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151.
本文设计合成了两亲性Eu(Ⅲ)配合物(Eu L^3+)、两亲性香豆素衍生物(CA)以及荧光素修饰的透明质酸(HA-FA).Eu L^3+和CA可在水中共组装形成带正电荷的囊泡型荧光纳米界面(Eu L^3+/CA).HA-FA可通过静电引力络合在Eu L^3+/CA表面,促使CA与FA之间发生有效的荧光共振能量转移,体系的荧光发射以荧光素的绿色荧光为主.当肿瘤细胞标识物CD44蛋白与络合在囊泡表面上的透明质酸发生特异相互作用后,降低了CA与FA之间的能量转移效率,体系的荧光发射从绿色转变为蓝色.据此,实现了对CD44的高灵敏检测(DL=1.79×10^-7g/m L),而所测试的氨基酸、蛋白质等生物分子几乎不对荧光纳米界面的荧光性质产生影响.基于此,我们成功地将Eu L^3+/CA/HA-FA用于人乳腺癌细胞MCF-7和MDA-MB-231悬浮液中CD44蛋白的高效检测,该工作为构建新型CD44蛋白荧光探针提供了思路,为癌症早期诊断和治疗奠定了基础. 相似文献
152.
G Mukherjee P Singh C Ganguri S Sharma HB Singh N Goel UP Singh RJ Butcher 《Inorganic chemistry》2012,51(15):8128-8140
The synthesis and characterization of the complexes of Cu(I), Ag(I), Cu(II), and Co(II) ions with 1,2,5-selenadiazolopyridine (psd) is reported. The following complexes have been prepared: [Cu(2)(psd)(3)(CH(3)CN)(2)](2+)2(PF(6)(-)); [(CuCl)(2)(psd)(3)]; [Cu(2)(psd)(6)](2+)2(ClO(4))(-); [Ag(2)(psd)(2)](2+)2(NO(3))(-); [Ag(2)(psd)(2)](2+)2(CF(3)COO)(-); [Cu(psd)(2)(H(2)O)(3)](2+)2(ClO(4))(-)·(psd)(2); [Cu(psd)(4)(H(2)O)](2+)2(ClO(4))(-)·(CHCl(3)); [Cu(psd)(2)(H(2)O)(3)](2+)2(NO(3))(-)·(H(2)O)·(psd)(2), and [Co(psd)(2)(H(2)O)(4)](2+)2(ClO(4))(-)·(psd)(2). The electronic structure of ligand psd, in particular the bond order of Se-N bonds, has been probed by X-ray diffraction, (77)Se NMR, and computational studies. A detailed analysis of the crystal structures of the ligand and the complexes revealed interesting supramolecular assembly. The assembly was further facilitated by the presence of neutral ligands for some complexes (Cu(II) and Co(II)). The molecular structure of the ligand showed that it was present as a dimer in the solid state where the monomers were linked by strong secondary bonding Se···N interactions. The crystal structures of Cu(I) and Ag(I) complexes revealed the dinuclear nature with characteristic metallophilic interactions [M···M] (M = Cu, Ag), while the Cu(II) and Co(II) complexes were mononuclear. The presence of M···M interactions has been further probed by Atoms in Molecules (AIM) calculations. The paramagnetic Cu(II) and Co(II) complexes have been characterized by UV-vis, ESI spectroscopy, and room temperature magnetic measurements. 相似文献
153.
U. Pandey A. Mukherjee G. Samuel S. Banerjee H. D. Sarma M. Venkatesh 《Journal of Radioanalytical and Nuclear Chemistry》2008,275(2):243-246
Lanreotide, a somatostatin analogue, was radioiodinated with 125I to explore the possibility of using 123I labeled lanreotide as a diagnostic radiopharmaceutical for tumors overexpressing somatostatin (SST) receptors. Radioiodination
was carried out with 125I using chloramine T as the oxidant. The labeling yield was >90%. Characterization of 125I-Lanreotide was carried out by paper electrophoresis as well as HPLC. 125I-Lanreotide was purified by chromatography using a C18 Sep-Pak column. Radiochemical purity of the purified 125I-Lanreotide thus obtained was >99%. Significant tumor uptake of 125I-Lanreotide was observed in C57BL/6 mice bearing melanoma. 相似文献
154.
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156.
