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多聚配合物法制备三氧化钨电致变色膜 被引量:14
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作者 张明春 王海红 +2 位作者 杨书廷 赵林治 丁立 《功能材料》 EI CAS CSCD 1995年第2期147-150,共4页
本文采用多聚配合物法制备三氧化钨电致变色膜。浸涂液是在离子交换后的钨酸溶液中加入双氧水。在不同的温度处理下可得到非晶态和晶态氧化钨电致变色膜,对制得的膜进行了光学及电化学测定。并对材料热处理过程进行了红外分析、热重-... 本文采用多聚配合物法制备三氧化钨电致变色膜。浸涂液是在离子交换后的钨酸溶液中加入双氧水。在不同的温度处理下可得到非晶态和晶态氧化钨电致变色膜,对制得的膜进行了光学及电化学测定。并对材料热处理过程进行了红外分析、热重-差热分析、x射线衍射分析及扫描电镜形貌观察。实验表明,用该法制得的氧化钨膜其电致变色特性可与其它方法制备的膜相媲美。 展开更多
关键词 多聚配合物 三氧化钨 电致变色膜
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多聚配合物[Cd(β-ala)Cl_2]的合成与晶体结构
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作者 余小岚 童叶翔 +1 位作者 陈小明 麦松威 《中山大学学报(自然科学版)》 CAS CSCD 北大核心 1997年第3期114-116,共3页
多聚配合物[Cd(β-ala)Cl2]用CdCl2与β-丙氨酸(β-ala,H3N+CH2CH2CO2-)在水溶液反应制得,并用单晶结构分析法测定其结构.该配合物的化学式为C3H7CdCl2NO2,属正交晶系,空间群... 多聚配合物[Cd(β-ala)Cl2]用CdCl2与β-丙氨酸(β-ala,H3N+CH2CH2CO2-)在水溶液反应制得,并用单晶结构分析法测定其结构.该配合物的化学式为C3H7CdCl2NO2,属正交晶系,空间群为Pnma(No.62),a=694.4(1),b=796.3(2),c=1293.1(3)pm,V=0.7150(6)nm3,Z=4,Mr=272.40,Dc=2.530Mg/m3,用834独立衍射数据对结构进行精化,最后残差因子R1=0.0421.结果表明,每个镉离子与4个Cl和2个β-ala的羧基氧原子配位,呈变形八面体结构.每对镉离子由2个Cl和1个双齿羧基桥连。 展开更多
关键词 晶体结构 多聚配合物 聚羧基镉配合 合成
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间苯二甲酸阴离子桥链锌多聚配合物的合成与表征(英文)
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作者 王舜 胡茂林 +3 位作者 林德峰 刘妙昌 林铃春 黄珠连 《合成化学》 CAS CSCD 2001年第1期9-11,33,共4页
合成了一种以间苯二甲酸阴离子桥链锌的多聚配合物 ,通过元素分析、IR,UV和差热分析确定其可能结构为一维链状、三维网状的空间结构 ,并推测其分子式为 [Zn( m- C8H4 O4 ) 2 /2 H2 O]n。
关键词 间苯二甲酸阴离子 多聚配合物 桥连配体 合成 表征
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邻苯二甲酸根桥联铜多聚配合物的谱学性质与成键状况
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作者 陈琳 田俐 《湘潭师范学院学报(自然科学版)》 2003年第2期59-61,共3页
对邻苯二甲酸根桥联铜多聚配合物{[Cu(phth)(phen)(H_2O)」·H_2O}(Phth表示邻苯二甲酸根二阶阴离子;phen表示1,10-邻菲咯啉)进行了红外光谱和紫外可见光谱研究,探讨了配位中心铜(Ⅱ)离子的成键状况。结果表明,铜与配位原子N、O形... 对邻苯二甲酸根桥联铜多聚配合物{[Cu(phth)(phen)(H_2O)」·H_2O}(Phth表示邻苯二甲酸根二阶阴离子;phen表示1,10-邻菲咯啉)进行了红外光谱和紫外可见光谱研究,探讨了配位中心铜(Ⅱ)离子的成键状况。结果表明,铜与配位原子N、O形成一个畸变的四方锥结构。 展开更多
关键词 邻苯二甲酸根桥联铜多聚配合物 谱学性质 红外光谱 紫外可见光谱 成键状况 配位结构
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草酸根桥联一维多聚铜配合物的合成及晶体结构(英文)
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作者 张桂玲 李延团 +1 位作者 罗绪强 吴智勇 《化学研究》 CAS 2008年第1期47-51,共5页
合成了草酸根(ox)桥联[Cu(tmen)]2+单元(tmen为N,N,N′,N′-四甲基乙二胺)的一维多聚铜配合物.X-ray单晶衍射表明,该配合物由Cu(Ⅱ)和四个ox氧原子、tmen的两个氮原子配位形成畸变的八面体构型.Cu…Cu间距为0.560 95(34)nm和0.565 94(40... 合成了草酸根(ox)桥联[Cu(tmen)]2+单元(tmen为N,N,N′,N′-四甲基乙二胺)的一维多聚铜配合物.X-ray单晶衍射表明,该配合物由Cu(Ⅱ)和四个ox氧原子、tmen的两个氮原子配位形成畸变的八面体构型.Cu…Cu间距为0.560 95(34)nm和0.565 94(40)nm.水分子和草酸根间氢键可以使该配合物形成三维超分子结构. 展开更多
关键词 多聚配合 N N N’ N’-四甲基乙二胺 晶体结构 草酸根桥联
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[Cu(C_(12)H_8N_2)(H_2O)(C_4H_4O_4)]·2H_2O的合成和晶体结构 被引量:16
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作者 郑岳青 孙杰 林建利 《化学学报》 SCIE CAS CSCD 北大核心 2000年第9期1131-1135,共5页
将适量邻菲啰啉、丁二酸和CuCl_2·2H_2O(摩尔比=1:1:1)溶于水和甲醇的混合溶剂[V(水):V(甲醇)=1:1]后,滴加NaOH溶液至pH=4.8.滤去沉淀物后,滤液于室温下缓慢蒸发得蓝色细长[Cu(phen)(H_2O)(C_4H_4O_4)]·2H_2O晶体.晶体属三斜... 将适量邻菲啰啉、丁二酸和CuCl_2·2H_2O(摩尔比=1:1:1)溶于水和甲醇的混合溶剂[V(水):V(甲醇)=1:1]后,滴加NaOH溶液至pH=4.8.滤去沉淀物后,滤液于室温下缓慢蒸发得蓝色细长[Cu(phen)(H_2O)(C_4H_4O_4)]·2H_2O晶体.晶体属三斜晶系,P1(No.2)空间群.晶胞参数a=0.7462(1)nm,b=0.9959(1)nm,c=1.2266(1)nm,α=75.02(1)°,β=82.38(1)°,γ=74.76(1)°,V=0.8475(2)nm^3,Z=2,D_c=1.622g/cm^3,F(000)=426,3882个独立衍射点中,2789个可观测点满足F_0~2≥2σ(F_0~2),R=0.0450,wR^2=0.0951.配合物内每个Cu与邻菲啰啉螯合配体中的2个N原子、来自不同羧酸根的2个羧基O和1个水分子O原子配位,形成扭曲的四方锥体,其中一羧基O位于锥顶[d(Ci—N)=0.2006(3)0 .2032(3)nm;赤道d(Cu—0)=0.1972(2),0.1973(2)nm;轴向d(Cu—O)=0.2210(2)nm].双齿桥联丁二酸根连接Cu原子形成平行于[100]方向的多聚超分子链_∞~1[Cu(phen)_2(H_2O)(C_4H_4O_4)_(2/2)].紧邻链分子上的邻菲啰啉配体互相穿插产生芳环堆积作用,并形成沿[100]方向无限延伸的超分子双链_∞~1[Cu(phen)_2(H_2O)·(C_4H_4O_4)_(2/2)]_2.芳环堆积间距交替为0.366nm和0.380nm.未配位的H_2O分子位于超分子双链之间. 展开更多
