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多酸超分子化合物的合成及液晶性质 被引量:38
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作者 毕丽华 黄如丹 +2 位作者 王恩波 李阳光 刘景华 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 1999年第9期1352-1353,共2页
A new heteropoly supermolecular compound was synthesized and characterized by elemental analysis, IR and TG-DSC. Six vibrational bands of organic groups were observed in IR spectra and the characteristic bands of hete... A new heteropoly supermolecular compound was synthesized and characterized by elemental analysis, IR and TG-DSC. Six vibrational bands of organic groups were observed in IR spectra and the characteristic bands of heteropoly anion are shifted to a higher frequency as the result of electronic delocalization in the heteropoly anion. The liquid crystal behavior of heteropoly supermolecular compound in organic solvent was firstly studied. When the observation was carried out under the polarimicroscope, the liquid crystal was showed as the smectic phase, which is characterized by heterothermal as well as wide angle XRD. 展开更多
关键词 超分子 合成 溶致溶晶 液晶性质 多酸 杂多酸
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自组装超分子膜修饰电极的研制及分析应用 被引量:5
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作者 杜丹 王升富 《化学研究与应用》 CAS CSCD 北大核心 2001年第6期617-622,共6页
阐述了自组装超分子膜修饰电极的发展概况及超分子体系形成的理论基础 ,并对自组装超分子膜修饰电极的特点、电化学行为、功能膜的制备和表征方法以及它在电催化、生物传感器、离子选择性电极等方面的应用进行了综述。参考文献
关键词 自组装膜 超分子 膜修饰电极 制备 电分析化学
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适用于页岩气井压裂的超分子增黏滑溜水 被引量:8
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作者 钱斌 张照阳 +1 位作者 尹丛彬 何启平 《天然气工业》 EI CAS CSCD 北大核心 2021年第11期97-103,共7页
针对页岩气井压裂施工排量大、液量大的特点,为了实现压裂液稠化剂在不同水质条件下速溶、高效降阻,可以有效利用河水或邻井返排液直接配液,从而达到扩大适用水源、降低水资源消耗以及降低返排液处理成本的目的。为此,以丙烯酰胺等单体... 针对页岩气井压裂施工排量大、液量大的特点,为了实现压裂液稠化剂在不同水质条件下速溶、高效降阻,可以有效利用河水或邻井返排液直接配液,从而达到扩大适用水源、降低水资源消耗以及降低返排液处理成本的目的。为此,以丙烯酰胺等单体为主要原料,研发了一种超分子滑溜水稠化剂——YS-1,对其性能进行了评价,并成功应用于现场施工。应用效果表明:①YS-1可以在不同的水质中速溶,并且具有良好的携砂性和耐盐性;②当浓度超过0.15%时,YS-1的黏度大幅度增加,可通过浓度的变化实现低黏滑溜水、中黏线性胶和高黏交联液的转变;③在常温与100℃条件下,经过2~3个40 s^(-1)与500 s^(-1)的变剪切循环周期后,YS-1溶液的黏度一直保持稳定,表现出了良好的抗剪切性;④0.05%~0.12%YS-1溶液的降阻率可超过70%,并且在10×10^(4)mg/L矿化度的盐水溶液中仍然能保持良好的降阻性能。结论认为,超分子变黏滑溜水YS-1可以在清水、现场返排液的水质条件下能够快速溶解,拥有良好的溶解性,利用邻井返排液配液后进行现场压裂,施工压力平稳,既节省了水资源,又节省了配液时间,大幅度提高了施工效率,具有较好的推广应用价值。 展开更多
关键词 超分子 滑溜水 增黏 重复利用 页岩气 压裂(岩石) 降阻 抗剪切性
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DBS类凝胶因子的合成及性能 被引量:4
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作者 邓鹏飞 冯亚青 +1 位作者 薛福华 宋健 《精细化工》 EI CAS CSCD 北大核心 2007年第11期1056-1060,共5页
以取代的苯甲醛和山梨醇为原料,环己烷为溶剂和夹带剂,甲醇为促进剂,对甲苯磺酸为催化剂,用共沸脱水法合成了1,3∶2,4-O-二苄叉-D-山梨醇(DBS),收率91.2%;1,3∶2,4-O-二(4-甲基苄叉)-D-山梨醇(MDBS),收率90.5%;1,3∶2,4-O-二(3,4-二甲... 以取代的苯甲醛和山梨醇为原料,环己烷为溶剂和夹带剂,甲醇为促进剂,对甲苯磺酸为催化剂,用共沸脱水法合成了1,3∶2,4-O-二苄叉-D-山梨醇(DBS),收率91.2%;1,3∶2,4-O-二(4-甲基苄叉)-D-山梨醇(MDBS),收率90.5%;1,3∶2,4-O-二(3,4-二甲基苄叉)-D-山梨醇(DMDBS),收率89.0%。用原甲酸三甲酯作化学脱水剂,合成了1,3∶2,4-O-二(2,4,6-三甲基苄叉)-D-山梨醇(2,4,6-TMDBS),收率37.1%;1,3∶2,4-O-二(2,4,5-三甲基苄叉)-D-山梨醇(2,4,5-TMDBS),收率30.9%;1,3∶2,4-O-二(5,6,7,8-四氢萘-2-亚甲叉)-D-山梨醇(DTHNS),收率74.1%。其结构经1HNMR确认。测定了它们对21种有机溶剂的凝胶性能。发现苯环上取代基的位置、数量、大小等因素对凝胶性能有重要影响。2,4,6-TMDBS无凝胶性能,其余化合物对多种溶剂具有良好的凝胶性能,DTHNS对非极性化合物有极优良的凝胶性能。测试并比较了上述化合物的最低凝胶浓度,证实了凝胶-溶胶解缔温度随凝胶因子质量分数增加而增加;随着溶剂(一元直链伯醇)碳原子数的增加而增加。 展开更多
