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61.
Hybrid censoring scheme is a combination of Type‐I and Type‐II censoring schemes. Determination of optimum hybrid censoring scheme is an important practical issue in designing life testing experiments to enhance the information on reliability of the product. In this work, we consider determination of optimum life testing plans under hybrid censoring scheme by minimizing the total cost associated with the experiment. It is shown that the proposed cost function is scale invariant for some selected distributions. Optimum solution cannot be obtained analytically. We propose a method for obtaining the optimum solution and consider Weibull distribution for illustration. We also studied the sensitivity of the optimal solution to the misspecification of parameter values and cost components through a well‐designed sensitivity analysis. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
62.
Manojit Chattopadhyay Subrata Kumar Mitra 《Computational & Mathematical Organization Theory》2017,23(4):451-474
Measuring performance of microfinance institutions (MFIs) is challenging as MFIs must achieve the twin objectives of outreach and sustainability. We propose a new measure to capture the performance of MFIs by placing their twin achievements in a 2 × 2 grid of a classification matrix. To make a dichotomous classification, MFIs that meet both their twin objectives are classified as ‘1’ and MFIs who could not meet their dual objectives simultaneously are designated as ‘0’. Six classifiers are applied to analyze the operating and financial characteristics of MFIs that can offer a predictive modeling solution in achieving their objectives and the results of the classifiers are comprehended using technique for order preference by similarity to ideal solution to identify an appropriate classifier based on ranking of measures of performance. Out of six classifiers applied in the study, kernel lab-support vector machines achieved highest accuracy and lowest classification error rate that discriminates the best achievement of the MFIs’ twin objective. MFIs can use both these steps to identify whether they are on the right path to attaining their multiple objectives from their operating characteristics. 相似文献
63.
In this work, we completely characterize (1) permutation binomials of the form \(x^{{{2^n -1}\over {2^t-1}}+1}+ ax \in \mathbb {F}_{2^n}[x], n = 2^st, a \in \mathbb {F}_{2^{2t}}^{*}\), and (2) permutation trinomials of the form \(x^{2^s+1}+x^{2^{s-1}+1}+\alpha x \in \mathbb {F}_{2^t}[x]\), where s, t are positive integers. The first result, which was our primary motivation, is a consequence of the second result. The second result may be of independent interest. 相似文献
64.
Amit Kumar Trevor Janes Subrata Chakraborty Prosenjit Daw Niklas vonWolff Raanan Carmieli Yael Diskin‐Posner David Milstein 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(11):3411-3415
We report a C?C bond‐forming reaction between benzyl alcohols and alkynes in the presence of a catalytic amount of KOtBu to form α‐alkylated ketones in which the C=O group is located on the side derived from the alcohol. The reaction proceeds under thermal conditions (125 °C) and produces no waste, making the reaction highly atom efficient, environmentally benign, and sustainable. Based on our mechanistic investigations, we propose that the reaction proceeds through radical pathways. 相似文献
65.
Bera Pulakesh Saha Nityananda Kumar Sanjay Banerjee D. Bhattacharya R. 《Transition Metal Chemistry》1999,24(4):425-430
New iron(III) complexes of 5-methyl-3-formylpyrazole thiosemicarbazone (HMPzTS) and 5-methyl-3-formylpyrazole-4-phenylthiosemicarbazone (HMPzPTS), namely [Fe(MPzTS)2]X and [Fe(MPzPTS)2]X respectively, where X=Cl, NO3, SCN and ClO4, have been synthesised and physico-chemically characterised by magnetic measurements (polycrystalline state), electronic, i.r., e.s.r. and Mössbauer spectra. All are cationic complexes containing two monoprotonic tridentate ligands with NNS donor sites and an anionic counterpart; they behave as 1:1 electrolytes in MeOH/DMF. Coordination to central iron(III) via the pyrazolyl nitrogen (2N), the azomethine nitrogen and the thiolato sulphur atom is confirmed in the complexes from i.r. data. E.s.r. data (RT & LNT) reveal the presence of a spin-paired iron(III) cation with d2
xyd2
yzd1
xy configuration. The 57Fe Mössbauer spectral data (RT) are commensurate with the presence of two iron(III) spin states, the percentage of each being dependent upon the counterion of the species. 相似文献
66.
Shubhamoy Chowdhury Arnab Bhattacharya Pinki Saha Smita Majumder E. Suresh 《Journal of Coordination Chemistry》2016,69(24):3664-3676
Employing 1-(2-methoxybenzyl)-2-(2-methoxyphenyl)-1H-benzimidazole (bpb) as a monodentate ligand, a new greenish-blue copper(II) complex, [Cu(bpb)2(NO3)2] (1a), has been synthesized. 1a has been characterized analytically and spectroscopically. The X-ray crystal structure of 1a reveals that it adopts a cis disposition with respect to the ligands. The solid state structure of 1a is stabilized by intramolecular offset face-to-face π–π stacking. Non-covalent supramolecular edge-to-face C–H?π interactions with neighboring molecules give 1-D supramolecular chains that further lead to the formation of an assembled 3-D supramolecular metal-organic framework via hydrogen bonding interactions. 1a shows blue fluorescence most likely due to intramolecular offset face-to-face π–π stacking. At room temperature, 1a is one-electron paramagnetic. It shows a rhombic EPR spectrum with g1 = 2.12, g2 = 2.42, and g3 = 2.52 in the solid state at liquid nitrogen temperature. In cyclic voltammetry, 1a displays a one-electron oxidative Cu(II)/Cu(III) couple. Our DFT calculations, corroborate the observed experimental results of 1a. 相似文献
67.
