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561.
Radovanovic PV Norberg NS McNally KE Gamelin DR 《Journal of the American Chemical Society》2002,124(51):15192-15193
Methods for introducing new magnetic, optical, electronic, photophysical, or photochemical properties to semiconductor nanocrystals are attracting intense applications-oriented interest. In this communication, we report the preparation and electronic absorption spectroscopy of colloidal ZnO DMS-QDs. Our synthetic procedure involves modification of literature methods known to yield highly crystalline and relatively monodisperse nanocrystals of pure ZnO to allow introduction of transition-metal dopants. We use ligand-field electronic absorption spectroscopy as a dopant-specific optical probe to monitor dopant incorporation during nanocrystal growth and to verify internal substitutional doping in Co2+:ZnO and Ni2+:ZnO DMS-QDs. To the best of our knowledge, these are the first free-standing oxide DMS-QDs reported. The synthesis of colloidal oxide DMS-QDs introduces a new category of magnetic semiconductor materials available for detailed physical study and application in nanotechnology. 相似文献
562.
Dodi K Gerothanassis IP Hadjiliadis N Schreiber A Bau R Butler IS Barrie PJ 《Inorganic chemistry》1996,35(22):6513-6519
The binding sites of Zn(2+), Cd(2+), and Hg(2+) in complexes with 2-(alpha-hydroxybenzyl)thiamine monophosphate chloride, (LH)(+)Cl(-), have been investigated in the solid state [2-(alpha-hydroxybenzyl)thiamin monophosphate chloride monoprotonated at the phosphate group and protonated at N(1)' is denoted as (LH)(+)Cl(-); therefore, the ligand monoprotonated at the phosphate group and deprotonated at N(1)' is L]. Complexes of formulae MLCl(2), M(LH)Cl(3), and (MCl(4))(2)(-)(LH)(2)(+) (M = Zn(2+), Cd(2+), and Hg(2+)) were isolated in aqueous and methanolic solutions, depending on pH. The crystal structure of the complex of formula HgL(2)Cl(2) was solved, together with that of the free ligand (LH)(+)Cl(-), by X-ray crystallography. HgL(2)Cl(2) crystallizes in C2/c, with a = 32.968(6) ?, b = 7.477(2) ?, c = 21.471(4) ?, beta = 118.19(1) degrees, V = 4665(2) ?(3), and Z = 4. (LH)(+)Cl(-) crystallizes in Cc, with a = 10.951(3) ?, b = 17.579(4) ?, c = 13.373(3) ?, beta = 105.36(2) degrees, V = 2482.4(10) ?(3), and Z = 4. Mercury(II) binds to the N(1') of the pyrimidine ring. Both ligands are in the S conformation [Phi(T) = -98.1(9) degrees and Phi(P) = 176.1(10) degrees for HgL(2)Cl(2) and Phi(T) = 104.1(5) degrees and Phi(P) = 171.9(6) degrees for (LH)(+)Cl(-)]. (31)P and (13)C NMR spectra, together with vibrational spectra (IR/Raman), are used to deduce the binding sites of the metal and the protonation states of the ligand at various pH values. It is found that solid-state (31)P NMR spectroscopy is particularly useful in characterizing these complexes as the (31)P shielding tensors are sensitive to the state of the phosphate group. On the other hand, the (31)P NMR spectra indicate that direct bonding between Zn(2+) and Cd(2+) to the phosphate can occur under certain preparation conditions. Solid-state (13)C NMR and vibrational (IR/Raman) spectroscopic results are also in agreement with the other techniques. 相似文献
563.
Brian Brookman Ioannis Papadakis Alan Squirrell Steve Evans Steve Ellison Ulf Örnemark Nick Boley Anita Schmidt Ellen van Berkel Barry Tylee Mike Noble Michael Koch Dan Tholen 《Accreditation and quality assurance》2004,9(10):635-641
A summary of the working group (WG) discussions on proficiency testing (PT) and external quality assessment (EQA) held at the joint EURACHEM/CITAC/EQALM workshop, Bracknell, UK, 16–18 February 2003 is provided. The nine WGs covered a range of issues concerned with current practice and future directions; PT/EQA as a tool for regulators (WG1); PT/EQA as a tool for accreditation (WG2); evaluation of performance and uncertainty (WG3); frequency of PT/EQA participation (WG4); selection of appropriate PT/EQA schemes (WG5); added value of PT/EQA and cost benefit evaluation (WG6); global harmonisation and rationalisation (WG7); new technical areas and challenges in PT/EQA (WG8); and accreditation of PT/EQA providers (WG9). Participants with different backgrounds were on each WG in order to capture a range of views and experience from different sectors. The discussions reflected on the keynote lectures and built, in many cases, on discussions at previous workshops in 2000 and 2002. 相似文献
564.
565.
Robin B. English Raymond J. Haines Nick D. Steen 《Journal of organometallic chemistry》1982,238(3):C34-C36
Reaction of [{Rh(μ-Cl)(CO)2}2] with PPh2H in CO-saturated ethanol yields [Rh3(μ-PPh2)3 (CO)6 (PPh2H)], a red trinuclear cluster of rhodium containing a near-planar six-membered Rh3P3 ring; this compound reversibly undergoes elimination of CO and PPh2H to afford [Rh3(μ-PPh2)3(CO)5]. 相似文献
566.
