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1.
Yutaka Morita Manfred Hesse Hans Schmid Avijit Banerji Julie Banerji Asima Chatterjee Willi E. Oberhnsli 《Helvetica chimica acta》1977,60(4):1419-1434
Alstonia scholaris: The structure of the indole alkaloid nareline Besides the known akuammidine, picralinal, picrinine and pseudoakuammigine a new indole alkaloid called nareline (M=352) was isolated from Alstonia scholaris R. BR. , which belongs to the plant family of Apocynaceae. Its structure 2 was deduced by single crystal X-ray diffraction. 2 represents the absolute configuration. The spectroscopic data of 2 and its derivatives (Scheme 1) as well as their chemical behavior support this structure. In biogenetic sense nareline is related to the bases akuammiline ( 4 ) and picraline ( 5 ) (Scheme 2). In contrast to those the C-atom 5 is exocyclic and represents an aldehyde group which forms together with the oxygen atom of the N (4)-hydroxylamine group a cyclic half acetale. - By oxidation (CrO3/CH3COOH) of 2 the oxindol derivative 19 (oxonareline) is formed which contains a cyclic acetal as a partial structure element (Scheme 4). 相似文献
2.
Shyamaprosad Goswami Abhishek Manna Sima Paul Avijit K. Das Prasanta K. Nandi Anup Kumar Maity Partha Saha 《Tetrahedron letters》2014
5(Benzothiazol-2-yl)-4-hydroxyisophthalaldehyde (BHI), an intense ESIPT containing molecule in mixed media loses its properties due to resonance-assisted H-bond (RAHB) in absolute water. Due to resonance-assisted H-bond the o-aldehyde is more reactive than the other one. With addition of cysteine/homocysteine into this solution the o-aldehyde group gets transformed into thiazolidine/thiazine ring, respectively, and the phenolic proton becomes free enough for transfer to nitrogen of the benzothiazole ring in excited state, that is, the ESIPT of BHI is turned on. Thus we can detect cysteine/homocysteine in water as well as in live cells. 相似文献
3.
Monte Carlo simulation is a very powerful tool for simulation of transient and steady state crystal size distribution (CSD) in a continuous crystallizer under stochastic dispersion effects. In the present work, transient CSD in a continuous crystallizer has been reported when shape factor and growth rate dispersions conform to normal distribution. For the steady state run, the algorithm reported by Sen Gupta and Dutta elsewhere has been used to validate the results obtained in the present work when the steady state is reached. 相似文献
4.
Saha A Mukherjee AK 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2004,60(8-9):1731-1737
The formation of charge transfer (CT) complexes of 4-acetamidophenol (commonly called 'paracetamol') and a series of quinones (including Vitamin K3) has been studied spectrophotometrically in ethanol medium. The vertical ionisation potential of paracetamol and the degrees of charge transfer of the complexes in their ground state has been estimated from the trends in the charge transfer bands. The oscillator and transition dipole strengths of the complexes have been determined from the CT absorption spectra at 298 K. The complexes have been found by Job's method of continuous variation to have the uncommon 2:1 (paracetamol:quinone) stoichiometry in each case. The enthalpies and entropies of formation of the complexes have been obtained by determining their formation constants at five different temperatures. 相似文献
5.
Fix a smooth very ample curve C on a K3 or abelian surface X. Let $ \mathcal{M} $ denote the
moduli space of pairs of the form (F, s), where F is a stable sheaf over X whose Hilbert polynomial
coincides with that of the direct image, by the inclusion map of C in X, of a line bundle of degree d
over C, and s is a nonzero section of F. Assume d to be sufficiently large such that F has a nonzero
section. The pullback of the Mukai symplectic form on moduli spaces of stable sheaves over X is
a holomorphic 2-form on $ \mathcal{M} $. On the other hand, $ \mathcal{M} $ has a map to a Hilbert scheme parametrizing
0-dimensional subschemes of X that sends (F, s) to the divisor, defined by s, on the curve defined
by the support of F. We prove that the above 2-form on $ \mathcal{M} $ coincides with the pullback of the
symplectic form on the Hilbert scheme. 相似文献
6.
A series of unexpected cycloadducts along with normal cycloadducts have been isolated from the 1,3-dipolar cycloaddition of 3,4-dehydromorpholine N-oxide to piperidides of cinnamic acid and para-substituted cinnamic acids and these were analyzed by X-ray crystallography to reveal novel solid-state structures. At first, 1:1 cycloadducts were formed which underwent in situ nucleophilic attack by another reduced nitrone moiety. A plausible iminium-oxonium ion mechanism has been proposed. 相似文献
7.