Anion‐Directed Copper(II) Metallocages,Coordination Chain,and Complex Double Salt: Structures,Magnetic Properties,EPR Spectra,and Density Functional Study 下载免费PDF全文
Prof. Dr. Jing‐Yun Wu Ming‐Shiou Zhong Prof. Dr. Ming‐Hsi Chiang Dr. Dibyendu Bhattacharya Yen‐Wei Lee Prof. Dr. Long‐Li Lai 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(21):7238-7247
A series of CuII metallo‐assemblies showing anion‐directed structural variations, including five metallocages [(Gn?)?{Cu2(Hdpma)4}](8?n)+(A?)8?n (Gn?=NO3?, ClO4?, SiF62?, BF4?, SO42?; A?=NO3?, ClO4?, BF4?, CH3SO4?; Hdpma=bis(3‐pyridylmethyl)ammonium cation), a complex double salt, namely, (H3dpma)4(CuCl4)5Cl2, and a coordination chain, namely, [Cu2(dpma)(OAc)4], are reported. The influence of the anion can be explained by its coordinating ability, the affinity of which for the CuII center interferes significantly with metallocage formation, and its shape, which offers host–guest recognition ability to engage in weak metal–anion coordination and hydrogen bonding to the organic ligand, which are responsible for metallocage templation. EPR studies of these metallocages in the powder phase at room temperature and 77 K showed a trend of the g values (g||>2.10>g⊥>2.00) indicating a ‐based ground state with square‐pyramidal geometry for the CuII centers. The magnetism of these metallocages can be interpreted as the result of a combination of relatively small magnetic coupling integrals and a substantial contribution of temperature‐independent paramagnetism (TIP). The weak magnetic interaction is corroborated by the results of DFT calculations and the EPR spectra. Availability of the low‐lying state for spin population was confirmed by a magnetization study, which revealed a magnetic moment approaching 2Nβ, which would explain the presence of the larger TIP term. 相似文献
68.
We report the first experimental and theoretical study of gas phase excited electronic state decomposition of a furazan based, high nitrogen content energetic material, 3,3'-diamino-4,4'-azoxyfurazan (DAAF), and its model systems, diaminofurazan (DAF) and furazan (C2H2N2O). DAAF has received major attention as an insensitive high energy explosive; however, the mechanism and dynamics of the decomposition of this material are not clear yet. In order to understand the initial decomposition mechanism of DAAF and those of its model systems, nanosecond energy resolved and femtosecond time resolved spectroscopies and complete active space self-consistent field (CASSCF) calculations have been employed to investigate the excited electronic state decomposition of these materials. The NO molecule is observed as an initial decomposition product from DAAF and its model systems at three UV excitation wavelengths (226, 236, and 248 nm) with a pulse duration of 8 ns. Energies of the three excitation wavelengths coincide with the (0-0), (0-1), and (0-2) vibronic bands of the NO A 2Sigma+<--X 2Pi electronic transition, respectively. A unique excitation wavelength independent dissociation channel is observed for DAAF, which generates the NO product with a rotationally cold (20 K) and a vibrationally hot (1265 K) distribution. On the contrary, excitation wavelength dependent dissociation channels are observed for the model systems, which generate the NO product with both rotationally cold and hot distributions depending on the excitation wavelengths. Potential energy surface calculations at the CASSCF level of theory illustrates that two conical intersections between the excited and ground electronic states are involved in two different excitation wavelength dependent dissociation channels for the model systems. Femtosecond pump-probe experiments at 226 nm reveal that the NO molecule is still the main observed decomposition product from the materials of interest and that the formation dynamics of the NO product is faster than 180 fs. Two additional fragments are observed from furazan with mass of 40 amu (C2H2N) and 28 amu (CH2N) employing femtosecond laser ionization. This observation suggests a five-membered heterocyclic furazan ring opening mechanism with rupture of a CN and a NO bond, yielding NO as a major decomposition product. NH2 is not observed as a secondary decomposition product of DAAF and DAF. 相似文献
69.
Xiao-Tao Chen Bishan Zhou Samit K. Bhattacharya Clare E. Gutteridge Thomas R. R. Pettus Samuel J. Danishefsky 《Angewandte Chemie (International ed. in English)》1998,37(6):789-792
An “sp 2 –sp 3 Stille coupling” of the vinyl triflate 1 and the stannyl compound 2 is a key step toward the completion of the total synthesis of eleutherobin, a natural product exhibiting taxol-like cytotoxic activity. 相似文献
70.
Bagkar N Choudhury S Bhattacharya S Yakhmi JV 《The journal of physical chemistry. B》2008,112(20):6467-6472
We report here the synthesis of nickel hexacyanoferrate (NiHCF) crystals using calf thymus DNA (CT-DNA) as a template. The double-stranded CT-DNA has been used as a template to self-assemble NiHCF crystals and to produce aggregates having different morphologies at different temperatures. The guided self-assembly behavior of DNA was studied at different temperatures by scanning electron microscopy. The cube-shaped crystals of NiHCF with an average diameter of 400 nm are observed along the DNA framework at room temperature; however, at higher temperatures, the morphology of NiHCF changed from open tubular to dendrimer. The intermediate temperatures show long chains (up to many micrometers) and spherical structures of NiHCF crystals. The micrometer long DNA template plays a key role in the formation of extended arrays of NiHCF crystals, suggesting that the templating action is retained even at the higher temperatures. 相似文献