关键词 超分子 山梨醇 缩醛 凝胶因子 功能材料
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混合配体配合物镉(Ⅱ)-邻菲罗啉-丙二酸根异构体的结构特征研究 被引量:4
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作者 孙亚光 魏德洲 +1 位作者 高恩君 丁茯 《化学学报》 SCIE CAS CSCD 北大核心 2004年第16期1569-1572,共4页
由硝酸镉、邻菲罗啉和丙二酸混合反应 ,得到无色透明单晶 .经X射线单晶衍射法测定了该晶体的分子结构 ,在 1个晶胞中存在两个混合配体配合物异构体 ,其组成为C2 7H18O4N4Cd .晶体学数据为 :三斜晶系 ,P 1空间群 .a =0 14 43 2 ( 5 )nm ... 由硝酸镉、邻菲罗啉和丙二酸混合反应 ,得到无色透明单晶 .经X射线单晶衍射法测定了该晶体的分子结构 ,在 1个晶胞中存在两个混合配体配合物异构体 ,其组成为C2 7H18O4N4Cd .晶体学数据为 :三斜晶系 ,P 1空间群 .a =0 14 43 2 ( 5 )nm ,b =0 15 5 17( 5 )nm ,c =0 160 98( 6)nm ,α =10 7 0 48( 6)° ,β =98 989( 6)° ,γ =116 481( 6)° ,Z =2 ,F( 0 0 0 ) =12 87,Dc=1 45 3g/cm3 ,μ =0 80 2mm-1,R1=0 0 64 5 ,wR2 =0 175 6.该异构体的差别在于丙二酸根中 2个羧基中各 1个氧原子配位 ( 1)或 1个羧基中 2个氧原子同时配位 ( 2 ) .1和 2之间靠氢键和π 展开更多
关键词 混合配体 镉配合物 邻菲罗啉 丙二酸 异构体 分子结构 超分子化合物
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长链烷基钴肟与β-环糊精超分子化合物的合成与性质研究 被引量:3
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作者 向平 罗来斌 +1 位作者 陈瑛 陈慧兰 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 1997年第11期1753-1755,共3页
Two supermolecular adducts involving p-cyclodextrin(β-CD) and long carbonchain alkyl (aqua) cobaltoximes (R= C6H13 and C8H17 ) have been synthesized for the firsttime and characterized by elementary analysis, UV-Vis ... Two supermolecular adducts involving p-cyclodextrin(β-CD) and long carbonchain alkyl (aqua) cobaltoximes (R= C6H13 and C8H17 ) have been synthesized for the firsttime and characterized by elementary analysis, UV-Vis and H NMR. We used the cyclicvoltammetry methods to characterize the electrochemical behaviour of the inclusion process.In addition, their formation constant Ka was quantitatively determined by using UV-Vismethods. It has been shown that the longer the carbon chain of the alkyl groups are, themore stable the inclusion complexes are. furthermore, by adding n-C8H17Co (DH)2H2O/β-CDto the aqueous solution, it has been found that the formation constant decreased. 展开更多
关键词 烷基钴肟 环糊精 超分子 分子识别
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水分子桥连的二维配位聚合物[(C_8H_(16)CoO_7)·2.5(H_2O)]_n的合成与晶体结构 被引量:3
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作者 秦小焕 桂柳成 +2 位作者 邹华红 胡坤 黄富平 《广西师范大学学报(自然科学版)》 CAS 北大核心 2014年第1期105-109,共5页
用溶剂热法,以1,4-环己烷二羧酸为配体合成一个新的配合物[(C8H16CoO7)·2.5(H2O)]n.Ⅹ-射线单晶衍射分析表明,晶体属单斜晶系,空间群为P21/c,晶胞参数a=0.981 0(2) nm,b=1.674 5(3) nm,c=0.808 20(16) nm,β=93.64(3)&... 用溶剂热法,以1,4-环己烷二羧酸为配体合成一个新的配合物[(C8H16CoO7)·2.5(H2O)]n.Ⅹ-射线单晶衍射分析表明,晶体属单斜晶系,空间群为P21/c,晶胞参数a=0.981 0(2) nm,b=1.674 5(3) nm,c=0.808 20(16) nm,β=93.64(3)°,V=1.324 9(4) nm3,Z=2.在配合物中,中心离子Co(Ⅱ)与6个氧原子形成六配位,其中2个氧原子分别来自2个羧酸,另外4个氧原子来自配位水(Co-O键长范围0.201 7(5)~0.224 1(4) nm,O-Co-O键角范围86.16(17)°~178.94(19)°),中心Co(Ⅱ)与6个配位氧原子形成畸变八面体配位构型,羧酸配体上两边的氧原子分别与Co(Ⅱ)形成单齿配位.金属钴之间通过羧酸桥连形成一维链,链与链之间通过水分子桥连形成二维结构,层与层之间通过氢键连接形成三维超分子结构. 展开更多
关键词 溶剂热法 配位聚合物 羧酸配体 合成 超分子结构
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新型钼磷酸超分子化合物的合成和性质
