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聚氨酯催化剂双(N,N-二甲胺基乙基)醚合成工艺研究进展 被引量:1
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作者 李向东 尹永波 +2 位作者 郭林 唐勇 宋丽凤 《塑料助剂》 2017年第1期13-17,共5页
综述了一种聚氨酯催化剂双(N,N-二甲胺基乙基)醚的合成方法。并对各种不同的合成工艺方法进行了对比分析,指出了各种工艺方法的优缺点。最后,对双(N,N-二甲胺基乙基)醚合成技术方法进行了展望。
关键词 聚氨酯 合成工艺 催化剂 双(N N-二甲胺基乙基)醚
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(N,N-二甲胺基乙基)丙烯酸酯在炭黑表面接枝聚合研究 被引量:1
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作者 蒋子铎 周爱军 吴璧耀 《武汉化工学院学报》 1996年第1期1-4,共4页
利用Ce(4+)和炭黑表面的羟甲基组成的氧化还原体系,探讨了(N,N-二甲胺基乙基)丙烯酸酯在炭黑表面的接枝聚合机理。研究表明单体和硝酸的浓度以及铈离子的用量对该反应有显著的影响。傅立叶红外光谱分析和透射电子显微镜分... 利用Ce(4+)和炭黑表面的羟甲基组成的氧化还原体系,探讨了(N,N-二甲胺基乙基)丙烯酸酯在炭黑表面的接枝聚合机理。研究表明单体和硝酸的浓度以及铈离子的用量对该反应有显著的影响。傅立叶红外光谱分析和透射电子显微镜分析表明,在接枝改性炭黑表面存在着聚(N,N-二甲胺基乙基)丙烯酸酯。 展开更多
关键词 接枝聚合 炭黑 二甲胺基乙基 丙烯酸酯 改性
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O-(2-二甲胺基乙基)羟胺二盐酸盐的合成
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作者 黄旭虎 《广东化工》 CAS 2020年第5期81-82,共2页
以二苯甲酮肟和N,N-二甲基-2-氯乙胺盐酸盐为原料合成了O-(2-二甲胺基乙基)-二苯基甲肟,然后再用盐酸水解得到了目标化合物O-(2-二甲胺基乙基)羟胺二盐酸盐。对反应条件进行了优化,两步反应总收率65%,并且用~1H-NMR和^(13)C-NMR对目标... 以二苯甲酮肟和N,N-二甲基-2-氯乙胺盐酸盐为原料合成了O-(2-二甲胺基乙基)-二苯基甲肟,然后再用盐酸水解得到了目标化合物O-(2-二甲胺基乙基)羟胺二盐酸盐。对反应条件进行了优化,两步反应总收率65%,并且用~1H-NMR和^(13)C-NMR对目标化合物进行了结构表征。 展开更多
关键词 O-(2-二甲胺基乙基)羟胺二盐酸盐 合成 结构表征
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原子转移自由基聚合法合成磺基甜菜碱型两性离子均聚物
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作者 王洪军 万芯瑗 +1 位作者 杨建 李洁华 《高分子材料科学与工程》 EI CAS CSCD 北大核心 2013年第7期5-8,共4页
为了实现两性离子可控聚合,文中以溴异丁酰基-叔丁氧碳基乙二胺(BDBBr)为引发剂,溴化亚铜为催化剂,2,2’-联吡啶(Bpy)为配体,用原子转移自由基法(ATRP)将3-(2-甲基丙烯酰氧乙基二甲胺基)丙磺酸盐(DMAPS)进行聚合,考察了溶剂体系、反应... 为了实现两性离子可控聚合,文中以溴异丁酰基-叔丁氧碳基乙二胺(BDBBr)为引发剂,溴化亚铜为催化剂,2,2’-联吡啶(Bpy)为配体,用原子转移自由基法(ATRP)将3-(2-甲基丙烯酰氧乙基二甲胺基)丙磺酸盐(DMAPS)进行聚合,考察了溶剂体系、反应温度和反应时间对聚合反应的影响,用凝胶渗透色谱仪(GPC)测定了分子量和分子量分布。研究结果表明,在良溶剂体系三氟乙醇/异丙醇=20∶1(体积比)和室温30℃条件下,得到目标聚合度Xn=50和Xn=100的磺酸盐两性离子聚合物。反应温度为60℃的聚合物比温度为30℃的聚合物的相对分子质量更低,分子量分布更宽。随着时间的延长,聚合物的相对分子质量有变大且转化率逐渐升高的趋势。 展开更多
关键词 两性离子聚合物 3-(2-甲丙烯酰氧二甲胺基)丙磺酸盐 原子转移自由聚合
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不饱和季铵盐的加压制备法 被引量:2
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作者 鲁红 冯大春 尹家贵 《化学试剂》 CAS CSCD 北大核心 2001年第6期362-363,369,共3页
介绍一种在一定压力下 ,制取不饱和季铵盐的通用方法 ,并用二甲胺基乙基丙烯酸酯 ( DMAEA)和一氯甲烷为原料 ,制取丙烯酸乙酯基三甲基氯化铵 ( DMAEA-Q)
关键词 不饱和季铵盐 二甲胺基乙基丙烯酸酯 一氯甲烷 丙烯酸三甲氯化铵 加压制备
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Solid-Liquid Equilibrium of Terephthalic Acid in Several Solvents 被引量:15
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作者 马沛生 陈明鸣 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2003年第3期334-337,共4页
Terephthalic acid(PTA) is practically one of the main materials of polyester. Its corresponding solid-liquid equilibrium data will provide essential support for industry design and further theoretical studies. In this... Terephthalic acid(PTA) is practically one of the main materials of polyester. Its corresponding solid-liquid equilibrium data will provide essential support for industry design and further theoretical studies. In this work,solid-liquid equilibriums of terephthalic acid in four solvents, N,N-dimethylformamide, N,N-dimethylacetamide,dimethylsulphoxide and N-methyl-2-ketopyrrolidene, were determined in the temperature range from 293.15 K to 364.6 K by dynamic method. All these data were regressed by λh model, Wilson model and NRTL model, average absolute relative deviations of which are 1.25%, 15.02% and 7.22% respectively. It indicates that λh model is mostsuitable for description of the solid-liquid equilibrium containing PTA. 展开更多
关键词 solid-liquid equilibrium terephthalic acid λh model
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Synthesis and Crystal Structure of a New Hexadentate Ligand N,N'-Bis(di(2-pyridyl)methyl)ethylenediamine
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作者 YEBao-Hui CHENXiao-Ming 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2004年第3期242-246,共5页
