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961.
Abbott LC Batchelor SN Oakes J Gilbert BC Whitwood AC Lindsay Smith JR Moore JN 《The journal of physical chemistry. A》2005,109(12):2894-2905
The structure and bonding of the azo dye Orange II (Acid Orange 7) in parent and reduced forms have been studied using NMR, infrared, Raman, UV-visible, and electron paramagnetic resonance (EPR) spectroscopy, allied with density functional theory (DFT) calculations on three hydrazone models (no sulfonate, anionic sulfonate, and protonated sulfonate) and one azo model (protonated sulfonate). The calculated structures of the three hydrazone models are similar to each other and that of the model without a sulfonate group (Solvent Yellow 14) closely matches its reported crystal structure. The 1H and 13C NMR resonances of Orange II, assigned directly from 1D and 2D experimental data, indicate that it is present as > or = 95% hydrazone in aqueous solution, and as a ca. 70:30 hydrazone:azo mixture in dimethyl sulfoxide at 300 K. Overall, the experimental data from Orange II are matched well by calculations on the hydrazone model with a protonated sulfonate group; the IR, Raman, and UV-visible spectra of Orange II are assigned to specific vibrational modes and electronic transitions calculated for this model. The EPR spectrum obtained on one-electron reduction of Orange II by the 2-hydroxy-2-propyl radical (*CMe2OH) at pH 4 is attributed to the hydrazyl radical produced on protonation of the radical anion. Calculations on reduced forms of the model dyes support this assignment, with electron spin density on the two nitrogen atoms and the naphthyl ring; in addition, they provide estimates of the structures, vibrational spectra, and electronic transitions of the radicals. 相似文献
962.
David A. Leigh M. ngeles F. Morales Emilio M. Prez Jenny K. Y. Wong Carlos G. Saiz Alexandra M. Z. Slawin Adrian J. Carmichael David M. Haddleton A. Manfred Brouwer Wybren Jan Buma George W. H. Wurpel Salvador Len Francesco Zerbetto 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2005,117(20):3122-3127
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One‐Electron Oxidation of [M(PtBu3)2] (M=Pd,Pt): Isolation of Monomeric [Pd(PtBu3)2]+ and Redox‐Promoted C−H Bond Cyclometalation 下载免费PDF全文
Dr. Thibault Troadec Sze‐yin Tan Dr. Christopher J. Wedge Dr. Jonathan P. Rourke Prof. Dr. Patrick R. Unwin Dr. Adrian B. Chaplin 《Angewandte Chemie (International ed. in English)》2016,55(11):3754-3757
Oxidation of zero‐valent phosphine complexes [M(PtBu3)2] (M=Pd, Pt) has been investigated in 1,2‐difluorobenzene solution using cyclic voltammetry and subsequently using the ferrocenium cation as a chemical redox agent. In the case of palladium, a mononuclear paramagnetic PdI derivative was readily isolated from solution and fully characterized (EPR, X‐ray crystallography). While in situ electrochemical measurements are consistent with initial one‐electron oxidation, the heavier congener undergoes C?H bond cyclometalation and ultimately affords the 14 valence‐electron PtII complex [Pt(κ2PC‐PtBu2CMe2CH2)(PtBu3)]+ with concomitant formation of [Pt(PtBu3)2H]+. 相似文献
965.
R. Nicholas Carmean C. Adrian Figg Troy E. Becker Prof. Brent S. Sumerlin 《Angewandte Chemie (International ed. in English)》2016,55(30):8624-8629
A biphasic one‐pot polymerization method enables the preparation of block copolymers from monomers with similar and competitive reactivities without the addition of external materials. AB diblock copolymers were prepared by encapsulating a frozen solution of monomer B on the bottom of a reaction vessel, while the solution polymerization of monomer A was conducted in a liquid layer above. Physical separation between the solid and liquid phases permitted only homopolymerization of monomer A until heating above the melting point of the lower phase, which released monomer B, allowing the addition of the second block to occur. The triggered release of monomer B allowed for chain extension without additional deoxygenation steps or exogenous monomer addition. A method for the closed (i.e., without addition of external reagents) one‐pot synthesis of block copolymers with conventional glassware using straightforward experimental techniques has thus been developed. 相似文献
966.
David A. Leigh M. ngeles F. Morales Emilio M. Prez Jenny K. Y. Wong Carlos G. Saiz Alexandra M. Z. Slawin Adrian J. Carmichael David M. Haddleton A. Manfred Brouwer Wybren Jan Buma George W. H. Wurpel Salvador Len Francesco Zerbetto 《Angewandte Chemie (International ed. in English)》2005,44(20):2985-2985
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We propose a new technique for processing the heterodyne beat signals obtained in interferometry by sinusoidal modulation of the optical path difference. This technique achieves a high degree of signal stabilization with respect to phase drifts, while removing earlier restrictions imposed on the modulation index. Four Fourier harmonics of the interference signal allow the determination of the current modulation index, and then the coherent component of the intensity can be calculated. The method was tested both numerically and experimentally, and compared to a previous technique that uses the same input data. The effects of phase drifts are canceled on a wide range of the modulation index values, while the reference method achieves the same performance only for particular isolated values. A simplified version of the method is proposed for cases when the signal-to-noise ratio is low.On leave from the National Institute for Laser, Plasma, and Radiation Physics, PO Box MG-36, Bucharest, Romania. 相似文献