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Achieving a superior Na storage performance of Fe-based Prussian blue cathode by coating perylene tetracarboxylic dianhydride amine
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作者 Xin-Yuan Fu Lu-Lu Zhang +6 位作者 Zhao-Yao Chen Yunkai Xu Junxiu Wu Cheng-Cheng Wang Xiao-Kai Ding Xue-Lin Yang Jun Lu 《Carbon Energy》 SCIE EI CAS CSCD 2024年第5期53-64,共12页
Fe-based Prussian blue(Fe-PB)cathode material shows great application potential in sodium(Na)-ion batteries due to its high theoretical capacity,long cycle life,low cost,and simple preparation process.However,the crys... Fe-based Prussian blue(Fe-PB)cathode material shows great application potential in sodium(Na)-ion batteries due to its high theoretical capacity,long cycle life,low cost,and simple preparation process.However,the crystalline water and vacancies of Fe-PB lattice,the low electrical conductivity,and the dissolution of metal ions lead to limited capacity and poor cycling stability.In this work,a perylene tetracarboxylic dianhydride amine(PTCDA)coating layer is successfully fabricated on the surface of Fe-PB by a liquid-phase method.The aminated PTCDA(PTCA)coating not only increases the specific surface area and electronic conductivity but also effectively reduces the crystalline water and vacancies,which avoids the erosion of Fe-PB by electrolyte.Consequently,the PTCA layer reduces the charge transfer resistance,enhances the Na-ion diffusion coefficient,and improves the structure stability.The PTCA-coated Fe-PB exhibits superior Na storage performance with a first discharge capacity of 145.2 mAh g^(−1) at 100 mA g^(−1).Long cycling tests exhibit minimal capacity decay of 0.027%per cycle over 1000 cycles at 1 A g^(−1).Therefore,this PTCA coating strategy has shown promising competence in enhancing the electrochemical performance of Fe-PB,which can potentially serve as a universal electrode coating strategy for Na-ion batteries. 展开更多
关键词 cathode material COATING Fe-based Prussian blue Na-ion batteries perylene tetracarboxylic dianhydride amine
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高压拉曼光谱研究均苯四甲酸二酐
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作者 丛广宇 李东飞 刘嘉睿 《光谱学与光谱分析》 SCIE EI CAS CSCD 北大核心 2024年第9期2434-2438,共5页
