DALTON TRANSACTIONS
·
2020
·Vol. 50
·期 3
·1060-1068
·
IF 4.174
Run-Ze Yuan,Peng-Fei Cui,Shu-Ting Guo,Guo-Xin Jin
Herein, we describe the synthesis of tetraphenylphosphonium o-carboranyl dithiocarboxylate (Ligand 1) and methyldithiocarboxyl-o-carborane (Ligand 2). The complexes [Cp*M(o-C2B10H11CS2)Cl] (M = Ir (3); Rh (4)) and [Cp*M(o-C2B10H11CS2)2] (M = Ir (5); Rh (6)) have been synthesized based on Ligand 1. The selective B–H bond activation of Ligand 2 has also been explored, leading to the synthesis of the B–H activated complex [Cp*Ir(o-C2B10H10CS2CH3)Cl] (7) and four of its substituted derivatives (8, 9, 10 and 11). All of these compounds have been characterised through single-crystal X-ray diffraction, NMR, IR spectroscopy and elemental analysis.
研究领域:
无机化学
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配位化学
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2015
·Vol. 132
·期 28
·
IF 1.768
Yumeng Luo,Yafei Lu,Ning Li,Yun Li,Xiaoa Zhang,Shicheng Qi
Novel segmented carborane-containing polyurethane (PUR 2–5) is synthesized from hydroxyl-terminated carborane-containing prepolymer (P3) as soft segment and isocyanate-terminated carborane-containing prepolymer (P5) as hard segment by different ratio of P3 and P5. The prepared carborane-containing polyarylesters and polyurethanes (PURs) are characterized by Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy (NMR). Their mechanical properties and thermal stability are measured, while the dosage of carborane biphenol is 5–10 wt %, the tensile strength is up to 20 MPa, and thermal gravimetric analyzer (TGA) curves indicate that the carborane group effectively reduces the degradation rate of carborane-containing polyurethane, which is fairly stable above 300°C and with char yield exceeding 40%. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 42227.
研究领域:
材料科学
·
高分子化学
✓ 已验证
产品关联
DOI
高影响因子
INORGANIC CHEMISTRY
·
2025
·
IF 4.7
Qiang-Qiang Ma,Peng Zhou,Yizhen Liu,Zuowei Xie
Transition metal catalyzed selective cage B–H functionalization of carboranes has made significant progress in recent years, giving rise to the efficient synthesis of a large variety of cage B-functionalized carboranes including alkenylation, arylation, alkynylation, borylation, hydroxylation, acyloxylation, amination, and halogenation. However, the mechanisms of these catalytic B–X coupling reactions are not well understood. Herein, we describe the isolation and characterization of the catalytically relevant o-carborane based palladium(II) metallacycle, disclosing the details of Pd-catalyzed B–H functionalization of o-carboranes. As a result, highly selective catalytic B(3,6)-dihalogenation, -dimethylation, and -diarylation of o-carboranes have been achieved.
研究领域:
有机化学
·
过渡金属催化
·
材料化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHINESE JOURNAL OF POLYMER SCIENCE
·
2017
·Vol. 35
·期 12
·1463-1473
·
IF 1.692
Yang Zhen,Li Ning,Yang Xiao-xue,Zhang Xiao-a,Jiang Sheng-ling,Lyu Ya-fei
o -Carborane-containing poly(hydroxy ethers) ( P1 , P2 and P3 ) were synthesized via “advancement reaction” of o -carborane-containing bisphenol ( 4 ) and diglycidyl ether of bisphenols (DGEBA and 1 ). FTIR and 1 H-, 13 C-, and 11 B-NMR were utilized to characterize the obtained polymers. TGA test was conducted under nitrogen and air. It is found that the shielding effect of carborane moiety on its adjacent aromatic structures contributes to high initial decomposition temperatures, while oxygen in air has an adverse effect on the initial decomposition temperature. The oxygen can combine with polymer chain to form peroxide and hydroperoxide groups, which are more reactive during the degradation process. Besides, o -carborane-containing poly(hydroxy ethers) have high char yield at elevated temperatures. The boron atom combines with oxygen from the polymer structure or/and from air, thus to form a three-dimensional network linked with B—O—B and B—C bonds, and retain the polymer weight to a large extent.