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作者 靳素荣 姚映钦 李刚 《华中科技大学学报(自然科学版)》 EI CAS CSCD 北大核心 2002年第5期105-107,共3页
首次合成了亚甲蓝的Keggin结构杂多酸超分子化合物 (MB) 3 [PMo12 O40 ]2 ·4H2 O和 (MB) 3 PMo11FeO40·5H2 O .用元素分析 ,IR ,Vis UV ,XRD和TG DTA等方法对标题化合物的结构和性质进行了研究 .结果显示 :杂多阴离子仍保持... 首次合成了亚甲蓝的Keggin结构杂多酸超分子化合物 (MB) 3 [PMo12 O40 ]2 ·4H2 O和 (MB) 3 PMo11FeO40·5H2 O .用元素分析 ,IR ,Vis UV ,XRD和TG DTA等方法对标题化合物的结构和性质进行了研究 .结果显示 :杂多阴离子仍保持完整的Keggin型结构 ,有机阳离子与杂多阴离子以静电引力作用形成超分子化合物 ,具有良好的光致变色性能 。 展开更多
关键词 杂多酸 超分子 光致变色
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SHG from centrosymmetric supermolecular crystal
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作者 郭文生 刘祁涛 +4 位作者 邵宗书 郭放 周广勇 魏春生 王东 《Science China Chemistry》 SCIE EI CAS 2002年第3期267-274,共8页
Supermolecular crystal composed of p-nitrophenol, hexamethylenetetramine, phosphoric acid and water was obtained by supermolecular assembly. The crystal has a centrosymmetric structure with space group P21/c. The rela... Supermolecular crystal composed of p-nitrophenol, hexamethylenetetramine, phosphoric acid and water was obtained by supermolecular assembly. The crystal has a centrosymmetric structure with space group P21/c. The relative intensity and integral value of green frequency doubling of light from the crystal powder compared with that from KDP powder measured by pico-second Nd:YAG laser are 757.3 (KDP: 183.4) and 1771.7 (KDP: 423.98), respectively. In supermolecular crystal, due to the arrangement of centrosymmetric p-nitrophenol molecules in the inorganic-organic host framework formed by hexamethylenetetramine, phosphoric acid and water, the distances between the p-nitrophenol molecules with centrosymmetry are changed (N1A-O1A: 0.8158 nm, N1B’-O1B: 1.4450 nm, N1A-N1A’: 0.5837 nm, N1B’-N1B: 0.6898 nm), and the interaction between the dipoles becomes weak, which is easy for the ground state to turn into the excited state charge separated form, and generate the stable asymmetrical distribution of π-electron cloud density of quinonal structure, thus exhibiting SHG effect. 展开更多
关键词 supermolecular CRYSTAL SHG EFFECT centrosymmetry p-nitrophenol.
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Entanglement in the supermolecular dimer [Mn4]2
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作者 许长谭 陈刚 +1 位作者 贺明明 梁九卿 《Chinese Physics B》 SCIE EI CAS CSCD 2006年第12期2828-2834,共7页
This paper investigates the entanglement in the supermolecular dimer [Mn4]2 consisting of a pair of single molecular magnets with antiferromagnetic exchange-coupllng J. The conventional yon Neumann entropy as a functi... This paper investigates the entanglement in the supermolecular dimer [Mn4]2 consisting of a pair of single molecular magnets with antiferromagnetic exchange-coupllng J. The conventional yon Neumann entropy as a function of the exchange-coupling is calculated explicitly for all eigenstates with the quantum number range from M = M1 + M2 = -9 to 0. It is shown that the yon Neumann entropy is not a monotonic function of the coupling strength. However, it is significant that the entropy of entanglement has the maximum values and the minimum values for most eigenstates, which is extremely useful in the quantum computing. It also presents the time-evolution of entanglement from various initial states. The results are useful in the design of devices based on the entanglement of two molecular magnets. 展开更多
