GO show higher power conversion efficiency performance and better long-term stability compared to those without GO. The DSSC based on the composite electrolytes which contain 2 wt% of GO show an overall power conversion efficiency of 4.83% under simulated AM 1.5 solar spectrum irradiation. The superior long-term stability of the DSSCs indicates that this type of composite electrolyte could overcome the drawbacks of volatile liquid electrolytes, and offer a feasible method to fabricate DSSCs in future practical applications.
Extraordinary aspects of bromo-functionalized multi-walled carbon nanotubes as initiator for polymerization of ionic liquid monomers
Chang, Yu-Hsun,Lin, Pei-Yi,Wu, Ming-Sung,Lin, King-Fu
, p. 2008 - 2014 (2012)
Two ionic liquid monomers, 1-(2-acryloyloxy-ethyl)-3-methyl-imidazol-1-ium iodide (AMImI) and 1-(2-acryloyloxy-ethyl)-3-methyl-benzoimidazol-1-ium iodide (AMBImI), were synthesized and polymerized through atom transfer radical polymerization (ATRP). Poly(AMImI)-grafted multi-walled carbon nanotubes (denoted as MWCNT-poly(AMImI)) could also be fabricated through "grafting from" method of ATRP using bromo-functionalized MWCNT (denoted as MWCNT-Br) as initiator but MWCNT-poly(AMBImI) could not. Based on the thermogravimetric analysis and high resolution transmission electron microscopy, AMBImI monomer has encapsulated the MWCNT-Br probably through the π-π and cation-π interactions invalidating the initiation capability of MWCNT-Br. Besides, by mixing AMBImI with MWCNT-Br directly at room temperature, the MWCNT-Br was coated with a thin layer of AMBImI, whereas MWCNT-Br could not physisorb AMImI. Both MWCNT-poly(AMImI) and AMBImI-encapsulated MWCNT were dispersed well in 1-methyl-3-propylimidazolium iodide ionic liquid.
Photocatalytic C-F Bond Borylation of Polyfluoroarenes with NHC-boranes
Chen, Kai,Chen, Xiao-Qing,Hu, Yuan-Zhuo,Xia, Peng-Ju,Xiang, Hao-Yue,Xiao, Jun-An,Yang, Hua,Ye, Zhi-Peng
supporting information, p. 1742 - 1747 (2020/03/24)
The first photoredox-catalyzed defluoroborylation of polyfluoroarenes with NHC-BH3 has been facilely achieved at room temperature via a single-electron-transfer (SET)/radical addition pathway. This new strategy makes full use of the advantage of photoredox catalysis to generate the key boryl radical via direct activation of a B-H bond. Good functional group tolerance and high regioselectivity offer this protocol incomparable advantages in preparing a wide array of valuable polyfluoroarylboron compounds. Moreover, both computational and experimental studies were performed to illustrate the reaction mechanism.