测量了常温常压下的均苯四甲酸二酐的拉曼光谱,并对所测量的各个拉曼谱线进行归属认证。获得了从常压到24GPa压强条件下的原位拉曼光谱,通过频率-压强关系曲线可以得出该材料在2Gpa存在晶体结构相变,定义了均苯四甲酸二酐在低于2GPa压... 测量了常温常压下的均苯四甲酸二酐的拉曼光谱,并对所测量的各个拉曼谱线进行归属认证。获得了从常压到24GPa压强条件下的原位拉曼光谱,通过频率-压强关系曲线可以得出该材料在2Gpa存在晶体结构相变,定义了均苯四甲酸二酐在低于2GPa压强条件的晶体结构为相Ⅰ,高于2GPa压强条件的晶体结构相为相Ⅱ。在相变前后,绝大多数的拉曼谱线频率-压强曲线斜率变小,说明与相Ⅰ相比,各官能团对压强的敏感程度下降,相Ⅱ的分子晶体具有更紧密的堆积结构。拉曼光谱强度能够给出丰富的材料结构信息,通过对C—O伸缩振动的倍频(常压位于1837cm^(-1))和C=O伸缩振动基频(常压位于1865cm^(-1))的相对拉曼光谱强度随压强的变化规律进行分析,发现两拉曼谱线强度比在2GPa附近存在突变,为均苯四甲酸二酐在2GPa附近发生结构相变提供了实验依据。 展开更多
关键词 拉曼光谱 高压 相变 均苯四甲酸二酐
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高性能PET珠粒泡沫的制备及机理
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作者 任祥锋 徐大伟 王琪 《塑料工业》 CAS CSCD 北大核心 2024年第6期164-172,共9页
聚对苯二甲酸乙二醇酯(PET)高温熔体强度低,难以通过超临界二氧化碳(scCO_(2))发泡技术制备高强度、高膨胀率的珠粒泡沫材料。本文建立了一种基于原位熔体增强的发泡新技术,利用聚对苯二甲酸丁二醇酯(PBT)有效负载扩链剂均苯四甲酸二酐(... 聚对苯二甲酸乙二醇酯(PET)高温熔体强度低,难以通过超临界二氧化碳(scCO_(2))发泡技术制备高强度、高膨胀率的珠粒泡沫材料。本文建立了一种基于原位熔体增强的发泡新技术,利用聚对苯二甲酸丁二醇酯(PBT)有效负载扩链剂均苯四甲酸二酐(PMDA)得到扩链剂负载母粒(PMDA-MB)。通过PMDA-MB与PET的共混挤出制备了改性PET,有效地延长并支化PET分子链,大幅度地提升了熔体黏度,有效地改善了PET的发泡性能。进一步通过scCO_(2)珠粒发泡技术制备了具有优异的泡孔结构和高膨胀率的PET泡沫材料。结果表明,当PMDA-MB的质量分数为3%、发泡温度为244℃、发泡压力为25 MPa时,所得PET泡沫平均泡孔尺寸为100.8μm,泡孔密度1.91×10^(6)个/cm^(3),膨胀率达15.2,而且该PET珠粒泡沫材料的力学性能优良,拉伸强度达2.54 MPa,压缩强度达4.08 MPa。 展开更多
关键词 聚对苯二甲酸乙二醇酯 聚对苯二甲酸丁二醇酯 均苯四甲酸二酐 原位熔体增强 超临界二氧化碳 珠粒发泡
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Synthesis of a New Aromatic Dianhydride Containing Pyridine Ring and Related Polyimide
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作者 Xiao Long WANG Shu Jiang ZHANG Yan Feng LI Tao MA Yu SHAO Xin ZHAO 《Chinese Chemical Letters》 SCIE CAS CSCD 2006年第3期305-306,共2页
A new aromatic dianhydride monomer containing pyridine moiety, 2,6-bis[4'-(3",4"- dicarboxyphenoxy)benzoyl]-pyridine dianhydride (Md), was synthesized in four steps, starting from 2,6-pyridinedicarboxyl chlorid... A new aromatic dianhydride monomer containing pyridine moiety, 2,6-bis[4'-(3",4"- dicarboxyphenoxy)benzoyl]-pyridine dianhydride (Md), was synthesized in four steps, starting from 2,6-pyridinedicarboxyl chloride. A novel pyridine-containing polyimide was prepared via polycondensation of Md with ODA by two-step method. The resulting polyimide exhibits excellent solubility, film-forming capability and high thermal resistance. 展开更多
关键词 Polyimides pyridine-containing monomer synthesis aromatic dianhydride.
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含苝环有机半导体的光催化分解水研究进展
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作者 于卉 卢金荣 《分子催化(中英文)》 CAS CSCD 北大核心 2024年第1期81-92,I0004,共13页
光催化分解水是太阳能向化学能转换的一种重要方式,其中高效稳定光催化剂的研制至关重要.具有平面共轭结构的苝类有机小分子是一类富含π电子的n-型半导体,具有结构易修饰、可见光吸收强以及光热稳定性高等优点,近年来在光催化领域研究... 光催化分解水是太阳能向化学能转换的一种重要方式,其中高效稳定光催化剂的研制至关重要.具有平面共轭结构的苝类有机小分子是一类富含π电子的n-型半导体,具有结构易修饰、可见光吸收强以及光热稳定性高等优点,近年来在光催化领域研究广泛.我们总结了4类含有苝环结构的有机小分子苝四甲酸二酐、苝二酰亚胺、苝单酰亚胺以及苝四酸的特点.此外,从分子结构修饰、构筑聚合物、金属辅助、与其它材料复合及改变组装条件这几种方式对材料在光催化分解水方面的研究进展进行了综述,并对含有苝环结构的有机半导体材料在光催化分解水方面存在的问题和前景进行了分析和展望. 展开更多