关键词 ENTANGLEMENT supermolecular dimer [Mn4]2 EXCHANGE-COUPLING time-evolution of entanglement
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A Review of Studies of Polymeric Membranes by Positron Annihilation Lifetime Spectroscopy
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作者 Htwe Htwe +3 位作者 Yin 阴泽杰 马卫涛 朱大鸣 《Plasma Science and Technology》 SCIE EI CAS CSCD 2005年第5期3062-3064,共3页
A review is presented of studies of polymeric membranes by applying positron annihilation lifetime spectroscopy (PALS). PALS has been used to study subnanometer-sized holes, to determine their size distribution and ... A review is presented of studies of polymeric membranes by applying positron annihilation lifetime spectroscopy (PALS). PALS has been used to study subnanometer-sized holes, to determine their size distribution and free-volume fractions, and to probe molecular-sized vacancies in glassy polymers. At present, PALS is believed to be a highly effective physical method for the examination of polymeric membranes. 展开更多
关键词 polymeric membrane applying positron annihilation lifetime spectroscopy(PALS) nuclear track DESALINATION PERMEABILITY reverse osmosis supermolecular struc-ture
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SYNTHESIS OF LADDERLIKE POLYHYDROXYPROPYLSILSESQUIOXANE
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作者 Huai-zhong Pan Chun-qing Liu +6 位作者 Zhong Jin Ming Cao Jian-hua Luo Ping Xie Rong-ben Zhang Yu-hui Lin Neal Tai-sheng Chung Center for Molecular Science, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China Institute of Materials Research and Engineering, Singapore 117602, Singapore 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2000年第5期453-457,共5页
Ladderlike polyhydroxypropylsilsesquioxane (HO-T) was synthesized by alcoholysis of ladderlike poly(3-propionyloxy-propyl)silsesquioxane. The HO-T was characterized by GPC, IR, NMR, DSC, TGA and X-ray diffraction meth... Ladderlike polyhydroxypropylsilsesquioxane (HO-T) was synthesized by alcoholysis of ladderlike poly(3-propionyloxy-propyl)silsesquioxane. The HO-T was characterized by GPC, IR, NMR, DSC, TGA and X-ray diffraction methods. Through hydrogen-bonding interaction, ladderlike polymer (HO-T) can form a supramolecular complex with somewhat regular structure. 展开更多
关键词 ladderlike polyhydroxypropylsilsesquioxane hydrogen-bond interaction supermolecular complex
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Studies of Ce(Ⅲ)-ALC-F Interacting with Herring Sperm DNA by Electrochemical, Fluorimetric and UV-spectrophotometric Method
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作者 GuangHanLU WeiLIU ChuanYinLIU LiPingJIANG FengSONG 《Chinese Chemical Letters》 SCIE CAS CSCD 2004年第4期443-446,共4页