研究领域:
材料科学
·
高分子化学
✓ 已验证
产品关联
DOI
高影响因子
CHINESE JOURNAL OF POLYMER SCIENCE
·
2016
·Vol. 34
·期 9
·1103-1116
·
IF 1.811
Han Guo,Yang Zhen,Yang Xiao-xue,Zhang Xiao-a,Jiang Sheng-ling,Lu Ya-fei
Carborane bisphenol novolacs ( 3 and 4 ) were synthesized in the presence of acid catalyst from carborane bisphenols ( 5 and 6 ) and formaldehyde. Further epoxidization of carborane bisphenol novolacs with epichlorohydrin gave carborane bisphenol epoxy novolacs ( 1 and 2 ). The molecular weight and epoxy value of obtained resins were determined using the molecular weight of their precursors. The epoxy values of 1 and 2 were 0.48 and 0.52 respectively, higher than the maximum theoretical epoxy value (0.45) of difunctional carborane bisphenol epoxy resins. FTIR and NMR were utilized to characterize 1 and 2 . The curing behaviors were also studied by DSC and the optimized curing conditions were obtained. TGA analysis indicated that carborane moiety could shield its adjacent organic structures against initial decomposition. On the other hand, B―H on carborane cage could react with oxygen to form a three-dimensional network linked by B―O―B and B―C bonds, which further blocked the movement of formed radicals and thus the degradation process was inhibited.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
POLYMER INTERNATIONAL
·
2015
·Vol. 64
·期 12
·1715-1721
·
IF 2.409
Tao Xing,Kai Zhang
Novel carborane polyimides were synthesized and studied. Aromatic meta -carborane diamines of different structures were initially prepared. Polymerization of these new diamines with the commercially available 4,4′-oxydiphthalic dianhydride led to meta -carborane polyimides with various structures and thermal properties. The amorphous polymers obtained are of moderate molecular weight and show good solubility in organic solvents. Thermal analyses of these polyimides reveal that they have moderate to ultrahigh thermal stability depending on their specific structures, with 5% decomposition temperatures ranging from 382 to 786 °C in nitrogen. Different thermal properties of these polyimides are observed when the analyses are performed in dry air, with 5% decomposition temperatures shifting to temperatures ranging from 388 to 1128 °C. Due to the ever-present requirement of higher performance polymers in fields like aerospace and defense, the methods developed here could be an impetus for the development of these industries. © 2015 Society of Chemical Industry
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
Polymer Chemistry
·
2022
·Vol. 13
·期 10
·1328-1334
·
IF 5.364
Lihua Zhao,Tianhao Li,Bijie Wang,Ke Chen,Xiao Hu,Ming Liu,Liu He,Qing Huang,Yujie Song
Poly(siloxane–carborane)s are a class of polymeric materials which can be used for harsh environments. Poly(cyclosiloxane–carborane)s were prepared through the hydrosilylation of cyclosiloxanes and vinyl modified carboranes. The structure of the as-prepared carborane cyclosiloxane hybrid polymers (CcHPs) could be controlled through changing the ratio of monomers, and the CcHPs showed good thermal stability as well as anti-oxidation properties. The carbon fiber coated with CcHPs could resist high temperature in air, and only 10 wt% loss was observed at 1000 °C. The coated carbon foam could retain its shape and size after burning for 2 min, demonstrating the potential applications of CcHPs as protective coatings for harsh environments.