关键词 苝四甲酸二酐 苝二酰亚胺 苝单酰亚胺 苝四酸 光催化水分解
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焙烧温度对均四甲苯气相氧化制均苯四甲酸二酐钒钛氧化物催化剂的影响
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作者 方敏 顾龙勤 +1 位作者 王昂 陈炳旭 《工业催化》 CAS 2024年第7期49-53,共5页
采用浸渍法经不同焙烧温度制备钒钛氧化物催化剂,以XRD、Raman和H_(2)-TPR等对催化剂物理化学性能进行表征,并在固定床装置上评价催化剂均四甲苯气相氧化反应性能。结果表明,钒钛氧化物催化剂中钒以TiO_(2)表面VO_(x)物种和晶体V_(2)O_... 采用浸渍法经不同焙烧温度制备钒钛氧化物催化剂,以XRD、Raman和H_(2)-TPR等对催化剂物理化学性能进行表征,并在固定床装置上评价催化剂均四甲苯气相氧化反应性能。结果表明,钒钛氧化物催化剂中钒以TiO_(2)表面VO_(x)物种和晶体V_(2)O_(5)存在,焙烧温度可调变催化剂中表面VO_(x)物种和晶体V_(2)O_(5)的比例,焙烧温度越高,多聚的表面VO_(x)物种或晶体V_(2)O_(5)越多。500℃焙烧条件制备的催化剂具有合适的可还原性,弱酸位点相对较多,在均四甲苯气相氧化中性能最优,均酐质量收率可达85.8%。 展开更多
关键词 催化剂工程 钒钛氧化物催化剂 均苯四甲酸二酐 气相氧化 焙烧温度
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3,3’,4,4’-联苯四甲酸二酐的合成
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作者 张秀红 付裕轩 +3 位作者 张恒 王培奇 陈思礼 彭浚峰 《应用化工》 CAS CSCD 北大核心 2024年第10期2372-2375,共4页
3,3’,4,4’-联苯四甲酸二酐是高性能材料聚酰亚胺的前体。采用格氏试剂偶联的方法对3,3’,4,4’-联苯四甲酸二酐的合成进行了研究。首先4-溴邻二甲苯与金属镁反应制备格氏试剂,然后在三氟甲磺酸铁催化下,格氏试剂自身偶联制得3,3’,4,4... 3,3’,4,4’-联苯四甲酸二酐是高性能材料聚酰亚胺的前体。采用格氏试剂偶联的方法对3,3’,4,4’-联苯四甲酸二酐的合成进行了研究。首先4-溴邻二甲苯与金属镁反应制备格氏试剂,然后在三氟甲磺酸铁催化下,格氏试剂自身偶联制得3,3’,4,4’-四甲基联苯;3,3’,4,4’-四甲基联苯经氧化、脱水制得3,3’,4,4’-联苯四甲酸二酐。考察了实验中关键因素的影响,确定了偶联最佳反应条件并对反应机理进行了解析。结果表明,偶联反应温度为60℃,反应时间为8 h时,3,3’,4,4’-四甲基联苯的收率达到83%。3,3’,4,4’-联苯四甲酸二酐的收率为78%。机理分析表明格氏试剂在铁催化剂和1,2-二氯乙烷作用下,发生了自偶联反应制备了3,3’,4,4’-四甲基联苯。 展开更多
关键词 聚酰亚胺 3 3’ 4 4’-联苯四甲酸二酐 4-溴邻二甲苯 格氏试剂 偶联反应
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超早强型聚羧酸减水剂的制备及性能研究
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作者 康净鑫 陈吓敏 李芳 《新型建筑材料》 2024年第10期47-51,共5页
将环状二酸酐醇解制备端羟基接枝羧基的聚醚大单体CA-HPEG,再与氨基硅氧烷进行酰胺化反应制得改性聚醚LPEG,将LPEG与酰胺类单体引入共聚反应中,制备长侧链、短主链的超早强型聚羧酸减水剂SPE。对SPE进行工艺优化,并探讨SPE对水泥净浆流... 将环状二酸酐醇解制备端羟基接枝羧基的聚醚大单体CA-HPEG,再与氨基硅氧烷进行酰胺化反应制得改性聚醚LPEG,将LPEG与酰胺类单体引入共聚反应中,制备长侧链、短主链的超早强型聚羧酸减水剂SPE。对SPE进行工艺优化,并探讨SPE对水泥净浆流动度、砂浆早期强度及混凝土拌合物性能的影响,然后通过傅里叶红外光谱对LPEG及SPE的结构进行表征,X射线衍射仪对SPE的水泥水化产物进行分析。结果表明,改性聚醚CA-HPEG的最佳酯化条件为:n(1,2-环己二甲酸酐)∶n(HPEG5000)为2∶1,反应时间为2h,反应温度为60℃。SPE的最佳合成工艺参数为:n(LPEG)∶n(HPEG5000)=2∶3,n(AA)∶n(AM)=3∶1,n(AA+AM)∶n(LPEG+HPEG5000)=4.5,引发剂APS用量为聚醚单体质量的0.45%,链转移剂用量为聚醚单体质量的0.25%,反应温度为常温,滴加时间为3 h。最佳工艺合成的减水剂对混凝土的初凝及终凝时间均有较好的缩短效果,并且早期抗压强度增强效果明显。 展开更多
关键词 环状二酸酐醇解 氨基硅氧烷 超早强型聚羧酸减水剂 终凝时间
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脱卤法制备联苯四甲酸二酐反应关键影响因素研究
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作者 王建华 《当代化工研究》 CAS 2024年第6期36-38,共3页
