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41.
Cheng-Zong Kuo Li-Yun Hsu Yu-Shan Chen Dr. Kenta Goto Dr. Subhendu Maity Dr. Yi-Hung Liu Prof. Shie-Ming Peng Dr. Kien Voon Kong Prof. Teruo Shinmyozu Prof. Jye-Shane Yang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(50):11511-11521
Anthracene–pentiptycene hybrid systems 1-Cn , where n refers to the number of carbon atoms in the linear alkyl chain, crystallize in three different polymorphs, denoted Y (yellow), G (green), and B (blue) forms in terms of the fluorescence color. While all Y-form crystals show the same yellow-to-blue fluorescence color response to the photomechanical stress generated by the anthracene [4+4] photodimerization reaction, the four G forms exhibit distinct photomechanofluorochromism (PMFC): from green to blue for G-1-C4 , to orange for G-1-C7 , to red for G-1-C8 , and to red then blue for G-1-C9 , and the B forms show no photochromic activity. The intriguing RGB three-color PMFC and abnormal topochemical reactivity of G-1-C9 are attributed to inherent softness of the crystal lattice. 相似文献
42.
Tripathy Debajani Chakroborty Subhendu Gadtya Ankita Subhrasmita Mahaling Ram Naresh Moharana Srikanta Barik Arundhati Pal Kaushik 《The European physical journal. E, Soft matter》2023,46(3):1-13
The European Physical Journal E - We discuss the lateral dynamics of two active force dipoles, which interact with each other via hydrodynamic interactions in a thin fluid layer that is active and... 相似文献
43.
Subhendu?Biswas Kamala?Mitra Shyamal?K.?Chattopadhyay Bibhutosh?AdhikaryEmail author C.?Robert.?Lucas 《Transition Metal Chemistry》2005,30(4):393-398
A number of mononuclear manganese(II) and manganese(III) complexes have been synthesized from tridentate N2O aminophenol ligands (HL1–HL5) formed by reduction of corresponding Schiff bases with NaBH4. Three types of tridentate N2O aminophenols have been prepared by reducing with NaBH4which are (a) Schiff bases obtained by bromo salicylaldehyde reaction with N,N-dimethyl/N,N-diethyl ethylene diamine (HL1, HL2), (b) Schiff bases obtained by condensing salicylaldehyde/bromo salicylaldehyde and picolyl amine (HL3, HL4), (c) pyridine-2-aldehyde and 2-aminophenol (HL5). All the manganese complexes have been prepared by direct addition of manganese perchlorate to the corresponding ligands and were characterized by the combination of i.r., u.v.–vis spectroscopy, magnetic moments and electrochemical studies. The u.v.–vis spectra of all of the manganese(III) complexes show two weak d–d transitions in the 630–520 nm region, which support a distorted octahedral geometry. The electron transfer properties of all of the manganese(III) complexes (1–4 and 6) exhibit mostly similar characteristics consisting two redox couples corresponding to the MnIII → MnII reductions and MnIII → MnIV oxidations. The electronic effect on the potential has also been studied by changing different substituents in the ligands. In all cases, an electron-donating group stabilizes the higher oxidation state and electron withdrawing group prefers the lower oxidation state. The cyclic voltammogram of [MnII(L5)2] shows an irreversible oxidation MnII → MnIII at −0.88 V, followed by another quasi-reversible oxidation MnIII → MnIV at +0.48 V. The manganese(III) complex (3) [Mn(L3)2]ClO4has been characterized by X-ray crystallography. 相似文献
44.
Mallick A Haldar B Maiti S Bera SC Chattopadhyay N 《The journal of physical chemistry. B》2005,109(30):14675-14682
Photophysical properties of 3-acetyl-4-oxo-6,7-dihydro-12H-indolo[2,3-a]quinolizine (AODIQ), a bioactive molecule, has been investigated in well-characterized, monodispersed biomimicking nanocavities formed by sodium bis(2-ethylhexyl)sulfosuccinate (AOT) in heptane using steady-state and picosecond time resolved fluorescence and fluorescence anisotropy. The emission behavior of AODIQ is very much dependent upon the water/surfactant mole ratio (W), i.e., on the water pool size of the reverse micellar core. AODIQ exhibits a sharp decrease in fluorescence anisotropy with increasing W, implying that the overall motional restriction experienced by the molecule is decreased with increased hydration. Some of the depth-dependent relevant fluorescence parameters, namely, fluorescence maxima and fluorescence anisotropy (r), have been monitored for exploiting the distribution and microenvironment around the probe in the reverse micelles. Fluorescence spectral position and fluorescence quenching studies suggest that the probe does not penetrate into the reverse micellar core; rather it binds at the interfacial region. Quantitaive estimates of the micropolarity and microviscosity at the binding sites of the probe molecule have been determined as a function of W. 相似文献
45.
