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Shahan Zeb Khan Muhammad Kashif Amir Imdad Ullah Asma Aamir John M. Pezzuto Tamara Kondratyuk Francine Bélanger‐Gariepy Akbar Ali Sajid Khan Zia‐ur‐Rehman 《应用有机金属化学》2016,30(6):392-398
Two new heteroleptic palladium(II) complexes have been synthesized by reacting equimolar quantities of palladium(II) chloride, sodium 4‐(2‐methoxyphenyl)piperazine‐1‐carbodithioate and diphenyl‐p‐tolylphosphine ( 1 ) or tri‐p‐tolylphosphine ( 2 ). Complexes 1 and 2 have been characterized using elemental analysis, Fourier transform infrared spectroscopy, multinuclear NMR (1H, 13C and 31P) spectroscopy and single‐crystal X‐ray analysis. The latter technique confirms a pseudo square‐planar geometry in which two adjacent positions are occupied by bidentate dithiocarbamate while chloro and substituted triphenylphosphine are present at the remaining two positions. The anticancer activity of both complexes against five different cancer cell lines (LU – human lung carcinoma, established at UIC, Department of Surgical Oncology; MCF7 – human breast adenocarcinoma, ATCC number HTB‐22?; MDA‐MB‐231 – human breast adenocarcinoma, ATCC number HTB‐26?; Hepa‐1c1c7 – mouse liver hepatoma, ATCC number CRL‐2026?; PC‐3 – human prostate adenocarcinoma, ATCC number CRL‐1435?) was determined by MTT assay, revealing 2 has higher activity than 1 . A drug–calf thymus DNA binding study with UV–visible spectroscopy reveals a higher DNA binding affinity of 2 (3.511 × 104 M?1) than 1 (4.213 × 103 M?1). Density functional theory studies confirm the relatively more stable nature of 2 than 1 . Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
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Dr. Ji-Rong Huang Dr. Muhammad Sohail Dr. Tohru Taniguchi Prof. Dr. Kenji Monde Prof. Dr. Fujie Tanaka 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(21):5947-5951
Spiro[4,5]decanes and polycyclic compounds bearing spiro[4,5]decane systems are important biofunctional molecules. Described are diastereoselective formal (4+1) cycloaddition reactions to afford oxindole-functionalized spiro[4,5]decanes and organocatalytic enantioselective Michael–Henry cascade reactions of the (4+1) cycloaddition products to generate spirooxindole polycyclic derivatives bearing the spiro[4,5]decane system. Spiro[4,5]decanes bearing oxindoles containing three stereogenic centers and spirooxindole polycycles having seven stereogenic centers, including two all-carbon chiral quaternary centers and one tetrasubstituted chiral carbon center, were obtained with high diastereo- and enantioselectivities. 相似文献
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We propose a new scheme for the coherent control of birefringent light pulses propagation in a four-level atomic medium. We modify the splitting of a light pulse by controlling the electric and magnetic responses. The Doppler broadening effect is also noted on the propagation of the birefringent pulses. The dispersions of the birefringence beams are oppositely manipulated for delay and advancement of time at a Doppler width of 10γ. A time gap is created between the birefringence beams, which protects from hacking of information. The time gap is then closed to restore the pulse into the original form by a reverse manipulation of the dispersion of the birefringence beams, i.e., introducing another medium whose transfer function is the complex conjugate of that of the original medium. The results are useful for secure communication technology. 相似文献
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