聚酰亚胺模塑料具有良好的热稳定性、化学稳定性和机械性能,广泛应用于食品、药品、化妆品等精细化工产品的生产过程,相关研究日益增加。作为联苯型聚酰亚胺的关键原料,联苯四甲酸二酐的制备过程日益受到关注。在各种制备方法中,脱卤偶... 聚酰亚胺模塑料具有良好的热稳定性、化学稳定性和机械性能,广泛应用于食品、药品、化妆品等精细化工产品的生产过程,相关研究日益增加。作为联苯型聚酰亚胺的关键原料,联苯四甲酸二酐的制备过程日益受到关注。在各种制备方法中,脱卤偶联法过程反应条件温和,产品收率高,纯度好,相关研究较多。本研究以卤代邻苯二甲酸酐为原料,以钯碳作为催化剂,在盐酸羟胺还原剂参与的条件下,采用脱卤偶联法制备了联苯四甲酸二酐,系统考察了卤代烃类型、催化剂类型、催化剂用量、还原剂用量、反应气氛、反应温度、反应时长、成酐方式等关键影响因素对产物收率的影响,获得了适宜的脱卤偶联制备联苯四甲酸二酐的反应条件。 展开更多
关键词 联苯四甲酸二酐 脱卤偶联法 卤代邻苯二甲酸酐 钯碳作为催化剂 盐酸羟胺还原剂
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SYNTHESIS AND CHARACTERIZATION OF ORGANSOLUBLE POLYIMIDE AND COPOLYIMIDES FROM ALICYCLIC DIANHYDRIDE 被引量:5
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作者 黄卫 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2007年第4期409-417,共9页
A kind of highly organsoluble polyimide and copolyimides were successfully synthesized from bicyclo(2.2.2)-oct- 7-ene-2,3,5,6-tetracarboxylic dianhydride (BCDA), the commercial diamine 4,4'-methylenedianiline (... A kind of highly organsoluble polyimide and copolyimides were successfully synthesized from bicyclo(2.2.2)-oct- 7-ene-2,3,5,6-tetracarboxylic dianhydride (BCDA), the commercial diamine 4,4'-methylenedianiline (MDA) and the designed diamine 4,4'-methylenebis-(2-tert-butylaniline) (MBTBA). The polyimide from BCDA and MBTBA is highly soluble in conventional low boiling point solvents (such as chloroform, tetrahydrofuran) at room temperature. But the solubility of the copolyimides in conventional solvents decreased with the molar ratio of MBTBA and MDA decreased. When the molar ratio of MBTBA and MDA was larger than 7/3, the copolyimides can be soluble in low boiling point solvents at room temperature to form a transparent, flexible, tough film by solution casting. When the molar ratio of MBTBA and MDA was between 7/3 and 1/9, they can only be soluble in hot dipolar aprotic solvents (such as DMF, NMP etc.) and form films too. The copolyimide was only soluble in m-cresol when the molar ratio of MBTBA and MDA was lower than 1/9. The number-average molecular weights of the soluble copolyimides were larger than 5.8 × 1064 g/mol by GPC and their polydispersity indices were higher than 1.4. Only one glass transition temperature of these copolyimides was detected around 400℃ by DMA. The copolyimides did not show appreciable decomposition up to 430℃ in N2. 展开更多
关键词 Polyimides Bicyclo(2.2.2)-oct-7-ene-2 3 5 6-tetracarboxylic dianhydride 4 4'-Methylenebis-(2-tert-butylaniline) 4 4'-Methylenedianiline.