46.
Two sets of solutions for a static incoherent charge distribution with spheroidal symmetry are presented. In one set, the charge distribution can be bounded and the charge-to-mass-density ratio is unity everywhere in relativistic units. In the other, the distribution pervades the entire space and the ratio of charge to mass-density also varies at different points.U.G.C. Teacher-fellow, on leave from Physics Department, B.N. Mahavidyalaya, Itachuna, Hooghly, India. 相似文献
47.
Daniel H. Cortes Subhendu K. Datta Osama M. Mukdadi 《International Journal of Solids and Structures》2008,45(18-19):5088-5102
In this work, we study the dispersion of elastic waves in piezoelectric infinite plates with ferroelectric inversion layers. The motivation is to analyze the effect of ferroelectric inversion layers on wave dispersion and resonant behavior under impulsive line loads. A semi-analytical finite-element (SAFE) method has been adopted to analyze the problem. Two model problems are considered for analysis. In one, the plate is composed of a layer of 36° rotated y-cut LiNbO3 with a ferroelectric inversion layer. In the other, material is PZT-4 with a ferroelectric inversion layer. Comparison with experimental results, reported in the literature for isotropic materials, shows a very good agreement with theoretical predictions obtained using SAFE method. Furthermore, comparison of the resonance frequencies of the S1 modes, calculated using KLM approximation (f0 = Cd/2h) and SAFE method, are illustrated for each problem. The frequency spectra of the surface displacements show that resonant peaks occur at frequencies where the group velocity vanishes and the phase velocity remains finite, i.e., a minimum in the dispersion curve below the cut-off frequency. The effect of the ratio of the thicknesses of the inversion layer (IL) and the plate on the frequencies and strength of the resonant peaks is examined. It is observed that for PZT-4 with 50% IL to plate thickness ratio the frequency for the second resonant peak is about twice that for the first one. Results are presented showing the dependence of resonant frequencies on the material properties and anisotropy. Materials selection for single-element harmonic ultrasound transducers is a very important factor for optimum design of transducers with multiple thickness-mode resonant frequencies. The theoretical analysis presented in this study should provide a means for optimum ultrasound transducer design for harmonic imaging in medical applications. 相似文献
48.
An acid-catalyzed modular synthesis of substituted 5H-dibenz[c,e]azepines from a biaryl allylbenzamides prepared from the MBH adducts via a cascade dearoylation and intramolecular cyclization is described. The utility of the product for preparing 7,9-dihydro-4bH-dibenz[c,e]pyrrolo[1,2-a]azepine is also presented. 相似文献
49.
Krishnendu B. Sahu Arindam Maity Shyamal Mondal Rupankar Paira Pritam Saha Subhendu Naskar Abhijit Hazra Sukdeb Banerjee Nirup B. Mondal 《Journal of heterocyclic chemistry》2013,50(Z1):E148-E155
A basic alumina‐supported microwave assisted simple methodology has been developed for the synthesis of aryl‐heteroaryl methanes (benzylated quinolones) via transition metal catalyzed cross‐coupling reaction of halo substituted polynuclear oxa‐aza quinolones with benzyl indium, an organometallic reagent easily derived from commercially available benzyl bromide. 相似文献
50.
Radiation‐assisted controlled grafting and reaction parameter optimization of an industrially important polyolefin elastomer (POE)
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Controlled (low degree) grafting of a polar group to a non‐polar polymer or reverse is an important means to change the polarity of the base polymer, maintaining the properties of the polymer. In the present study, a polar monomer, methacrylic acid (MAA), was grafted onto three different types of “Engages” (a special type of polyolefin elastomer) in aqueous medium by gamma radiation. Grafting parameters (total dose, MAA concentration, and Mohr's salt concentration) were optimized for the desired amount of low‐degree grafting (less than 15 wt%). The grafting yields were measured gravimetrically. Pure and grafted Engages were characterized by Fourier transformed infrared spectroscopy, contact angle measurement, and scanning electron microscope. Fourier transformed infrared spectroscopy spectra confirmed the successful grafting of MAA onto the Engages. For all three, the best yields were found at 3‐kGy gamma radiation dose, 25‐vol% MAA, and 20‐mM Mohr's salt concentration. The grafting efficiencies follow a descending trend like Engage 8150 > Engage 7447 > Engage 8003. From contact angle measurement, it was seen that the hydrophilicities of all Engage surfaces were increased after grafting. Scanning electron microscope illustrated the best distribution of grafted MAA molecules to be on Engage 8150 surface followed by Engage 7447 and Engage 8003, respectively. The tensile testing results suggested that the mechanical properties of the base polymers remained almost unchanged after grafting. Thus, without detrimenting any basic properties, polyolefin elastomers can be grafted to achieve desired yield by an environmental‐friendly method, gamma radiation grafting, in aqueous media. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献