关键词 配合 合成 晶体结构 多聚超分子配合
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A Pd-metalated porous organic polymer as a highly efficient heterogeneous catalyst for C–C couplings 被引量:3
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作者 戴志锋 陈芳 +4 位作者 孙琦 纪妍妍 王亮 孟祥举 肖丰收 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2016年第1期54-60,共7页
An efficient catalyst system based on a Pd-metalated porous organic polymer bearing phenanthroline ligands was designed and synthesized.This catalyst was applied to various C–C bond-forming reactions,including the Su... An efficient catalyst system based on a Pd-metalated porous organic polymer bearing phenanthroline ligands was designed and synthesized.This catalyst was applied to various C–C bond-forming reactions,including the Suzuki,Heck and Sonogashira couplings,and afforded the corresponding products while exhibiting excellent activities and selectivities.More importantly,this catalyst can be readily recycled.These features show that such catalysts have significant potential applications in the future. 展开更多
关键词 Porous organic polymer Phenanthroline ligand Carbon–carbon couplings Pd-based heterogeneous catalyst
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Porous coordination polymers based on three planar rigid ligands 被引量:12
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作者 ZHONG DiChang LU TongBu 《Science China Chemistry》 SCIE EI CAS 2011年第9期1395-1406,共12页
During the last two decades,porous coordination polymers(PCPs),usually called as metal-organic frameworks(MOFs),have been developed rapidly due to their versatile structural diversities and potential physical and chem... During the last two decades,porous coordination polymers(PCPs),usually called as metal-organic frameworks(MOFs),have been developed rapidly due to their versatile structural diversities and potential physical and chemical functions.This article provides a short review of recent advances in the design and constructions of porous coordination polymers based on three planar rigid ligands,including imidazole-4,5-dicarboxlate(H3IDC),1H-tetrazole(HTz),as well as 1H-tetrazole-5-carboxylate(H2Tzc).Their preparations,crystal structures,and desirable properties have been reviewed. 展开更多
关键词 porous coordination polymers metal-organic frameworks planar rigid ligands imidazole-4 5-dicarboxlate 1H-tetrazole 1H-tetrazole-5-carboxylate
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Polymer solar cells with an inverted device configuration using polyhedral oligomeric silsesquioxane-[60]fullerene dyad as a novel electron acceptor 被引量:3
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作者 ZHANG Wen-Bin TU YingFeng +3 位作者 SUN Hao-Jan YUE Kan GONG Xiong CHENG Stephen Z. D. 《Science China Chemistry》 SCIE EI CAS 2012年第5期749-754,共6页