The reaction of di(2-pyridyl)ketone with ethylenediamine produced hexadentate Schiff base 1 which can be reduced to form a new ligand N,N-bis(di(2-pyridyl)-methyl)ethylene- diamine (BDPM) in ethanol solution. The two ... The reaction of di(2-pyridyl)ketone with ethylenediamine produced hexadentate Schiff base 1 which can be reduced to form a new ligand N,N-bis(di(2-pyridyl)-methyl)ethylene- diamine (BDPM) in ethanol solution. The two compounds were characterized by elemental analyses and spectroscopic methods. Their structures were determined by X-ray diffraction study. Crystal data for 1: C24H20N6, Mr = 392.5, monoclinic, P21/c, a = 13.871(3), b = 13.510(2), c = 12.153(2) ? b = 112.97(2)? Z = 4, V = 2094.1(6) ?, Dc = 1.245 g/cm3, m(MoKa) = 0.078 mm-1, F(000) = 824, the final R = 0.0545 and wR = 0.0557 for 2048 observed reflections (I > 2s(I)); for BDPM: C24H24N6, Mr = 396.49, monoclinic, C2/c, a = 21.411(3), b = 8.053(1), c = 11.868(1) ? b = 92.63(1)? Z = 4, V = 2044.2(4) 3, Dc = 1.288 g/cm3, m(MoKa) = 0.080 mm-1, F(000) = 840, the final R = 0.0401 and wR = 0.0939 for 1673 observed reflections (I > 2s(I)). 展开更多
关键词 synthesis crystal structure hexadentate ligand di-2-pyridyl ketone
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Development of efficient solid chiral catalysts with designable linkage for asymmetric transfer hydrogenation of quinoline derivatives 被引量:1
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作者 Yiqi Ren Lin Tao +3 位作者 Chunzhi Li Sanjeevi Jayakumar He Li Qihua Yang 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2021年第9期1576-1585,共10页
Developing chiral solid catalysts for asymmetric catalysis is desirable for the elimination of homogeneous catalysis flaws but remains an immense challenge.Herein,we report the immobilization of TsDPEN on SBA‐15 with... Developing chiral solid catalysts for asymmetric catalysis is desirable for the elimination of homogeneous catalysis flaws but remains an immense challenge.Herein,we report the immobilization of TsDPEN on SBA‐15 with an ionic liquid(IL)linkage via the one‐pot reaction of imidazole‐TsDPEN‐N‐Boc with 3‐(trimethoxysilyl)propyl bromide in the SBA‐15 mesopores.After coordination to Rh,the chiral solid catalysts could efficiently catalyze quinoline transfer hydrogenation,achieving 97%conversion with 93%ee,which was comparable to their homogeneous counterparts.The chiral solid catalyst with the IL linkage afforded much higher turnover frequency than that without the IL linkage(93 h^(–1)vs.33 h^(–1)),attributed to the phase transfer and formate‐enriching ability of the IL linkage.Furthermore,the effect of the pH on the reaction rate of the solid catalyst was investigated,preventing reaction rate retardation during the catalytic process.The tuning of the linkage group is an efficient approach for catalytic activity improvement of immobilized chiral catalysts. 展开更多
关键词 Heterogeneous asymmetric catalysis Asymmetric transfer hydrogenation QUINOLINES IMIDAZOLATE Ionic liquid N‐(p‐toluenesulfonyl)‐1 2‐diphenylethylenediamine
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Synthesis and Crystal Structure of Neodymium Complex [Nd(C_6H_4OHCHNC_2H_4NCHC_6H_4OH)(NO_3)_3(CH_3SOCH_3)] 被引量:1
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作者 张敏 张崇起 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1996年第5期411-414,共4页
The title complex was obtained by reaction of hydrated neodymium(Ⅲ) nitrate with N,N-disalicyclideneethylenediamine in DMSO. The complex [Nd(C_6H_4OHCHNC_2H_4NCHC_6H_4OH)(NO_3)_3(CH_3SOCH_3)] crystallizes in monoclin... The title complex was obtained by reaction of hydrated neodymium(Ⅲ) nitrate with N,N-disalicyclideneethylenediamine in DMSO. The complex [Nd(C_6H_4OHCHNC_2H_4NCHC_6H_4OH)(NO_3)_3(CH_3SOCH_3)] crystallizes in monoclinic system, space group- P2_1/n, a=9.663(2), b=16.610(6),c=16.322(5),β=102.77(2)°,V=2555(3),M_r=676.71,Z=4,Dx=1.759 gcm-3. The coordination number of Nd(Ⅲ) is 9 with the geometry of a monocapped square antiprism.All of coordination atoms are oxygen atoms from three bidentate nitrate groups, two dischiff base molecules and one DMSO molecule. 展开更多
关键词 neodymium complex N N-disalicylideneethylenediamine dimethyl sulfoxide crystal structure
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