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V. Balamurugan Jhumpa Mukherjee Maninder Singh Hundal Rabindranath Mukherjee 《Structural chemistry》2007,18(2):133-144
New MnII/CuII/ZnII complexes [(L1)MnCl2] (1), [(L2)CuCl2]·0.5H2O (2) and [(L2)ZnCl(H2O)][ClO4] (3), containing (2-pyridyl)alkylamine ligands, N-methyl-N,N-bis(2-pyridylmethyl)amine (L1) and methyl[2-(2-pyridyl)ethyl](2-pyridylmethyl)amine (L2), have been prepared and characterized, including X-ray crystallography. The most striking feature of the structures of these
complexes is the formation of molecular ladder and lamellar topology through the crystal packing arrangement, determined by
both strong O–H···Cl and weak (however, multiple) C–H···Cl hydrogen-bonding interactions, to maintain the neutral/cationic
metal-ligand coordination units linked to each other. In 3, additional secondary interactions are observed involving coordinated solvent and the counter-ion. The results presented
here demonstrate that (i) the choice of organic ligands to provide flexibility and inherent potential to participate in hydrogen-bonding
interactions, (ii) the coordination geometry preferences of metal ions, (iii) the number of metal-bound chloride ion and (iv)
the presence of solvent/counter-anion have a great influence on supramolecular network topology. 相似文献
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S. Trippett 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1):89-98
Abstract In order to dicuss mechanism in organophosphorus chemistry a number of assumptions have to be made. Among them are: (a) that substitutions at tetrahedral phosphorus proceed via five-coordinate intermediates; (b) these intermediates are trigonal bipyramidal; (c) they are formed by apical attack and decompose by apical loss; and (d) if sufficiently long-lived, they may undergo permutational isomerization, that is the ligands may alter their relative dispositions round the phosphorus, before going on to products or back to reactants. Assuming that the course of a given substitution is dictated primarily by thermodynamic considerations, in order to understand the course of that substitution one needs to know how to assess the relative stabilities of the four isomeric tbps (trigonal bipyramids) that can be formed initially and of the others that could be formed by subsequent isomerization, the barriers to those isomerizations, and the relative rates of the various product-forming steps. We have concentrated on the first of these factors and this lecture describes our attempts to provide the necessary data. The energy difference between two isomeric tbps can be analyzed in terms of changes in the relative apicophilicities1 of the groups occupying apical positions, changes in ring-strain as small rings move between apical-equatorial and diequatorial positions, and changes in steric strain. I shall consider each of these in turn. Ligand subset symmetry may also have to be taken into account.1,2 相似文献
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Shun-Yang Yu Yan-Cang Li Tao Xiong Qun Yuan Yong-Ming Liu Zhong-Yi Yuan Yi Xiao 《中国化学快报》2014,25(2):364-366
In recent years, there has been a pronounced interest in solid-contact ion-selective electrodes (SC-ISEs), with emphasis on the use of conducting polymers as ion-to-electron transducer. In this work, a ladder conjugated polymer, thieno[3,2-b]thiophene (LCPT), was investigated in fabricating Cu2+-selective electrodes for the first time. The resulting electrodes were characterized by electrochemical impedance spectroscopy (EIS), chronopotentiometry, and the water layer test. Results proved that the active LCPT facilitates the ion-to-electron transduction, and avoids the detrimental aqueous layer formed at the interface of SC-ISEs. 相似文献
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You Zhi WAN Ying Hua LIU Ping XIE Rong Ben ZHANG* Department of Applied Chemistry School of Science Beijing University of Chemical Technology Beijing State Key Laboratory of Polymer Physics Chemistry Joint Laboratory of Polymer Science Materials Institute of Chemistry Chinese Academy of Sciences Beijing 《中国化学快报》2006,17(10):1361-1364
Ladder polysiloxanes (LPS) including both oxygen-bridged ladder polysilsesquioxanes (LPSQ) and organo-bridged ladder polysiloxanes (OLPS) are very important materials because of their excellent properties1. Adrianov et al. in 1960 attempted to prepare 1, … 相似文献
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FENG Yu-zhong QI Sheng-li LIU Jing-jing WU Zhan-peng YANG Xiao-ping JIN Ri-guang WU De-zhen State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China 《高等学校化学研究》2011,(3):516-519
Soluble and ordered ladder like polyphenylsilsesquioxane was synthesized by a two-step sol-gel method including hydrolysis and polycondensation. The procedure was monitored by Fourier transform infrared spectroscopy and the presence of the ladder like structure was confirmed by X-ray techniques. 29Si NMR analysis shows a very narrow half peak width(δ<4) at δ -78.866 of the main chain unit C6H5SiO3/2 of polyphenylsilsesquioxane, indicating that the polyphenylsilsesquioxane has ordered ladder like structures ... 相似文献
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Eric C.K. Cheung 《Insurance: Mathematics and Economics》2010,46(1):117-126
The structure of various Gerber-Shiu functions in Sparre Andersen models allowing for possible dependence between claim sizes and interclaim times is examined. The penalty function is assumed to depend on some or all of the surplus immediately prior to ruin, the deficit at ruin, the minimum surplus before ruin, and the surplus immediately after the second last claim before ruin. Defective joint and marginal distributions involving these quantities are derived. Many of the properties in the Sparre Andersen model without dependence are seen to hold in the present model as well. A discussion of Lundberg’s fundamental equation and the generalized adjustment coefficient is given, and the connection to a defective renewal equation is considered. The usual Sparre Andersen model without dependence is also discussed, and in particular the case with exponential claim sizes is considered. 相似文献
10.
We study the effect of external potential on transport properties of the fermionic two-leg ladder model. The response of the system to a local perturbation is strongly dependent on the ground state properties of the system and especially on the dominant correlations. We categorize all phases and transitions in the model (for incommensurate filling) and introduce “hopping-driven transitions” that the system undergoes as the inter-chain hopping is increased from zero. We also describe the response of the system to an ionic potential. The physics of this effect is similar to that of the single impurity, except that the ionic potential can affect the bulk properties of the system and in particular induce true long range order. 相似文献