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191.
A novel two-dimensional complex, [Cu(bbdc)(phen)]·(H2O)(bbdc = 2-bromo-1,4-benzenedicarboxylate dianion; phen = 1,10-phenanthroline), has been synthesized and structurally characterized by single crystal X-ray analysis. The crystal structure consists of infinite chains of [Cu2(
4-bbdc)]2+ units connected by bis-monodentate bbdc ligands, the coordination mode of which [
4-bbdc] is very rare in the phenyldicarboxylate complexes. The substituent group of bbdc is believed to be the growth key of this coordination network. 相似文献
192.
CCl2自由基与H2O分子反应动力学研究 总被引:2,自引:0,他引:2
用213 nm激光光解CCl4产生CCl2自由基,用LP LIF技术测定了室温下基态CCl2自由基与H2O分子的反应速率常数为(5.45±0.95)×10-14 cm3•molecule-1•s-1.在G2MP2理论水平上计算了CCl2+H2O反应的最低单重态势能面,揭示了插入与加成 消除两种反应机理,得到了三个可能的产物通道:HCl+HClCO、HCl+trans ClCOH以及HCl+cis ClCOH.并用RRKM TST和传统过渡态理论计算了这三个通道的分支比及其温度效应.结果说明在低温下(273 K),插入机理的产物通道的分支比远大于加成 消除机理的产物通道, HCl+HClCO是主要产物,分支比为77.4%,其次是HCl+cis ClCOH,分支比为22.6%.而在高温下(3000 K),加成 消除机理的反应通道大于插入机理, HCl+trans ClCOH分支比为82.3%. 相似文献
193.
194.
Photocatalytic oxidation of water is a promising method to realize large-scale H2O2 production without a hazardous and energy-intensive process. In this study, we introduce a Pt/TiO2(anatase) photocatalyst to construct a simple and environmentally friendly system to achieve simultaneous H2 and H2O2 production. Both H2 and H2O2 are high-value chemicals, and their separation is automatic. Even without the assistance of a sacrificial agent, the system can reach an efficiency of 7410 and 5096 μmol g–1 h–1 (first 1 h) for H2 and H2O2, respectively, which is much higher than that of a commercial Pt/TiO2(anatase) system that has a similar morphology. This exceptional activity is attributed to the more favorable two-electron oxidation of water to H2O2, compared with the four-electron oxidation of water to O2. 相似文献
195.
196.
Qintong Huang Ningyue Chen Lichen Liu Karen S. Arias Sara Iborra Xianfeng Yi Chao Ma Weichi Liang Anmin Zheng Chuanqi Zhang Jibo Hu Zilin Cai Yi Liu Jiuxing Jiang Avelino Corma 《Chemical science》2020,11(44):12221
Aluminosilicate boggsite (Si/Al-BOG) has been hydrothermally synthesized without adding organic structure-directing agents (OSDAs) in the synthesis gel using the borosilicogermanium ITQ-47 (Si/B-ITQ-47) zeolite as seeds. The introduction of the costly and environmentally less benign phosphazene organic structure-directing agent is not required to grow the zeolite. Physicochemical characterization experiments show that Si/Al-BOG has good crystallinity, high surface area, tetrahedral Al3+ species, and acid sites. In order to test the catalytic performance of the zeolite, the synthesis of l,l-lactide from l-lactic acid was performed. Si/Al-BOG exhibits 88.2% conversion of l-lactic acid and 83.8% l,l-lactide selectivity, which are better than those of other zeolites studied up to now.Aluminosilicate boggsite (Si/Al-BOG) has been hydrothermally synthesized without adding organic structure-directing agents (OSDAs) in the synthesis gel using the borosilicogermanium ITQ-47 (Si/B-ITQ-47) zeolite as seeds. 相似文献
197.
Mao Jiang-Gao Huang Jin-Shun Ma Jian-Fang Ni Jia-Zuan 《Transition Metal Chemistry》1997,22(3):277-280
The reaction of diglycolic acid, O(CH2CO2H)2, with Cu(NO3)2·2H2O and lanthanoid nitrate hydrate produces a series of novel Ln–Cu mixed metal complexes, [Ln2Cu3{O(CH2CO2)2}6]·nH2O (Ln=La, Nd, n=9; Ln=Er, n=6), which have been characterized by elemental analysis, i.r. spectroscopy, magnetic measurements and X-ray crystallography. The Ln3+ and Cu2+ ions are connected by the carboxylate groups of the ligands, resulting in the formation of a complicated network. 相似文献
198.
Wen Ma Yu-Peng Tian Sheng-Yi Zhang Jie-Ying Wu Hoong-Kun Fun Suchada Chantrapromma 《Transition Metal Chemistry》2006,31(1):97-102
A new diferrocenyl-substituted macrocyclic ligand (H2L) and its complexes ML(M = CuII, NiII, ZnII, CdII) were prepared and characterized by IR, elemental analysis, absorption spectra and FAB mass spectra. The ferrocenyl-substituted
macrocyclic ligand was characterized by single crystal X-ray diffraction analysis. The superconjugative effect of the cyclopentadienyl
(CP) rings increase the activity of the hydrogen atoms in the tetra-azacyclotetradecane macrocyclic ligand. The imine nitrogen
atoms lose two protons and coordinate to the metal. The electrochemical properties of these compounds are discussed. 相似文献
199.
Yan Ouyang Wei Zhang Yue Ma Na Xu Dai-Zheng Liao Kazuyoshi Yoshimura Shi-Ping Yan 《Structural chemistry》2007,18(6):891-898
Two new tetranuclear complexes of macrocyclic oxamide [Cd(CuL)3](NO3)2·2.5H2O 1, [Mn(CuL)3(OH)2](ClO4)2·Mn(H2O)6·4.5H2O 2 (L = 1,4,8,11-tatraazacyclotradecanne-2,3-dione) have been synthesized, structurally characterized and preliminary investigated
by magnetic studies. The structures of the title complexes consist of a tetranuclear units MCu3 (M = Cd, Mn), the packing diagram shows two-dimensional and three-dimensional system through intermolecular weak interactions.
The temperature-dependent magnetic susceptibilities of complex 2 were analyzed by an approximate treatment leading to J = −33 cm−1, gCu = 2.10, gMn = 1.95 indicating antiferromagnetic exchange between Cu(II) and Mn(II) ions. 相似文献
200.
Summary A method is described for the determination of alkaloids in morning glory leaves by means of spectrophotofluorimetry. The total alkaloidal contents found in different batches of leaves ranged from 0.027 to 0.04%.
For part XIV see Mikrochim. Acta [Wien]1976 I, 227. 相似文献
Zusammenfassung Ein Verfahren zur Bestimmung der Gesamtalkaloide in den Blättern vonIpomoea violacea wurde angegeben. Spektralfluoreszenzmessungen ergaben für verschiedene Chargen solcher Blätter Gehalte von 0,027 bis 0,04%.
For part XIV see Mikrochim. Acta [Wien]1976 I, 227. 相似文献