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41.
Merlin C. E. Bandeira César V. Franco Emilse Martini 《Journal of Solid State Electrochemistry》1999,3(4):210-214
The present study focuses on the electronic and electrochemical features of a copolymer electrochemically grown from pyrrole
and trans-[RuCl2(pmp)4] monomers, where pmp = 3-(pyrrol-1-ylmethyl)pyridine. The results from electrochemical impedance spectroscopy analyses revealed
the redox behavior of the poly{pyrrole-trans-[RuCl2(pmp)4]} compound as well as the non-homogeneous nature of the extremely thin polymeric layers. An equivalent circuit is proposed
for an optimized film produced under the scope of the work.
Received: 4 May 1998 / Accepted: 24 August 1998 相似文献
42.
Bhattacharjee S Dong J Ma Y Hovde S Geiger JH Baker GL Bruening ML 《Langmuir : the ACS journal of surfaces and colloids》2012,28(17):6885-6892
Layer-by-layer polyelectrolyte adsorption is a simple, convenient method for introducing ion-exchange sites in porous membranes. This study demonstrates that adsorption of poly(acrylic acid) (PAA)-containing films at pH 3 rather than pH 5 increases the protein-binding capacity of such polyelectrolyte-modified membranes 3-6-fold. The low adsorption pH generates a high density of -COOH groups that function as either ion-exchange sites or points for covalent immobilization of metal-ion complexes that selectively bind tagged proteins. When functionalized with nitrilotriacetate (NTA)-Ni(2+) complexes, membranes containing PAA/polyethylenimine (PEI)/PAA films bind 93 mg of histidine(6)-tagged (His-tagged) ubiquitin per cm(3) of membrane. Additionally these membranes isolate His-tagged COP9 signalosome complex subunit 8 from cell extracts and show >90% recovery of His-tagged ubiquitin. Although modification with polyelectrolyte films occurs by simply passing polyelectrolyte solutions through the membrane for as little as 5 min, with low-pH deposition the protein binding capacities of such membranes are as high as for membranes modified with polymer brushes and 2-3-fold higher than for commercially available immobilized metal affinity chromatography (IMAC) resins. Moreover, the buffer permeabilities of polyelectrolyte-modified membranes that bind His-tagged protein are ~30% of the corresponding permeabilities of unmodified membranes, so protein capture can occur rapidly with low-pressure drops. Even at a solution linear velocity of 570 cm/h, membranes modified with PAA/PEI/PAA exhibit a lysozyme dynamic binding capacity (capacity at 10% breakthrough) of ~40 mg/cm(3). Preliminary studies suggest that these membranes are stable under depyrogenation conditions (1 M NaOH). 相似文献
43.
C. Colvard R. Fischer T.A. Gant M.V. Klein R. Merlin H. Morkoc A.C. Gossard 《Superlattices and Microstructures》1985,1(1):81-86
Phonon modes in GaAsAlxGa1?xAs superlattices simplify when the phonon wavevector q is perpendicular to the plane of the layers. We have studied such modes using a Raman back-scattering technique on SL's grown by MBE. The results are consistent with simple ideas of LA phonon freedom and LO phonon confinement suggested by one-dimensional lattice dynamical calculations. The longitudinal acoustic (LA) modes show zone folding due to mini-zone formation. Their frequencies occur in doublets linearly dependent on q and show little mini-gap formation. This is consistent with a picture of approximately free plane wave propagating through the interfaces with Raman coupling due to SL layering of the photoelastic coefficient. By contrast, Raman data on LO modes in small period GaAsAlAs SL's suggest that these modes are standing waves strongly confined in either GaAs or AlAs. 相似文献
44.
A recently published model of surface enhanced Raman scattering from adsorbed molecules on semiconductor surfaces is compared to our experimental results for amorphous carbon on PbTe. The model fails to account for the major features of the observed scattering. 相似文献
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Merlin Rosales Jesús A. Durn ngel Gonzlez Ins Pacheco Roberto A. Snchez-Delgado 《Journal of molecular catalysis. A, Chemical》2007,270(1-2):250-256
Cationic rhodium and iridium complexes of the type [M(COD)(PPh3)2]PF6 (M = Rh, 1a; Ir, 1b) are efficient precatalysts for the hydroformylation of 1-hexene to its corresponding aldehydes (heptanal and 2-methylhexanal), under mild pressures (2–5 bar) and temperatures (60 °C for Rh and 100 °C for Ir) in toluene solution; the linear to branched ratio (l/b) of the aldehydes in the hydroformylation reaction varies slightly (between 3.0 and 3.7 for Rh and close to 2 for Ir). Kinetic and mechanistic studies have been carried out using these cationic complexes as catalyst precursors. For both complexes, the reaction proceeds according to the rate law ri = K1K2K3k4[M][olef][H2][CO]/([CO]2 + K1[H2][CO] + K1K2K3[olef][H2]). Both complexes react rapidly with CO to produce the corresponding tricarbonyl species [M(CO)3(PPh3)2]PF6, M = Rh, 2a; Ir, 2b, and with syn-gas to yield [MH2(CO)2(PPh3)2]PF6, M = Rh, 3a; Ir, 3b, which originate by CO dissociation the species [MH2(CO)(PPh3)2]PF6 entering the corresponding catalytic cycle. All the experimental data are consistent with a general mechanism in which the transfer of the hydride to a coordinated olefin promoted by an entering CO molecule is the rate-determining step of the catalytic cycle. 相似文献
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