Takashi Saito Nick A. Hartell Hitoshi Muguruma Shu Hotta Satoshi Sasaki Masao Ito Isao Karube 《Photochemistry and photobiology》1998,68(5):745-748
We have investigated the light dose and time dependency of photodynamic cell membrane damage using electrophysiological methods. This study controls the level of cell membrane damage by precisely administration of the light dose. The photosensitizer used was 5′,5″-bis(aminomethyl)-2,2′:5′,2″-terthiophene dihydrochloride (BAT). A confocal laser scanning microscope was used to provide rapid light activation (<1 s) and the subsequent membrane damage was monitored using standard patch clamp techniques. In the presence of 49 μM BAT, light levels less than 0.94 J/cm2 led to a reversible depolarization (20 mV) and reduction of resistance (10%) within 3 s of illumination. Higher intensities of illumination (1.57 J/cm2) caused a complete and irreversible loss of membrane potential and cell membrane resistance within 8 s of illumination. The threshold dose of light required to induce cell death by illumination in the presence of BAT was increased in the presence of the antioxidant Trolox-C. 相似文献
567.
Polfer NC Paizs B Snoek LC Compagnon I Suhai S Meijer G von Helden G Oomens J 《Journal of the American Chemical Society》2005,127(23):8571-8579
Infrared multiple-photon dissociation spectroscopy is effected on the K(+) tagged aromatic amino acids tyrosine and phenylalanine, as well as the K(+) tagged peptides bradykinin fragment 1-5 and [Leu]-enkephalin. The fingerprint (800-1800 cm(-1)) infrared spectra of these species are compared to density-functional theory (DFT) calculated spectra to determine whether the complex is in the charge solvation (CS) or salt bridge (SB) (i.e. zwitterionic) configuration. For the aromatic amino acids the CS structure is favored and the tridentate N/O/ring structure is found to be the preferred binding geometry for K(+). The experimental and theoretical evidence for bradykinin fragment 1-5 tagged with K(+) suggests that the SB structure is favored; the calculations indicate a head-to-tail looped structure stabilized by a salt bridge between the protonated guanidine group and the deprotonated C-terminus, which allows K(+) to sit in a binding pocket with five C=O electrostatic interactions. For K(+) tagged [Leu]-enkephalin the spectroscopic evidence is not as clear. While the calculations clearly favor a CS structure and the observation of a weak carboxylic acid C=O stretching band in the infrared spectrum matches this finding, the prominence of a band at 1600 cm(-1) renders the analysis more ambiguous, and hence the presence of some salt bridge ions cannot be excluded. Another striking feature in the [Leu]-enkephalin spectrum is the high infrared activity of the tyrosine side-chain modes, which can be clearly identified from comparison to the [Tyr + K](+) experimental spectrum, but which is not reproduced by the DFT calculations. 相似文献
568.
Hawley JC Bampos N Sanders JK 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(21):5211-5222
Most of the porphyrin-recognition chemistry we have investigated previously has centred on kinetically labile metal-ligand interactions, such as Z-N and Ru-N. Our interest in the broader scope of molecular recognition required a metal with the ability to specifically recognise non-nitrogen-based ligands, with a significantly different binding interaction to distinguish it from nitrogen-based analogues. In this report we describe interactions of Sn(IV) porphyrins that bind oxygen-based ligands and for which the Sn(IV)bond;O bond is in slow exchange on the NMR timescale. A series of carboxylate complexes is employed to highlight the structural/geometric features of porphyrin monomers and cyclic oligomers. Where more than one porphyrin unit is present in a molecular scaffold, we report the effect of carboxylate binding on the complex when the two porphyrins contain different metals (typically Sn(IV) and Zn(II)). The unexpected spectroscopic and structural properties of the Sn(2)(9-anthroic acid)porphyrin dimer are also reported. 相似文献
569.
Nick Kozlovich Alexander Puzenko Yuriy Alexandrov Yuri Feldman 《Colloids and surfaces. A, Physicochemical and engineering aspects》1998,140(1-3):299-312
A statistical model of the dielectric polarization of ionic water-in-oil microemulsions is proposed. The model makes it possible to describe the effect of temperature and dispersed phase content on the static dielectric permittivity behavior of the microemulsions at a region far below percolation. With the help of this model, the microemulsions formed with the surfactant, sodium bis(2-ethylhexyl) sulfosuccinate (AOT), have been analyzed. The studied systems are considered to consist of nanometer-sized spherical non-interacting water droplets of equal size with negatively charged head groups
, staying at the interface and positive counterions Na+, distributed in the electrical diffuse double layer of the droplet interior. It can be conjectured that two different mechanisms, that provide an increase of the static dielectric permittivity as a function of temperature, may take place. These may be attributed either to the aggregation of droplets or the temperature growth of polarizability of non-interacting and therefore non-aggregating droplets dispersed in oil. The results support the hypothesis that the experimental temperature behavior of dielectric polarization far below the percolation region is only due to the polarization of a single droplet and not to an aggregation. The droplet polarizability is proportional to the fluctuation mean-square dipole moment of a droplet. It is shown that this mean-square dipole moment and the corresponding value of the dielectric increment, depend upon the equilibrium distribution of counterions within a diffuse double layer. The density distribution of ions is determined by the degree of the dissociation of the ionic surfactant. The dissociation of the ionic surfactant in the system has been analyzed numerically. The relationship between the constant of dissociation and the experimental dielectric permittivity has been ascertained. 相似文献
570.