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国家自然科学基金(20272062)

作品数:10 被引量:38H指数:3
相关作者:孙文华张文娟侯俊先唐秀波张天柱更多>>
相关机构:中国科学院兰州大学中国科学院福建物质结构研究所更多>>
发文基金:国家自然科学基金中国科学院“百人计划”更多>>
相关领域:理学化学工程更多>>

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10 条 记 录,以下是 1-10
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Synthesis and Characterization of {2-Formyl-6-[1-(2,4,6-trimethylphenyl)]-4- chlorophenoxy}_2Ni and Its Ethylene Oligomerization
2005年
The title nickel complex (C34H3oCl2N2NiO4, Mr = 660.21) has been synthesized and its crystal structure was determined by single-crystal X-ray structure analysis. It crystallizes in the monoclinic system, space group P21/n with a = 11.026(8), b = 11.491(8), c = 12.119(9) A°, β=91.328(13)°, Z= 2, V= 1535.0(19) ,A°^3, Dc = 1.428 g/cm^3, F(000) = 684 andμ(MoKa) = 0.848 mm^-1 The structure was refined to R = 0.0544 for 1813 observed reflections with I 〉 2σ(I) and wR =0.0867 for 3132 unique reflections. The molecule of the complex is high symmetrical. Ni(Ⅱ) atom is located in the symmetric center and coordinated to two phenolic oxygen and two imino nitrogen atoms, forming two six-membered rings. Upon activation with methylaluminoxane (MAO), it is active for ethylene oligomerization.
ZHANG Dong-HengDU Jian-LongHAN Ling-QinSUN Wen-Hua
关键词:SALICYLALDIMINE
2-羰基-4-氯-6-亚胺基苯酚中性镍配合物的合成和结构
<正> 后过渡金属催化剂用于烯烃聚合受到了学术界和工业界越来越多的关注。其中水杨醛亚胺类希夫碱与中性镍的配合物展现了较好的烯烃聚合催化活性。有鉴于此,我们通过4-氯-2,6-二羰基苯酚与取代苯胺在p-TsOH催化下在无水...
林奇张有明吴彪孙文华
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新型钯烯烃催化剂的合成和结构
<正> 后过渡金属配合物用于烯烃聚合和齐聚研究已成为近年来金属有机化学领域的一个热门课题,而围绕双亚胺吡啶类型的配体展开的后过渡金属配合物的合成及催化性能的研究引起了学术界和工业界的极大的兴趣。本文报道了一类新型的吡啶亚...
张文娟唐秀波高铁龙孙文华
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双吡啶亚胺双核镍配合物的合成、表征及其乙烯催化性能的研究
<正> 近年来,后过渡金属烯烃聚合催化剂的研究引起了广泛的关注。Brookhart小组曾报道α一二亚胺镍配合物和吡啶双亚胺铁、钴配合物对乙烯表现出高的齐聚活性。催化剂的活性和产物的特征在很大程度上依赖于催化剂中心金属和配...
介素云张天柱吴彪孙文华
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Synthesis and Crystal Structure of Bis-{N-[2-(6-ethylpyridyl)]-salicylideneiminato} Cobalt(Ⅱ)
2004年
The title complex 1, C28H26CoN4O2, crystallizes in the triclinic system, space group P with a = 9.506(3), b = 9.506(3), c = 14.837(5) ? a = 106.397(5), b = 106.012(5), g = 91.889(6), V = 1217.7(7) 3, Z = 2, Dc =1.390 g/cm3, Mr = 509.46, F(000) = 530, m(MoKa) = 0.738 mm-1, the final R = 0.0359 and wR = 0.0951 for 4275 observed reflections with I > 2s(I). The complex adopts a distorted tetrahedral coordination sphere around the cobalt atom.
杨海健王宏根孙文华
铁配合物催化的乙烯聚合与齐聚
<正> 在Brookhart与Gibson分别同时报道三齿氮配位铁催化剂催化乙烯聚合之后,后过渡金属配合物催化烯烃聚合的研究倍受学术界和聚烯烃工业界的关注。在多年铁配合物合成与催化乙烯研究过程中发现,配体的立体位阻和电子...
孙文华唐秀波张东恒介素云张闻马志
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酰腙钛配合物的合成及其催化乙烯聚合研究被引量:9
2004年
Aroylhydrazones,formed by condensation of benzoylhydrazine with benzoylaldehyde,2-methoxybenzoylaldehyde and 2,4-dimethoxybenzoylaldehyde,reacted with TiCl 4 to form their corresponding complexes.The titanium complexes were characterized by elementary analysis,IR,and 1H-NMR.Their catalytic properties for ethylene polymerization performed up to 104gPE/(molTi·h).The resultant PE was studied by DSC,GPC,WAXD,FT-IR analyses.The results reveal that the product obtained is a typical linear polyethylene.
侯俊先陈立谊唐秀波孙文华
关键词:均相催化苯甲酰肼对甲基苯磺酸
双水杨醛亚胺双核镍(Ⅱ)配合物降冰片烯加成聚合的研究被引量:6
2004年
A series of bridged ligand 4,4′-methylene-bis [2,6-dialkyl-N-(2-phenylmethylene)-anil] was efficiently synthesized by the condensation reaction of 4,4′-methylene-bis(2,6-disubstituted aniline) and salicyl aldehyde.They easily coordinated with Ni (Ⅱ) to form the title complexes,which were characterized by IR spectroscopy and elemental analysis.The complexes show good activities for vinyl polymerization of norbornene with methylalumoxane (MAO) as co-catalyst.The variations of complexes and catalytic parameters were investigated along with viscosimetric measurement of resultant polynorbornenes.
张东恒介素云张天柱侯俊先李伟赵东风孙文华
关键词:降冰片烯加成聚合甲基铝氧烷对甲苯磺酸
α-芳香亚胺-2-乙基-6-乙酯基吡啶金属配合物及其烯烃聚合催化研究
2004年
  从国际材料市场的发展来看,结构材料是支撑国防、航空航天、信息产业、国家建设和人们生活的重要物质基础之一,其中聚烯烃树脂材料约占高分子材料产量的一半.后过渡金属(铁、钴、镍、钯等)配合物用于烯烃催化研究可追溯至上世纪七十年代,其研究结果发展成了SHOP催化体系[1],被广泛用于工业生产线性α-烯烃.然而,由于后过渡金属容易导致β-氢消除反应,影响了乙烯聚合催化的发展.……
孙文华唐秀波高铁龙苏碧云吴彪张文娟赵建设马宏伟陈久桐
SILICA-SUPPORTED NICKEL AND ZIRCONIUM CATALYSTS FOR BRANCHED POLYETHYLENE被引量:2
2003年
8-Aminoquinoline nickel dichloride and bis(cyclopentadienyl)zirconium dichloride (Cp_2ZrCl_2) were supportedsimultaneously on silica to produce branched polyethylene successfully by combined polymerization. The supportedpolymerization results showed that the molecular weight of polyethylene increased while the molecular weight distributionbecame wider and the molecular chains of oligomers remaning in the final solution became shorter as compared to theoligomers obtained in polymerization processes with pure 8-aminoquinoline nickel dichloride catalysis, as well as theCp_2ZrCl_2 and nickel combination system. With decreasing amount of Ni catalyst in the supported catalyst, the molecular chains of oligomers in the resulting solution became shorter, while α-olefin selectivity increased.
孙文华
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