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A novel efficient synthetic method for 2,2′,3,3′-biphenyltetracarboxylic dianhydride 被引量:1
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作者 Shi Xu Yi Jian Men +2 位作者 Xiao Yan Ma Yan Jiang Guo Wei Gao 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第3期306-309,共4页
A novel approach to the synthesis of 2,2',3,3'-biphenyltetracarboxylic dianhydride is described. The target compound was prepared by a nickel-catalyzed couplirtg reaction of dimethy 3-chlorophthalate (3-DMCP) for ... A novel approach to the synthesis of 2,2',3,3'-biphenyltetracarboxylic dianhydride is described. The target compound was prepared by a nickel-catalyzed couplirtg reaction of dimethy 3-chlorophthalate (3-DMCP) for 4 h at 70-80 ℃, followed by subsequent hydrolysis of tetra-ester in acid solution and dehydration of tetra-acid, with overall yield of 68%. The structures of the products were characterized by IR, 1H NMR and ^13C NMR respectively. 展开更多
关键词 2 2' 3 3'-Biphenyltetracarboxylic dianhydride NICKEL-CATALYZED Coupling reaction
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Polyimide structure-Property Relationships I. Polyimide Properties υs Dianhydride Configuration 被引量:1
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作者 Yue Jin TONG Yan Xiang CHENG +2 位作者 Meng Xian DING Yan XING Yong Hua LIN (Changchun institute of Applied Chemistry, Acadenda Sinica, Changchun 130022) 《Chinese Chemical Letters》 SCIE CAS CSCD 1998年第10期971-972,共2页
X-ray crystal structures of 2,2',3,3'-and 3, 3',4,4'-biphenyltetracarboxylic dianhydride (2,2',3,3'- and 3,3',4,4'-BPDA) were determined. The dianhydride isomers have different symmetr... X-ray crystal structures of 2,2',3,3'-and 3, 3',4,4'-biphenyltetracarboxylic dianhydride (2,2',3,3'- and 3,3',4,4'-BPDA) were determined. The dianhydride isomers have different symmetry caused by difference in two anhydride group positions and the dihedral angles between the two phenyl rings are 62.9°for 2,2',3,3',-BPDA and 0°for 3,3',4,4'-BPDA respectively. The polyimides from 2,2',3,3'-BPDA exhibit enhanced solubility, higher thermal stability, and higher glasstransition temperature (Tg) compared with those from 3,3',4,4'-BPDA. 展开更多
关键词 polytimide dianhydride isomers x-ray single-crystal structure STRUCTURE-PROPERTY
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Modified disordered carbon prepared from 3,4,9,10-perylenetetracarboxylic dianhydride as an anode material for Li-ion batteries
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作者 Fei-biao Chen Bo-rong Wu +3 位作者 Yun-kui Xiong Wei-lin Liao Dao-Bin Mu Feng Wu 《International Journal of Minerals,Metallurgy and Materials》 SCIE EI CAS CSCD 2015年第2期203-209,共7页
To prepare an anode material for Li-ion batteries with high discharge capacity and good cycling stability, disordered carbon (DC) formed by calcinations of 3,4,9,10-perylenetetracarboxylic dianhydride was modified v... To prepare an anode material for Li-ion batteries with high discharge capacity and good cycling stability, disordered carbon (DC) formed by calcinations of 3,4,9,10-perylenetetracarboxylic dianhydride was modified via an acid treatment using a mixture of HNO3 and H2SO4. The modified disordered carbon (MDC) was characterized by Fourier-transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) analysis, Brtmaner-Emmett-Teller (BET) analysis, and scanning electron microscopy (SEM). FTIR spectra confirm the successful introduction of carbonyl groups onto the DC surface. Some pores appear in the columnar structure of MDC, as observed in SEM micro- graphs. Li+ ions intercalation/deintercalation is facilitated by the modified morphology. Electrochemical tests show that the MDC exhibits a significant improvement in discharge capacity and cycling stability. These results indicate that the MDC has strong potential for use as an anode material in Li-ion batteries. 展开更多
关键词 CARBON perylenetetracarboxylic dianhydride anode materials lithium-ion batteries
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Facile Synthetic Method and Crystal Structure of 2,3,3',4'-Biphenyltetracarboxylic Dianhydride
