排序方式: 共有30条查询结果,搜索用时 15 毫秒
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Alexopoulos T Allen C Anderson EW Areti H Banerjee S Beery PD Biswas NN Bujak A Carmony DD Carter T Cole P Choi Y De Bonte RJ Erwin AR Findeisen C Goshaw AT Gutay LJ Hirsch AS Hojvat C Kenney VP Lindsey CS LoSecco JM McMahon T McManus AP Morgan N Nelson KS Oh SH Piekarz J Porile NT Reeves D Scharenberg RP Stampke SR Stringfellow BC Thompson MA Turkot F Walker WD Wang CH Wesson DK 《Physical review letters》1990,64(9):991-994
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Lazarus EA Navratil GA Greenfield CM Strait EJ Austin ME Burrell KH Casper TA Baker DR DeBoo JC Doyle EJ Durst R Ferron JR Forest CB Gohil P Groebner RJ Heidbrink WW Hong R Houlberg WA Howald AW Hsieh C Hyatt AW Jackson GL Kim J Lao LL Lasnier CJ Leonard AW Lohr J La Haye RJ Maingi R Miller RL Murakami M Osborne TH Perkins LJ Petty CC Rettig CL Rhodes TL Rice BW Sabbagh SA Schissel DP Scoville JT Snider RT Staebler GM Stallard BW Stambaugh RD St John HE Stockdale RE Taylor PL Thomas DM 《Physical review letters》1996,77(13):2714-2717
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Richard J. M. Egberink Peter L. H. M. Cobben Willem Vverboom Sybolt Harkema David N. Reinhoudt 《Journal of inclusion phenomena and macrocyclic chemistry》1992,12(1-4):151-158
Preparations of the Högberg compounds (Ia–e) with functionalized box-like cavities, designed for complexation of soft cations like silver and copper(II), are described. The structure of1a was determined by X-ray analysis.This paper is dedicated to the memory of the late Dr C. J. Pedersen. 相似文献
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The rate of formation of cyclohexanone oxime from cyclohexanone and hydroxylamine and the rate of the reverse reaction, the hydrolysis of cyclohexanone oxime, were studied in the pH range 1–7. The relative position and the bell shape of the two experimental reaction-rate curves can be fully explained by supplementing the reaction mechanism proposed by Jencks for the oximation only with the reverse reaction, applying the principle of microscopic reversibility. An essential part of this mechanism is the intermediate formation of a 1:1 adduct of cyclohexanone and hydroxylamine. It is concluded that the concentration of this adduct is negligibly small under all the conditions used here. 相似文献
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Extensive new high-temperature, high-resolution FTIR emission spectroscopy measurements for the five common isotopomers of GeO are combined with previous diode laser and microwave measurements in combined isotopomer analyses. New Dunham expansion parameters and an accurate analytical potential energy function are determined for the ground X1Sigma+ state. Copyright 1999 Academic Press. 相似文献
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Metal–Organic Frameworks (MOFs) as Multivalent Materials: Size Control and Surface Functionalization by Monovalent Capping Ligands
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Timon Rijnaarts Raquel Mejia‐Ariza Richard J. M. Egberink Dr. Wies van Roosmalen Prof. Dr. Jurriaan Huskens 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(29):10296-10301
Control over particle size and composition are pivotal to tune the properties of metal organic frameworks (MOFs), for example, for biomedical applications. Particle‐size control and functionalization of MIL‐88A were achieved by using stoichiometric replacement of a small fraction of the divalent fumarate by monovalent capping ligands. A fluorine‐capping ligand was used to quantify the surface coverage of capping ligand at the surface of MIL‐88A. Size control at the nanoscale was achieved by using a monovalent carboxylic acid‐functionalized poly(ethylene glycol) (PEG‐COOH) ligand at different concentrations. Finally, a biotin–carboxylic acid capping ligand was used to functionalize MIL‐88A to bind fluorescently labeled streptavidin as an example towards bioapplications. 相似文献