研究领域:
材料科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING
·
2025
·
IF 8.9
Zichun Ding,Jianjian Jiao,Yuhang Wang,Runze Liu,Qing Wang,Jianing Guo,Siying Wang,Lishuai Zong,Xigao Jian,Jinyan Wang
Ultra heat-resistant phthalonitrile resin has faced serious challenges of the trade-off between temperature resistance and toughness and seriously affects its application in the field of temperature resistant structural composites. In this work, a kind of oligo (aryl ethers) containing phenyl-s-triazine and pendent amino group (AFT-Ph/PAFT-Ph) were first selected as modifier co-cured with phthalonitrile prepolymers containing a carborane (CEPN) to achieve synergistic improvement in toughness and heat resistance performance. The flexural and impact strengths of optimized composites reach 278.6 MPa and 58.4 kJ/m 2 , which are increased by 92.7 % and 1091.8 % compared to the blank contrast. The glass transition temperature ( T g ) remained consistent with that of the blank control group, both exceeding 550 ℃. Furthermore, the T d5% –N 2 shows a marginal increase from 706 ℃ in the blank contrast to 713 ℃ in the modified material. Simultaneously conducting research on the mechanism of collaborative improvement mentioned above.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
CHINESE JOURNAL OF POLYMER SCIENCE
·
2017
·Vol. 36
·期 1
·85-97
·
IF 1.692
Li Ning,Zeng Fang-Lei,Wang Yu,Qu De-Zhi,Zhang Chun,Li Juan,Huo Jin-Zhao,Bai Yong-Ping
In this study, two fluorinated polyurethanes (FPU) containing carborane groups in the main chains were firstly designed and synthesized via the reaction of hexamethylene diisocyanate trimer (HDI trimer) with fluorinated polyesters (CFPETs) having hydroxyl-terminated carborane groups at room temperature. The structures of carborane fluorinated polyesters (CFPETs) and polyurethanes (CFPUs) were characterized by gel permeation chromatography (GPC), Fourier transform infrared (FTIR) spectroscopy and nuclear magnetic resonance (NMR) measurements. The thermal stability, mechanical properties, Shore A hardness, solvent resistance and acid-alkali resistance of the carborane fluorinated polyurethane films were also studied. Thermogravimetric analysis (TGA) tests manifested that the introduction of carborane groups into the main chain of fluorinated polyurethane endowed the obtained fluorinated polyurethane with excellent thermal stability. The thermal decomposition temperature of carborane fluorinated polyurethane (CFPU) increased by 190 °C compared with that of the carborane-free fluorinated polyurethane (FPU). Even at 800 °C, CFPU showed the char yield of 66.5%, which was higher than that of FPU (34.3%). The carborane-containing fluorinated polyurethanes also showed excellent chemical resistance and prominent mechanical property even after the cured films being immersed into Jet aircraft oil or 37% HCl for 168 h or at high temperature (700 °C). It is found that the structural characteristics of carborane group and the compacted structure of CFPU effectively improve the thermal stability, mechanical property, solvent resistance and acid-alkali resistance of the carborane-free fluorinated polyurethane. These excellent properties make CFPU as the useful raw materials to prepare the high temperature resistant coatings or adhesives for automotive engines, engine or fuel tank of aircraft and other equipment working in high-temperature or high concentrations of acid-alkali environments.
研究领域:
材料科学
·
高分子化学
✓ 已验证
产品关联
DOI
高影响因子
DYES AND PIGMENTS
·
2020
·
IF 4.613
Huici Shan,Anjie Liu,Yan Lv,Xueyan Wu,Yongdong Ma,Xiaoping Jin,Jixi Guo
Four D−π−A dyads based on various imidazole derivatives donor and o -carborane acceptor moiety have been designed and synthesized for efficient tunable solid-state fluorescence and low-temperature phosphorescence. The results showed that four dyads are all AIEgens with dual emission properties in solution, highly solid-state emission, and low-temperature phosphorescence. The dual emissions were attributed to the locally excited (LE) and twisted intramolecular charge transfer (TICT) emission. The crystallographic measurements and theoretical calculations demonstrated that the strong phosphorescence with a long lifetime up to 2.18 s at low temperature may be attributed to the C–H⋅⋅⋅N, C–H⋅⋅⋅π interactions, strong TICT effect and the reduced vibration coupling by attaching a bulky carborane moiety to the chromophore .