8.
Unitary group adapted state specific multireference perturbation theory: Formulation and pilot applications
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Avijit Sen Sangita Sen Pradipta Kumar Samanta Debashis Mukherjee 《Journal of computational chemistry》2015,36(9):670-688
We present here a comprehensive account of the formulation and pilot applications of the second‐order perturbative analogue of the recently proposed unitary group adapted state‐specific multireference coupled cluster theory (UGA‐SSMRCC), which we call as the UGA‐SSMRPT2. We also discuss the essential similarities and differences between the UGA‐SSMRPT2 and the allied SA‐SSMRPT2. Our theory, like its parent UGA‐SSMRCC formalism, is size‐extensive. However, because of the noninvariance of the theory with respect to the transformation among the active orbitals, it requires the use of localized orbitals to ensure size‐consistency. We have demonstrated the performance of the formalism with a set of pilot applications, exploring (a) the accuracy of the potential energy surface (PES) of a set of small prototypical difficult molecules in their various low‐lying states, using natural, pseudocanonical and localized orbitals and compared the respective nonparallelity errors (NPE) and the mean average deviations (MAD) vis‐a‐vis the full CI results with the same basis; (b) the efficacy of localized active orbitals to ensure and demonstrate manifest size‐consistency with respect to fragmentation. We found that natural orbitals lead to the best overall PES, as evidenced by the NPE and MAD values. The MRMP2 results for individual states and of the MCQDPT2 for multiple states displaying avoided curve crossings are uniformly poorer as compared with the UGA‐SSMRPT2 results. The striking aspect of the size‐consistency check is the complete insensitivity of the sum of fragment energies with given fragment spin‐multiplicities, which are obtained as the asymptotic limit of super‐molecules with different coupled spins. © 2015 Wiley Periodicals, Inc. 相似文献
9.
Avijit Ghosh Prof. Mangalampalli Ravikanth 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(20):6386-6396
The synthesis, spectroscopic, and electrochemical properties of seven new PV–meso‐triarylcorroles ( 1 – 7 ) are reported. Compounds 1 – 7 were prepared by heating the corresponding free‐base corroles with POCl3 at reflux in pyridine. Hexacoordinate PV complexes of meso‐triarylcorroles were isolated that contained two axial hydroxy groups, unlike the PV complex of 8,12‐diethyl‐2,3,7,13,17,18‐hexamethylcorrole, which was pentacoordinate, or the PV complex of meso‐tetraphenylporphyrin, which was hexacoordinate with two axial chloro groups. 1H and 31P NMR spectroscopy in CDCl3 indicated that the hexacoordinated PV–meso‐triarylcorroles were prone to axial‐ligand dissociation to form pentacoordinated PV–meso‐triarylcorroles. However, in the presence of strongly coordinating solvents, such as CH3OH, THF, and DMSO, the PV–meso‐triarylcorroles preferred to exist in a hexacoordinated geometry in which the corresponding solvent molecules acted as axial ligands. X‐ray diffraction of two complexes confirmed the hexacoordination environment for PV–meso‐triarylcorroles. Their absorption spectra in two coordinating solvents revealed that PV–meso‐triarylcorroles showed a strong band at about 600 nm together with other bands, in contrast to PV–porphyrins, which showed weak bands in the visible region. These compounds were easier to oxidize and more difficult to reduce compared to PV–porphyrins. These compounds were brightly fluorescent, unlike the weakly fluorescent PV–porphyrins, and the quantum yields for selected PV–corroles were as high as AlIII and GaIII corroles, which are the best known fluorescent compounds among oligopyrrolic macrocycles. 相似文献
10.
Shyamaprosad Goswami Avijit Kumar Adak Subrata Jana John F. Gallagher 《Tetrahedron》2005,61(17):4289-4295
A series of symmetrical diamido biaryls has been synthesized in good yield by direct homocoupling of iodoarylbenzamides by palladium-catalysis. No cross product has been isolated from the reaction mixture of two different iodoarylbenzamides under similar conditions. However, only in the case of 2-iodo-N-phenylbenzamide, the intramolecularly coupled product phenanthridone has been isolated as a minor product along with the major intermolecularly coupled product. Biphenyl chiral diamides have been synthesized by this coupling method. This coupling reaction also works well with the reductive dimerization of functionalized heterocyclic compounds. Thus 6,6′-dipivaloylamino-3,3′-bipyridine and 6,6′-dimethyl-2,2′-bipyridine have been efficiently synthesized. In two cases, the X-ray crystal structures have been solved to establish the structures of symmetrical and chiral diamido biaryls and their supramolecular networks. 相似文献