A polyhedral oligomeric silsesquioxane-[60]fullerene (POSS-C60) dyad was designed and used as a novel electron acceptor for bulk heterojunction (BHJ) polymer solar cells (PSCs) with an inverted device configuration. T... A polyhedral oligomeric silsesquioxane-[60]fullerene (POSS-C60) dyad was designed and used as a novel electron acceptor for bulk heterojunction (BHJ) polymer solar cells (PSCs) with an inverted device configuration. The studies of time-resolved photoinduced absorption of the pristine thin film of poly[(4,4'-bis(2-ethylhexyl)dithieno[3,2-b:2',3'-d]silole)-2,6-diyl-alt-(4,7-bis (2-thienyl)-2,1,3-benzothiadiazole)-5,5'-diyl] (SiPCPDTBT) and the composite thin film of SiPCPDTBT:POSS-C60 indicated efficient electron transfer from SiPCPDTBT to POSS-C60 with inhibited back-transfer. BHJ PSCs made by SiPCPDTBT mixed with POSS-C60 yielded the power conversion efficiencies (PCEs) of 1.50%. Under the same operational conditions, PCEs observed from BHJ PSCs made by SiPCPDTBT mixed with [6,6]-phenyl-C61-butyric acid methyl ester were 0.92%. These results demonstrated that POSS-C60 is a potentially good electron acceptor for inverted BHJ PSCs. 展开更多
关键词 electron acceptor polyhedral oligomeric silsesquioxane FULLERENE polymer solar cells inverted device structure
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Recent advance in porous coordination polymers from the viewpoint of crystalline-state transformation 被引量:8
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作者 YIN Zheng ZENG MingHua 《Science China Chemistry》 SCIE EI CAS 2011年第9期1371-1394,共24页
Recently,research of crystalline-state transformation involving the removal/inclusion of guest molecules in porous coordination polymers(PCPs) was underway.Crystalline-state transformation,especially,single-crystal to... Recently,research of crystalline-state transformation involving the removal/inclusion of guest molecules in porous coordination polymers(PCPs) was underway.Crystalline-state transformation,especially,single-crystal to single-crystal(SC-SC) transformation as new method for the direct observation of host-guest chemistry,can reveal the intrinsic relevance and interaction between the framework and guest molecules.This review describes our work concerning PCPs and recent investigations of others,within the last four years,from the viewpoint of crystalline-state transformations of PCPs on guest removal or inclusion processes.Ligand substitution reaction and postsynthetic modification of PCPs in SC-SC fashion which were distinguished from conventional crystalline-state transformation triggered by guest removal or exchange were highlighted in this review.The research status of crystalline-state transformation in China was briefly introduced as well.Series of structure analysis techniques including single-crystal X-ray diffraction,powder X-ray diffraction,neutron diffraction,inelastic neutron scattering as well as the application of synchrotron radiation light source will inevitably promote the advance of study of crystalline-state transformation.And as a hotspot,deep investigations of crystalline-state transformation also help us to overcome the challenge of achieving multifunction and the correlation among them,such as sorption,magnetism,optical or electrical properties simultaneously in PCPs and contribute to design stimulate-oriented porous intelligent materials in the future. 展开更多
关键词 porous coordination polymer crystalline-state transformation ligand substitution reaction postsynthetic modification structure analysis techniques
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