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作者 YI Shi-xu GAO Guo-wei +3 位作者 YANG Mei-jia CHEN Hua WU Di-feng MEN Jian 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2012年第2期234-238,共5页
A facile method for the synthesis of 2,3,3',4'-biphenyltetracarboxylic dianhydride(a-BPDA) was reported,which comprises the steps of the dehalogenative coupling of dimethyl 4-chlorophthalate(4-DMCP) and dimethyl... A facile method for the synthesis of 2,3,3',4'-biphenyltetracarboxylic dianhydride(a-BPDA) was reported,which comprises the steps of the dehalogenative coupling of dimethyl 4-chlorophthalate(4-DMCP) and dimethyl 3-chlorophthalate(3-DMCP) catalyzed by low-cost(Ph 3 P) 2 NiCl 2,the hydrolysis of tetra-ester and the dehydration of tetra-acid.In contrast to the conventional methods,this method has the advantage of low cost,convenient manipulation,available condition,high purity and good overall yield.Moreover,the single crystal structure of a-BPDA was analyzed by X-ray diffraction method.The X-ray data suggest that a-BPDA is a rigid,non-coplanar and non-linear structure.It contains three crystallographically independent molecules,in which the dihedral angles of the two linked phenyl rings are 44.75(4)°,46.37(3)° and 42.32(3)°,respectively.The title molecule is governed by a stronger intermolecular interaction in contrast to van der Waals interaction because of the special positions of anhydride groups. 展开更多
关键词 2 3 3' 4'-Biphenyltetracarboxylic dianhydride Crystal structure Ni-catalyzation Dehalogenative coupling
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Hydrogen Bonding-Mediated Assembly of Perelene Dianhydride and Pyridine Derivatives
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作者 Shi Wu Qi-wen Teng 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 北大核心 2006年第1期76-78,共3页
Semi-empirical AMI method was used to study 1:1 and 1:2 hydrogen bond complexes formed with perylene dianhydride and pyridine derivatives. The weak interaction energy become bigger as the number of hydrogen bonds in... Semi-empirical AMI method was used to study 1:1 and 1:2 hydrogen bond complexes formed with perylene dianhydride and pyridine derivatives. The weak interaction energy become bigger as the number of hydrogen bonds increases. The donor groups on the host and electron-withdrawing groups on the guest molecules favor hydrogen bonding interactions, and the formation of hydrogen bonding leads to electron density flow from the host to the guest molecules. Electronic spectra of these complexes were computed using INDO/SCI method. Blue-shift of the clectronic absorption spectra for the complexes, comparing that of the host, takes place, and the first peaks for different complexes changed slightly. These are in agreement with the experimcntal results. The cause of blue-shift was discussed, and the electronic transitions were assigned based on theoretical calculations. The potential curve of double proton transfer in the complex was calculated, and the transition state and activated energy relative to the N H bond were obtained. 展开更多
关键词 Perylene dianhydride Hydrogen bonding assembly Electronic spectra AMI
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A Facile Synthetic Method for Biphenyltetracarboxylic Dianhydrides
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作者 XueEWU ChangLuGAO MengXianDING SuoBoZHANG LianXunGAO 《Chinese Chemical Letters》 SCIE CAS CSCD 2004年第7期787-790,共4页
We report a facile and high-yielding procedure for preparing biphenyltetracarboxylic dianhydrides (BPDAs). This method relies on a nickel-catalyzed electroreductive coupling reaction of dimethyl 3-chorophthalate (3-DM... We report a facile and high-yielding procedure for preparing biphenyltetracarboxylic dianhydrides (BPDAs). This method relies on a nickel-catalyzed electroreductive coupling reaction of dimethyl 3-chorophthalate (3-DMCP) and/or dimethyl 4-chorophthalate (4-DMCP) with subsequent hydrolysis of tetra-ester and dehydration of tetra-acid. 展开更多
关键词 Biphenyltetracarboxylic dianhydrides NICKEL-CATALYZED electroreductive coupling.
