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Quantum coherence captures the essential nature of a quantum system[1]and can serve as a resource for quantum information processing[2].Recent studies also provide evidence that long-lived quantum coherence is crucial for overcoming the classical limits of measurement accuracy in quantum metrology[3-5].However,in practice,the unavoidable interaction of a principal system with its surroundings results in decoherence in most situations.Consequently,the advantage of quantum coherence in empowering the performance of quantum tasks will disappear in a very short time interval,which remains one of the major obstacles in its potential application. 相似文献
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CdS sensitized NiO electrode was used as the photoactive cathode in a photoelectrochemical cell for water splitting,avoiding the use of a sacrificial electron donor.Photocurrent increment under visible light irradiation was observed after integration of[Co(dmgH)2(4-Me-py)Cl](1) to the photocathode,suggesting 1 could accept electrons from photoexcited CdS for water reduction and NiO could move the holes in the valence band of CdS to anode for water oxidation. 相似文献
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Reversibly light‐responsive biodegradable poly(carbonate) micelles constructed via CuAAC reaction 下载免费PDF全文
Ding Hu Hua Peng Yile Niu Yefei Li Yingchun Xia Ling Li Jingwen He Xiangyu Liu Xinnian Xia Yanbing Lu Weijian Xu 《Journal of polymer science. Part A, Polymer chemistry》2015,53(6):750-760
Light‐responsive poly(carbonate)s PEG113‐b‐PMPCn‐SP were synthesized via copper catalyzed azide‐alkyne cycloaddition reaction between azide‐modified spiropyran (SP‐N3) and amphiphilic copolymer PEG113‐b‐PMPCn. PEG113‐b‐PMPC25‐SP can self‐assemble to biocompatible micelles with an average diameter of ~96 nm and a critical aggregation concentration of 0.0148 mg mL?1. Under 365 nm UV light irradiation, the characteristic absorption intensity of merocyanine (MC) progressively increased and most of the micellar aggregations were disrupted within 10 min, suggesting the completion of the transformation of hydrophobic SP to hydrophilic MC. Subsequent exposuring the micelles to 620 nm visible light, spherical micelles aggregated again. The light‐controlled release and re‐encapsulation behaviors of coumarin 102‐loaded micelles were further investigated by fluorescence spectroscopy. This study provides a convenient way to construct smart poly(carbonate)s nanocarriers for controlled release and re‐encapsulation of hydrophobic drugs. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 750–760 相似文献
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Emily J. Hopkins Dr. Yurii Prots Dr. Ulrich Burkhardt Dr. Yves Watier Dr. Zhiwei Hu Dr. Chang‐Yang Kuo Dr. Jen‐Che Chiang Dr. Tun‐Wen Pi Dr. Arata Tanaka Prof. Liu Hao Tjeng Dr. Martin Valldor 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(21):7938-7943
Through a solid‐state reaction, a practically phase pure powder of Ba3V2S4O3 was obtained. The crystal structure was confirmed by X‐ray single‐crystal and synchrotron X‐ray powder diffraction (P63, a=10.1620(2), c=5.93212(1) Å). X‐ray absorption spectroscopy, in conjunction with multiplet calculations, clearly describes the vanadium in charge‐disproportionated VIIIS6 and VVSO3 coordinations. The compound is shown to be a strongly correlated Mott insulator, which contradicts previous predictions. Magnetic and specific heat measurements suggest dominant antiferromagnetic spin interactions concomitant with a weak residual ferromagnetic component, and that intrinsic geometric frustration prevents long‐range order from evolving. 相似文献
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Liquid chromatography mass spectrometry simultaneous determination of vindoline and catharanthine in rat plasma and its application to a pharmacokinetic study 下载免费PDF全文
Chongliang Lin Jinzhang Cai Xuezhi Yang Lufeng Hu Guanyang Lin 《Biomedical chromatography : BMC》2015,29(1):97-102
Vinblastine and vincristine, both of which are bisindole alkaloids derived from vindoline and catharanthine, have been used for cancer chemotherapy; their monomeric precursor molecules are vindoline and catharanthine. A simple and selective liquid chromatography mass spectrometry method for simultaneous determination of vindoline and catharanthine in rat plasma was developed. Chromatographic separation was achieved on a C18 (2.1 × 50 mm, 3.5 µm) column with acetonitrile–0.1% formic acid in water as mobile phase with gradient elution. The flow rate was set at 0.4 mL/min. An electrospray ionization source was applied and operated in positive ion mode; selective ion monitoring mode was used for quantification. Mean recoveries were in the range of 87.3–92.6% for vindoline in rat plasma and 88.5–96.5% for catharanthine. Matrix effects for vindoline and catharanthine were measured to be between 95.3 and 104.7%. Coefficients of variation of intra‐day and inter‐day precision were both <15%. The accuracy of the method ranged from 93.8 to 108.1%. The method was successfully applied in a pharmacokinetic study of vindoline and catharanthine in rats. The bioavailability of vindoline and catharanthine were 5.4 and 4.7%, respectively. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献