Ce(Ⅲ)-ALC-F complex can react with hsDNA to form an electrochemically non-active supermolecular complex Ce(Ⅲ)-ALC-F-DNA in the buffer solution of (CH2)6N4(pH=4.9), which results in the decrease of the peak current o... Ce(Ⅲ)-ALC-F complex can react with hsDNA to form an electrochemically non-active supermolecular complex Ce(Ⅲ)-ALC-F-DNA in the buffer solution of (CH2)6N4(pH=4.9), which results in the decrease of the peak current of Ce(Ⅲ)-ALC-F. This method can be applied to determine DNA concentration. In addition, by using fluorimetric and UV-spectrophotometric methods with studies of denatured DNA and the effect of NaCl solution , it is also found that the binding mode is intercalation. 展开更多
关键词 Ce(Ⅲ)-ALC-F electrochemically non-active supermolecular complex herring sperm DNA(hsDNA) FLUORIMETRY UV-SPECTROPHOTOMETRY intercalation.
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RELATION BETWEEN STRUCTURE OF PP DRAWN FILAMENT AND TEXTURING EFFECT
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作者 仲蕾兰 戚慰先 +1 位作者 江建明 曹正燕 《Journal of China Textile University(English Edition)》 EI CAS 1991年第1期48-54,共7页
The relationship between the structure of PP drawn filament and the crimp elasticity of tex-tured yarn is investigated.It is found that orientation,crystallinity,and especially,crystalline formof drawn filament are re... The relationship between the structure of PP drawn filament and the crimp elasticity of tex-tured yarn is investigated.It is found that orientation,crystallinity,and especially,crystalline formof drawn filament are related to crimp property of textured yarn.Lower crystallinity,moderateorientation and unstable para-crystalline structure are necessary for increasing crimp elasticity.Inaddition,the filament structure and properties before and after texturing are compared. 展开更多
关键词 polypropylene FIBRE FIBRE STRUCTURE TEXTURED YARN orientation supermolecular STRUCTURE false twist TEXTURING CRYSTALLINITY crystalline form crimp elasticity
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Studies on the Structures and Properties of Latent-crimp Copolyester Fibers
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作者 顾书英 李光 顾利霞 《Journal of China Textile University(English Edition)》 EI CAS 1998年第2期1-4,共4页
The internal causes of latent-crimp were analyzed bystudying the supermolecular structures of the standardpolyester fibers(PET),copolyester fibers(IPET)andtheir side-by-side composite fibers(PET/IPET)inthis paper.It i... The internal causes of latent-crimp were analyzed bystudying the supermolecular structures of the standardpolyester fibers(PET),copolyester fibers(IPET)andtheir side-by-side composite fibers(PET/IPET)inthis paper.It is concluded that IPET and PET/IPEThave better latent-crimp ability because of their asym-metric supermolecular structures.At the same time,they have good dyeability and mechanical properties.Soit is a simple and low cost process to manufacture latent-crimp continuous fibers by melt-spinning of the co-polyester IPET. 展开更多
关键词 COPOLYESTER LATENT - CRIMP supermolecular structure.
