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951.
Yun‐Yu Liu Guang‐Shan Zhu Guo‐Zhen Fan Shi‐Lun Qiu 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(4):m159-m160
In the title compound, poly[μ5‐pyrazine‐2,3‐dicarboxylato‐cadmium(II)], [Cd(C6H2N2O4)]n or [Cd(pdc)]n, where pdc is the pyrazine‐2,3‐dicarboxylate anion, the CdII atom is six‐coordinated by five carboxylate O atoms and one N atom from five different pdc ligands in a distorted octahedral CdO5N coordination geometry. Two CdII atoms are bridged by carboxylate groups of the pdc ligands to create a dimeric unit. The dimeric units are further connected by the pdc ligands to generate an interesting two‐dimensional structure. 相似文献
952.
Denifl S Ptasińska S Sonnweber B Scheier P Liu D Hagelberg F Mack J Scott LT Märk TD 《The Journal of chemical physics》2005,123(10):104308
Electron attachment to the polyaromatic hydrocarbons coronene and corannulene is studied in the electron energy range of about 0-14 eV using a high-resolution crossed electron-neutral beam setup. The major anions observed are the parent anions peaking at about 0 eV with cross sections of 3.8 x 10(-20) and 1 x 10(-19) m(2), respectively. The only fragment anions formed in coronene and corannulene are the dehydrogenated coronene and corannulene anions. Other anions observed in the negative mass spectra at about 0 eV can be ascribed to impurities of the sample. High-level quantum-mechanical studies are carried out for the determination of electron affinities, hydrogen binding energies, and structures of both molecules. The behavior of coronene and corannulene upon electron attachment is compared with that of other polyaromatic hydrocarbons studied previously. 相似文献
953.
Xiongyu Wu Xiaohong Liu Guangce Jiang Yongcheng Lin Willy Chan L. L. P. Vrijmoed 《Chemistry of Natural Compounds》2005,41(1):27-29
A novel metabolite 1, named xyloketal G, was isolated from cultures of marine derived mangrove fungus Xylaria sp. 2508. Its structure was elucidated by analysis of spectroscopic data.__________Published in Khimiya Prirodnykh Soedinenii, No. 1, pp. 22–23, January–February, 2005. 相似文献
954.
This paper reports the first example of diruthenium phosphonate with kagomé structure, namely, [NH3(CH2)4NH3][Ru2(hedpH(0.5))2].2H2O (hedp = 1-hydroxyethylidenediphosphonate). The compound contains kagomé layers that are linked by very strong hydrogen bonds into a nanoscale kagomé structure. Ferromagnetic interactions are mediated between the paramagnetic diruthenium units. 相似文献
955.
Chabinyc ML Salleo A Wu Y Liu P Ong BS Heeney M McCulloch I 《Journal of the American Chemical Society》2004,126(43):13928-13929
A method for the fabrication of polymeric thin-film transistors (TFTs) by lamination is described. Poly(dimethylsiloxane) stamps were used to delaminate thin films of semiconducting polymers from silicon wafers coated with a self-assembled monolayer (SAM) formed from octyltrichlorosilane. These supported films were laminated onto electrode structures to form coplanar TFTs. The fabrication process was used to make TFTs with poly(3-hexylthiophene), P3HT, and poly[5,5'-bis(3-dodecyl-2-thienyl)-2,2'-bithiophene], PQT-12. TFTs, where these polymers were laminated onto gate dielectrics coated with SAMs from octyltrichlorosilane, had effective field-effect mobilities of 0.03 and 0.005 cm2/(V s), respectively. TFTs where PQT-12 was laminated onto gate dielectrics that were not coated with a SAM also had mobility of 0.03 cm2/(V s). In contrast, TFTs fabricated by spin-coating PQT-12 onto the same structure had mobilities ranging from 10-3 to 10-4 cm2/(V s). These results suggest that the lower mobilities of polymer TFTs made with hydrophilic gate dielectrics are caused by molecular ordering in the semiconducting film rather than electronic effects of dipolar groups at the interface. 相似文献
956.
流动注射—化学发光法测定苯甲醛 总被引:1,自引:0,他引:1
依据苯甲醛增强没食子酸-过氧化氢-氢氧化钠体系化学发光的性质,建立了苯甲醛的流动注射化学发光分析法。 相似文献
957.
评进了当前中药徽量元素研究中的若干热点课题;1.微量元素与中药品种、产地的关系;2.微量元素与中药性味、归经,功效的关系;3.中药微量元素的存在状态;4.中药内有机成分与微量元素的相互关系;5.微量元素对中西药配伍的影响;6.微量元素的毒副作用.共引用文献29篇. 相似文献
958.
Xin‐Zhou Yang Li‐Gen Lin Chun‐Ping Tang Yong‐Qiang Liu Yang Ye 《Helvetica chimica acta》2007,90(2):318-325
Five new nonalkaloid constituents, a neolignan, japonin A ( 1 ), a macrocyclic lactone, japonin B ( 2 ), a (phenylethyl)benzoquinone, japonin C ( 3 ), a phenanthraquinone, japonin D ( 4 ), as well as a dihydrostilbene, stilbostemin M ( 5 ), were isolated from the roots of Stemona japonica, together with eight known compounds. Their structures were established by spectroscopic analyses. 相似文献
959.
Chen Luo Chenggang Zhou Jinping Wu T. J. Dhilip Kumar Naduvalath Balakrishnan Robert C. Forrey Hansong Cheng 《International journal of quantum chemistry》2007,107(7):1632-1641
Structures and physical properties of small palladium clusters Pdn up to n = 15 and several selected larger clusters were studied using density functional theory under the generalized gradient approximation. It was found that small Pdn clusters begin to grow 3‐dimensionally at n = 4 and evolve into symmetric geometric configurations, such as icosahedral and fcc‐like, near n = 15. Several isomers with nearly degenerate average binding energies were found to coexist and the physical properties of these clusters were calculated. For several selected isomers, relatively moderate energy barriers for structural interchange for a given cluster size were found, implying that isomerization could readily occur under ambient conditions. © 2007 Wiley Periodicals, Inc. Int J Quantum Chem, 2007 相似文献
960.
Guang‐Fei Liu Lin‐Lin Li Yong Zhang Jian‐Ping Lang Seik Weng Ng 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(1):m1-m3
The title compound, [Cu(ClO4)2(C4H9N3O2)2][Cu(C4H9N3O2)2(CH4O)2](ClO4)2·2CH3OH, comprises two independent CuII species lying on different inversion sites. In the Cu complexes, a distorted octahedral geometry arises (from basic square‐planar N4 coordination) from the weak coordination of two perchlorate ions (as Cu—O) in one species and two methanol molecules in the other (also as Cu—O). Interactions between the O atoms of the perchlorate anions or methanol groups and the imide or amine NH groups afford an extensive intermolecular hydrogen‐bonding network. 相似文献