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31.
Debprasad Patra Poulami Pattanayak Jahar Lal Pratihar Surajit Chattopadhyay 《Polyhedron》2007,26(18):5484-5490
The reactions of HL 1 [where HL is 1N-(2-pyridyl-2-methyl)-2-arylazoaniline and is formulated as ArN = NC6H4N(H)(CH2C5H4N); Ar = C6H5 (for HL1) or p-MeC6H4 (for HL2) or p-ClC6H4 (for HL3)] with K2PtCl4 and Co(ClO4)3 · 6H2O afforded the (L)PtCl and [(L)2Co]ClO4 complexes, respectively. The HL ligands bind the platinum(II) and cobalt(III) centres in a tridentate (N,N,N) fashion, forming new diazoketiminato chelates upon dissociating the amino proton. The X-ray structures of (L3)PtCl and [(L3)2Co]ClO4 were determined. Redox properties of the new complexes have been examined. 相似文献
32.
Chaudhuri RK Freed KF Hose G Piecuch P Kowalski K Włoch M Chattopadhyay S Mukherjee D Rolik Z Szabados A Tóth G Surján PR 《The Journal of chemical physics》2005,122(13):134105
Tests have been made to benchmark and assess the relative accuracies of low-order multireference perturbation theories as compared to coupled cluster (CC) and full configuration interaction (FCI) methods. Test calculations include the ground and some excited states of the Be, H(2), BeH(2), CH(2), and SiH(2) systems. Comparisons with FCI and CC calculations show that in most cases the effective valence shell Hamiltonian (H(v)) method is more accurate than other low-order multireference perturbation theories, although none of the perturbative methods is as accurate as the CC approximations. We also briefly discuss some of the basic differences among the multireference perturbation theories considered in this work. 相似文献
33.
34.
The anisotropy of the magnetic susceptibility of CuO has been measured. In both, the paramagnetic and the antiferromagnetic state the susceptibility can be described to a good approximation by
相似文献
35.
Sumanta Bhattacharya Sandip K. Nayak Subrata Chattopadhyay Manas Banerjee 《Journal of solution chemistry》2006,35(4):485-506
Supramolecular complexes of [60]- and [70]fullerenes with various meso-tetraphenylporphyrins in toluene solutions have been studied by electronic absorption spectroscopy. Charge transfer (CT) absorption bands are observed in the visible region. Vertical ionization potentials (I
D
V) of the meso-tetraphenylporphyrins are reported from a study of EDA interaction of these porphyrins with a number of electron acceptors like o-chloranil, p-chloranil, 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) and vitamin K. The dependence of the CT transition energy on the donor ionization potential has been utilized to estimate the vertical electron affinities (E
A
V) of [60]- and [70]fullerenes in solution. The value of E
A
V for [60]fullerene is found to be 0.10 eV lower in magnitude than that of [70]fullerene. We have extracted degrees of CT, and oscillator and transition dipole strengths of the fullerenes/meso-tetraphenylporphyrins complexes. The experimental results show that the CT complexes studied here have a neutral character in their ground states. Electronic coupling elements have been determined for fullerene/meso-tetraphenylporphyrin complexes. Values of the solvent reorganization energy indicate that the electron transfer process takes place at a faster rate in the case of [70]fullerene/meso-tetraphenylporphyrin complexes. 相似文献
36.
Abstract— Triplet-and singlet-related photoprocesses of pyrene-1-aldehyde (PA) in various solvents have been investigated in detail using 337.1 and 355 nm laser flash photolysis in conjunction with time-correlated determination of fluorescence lifetimes (τ
37.
Mallick A Haldar B Maiti S Chattopadhyay N 《Journal of colloid and interface science》2004,278(1):215-223
Photophysical properties of 3-acetyl-4-oxo-6,7-dihydro-12H indolo-[2,3-a] quinolizine (AODIQ) have been studied in different aqueous micellar environments using steady-state and time-resolved emission spectroscopy. The charge transfer (CT) fluorescence exhibits appreciable hypsochromic shift, along with an enhancement in the fluorescence intensity in all the micellar media. This is associated with an increase in the fluorescence anisotropy (r), which suggests that the fluorophore molecule experiences motionally restricted environments upon binding with the micelles. Fluorescence spectral position and fluorescence quenching studies suggest that the fluorescing moiety does not penetrate into the core of the micellar units; rather it binds at the micelle-water interfacial region. The binding constant and free energy change during probe-micelle binding have been evaluated from relevant fluorescence data. Light has been thrown on the mode of action of urea on micelle bound probes. The results are interpreted in terms of the model that urea displaces water molecules from the micellar interface and the consequent destabilization leads to the expulsion of the probe molecules from the interfacial region. Polarity and viscosity of the microenvironments around the probe have been determined in the micellar systems. 相似文献
38.
An extremely short synthesis of 2,2-dimethyl-3-hydroxymethyl cyclopentanone 2 (R1 = R2 = Me), an advanced intermediate in the synthesis of the pheromone planococcyl acetate 3, is described. 相似文献
39.
JPC – Journal of Planar Chromatography – Modern TLC - The four new spray reagents (Benzoic acid and some of its parahaloderivatives) have been introduced. These reagents enable... 相似文献
40.
Tanay Chattopadhyay Cláudia Reis Paulo André António Teixeira 《Optics Communications》2012,285(9):2266-2275
A novel scheme for an all-optical clocked D flip-flop, with very low complexity, is proposed and numerically demonstrated. This new flip-flop configuration is based on a semiconductor optical amplifier — Mach–Zehnder interferometer (SOA-MZI), with a feedback loop, and presents two stable states determined by the phase shift between the two MZI arms. 相似文献
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