研究领域:
化学
·
材料科学
✓ 已验证
DOI
高影响因子
JOURNAL OF ADHESION SCIENCE AND TECHNOLOGY
·
2023
·
IF 2.3
Luyao Wang,Xiaoyu Zhang,Yi Guo,Jiahao Gao,Binghao Ma,Fanglei Zeng,Hailong Liu,Ning Li,Gang Yi,Zhongwei Wang
The long-term use temperature of the traditional high-temperature adhesive can only reach about 280 °C, and it cannot be used in extreme environments such as acid and alkali for a long time, which greatly limits its application in aerospace and other fields. Because of its unique three-dimensional structure, carborane has excellent thermal stability and chemical stability. Based on this, first, this article introduced carborane monomer into polyurethane structure, using indirect copolymerization method, Hydroxyl carborane derivative (m8) and conventional polyether diols were used as soft segments. By adjusting the introduction ratio of m8, a series of copolymerized carborane polyurethane (Co-CBR-PU) with controllable thermal and mechanical properties were successfully prepared. Its structure and molecular weight were characterized by FTIR and gel permeation chromatography (GPC), its surface morphology were observed by SEM. The thermal stability and mechanical properties were studied by thermogravimetric test, tensile test and rheological dynamic mechanical analysis test., and its activity, solvent resistance and hydrophobic properties were studied by finger contact method, solvent resistance test and contact Angle test. Second, the high temperature resistant carborane polyurethane adhesive (PUAS) was prepared using Co-CBR-PU as matrix and its adhesion was studied. The results show that a series of Co-CBR-PU has good high temperature resistance, mechanical properties and solvent resistance after adding carborane monomer, and its various properties were optimal when the addition amount of m8 was 15 wt%. The carborane PUAS prepared by using it as the substrate has excellent high temperature adhesion to different adhesive parts. The aim of this study is to reduce the cost of synthesis of carborane polyurethane by regulating the proportion of carborane, and then realize the industrial trial production of high temperature resistant carborane adhesive.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
CHINESE JOURNAL OF CHEMISTRY
·
2022
·Vol. 41
·期 3
·307-313
·
IF 5.56
Run-Ze Yuan,Peng-Fei Cui,Yue-Jian Lin,Guo-Xin Jin
Comprehensive Summary Herein, we describe the synthesis of a carborane-supported octanuclear palladacycle complex, Pd 8 ( o -C 2 B 10 H 10 CS 2 CH 3 ) 4 Cl 4 (CH 3 CN) 4 (complex 1 ), with B(3)–H activations on o -carborane ligand. The substitution reaction of 1 has been explored, and three of its substituted complexes Pd 8 ( o -C 2 B 10 H 10 CS 2 CH 3 ) 4 Cl 4 (L) 4 (L = t BuNC, 2 ; L = C 5 H 5 N, 3 ; L = C 4 H 8 S, 4 ) have been synthesized. The m - and p -carborane disubstituted ligands m - and p -C 2 B 10 H 10 (CS 2 CH 3 ) 2 (ligands 5 and 6 ) as well as their B—H activated carborane complexes [ m -C 2 B 10 H 9 (CS 2 CH 3 ) 2 PdCl] ( 7 ) and [ p -C 2 B 10 H 8 (CS 2 CH 3 ) 2 ][PdCl( t BuNC)] 2 ( 8 ) have also been synthesized by the similar method. All of these complexes have been characterized, including X-ray single crystal diffraction, NMR spectroscopy, IR spectroscopy and elemental analysis methods.
研究领域:
无机化学
·
材料科学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）