Vibha Mishra Rabindranath Mukherjee Jorge Linares Epiphane Codjovi Fran?ois Varret Max Lawson-Daku 《Hyperfine Interactions》2009,188(1-3):71-78
The spin-transition (1A1?5T2) behaviour of a new mononuclear iron(II) compound [FeII(L)3][PF6]2[L = 2-[3-(2′-pyridyl)pyrazole-1-ylmethyl]pyridine] has been investigated by 57Fe Mössbauer spectroscopy. Analysis of the Mössbauer spectra revealed low value of the quadrupole splitting of the high-spin state which reflects iron(II) to be in nearly cubic lattice site. Mössbauer spectra under light show the light-induced excited spin state trapping effect and the observed quadrupole splitting of the metastable high-spin state is found little sensitive to the high-spin fraction value. DFT calculations are in progress to document the almost cubic nature of the ligand-field acting on the iron atom. 相似文献
157.
Kousik Mukherjee Ajit Kumar Meikap Dharmadas Kumbhakar 《Optical and Quantum Electronics》2012,43(6-10):101-107
A method of all optical frequency encoded single bit memory unit is proposed and described using difference frequency generation only in non linear materials. The unit can store a single bit in frequency encoded format and thus maintains the same state when input is withdrawn. To change the state of the information of the memory unit the input should be changed. The proposed memory unit employs difference frequency generation for its operation and is very fast, the speed of operation is limited by the difference frequency generation process. 相似文献
158.
R. Khare P.K. Shukla G.K. Mishra C. Mukherjee S. Talwar V.K. Dubey P. Saxena J.K. Mittal 《Optics Communications》2009,282(19):3850-3853
We present an analytical and experimental study of a novel confocal optical pulse stretcher (COPS). The simple and passive pulse stretcher consists of two concave mirrors and a scraper beam-splitter and its optical configuration ensures a perfect spatial overlapping of laser pulses at the beam-splitter. The pulse stretcher is compact and suitable for laser pulses of large divergences. The confocal optical pulse stretcher is demonstrated on a pulsed copper vapour laser to convert a 40 ns (1/e2 % points) pulse into a 55 ns with reduction of peak power by a factor of 1.375 without loss of pulse energy. 相似文献
159.
Asymmetric,Three‐Component,One‐Pot Synthesis of Spiropyrazolones and 2,5‐Chromenediones from Aldol Condensation/NHC‐Catalyzed Annulation Reactions
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Dr. Lei Wang Sun Li Dr. Pankaj Chauhan Dr. Daniel Hack Arne R. Philipps Dr. Rakesh Puttreddy Prof. Dr. Kari Rissanen Prof. Dr. Gerhard Raabe Prof. Dr. Dieter Enders 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(15):5123-5127
A novel one‐pot, three‐component diastereo‐ and enantioselective synthesis of spiropyrazolones has been developed involving the aldol condensation of an enal to generate α,β‐unsaturated pyrazolones, which react with a second equivalent of enal through an N‐heterocyclic carbene (NHC)‐catalyzed [3+2] annulation. The desired spirocyclopentane pyrazolones are obtained in moderate to good yields and good to excellent stereoselectivities. Alternatively, starting from cyclic 1,3‐diketones, 2,5‐chromenediones are available through [2+4] annulation. 相似文献
160.
M. Mukherjee D. Beck K. Blaum G. Bollen J. Dilling S. George F. Herfurth A. Herlert A. Kellerbauer H. -J. Kluge S. Schwarz L. Schweikhard C. Yazidjian 《The European Physical Journal A - Hadrons and Nuclei》2008,35(1):1-29
ISOLTRAP is a Penning trap mass spectrometer for high-precision mass measurements on short-lived nuclides installed at the
on-line isotope separator ISOLDE at CERN. The masses of close to 300 radionuclides have been determined up to now. The applicability
of Penning trap mass spectrometry to mass measurements of exotic nuclei has been extended considerably at ISOLTRAP by improving
and developing this double Penning trap mass spectrometer over the past two decades. The accurate determination of nuclear
binding energies far from stability includes nuclei that are produced at rates less than 100 ions/s and with half-lives well
below 100ms. The mass-resolving power reaches 107 corresponding to 10keV for medium heavy nuclei and the uncertainty of the resulting mass values has been pushed down to below
10-8. The article describes technical developments achieved since 1996 and the present performance of ISOLTRAP. 相似文献