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Microwave Accelerated Synthesis of 2,2',3,3'-Biphenyltetracarboxylic Dianhydride
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作者 HUANG Yuan-yuan SHAO Tao +1 位作者 MEN Jian GAO Guo-wei 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2012年第3期364-365,共2页
Polyimides have been widely used in aerospace and mi- croelectronics due to their excellent mechanical properties and thermo oxidative stability^[1]. However, most of aromatic polyi- mides are severe difficult to proc... Polyimides have been widely used in aerospace and mi- croelectronics due to their excellent mechanical properties and thermo oxidative stability^[1]. However, most of aromatic polyi- mides are severe difficult to process because of their bad solu- bility in common solvents and intractable in their fully imidized forms, which restrict their applications and developments^[2,3]. Therefore, many investigations were focused on improving the dissolvability of polyimides and it was found that the excellent solubilizing units could be obtained from substituted biphenyls^[4-7]. Biphenyltetracarboxylic dianhydrides(BPDAs) are the most important monomers for the synthesis of these compounds. Among them, the synthesis of 2,3,3',4'-/3,3',4,4'- biphenyltetracarboxylic dianhydride has been widely investi- gated, but only a few literatures reported the synthesis of 2,2',3,3'-biphenyltetracarboxylic dianhydride(i-BPDA)^[8-10]. 展开更多
关键词 2 2' 3 3'-Biphenyltetracarboxylic dianhydride NICKEL-CATALYZED Microwave synthesis
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The Crystal Structure of Biphenyltetracarboxylic Dianhydride Isomers
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作者 童跃进 关怀民 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1999年第5期393-397,共5页
Biphenyltetracarboxylic dianhydride (2,2',3,3' BPDA), C 16 H 6O 6, M r =294.21, monoclinic, P2 1/c, a=11.694(2), b=8.111(2), c=13 494(3) , β=103.47(3)°, V=1244.7(4) 3, Z=4, D c =1.57... Biphenyltetracarboxylic dianhydride (2,2',3,3' BPDA), C 16 H 6O 6, M r =294.21, monoclinic, P2 1/c, a=11.694(2), b=8.111(2), c=13 494(3) , β=103.47(3)°, V=1244.7(4) 3, Z=4, D c =1.570 g/cm 3 , F (000)=450, Mo Kα radiation( λ =0.71073), μ (Mo Kα )=0.092 mm -1 , R =0.0329 for 2180 observed reflections 〔 I>2σ(I) 〕. 3,3',4,4' Biphenyltetracarboxylic dianhydride (3,3',4,4' BPDA), C 16 H 6O 6, M r =294.21, monoclinic, P2 1/n, a=6.8720(14), b=5.1870(10), c=17.288(4), β=94.96(3)°, V= 613.9(2) 3, Z=2, D c =1 592 gcm -3 , F(000)=300 , μ (Mo Kα )=0.125mm -1 , R =0.0331 for 1079 observed reflections〔 I>2σ(I) 〕. The dianhydride isomers have different symmetry caused by alternating two anhydride group positions and the dihedral angle between the two phenyl rings are 62.9°for 2,2',3,3', BPDA and 0°for 3,3',4,4' BPDA respectively. 展开更多
关键词 crystal structure biphenyltetracarboxylic dianhydride ISOMERS
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A Di-D-Fructose Dianhydride-Enriched Caramel Modulates Pig Fecal Microbiota Composition
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作者 Luis A. Rubio María Jesús Peinado +4 位作者 Ana Echávarri Raquel Ruiz Elena Suárez-Pereira Carmen Ortiz Mellet José M. García Fernández 《Advances in Microbiology》 2014年第5期242-251,共10页
