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1.
Edelsbacher Philipp Redhammer Gnther Monkowius Uwe 《Monatshefte für Chemie / Chemical Monthly》2020,151(4):543-547
Monatshefte für Chemie - Chemical Monthly - Four members of a new series of paddle-wheel copper(II) complexes bearing cyclobutanecarboxylate as bridging ligand with pyridine derived ligands in... 相似文献
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Albrecht H Binder U Harder G Lembke-Koppitz I Philipp A Schmidt-Parzefall W Schröder H Schulz HD Wurth R Donker JP Drescher A Matthiesen U Scheck H Spaan B Spengler J Wegener aD Gabriel JC Schubert KR Stiewe J Waldi R Weseler S Brown NN Edwards KW Frisken WR Fukunaga C Gilkinson DJ Gingrich DM Goddard M Kapitza H Kim PC Kutschke R MacFarlane DB McKenna JA McLean KW Nilsson AW Orr RS Padley P Patel PM Prentice JD Seywerd HC Stacey BJ Yoon T Yun JC Ammar R Coppage D Davis R Kanekal S Kwak N 《Physical review letters》1986,56(6):549-552
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W. Kiridena C. DeKay N. D. Villiere W. W. Koziol C. F. Poole 《Chromatographia》2005,61(11-12):587-593
The solvation parameter model is used to establish the contribution of cohesion, dipole-type and hydrogen-bonding interactions to the retention mechanism on an XTerra MS C18 stationary phase with acetonitrile-water, methanol-water and tetrahydrofuran-water mobile phases containing from 10 to 70% (v/v) organic solvent. Solute size and electron lone pair interactions are responsible for retention while dipole-type and hydrogen-bonding interactions result in lower retention. The volume fraction of water in the mobile phase plays a dominant role in the retention mechanism. However, the change in values of the system constants of the solvation parameter model cannot be explained entirely by assuming the principle role of the organic solvent is to act as a diluent for the mobile phase. Selective solvation of the stationary phase by the organic solvent and the ability of the organic solvent to extract water into the stationary phase, and/or the absorption of water-organic solvent complexes by the stationary phase, are important in accounting for the details revealed about the retention mechanism by the solvation parameter model. A qualitative picture of the above solvent effects, compatible with current knowledge of solvent and stationary phase properties, is presented. 相似文献
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Pablo Wessig Philipp Wettstein Bernd Giese Markus Neuburger Margaretha Zehnder 《Helvetica chimica acta》1994,77(3):829-837
The chiral N-(2-benzoylethyl)-N-tosylglycinamides 1a-c were prepared from the C2-symmetric pyrrolidines 5a-c . Irradiation of these ketones 1a-c gave cis-3-hydroxyprolinamides 10-12 in moderate to good yields (Scheme 3). The de of the photocyclizations depended on the size of the substituents in positions C(2) and C(5) of the chiral pyrrolidine auxiliaries. In addition, the de varied with the reaction temperature, allowing the determination of activation-parameter differences. The structure of products 10-12 were established by NMR and X-ray analyses. 相似文献
9.
Haiss W Raisch P Schiffrin DJ Bitsch L Nichols RJ 《Faraday discussions》2002,(121):167-80; discussion 229-51
In situ FTIR spectroscopy has been used in the attenuated total reflectance (ATR) mode to investigate the surface chemistry of etching Si(100) surfaces in aqueous KOH. The effect of solution concentration and electrode potential on the Si-H vibrations has been explored and the experimental results compared with density functional theory calculations. In addition. the kinetics of surface passivation of n-Si(100) has been investigated using FTIR spectroscopy. 相似文献
10.
The solvation parameter model is used to elucidate the retention mechanism on a perfluorohexylpropylsiloxane-bonded (Fluophase
RP) and octadecylsiloxane-bonded (Betasil C18) stationary phases based on the same silica substrate with acetonitrile–water
and methanol–water mobile phase compositions. Dewetting affects the retention properties of Fluophase RP at mobile phase compositions
containing less than 20% (v/v) acetonitrile or 40% (v/v) methanol. It results in a loss of retention due to an unfavorable change in the phase ratio as well as changes in specific
intermolecular interactions. Steric repulsion reduces retention of bulky solutes on fully solvated Betasil C18 with methanol–water
(but not acetonitrile–water) mobile phase compositions but is not important for Fluophase RP. The retention of weak bases
is affected by ion-exchange interactions on Fluophase RP with acetonitrile–water, and to a lesser extent, methanol-water mobile
phases but these are weak at best for Betasil C18. The system constants of the solvation parameter model and retention factor
scatter plots are used to compare selectivity differences for Fluophase RP, Betasil C18 and a perfluorophenylpropylsiloxane-bonded
silica stationary phase Discovery HS F5 for conditions where incomplete solvation, steric repulsion and ion-exchange do not
significantly contribute to the retention mechanism. Lower retention on Fluophase RP results from weaker dispersion and/or
higher cohesion moderated to different extents by polar interactions since solvated Fluophase RP is a stronger hydrogen-bond
acid and more dipolar/polarizable than Betasil C18. Retention factors for acetonitrile–water mobile phases are highly correlated
for Fluophase RP and Betasil C18 except for compounds with a large excess molar refraction and weak hydrogen-bonding capability.
Selectivity differences are more significant for methanol–water mobile phases. Retention factors on Fluophase RP are strongly
correlated with those on Discovery HSF5 for acetonitrile–water mobile phases while methanol–water mobile phases retention
on Fluophase RP is a poor predictor of the retention order on Discovery HS F5. 相似文献