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THE INFLUENCE OF DRAWING CONDITIONS OF PET POY ON STRUCTURE AND PROPERTY OF THE FIBER
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作者 穆淑华 《Journal of China Textile University(English Edition)》 EI CAS 1990年第3期33-40,共8页
Drawing tests upon PET POY have been made by using dynamic thermal stress analyser,which show that the dynamic thermal stress of fiber is readily affected by drawing conditions. Aseries of samples have been obtained u... Drawing tests upon PET POY have been made by using dynamic thermal stress analyser,which show that the dynamic thermal stress of fiber is readily affected by drawing conditions. Aseries of samples have been obtained under different drawing velocities, drawing temperatures anddraw ratios. The variations of structural factors of fiber such as the orientation, crystallinity,crystallite size and the thermal shrinkage have been measured. It is proved through experimentsthat the thermal shrinkage(Y) of the drawn fiber of PET POY is influenced by the orientation (rep-resented by sonic velocity x<sub>1</sub>) and crystallinity (x<sub>2</sub>) of the fiber. The quantitative relationship is es-tablished using the binary regression method: Y=10.2246+2.2030x<sub>1</sub>-26.2670x<sub>2</sub> The mechanical properties such as tenacity, elongation, yield stress, initial modulus and the te-nacity at 10% elongation, etc. have also been measured. The relations between the tenacity at 10%elongation (D) and drawing velocity(V), draw ratio (DR), drawing temperature (T), and sonic ve-locity and crystallinity have been obtained using a method of mathematical statistics: D=4.594-0.009 6V , D=-8.937+7.170DR, D=2.866+0.00629T, D=-7.34+2.866x<sub>1</sub>+6.314x<sub>2</sub> These equations fit well with data from the experiments. This work will be benefical to the control of quality of products and the development of newproducts. 展开更多
关键词 POLYESTER supermolecular structure DRAWING THERMAL SHRINKAGE dynamic THERMAL stress TENACITY at 10% ELONGATION
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STUDY ON POLYPYRROLE-VISCOSE CONDUCTING FIBER
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作者 江建明 张玉梅 李光 《Journal of China Textile University(English Edition)》 EI CAS 1996年第1期1-8,共8页
The conductivity of Polypyrrole-viscose conducting fiber prepared with author’s method can be shown up to as high as 2.106x10<sup>-2</sup> S/cm. The main factors influencing the conductivity are the conce... The conductivity of Polypyrrole-viscose conducting fiber prepared with author’s method can be shown up to as high as 2.106x10<sup>-2</sup> S/cm. The main factors influencing the conductivity are the concentration of FeCl<sub>3</sub> used as dopant and initiator, the treatment time of viscose fiber as base material in FeCl<sub>3</sub> solution, temperature and polymerization time. It is found that the orientation and crystallization degree of viscose fiber keep constant before and after conducting treatment and the mechanical properties of conducting fiber is the same as that of base material. In addition, the distribution of polypyrrole in viscose fiber, and its effect on the conductivity were investigated in details by TEM. 展开更多
关键词 VISCOSE CONDUCTING fiber mechanical properties supermolecular structures POLYPYRROLE CONDUCTIVITY BASE POLYMER