A correlation has been previously described between bifidobacteria counts before and after the use of a dietary additive in human studies. However, to our knowledge no information on this topic has yet been reported i... A correlation has been previously described between bifidobacteria counts before and after the use of a dietary additive in human studies. However, to our knowledge no information on this topic has yet been reported in animals, and no information exists either on similar possible correlations of bacterial groups other than bifidobacteria. The potential prebiotic effects of di-D-fructose dianhydride (DFA)-enriched caramels have been previously reported in laboratory animals, poultry and pigs. In the present work, twelve growing male castrated pigs (41.8 ± 1.9 kg mean BW) were fed in succession on a control (no additive) or DFA-enriched caramel (20 g/kg) containing diets. Another group of 10 pigs (38.0 ± 3.7 kg mean BW) fed on a control diet without any additive was used as negative control. Bacterial log10 number of copies of the 16S rRNA gene was determined in fecal samples by using qPCR. Increased (P10 number of copies were determined in fecal samples of pigs fed on the caramel containing diet compared with non-caramel controls. In addition, for all bacterial groups studied microbiological values co-variated with initial counts and, except for enterobacteria, variations in the fecal bacterial numbers after caramel supplementation correlated (P< 0.05) with the fecal numbers before supplementation. In conclusion, the supplementation of pig diets with DFA-enriched caramels induced significant increases in the fecal number of copies of bacterial groups regarded as beneficial, and variations in the fecal number of copies correlated with the initial fecal number of copies. 展开更多
关键词 Di-D-Fructose dianhydrideS Fecal Microbiota Correlations PIG Prebiotics
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Effects of difructose dianhydride (DFA)-Ⅳ on in vitro fertilization in pigs
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作者 Young-Joo Yi S. Kamala-Kannan +2 位作者 Jeong-Muk Lim Byung-Taek Oh Sang-Myeong Lee 《The Journal of Biomedical Research》 CAS CSCD 2017年第5期453-461,共9页
Difructose dianhydride Ⅳ(DFA-Ⅳ) is produced from levan, which is a natural polysaccharide that belongs to the fructan family, through the activity of levan fructotransferase(LF) derived from microorganisms. Recently... Difructose dianhydride Ⅳ(DFA-Ⅳ) is produced from levan, which is a natural polysaccharide that belongs to the fructan family, through the activity of levan fructotransferase(LF) derived from microorganisms. Recently, DFA-Ⅳ has been expected to have diverse applications in the food and medical industry. Here, we examined the potential application of DFA-Ⅳ for in vitro fertilization(ⅣF) in pigs. In the assessment of acrosomal integrity during incubation, intact acrosomal or viable spermatozoa were highly sustained in 0.1% or 0.25% DFA-Ⅳ(69.8%-70.8%,P<0.05). Reactive oxygen species(ROS) levels during sperm incubation decreased following the addition of DFA-Ⅳ, and 0.1 %-0.5% DFA-Ⅳ in particular significantly decreased ROS production relative to that seen with no addition or 0.75% DFA-Ⅳ. Total fertilization(mono + polyspermic oocyte) rate was significantly higher in the addition of0.1% DFA-Ⅳ(94.2%) than with other concentrations(71.8%-86.7%, P<0.05). When using reduced ⅣF times and lower sperm numbers, we found that addition of 0.1%-0.5% DFA-Ⅳ significantly increased the fertilization rate(P<0.05). Fertilized oocytes treated with 0.1% DFA-Ⅳ exhibited higher embryonic development and blastocyst formation than those treated with other concentrations(P<0.05). Consequently, the addition of DFA-Ⅳ during ⅣF improved fertilization and embryonic development, suggesting the possible use of novel sugars for enhancement of assisted reproductive technology(ART) in mammals. 展开更多
关键词 difructose dianhydride-Ⅳ SPERMATOZOA in vitro fertilization EMBRYO PIG
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