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Effective sugar-derived organic gelator for three different types of lubricant oils to improve tribological performance 被引量:2
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作者 Ruochong ZHANG Xuqing LIU +2 位作者 Zhiguang GUO Meirong CAI Lei SHI 《Friction》 SCIE CSCD 2020年第6期1025-1038,共14页
In this study,the gelling ability and lubrication performance of N-octadecyl-D-gluconamides(NOG)in liquid paraffin(LP),pentaerythritol oleate(PE-OA),and polyethylene glycol(PEG)oils were systemically investigated.The ... In this study,the gelling ability and lubrication performance of N-octadecyl-D-gluconamides(NOG)in liquid paraffin(LP),pentaerythritol oleate(PE-OA),and polyethylene glycol(PEG)oils were systemically investigated.The NOG,which could gelate the investigated oils,was successfully synthesized by a one-step method.The prepared gel lubricants were completely thermoreversible and exhibited improved thermal stability,according to the thermogravimetry analysis(TGA)reports.Rheological tests confirmed that the NOG gelator could effectively regulate the rheological behavior of the base oils.Tribological evaluation suggested that NOG,as an additive in the three types of base oils,could remarkably reduce the friction and wear in steel contacts.A plausible mechanism for the improved performances was proposed based on the mechanical strength of the gels and the formation of the boundary-lubricating film on the worn surface.The results indicated that NOG is a potential gelator for preparing gel lubricants with excellent tribological properties and environment-friendly characteristics. 展开更多
关键词 gel lubricant supermolecular assembly rheological property tribological performance lubricating mechanism
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两种钴离子支撑钼磷多金属氧酸盐的水热合成及晶体结构 被引量:2
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作者 张羽男 周百斌 +1 位作者 沙靖全 苏占华 《分子科学学报》 CAS CSCD 北大核心 2011年第1期7-13,共7页
利用水热技术合成了2个新型钴支撑的磷钼多金属氧酸盐超分子化合物:(C2N2H10)5[(P4Mo6O25(OH)6)2Co](1)和(Co(H2O)6)2(C5NH6)6[(P4Mo6O25(OH)6)2Co]·10H2O(2).并通过元素分析、红外光谱、热重分析和X射线单晶衍射对2个化合物进行... 利用水热技术合成了2个新型钴支撑的磷钼多金属氧酸盐超分子化合物:(C2N2H10)5[(P4Mo6O25(OH)6)2Co](1)和(Co(H2O)6)2(C5NH6)6[(P4Mo6O25(OH)6)2Co]·10H2O(2).并通过元素分析、红外光谱、热重分析和X射线单晶衍射对2个化合物进行了表征.结果表明:化合物1属于三斜晶系,P-1空间群;晶胞参数a=1.179 9(2)nm,b=1.337 7(2)nm,c=1.479 7(3)nm,α=73.435(2)°,β=74.383(2)°,γ=66.499(2)°,V=2.020 5(6)nm3,F(000)=1 327,Z=1;化合物2属于属于三斜晶系,P-1空间群;晶胞参数a=1.220 68(11)nm,b=1.381 08(13)nm,c=1.687 18(15)nm,α=92.275(1)°,β=104.774(1)°,γ=114.475(1)°,V=2.468 8(4)nm3,F(000)=1 649,Z=1. 展开更多
关键词 水热合成 超分子 晶体结构 多金属氧酸盐
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二维层状超分子配合物[VO(acac)_2(H_2O)]·(C_9H_(11)N_3OS)的合成、晶体结构及性质 被引量:2
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作者 刘芳 周荫庄 《首都师范大学学报(自然科学版)》 2011年第6期32-36,共5页
甲醇和水混合溶剂中,邻羟基苯乙酮缩氨基硫脲(L=C9H11N3OS)和乙酰丙酮氧钒VO(acac)2,在醋酸钠存在下反应,得到一种新颖的二维层状超分子配合物[VO(acac)2(H2O)].(C9H11 N3OS).通过红外光谱和X-射线单晶衍射对其进行结构表征.该晶体属三... 甲醇和水混合溶剂中,邻羟基苯乙酮缩氨基硫脲(L=C9H11N3OS)和乙酰丙酮氧钒VO(acac)2,在醋酸钠存在下反应,得到一种新颖的二维层状超分子配合物[VO(acac)2(H2O)].(C9H11 N3OS).通过红外光谱和X-射线单晶衍射对其进行结构表征.该晶体属三斜晶系,P1-空间群,晶胞参数为:a=0.780 87(9)nm,b=1.232 82(13)nm,c=1.337 4(2)nm,α=108.708(8)°,β=91.299(8)°,γ=107.652(6)°,V=1.151 7(3)nm3,Z=2,Dc=1.420 g.cm-3,μ=0.565 mm-1,F(000)=514,R1=0.051 6,ωR2=1.102 2.其中钒中心为六配位的近乎理想的八面体构型.通过氢键和π-π相互作用形成独特的二维层状超分子结构.同时研究了该配合物的荧光性质和热稳定性.CCDC:764394. 展开更多
关键词 钒(Ⅳ)配合物 缩氨基硫脲 超分子 晶体结构
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